5322 NP_001070868 L561I not found in SNVbox database
6800 NP_109597 R262Q not found in SNVbox database
7173 NP_001070868 R689W not found in SNVbox database
8521 NP_705833 L468R not found in SNVbox database
476 NP_705833 G569V not found in SNVbox database
1305 NP_001070868 K621E not found in SNVbox database
1713 NP_001070868 D603E not found in SNVbox database
2180 NP_001070868 D304N not found in SNVbox database
3500 NP_001070868 T624S not found in SNVbox database
4469 NP_001070868 R640H not found in SNVbox database
4484 NP_705833 L38F not found in SNVbox database
4558 NP_001070868 G663R not found in SNVbox database
4659 NP_705833 E56K not found in SNVbox database
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:58864528 G>A maps to NM_130786.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr19:58861778 G>A maps to NM_130786.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:52610432 G>A maps to NM_001198819.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:52580382 G>A maps to NM_138932.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:52580382 G>A maps to NM_138932.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:52575868 G>T maps to NM_138932.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:52566611 G>T maps to NM_138932.2 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr16:7760695 A>G maps to NM_145891.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr16:7568384 C>T maps to NM_145891.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr16:7726831 C>A maps to NM_145891.2 Y350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr16:7383010 G>A maps to NM_145891.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:7743331 C>T maps to NM_145893.2 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:9262475 G>T maps to NM_000014.4 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:9229939 A>G did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:9230365 C>T maps to NM_000014.4 W1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:9246170 T>C maps to NM_000014.4 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:9264793 A>G maps to NM_000014.4 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:9264787 G>A maps to NM_000014.4 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:9260158 A>G maps to NM_000014.4 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:9258855 T>C maps to NM_000014.4 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:9242596 G>A maps to NM_000014.4 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr12:9260176 G>A maps to NM_000014.4 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr12:9013552 T>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:8976342 G>T maps to NM_144670.3 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr12:8990975 C>A maps to NM_144670.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:8976419 G>A maps to NM_144670.3 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:9009772 C>A maps to NM_144670.3 G954G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:8975954 C>A maps to NM_144670.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:8988857 G>A maps to NM_144670.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:9004867 C>A maps to NM_144670.3 T842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr12:8991766 C>A maps to NM_144670.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:9016513 C>T maps to NM_144670.3 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:8975301 G>T maps to NM_144670.3 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr12:9004511 G>A maps to NM_144670.3 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr12:9020911 A>G maps to NM_144670.3 Q1340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:8995917 C>A maps to NM_144670.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr22:43089432 G>A maps to NM_017436.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr22:43089135 G>A maps to NM_017436.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:43088985 C>T maps to NM_017436.4 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr22:43089399 G>A maps to NM_017436.4 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:53714425 A>G maps to NM_015665.5 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:125558512 T>C maps to NM_023928.3 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:12726292 G>A maps to NM_001013630.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:170988515 G>A maps to ENST00000509167 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:67501868 G>T maps to NM_024666.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:67524223 C>A maps to NM_024666.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:69746145 C>T maps to NM_014911.3 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:69736571 T>C maps to NM_014911.3 Q599Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr2:69752181 C>T maps to NM_014911.3 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:219131180 G>A maps to ENST00000444053 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:74465821 C>T maps to NM_001166579.1 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:70288538 G>A maps to ENST00000418685 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr16:70287896 C>T maps to ENST00000418685 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:70288538 G>A maps to ENST00000418685 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:70305733 G>A maps to ENST00000418685 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:44275059 G>A maps to NM_020745.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:44270903 T>C maps to NM_020745.2 P718P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3555-01A-01W-0831-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:44272836 G>A maps to NM_020745.2 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:44271021 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr6:44272507 G>A maps to NM_020745.2 D542D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CM-6162-01A-11D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:41106924 A>G maps to NM_001136042.2 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:57219750 C>T maps to NM_181806.2 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:57215675 C>T maps to NM_181806.2 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:57219642 C>T maps to NM_181806.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:57216119 A>G maps to NM_181806.2 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:57209808 G>T maps to NM_181806.2 V898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:57208998 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:57204783 G>A maps to NM_181806.2 F1027F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr7:121755212 G>A maps to NM_005763.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:121756950 C>A maps to NM_005763.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:121721592 C>T maps to NM_005763.3 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:121758661 T>C maps to NM_005763.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:121718952 A>G maps to NM_005763.3 D816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:35307577 A>G maps to NM_012138.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:35343935 T>C maps to NM_012138.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr17:35310579 C>T maps to NM_012138.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:79094540 G>T maps to NM_001080395.2 S1065S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:79098552 C>T maps to NM_001080395.2 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr17:79100321 C>A maps to NM_001080395.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:79094324 G>A maps to NM_001080395.2 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:8873400 C>T maps to NM_001127448.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr9:107602686 G>A maps to NM_005502.3 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr9:107620892 T>C maps to NM_005502.3 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr9:107571799 G>A maps to NM_005502.3 A1407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:107593985 G>A maps to NM_005502.3 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr9:107593312 G>A maps to NM_005502.3 Y595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:107566929 C>T maps to NM_005502.3 T1512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:107555525 G>A maps to NM_005502.3 F1854F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:107562119 C>T maps to NM_005502.3 Q1641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:107571778 G>A maps to NM_005502.3 F1414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:107593904 A>G maps to NM_005502.3 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:107555516 G>A maps to NM_005502.3 A1857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:107584853 A>G maps to NM_005502.3 D917D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr9:107560699 A>G did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:67148194 A>C maps to NM_080282.3 A1462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:67187392 A>G maps to NM_080282.3 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:67183904 T>C maps to NM_080282.3 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:67197726 G>T maps to NM_080282.3 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr17:67178329 C>T maps to NM_080282.3 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:67181743 C>A maps to NM_080282.3 E791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr17:67183847 C>T maps to NM_080282.3 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:215843526 C>T did not map to a codon.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr2:215884379 C>T maps to NM_173076.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:215914495 C>A maps to NM_173076.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:215876262 G>T maps to NM_173076.2 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:215818729 G>A maps to NM_173076.2 V2165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:215914347 A>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:215821481 T>C maps to NM_173076.2 V2046V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr2:215848423 A>G maps to NM_173076.2 G1443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:215868933 G>T maps to NM_173076.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr2:215845344 C>T maps to NM_173076.2 T1534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:215840683 T>G maps to NM_173076.2 R1736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:215890459 A>C maps to NM_173076.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:215797435 C>T maps to NM_173076.2 K2570K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:215809801 C>T maps to NM_173076.2 P2422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr2:215914347 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:215866461 C>A did not map to a codon.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:215845317 C>T maps to NM_173076.2 L1543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:215802331 G>A maps to NM_173076.2 R2482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:215868931 C>T did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr2:215798885 G>A maps to NM_173076.2 V2532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:215880275 G>A maps to NM_173076.2 Q632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:48285545 T>C maps to NM_152701.3 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:48375071 G>A maps to NM_152701.3 L3351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:48259006 T>A maps to NM_152701.3 L115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:48494820 C>A maps to NM_152701.3 T4251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:48352728 C>T maps to NM_152701.3 S3194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr7:48528918 T>C maps to NM_152701.3 P4423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:48416146 G>A maps to NM_152701.3 W3771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:48315689 G>T maps to NM_152701.3 E2143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:48313214 G>T maps to NM_152701.3 E1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:48314155 T>C maps to NM_152701.3 G1631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:48319386 G>T maps to NM_152701.3 E2866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:48285121 C>T maps to NM_152701.3 C468C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:48318816 G>T maps to NM_152701.3 E2676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr7:48506561 C>T maps to NM_152701.3 G4275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr7:48428793 C>T maps to NM_152701.3 N3877N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr7:48311512 C>T maps to NM_152701.3 D750D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:48318758 G>A maps to NM_152701.3 A2656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:48314104 T>C maps to NM_152701.3 N1614N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:48556477 G>A did not map to a codon.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr7:48259086 C>T maps to NM_152701.3 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr7:48390273 C>T maps to NM_152701.3 G3413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:48269451 G>A maps to NM_152701.3 W221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:48626781 C>T maps to NM_152701.3 L4846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:48317838 G>T maps to NM_152701.3 E2350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr7:48318434 C>T maps to NM_152701.3 T2548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr7:48682889 T>C maps to NM_152701.3 G4948G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr7:48314635 C>T maps to NM_152701.3 F1791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:48411859 C>T maps to NM_152701.3 A3633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr7:48313813 C>T maps to NM_152701.3 S1517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:48318848 C>T maps to NM_152701.3 N2686N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr7:48353920 C>T maps to NM_152701.3 S3258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:48318434 C>T maps to NM_152701.3 T2548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:48314512 T>C maps to NM_152701.3 L1750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr7:48431529 G>A maps to NM_152701.3 T3889T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:139906726 C>T maps to ENST00000355090 P1793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:139906957 G>A maps to ENST00000355090 I1752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:139905558 T>G did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:139911462 G>A maps to ENST00000355090 D919D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:139910918 C>T maps to ENST00000355090 E1006E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr9:139904515 C>T maps to ENST00000355090 A2168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:139906451 G>A maps to ENST00000355090 V1823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:139910136 C>T maps to ENST00000355090 K1198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:2350119 C>A maps to NM_001089.2 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr16:2376023 C>T maps to NM_001089.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr16:2339470 G>T maps to NM_001089.2 I888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr16:2347793 G>A maps to NM_001089.2 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:2369737 C>A maps to NM_001089.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:2336921 G>A maps to NM_001089.2 G1017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:2334935 G>A maps to NM_001089.2 L1183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:2326737 C>T maps to NM_001089.2 S1684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:2334978 G>A maps to NM_001089.2 D1168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr1:94505620 T>A maps to NM_000350.2 L1195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:94471007 C>A maps to NM_000350.2 E2046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:94544217 G>T maps to NM_000350.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr1:94487242 C>A maps to NM_000350.2 E1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:94497435 C>T maps to NM_000350.2 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:94495009 C>T maps to NM_000350.2 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:94497336 C>T maps to NM_000350.2 A1375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:94517195 G>A maps to NM_000350.2 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:94528146 G>T maps to NM_000350.2 C641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:94485239 G>A maps to NM_000350.2 V1698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:94497578 C>A maps to NM_000350.2 E1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:94471002 G>A maps to NM_000350.2 I2047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:94480236 G>T maps to NM_000350.2 V1774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:94546199 G>T maps to NM_000350.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr1:94476438 C>T maps to NM_000350.2 K1877K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:94564520 C>T maps to NM_000350.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:94485176 G>A maps to NM_000350.2 S1719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:94574255 G>A maps to NM_000350.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr1:94496610 G>A maps to NM_000350.2 G1398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:94487497 T>C maps to NM_000350.2 G1559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:94508386 G>A maps to NM_000350.2 D1086D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr1:94502895 A>G maps to NM_000350.2 N1206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:94522177 G>A maps to NM_000350.2 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:94487499 C>A maps to NM_000350.2 G1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:94497527 G>A maps to NM_000350.2 Q1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr17:67257280 C>A maps to ENST00000392677 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:67252411 C>T maps to ENST00000392677 T1249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:67250468 C>A maps to ENST00000392677 E1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:67309335 A>G maps to ENST00000392677 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:67286061 C>A maps to ENST00000392677 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr17:67270115 A>G maps to ENST00000392677 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:67136790 C>T maps to NM_080284.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:67130781 C>A maps to NM_080284.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:67075193 C>A maps to NM_080284.2 E1592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:67096963 G>A maps to NM_080284.2 R996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr17:67092919 C>T maps to NM_080284.2 W1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr17:67084326 G>A maps to NM_080284.2 R1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:1062245 G>T maps to NM_019112.3 L1882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:1047289 C>T maps to NM_019112.3 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:1062267 C>T maps to NM_019112.3 L1890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:1044670 C>T maps to NM_019112.3 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:1047595 C>T maps to NM_019112.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:1055215 C>T maps to NM_019112.3 P1357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:1053355 G>A maps to NM_019112.3 Q1083Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:1047277 T>C maps to NM_019112.3 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr19:1043342 C>T maps to NM_019112.3 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:66890430 T>C maps to NM_007168.2 A933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:66864486 G>A maps to NM_007168.2 S1534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:66878853 A>G maps to NM_007168.2 S1198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:66890311 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:66914236 G>A maps to NM_007168.2 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:66891116 G>A maps to NM_007168.2 H894H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:66928607 T>C maps to NM_007168.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr17:67024674 C>G did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:67016638 G>A maps to NM_080283.3 H830H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:67016608 C>T maps to NM_080283.3 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:67016614 G>A maps to NM_080283.3 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:66986991 G>A maps to NM_080283.3 R1275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:66981060 C>T maps to NM_080283.3 S1448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr17:66989216 A>C maps to NM_080283.3 P1188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:67028258 C>A maps to NM_080283.3 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:67028402 G>A maps to NM_080283.3 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:67039645 G>A maps to NM_080283.3 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr17:67047174 C>T maps to NM_080283.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:66982447 G>A maps to NM_080283.3 S1355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr17:67028402 G>A maps to NM_080283.3 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr7:87145947 G>A maps to NM_000927.3 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:87178780 C>T maps to NM_000927.3 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr7:87168615 G>A maps to NM_000927.3 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr7:87173489 T>C maps to NM_000927.3 G722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:87173489 T>C maps to NM_000927.3 G722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr7:87190655 A>G maps to NM_000927.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr7:87195424 G>A maps to NM_000927.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:229667404 T>C maps to NM_012089.2 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:229661731 G>A maps to NM_012089.2 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:229667404 T>C maps to NM_012089.2 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:169791764 C>T maps to NM_003742.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:169826013 C>T maps to NM_003742.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:169851888 G>T maps to NM_003742.2 S194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:169830284 T>C maps to NM_003742.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:169792925 G>A maps to NM_003742.2 I876I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:169787306 C>T maps to NM_003742.2 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:169842645 C>A maps to NM_003742.2 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:169781228 G>A maps to NM_003742.2 R1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr2:169781226 T>C maps to NM_003742.2 R1235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:169788949 G>T maps to NM_003742.2 R1050R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:169783755 A>G maps to NM_003742.2 Y1176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:87081079 A>G maps to NM_018849.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:87046647 C>A maps to NM_018849.2 E888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr7:87083891 C>T maps to NM_018849.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:87079354 G>A maps to NM_018849.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:87082365 G>A maps to NM_018849.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr7:87056074 G>T maps to NM_018849.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr7:20691090 C>T maps to NM_001163941.1 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr7:20691165 C>T maps to NM_001163941.1 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:20782555 C>T maps to NM_001163941.1 R1027R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:20795129 C>T maps to NM_001163941.1 N1219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr7:20738043 A>G maps to NM_001163941.1 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr7:20782526 C>T maps to NM_001163941.1 R1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr7:20738043 A>G maps to NM_001163941.1 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr2:220083281 A>C maps to NM_005689.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:220074986 G>A maps to NM_005689.2 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:220078003 G>A maps to NM_005689.2 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:220082507 G>A maps to NM_005689.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:220078604 G>A maps to NM_005689.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:220075486 G>A maps to NM_005689.2 R734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:220074707 T>C maps to NM_005689.2 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:220079110 C>T maps to NM_005689.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:74293779 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:74288923 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:74273303 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:74280119 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:74290311 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:74318889 C>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:74295430 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:74282221 C>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:150733234 G>A maps to ENST00000297504 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr7:150730778 C>A maps to ENST00000297504 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:150731635 C>T maps to ENST00000297504 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:123416858 G>A maps to NM_203444.2 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:123433275 G>A maps to NM_203444.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr16:16205395 G>A maps to ENST00000399408 T1022T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:16218762 C>G maps to ENST00000399408 Y1246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr16:16146606 A>G maps to ENST00000399408 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:16215989 C>T maps to ENST00000399408 D1193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:16215887 C>T maps to ENST00000399408 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:16200717 G>A maps to ENST00000399408 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:16165539 T>C maps to ENST00000399408 H622H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:16230393 G>A maps to ENST00000399408 S1405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:16142036 G>A maps to ENST00000399408 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:16208699 C>T maps to ENST00000399408 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr16:16162131 C>G maps to ENST00000399408 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr16:16205317 T>C maps to ENST00000399408 H996H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr6:43400986 C>T maps to NM_033450.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:43399922 C>T maps to NM_033450.2 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:43403512 C>T maps to NM_033450.2 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:43415477 G>A maps to NM_033450.2 A1226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr6:43414146 C>T maps to NM_033450.2 I1141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:43412974 C>A maps to NM_033450.2 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:43400515 C>T maps to NM_033450.2 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr16:48245002 G>A maps to NM_032583.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:48248902 G>A maps to NM_032583.3 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:48201511 C>T maps to NM_032583.3 Q1317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:48204878 C>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:48261823 G>A maps to NM_032583.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr16:48177960 C>T maps to NM_033226.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr16:48138246 C>T maps to NM_033226.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:48119526 G>A maps to NM_033226.2 R1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:48145382 C>A maps to NM_033226.2 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:48174663 C>T maps to NM_033226.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:48177912 C>T maps to NM_033226.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr16:48141283 G>A maps to NM_033226.2 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr16:48173232 C>T maps to NM_033226.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:101590127 C>T maps to NM_000392.3 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:101556952 G>A maps to NM_000392.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:101577087 G>A maps to NM_000392.3 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:101569956 C>T maps to NM_000392.3 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:101551995 C>T maps to NM_000392.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:101590550 C>T maps to NM_000392.3 D942D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:101544387 G>A maps to NM_000392.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:101591510 C>A maps to NM_000392.3 I1009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr10:101578641 T>C maps to NM_000392.3 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:101578641 T>C maps to NM_000392.3 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr10:101577096 G>A maps to NM_000392.3 W709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:101591417 G>A maps to NM_000392.3 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr10:101596038 C>T maps to NM_000392.3 T1202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:48746536 C>T maps to NM_003786.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:48753744 C>T maps to NM_003786.3 S1058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:48765037 C>A maps to NM_003786.3 T1474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:48734097 G>A maps to NM_003786.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:48752838 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:48755241 C>A maps to NM_003786.3 I1172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr13:95840745 G>A maps to NM_005845.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr13:95686891 T>C maps to NM_005845.3 A1279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:95673843 G>A maps to NM_005845.3 F1321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr13:95815373 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:95816648 G>A maps to NM_005845.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr13:95815374 C>T did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr13:95686891 T>C maps to NM_005845.3 A1279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr13:95815374 C>T did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr13:95815373 A>C did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr13:95815374 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:183670975 G>A maps to NM_005688.2 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:183679307 C>T maps to NM_005688.2 P790P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:183645174 G>A maps to NM_005688.2 F1330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:183706418 G>A maps to NM_005688.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:183639141 G>A maps to NM_005688.2 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:183660587 A>G maps to NM_005688.2 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:183667629 C>T maps to NM_005688.2 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:16253347 C>T maps to NM_001171.5 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:16291967 G>A maps to NM_001171.5 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr16:16244070 C>T maps to NM_001171.5 V1477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr16:16315526 G>A maps to NM_001171.5 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:16248612 G>A maps to NM_001171.5 L1360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:16271459 T>G maps to NM_001171.5 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr16:16278886 G>A maps to NM_001171.5 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:17496473 G>A maps to ENST00000302539 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:17418531 G>A maps to ENST00000302539 S1351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:17414671 G>A maps to ENST00000302539 R1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:17424299 C>T maps to ENST00000302539 R1187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:17452470 G>A maps to ENST00000302539 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr11:17434262 G>A maps to ENST00000302539 R837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:17483201 G>A maps to ENST00000302539 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr11:17483315 G>A maps to ENST00000302539 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:17426165 G>T maps to ENST00000302539 V1151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:17452410 C>T maps to ENST00000302539 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:17416761 G>A maps to ENST00000302539 I1457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:22078906 G>A maps to NM_005691.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:21954111 G>A maps to NM_020297.2 R1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:22068667 T>C maps to NM_005691.2 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr12:22086846 G>A maps to NM_005691.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:22012525 G>T maps to NM_005691.2 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:22061064 C>T maps to NM_005691.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:153008756 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:153006172 G>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:153009113 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:153005590 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr23:153002627 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:152994809 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:152990900 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:152994811 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:152991510 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:40013030 T>C maps to NM_005164.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr12:39979966 A>G maps to NM_005164.3 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr12:39980005 C>A maps to NM_005164.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:40012547 G>A maps to NM_005164.3 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:39997785 G>A maps to NM_005164.3 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:39997728 G>A maps to NM_005164.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr12:40013090 C>A maps to NM_005164.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr12:39980005 C>T maps to NM_005164.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr1:94972161 C>T maps to ENST00000454898 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:74766250 C>A maps to NM_005050.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:74762569 C>A maps to NM_005050.3 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:74761870 C>T maps to NM_005050.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:74764631 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:74764631 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr4:146025660 C>T maps to NM_002940.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:146041198 T>C maps to NM_002940.2 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:30546299 G>A maps to NM_001025091.1 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:30558318 C>T maps to NM_001025091.1 I793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:30554260 C>T maps to NM_001025091.1 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr6:30553069 G>A maps to NM_001025091.1 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:30553367 C>T maps to NM_001025091.1 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr7:150912141 G>A maps to NM_005692.3 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:150915851 G>A maps to NM_005692.3 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:150912141 G>A maps to NM_005692.3 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:183911218 C>T maps to NM_018358.2 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:183908976 C>T maps to NM_018358.2 Y501Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:183906139 C>T maps to NM_018358.2 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:183909025 G>T maps to NM_018358.2 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr21:43711633 C>T maps to NM_004915.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr21:43708057 C>A maps to NM_004915.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:43716282 C>T maps to NM_004915.3 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr21:43710216 C>T maps to NM_004915.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr21:43710218 G>A maps to NM_004915.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr4:89053005 A>G maps to NM_004827.2 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:89013496 G>A maps to NM_004827.2 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:89034592 A>T maps to NM_004827.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr4:89036208 A>G maps to NM_004827.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr11:119027068 G>A maps to NM_001142505.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr11:119024775 C>T maps to NM_001142505.1 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:119027113 C>A maps to NM_001142505.1 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:119024814 T>C maps to NM_001142505.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:44058952 C>T maps to NM_022436.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:44047052 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:44051193 C>A maps to NM_022436.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:44051091 G>A maps to NM_022436.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr2:44078889 C>T maps to NM_022437.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:44078795 C>A maps to NM_022437.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:44099256 C>T maps to NM_022437.2 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:111705828 C>T maps to NM_018394.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:111705849 T>G maps to NM_018394.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:73150966 C>T maps to NM_148912.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:73151392 G>A maps to NM_148912.2 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:73151383 G>A maps to NM_148912.2 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr20:25300887 G>T maps to NM_015600.3 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr14:51368611 C>A maps to ENST00000337334 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:51347253 A>G maps to ENST00000337334 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr13:108882411 C>T maps to NM_032859.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr13:108881820 A>G maps to NM_032859.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr13:108882090 C>T maps to NM_032859.2 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr15:89738521 C>A maps to NM_152924.4 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:89719193 C>T maps to NM_152924.4 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:19282289 C>A maps to NM_138340.4 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr14:23072500 C>T maps to NM_022060.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr14:23075355 G>A maps to NM_022060.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr14:23078737 C>A maps to NM_022060.2 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:58260428 G>T maps to NM_020676.5 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:17411867 A>G maps to NM_024527.4 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr10:27037564 G>A maps to NM_005470.3 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:204267311 G>A maps to ENST00000295851 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr2:204291954 A>G maps to ENST00000295851 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:47295133 A>C maps to NM_016428.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:47288172 C>T maps to NM_016428.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:100605106 A>G maps to ENST00000471714 C181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr3:100489782 T>C maps to ENST00000471714 R1506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:100489784 G>A maps to ENST00000471714 R1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr3:100471736 C>T maps to ENST00000471714 E1663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:100581169 G>A maps to ENST00000471714 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:100471643 G>A maps to ENST00000471714 S1694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:100489784 G>A maps to ENST00000471714 R1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:100494174 G>T maps to ENST00000471714 I1437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:100645176 G>A maps to ENST00000471714 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr3:100712147 G>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:133760832 C>T maps to NM_007313.2 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:133760742 C>T maps to NM_007313.2 I1041I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:133759405 C>T maps to NM_007313.2 R596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:133755461 G>A maps to NM_007313.2 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:133729568 C>T maps to NM_007313.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr9:133738358 C>A maps to NM_007313.2 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:133730431 A>G maps to NM_007313.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:133755914 C>T maps to NM_007313.2 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:133750419 C>A maps to NM_007313.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:133760373 G>A maps to NM_007313.2 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr9:133750320 G>A maps to NM_007313.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr9:133750356 T>C maps to NM_007313.2 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr9:133750318 C>T maps to NM_007313.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:133760817 C>T maps to NM_007313.2 S1066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr9:133760391 C>T maps to NM_007313.2 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr1:179084016 T>C maps to NM_007314.3 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:179100515 A>G maps to NM_007314.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:179100581 T>C maps to NM_007314.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:179100565 C>A maps to NM_007314.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:179077545 G>A maps to NM_007314.3 D952D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:179090855 G>A maps to NM_007314.3 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:179087843 C>T maps to NM_007314.3 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:179078211 G>A maps to NM_007314.3 D730D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:179084016 T>C maps to NM_007314.3 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr1:179084016 T>C maps to NM_007314.3 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:179095520 T>C maps to NM_007314.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:116196051 G>A maps to ENST00000277895 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:8082515 G>A maps to NM_001130083.1 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:8089974 G>A maps to NM_001130083.1 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:8098968 C>T maps to NM_001130083.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr4:8098824 C>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:8089974 G>A maps to NM_001130083.1 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:148596587 G>T maps to NM_014945.2 G246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:148612862 C>T maps to NM_014945.2 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:148577902 C>T maps to NM_014945.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:148624519 G>A maps to NM_014945.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:136137512 C>T maps to NM_020469.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:150558218 C>T maps to ENST00000416793 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr17:995066 G>A maps to NM_021962.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:910518 T>C maps to NM_021962.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:1003930 C>T maps to NM_021962.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr17:986852 A>T maps to NM_021962.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:960286 A>T maps to NM_021962.2 C479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:959344 A>G maps to NM_021962.2 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:913998 G>T maps to NM_021962.2 R736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:970418 G>A maps to NM_021962.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr8:107773723 C>T maps to NM_139166.4 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:107782175 C>T maps to NM_139166.4 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:26597309 G>T maps to NM_013375.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:127399218 C>T maps to NM_172027.2 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:34378257 C>T maps to NM_145804.2 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:34180875 G>A maps to NM_145804.2 I888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:38173084 A>G did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:47329179 G>A maps to NM_006111.2 Y20Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr18:47310297 A>G maps to NM_006111.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr18:47310297 A>G maps to NM_006111.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr18:47310297 A>G maps to NM_006111.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr17:35687261 T>C maps to NM_198834.1 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr17:35591952 T>G maps to NM_198834.1 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr17:35591931 G>A maps to NM_198834.1 H1068H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:35631121 C>A maps to NM_198834.1 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:35470056 G>T maps to NM_198834.1 R2140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:35454848 T>A maps to NM_198834.1 L2212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:35583270 G>A maps to NM_198834.1 R1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr17:35518873 G>T maps to NM_198834.1 R1724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr12:109698369 G>A maps to NM_001093.3 P2194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr12:109660388 A>G maps to NM_001093.3 K1214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:109610081 G>A maps to NM_001093.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:109605762 C>A maps to NM_001093.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:109577533 C>T maps to NM_001093.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:109692075 G>T maps to NM_001093.3 E2035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:109577290 G>A maps to NM_001093.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:112186253 G>A maps to NM_001136538.1 T904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:112184980 C>T maps to NM_001136538.1 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr12:112147427 T>C maps to NM_001136538.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:112171750 A>G maps to NM_001136538.1 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr12:112147427 T>C maps to NM_001136538.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr12:112147427 T>C maps to NM_001136538.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr12:112147427 T>C maps to NM_001136538.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:132358364 G>A maps to NM_032169.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr3:132322121 T>C maps to NM_032169.4 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr3:132360862 G>A maps to NM_032169.4 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr11:134128471 G>A maps to NM_014384.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:134127058 C>T maps to NM_014384.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:128628952 C>T maps to NM_014049.4 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:128625013 C>T maps to NM_014049.4 I400I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D5-6540-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:211057583 G>A maps to NM_001608.3 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:76215192 C>T maps to ENST00000370834 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:76216212 C>T maps to ENST00000370834 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:76198535 A>G did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr1:76205780 A>G maps to ENST00000370834 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr1:76205780 A>G maps to ENST00000370834 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:121174937 C>T maps to NM_000017.2 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:121177211 G>A maps to NM_000017.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:124812605 C>T maps to NM_001609.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr10:124800807 T>A maps to NM_001609.3 Y198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:124802683 C>A maps to NM_001609.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr10:124802683 C>A maps to NM_001609.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr10:124810617 A>G maps to NM_001609.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:7127039 C>A maps to ENST00000356839 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:7123996 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:89400882 A>G maps to NM_013227.3 A1689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:89392864 C>T maps to NM_013227.3 C643C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr15:89381930 G>A maps to NM_013227.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr15:89402046 G>A maps to NM_013227.3 G2077G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr15:89401782 C>T maps to NM_013227.3 S1989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:89386584 G>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:89395064 C>T maps to NM_013227.3 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:7250183 G>A maps to NM_014716.3 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:195022851 C>A maps to NM_012287.5 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:195101757 C>A maps to NM_012287.5 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:195016437 T>C maps to NM_012287.5 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr3:195016575 T>C maps to NM_012287.5 K511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr3:195027308 G>A maps to NM_012287.5 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:1230827 G>A maps to NM_030649.2 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:1233772 G>A maps to NM_030649.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:1231968 G>A maps to NM_030649.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:1233204 G>A maps to NM_030649.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:1231944 G>A maps to NM_030649.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:108005950 T>C maps to NM_000019.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:108009659 C>A maps to NM_000019.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr11:108004591 T>C maps to NM_000019.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:108010833 C>T maps to NM_000019.3 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:108014719 C>T maps to NM_000019.3 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:226334447 G>A maps to NM_022735.3 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:43216506 A>G maps to NM_001135706.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:27499983 A>G maps to ENST00000375888 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr10:27493439 C>T maps to ENST00000375888 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:27497252 G>A maps to ENST00000375888 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:27506963 C>T maps to ENST00000375888 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:180471299 A>G maps to NM_032360.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:31348258 C>T maps to NM_183377.1 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:32483421 G>A maps to NM_001094.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr17:32483404 G>A maps to NM_001094.4 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:32483385 G>A maps to NM_001094.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:50471864 C>T maps to NM_020039.2 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:50475044 C>A maps to NM_020039.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr12:50472719 C>T maps to NM_020039.2 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:150747999 C>T maps to NM_020321.2 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:150749526 C>T maps to NM_020321.2 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr7:150749266 G>A maps to NM_020321.2 K467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:150748980 G>A maps to NM_020321.2 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr7:150746491 G>T maps to NM_020321.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:150747233 C>T maps to NM_020321.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr7:150749757 C>T maps to NM_020321.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:150747658 G>T maps to NM_020321.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:220402675 C>T maps to NM_018674.4 R637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:220396589 G>A maps to NM_018674.4 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:220401790 G>A maps to NM_018674.4 E538E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:156757926 C>T maps to NM_017419.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:44097101 G>A maps to NM_032592.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:44101104 T>C maps to NM_032592.3 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr11:44104785 A>G maps to NM_032592.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:44092822 C>T maps to NM_032592.3 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:44105041 G>A maps to NM_032592.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:44079990 C>T maps to NM_001031854.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:44080227 G>T maps to NM_001031854.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr11:44081457 A>C maps to NM_001031854.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:44072139 G>A maps to NM_001031854.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:67693651 G>A maps to NM_001082486.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:61574338 G>A maps to NM_000789.3 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:61558934 C>T maps to NM_000789.3 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr17:61557142 C>T maps to NM_000789.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:15593881 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:15596417 A>G did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:15582186 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:15599403 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:15589758 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:15588431 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:15599442 G>C did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:15591549 T>C did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:15596407 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:15589746 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:15582271 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:15585934 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:15591490 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:15609902 G>A did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:15596408 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:15591536 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:6309775 C>T maps to NM_133492.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr19:6307228 C>T maps to NM_133492.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr9:19424800 C>T maps to NM_001010887.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:76696755 A>G maps to NM_018367.5 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:76731340 G>A maps to NM_018367.5 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:100491166 C>T maps to NM_000665.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr7:100490872 C>A maps to NM_000665.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:100491610 C>T maps to NM_000665.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr14:23549649 C>T maps to NM_014977.3 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr14:23530626 G>T maps to NM_014977.3 R1160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:23530358 C>A maps to NM_014977.3 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:23531678 G>A maps to NM_014977.3 T1037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr14:23549703 C>A maps to NM_014977.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:135616875 C>T maps to NM_138326.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:135621047 C>T maps to NM_138326.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:32405518 C>T maps to NM_002197.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:32418468 G>A maps to NM_002197.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:32418177 C>T maps to NM_002197.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr22:41920873 G>T maps to ENST00000396512 G528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr22:41919905 C>T maps to ENST00000396512 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr22:41922429 C>T maps to ENST00000396512 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:41919276 G>A maps to ENST00000396512 W480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:55072842 C>T maps to NM_015547.3 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:55058257 G>A maps to NM_015547.3 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:55096498 C>T maps to NM_015547.3 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:80643603 A>T maps to NM_130767.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:80641771 G>A maps to NM_130767.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:80640028 A>G maps to NM_130767.2 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:80628424 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:80626685 C>A maps to NM_130767.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00W-01A-01W-A005-10 chr5:80643666 A>G maps to NM_130767.2 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:80631701 C>A maps to NM_130767.2 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:74061988 C>T maps to NM_152331.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:44470596 T>C did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr20:44472358 G>A maps to NM_005469.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr20:44477252 C>T maps to NM_005469.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr23:23731271 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:23723951 A>G did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:23723951 A>G did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:23722859 C>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:23724821 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:23751330 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:23731271 A>G did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:23723951 A>G did not map to a codon.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr17:73945441 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr17:73945295 A>C did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:58520689 T>C maps to NM_003500.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:58510205 G>T maps to NM_003500.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:8394084 C>T maps to NM_003501.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:8401375 G>A maps to NM_003501.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:8412055 G>A maps to NM_003501.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:8368723 G>A maps to NM_003501.2 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:111562875 G>A maps to NM_001142807.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:111551741 C>A maps to NM_001142807.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:111542322 G>A maps to NM_001142807.1 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:277234 C>T maps to NM_004300.3 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:277273 C>A maps to NM_004300.3 C149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:11687266 G>A maps to NM_001111036.1 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:147126329 C>T maps to NM_016361.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:147122001 G>T maps to NM_016361.3 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:147126383 C>A maps to NM_016361.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr3:141011878 C>T maps to NM_001037172.1 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:140997319 C>T maps to NM_001037172.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr3:132086608 G>A maps to NM_001134194.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:51176728 C>T maps to NM_001097.2 N22N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr22:51178319 G>A maps to NM_001097.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:51182576 C>T maps to NM_001097.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr22:51176734 G>A maps to NM_001097.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:6747453 G>A maps to NM_032489.2 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:6749517 G>A maps to NM_032489.2 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:6747453 G>A maps to NM_032489.2 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:6753598 C>T maps to NM_032489.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr12:6747453 G>A maps to NM_032489.2 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:6749535 G>T maps to NM_032489.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:6748203 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:70832213 G>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:70823718 G>A did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:70823979 T>C did not map to a codon.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr23:70823979 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:70824219 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:70832372 A>G did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:70823893 A>G did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr23:70800721 C>T did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:70812014 T>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:70824341 T>C did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:70823979 T>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:70823470 C>T did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr23:70828951 C>A did not map to a codon.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr23:70824341 T>C did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:70828875 A>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:70823564 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:70824341 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:70825523 C>T did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:70824341 T>C did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:125547743 C>T maps to NM_001612.5 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr15:78463863 C>T maps to NM_015162.4 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr15:78486311 C>T maps to NM_015162.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr15:78472019 C>T maps to NM_015162.4 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:78526728 C>A maps to NM_015162.4 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr15:78466768 A>G maps to NM_015162.4 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr15:78486311 C>T maps to NM_015162.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:6183070 C>T maps to NM_030924.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:6166025 C>T maps to NM_030924.3 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:6185581 C>T maps to NM_030924.3 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:6190667 A>C maps to NM_030924.3 *667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:6182868 C>T maps to NM_030924.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr17:48538073 C>T maps to ENST00000427954 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:48549865 C>T maps to ENST00000427954 C492C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:48503633 C>T maps to ENST00000427954 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:48548453 G>A maps to ENST00000427954 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr17:48539855 G>A maps to ENST00000427954 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr16:89167139 G>C maps to NM_174917.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr4:185689496 T>C maps to NM_001995.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:185724637 G>A maps to NM_001995.2 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr4:185697679 G>A maps to NM_001995.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:185705137 G>A maps to NM_001995.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:185687076 G>A maps to NM_001995.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:223791884 T>G maps to NM_203372.1 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:223786007 T>C maps to NM_203372.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr2:223786007 T>C maps to NM_203372.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:108926077 G>A did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:108926671 A>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:108924288 G>T did not map to a codon.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr23:108902681 C>T did not map to a codon.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr23:108906629 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:108902600 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:108926625 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:108906570 T>G did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:108926077 G>A did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:108921571 C>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:108924287 A>G did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:108926078 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:108887258 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr23:108924288 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:108906467 G>T did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:108926520 G>A did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr10:114154766 G>C maps to NM_016234.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:114182168 T>C maps to NM_016234.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:131298299 G>A maps to NM_001009185.1 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:131302210 T>C maps to NM_001009185.1 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:131302158 G>A maps to NM_001009185.1 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr16:20693654 C>T maps to NM_052956.2 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:20634873 C>T maps to NM_052956.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr16:20702393 T>C maps to NM_052956.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr16:20702393 T>C maps to NM_052956.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:20651869 G>A maps to NM_052956.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr16:20486998 C>T maps to NM_001010845.2 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:20471591 T>C maps to NM_001010845.2 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:20477042 C>T maps to NM_001010845.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr16:20471448 C>T maps to NM_001010845.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:20477042 C>T maps to NM_001010845.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:20482939 G>T maps to NM_001010845.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr16:20497943 C>T maps to NM_001010845.2 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr16:20548585 C>T maps to NM_182617.3 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:20566706 C>T maps to NM_182617.3 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr16:20548585 C>T maps to NM_182617.3 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr16:20554286 A>G maps to NM_182617.3 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr16:20554286 A>G maps to NM_182617.3 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:20548635 G>A maps to NM_182617.3 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr16:20797536 C>T maps to NM_202000.2 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr16:20781478 C>T maps to NM_005622.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr12:7469870 C>T maps to NM_001080454.1 C253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:7473343 G>A maps to NM_001080454.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:7475859 G>T maps to NM_001080454.1 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:7480897 G>T maps to NM_001080454.1 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:7476928 G>T maps to NM_001080454.1 G457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr16:20448398 C>A maps to NM_017888.2 S445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr16:20430598 G>A maps to NM_017888.2 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr16:20432624 C>T maps to NM_017888.2 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:20441124 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:20448643 C>A maps to NM_017888.2 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr20:25011503 C>T maps to NM_032501.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:25002127 G>A maps to NM_032501.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:25004116 G>A maps to NM_032501.2 D264D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CK-5913-01A-11D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:33514684 G>T maps to NM_001076552.2 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:81532923 T>C maps to NM_024560.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:81610680 G>A maps to NM_024560.2 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr12:81593215 G>A maps to NM_024560.2 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr12:81647174 A>G maps to NM_024560.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:81647353 C>T maps to NM_024560.2 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:81593147 C>T maps to NM_024560.2 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:81503337 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:81503390 G>T maps to NM_024560.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:81647322 T>C maps to NM_024560.2 V623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:81528629 C>T maps to NM_024560.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:229567867 G>A maps to NM_001100.3 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:229567822 G>A maps to NM_001100.3 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:229568814 G>A maps to NM_001100.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:229568321 G>A maps to NM_001100.3 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:90707098 G>A maps to NM_001141945.1 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr7:5568992 C>A maps to NM_001101.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:5567715 G>A maps to NM_001101.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:56778141 T>C maps to NM_001017992.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:56777676 G>A maps to NM_001017992.2 C286C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:56777652 G>T maps to NM_001017992.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:35085653 G>A maps to NM_005159.4 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:35086967 G>A maps to NM_005159.4 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:35083347 G>T maps to NM_005159.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:79478018 G>A maps to NM_001614.2 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:79478649 A>G maps to NM_001614.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:74143865 C>T maps to NM_001615.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:179287852 A>G did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:179291193 T>C maps to NM_004301.3 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:179294682 G>A maps to NM_004301.3 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:100252641 C>T maps to NM_016188.4 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:100252713 G>A maps to NM_016188.4 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr7:100253176 G>A maps to NM_016188.4 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr7:100243870 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr7:100253092 G>A maps to NM_016188.4 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:100253062 C>T maps to NM_016188.4 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:111625207 G>A maps to NM_006687.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:111617853 G>A maps to NM_006686.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:111618015 G>A maps to NM_006686.3 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:18152557 G>A maps to NM_030812.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:18153007 G>A maps to NM_030812.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:8808925 G>A maps to NM_178525.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr19:8808430 G>A maps to NM_178525.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr14:69341668 C>T maps to NM_001130004.1 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr14:69376752 G>T maps to NM_001130004.1 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr14:69376752 G>T maps to NM_001130004.1 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:236918363 C>T maps to NM_001103.2 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:236924370 C>A maps to NM_001103.2 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:236906323 G>A maps to NM_001103.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:236907965 G>A maps to NM_001103.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:236902624 G>A maps to NM_001103.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:236925807 G>A maps to NM_001103.2 Q858Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr1:236899007 G>A maps to NM_001103.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:236912554 G>A maps to NM_001103.2 E549E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:236920871 G>A maps to NM_001103.2 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:236883483 G>A maps to NM_001103.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:236924421 C>T maps to NM_001103.2 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:236918422 C>T maps to NM_001103.2 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:66330367 C>T maps to NM_001104.1 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:66328147 G>A maps to NM_001104.1 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr11:66328762 C>T maps to NM_001104.1 N642N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:66330534 C>T maps to NM_001104.1 R859R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:66328753 G>A maps to NM_001104.1 Q639Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:66329500 C>T maps to NM_001104.1 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:66330310 C>T maps to NM_001104.1 N811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:39191316 C>T maps to NM_004924.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:39219736 C>T maps to NM_004924.3 T840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:39205201 G>A did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr14:58669570 A>G did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr14:58697128 G>A maps to NM_018477.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr10:104247969 G>A maps to NM_005736.3 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:98277047 C>A maps to NM_005735.3 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:98274991 A>G maps to NM_005735.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:98275015 A>G maps to NM_005735.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:98277065 C>A maps to NM_005735.3 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:65478168 T>C maps to NM_001005386.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:114709343 T>C maps to NM_005721.3 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:114697555 C>T maps to NM_005721.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:152497715 C>T maps to NM_020445.4 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:37378855 G>A maps to NM_024855.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:37384639 G>A maps to NM_024855.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:100598810 C>A maps to NM_022496.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr12:100612251 G>A maps to NM_022496.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:53908260 C>A maps to NM_022899.4 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:53911333 A>G maps to NM_022899.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:127185753 C>A did not map to a codon.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr23:127185064 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:127186116 T>C did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:127185122 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:127185348 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:127185067 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:127186026 C>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:127186073 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr23:127185494 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr23:127185238 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:127186017 G>A did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:127186024 T>C did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr23:127185238 T>C did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:127185493 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:127185794 T>C did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:127185062 A>G did not map to a codon.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr1:2938453 C>A maps to NM_080431.4 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:2938633 C>T maps to NM_080431.4 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:2938561 C>T maps to NM_080431.4 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:158617467 G>A maps to NM_001111067.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:158626922 C>T maps to NM_001111067.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:158634840 A>G maps to NM_001111067.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr12:52377794 G>A maps to NM_020328.3 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:52385765 C>T maps to NM_020328.3 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:52380694 T>G maps to NM_020328.3 Y451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:52385714 C>T maps to NM_020328.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:52385714 C>T maps to NM_020328.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr12:52385714 C>T maps to NM_020328.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:158406683 A>G maps to NM_145259.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr2:158390507 G>A maps to NM_145259.2 N468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr2:158395159 C>T maps to NM_145259.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:158443864 A>G maps to NM_145259.2 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr2:158401099 C>T maps to NM_145259.2 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:148674877 C>T maps to NM_001616.3 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:148680543 T>C maps to NM_001616.3 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:148674865 G>A maps to NM_001616.3 W229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:148674904 G>A maps to NM_001616.3 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr2:148674941 C>T maps to NM_001616.3 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:148657096 G>T maps to NM_001616.3 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr3:38521287 C>T maps to NM_001106.3 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr3:38519663 C>T maps to NM_001106.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:38521170 C>A maps to NM_001106.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:38523753 C>A maps to NM_001106.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:38521243 C>T maps to NM_001106.3 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:38524729 G>T maps to NM_001106.3 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:52306961 G>T maps to NM_001077401.1 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:52021348 A>G maps to ENST00000463937 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:67412827 G>T maps to NM_080658.1 C152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr14:75530246 C>A maps to NM_001107.3 G4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:43254297 C>T maps to NM_000022.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:43252920 G>A maps to NM_000022.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr20:43255176 G>A maps to NM_000022.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:123329153 T>C maps to NM_139243.3 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr4:123342496 A>G maps to NM_139243.3 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:123342439 A>G maps to NM_139243.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:84228717 C>T maps to NM_139174.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:84230549 G>A maps to NM_139174.3 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr16:84229153 C>T maps to NM_139174.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:84229285 C>T maps to NM_139174.3 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr16:84228717 C>T maps to NM_139174.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:58933009 G>A maps to NM_001110.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr15:58889826 C>T maps to NM_001110.2 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:42855595 G>A maps to NM_002390.4 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr10:127843849 C>T maps to NM_003474.4 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr10:127782639 G>A maps to NM_003474.4 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:128019054 T>G maps to NM_003474.4 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:127967511 C>A maps to NM_003474.4 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:127737878 G>A maps to NM_003474.4 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr10:127782694 G>C maps to NM_003474.4 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:155034761 G>A maps to NM_207197.1 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:155029741 C>T maps to NM_207197.1 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:155030532 C>T maps to NM_207197.1 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:155028557 C>T maps to NM_207197.1 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:155034447 G>A maps to NM_207197.1 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr1:155029720 C>A maps to NM_207197.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr2:9676855 C>T maps to NM_003183.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:9658247 T>C maps to NM_003183.4 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:9633024 A>G did not map to a codon.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr8:39502936 T>C maps to NM_014237.2 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:39495981 A>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:39525650 T>C maps to NM_014237.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr8:39502936 T>C maps to NM_014237.2 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr8:39581384 A>G maps to NM_014237.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr8:39581384 A>G maps to NM_014237.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr8:39537672 T>C maps to NM_014237.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr8:39537615 C>T maps to NM_014237.2 D564D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr8:39467065 A>T maps to NM_014237.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr5:156917412 C>T maps to ENST00000430702 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:156964947 G>A maps to ENST00000430702 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr5:156932771 G>A maps to ENST00000430702 H347H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr5:156936319 G>T maps to ENST00000430702 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:39624522 C>A maps to NM_001464.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:39646226 G>A maps to NM_001464.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:39613369 T>C maps to NM_001464.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:39604067 G>A maps to NM_001464.3 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr8:39679163 T>C maps to NM_001464.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr8:39613300 A>G maps to NM_001464.3 H581H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:39644501 A>G maps to NM_001464.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:70990832 G>A maps to NM_003814.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:70990283 C>T maps to NM_003814.4 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr14:70990472 G>A maps to NM_003814.4 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr14:70924866 C>T maps to NM_003813.2 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:70925424 C>T maps to NM_003813.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:70925120 C>A maps to NM_003813.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:70924431 C>T maps to NM_003813.2 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:70925419 G>T maps to NM_003813.2 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:70924266 C>T maps to NM_003813.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:70926358 G>T maps to NM_003813.2 E715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:87762256 C>T maps to NM_021723.3 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:87811336 T>C maps to NM_021723.3 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr7:87762211 G>A maps to NM_021723.3 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr7:87797509 C>T maps to NM_021723.3 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:87762211 G>A maps to NM_021723.3 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:207437915 T>C maps to NM_003812.2 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:207310094 G>A maps to NM_003812.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr2:207437915 T>C maps to NM_003812.2 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:24193083 C>T maps to NM_014265.4 H499H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr8:24199149 G>A maps to NM_014265.4 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:24167465 T>C maps to NM_014265.4 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr8:24199173 G>C maps to NM_014265.4 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:175898277 T>C maps to NM_014269.4 C534C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr4:175897680 T>C maps to NM_014269.4 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:175897680 T>C maps to NM_014269.4 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:175898442 G>T maps to NM_014269.4 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:175897210 G>T maps to NM_014269.4 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:175898448 G>A maps to NM_014269.4 K591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr4:175898991 G>T maps to NM_014269.4 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:175896954 G>A maps to NM_014269.4 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr4:175897680 T>C maps to NM_014269.4 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr4:175896768 G>T maps to NM_014269.4 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr4:175897768 A>T maps to NM_014269.4 K365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:175897950 T>C maps to NM_014269.4 C425C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:175897680 T>C maps to NM_014269.4 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:175899082 C>T maps to NM_014269.4 Q803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr4:175898277 T>C maps to NM_014269.4 C534C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr4:175897560 A>G maps to NM_014269.4 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr4:175898277 T>C maps to NM_014269.4 C534C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr4:175898433 C>T maps to NM_014269.4 Y586Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:120438506 G>T maps to NM_021794.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:120438329 G>T maps to NM_021794.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:120438692 G>A maps to NM_021794.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:120437573 A>G maps to NM_021794.2 N462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr8:39114859 C>T maps to NM_145004.5 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:39079202 G>A maps to NM_145004.5 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:3654116 G>T maps to NM_025220.2 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:3654719 G>A maps to NM_025220.2 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:24359067 G>A maps to ENST00000380789 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:24344701 T>C maps to ENST00000380789 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:24365021 C>T maps to ENST00000380789 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:24349483 C>G maps to ENST00000380789 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:24339815 A>G maps to ENST00000380789 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:24365048 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:24342870 T>C maps to ENST00000380789 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:24349523 G>T maps to ENST00000380789 G489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:24324310 G>T did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr8:24324386 G>A maps to ENST00000380789 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr8:24358397 C>T maps to ENST00000380789 Q700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr10:135085434 G>A maps to NM_001109.4 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:38899485 T>C maps to NM_003816.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:38961209 C>A maps to NM_003816.2 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr8:38928859 T>C maps to NM_003816.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:38869200 G>T maps to NM_003816.2 G74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:24254939 C>T maps to NM_014479.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:24254935 A>G maps to NM_014479.3 P198P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3984-01A-02W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:24242067 C>T maps to NM_014479.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:24255198 G>T maps to NM_014479.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr21:28210224 G>T maps to NM_006988.3 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr21:28212320 G>A maps to NM_006988.3 C575C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:28212813 G>A maps to NM_006988.3 Y482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr21:28213371 C>T maps to NM_006988.3 Q441Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:28216553 T>C maps to NM_006988.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:28210819 A>G maps to NM_006988.3 C714C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr21:28214912 G>A maps to NM_006988.3 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:8657733 C>T maps to NM_030957.2 W500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:8651509 G>A maps to NM_030957.2 R779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:8661198 G>A maps to NM_030957.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:8661469 C>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:8661932 G>A maps to NM_030957.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:8662192 T>C maps to NM_030957.2 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:33576743 C>T maps to NM_030955.2 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:33549440 G>A maps to NM_030955.2 C1391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:33649705 C>T maps to NM_030955.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:33616037 C>T maps to NM_030955.2 W761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:33630980 G>A maps to NM_030955.2 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:33577193 G>A maps to NM_030955.2 C979C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:33534962 G>A maps to NM_030955.2 N1527N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:33881334 G>T maps to NM_030955.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:33577193 G>A maps to NM_030955.2 C979C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr5:33684026 T>C maps to NM_030955.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:33630923 G>A maps to NM_030955.2 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:33649062 C>T maps to NM_030955.2 W448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr5:33881280 C>T maps to NM_030955.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr5:33577193 G>A maps to NM_030955.2 C979C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:136319718 G>A maps to NM_139025.3 W1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:136291110 G>A maps to NM_139025.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:136291317 G>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:136287583 G>T maps to NM_139025.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:136289528 C>T maps to NM_139025.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr9:136291062 C>T maps to NM_139025.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr9:136301995 G>A maps to NM_139025.3 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:72517836 C>T maps to NM_139155.2 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:72513564 G>A maps to NM_139155.2 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:72513720 A>G maps to NM_139155.2 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:72489102 C>T maps to NM_139155.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:72434612 A>G maps to NM_139155.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:130332614 C>T maps to NM_139055.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr11:130319401 G>A maps to NM_139055.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:5209319 C>T maps to NM_139056.2 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:5200310 T>C maps to NM_139056.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:5306762 G>A maps to NM_139056.2 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:5242284 C>T maps to NM_139056.2 C881C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr5:5235250 C>T maps to NM_139056.2 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:5222990 T>C maps to NM_139056.2 H565H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr5:5319208 C>T maps to NM_139056.2 Y1211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:5239325 C>T maps to NM_139056.2 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:5303422 C>T maps to NM_139056.2 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:100672324 C>T maps to NM_139057.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr15:100802559 A>G maps to NM_139057.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr15:100589135 G>A maps to NM_139057.2 N839N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:100516343 G>A maps to NM_139057.2 C1011C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:100533366 G>A maps to NM_139057.2 T945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr15:100739608 A>G maps to NM_139057.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:77353778 C>T maps to NM_199355.2 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr16:77465437 G>A maps to NM_199355.2 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr16:77353781 G>A maps to NM_199355.2 Y832Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:77401506 G>A maps to NM_199355.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr16:77334178 G>A maps to NM_199355.2 C885C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:77401473 G>T maps to NM_199355.2 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:77465419 C>T maps to NM_199355.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr16:77389927 C>A maps to NM_199355.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr16:77317954 G>T maps to NM_199355.2 C1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:77334297 G>A maps to NM_199355.2 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:77323236 T>C maps to NM_199355.2 S1158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:77465344 G>T maps to NM_199355.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr5:128957998 G>A maps to NM_133638.3 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:129070677 T>C maps to NM_133638.3 H1116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:128932343 G>T maps to NM_133638.3 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr5:129072865 A>G maps to NM_133638.3 E1193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:128990050 T>G maps to NM_133638.3 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:128983513 A>T maps to NM_133638.3 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:129070665 C>T maps to NM_133638.3 I1112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:128990098 A>G maps to NM_133638.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr5:178771019 G>A maps to NM_014244.4 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:178557031 T>C maps to NM_014244.4 K786K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr5:178541161 G>A maps to NM_014244.4 N1114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr5:178555068 G>T maps to NM_014244.4 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr5:178562942 G>A maps to NM_014244.4 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:178564800 C>T maps to NM_014244.4 Q640Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:178559841 G>A maps to NM_014244.4 C715C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr5:178581123 C>T maps to NM_014244.4 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr5:178564905 G>A maps to NM_014244.4 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr5:178552066 G>A maps to NM_014244.4 H955H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:178562921 G>A maps to NM_014244.4 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr5:178541176 C>T maps to NM_014244.4 P1109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr5:178579178 C>G maps to NM_014244.4 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:178579178 C>T maps to NM_014244.4 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr5:178770827 G>A maps to NM_014244.4 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr5:178556950 G>A maps to NM_014244.4 H813H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:178540951 C>T maps to NM_014244.4 P1184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr5:178771028 C>T maps to NM_014244.4 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:178555110 C>T maps to NM_014244.4 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:43833713 C>A maps to ENST00000389420 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:43837615 T>A maps to ENST00000389420 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:43826490 G>T maps to ENST00000389420 Y948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:43823439 G>A maps to ENST00000389420 R1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:43824240 G>A maps to ENST00000389420 R1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr12:43777689 G>A maps to ENST00000389420 Q1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:43826229 A>C maps to ENST00000389420 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:43833713 C>A maps to ENST00000389420 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:43858494 C>A maps to ENST00000389420 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:43884225 A>G maps to ENST00000389420 C363C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr12:43944960 G>A maps to ENST00000389420 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr12:43763094 G>A maps to ENST00000389420 Q1846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:43777662 G>A maps to ENST00000389420 R1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:43825178 C>A maps to ENST00000389420 E1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:43887035 A>G maps to ENST00000389420 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:43822184 G>A maps to ENST00000389420 S1268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:43826147 C>A maps to ENST00000389420 E1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr12:43846437 A>G maps to ENST00000389420 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:43771224 G>A maps to ENST00000389420 Y1646Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:43833825 A>T maps to ENST00000389420 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr4:73176815 C>T maps to NM_014243.1 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:73176815 C>T maps to NM_014243.1 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:73176815 C>T maps to NM_014243.1 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:73414443 C>T maps to NM_014243.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr4:73156637 G>A maps to NM_014243.1 P955P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:73179509 C>T maps to NM_014243.1 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:73185648 T>G maps to NM_014243.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:73205300 A>G maps to NM_014243.1 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr4:73171755 A>G maps to NM_014243.1 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr4:73169735 C>T maps to NM_014243.1 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr4:73171755 A>G maps to NM_014243.1 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:161161161 G>A maps to NM_005099.4 R760R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr21:28338026 C>A maps to NM_007038.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr21:28307003 G>T maps to NM_007038.3 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:28338170 G>A maps to NM_007038.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:28338242 G>A maps to NM_007038.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr21:28306865 C>T maps to NM_007038.3 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr21:28302335 G>A maps to NM_007038.3 C698C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr21:28337608 C>A maps to NM_007038.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr21:28338242 G>A maps to NM_007038.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr21:28306825 G>A maps to NM_007038.3 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr21:28338200 G>A maps to NM_007038.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr21:28338170 G>A maps to NM_007038.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:28338353 C>T maps to NM_007038.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:64511156 G>A maps to NM_197941.2 I810I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:64556486 A>C maps to NM_197941.2 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:64447731 C>T maps to NM_197941.2 V1095V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:64466557 G>A maps to NM_197941.2 Q1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr15:79068579 C>A maps to ENST00000258883 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr15:79080691 G>A maps to ENST00000258883 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr15:79058178 A>G maps to ENST00000258883 G1358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:79092764 G>A maps to ENST00000258883 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:79092830 C>T maps to ENST00000258883 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:130281312 G>A maps to NM_007037.4 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:130297695 C>T maps to NM_007037.4 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:130278671 G>A maps to NM_007037.4 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:130289127 C>T maps to NM_007037.4 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr11:130275572 G>A maps to NM_007037.4 A850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr3:64527267 T>A maps to NM_182920.1 V1742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:64640051 C>T maps to NM_182920.1 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr3:64606904 G>A maps to NM_182920.1 R900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:64666901 T>C maps to NM_182920.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:64507915 C>A maps to NM_182920.1 G1913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:64547346 G>T maps to NM_182920.1 T1535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:64606844 G>T maps to NM_182920.1 R920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:64606836 G>A maps to NM_182920.1 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr3:64547346 G>T maps to NM_182920.1 T1535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr3:64619472 G>A maps to NM_182920.1 R647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr9:18753367 C>T maps to NM_001040272.4 C693C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:18906803 G>A maps to NM_001040272.4 V1692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:18775763 C>T maps to NM_001040272.4 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:18533266 C>T maps to NM_001040272.4 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:18533262 T>C maps to NM_001040272.4 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:18795427 C>A maps to NM_001040272.4 I1237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr9:18684798 G>C maps to NM_052866.3 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:18574168 G>T maps to NM_001040272.4 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:18770601 T>C maps to NM_001040272.4 C740C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:18574168 G>T maps to NM_001040272.4 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:18770667 C>T maps to NM_001040272.4 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr9:18504909 C>T maps to NM_001040272.4 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:18574170 A>G maps to NM_001040272.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr9:18574170 A>G maps to NM_001040272.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr9:18657647 G>T maps to NM_001040272.4 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:136438987 C>T maps to ENST00000393061 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:136404995 G>A did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr9:136405807 C>T maps to ENST00000393061 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:136433532 C>T maps to ENST00000393061 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:136412259 G>A maps to ENST00000393061 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:84694028 C>T maps to NM_207517.2 C1499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr15:84581894 G>A maps to NM_207517.2 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr15:84652082 C>T maps to NM_207517.2 Q1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr15:84488783 C>A maps to NM_207517.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:84659916 C>T maps to NM_207517.2 I1308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:84539704 C>A maps to NM_207517.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:84582092 C>T maps to NM_207517.2 Y650Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr15:84488783 C>A maps to NM_207517.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:84694109 A>G maps to NM_207517.2 A1526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr15:84553919 G>A maps to NM_207517.2 W343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr15:84324538 G>A maps to NM_207517.2 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:84566626 C>T maps to NM_207517.2 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr15:84527522 G>T maps to NM_207517.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr15:84705704 T>A maps to NM_207517.2 I1645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:84581879 G>A maps to NM_207517.2 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:150526087 C>T maps to ENST00000369039 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:150529434 C>T maps to ENST00000369039 N613N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:150526087 C>T maps to ENST00000369039 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:150526264 G>A maps to ENST00000369039 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:150525555 G>A maps to ENST00000369039 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr1:150531082 G>T maps to ENST00000369039 G862G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:1507270 G>A maps to NM_213604.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:966265 G>A maps to NM_006869.2 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:29283266 C>T maps to ENST00000394782 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr17:29281570 C>T maps to ENST00000394782 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr17:29272007 G>T maps to ENST00000394782 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:29281501 G>T maps to ENST00000394782 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr17:29283317 C>T maps to ENST00000394782 Y320Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:154562392 A>G maps to ENST00000292205 T879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr1:154574858 G>A maps to ENST00000292205 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:154560637 A>G maps to ENST00000292205 N1037N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:154574367 A>G maps to ENST00000292205 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:154574367 A>G maps to ENST00000292205 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:154562392 A>G maps to ENST00000292205 T879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr21:46602599 C>T maps to NM_015833.3 C393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr21:46595933 G>A maps to NM_015833.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr21:46596152 T>G maps to NM_015833.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:1246062 G>A maps to NM_018702.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:1279725 G>A maps to NM_018702.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:1245951 G>A maps to NM_018702.2 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:1405669 C>T maps to NM_018702.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr16:75646370 G>A maps to NM_012091.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:75646613 G>A maps to NM_012091.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr16:75651142 T>C maps to NM_012091.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr19:1912939 C>T maps to NM_138422.1 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:33549680 C>T maps to ENST00000373441 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:33549626 C>T maps to ENST00000373441 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr14:78392247 C>T maps to NM_020421.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:140373518 G>A maps to NM_052853.3 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:140373165 C>T maps to NM_052853.3 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:140394518 G>A maps to NM_052853.3 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:41220185 G>T maps to NM_024876.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:41198067 G>A maps to NM_024876.3 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr19:41216021 C>A maps to NM_024876.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr8:145616371 C>G maps to NM_174922.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:145616595 G>A maps to NM_174922.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr7:45725775 C>T maps to NM_021116.2 Y763Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:45744181 C>T maps to NM_021116.2 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:45632458 G>A maps to NM_021116.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr7:45750181 C>T maps to NM_021116.2 Y996Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:45662326 C>T maps to NM_021116.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:45699745 C>T maps to NM_021116.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:45697379 G>T maps to NM_021116.2 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:45742988 A>G maps to NM_021116.2 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:167814852 G>A maps to NM_018417.4 N985N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:167814993 G>A maps to NM_018417.4 Y938Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr1:167852755 G>A maps to NM_018417.4 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:167793976 G>A maps to NM_018417.4 G1289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:167829050 C>T maps to NM_018417.4 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:167778932 G>A maps to NM_018417.4 T1605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:167779025 C>T maps to NM_018417.4 T1574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:167802283 G>A maps to NM_018417.4 V1178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:167815496 G>T maps to NM_018417.4 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:167839592 A>G maps to NM_018417.4 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:167852755 G>A maps to NM_018417.4 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr5:7727284 C>A maps to NM_020546.2 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:7396597 C>T maps to NM_020546.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:7802383 G>A maps to NM_020546.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr5:7802410 C>T maps to NM_020546.2 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr5:7789858 C>T maps to NM_020546.2 N858N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:7520954 C>T maps to NM_020546.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:7414705 G>A maps to NM_020546.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:7817086 C>T maps to NM_020546.2 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr5:7695918 G>A maps to NM_020546.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:7695882 C>T maps to NM_020546.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:7789867 C>T maps to NM_020546.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:7826971 C>T maps to NM_020546.2 N1088N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:7802365 C>T maps to NM_020546.2 V888V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:7789867 C>T maps to NM_020546.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:7724693 A>C maps to NM_020546.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:25047357 G>A maps to NM_004036.3 H875H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:25141469 C>A maps to NM_004036.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:25141679 C>T maps to NM_004036.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:25059815 C>T maps to NM_004036.3 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:25044452 C>T maps to NM_004036.3 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:25046125 A>G maps to NM_004036.3 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:25057802 G>T maps to NM_004036.3 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr14:24791316 A>C maps to NM_139247.3 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:24787943 G>A maps to NM_139247.3 A999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:24801826 G>A maps to NM_139247.3 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:123018971 G>A maps to NM_183357.2 N965N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:123166519 G>A maps to NM_183357.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:123014981 G>A maps to NM_183357.2 H1004H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:123022949 G>T maps to NM_183357.2 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:123005606 A>G maps to NM_183357.2 P1194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:123010121 G>A maps to NM_183357.2 R1055R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:49170329 G>A maps to NM_015270.3 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr12:49164714 G>T maps to NM_015270.3 I1030I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr12:49176638 C>G maps to NM_015270.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr12:49176557 C>T maps to NM_015270.3 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:50349013 C>T maps to NM_001114.3 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:50325726 C>T maps to NM_001114.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr16:50346928 C>A maps to NM_001114.3 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:50339756 C>T maps to NM_001114.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr8:132052131 G>A maps to NM_001115.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr8:131793085 G>A maps to NM_001115.2 G1102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:131792904 C>A maps to NM_001115.2 G1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr8:131916176 A>C maps to NM_001115.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:131921973 G>A maps to NM_001115.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr8:132051772 G>A maps to NM_001115.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr8:131792812 G>A maps to NM_001115.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr8:131795990 C>A maps to NM_001115.2 E1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:131812677 G>A maps to NM_001115.2 F1018F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:131896893 G>A maps to NM_001115.2 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:131921973 G>A maps to NM_001115.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:132052012 G>A maps to NM_001115.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:132051721 C>T maps to NM_001115.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr16:4163979 G>A maps to NM_001116.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:4042331 G>A maps to NM_001116.3 N674N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:4016009 G>A maps to NM_001116.3 D1276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:4027523 G>A maps to NM_001116.3 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr16:4043427 G>A maps to NM_001116.3 D656D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:4164269 C>A maps to NM_001116.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:4015907 T>C maps to NM_001116.3 R1310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:4024695 C>T maps to NM_001116.3 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr16:4042223 C>T maps to NM_001116.3 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:4029173 C>T maps to NM_001116.3 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:4016177 G>A maps to NM_001116.3 G1220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:31125011 G>A maps to ENST00000409489 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr7:31125023 G>A maps to ENST00000409489 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:2930141 C>T maps to NM_014189.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr4:2916684 C>A maps to NM_014189.2 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:70890766 C>T maps to NM_001185054.1 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr2:70931501 C>T maps to NM_001185054.1 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:70890805 C>T maps to NM_001185054.1 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:70933507 C>T maps to NM_001185054.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr2:70919534 C>T maps to NM_001185054.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr2:70903945 G>A maps to NM_001185054.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:70933561 C>T maps to NM_001185055.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:70905960 G>A maps to NM_001185054.1 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:70905958 T>C maps to NM_001185054.1 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:70905960 G>A maps to NM_001185054.1 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:111872674 T>C did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr10:111860546 C>T maps to NM_016824.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr4:100205627 C>T maps to NM_000667.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr4:100235223 A>G maps to NM_000668.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr4:100235022 T>G maps to NM_000668.4 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr4:100229008 G>A maps to NM_000668.4 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:100260857 C>A maps to NM_000669.3 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:100266406 C>T maps to NM_000669.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr4:100260870 G>A maps to NM_000669.3 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:99996086 T>C maps to NM_000671.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:99993587 G>A maps to NM_000671.3 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr4:99993585 T>C maps to NM_000671.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:100348986 G>T maps to NM_000673.4 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:100341929 G>A maps to NM_000673.4 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:100349031 T>C maps to NM_000673.4 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:67372690 G>A maps to NM_144650.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:67372615 C>T maps to NM_144650.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr8:67357524 C>T maps to NM_144650.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr8:67366350 T>C maps to NM_144650.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr8:67366350 T>C maps to NM_144650.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:186572480 T>C maps to NM_004797.3 H241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:10328067 C>T maps to NM_001124.1 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr22:50921008 C>A maps to NM_024866.4 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:49520436 C>A maps to NM_181442.1 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:49509471 T>C maps to NM_181442.1 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:49508154 G>T maps to NM_181442.1 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr18:77894435 T>C maps to NM_014913.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:77896553 T>C maps to NM_014913.3 D1086D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:77894213 A>T maps to NM_014913.3 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr18:77894435 T>C maps to NM_014913.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr18:77894435 T>A maps to NM_014913.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:64565350 G>T maps to NM_032804.5 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:64565385 G>A maps to NM_032804.5 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:203134418 G>A maps to NM_001048230.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:203134554 G>T maps to NM_001048230.1 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:203098124 G>A maps to NM_001048230.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:203134421 G>A maps to NM_001048230.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:203134712 G>A maps to NM_001048230.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr22:24837096 C>T maps to NM_000675.4 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr22:24836790 G>A maps to NM_000675.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr22:24836787 G>A maps to NM_000675.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr17:15878601 C>A maps to NM_000676.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:15848597 G>T maps to NM_000676.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:15848636 C>T maps to NM_000676.2 N25N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:15878496 T>C maps to NM_000676.2 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:15878010 G>T maps to NM_000676.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:112031413 C>T maps to NM_020683.6 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:119305270 C>T maps to NM_001125.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:114078553 A>G maps to NM_138430.3 C295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:36557308 C>T maps to NM_017825.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:36558052 C>T maps to NM_017825.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:26627770 G>A maps to NM_000680.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:26722390 G>T maps to ENST00000356368 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:26722150 C>T maps to ENST00000356368 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr8:26721997 G>A maps to ENST00000356368 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:26722228 G>A maps to ENST00000356368 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:26627980 C>T maps to ENST00000356368 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:26628124 G>T maps to ENST00000356368 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:26722366 C>T maps to ENST00000356368 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr8:26627704 G>A maps to NM_000680.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:159344496 C>T maps to NM_000679.3 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:159344091 C>T maps to NM_000679.3 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr20:4228635 G>A maps to NM_000678.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:112838329 C>T maps to NM_000681.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:112838296 C>T maps to NM_000681.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:96781639 C>T maps to NM_000682.5 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr2:96781594 C>A maps to NM_000682.5 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:96781612 G>A maps to NM_000682.5 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:3768986 C>A maps to NM_000683.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr10:115804409 G>A maps to NM_000684.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:148206774 C>T maps to NM_000024.5 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:148207020 C>T maps to NM_000024.5 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr8:37823747 G>A maps to NM_000025.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:37823657 G>A maps to NM_000025.2 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr8:37822937 C>T maps to NM_000025.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:67051377 C>T maps to NM_001619.3 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr22:26074866 T>C maps to NM_005160.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:26083621 C>T maps to NM_005160.3 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:26107096 C>T maps to NM_005160.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr22:26086208 T>C maps to NM_005160.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr22:26074866 T>C maps to NM_005160.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr22:26114242 C>T maps to NM_005160.3 H562H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr22:26074866 T>C maps to NM_005160.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr22:26074866 T>C maps to NM_005160.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr20:60882684 A>G maps to NM_175573.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:60879584 C>T maps to NM_175573.1 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:40754874 C>T maps to ENST00000428371 Q591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:40762492 C>T maps to NM_000026.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:40762492 C>T maps to NM_000026.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr22:40745999 T>C maps to ENST00000428371 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr22:40745999 T>C maps to ENST00000428371 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:244587289 G>A maps to NM_001126.3 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:244574618 G>A maps to NM_001126.3 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:244587340 G>A maps to NM_001126.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:244587340 G>A maps to NM_001126.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:244587340 G>A maps to NM_001126.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:105207578 C>T maps to NM_199165.1 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:105209438 G>A maps to NM_199165.1 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:105212645 C>T maps to NM_199165.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:105209528 G>A did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr7:44152233 C>T maps to NM_001129.3 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr7:44151763 G>A maps to NM_001129.3 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:44152233 C>T maps to NM_001129.3 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr7:44153418 C>T maps to NM_001129.3 T1012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:19626225 A>T maps to NM_001114176.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:89172518 G>A maps to NM_022767.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:3057709 A>G maps to NM_198969.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr4:7820854 G>C maps to NM_001134647.1 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr4:7780552 C>T maps to NM_001134647.1 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:7811443 C>T maps to NM_001134647.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:148687127 C>T maps to NM_152406.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr5:148695849 G>A maps to NM_152406.2 E417E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:148685905 C>T maps to NM_152406.2 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr5:148686977 C>T maps to NM_152406.2 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:116068255 G>A maps to NM_001001936.1 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:116075495 G>A maps to NM_001001936.1 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:116057095 G>A maps to NM_001001936.1 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:87968100 C>T maps to NM_001166693.1 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:88052294 G>T maps to NM_001166693.1 G1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr4:88056831 A>G maps to NM_001166693.1 Q1212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:88036156 C>T maps to NM_001166693.1 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:148059503 C>T did not map to a codon.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr23:147743524 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:147919256 G>T did not map to a codon.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr23:147743552 T>G did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:147743979 C>T did not map to a codon.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr23:147743445 A>G did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:148037697 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:147743553 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:148044282 A>G did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:148055086 G>A did not map to a codon.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr23:147743458 G>T did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr23:148039900 A>C did not map to a codon.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr23:148037779 G>A did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:148068926 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:148055005 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:147967475 G>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:147733535 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:148044264 C>A did not map to a codon.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr23:148037295 C>T did not map to a codon.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr23:148037644 G>A did not map to a codon.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr23:148037869 C>A did not map to a codon.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr23:148037374 C>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:147743717 C>A did not map to a codon.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr23:148048394 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:148062284 C>T did not map to a codon.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr23:147744007 G>A did not map to a codon.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr23:148039900 A>T did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:148035226 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:147743635 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:148038045 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr23:148037696 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:148068916 C>A did not map to a codon.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr23:148039911 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:148059904 T>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:148037756 C>T did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr23:148049173 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:148059507 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:147919203 T>C did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:148037200 G>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:148037387 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:147919205 C>T did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:148072797 C>A did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:148048382 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:100182038 G>T maps to NM_001025108.1 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:100185367 A>G maps to NM_001025108.1 S1001S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:100182038 G>T maps to NM_001025108.1 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:100623901 G>T maps to NM_001025108.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:100170797 G>A maps to NM_001025108.1 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:100182037 C>T maps to NM_001025108.1 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:100209980 G>A maps to NM_001025108.1 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr2:100210307 G>A maps to NM_001025108.1 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:100170917 G>A maps to NM_001025108.1 N1163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr5:132232704 T>C maps to NM_014423.3 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:132232500 G>A maps to NM_014423.3 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:132228028 T>A maps to NM_014423.3 K822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr5:132270222 A>G maps to NM_014423.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr5:132270222 A>G maps to NM_014423.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr5:132270222 A>G maps to NM_014423.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr5:132232704 T>C maps to NM_014423.3 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr5:132270222 A>G maps to NM_014423.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:12337410 G>A maps to NM_006796.2 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:12358776 C>T maps to NM_006796.2 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:12329685 C>A maps to NM_006796.2 E758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:12337432 T>C maps to NM_006796.2 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:12344229 C>T maps to NM_006796.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:12351082 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:74357771 C>T maps to NM_001133.2 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr4:74351670 A>G maps to NM_001133.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr4:74353499 G>A maps to NM_001133.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:76198670 C>T maps to NM_001145526.1 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:76183474 T>C maps to NM_001145526.1 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr4:74318182 C>T maps to NM_001134.1 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:74318131 C>T maps to NM_001134.1 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:64819162 C>T maps to ENST00000422803 D936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:64779655 G>T maps to ENST00000422803 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:64778947 G>T maps to ENST00000422803 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:178355597 G>A maps to NM_000027.3 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:236706490 C>T maps to NM_001037131.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:236708117 G>A maps to NM_001037131.1 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:236839520 C>T maps to NM_001037131.1 D479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:236659082 C>T maps to NM_001037131.1 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr2:237032579 G>A maps to NM_001037131.1 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:236957901 G>A maps to NM_001037131.1 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:88769385 C>T maps to NM_133447.1 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:58128169 C>A maps to NM_001122772.1 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr12:58124350 C>T maps to NM_001122772.1 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:58135848 A>G maps to NM_014770.2 H2H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:58121321 G>T maps to NM_001122772.1 I967I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:58124397 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:58125148 G>A maps to NM_001122772.1 N715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:58124634 G>T maps to NM_001122772.1 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr12:58123530 G>A maps to NM_001122772.1 D816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr7:150840640 C>T maps to NM_031946.4 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:150814832 C>T maps to NM_031946.4 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:150831564 C>T maps to NM_031946.4 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr7:150815601 G>A maps to NM_031946.4 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:150837145 C>A maps to NM_031946.4 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr7:150840640 C>T maps to NM_031946.4 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr7:150840511 G>T maps to NM_031946.4 G786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:46321473 G>A maps to ENST00000355953 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:51465444 G>A maps to ENST00000416142 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:86814892 C>T maps to NM_152336.2 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:86807808 C>T maps to NM_152336.2 D423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:87531319 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:86702185 A>C maps to NM_152336.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:86807790 G>A maps to NM_152336.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr15:87097659 G>A maps to NM_152336.2 E916E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:47681861 T>A maps to ENST00000357610 K860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:47711986 A>C maps to ENST00000357610 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:47707504 G>A maps to ENST00000357610 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:49119052 G>A maps to NM_032785.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:50162982 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:49119124 T>C did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:49052673 A>T maps to ENST00000416121 C268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr2:27278094 C>T maps to NM_021831.5 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:27290366 C>T maps to NM_021831.5 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr2:27291578 A>G maps to NM_021831.5 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:27278918 C>T maps to NM_021831.5 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr2:27281305 G>A maps to NM_021831.5 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:32150768 G>A maps to ENST00000375070 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:228389530 C>T maps to NM_001135187.1 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:228399681 C>T maps to NM_001135187.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:228356263 C>T maps to NM_001135187.1 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:228398469 G>A maps to NM_001135187.1 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:76330319 G>A maps to NM_018046.4 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr7:141315311 A>G maps to NM_018238.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr1:100349685 A>G maps to ENST00000311030 E774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:100345591 C>A maps to ENST00000311030 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:100327972 G>T maps to ENST00000311030 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:100347095 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:100340250 C>T maps to ENST00000311030 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr1:100349685 A>G maps to ENST00000311030 E774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:100349685 A>G maps to ENST00000311030 E774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:100349685 A>G maps to ENST00000311030 E774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr1:15900148 G>C maps to NM_024758.3 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr1:15901279 G>A maps to NM_024758.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:15905500 G>A maps to NM_024758.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:15904212 C>T maps to NM_024758.3 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:15911216 A>G maps to NM_024758.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:32137082 G>A maps to NM_032741.4 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:32137187 C>T maps to NM_032741.4 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:139571063 G>A maps to NM_006412.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:139571096 G>A maps to NM_006412.3 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr21:45390598 G>A maps to NM_001037553.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:45389132 C>T maps to NM_001037553.1 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr21:45391347 G>A maps to NM_001037553.1 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:161587354 G>A maps to NM_020133.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:161560604 C>T maps to NM_020133.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:161575339 G>A maps to NM_020133.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr8:6605332 G>A maps to NM_018361.3 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:6612680 C>T maps to NM_018361.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr8:6605347 G>A maps to NM_018361.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:6590132 C>T maps to NM_018361.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:6612620 C>T maps to NM_018361.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr8:6612657 A>C maps to NM_018361.3 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:41467378 C>T maps to NM_178819.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:84518017 G>T maps to NM_032717.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:84509417 C>T maps to NM_032717.3 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:84519855 A>C maps to NM_032717.3 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:84457783 C>T maps to NM_032717.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:78805483 T>C maps to NM_001013619.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:78805531 T>G maps to NM_001013619.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:178362465 C>T maps to NM_003659.3 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:178299105 T>C maps to NM_003659.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:178326733 T>C maps to NM_003659.3 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr2:178305756 A>G maps to NM_003659.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr2:178364458 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:977502 C>T maps to NM_198576.2 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:987180 C>T maps to NM_198576.2 N1879N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:981164 G>A maps to NM_198576.2 T863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:980778 C>A maps to NM_198576.2 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr1:982770 G>A maps to NM_198576.2 T1151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr1:980568 G>A maps to NM_198576.2 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:67517229 G>A maps to NM_001138.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:230846503 A>G maps to NM_000029.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:230839953 G>A maps to NM_000029.3 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:230839053 C>A maps to NM_000029.3 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:88193951 G>A maps to ENST00000395847 F1075F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:88204551 G>T maps to ENST00000395847 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr9:88203271 T>C maps to ENST00000395847 R948R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:88247985 G>T maps to ENST00000395847 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:88292446 A>G maps to ENST00000395847 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:88247911 A>G maps to ENST00000395847 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr9:88236186 G>A maps to ENST00000395847 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:115304184 C>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:115303975 A>G did not map to a codon.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr23:115304082 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:115304068 T>G did not map to a codon.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr23:115303650 T>A did not map to a codon.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr23:115304580 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:115304469 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:115303748 A>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:115304581 G>A did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:115304581 G>A did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:115304580 C>T did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:115304186 T>C did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr23:115304185 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:241817500 C>T maps to NM_000030.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr2:241817524 C>T maps to NM_000030.2 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:35047955 C>T maps to NM_031900.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:35039604 G>T maps to NM_031900.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr5:35014155 G>A maps to NM_031900.3 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr5:35003912 G>A maps to NM_031900.3 C464C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:35047955 C>A maps to NM_031900.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:109663681 G>A maps to NM_031279.3 C486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:109680984 G>A maps to NM_031279.3 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:109669168 T>C maps to NM_031279.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr4:109669168 T>C maps to NM_031279.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr4:109669168 T>C maps to NM_031279.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr4:109675859 G>T maps to NM_031279.3 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr5:177652372 G>A maps to NM_153373.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:177649538 G>T maps to NM_153373.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:247014084 C>T maps to ENST00000428671 T1779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:247079628 G>A maps to ENST00000428671 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:247014366 A>G maps to ENST00000428671 S1685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:247040540 T>C maps to ENST00000428671 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr1:247014366 A>G maps to ENST00000428671 S1685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr1:247014366 A>G maps to ENST00000428671 S1685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:247071040 A>G maps to ENST00000428671 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:247025322 G>A maps to ENST00000428671 R1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:247014537 G>A maps to ENST00000428671 S1628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr20:32883281 C>T maps to NM_000687.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:32883266 A>T maps to NM_000687.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr20:32878666 G>A maps to NM_000687.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:32880257 G>T maps to NM_000687.2 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr1:110560607 C>A maps to NM_006621.4 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:110559336 G>A maps to NM_006621.4 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:129037101 C>T maps to NM_015328.3 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:129019505 G>T maps to NM_015328.3 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:129028933 G>A maps to NM_015328.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:129029018 G>T maps to NM_015328.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:129053510 C>A maps to NM_015328.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:27875812 G>A maps to NM_001029882.2 C938C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr1:27875386 A>T maps to NM_001029882.2 S1080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:27875056 T>C maps to NM_001029882.2 S1190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:27878506 G>T maps to NM_001029882.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:27876985 G>A maps to NM_001029882.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:27877069 C>T maps to NM_001029882.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:27877792 G>A maps to NM_001029882.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:27878431 T>C maps to NM_001029882.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:27874573 C>T maps to NM_001029882.2 P1351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr6:135749839 A>G maps to NM_017651.4 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr6:135763774 G>A maps to NM_017651.4 H619H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:135787348 C>A maps to NM_017651.4 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr6:135787487 A>G maps to NM_017651.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:135644339 T>C maps to NM_017651.4 G1096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr6:135749839 A>G maps to NM_017651.4 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr11:62296449 C>T maps to NM_001620.1 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:62294103 G>A maps to NM_001620.1 G2595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:62286993 G>A maps to NM_001620.1 I4965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:62287413 G>A maps to NM_001620.1 I4825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:62287827 T>C maps to NM_001620.1 K4687K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:62292855 C>A maps to NM_001620.1 V3011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:62286459 G>T maps to NM_001620.1 V5143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:62287212 G>A maps to NM_001620.1 F4892F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:62286993 G>A maps to NM_001620.1 I4965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:62289563 C>A maps to NM_001620.1 E4109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:62290899 C>T maps to NM_001620.1 E3663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:62297259 T>A maps to NM_001620.1 G1543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:62289852 G>T maps to NM_001620.1 G4012G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:62286113 G>A maps to NM_001620.1 L5259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:62286513 A>G maps to NM_001620.1 S5125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:62286495 G>A maps to NM_001620.1 V5131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:62299269 C>T maps to NM_001620.1 W873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:62299350 C>T maps to NM_001620.1 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:62289522 C>T maps to NM_001620.1 L4122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:62289524 G>A maps to NM_001620.1 L4122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:62286942 A>G maps to NM_001620.1 F4982F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:62296449 C>T maps to NM_001620.1 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:62287677 G>A maps to NM_001620.1 G4737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr11:62287401 G>A maps to NM_001620.1 D4829D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr11:62285124 C>T maps to NM_001620.1 L5588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:105409181 C>T maps to NM_138420.2 P4202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr14:105416462 C>T maps to NM_138420.2 A1775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:105411302 C>T maps to NM_138420.2 S3495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:105416057 A>G maps to NM_138420.2 D1910D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:105421013 C>T maps to NM_138420.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:105408632 C>T maps to NM_138420.2 Q4385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr14:105412262 G>A maps to NM_138420.2 A3175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr14:105417779 C>T maps to NM_138420.2 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr14:105409037 C>T maps to NM_138420.2 A4250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr14:105411250 G>A maps to NM_138420.2 Q3513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:105408518 G>A maps to NM_138420.2 D4423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:105410996 G>A maps to NM_138420.2 V3597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:105412823 G>A maps to NM_138420.2 F2988F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:105415451 G>A maps to NM_138420.2 V2112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:105415766 G>A maps to NM_138420.2 I2007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr14:105416252 C>T maps to NM_138420.2 S1845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:105409988 G>A maps to NM_138420.2 S3933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:105411152 G>A maps to NM_138420.2 P3545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:105411782 C>T maps to NM_138420.2 A3335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:105416648 G>A maps to NM_138420.2 A1713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:105411254 G>A maps to NM_138420.2 S3511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:105409985 C>T maps to NM_138420.2 V3934V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:105416690 C>T maps to NM_138420.2 G1699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:105421937 C>T maps to NM_138420.2 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr14:105415232 G>A maps to NM_138420.2 A2185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:105413903 C>T maps to NM_138420.2 A2628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:105414467 G>A maps to NM_138420.2 P2440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr14:105414314 C>T maps to NM_138420.2 P2491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:105408032 G>A maps to NM_138420.2 P4585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:17378624 A>C maps to NM_001621.4 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:17349712 C>T maps to NM_001621.4 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr7:17382603 T>C maps to NM_001621.4 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:17370461 C>T maps to NM_001621.4 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:17382603 T>C maps to NM_001621.4 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr7:17382603 T>C maps to NM_001621.4 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr7:17382603 T>C maps to NM_001621.4 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:433965 A>G did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr5:434621 C>T maps to NM_020731.3 H611H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:186331019 G>A maps to ENST00000273784 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:186333472 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:186338616 G>A maps to ENST00000273784 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr3:186338466 C>T maps to ENST00000273784 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr12:8758006 G>A maps to NM_020661.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:8758078 G>A maps to NM_020661.2 N53N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:222867563 A>G maps to NM_022831.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:129263596 T>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:129283519 A>G did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:129283519 A>G did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:129283453 G>A did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:129299597 A>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:129272595 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:129274570 C>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:129283519 A>G did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:129263994 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:129265758 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:129271122 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:129283520 T>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:129271123 G>T did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:129263595 T>C did not map to a codon.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr23:129283520 T>C did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:129271122 G>T did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:129271122 G>A did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:129263595 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:129283519 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:129271122 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:129283532 G>T did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:129271122 G>A did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:129273833 C>A did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:129263594 C>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:71874808 G>A maps to NM_032797.5 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:21330798 C>T maps to NM_144704.2 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:21327653 G>A maps to NM_144704.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr22:21329041 C>T maps to NM_144704.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:143605290 G>A maps to NM_016108.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:106992557 C>T maps to NM_001624.2 R1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:106992491 C>T maps to NM_001624.2 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:106968376 A>G maps to NM_001624.2 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:107009237 C>T maps to NM_001624.2 R1593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:106967686 A>C maps to NM_001624.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:106968097 A>G maps to NM_001624.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:106973036 C>A maps to NM_001624.2 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:106960726 C>T maps to NM_001624.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr6:106968505 T>C maps to NM_001624.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr1:26664940 G>A maps to NM_001039775.3 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:26658051 G>A maps to NM_001039775.3 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr1:26650702 G>A maps to NM_001039775.3 A1559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:159032496 G>T maps to NM_004833.1 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:159035965 C>A maps to NM_004833.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:159033349 G>A maps to NM_004833.1 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:107248642 C>T maps to NM_001142416.1 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:6063210 A>G maps to NM_006303.3 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:4832546 G>A maps to NM_018836.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:4829943 C>T maps to NM_018836.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:4772523 G>A maps to NM_018836.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:4772688 G>A maps to NM_018836.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:33480161 G>A maps to NM_001625.3 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:4719245 C>T maps to NM_016282.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:4722617 G>A maps to NM_016282.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr9:4741075 G>A maps to NM_016282.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:65691784 G>A maps to NM_013410.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:65691814 T>C maps to NM_013410.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:77883339 T>C maps to NM_174858.1 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:77883327 A>G maps to NM_174858.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:78001626 C>T maps to NM_174858.1 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:77759476 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr14:96953317 C>A maps to NM_152327.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:96875238 G>A maps to NM_152327.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr14:96917801 G>A maps to NM_152327.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:96875277 C>A maps to NM_152327.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:55183367 C>T maps to ENST00000427138 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:55194232 C>A maps to ENST00000427138 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr17:19839631 A>T maps to NM_007202.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:19839690 A>G maps to NM_007202.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr17:19827746 T>C maps to NM_007202.2 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:19839688 T>C maps to NM_007202.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr13:42877609 A>G maps to NM_016248.2 A1576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr13:42877912 C>T maps to NM_016248.2 I1677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:42875392 T>C maps to NM_016248.2 C837C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:42871242 T>C maps to NM_016248.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:42877859 G>T maps to NM_016248.2 E1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:42876272 G>T maps to NM_016248.2 E1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr6:151672213 C>T maps to NM_005100.3 V896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:151669939 G>A maps to NM_005100.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:151672534 G>A maps to NM_005100.3 V1003V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:151673068 C>T maps to NM_005100.3 D1181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr6:151670377 G>A maps to NM_005100.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:151671725 G>T maps to NM_005100.3 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:151673890 G>A maps to NM_005100.3 E1455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:151674610 G>A maps to NM_005100.3 P1695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:151670380 T>C maps to NM_005100.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr6:151672776 C>A maps to NM_005100.3 S1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr6:151672642 T>C maps to NM_005100.3 T1039T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr6:151670303 C>T maps to NM_005100.3 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr6:151673257 G>A maps to NM_005100.3 E1244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:151671214 C>T maps to NM_005100.3 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr15:86118502 T>C maps to NM_006738.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:86228046 A>G maps to NM_006738.4 K1748K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr15:86273921 A>G maps to NM_006738.4 K2426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr15:86286790 G>A maps to NM_006738.4 S2713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr15:86253846 C>A maps to NM_006738.4 S1861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr15:86266519 G>C maps to NM_006738.4 V2242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:119048781 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:119054484 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:119054495 A>C did not map to a codon.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr9:112900133 C>T maps to NM_007203.4 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:112899186 G>T maps to NM_007203.4 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:112898624 C>T maps to NM_007203.4 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr9:112918755 C>T maps to NM_007203.4 R1051R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:112899527 G>A maps to NM_007203.4 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:112898666 C>A maps to NM_007203.4 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr9:112899527 G>A maps to NM_007203.4 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr12:4737860 C>A maps to NM_006422.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:4736311 C>A maps to NM_006422.2 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr12:4737041 G>A maps to NM_006422.2 H342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:4736171 C>T maps to NM_006422.2 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:4724973 G>A maps to NM_006422.2 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:49958342 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:49958928 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:49957284 G>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:49958791 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:49958206 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:49957593 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:49958421 G>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:49958748 G>A did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:49958205 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:49958921 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:49958600 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:49961556 C>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:49958442 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:49957703 A>G did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr23:49957692 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:49961618 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:49957692 G>T did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:49958749 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:49958900 A>G did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr14:64935669 C>T maps to NM_004857.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:64936051 G>T maps to NM_004857.3 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:64936051 G>T maps to NM_004857.3 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:33165303 G>A maps to NM_004274.4 Q996Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr14:33292208 C>T maps to NM_004274.4 S1730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr14:32902866 C>T maps to NM_004274.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr14:33147545 A>G maps to NM_004274.4 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr14:33293450 G>T maps to NM_004274.4 S2144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr14:33290897 T>C maps to NM_004274.4 N1293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:32902839 C>T maps to NM_004274.4 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:33242900 C>A maps to NM_004274.4 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:33292343 C>T maps to NM_004274.4 D1775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr14:33293555 T>C maps to NM_004274.4 S2179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:33014666 C>T maps to NM_004274.4 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:33293817 G>T maps to NM_004274.4 E2267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:33014897 G>T maps to NM_004274.4 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:33291578 A>G maps to NM_004274.4 P1520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr14:33015179 T>C maps to NM_004274.4 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr14:33293555 T>C maps to NM_004274.4 S2179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr14:33291578 A>G maps to NM_004274.4 P1520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:33242907 C>T maps to NM_004274.4 R1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr14:33015179 T>C maps to NM_004274.4 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr14:33147545 A>G maps to NM_004274.4 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr14:33291438 C>T maps to NM_004274.4 Q1474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr14:33291989 C>A maps to NM_004274.4 I1657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:131602739 G>A maps to ENST00000431975 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:131490292 G>T maps to ENST00000431975 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr6:131602691 C>T maps to ENST00000431975 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr6:131490396 A>G maps to ENST00000431975 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr6:131490396 A>T maps to ENST00000431975 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:15465890 G>A maps to NM_005858.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:15465905 C>T maps to NM_005858.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:15484054 G>A maps to NM_005858.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:15484003 G>A maps to NM_005858.2 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr19:15508590 C>T maps to NM_014371.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:15511139 A>G maps to NM_014371.2 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr7:91674348 A>G maps to NM_005751.4 R1730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr7:91631175 C>T maps to NM_005751.4 R649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:91726632 C>T maps to NM_005751.4 R3454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:91682215 C>T maps to NM_005751.4 R1849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr7:91726991 A>G maps to NM_005751.4 K3497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:91630311 G>T maps to NM_005751.4 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:91631426 A>G maps to NM_005751.4 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:91711865 G>T maps to NM_005751.4 E2684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:91652167 T>C maps to NM_005751.4 L1331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:91652291 C>T maps to NM_005751.4 Q1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:91630472 C>T maps to NM_005751.4 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:91700277 A>G maps to NM_005751.4 V2189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:91731943 C>T maps to NM_005751.4 R3712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:91603143 T>C maps to NM_005751.4 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:91641909 G>A maps to NM_005751.4 Q1162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:91711951 T>C maps to NM_005751.4 A2712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr7:91667979 T>G maps to NM_005751.4 L1529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:91682256 T>C maps to NM_005751.4 S1862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr7:91722505 G>T maps to NM_005751.4 E3152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr7:91674348 A>G maps to NM_005751.4 R1730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr7:91711951 T>C maps to NM_005751.4 A2712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr6:109837155 A>G maps to NM_001145128.2 F1323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:109962806 G>A maps to NM_001145128.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:109993197 G>A maps to NM_001145128.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:109818756 A>C maps to NM_001145128.2 A1742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:109835534 C>A maps to NM_001145128.2 E1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:109940433 G>A maps to NM_001145128.2 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr6:109995407 A>G maps to NM_001145128.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr6:109996870 C>T maps to NM_001145128.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr6:109854527 C>A maps to NM_001145128.2 E1166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:109871411 C>A maps to NM_001145128.2 G949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:109854525 T>C maps to NM_001145128.2 E1166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:88385617 A>G maps to NM_018064.3 H187H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr9:117120254 G>A maps to NM_030767.4 I895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:117113142 G>A maps to NM_030767.4 R1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr9:117119198 T>C maps to NM_030767.4 E930E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:117139234 C>T maps to NM_030767.4 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:109395256 C>T maps to NM_152763.3 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:109391429 C>A maps to NM_152763.3 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:46027471 G>A maps to NM_153326.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:46032599 C>T maps to NM_153326.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:134133182 G>A maps to NM_001628.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:134133769 C>T maps to NM_001628.2 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:134130003 G>T maps to NM_001628.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:134133182 G>A maps to NM_001628.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr7:134217820 G>A maps to NM_020299.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr7:134221873 G>A maps to NM_020299.4 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:134223760 C>T maps to NM_020299.4 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:134252930 G>T maps to ENST00000418096 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:5014390 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:5008131 C>T maps to NM_001353.5 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr10:5008131 C>T maps to NM_001353.5 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr10:5008131 C>T maps to NM_001353.5 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr10:5043830 C>A maps to NM_001354.4 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:5141526 G>A maps to NM_003739.4 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:5247766 C>T maps to NM_001818.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:5247766 C>T maps to NM_001818.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:137792314 G>T maps to NM_005989.3 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:4877926 C>T maps to NM_001040177.1 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:19632583 G>A maps to NM_003689.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:105240284 G>A maps to NM_001014432.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr14:105240257 G>A maps to NM_001014432.1 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:105239665 G>A maps to NM_001014432.1 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr19:50376401 G>A maps to ENST00000391835 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:40741936 G>A maps to NM_001626.3 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:40761147 C>T maps to NM_001626.3 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:40740993 C>A maps to NM_001626.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:40747961 G>A maps to NM_001626.3 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:40741045 T>C maps to NM_001626.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:40761147 C>T maps to NM_001626.3 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:40743923 C>T maps to NM_001626.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:243668607 G>A maps to NM_005465.3 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:116151290 G>C maps to ENST00000277315 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr9:116151290 G>A maps to ENST00000277315 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:55042153 T>C did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:55044055 A>G did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:55044077 C>T did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr23:55039969 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:55039972 G>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:55047635 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:55046844 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:55047633 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:55043986 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:55051257 G>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:55044077 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:55041425 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:74281974 C>T maps to NM_000477.5 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:74276060 G>A maps to NM_000477.5 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr4:74279228 C>T maps to NM_000477.5 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:74281974 C>T maps to NM_000477.5 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:74276114 T>C maps to NM_000477.5 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr4:74276114 T>C maps to NM_000477.5 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:74276114 T>C maps to NM_000477.5 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr4:74275110 T>C maps to NM_000477.5 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr4:74276114 T>C maps to NM_000477.5 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:105252517 A>G maps to NM_001627.2 L177L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AD-6899-01A-11D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:105239010 T>G maps to NM_001627.2 Y58*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D5-6923-01A-11D-1924-10. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-DM-A1HA-01A-11D-A152-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:105271366 T>C maps to NM_001627.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:49969084 C>T maps to NM_153329.3 N553N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:49967706 C>T maps to NM_153329.3 H455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr19:49965879 G>A maps to NM_153329.3 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:49967706 C>T maps to NM_153329.3 H455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:49967406 C>A maps to NM_153329.3 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:97376278 G>T maps to NM_002860.3 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:97397088 G>A maps to NM_002860.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:97366613 G>A maps to NM_002860.3 R765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr9:75543930 C>A maps to NM_000689.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:75527002 G>T maps to NM_000689.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:58247397 G>C maps to NM_003888.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr15:58256268 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:101434181 G>T maps to NM_000693.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr15:101440828 C>T maps to NM_000693.2 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:38396959 C>T maps to NM_000692.3 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:125869308 C>T maps to ENST00000273450 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:125879750 G>A maps to ENST00000273450 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr3:125826003 G>A maps to ENST00000273450 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:125850316 C>T maps to ENST00000273450 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:125873402 A>T maps to ENST00000273450 C248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:125877288 C>T maps to ENST00000273450 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:125876302 C>T maps to ENST00000273450 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr3:125826048 G>A maps to ENST00000273450 D806D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:105434388 G>A maps to NM_001034173.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:105420515 G>A maps to NM_001034173.3 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:105455464 C>T maps to NM_001034173.3 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:105464409 G>A maps to NM_001034173.3 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:105454759 T>G maps to NM_001034173.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:19575148 T>C maps to NM_001031806.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr17:19566799 G>A maps to NM_001031806.1 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr17:19575148 T>C maps to NM_001031806.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr17:19575148 T>C maps to NM_001031806.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:67786360 A>C maps to NM_001161473.1 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:67431175 G>A maps to NM_001031615.1 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:19202916 T>C maps to NM_003748.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:19215894 A>G maps to NM_003748.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:19203969 C>T maps to NM_003748.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:24520642 C>T maps to NM_170740.1 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:24532349 C>T maps to NM_170740.1 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:24520765 T>G maps to NM_170740.1 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr6:24515537 G>A maps to NM_170740.1 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr6:24533774 G>A maps to NM_170740.1 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr14:74534116 C>T maps to NM_005589.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:125904008 G>T maps to NM_001182.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:125885885 A>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:125895024 G>T maps to NM_001182.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:125885901 G>T maps to NM_001182.3 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr5:125887745 A>G maps to NM_001182.3 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:135239873 A>T maps to NM_022568.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr6:135265011 C>T maps to NM_022568.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:165651347 G>T maps to NM_000696.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:104192138 G>A maps to NM_000035.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:104184120 C>T maps to NM_000035.3 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:5128853 G>A maps to NM_019109.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:5122058 G>A did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr16:5132656 T>C maps to NM_019109.4 C390C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:34179048 G>A maps to NM_032834.3 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:34179139 T>C maps to NM_032834.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:38714423 C>T maps to NM_001013620.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:38714657 T>G maps to NM_001013620.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:38714423 C>T maps to NM_001013620.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr12:38714631 T>C maps to NM_001013620.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:38714999 A>G maps to NM_001013620.3 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:52599065 T>C maps to NM_001004127.2 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:52593264 A>G maps to NM_001004127.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr13:52593264 A>G maps to NM_001004127.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:110963367 G>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:110970860 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:110971417 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:110987992 A>T did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:110970905 C>A did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:111000948 T>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:110987992 A>T did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:110987998 T>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:110931223 A>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:110988022 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:110970569 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:110925418 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:110988004 T>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:110956512 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr23:110970046 G>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:110928263 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:110964890 G>A did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr23:110987995 A>T did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:111003079 G>T did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:110987995 A>T did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:110970893 T>C did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:110987995 A>T did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:111000948 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:111000949 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:110961350 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:111003073 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:95448769 G>A maps to NM_144988.3 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:183963387 G>A maps to NM_005787.5 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr13:37526711 G>A maps to NM_013338.4 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:37539737 C>T maps to NM_013338.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:63902531 G>A maps to ENST00000263440 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:63881567 G>A maps to ENST00000263440 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:63881555 G>A maps to ENST00000263440 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:77815465 C>T maps to NM_024079.4 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:77838456 G>A maps to NM_024079.4 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:77823707 G>A maps to NM_024079.4 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:111711401 G>A maps to ENST00000428306 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr11:111724115 T>C maps to ENST00000428306 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr11:111724115 T>C maps to ENST00000428306 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr11:111724115 T>C maps to ENST00000428306 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr11:111680488 G>A maps to ENST00000428306 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:29917878 A>G maps to NM_004304.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr2:29446382 T>A maps to NM_004304.3 K1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:29455170 T>C maps to NM_004304.3 A877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:29416569 G>T maps to NM_004304.3 I1461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr2:29445424 G>A maps to NM_004304.3 S1136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr2:29443697 T>C maps to NM_004304.3 K1173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr2:29455173 G>A maps to NM_004304.3 A876A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr2:29498048 T>A maps to NM_004304.3 R653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:29940474 G>A maps to NM_004304.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr2:29519767 G>A maps to NM_004304.3 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:29606700 G>A maps to NM_004304.3 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:29462662 G>A maps to NM_004304.3 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:29519818 G>A maps to NM_004304.3 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:29606678 G>A maps to NM_004304.3 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:30143306 C>T maps to NM_004304.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:29416368 G>A maps to NM_004304.3 H1528H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:29940444 A>T maps to NM_004304.3 Y262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr2:29498349 C>T maps to NM_004304.3 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:29446229 G>T maps to NM_004304.3 R1113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr2:29541190 C>T maps to NM_004304.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:29473981 G>A maps to NM_004304.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr2:29432662 T>C maps to NM_004304.3 R1275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr2:29416320 G>A maps to NM_004304.3 N1544N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr2:29445211 G>T maps to NM_004304.3 I1171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr2:29541190 C>A maps to NM_004304.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr2:29436890 G>T maps to NM_004304.3 A1234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:29541190 C>A maps to NM_004304.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:109530488 C>A maps to NM_001145375.1 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:43923166 C>T maps to NM_139178.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:102097990 C>T maps to NM_017621.3 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:102100113 G>A maps to NM_017621.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:18098292 T>G maps to ENST00000261650 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:18110176 C>T maps to ENST00000261650 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:107427548 C>A maps to ENST00000417449 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:107375478 C>A maps to ENST00000417449 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:3726106 G>A maps to ENST00000403787 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:3727550 C>T maps to ENST00000403787 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr2:3749153 A>G maps to ENST00000403787 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:73678837 C>T maps to NM_015120.4 D1727D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:73653608 C>T maps to NM_015120.4 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:73675156 T>A maps to NM_015120.4 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr2:73717194 G>A maps to NM_015120.4 P2702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:73716867 T>C maps to NM_015120.4 H2593H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:73828376 C>T maps to NM_015120.4 N3975N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:73800037 G>A maps to NM_015120.4 R3677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:73675232 G>T maps to NM_015120.4 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:73718040 T>C maps to NM_015120.4 F2984F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:73718580 C>T maps to NM_015120.4 F3164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:73677628 G>T maps to NM_015120.4 V1324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:73676230 G>A maps to NM_015120.4 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:73680673 G>A maps to NM_015120.4 T2339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:73651832 C>A maps to NM_015120.4 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:73717424 C>A maps to NM_015120.4 S2779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr2:73679560 T>C maps to NM_015120.4 P1968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:73679818 T>C maps to NM_015120.4 N2054N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:73676995 T>C maps to NM_015120.4 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:73799824 G>A maps to NM_015120.4 E3606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr2:73716957 C>T maps to NM_015120.4 A2623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:73679098 C>G maps to NM_015120.4 S1814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:73676551 G>A maps to NM_015120.4 Q965Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:73677832 A>G maps to NM_015120.4 Q1392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:73653608 C>T maps to NM_015120.4 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:6900227 C>T maps to NM_000697.2 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:6909199 C>T maps to NM_000697.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:6903659 T>C maps to NM_000697.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:6902758 C>T maps to NM_000697.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:6913096 A>G maps to NM_000697.2 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr17:7990679 C>A maps to NM_001139.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:7976992 A>G maps to NM_001139.2 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr17:7979503 A>G maps to NM_001139.2 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:7976220 C>T maps to NM_001139.2 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:7976247 C>T maps to NM_001139.2 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:7979608 C>T maps to NM_001139.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr17:4534948 G>A maps to NM_001140.3 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:4535209 G>A maps to NM_001140.3 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:4535336 A>G maps to NM_001140.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:4539179 G>A maps to NM_001140.3 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:4540430 T>C maps to NM_001140.3 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:4540412 G>T maps to NM_001140.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr17:7950307 T>C maps to NM_001141.2 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:7942759 C>T maps to NM_001141.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr17:7948892 C>T maps to NM_001141.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr10:45891366 A>G maps to NM_000698.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:45877941 C>T maps to NM_000698.2 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:45878097 C>T maps to NM_000698.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr10:45877980 G>A maps to NM_000698.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:45891355 G>T maps to NM_000698.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr10:45878103 C>T maps to NM_000698.2 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:45877968 C>T maps to NM_000698.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:8020175 G>T maps to ENST00000380149 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:8007504 T>C maps to ENST00000380149 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:8012556 G>A maps to ENST00000380149 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr17:8012523 G>A maps to ENST00000380149 D666D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:8011846 C>T maps to ENST00000380149 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:8020130 A>G maps to ENST00000380149 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:7999968 G>T maps to ENST00000380149 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr2:233322984 G>T maps to NM_001631.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr2:233323597 G>A maps to NM_001631.3 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:233322984 G>A maps to NM_001631.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:233323375 C>A maps to NM_001631.3 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:113333026 G>T maps to NM_025144.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:113352091 T>C maps to NM_025144.3 H463H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:113351827 C>T maps to NM_025144.3 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr18:56184319 C>T maps to NM_052947.3 T1920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr18:56202933 C>T maps to NM_052947.3 L1495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr18:56204409 C>T maps to NM_052947.3 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr18:56205084 G>T maps to NM_052947.3 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr18:56202375 C>T maps to NM_052947.3 A1681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:56274624 G>A maps to NM_052947.3 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr18:56184259 G>A maps to NM_052947.3 H1940H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:56203131 G>A maps to NM_052947.3 G1429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:56247689 G>A maps to NM_052947.3 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr18:56246465 C>A maps to NM_052947.3 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr18:56204114 G>A maps to NM_052947.3 Q1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr18:56204592 T>C maps to NM_052947.3 E942E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:56246909 G>A maps to NM_052947.3 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr18:56246165 G>A maps to NM_052947.3 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:85382950 C>T maps to NM_020778.4 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:85401247 A>G maps to NM_020778.4 G1295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:85400116 G>A maps to NM_020778.4 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr15:85383454 G>A maps to NM_020778.4 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr15:85400842 T>C maps to NM_020778.4 D1160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:85399648 T>C maps to NM_020778.4 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:85370762 G>A maps to NM_020778.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr15:85401517 T>A maps to NM_020778.4 P1385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:21903981 C>T maps to NM_000478.4 H472H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:21889685 C>T maps to NM_000478.4 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:21887155 G>A maps to NM_000478.4 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr1:21889697 C>T maps to NM_000478.4 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr2:233246012 C>T maps to NM_001632.3 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr2:233245140 T>C maps to NM_001632.3 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:233274359 C>T maps to NM_031313.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:202569241 G>A maps to NM_020919.3 H1591H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:202614432 A>G did not map to a codon.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr2:202587822 G>A maps to NM_020919.3 S1215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:202574758 G>T maps to NM_020919.3 A1375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:202569301 T>C maps to NM_020919.3 K1571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:202593906 C>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:202592489 C>T maps to NM_020919.3 T950T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr2:202619284 T>C maps to NM_020919.3 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr3:46721931 C>T maps to NM_147129.3 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:46719777 G>T maps to NM_147129.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:46723045 G>A maps to NM_147129.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:46717820 G>A maps to NM_147129.3 Y700Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:46722887 G>A maps to NM_147129.3 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr3:46721988 G>A maps to NM_147129.3 H493H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr2:202352478 C>T maps to NM_001168221.1 P1773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:202466488 G>A maps to NM_001168221.1 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:202400899 G>A maps to NM_001168221.1 N450N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:202436668 G>A maps to NM_001168221.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:202352429 G>A maps to NM_001168221.1 R1790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:202412329 C>A maps to NM_001168221.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr2:202483769 C>T maps to NM_001168221.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr2:202401013 C>A maps to NM_001168221.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:202172322 G>A maps to NM_139163.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:202173901 G>A maps to NM_139163.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:202172307 T>C maps to NM_139163.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:202208957 G>A maps to NM_139163.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:202195245 C>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:202172307 T>C maps to NM_139163.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr2:202208955 T>C maps to NM_139163.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr2:202498080 C>T maps to ENST00000409099 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:203807551 T>C maps to NM_024744.14 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:85674185 C>T maps to NM_006982.2 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:85680719 T>C maps to NM_006982.2 Y207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:110603357 C>T maps to NM_006492.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr1:110604182 G>T maps to NM_006492.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:33521100 G>A maps to NM_152462.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:11188668 G>A maps to NM_054028.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:7385419 C>T maps to NM_001102614.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr5:33989380 G>A maps to NM_001167595.1 D322D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CK-6746-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr4:71472191 C>T maps to NM_016519.4 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:71471987 C>T maps to NM_016519.4 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:71471999 C>T maps to NM_016519.4 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:116831993 C>T maps to NM_001633.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr9:116836361 C>T maps to NM_001633.3 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr9:116840458 G>A maps to NM_001633.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr11:46439590 G>A maps to ENST00000458649 N996N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr11:46567212 G>A maps to ENST00000458649 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:46564498 C>T maps to ENST00000458649 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:46455112 G>A maps to ENST00000458649 R963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:46529901 G>A maps to ENST00000458649 Y726Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr12:96350677 C>T maps to NM_152435.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:96346564 G>T maps to NM_152435.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:96356152 G>A maps to NM_152435.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:96350698 C>T maps to NM_152435.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:2579037 C>T maps to NM_001145815.1 P391P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AZ-6601-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:2580609 G>A maps to NM_001145815.1 T545T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:11316901 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:11316981 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:2249537 C>T maps to NM_000479.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:2251742 C>T maps to NM_000479.3 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:53818997 C>G maps to NM_020547.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:53818568 C>T maps to NM_020547.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:118083238 C>T maps to NM_001098526.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:110050403 T>C maps to NM_020703.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:110051426 G>A maps to NM_020703.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:110051165 A>G maps to NM_020703.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr1:110050859 G>A maps to NM_020703.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:47471240 G>A maps to NM_001143668.1 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr12:47471456 C>T maps to NM_001143668.1 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr12:47472367 A>G maps to NM_001143668.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:47472367 A>G maps to NM_001143668.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:49756601 C>T maps to NM_198722.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:49756634 G>A maps to NM_198722.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:49756352 G>A maps to NM_198722.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:109445739 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:109445699 T>C did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:128631637 G>A maps to NM_031445.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:128628467 G>A maps to NM_031445.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr2:128627061 T>C maps to NM_031445.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr14:103389066 C>T maps to NM_030943.3 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:31850808 G>T maps to NM_001113402.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:31842007 G>A maps to NM_001113402.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:112034008 C>T did not map to a codon.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr23:112054558 T>C did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:112066114 G>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:112022307 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:112024257 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:112022856 G>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:112024269 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:112033861 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:112053119 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:112022765 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:112065720 T>C did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr23:112066059 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:112065759 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:112022814 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr23:112021860 T>C did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr11:94532787 C>T maps to NM_130847.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:94532970 G>A maps to NM_130847.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr11:94528287 T>A maps to NM_130847.2 L54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:94533342 G>A maps to NM_130847.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:94583283 G>T maps to NM_130847.2 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:94528270 G>A maps to NM_130847.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:94597938 C>T maps to NM_130847.2 Y725Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:94602447 C>A maps to NM_130847.2 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr11:94554842 C>T maps to NM_130847.2 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr11:94602576 G>A maps to NM_130847.2 T901T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:134086427 G>A maps to ENST00000514516 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:134079138 G>A maps to ENST00000514516 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:134079063 C>T maps to ENST00000514516 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:115220553 C>A maps to NM_000036.2 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:115229484 G>A maps to NM_000036.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:115216604 A>G maps to NM_000036.2 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:110170838 C>A maps to ENST00000393689 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr1:110170089 A>G maps to ENST00000393689 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:110173662 C>T maps to ENST00000393689 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:110172892 C>T maps to ENST00000393689 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:10506535 C>A maps to NM_000480.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:10500071 G>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:10523122 C>T maps to NM_000480.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr7:38670905 G>A maps to NM_001635.3 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:38505083 G>A maps to NM_001635.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr7:38433613 T>C maps to NM_001635.3 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:38505101 G>A maps to NM_001635.3 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:38574563 G>A maps to NM_001635.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:38543282 G>A maps to NM_001635.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:38433622 G>A maps to NM_001635.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:38574602 T>C maps to NM_001635.3 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:38502643 C>T maps to NM_001635.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:49459683 C>T maps to NM_000481.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:49455005 G>T maps to NM_000481.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:49456806 G>A maps to NM_000481.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:71384511 A>G maps to NM_212557.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:71388515 G>A maps to NM_212557.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr1:104166589 C>T maps to ENST00000305865 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:2752094 C>T maps to NM_133463.1 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:2748264 G>A maps to NM_133463.1 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr7:2752151 G>A maps to NM_133463.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:2748715 C>T maps to NM_133463.1 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:112638396 C>T maps to NM_022662.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:112592218 T>G maps to NM_022662.2 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:112545839 C>T maps to NM_022662.2 P1590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:146017245 A>C maps to NM_014885.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr4:145985783 A>G maps to NM_014885.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:140079404 G>A maps to NM_013366.3 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:140069727 G>A maps to NM_013366.3 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr4:25390356 A>G maps to ENST00000510092 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:25390132 C>A maps to ENST00000510092 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:25419838 C>T maps to ENST00000510092 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr4:25379093 A>C maps to ENST00000510092 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:121764934 G>A maps to NM_016237.4 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr12:121773427 G>C maps to NM_016237.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr12:121756397 A>G maps to NM_016237.4 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr12:121768433 A>G maps to NM_016237.4 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:110820735 G>A maps to NM_016238.2 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:110819602 A>G maps to NM_016238.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:77275489 A>G maps to NM_015305.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:77255720 C>T maps to NM_015305.3 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:213178539 C>T maps to NM_144567.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:213178593 G>A maps to NM_144567.3 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr1:213170545 C>T maps to NM_144567.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr8:108348475 A>G maps to NM_001146.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:6377501 G>T maps to NM_001147.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:6378783 C>T maps to NM_001147.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:6372208 C>A maps to NM_001147.2 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr20:854939 T>C maps to NM_015985.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr20:853740 G>A maps to NM_015985.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:178834295 G>A maps to NM_004673.3 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr1:178834374 G>A maps to NM_004673.3 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:129870763 G>A maps to NM_012098.2 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr9:129851331 G>C maps to NM_012098.2 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:129851285 G>A maps to NM_012098.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:101765792 C>A maps to NM_178127.4 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr11:101765643 A>G maps to NM_178127.4 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:101777906 A>C maps to NM_178127.4 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:10205578 C>T maps to NM_031917.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:10204055 G>A maps to NM_031917.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:41566367 G>A maps to ENST00000415018 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:41513260 C>T maps to NM_020476.2 S1877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:41545713 C>T maps to ENST00000415018 K1406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:41577199 G>T maps to ENST00000415018 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr8:41591494 T>C maps to ENST00000415018 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:41573226 A>G maps to ENST00000415018 H515H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr8:41552253 C>T maps to ENST00000415018 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr8:41542062 A>G maps to ENST00000415018 N1512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr8:41543688 A>G maps to ENST00000415018 R1457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:41553927 C>G maps to ENST00000415018 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:41553954 C>T maps to ENST00000415018 P962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:41554080 G>A maps to ENST00000415018 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:41582069 C>T maps to ENST00000415018 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr8:41552770 G>A maps to ENST00000415018 N1013N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr8:41552253 C>T maps to ENST00000415018 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr8:41522454 G>A maps to NM_020478.4 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:41580726 A>G maps to ENST00000415018 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr8:41583311 C>A maps to ENST00000415018 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:41554095 C>A maps to ENST00000415018 V915V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr8:41543688 A>G maps to ENST00000415018 R1457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:41552850 T>G did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr8:41554023 C>T maps to ENST00000415018 P939P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr8:41583365 C>T maps to ENST00000415018 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr8:41543688 A>G maps to ENST00000415018 R1457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:41566382 C>T maps to ENST00000415018 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:114274615 T>A maps to NM_001148.4 Y1614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr4:114290873 G>A maps to NM_001148.4 P3841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr4:113970949 G>A maps to NM_001148.4 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr4:114279790 G>A maps to NM_001148.4 A3339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:114177075 C>T maps to NM_001148.4 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr4:114284515 C>T maps to NM_001148.4 F3593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr4:114274778 C>T maps to NM_001148.4 L1669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:114282000 G>A maps to NM_001148.4 R3568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:114276313 C>T maps to NM_001148.4 L2180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:114277406 G>T maps to NM_001148.4 E2545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:114158159 A>G maps to NM_001148.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:114213657 C>T maps to NM_001148.4 N788N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr4:114279263 G>T maps to NM_001148.4 E3164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr4:114294250 C>T maps to NM_001148.4 D3872D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:114290888 C>T maps to NM_001148.4 L3846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:114294472 C>A maps to NM_001148.4 S3909S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:114286264 A>G maps to NM_001148.4 T3653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr4:114186087 C>T maps to NM_001148.4 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr4:114278342 G>T maps to NM_001148.4 E2857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr4:114275155 G>A maps to NM_001148.4 K1794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr4:114251429 C>T maps to NM_001148.4 R977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr4:114277912 C>T maps to NM_001148.4 V2713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr10:61829382 A>G maps to NM_020987.2 C3752C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr10:61967901 A>G maps to NM_020987.2 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:61847918 G>A maps to NM_020987.2 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr10:61829382 A>G maps to NM_020987.2 C3752C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:61959949 G>A maps to NM_020987.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr10:61832211 C>T maps to NM_020987.2 V2809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:61829889 C>T maps to NM_020987.2 T3583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:61830474 G>A maps to NM_020987.2 N3388N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:61958199 T>C maps to NM_020987.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:62149253 C>A maps to NM_020987.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:61831359 G>A maps to NM_020987.2 P3093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:61834883 G>A maps to NM_020987.2 L1919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:62023721 C>T maps to NM_020987.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr10:61829382 A>G maps to NM_020987.2 C3752C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:61967886 G>A maps to NM_020987.2 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:61994474 G>A maps to NM_020987.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:61833636 G>A maps to NM_020987.2 I2334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr10:61834056 A>G maps to NM_020987.2 P2194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:61829382 A>G maps to NM_020987.2 C3752C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr10:61829382 A>G maps to NM_020987.2 C3752C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:61868655 G>T maps to NM_020987.2 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:61832211 C>T maps to NM_020987.2 V2809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:61967940 G>A maps to NM_020987.2 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:190602524 T>C maps to NM_144708.3 L1180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:190608072 G>T maps to NM_144708.3 E1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:190592694 A>T maps to NM_144708.3 K917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:190593548 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:190569857 G>A maps to NM_144708.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:190608162 C>T maps to NM_144708.3 Q1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:190608164 A>G maps to NM_144708.3 Q1325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr2:190608164 A>G maps to NM_144708.3 Q1325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr15:65214163 A>G maps to NM_182703.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr15:65239744 G>A maps to NM_182703.3 W428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:65242155 C>T maps to NM_182703.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:54403596 C>T maps to NM_153228.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:54431391 C>T maps to NM_153228.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:54431318 C>A maps to NM_153228.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:54452043 C>T maps to NM_153228.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr17:54428210 C>T maps to NM_153228.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:54450137 C>T maps to NM_153228.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:4139121 G>A maps to NM_016376.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:4100822 G>A maps to NM_016376.3 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:4111302 C>T maps to NM_016376.3 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:4109748 G>A maps to NM_016376.3 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr17:4083021 G>A maps to NM_016376.3 N798N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:4087185 G>A maps to NM_016376.3 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:139866559 G>A maps to ENST00000253810 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:139887522 C>T maps to ENST00000253810 G1235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:139838289 A>G maps to ENST00000253810 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:139905674 G>A maps to ENST00000253810 G1529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr5:139917755 T>C maps to ENST00000253810 H2455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:139866559 G>A maps to ENST00000253810 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:139876831 G>A maps to ENST00000253810 T991T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:139838388 C>A maps to ENST00000253810 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:139887480 G>A maps to ENST00000253810 E1221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:139884482 C>T maps to ENST00000253810 Q1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:139838232 T>C maps to ENST00000253810 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr5:139917025 A>G maps to ENST00000253810 Q2377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:92020505 C>T maps to NM_019004.1 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:113270839 C>T maps to NM_178510.1 Q717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:113258695 C>T maps to NM_178510.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:113264227 G>T maps to NM_178510.1 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:113270367 C>T maps to NM_178510.1 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:113270400 G>A maps to NM_178510.1 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr19:17394220 C>T maps to NM_152363.4 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:17394931 T>C maps to NM_152363.4 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr12:133304673 C>T maps to NM_015114.1 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:241496641 C>T maps to ENST00000401804 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr2:241447027 G>T maps to ENST00000401804 A825A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:241494441 C>T maps to ENST00000401804 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:241468548 A>G maps to ENST00000401804 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:241465687 G>A maps to ENST00000401804 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:16666736 G>A maps to NM_020319.2 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:16644474 C>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:72856979 G>T maps to NM_023039.4 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:72851348 G>A maps to NM_023039.4 H192H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:72850780 G>A maps to NM_023039.4 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr10:92675392 T>G maps to NM_014391.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:92679967 C>A maps to NM_014391.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr13:111545610 C>T did not map to a codon.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr16:89346532 C>T maps to NM_013275.4 P2139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:89345818 G>A maps to NM_013275.4 D2377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:89348650 G>A maps to NM_013275.4 S1433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:89349262 C>T maps to NM_013275.4 T1229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:89352450 C>T maps to NM_013275.4 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr16:89348413 G>A maps to NM_013275.4 R1512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:89345632 G>A maps to NM_013275.4 F2439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr16:89354947 G>A maps to NM_013275.4 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr16:89345605 G>A maps to NM_013275.4 I2448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr16:89354971 C>T maps to NM_013275.4 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr16:89357084 G>A maps to NM_013275.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:89347189 C>A maps to NM_013275.4 T1920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:89349018 G>A maps to NM_013275.4 R1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:89347750 C>T maps to NM_013275.4 A1733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:89347804 G>A maps to NM_013275.4 Y1715Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:89350090 G>A maps to NM_013275.4 D953D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:9211612 G>A maps to NM_015208.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:9257446 A>G maps to NM_015208.3 P1394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:9254527 C>A maps to NM_015208.3 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:9257180 G>T maps to NM_015208.3 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:9257186 C>T maps to NM_015208.3 R1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:9211580 G>T did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr18:9256519 C>T maps to NM_015208.3 S1085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr18:9255368 A>T maps to NM_015208.3 K702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr18:9255448 A>G maps to NM_015208.3 K728K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:110467369 G>A maps to NM_033121.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:110461849 G>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:110456189 C>T maps to NM_033121.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:27936393 C>A maps to NM_152345.4 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:70728528 A>G maps to NM_030816.4 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:70766509 C>T maps to NM_030816.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:67068553 T>C maps to NM_207354.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr11:67068553 T>C maps to NM_207354.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:67069608 C>T maps to NM_207354.2 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:67068553 T>C maps to NM_207354.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:5929900 G>A maps to NM_001009941.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:5929834 A>G maps to NM_001009941.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:5929963 G>A maps to NM_001009941.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:5931161 C>T maps to NM_001009941.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:5925067 C>T maps to NM_001009941.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:5924971 A>G maps to NM_001009941.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:74014557 T>C maps to NM_032217.3 E513E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:74019690 C>A maps to NM_032217.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:73956407 G>A maps to NM_032217.3 Q2313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:74014556 C>A maps to NM_032217.3 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:73957884 T>G maps to NM_032217.3 S1820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:73957209 G>A maps to NM_032217.3 S2045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:74005392 C>T maps to NM_032217.3 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:74124064 G>A maps to NM_032217.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:73944446 C>T maps to NM_032217.3 T2440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:74005853 C>A maps to NM_032217.3 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:74019690 C>T maps to NM_032217.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:74019690 C>T maps to NM_032217.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:99338334 C>T maps to NM_020349.2 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:90591678 C>T maps to NM_144590.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr19:4216000 C>T maps to ENST00000262970 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:4216018 T>C maps to ENST00000262970 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:4217212 G>T maps to ENST00000262970 G776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:27328934 C>T maps to NM_014915.2 E778E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:27366332 G>A maps to NM_014915.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:27306673 T>C maps to NM_014915.2 L1421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:27356143 C>T maps to NM_014915.2 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:27350070 A>G did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr10:27337755 G>T maps to NM_014915.2 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:33096770 G>A maps to NM_032139.2 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:15762451 T>C maps to NM_015199.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:15727736 T>C maps to NM_015199.3 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr3:15727736 T>C maps to NM_015199.3 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:15807806 G>A maps to NM_015199.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:37506799 G>A maps to ENST00000374660 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr10:37486215 C>T maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:37490200 A>G maps to ENST00000374660 V1002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr10:37482112 G>C did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:37490212 A>G maps to ENST00000374660 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:37436299 T>C maps to ENST00000374660 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:37508137 G>A maps to ENST00000374660 G1229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr10:37455537 C>T maps to ENST00000374660 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr10:37488680 C>T maps to ENST00000374660 Q978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:37442559 G>T maps to ENST00000374660 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr10:37486215 C>T maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:37422906 A>G maps to ENST00000374660 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:37486215 C>A maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr10:37486215 C>A maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:37422906 A>G maps to ENST00000374660 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr10:37451765 A>G maps to ENST00000374660 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr10:37486215 C>A maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:37486215 C>A maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr10:37486215 C>T maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr10:37486215 C>A maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr10:37486215 C>T maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr18:14797845 C>T maps to NM_001145029.1 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:14791464 C>T maps to NM_001145029.1 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:14852181 A>G maps to NM_001145029.1 E1294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr18:14752923 G>A maps to NM_001145029.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:94030707 C>A maps to NM_032290.3 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:94024344 A>G maps to NM_032290.3 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:94014611 C>T maps to NM_032290.3 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:94001563 A>G did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr5:94022410 T>C maps to NM_032290.3 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:52283234 G>A maps to NM_182608.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr12:52285010 C>T maps to NM_182608.3 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:52283273 C>T maps to NM_001130015.1 C80C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:52282035 C>T maps to NM_182608.3 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:145473954 G>A maps to NM_001039888.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:79855250 C>T maps to NM_001004441.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:145549324 T>C maps to NM_144698.3 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:145555807 G>A maps to NM_144698.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:145560245 G>C maps to NM_144698.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:145566745 G>T maps to NM_144698.3 E950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:97784178 C>T maps to NM_001164315.1 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr2:98197004 A>G maps to NM_025190.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:98132210 C>A maps to NM_025190.3 E869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:97520142 G>A maps to NM_016466.5 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:97519206 C>T maps to NM_016466.5 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:48774410 G>A maps to NM_052855.3 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:82935966 G>A maps to ENST00000260047 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:82947449 T>C maps to ENST00000260047 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:132150839 G>A maps to NM_175873.4 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr2:197951414 G>A maps to NM_001195144.1 D435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:197878289 G>A maps to NM_001195144.1 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:197878247 T>C maps to NM_001195144.1 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:197986250 G>T maps to NM_001195144.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:197863697 G>A maps to NM_001195144.1 N866N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:197863733 G>T maps to NM_001195144.1 C854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:197990156 G>A maps to NM_001195144.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:197870556 C>A maps to NM_001195144.1 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:173579319 A>G maps to ENST00000367712 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:173616054 C>T maps to ENST00000367712 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:101541898 G>A maps to NM_198401.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:101541860 G>A maps to NM_198401.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:101541860 G>A maps to NM_198401.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:94231406 G>A maps to NM_017704.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr20:10036250 T>C maps to NM_198798.1 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:10025154 C>T maps to NM_198798.1 H220H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr20:10019236 A>C maps to NM_198798.1 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr20:10033775 C>T maps to NM_198798.1 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr20:10030770 G>T maps to NM_198798.1 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:125593422 G>A maps to NM_020337.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:125592222 G>A maps to NM_020337.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:125590198 C>T maps to NM_020337.2 K1411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:125592205 A>G maps to NM_020337.2 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:125591554 A>G maps to NM_020337.2 L959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:56649627 G>A maps to NM_173595.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:56648406 A>G maps to NM_173595.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:56651620 G>A maps to NM_173595.3 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:71206990 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr2:71212288 G>A maps to NM_001115116.1 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:71209122 C>T maps to NM_001115116.1 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:55422834 G>A maps to NM_024669.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:55455692 C>T maps to NM_024669.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:110373604 G>A maps to NM_023016.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:118893450 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:118893412 T>C did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:118893349 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:117876199 A>C maps to ENST00000357099 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr6:34952859 T>C maps to NM_015245.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:34935090 C>T maps to NM_015245.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:35048768 A>G did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr6:35047312 C>T maps to NM_015245.2 D768D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:35047671 G>A maps to NM_015245.2 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:34949576 C>T maps to NM_015245.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr6:34985641 C>T maps to NM_015245.2 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr6:35051280 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:34953006 G>A maps to NM_015245.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:35047617 C>T maps to NM_015245.2 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:100169337 G>A maps to NM_152788.3 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:99640603 C>A maps to NM_152788.3 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr12:100166796 G>T maps to NM_152788.3 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:99478701 C>G did not map to a codon.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr12:99201660 G>A maps to NM_181670.2 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:100048862 G>A maps to NM_152788.3 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr12:100048909 C>A maps to NM_152788.3 G403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:99223050 G>A maps to NM_152788.3 D989D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:4764130 C>T maps to NM_133450.2 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:4776985 A>G maps to NM_133450.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr16:4747085 C>G maps to NM_133450.2 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:101547143 G>A maps to ENST00000375018 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr9:101552551 G>A maps to ENST00000375018 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr9:101552602 C>T maps to ENST00000375018 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr9:101533310 A>C maps to ENST00000375018 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr2:220095080 C>T maps to NM_001042410.1 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr2:220099842 T>C maps to NM_001042410.1 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr7:36462287 C>T maps to NM_018685.2 N782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr7:36460247 T>C maps to NM_018685.2 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:36438784 G>A maps to NM_018685.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr7:36466558 A>T maps to NM_018685.2 R935R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:36458904 G>A maps to NM_018685.2 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr7:36483374 A>G maps to NM_018685.2 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:36466558 A>G maps to NM_018685.2 R935R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr7:36483374 A>G maps to NM_018685.2 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr7:36466556 C>T maps to NM_018685.2 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr11:69972211 C>T maps to NM_018043.5 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr11:69934096 G>A maps to NM_018043.5 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:70028642 G>A maps to NM_018043.5 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:70026155 C>A maps to NM_018043.5 I799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:70028642 G>A maps to NM_018043.5 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr11:69972184 G>A maps to NM_018043.5 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr11:69972274 C>T maps to NM_018043.5 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr11:69978153 G>A maps to NM_018043.5 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:70007370 G>A maps to NM_018043.5 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:43602845 C>A maps to NM_018075.3 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:5724461 C>T maps to ENST00000356134 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:5722087 G>A maps to ENST00000356134 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:5941724 G>A maps to ENST00000356134 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:5687595 C>T maps to ENST00000356134 R775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr12:5841760 T>G maps to ENST00000356134 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr11:26538390 C>T maps to NM_031418.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:26681883 C>T maps to NM_031418.2 R947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:101336253 G>T maps to ENST00000392977 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr12:101473024 G>A maps to ENST00000392977 W456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr12:101505455 A>G maps to ENST00000392977 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr12:101505350 T>C maps to ENST00000392977 Y771Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:101490422 A>G maps to ENST00000392977 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr12:101505350 T>C maps to ENST00000392977 Y771Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:101477520 A>G maps to ENST00000392977 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr12:101473016 T>A maps to ENST00000392977 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:22239800 C>T maps to NM_213599.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:22249050 A>G maps to NM_213599.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr11:22272304 T>A maps to NM_213599.2 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:22272295 C>A maps to NM_213599.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr11:22283795 C>A maps to NM_213599.2 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr11:22294384 T>C maps to NM_213599.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:22296290 C>T maps to NM_213599.2 C804C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr11:22294384 T>C maps to NM_213599.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr11:22283801 T>C maps to NM_213599.2 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:22284541 A>T maps to NM_213599.2 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr11:22276995 A>G maps to NM_213599.2 E420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:45810497 C>T maps to NM_001142679.1 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:45761563 C>T maps to NM_001142679.1 C364C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:45810569 A>G maps to NM_001142679.1 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:45741977 C>T maps to NM_001142679.1 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:242148794 C>T maps to NM_001001891.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr2:242147066 C>T maps to NM_001001891.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:242163196 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:242149780 G>A maps to NM_001001891.3 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:242129576 C>T maps to NM_001001891.3 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:242149756 C>T maps to NM_001001891.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr2:242148959 G>A maps to NM_001001891.3 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:242157242 C>A maps to NM_001001891.3 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:17435832 A>G maps to NM_020959.2 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:17443978 G>A maps to NM_020959.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:17441024 G>A maps to NM_020959.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:17443938 C>A maps to NM_020959.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:17443966 G>T maps to NM_020959.2 C144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:419628 G>A maps to NM_001012302.2 Y629Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:428139 G>A maps to NM_001012302.2 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr11:428519 C>T maps to NM_001012302.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr11:433873 G>T maps to NM_001012302.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr9:100760917 A>G maps to NM_006401.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:165118736 C>A maps to NM_012403.1 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:90346940 G>A maps to NM_001150.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:90347137 C>T maps to NM_001150.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:90335551 G>A maps to NM_001150.2 H789H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr15:90349529 G>A maps to NM_001150.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:90335515 G>A maps to NM_001150.2 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr15:90349529 G>T maps to NM_001150.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:90346952 C>T maps to NM_001150.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:69409701 G>A maps to NM_032208.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:69350183 C>T maps to NM_032208.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:69300211 C>A maps to NM_032208.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:69329976 C>A maps to NM_032208.2 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:69472418 C>T maps to NM_032208.2 N499N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:69472436 G>A maps to NM_032208.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:69297802 A>G maps to NM_032208.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr4:80976540 A>G maps to NM_001145794.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:46122028 G>A maps to NM_001128324.1 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:75781106 C>T maps to NM_000700.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:75775255 G>A maps to NM_000700.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr4:169049306 C>T maps to NM_007193.3 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:169102844 C>T maps to NM_007193.3 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:169049237 C>T maps to NM_007193.3 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:81923883 C>A maps to NM_145869.1 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:81925953 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:124714947 G>T maps to NM_001003954.1 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:79525441 T>G maps to NM_005139.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:70037805 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:150501737 G>A maps to NM_001155.4 Y439Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:150509048 G>T maps to NM_001155.4 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:150502503 G>A maps to NM_001155.4 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:150512045 G>A maps to NM_001155.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:75143370 C>T maps to NM_004034.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:47754734 T>C maps to NM_001630.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:150956842 C>T maps to NM_003568.2 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:36570111 C>T maps to NM_001177506.1 E478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:40998103 T>C maps to NM_009590.2 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr17:40997488 G>C maps to NM_009590.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr17:40997899 T>G maps to NM_009590.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:40997218 G>A maps to NM_009590.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:40997945 C>T maps to NM_009590.2 R435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:40997575 G>A maps to NM_009590.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:41004928 C>T maps to NM_003734.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:41004721 T>C maps to NM_003734.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr17:41008320 T>C maps to NM_003734.2 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr17:41008434 C>T maps to NM_003734.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr17:41008390 C>T maps to NM_003734.2 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr17:41004661 G>A maps to NM_003734.2 Q434Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr17:41004721 T>C maps to NM_003734.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr17:41008476 C>T maps to NM_003734.2 C734C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:201515842 A>G maps to NM_001159.3 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:201450842 G>A maps to NM_001159.3 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:201527661 T>C maps to NM_001159.3 V1171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:201485473 C>T maps to NM_001159.3 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:201505906 C>T maps to NM_001159.3 F885F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:113181937 G>T maps to NM_018569.4 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:113186910 C>T maps to NM_018569.4 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr22:29736662 G>A maps to NM_001127.3 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr22:29745284 G>A maps to NM_001127.3 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr22:29747801 C>T maps to NM_001127.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr22:29755935 G>A maps to NM_001127.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr22:29736662 G>A maps to NM_001127.3 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:29745278 G>A maps to NM_001127.3 Y455Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:29726420 G>A maps to NM_001127.3 N904N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr22:29737635 T>C maps to NM_001127.3 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:71808492 C>T maps to ENST00000423132 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:71779387 C>T maps to ENST00000423132 Q643Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr16:71805131 G>A maps to ENST00000423132 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:71768553 C>T maps to ENST00000423132 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:71808375 G>T maps to ENST00000423132 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:71782161 A>G maps to ENST00000423132 C562C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:16344356 C>T maps to NM_001130524.1 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr19:16314402 G>A maps to NM_001130524.1 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:10694719 G>A maps to ENST00000453102 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr19:10691999 T>C maps to ENST00000453102 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:15870620 A>C did not map to a codon.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr23:15845473 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:15870606 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:50303256 C>T maps to NM_014203.2 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:959447 G>T maps to ENST00000332231 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:994080 C>T maps to ENST00000332231 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:992663 C>T maps to ENST00000332231 Y478Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr17:34036280 C>T maps to NM_001030006.1 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:33977569 C>T maps to NM_001030006.1 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:33966775 C>T maps to NM_001030006.1 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:34037325 T>C maps to NM_001030006.1 C871C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:33954700 C>T maps to NM_001030006.1 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr17:33977562 T>C maps to NM_001030006.1 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:183901277 C>T maps to ENST00000411763 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:47342047 G>A maps to NM_004069.3 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:47342727 G>A maps to NM_004069.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr19:47342016 G>A maps to NM_004069.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:77477329 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:77330246 G>A maps to NM_003664.3 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:77477428 C>A maps to NM_003664.3 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:77473164 A>G maps to NM_003664.3 N346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:83330927 G>A maps to NM_004644.3 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:83332639 G>A maps to NM_004644.3 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr15:83331584 G>A maps to NM_004644.3 R879R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:2151261 G>A maps to ENST00000355272 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr19:2132553 G>A maps to ENST00000355272 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:2120979 G>A maps to ENST00000355272 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:2121166 G>A maps to ENST00000355272 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:2120979 G>A maps to ENST00000355272 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:2111698 C>T maps to ENST00000355272 A972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:2115370 C>T maps to ENST00000355272 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:2138665 C>T maps to ENST00000355272 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:2110733 G>A maps to ENST00000355272 G1049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr19:2114771 T>G maps to ENST00000355272 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:42022946 C>T maps to NM_006803.3 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:42026548 C>A maps to NM_006803.3 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr5:115249090 A>G maps to NM_001284.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:115202450 G>T maps to NM_001284.2 G52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:114437899 G>A maps to NM_006594.2 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr1:114442769 A>G maps to NM_006594.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr1:114444377 T>C maps to NM_006594.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:51291414 T>C maps to NM_007347.3 A1017A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:51221221 A>T maps to NM_007347.3 K187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:51291378 T>C maps to NM_007347.3 G1005G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:51290053 G>T maps to NM_007347.3 E960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:99703093 C>T maps to ENST00000429084 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:99700368 C>T maps to ENST00000429084 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:31549816 C>T maps to NM_007077.3 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:99071220 G>A maps to NM_181861.1 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr12:99061304 G>A maps to NM_181861.1 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr12:99043373 A>G maps to NM_181861.1 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:99097276 G>A maps to NM_181861.1 E865E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:99071220 G>A maps to NM_181861.1 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:99093196 G>A maps to NM_181861.1 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:99059361 A>G maps to NM_181861.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:99076931 T>C maps to NM_181861.1 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr12:99043373 A>G maps to NM_181861.1 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:99043373 A>G maps to NM_181861.1 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:99065434 T>G maps to NM_181861.1 Y577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr12:99043373 A>G maps to NM_181861.1 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr9:72064690 C>A maps to NM_001163.3 G664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr9:72132060 G>A maps to NM_001163.3 N22N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:72071174 G>A maps to NM_001163.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:72067052 C>T maps to NM_001163.3 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:72131085 C>T maps to NM_001163.3 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr9:72082870 G>T maps to NM_001163.3 C450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr15:29346704 C>T maps to NM_005503.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:29346521 G>A maps to NM_005503.3 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:29346287 C>T maps to NM_005503.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:29393815 C>T maps to NM_005503.3 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:29346353 C>T maps to NM_005503.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:29346773 C>T maps to NM_005503.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr15:29346110 C>T maps to NM_005503.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr15:29397622 G>T maps to NM_005503.3 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:3751530 C>T maps to NM_004886.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:3760055 G>A maps to NM_004886.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr19:3760130 G>A maps to NM_004886.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr11:6432199 G>A maps to ENST00000389906 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:6432331 C>T maps to ENST00000389906 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:6417404 G>T maps to ENST00000389906 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:6422650 G>C maps to ENST00000389906 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:6424728 C>A maps to ENST00000389906 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:6432526 G>A maps to ENST00000389906 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:6417099 G>A maps to ENST00000389906 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:26802504 C>A maps to NM_019043.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:26800677 C>T maps to NM_019043.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:26802501 A>G maps to NM_019043.3 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr10:26825056 T>C maps to NM_019043.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:26789988 T>C maps to NM_019043.3 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr10:26789988 T>C maps to NM_019043.3 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr10:26822411 T>G maps to NM_019043.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:26789884 C>T maps to NM_019043.3 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:41015996 C>T maps to NM_004307.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:40829236 C>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:41016251 G>A maps to NM_004307.1 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr5:139942027 C>T maps to ENST00000354402 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr5:112137037 A>G maps to NM_001127510.2 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr5:112164585 C>T maps to NM_001127510.2 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr5:112162833 C>T maps to NM_001127510.2 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr5:112173703 C>T maps to NM_001127510.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr5:112128192 A>G maps to NM_001127510.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr5:112175214 A>G maps to NM_001127510.2 K1308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr5:112173369 A>G maps to NM_001127510.2 K693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr5:112174240 G>T maps to NM_001127510.2 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr5:112173387 G>A maps to NM_001127510.2 W699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr5:112174023 A>G maps to NM_001127510.2 E911E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr5:112175133 A>G maps to NM_001127510.2 S1281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr5:112175254 G>T maps to NM_001127510.2 E1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr5:112175208 A>G maps to NM_001127510.2 E1306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:112157671 T>C maps to NM_001127510.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:112175697 A>G maps to NM_001127510.2 Q1469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr5:112175641 G>T maps to NM_001127510.2 E1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr5:112175479 G>T maps to NM_001127510.2 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:112175855 T>G maps to NM_001127510.2 L1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:112175922 A>G maps to NM_001127510.2 E1544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr5:112175506 C>T maps to NM_001127510.2 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr5:112175220 G>A maps to NM_001127510.2 K1310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr5:112128192 A>G maps to NM_001127510.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr5:112175120 T>A maps to NM_001127510.2 L1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr5:112175680 G>T maps to NM_001127510.2 E1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr5:112175132 C>G maps to NM_001127510.2 S1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr5:112175389 C>T maps to NM_001127510.2 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:112175229 T>C maps to NM_001127510.2 T1313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr5:112174042 G>T maps to NM_001127510.2 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr5:112175814 T>C maps to NM_001127510.2 A1508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr5:112175465 C>A maps to NM_001127510.2 S1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr5:112174657 C>T maps to NM_001127510.2 Q1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr5:112177305 A>G maps to NM_001127510.2 S2005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3519-01A-02W-0831-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr5:112175206 G>T maps to NM_001127510.2 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr5:112175756 T>A maps to NM_001127510.2 L1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr5:112175520 C>A maps to NM_001127510.2 C1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr5:112174972 C>T maps to NM_001127510.2 Q1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr5:112175695 C>T maps to NM_001127510.2 Q1469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr5:112128190 C>T maps to NM_001127510.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr5:112174744 C>T maps to NM_001127510.2 Q1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr5:112173250 C>T maps to NM_001127510.2 Q654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr5:112174105 A>T maps to NM_001127510.2 K939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr5:112175410 G>T maps to NM_001127510.2 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr5:112174222 C>T maps to NM_001127510.2 Q978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr5:112175327 C>A maps to NM_001127510.2 S1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr5:112173703 C>T maps to NM_001127510.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr5:112175234 C>A maps to NM_001127510.2 S1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr5:112174095 C>A maps to NM_001127510.2 Y935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr5:112164585 C>T maps to NM_001127510.2 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr5:112175422 C>T maps to NM_001127510.2 Q1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr5:112175620 C>T maps to NM_001127510.2 Q1444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:112102087 T>C maps to NM_001127510.2 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:112128141 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:112157671 T>C maps to NM_001127510.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:112174632 A>G maps to NM_001127510.2 R1114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:112175389 C>T maps to NM_001127510.2 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr5:112128192 A>G maps to NM_001127510.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr5:112175340 A>G maps to NM_001127510.2 K1350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr5:112175520 C>T maps to NM_001127510.2 C1410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr5:112175550 C>A maps to NM_001127510.2 P1420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:112174413 A>G maps to NM_001127510.2 Q1041Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr5:112174267 A>T maps to NM_001127510.2 K993*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3679-01A-02W-0900-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr5:112174060 A>T maps to NM_001127510.2 R924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr5:112174240 G>T maps to NM_001127510.2 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr5:112174222 C>T maps to NM_001127510.2 Q978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr5:112175398 A>T maps to NM_001127510.2 K1370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr5:112174111 G>T maps to NM_001127510.2 E941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr5:112173703 C>T maps to NM_001127510.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr5:112175410 G>T maps to NM_001127510.2 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3697-01A-01D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:112174638 T>C maps to NM_001127510.2 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:112175215 G>T maps to NM_001127510.2 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr5:112111324 G>T did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr5:112154957 T>A maps to NM_001127510.2 L410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr5:112175121 A>G maps to NM_001127510.2 L1277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr5:112175538 C>T maps to NM_001127510.2 G1416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr5:112175512 G>T maps to NM_001127510.2 E1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:112175364 G>C maps to NM_001127510.2 A1358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr5:112175170 C>T maps to NM_001127510.2 Q1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr5:112175422 C>T maps to NM_001127510.2 Q1378*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3848-01A-01W-0900-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr5:112175397 C>A maps to NM_001127510.2 P1369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr5:112128200 T>A maps to NM_001127510.2 L235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr5:112175302 C>T maps to NM_001127510.2 Q1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr5:112175214 A>G maps to NM_001127510.2 K1308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:112154770 C>T maps to NM_001127510.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr5:112174393 C>T maps to NM_001127510.2 Q1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr5:112163700 C>T maps to NM_001127510.2 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr5:112174111 G>T maps to NM_001127510.2 E941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr5:112151203 C>T maps to NM_001127510.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr5:112175422 C>T maps to NM_001127510.2 Q1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr5:112175206 G>T maps to NM_001127510.2 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr5:112173991 C>T maps to NM_001127510.2 Q901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:112175215 G>T maps to NM_001127510.2 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr5:112173559 C>T maps to NM_001127510.2 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr5:112128190 C>T maps to NM_001127510.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr5:112151260 C>T maps to NM_001127510.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:112173282 T>G maps to NM_001127510.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3989-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr5:112173703 C>T maps to NM_001127510.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr5:112175302 C>T maps to NM_001127510.2 Q1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:112164585 C>T maps to NM_001127510.2 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr5:112175389 C>T maps to NM_001127510.2 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:112175132 C>A maps to NM_001127510.2 S1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:112175512 G>T maps to NM_001127510.2 E1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr5:112175389 C>T maps to NM_001127510.2 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00W-01A-01W-A005-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-A00Z-01A-01W-A005-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:112170664 C>T maps to NM_001127510.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:112176276 C>T maps to NM_001127510.2 I1662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr5:112175020 C>T maps to NM_001127510.2 Q1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr5:112174095 C>A maps to NM_001127510.2 Y935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr5:112175575 C>T maps to NM_001127510.2 Q1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr5:112154962 C>T maps to NM_001127510.2 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr5:112154941 C>T maps to NM_001127510.2 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr5:112173599 C>G maps to NM_001127510.2 S770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr5:112175361 A>G maps to NM_001127510.2 G1357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr5:112175619 T>C maps to NM_001127510.2 P1443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr5:112175410 G>T maps to NM_001127510.2 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr5:112173703 C>T maps to NM_001127510.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:112174118 C>A maps to NM_001127510.2 S943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr5:112175161 C>T maps to NM_001127510.2 Q1291*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AD-6888-01A-11D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:112175124 A>G maps to NM_001127510.2 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr5:112174095 C>A maps to NM_001127510.2 Y935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:112175980 T>C maps to NM_001127510.2 L1564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr5:112175479 G>T maps to NM_001127510.2 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr5:112174867 C>T maps to NM_001127510.2 Q1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr5:112175512 G>T maps to NM_001127510.2 E1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:112173957 A>G maps to NM_001127510.2 K889K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:112175321 C>A maps to NM_001127510.2 S1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:112175688 A>G maps to NM_001127510.2 G1466G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AU-6004-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:112173975 A>G maps to NM_001127510.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:112175193 C>T maps to NM_001127510.2 T1301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:112175302 C>T maps to NM_001127510.2 Q1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:112175730 G>A maps to NM_001127510.2 Q1480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:112175943 A>G maps to NM_001127510.2 K1551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr5:112173852 A>G maps to NM_001127510.2 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr5:112175175 A>G maps to NM_001127510.2 E1295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr5:112175229 T>C maps to NM_001127510.2 T1313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr5:112175550 C>T maps to NM_001127510.2 P1420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:112175409 T>C maps to NM_001127510.2 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:112173581 T>G maps to NM_001127510.2 L764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:112175465 C>A maps to NM_001127510.2 S1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:112174871 C>A maps to NM_001127510.2 S1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:112177999 C>T maps to NM_001127510.2 R2237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr5:112164615 C>A maps to NM_001127510.2 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AZ-4681-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr5:112151260 C>T maps to NM_001127510.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr5:112174164 A>G maps to NM_001127510.2 R958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr5:112175389 C>T maps to NM_001127510.2 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr5:112175140 G>T maps to NM_001127510.2 E1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr5:112175514 A>G maps to NM_001127510.2 E1408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr5:112175878 G>T maps to NM_001127510.2 E1530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:112174235 C>A maps to NM_001127510.2 S982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:112175085 A>G maps to NM_001127510.2 E1265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:112175170 C>T maps to NM_001127510.2 Q1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:112175206 G>T maps to NM_001127510.2 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:112179183 C>T maps to NM_001127510.2 S2631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:112174057 A>T maps to NM_001127510.2 R923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:112175217 A>G maps to NM_001127510.2 E1309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:112179000 A>G maps to NM_001127510.2 S2570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:112128190 C>T maps to NM_001127510.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:112151203 C>T maps to NM_001127510.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:112178910 A>G maps to NM_001127510.2 P2540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr5:112176816 A>G maps to NM_001127510.2 S1842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr5:112151260 C>T maps to NM_001127510.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr5:112162844 T>C maps to NM_001127510.2 C483C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr5:112175325 A>G maps to NM_001127510.2 E1345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr5:112116510 A>T maps to NM_001127510.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr5:112175281 A>T maps to NM_001127510.2 R1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr5:112175373 C>A maps to NM_001127510.2 P1361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr5:112175673 A>G maps to NM_001127510.2 E1461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr5:112175241 A>G maps to NM_001127510.2 E1317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr5:112155042 T>A did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr5:112116590 A>G maps to NM_001127510.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr5:112137047 G>T maps to NM_001127510.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:112154770 C>T maps to NM_001127510.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:112164585 C>T maps to NM_001127510.2 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:112175465 C>A maps to NM_001127510.2 S1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:112177048 C>T maps to NM_001127510.2 R1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:112179736 C>T maps to NM_001127510.2 R2816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:112116530 A>G maps to NM_001127510.2 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:112162853 T>C maps to NM_001127510.2 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:112174296 C>T maps to NM_001127510.2 A1002A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:112175673 A>G maps to NM_001127510.2 E1461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:112175679 A>G maps to NM_001127510.2 R1463R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CK-4947-01B-11D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr5:112175247 T>C maps to NM_001127510.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr5:112175622 A>G maps to NM_001127510.2 Q1444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr5:112175937 A>G maps to NM_001127510.2 Q1549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr5:112174047 A>G maps to NM_001127510.2 R919R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr5:112174465 G>T maps to NM_001127510.2 E1059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr5:112174917 A>G maps to NM_001127510.2 E1209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr5:112175634 C>A maps to NM_001127510.2 T1448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr5:112175298 A>G maps to NM_001127510.2 R1336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr5:112175389 C>T maps to NM_001127510.2 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:112151260 C>T maps to NM_001127510.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:112157674 A>G maps to NM_001127510.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:112175140 G>T maps to NM_001127510.2 E1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:112175640 A>G maps to NM_001127510.2 R1450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr5:112116590 A>G maps to NM_001127510.2 K212K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CK-5914-01A-11D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr5:112175215 G>T maps to NM_001127510.2 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr5:112175679 A>G maps to NM_001127510.2 R1463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr5:112155041 G>C did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr5:112175911 C>T maps to NM_001127510.2 Q1541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:112174491 A>G maps to NM_001127510.2 Q1067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:112175358 A>G maps to NM_001127510.2 S1356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr5:112176816 A>G maps to NM_001127510.2 S1842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr5:112174224 A>G maps to NM_001127510.2 Q978Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr5:112175234 C>A maps to NM_001127510.2 S1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr5:112175719 C>T maps to NM_001127510.2 Q1477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:112174524 T>C maps to NM_001127510.2 Y1078Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr5:112163643 A>T maps to NM_001127510.2 K523*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CM-5341-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr5:112174743 A>G maps to NM_001127510.2 E1151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr5:112177305 A>G maps to NM_001127510.2 S2005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr5:112175398 A>T maps to NM_001127510.2 K1370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr5:112175634 C>A maps to NM_001127510.2 T1448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr5:112174608 A>G maps to NM_001127510.2 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr5:112174725 A>G maps to NM_001127510.2 E1145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:112174812 T>C maps to NM_001127510.2 D1174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:112174917 A>G maps to NM_001127510.2 E1209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:112175391 G>A maps to NM_001127510.2 Q1367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:112175673 A>G maps to NM_001127510.2 E1461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:112174608 A>G maps to NM_001127510.2 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:112174683 A>G maps to NM_001127510.2 Q1131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:112175457 T>C maps to NM_001127510.2 S1389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:112175514 A>G maps to NM_001127510.2 E1408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:112177999 C>T maps to NM_001127510.2 R2237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr5:112174191 C>G maps to NM_001127510.2 V967V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr5:112175272 C>T maps to NM_001127510.2 Q1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr5:112175479 G>T maps to NM_001127510.2 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr5:112162895 T>C maps to NM_001127510.2 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr5:112174411 C>T maps to NM_001127510.2 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr5:112175448 A>G maps to NM_001127510.2 R1386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:112111323 A>G did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr5:112175067 A>T maps to NM_001127510.2 I1259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr5:112128190 C>T maps to NM_001127510.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr5:112175154 A>G maps to NM_001127510.2 G1288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr5:112175272 C>T maps to NM_001127510.2 Q1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr5:112175506 C>T maps to NM_001127510.2 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:112175686 G>T maps to NM_001127510.2 G1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr5:112173703 C>T maps to NM_001127510.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr5:112174110 G>A maps to NM_001127510.2 S940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr5:112175307 T>C maps to NM_001127510.2 G1339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr5:112175770 G>T maps to NM_001127510.2 E1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:112173369 A>G maps to NM_001127510.2 K693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:112175217 A>G maps to NM_001127510.2 E1309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:112175556 T>C maps to NM_001127510.2 D1422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CM-6172-01A-11D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr5:112175422 C>T maps to NM_001127510.2 Q1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr5:112175479 G>T maps to NM_001127510.2 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:112174111 G>T maps to NM_001127510.2 E941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr5:112170862 G>A did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr5:112176816 A>G maps to NM_001127510.2 S1842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr5:112175556 T>C maps to NM_001127510.2 D1422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr5:112174936 G>T maps to NM_001127510.2 E1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr5:112175695 C>T maps to NM_001127510.2 Q1469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr5:112175907 A>G maps to NM_001127510.2 S1539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr5:112173344 G>A maps to NM_001127510.2 W685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr5:112174785 A>G maps to NM_001127510.2 K1165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr5:112175241 A>G maps to NM_001127510.2 E1317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr5:112157674 A>T maps to NM_001127510.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr5:112175208 A>G maps to NM_001127510.2 E1306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr5:112175214 A>G maps to NM_001127510.2 K1308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:112174042 G>T maps to NM_001127510.2 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:112175649 T>A maps to NM_001127510.2 P1453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:112175756 T>A maps to NM_001127510.2 L1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr5:112174743 A>G maps to NM_001127510.2 E1151E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D5-6535-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:112173975 A>G maps to NM_001127510.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr5:112173369 A>G maps to NM_001127510.2 K693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr5:112175215 G>T maps to NM_001127510.2 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr5:112175241 A>G maps to NM_001127510.2 E1317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:112174386 A>G maps to NM_001127510.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:112175643 A>G maps to NM_001127510.2 E1451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr5:112128144 A>G maps to NM_001127510.2 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr5:112174725 A>G maps to NM_001127510.2 E1145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr5:112175389 C>T maps to NM_001127510.2 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr5:112128190 C>T maps to NM_001127510.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr5:112175118 A>G maps to NM_001127510.2 S1276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr5:112162803 G>A did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr5:112175357 C>G maps to NM_001127510.2 S1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr5:112175085 A>G maps to NM_001127510.2 E1265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr5:112175170 C>T maps to NM_001127510.2 Q1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr5:112128190 C>T maps to NM_001127510.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr5:112175161 C>T maps to NM_001127510.2 Q1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:112175247 T>C maps to NM_001127510.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr5:112174119 A>G maps to NM_001127510.2 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr5:112175235 A>G maps to NM_001127510.2 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr5:112175235 A>G maps to NM_001127510.2 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr5:112175271 A>G maps to NM_001127510.2 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr5:112175142 A>G maps to NM_001127510.2 E1284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr5:112175247 T>C maps to NM_001127510.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr5:112175479 G>T maps to NM_001127510.2 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr5:112174095 C>A maps to NM_001127510.2 Y935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr5:112175217 A>G maps to NM_001127510.2 E1309E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DM-A0XF-01A-11D-A152-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr5:112174915 G>T maps to NM_001127510.2 E1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr5:112175229 T>C maps to NM_001127510.2 T1313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr5:112175512 G>T maps to NM_001127510.2 E1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr5:112154990 G>A maps to NM_001127510.2 W421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:112175234 C>G maps to NM_001127510.2 S1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:112175751 T>C maps to NM_001127510.2 T1487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:112175920 G>T maps to NM_001127510.2 E1544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:112175643 A>G maps to NM_001127510.2 E1451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:112174436 G>A maps to NM_001127510.2 W1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:112174812 T>C maps to NM_001127510.2 D1174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:112175512 G>T maps to NM_001127510.2 E1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr5:112164615 C>T maps to NM_001127510.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:112175105 C>A maps to NM_001127510.2 S1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:112175313 T>C maps to NM_001127510.2 S1341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr5:112175389 C>T maps to NM_001127510.2 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr5:112173911 C>G maps to NM_001127510.2 S874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr5:112175512 G>T maps to NM_001127510.2 E1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr5:112176021 A>G maps to NM_001127510.2 E1577E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr5:112173703 C>T maps to NM_001127510.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr5:112175479 G>T maps to NM_001127510.2 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr5:112175506 C>T maps to NM_001127510.2 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr5:112154941 C>A maps to NM_001127510.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr5:112175325 A>G maps to NM_001127510.2 E1345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr5:112154722 C>T maps to NM_001127510.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr5:112176816 A>G maps to NM_001127510.2 S1842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr5:112175422 C>T maps to NM_001127510.2 Q1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr5:112174386 A>G maps to NM_001127510.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr5:112174812 T>C maps to NM_001127510.2 D1174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr5:112175214 A>G maps to NM_001127510.2 K1308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr5:112175907 A>G maps to NM_001127510.2 S1539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr5:112175124 A>G maps to NM_001127510.2 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr5:112174095 C>G maps to NM_001127510.2 Y935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr5:112154976 C>T maps to NM_001127510.2 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr5:112173276 A>G maps to NM_001127510.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr5:112175323 G>T maps to NM_001127510.2 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr5:112175622 A>G maps to NM_001127510.2 Q1444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr5:112174109 C>A maps to NM_001127510.2 S940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr5:112174095 C>A maps to NM_001127510.2 Y935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr5:112175575 C>T maps to NM_001127510.2 Q1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:112175152 G>T maps to NM_001127510.2 G1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:112175514 A>G maps to NM_001127510.2 E1408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:112175752 T>C maps to NM_001127510.2 L1488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr5:112175422 C>T maps to NM_001127510.2 Q1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr5:112175980 T>C maps to NM_001127510.2 L1564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:112175235 A>G maps to NM_001127510.2 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr5:112175123 C>A maps to NM_001127510.2 S1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr5:112175283 A>G maps to NM_001127510.2 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr5:112151203 C>T maps to NM_001127510.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr5:112175052 T>A maps to NM_001127510.2 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr5:112175298 A>G maps to NM_001127510.2 R1336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr5:112175490 G>A maps to NM_001127510.2 S1400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:112164585 C>T maps to NM_001127510.2 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:112175214 A>G maps to NM_001127510.2 K1308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr5:112170691 A>G maps to NM_001127510.2 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr5:112175254 G>T maps to NM_001127510.2 E1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr5:112175475 T>C maps to NM_001127510.2 S1395S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G4-6315-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:112128142 C>T maps to NM_001127510.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:112164617 A>G maps to NM_001127510.2 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:112175208 A>G maps to NM_001127510.2 E1306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:112175347 G>T maps to NM_001127510.2 E1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr5:112175161 C>T maps to NM_001127510.2 Q1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr5:112170862 G>A did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr5:112175313 T>C maps to NM_001127510.2 S1341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:112157674 A>G maps to NM_001127510.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:112175178 A>G maps to NM_001127510.2 A1296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr5:112175270 C>G maps to NM_001127510.2 S1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr5:112128190 C>T maps to NM_001127510.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr5:112175673 A>G maps to NM_001127510.2 E1461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr5:112175814 T>C maps to NM_001127510.2 A1508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:112173918 A>G maps to NM_001127510.2 R876R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:1466938 G>A maps to NM_005883.2 T1213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:1466992 G>A maps to NM_005883.2 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:1466938 G>A maps to NM_005883.2 T1213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr18:10487719 C>T maps to ENST00000423585 C461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:10471775 C>T maps to ENST00000423585 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr20:57036160 G>A maps to NM_153360.1 N397N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr20:57036118 G>A maps to NM_153360.1 Y411Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr20:57036199 G>C maps to NM_153360.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:159558137 C>T maps to NM_001639.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:159558237 C>T maps to NM_001639.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:49718601 G>A maps to ENST00000438011 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:49720278 C>T maps to ENST00000438011 C634C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:49713367 G>A maps to ENST00000438011 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:49712685 C>T maps to ENST00000438011 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:55033731 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:55028039 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:55032955 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:55033177 C>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:55028047 G>A did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:55033113 G>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:150240403 A>G maps to NM_001077628.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr15:63594625 C>A maps to NM_031301.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:63571504 C>T maps to NM_031301.3 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr15:63571413 A>G maps to NM_031301.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr11:43342381 A>G maps to NM_001142930.1 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:34910305 T>C maps to NM_015957.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr11:34904915 C>A maps to NM_015957.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:10493918 C>T maps to NM_198544.3 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:10511543 C>T maps to NM_198544.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr2:68765170 T>C maps to NM_173545.2 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:68765170 T>C maps to NM_173545.2 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:68717381 C>T maps to NM_173545.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:68765119 T>C maps to NM_173545.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:57003935 G>A maps to NM_005161.4 C181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:36362840 G>A maps to NM_001024807.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:36362930 C>T maps to NM_001024807.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr19:36365453 C>T maps to NM_001024807.1 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:156563825 C>T maps to ENST00000446584 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr1:156563680 C>T maps to ENST00000446584 D242D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3977-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:116692539 C>T maps to NM_000482.3 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:21225888 A>G maps to NM_000384.2 S4135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr2:21230895 G>A maps to NM_000384.2 F2948F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:21225417 G>C maps to NM_000384.2 T4292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:21242611 C>T maps to NM_000384.2 P994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:21236151 A>G maps to NM_000384.2 L1366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr2:21232386 A>G maps to NM_000384.2 N2451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:21229929 G>A maps to NM_000384.2 F3270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr2:21231276 C>T maps to NM_000384.2 P2821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr2:21228795 G>A maps to NM_000384.2 V3648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr2:21255245 C>T maps to NM_000384.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:21252573 C>T maps to NM_000384.2 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr2:21257691 A>G maps to NM_000384.2 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:21232485 T>C maps to NM_000384.2 K2418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:21225594 C>T maps to NM_000384.2 S4233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:21228132 G>A maps to NM_000384.2 F3869F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:21230013 G>A maps to NM_000384.2 L3242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:21234810 C>T maps to NM_000384.2 A1643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:21225495 G>T maps to NM_000384.2 I4266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:21230393 C>A maps to NM_000384.2 G3116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:21230679 C>T maps to NM_000384.2 R3020R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:21231591 G>A maps to NM_000384.2 I2716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:21230223 A>G maps to NM_000384.2 S3172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:21227437 T>C maps to NM_000384.2 G3966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:21230381 C>A maps to NM_000384.2 E3120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:21241885 C>A maps to NM_000384.2 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:21242656 G>A maps to NM_000384.2 G979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr2:21228795 G>A maps to NM_000384.2 V3648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr2:21251251 A>G maps to NM_000384.2 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:21224766 G>T maps to NM_000384.2 Y4509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:21225324 A>C maps to NM_000384.2 T4323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:21228198 G>A maps to NM_000384.2 I3847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:21250715 G>T maps to NM_000384.2 S684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:21256303 C>A maps to NM_000384.2 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr2:21230268 G>T maps to NM_000384.2 G3157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr2:21235488 C>T maps to NM_000384.2 T1417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr2:21232179 T>C maps to NM_000384.2 R2520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:21228860 T>A maps to NM_000384.2 K3627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:21228860 T>A maps to NM_000384.2 K3627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr2:21260913 A>G maps to NM_000384.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:21235158 G>T maps to NM_000384.2 L1527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr2:21233154 T>C maps to NM_000384.2 K2195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr2:21233154 T>C maps to NM_000384.2 K2195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:21247802 A>G did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr2:21232181 G>A maps to NM_000384.2 R2520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:21260931 C>T maps to NM_000384.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr2:21245842 C>T maps to NM_000384.2 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:21233250 G>T maps to NM_000384.2 A2163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:21233643 C>T maps to NM_000384.2 E2032E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:21234339 G>A maps to NM_000384.2 D1800D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:7802145 T>C maps to NM_001644.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:7805205 C>T maps to NM_001644.3 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:7803645 G>A maps to NM_001644.3 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:41021160 C>T maps to NM_006789.3 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:39357588 C>A maps to NM_001193289.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:39382079 G>T maps to ENST00000402182 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr22:39413826 C>T maps to ENST00000396762 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:39414353 C>T maps to ENST00000396762 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr22:39421628 C>T maps to NM_152426.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr22:39427874 C>T maps to NM_152426.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:39439082 C>A maps to NM_145298.5 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr22:39477056 C>T maps to NM_021822.3 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr22:39479813 G>A maps to NM_021822.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr22:39498028 A>G maps to NM_001166003.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr22:39497342 C>A maps to NM_001166003.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr22:39496300 C>T maps to NM_001166003.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:183617629 G>T maps to NM_203454.2 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr3:195295824 A>G maps to ENST00000421243 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:195306272 T>C maps to ENST00000421243 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr3:195295773 C>T maps to NM_001647.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr17:64224270 C>T maps to NM_000042.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr22:36662063 G>A maps to NM_145343.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr22:36624213 C>A maps to ENST00000451256 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:36624106 C>G maps to ENST00000451256 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr22:36541543 G>A maps to NM_145640.2 F109F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AY-6386-01A-21D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:36122759 C>T maps to NM_030642.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:84322131 G>T did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:84258933 G>A did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr21:27264120 G>A maps to NM_000484.3 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:27327991 G>A maps to NM_000484.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr21:27425587 G>A maps to NM_000484.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr21:27372414 A>T maps to NM_000484.3 C316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:58525147 G>A maps to NM_006380.2 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:57301816 A>G maps to NM_012096.2 E630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:57293901 C>T maps to NM_012096.2 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:57302458 G>T maps to NM_012096.2 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:57293074 G>T maps to NM_012096.2 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:57280177 T>C maps to NM_012096.2 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr3:57303657 C>T maps to NM_012096.2 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:57287767 T>C did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr12:105593206 G>A maps to NM_018171.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:105583830 C>T maps to NM_018171.3 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:105593256 C>A maps to NM_018171.3 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:88878265 G>A maps to NM_000485.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:88876156 G>A maps to NM_000485.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr7:30963108 C>T maps to ENST00000509504 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:154295461 C>T maps to NM_080429.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:241631510 C>T maps to ENST00000429564 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr2:241631753 C>T maps to ENST00000429564 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:241631576 G>A maps to ENST00000429564 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:241631642 C>T maps to ENST00000429564 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:241621921 C>T maps to NM_001102467.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:241622005 G>A maps to NM_001102467.1 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:50344951 C>T maps to NM_000486.5 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:24440746 C>A maps to NM_001650.4 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:24440759 G>T maps to NM_001650.4 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:25228721 C>T maps to NM_001169.2 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:25232822 C>T maps to NM_001169.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:25235801 C>T maps to NM_001169.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr16:25235708 G>A maps to NM_001169.2 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:58458910 C>T maps to NM_020980.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr15:58465354 G>A maps to NM_020980.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:115329443 G>T maps to NM_173800.4 G423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:115338989 G>A maps to NM_173800.4 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr5:115350987 C>T maps to NM_173800.4 G830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:115351417 C>T maps to NM_173800.4 V904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:115351367 G>T maps to NM_173800.4 E888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:115298919 C>T maps to NM_173800.4 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr5:115323553 A>G maps to NM_173800.4 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr5:115351065 T>A maps to NM_173800.4 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr15:35163006 G>A maps to NM_014691.2 R1238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:35212552 C>A maps to NM_014691.2 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:35212573 C>A maps to NM_014691.2 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr15:35166924 A>G maps to NM_014691.2 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:35219333 A>G maps to NM_014691.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr15:35166924 A>G maps to NM_014691.2 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:66937336 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:66765323 G>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:66937377 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:66937335 C>T did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:66941715 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:66942735 C>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:66765270 G>A did not map to a codon.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr23:66931381 T>C did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr23:66937452 G>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:66941804 A>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:66765078 C>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:66931275 C>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:66942786 C>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:66766584 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:66765794 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:66765852 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:66905871 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:66765032 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:66765157 T>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:66765081 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:66942787 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:66765777 C>T did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:66937330 T>C did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:66766502 T>C did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:66766109 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:66765528 C>A did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:66937460 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:66765157 T>A did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:66765794 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:66943542 C>T did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:66765163 A>T did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:66937332 A>G did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:66937390 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:66863122 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:66931462 T>A did not map to a codon.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr23:47429007 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:47426710 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:47430736 G>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:47424259 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:47426104 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:47428962 G>A did not map to a codon.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr23:47430311 G>A did not map to a codon.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr11:72408437 C>T maps to NM_001040118.2 S961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:72423598 C>T maps to NM_001040118.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:72423329 C>T maps to NM_001040118.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:72397215 G>T maps to NM_001040118.2 P1402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:72437819 C>T maps to NM_001040118.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:72422183 G>A maps to NM_001040118.2 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr11:72408368 G>A maps to NM_001040118.2 C984C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr11:72418301 G>A maps to NM_001040118.2 N547N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:72423502 G>A maps to NM_001040118.2 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:72423490 G>A maps to NM_001040118.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:72423329 C>T maps to NM_001040118.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr4:36212303 G>A maps to NM_015230.2 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:36189181 C>T maps to NM_015230.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr4:36085000 C>T maps to NM_015230.2 K1499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr4:36134965 C>T maps to NM_015230.2 W1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:36069843 G>T maps to NM_015230.2 S1600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:36152625 C>T maps to NM_015230.2 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:36162091 C>A maps to NM_015230.2 E811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr4:36069794 C>A maps to NM_015230.2 E1617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:36231002 T>A maps to NM_015230.2 K36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:36230519 C>A maps to NM_015230.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr4:36122933 G>T maps to NM_015230.2 S1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:36162091 C>A maps to NM_015230.2 E811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:36230883 T>C maps to NM_015230.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:36118697 A>G maps to NM_015230.2 C1341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:36230754 C>T maps to NM_015230.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:36118703 G>A maps to NM_015230.2 P1339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:36168551 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr4:36126563 A>G maps to NM_015230.2 I1222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr4:36230973 C>T maps to NM_015230.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:141039456 C>T maps to NM_022481.5 T1052T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:141052616 G>T maps to NM_022481.5 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:141051777 A>G maps to NM_022481.5 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:141039396 G>A maps to NM_022481.5 H1072H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:141059792 C>T maps to NM_022481.5 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:141059753 G>A maps to NM_022481.5 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:141049359 C>T maps to NM_022481.5 E756E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:141033739 G>T maps to NM_022481.5 S1471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:141033741 A>G maps to NM_022481.5 P1470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr5:141033867 T>C maps to NM_022481.5 T1428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:141039456 C>T maps to NM_022481.5 T1052T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:143694936 G>A maps to NM_015193.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr8:143694644 G>A maps to NM_015193.3 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:143695305 G>A maps to NM_015193.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr8:143694852 G>A maps to NM_015193.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:228285653 C>T maps to NM_001024228.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:127231326 C>T maps to NM_001662.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:127229599 C>A maps to NM_001662.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:61907981 C>T maps to NM_175609.1 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:61919086 G>A maps to NM_175609.1 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr11:47197404 A>G maps to NM_032389.3 N87N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:47189786 G>A maps to NM_032389.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr11:47187899 G>A maps to NM_032389.3 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr11:47196801 T>C maps to NM_032389.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr22:43213805 T>C maps to NM_014570.4 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr22:43213807 C>A maps to NM_014570.4 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr22:43213805 T>C maps to NM_014570.4 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr22:43213805 T>C maps to NM_014570.4 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:68204115 T>C maps to NM_006421.3 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr8:68179451 T>C maps to NM_006421.3 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr8:68200270 C>A maps to NM_006421.3 G316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr8:68150598 C>A maps to NM_006421.3 E1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr8:68137223 T>C maps to NM_006421.3 E1374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:68178256 C>A maps to NM_006421.3 E703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:68139530 G>A maps to NM_006421.3 R1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:68179664 C>A maps to NM_006421.3 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:68137223 T>C maps to NM_006421.3 E1374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr8:68179364 T>C maps to NM_006421.3 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr8:68137223 T>C maps to NM_006421.3 E1374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr8:68204115 T>C maps to NM_006421.3 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr8:68179364 T>C maps to NM_006421.3 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr8:68123820 A>G maps to NM_006421.3 I1572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr8:68130138 C>T maps to NM_006421.3 A1497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr8:68139372 G>T maps to NM_006421.3 V1305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr8:68179364 T>C maps to NM_006421.3 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr8:68184047 A>C maps to NM_006421.3 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr8:68200193 A>G maps to NM_006421.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr20:47605047 A>G maps to NM_006420.2 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:47585688 G>A maps to NM_006420.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr20:47592682 G>A maps to NM_006420.2 E635E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:47592632 G>T maps to NM_006420.2 E619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr20:47621657 A>C maps to NM_006420.2 R1162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr20:47626846 T>C maps to NM_006420.2 G1221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr20:47605047 A>G maps to NM_006420.2 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr20:47605047 A>G maps to NM_006420.2 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:47605047 A>G maps to NM_006420.2 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr4:153809372 C>T maps to NM_001025595.1 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:153793643 A>G maps to NM_001025595.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:6499302 C>T maps to NM_012402.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:6499048 G>A maps to NM_012402.2 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr20:62333229 C>T maps to NM_003224.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr14:68117615 T>C maps to NM_001172.3 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:121304870 T>C maps to NM_001012659.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr3:121304886 C>T maps to NM_001012659.1 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:46702230 C>G maps to NM_004308.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr11:46700962 G>A maps to NM_004308.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr4:148800392 G>A maps to NM_024605.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr4:148944514 A>G maps to NM_024605.3 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:148876465 G>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:32921922 G>A maps to NM_014783.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:32928049 C>T maps to NM_014783.3 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:32915737 C>T maps to NM_014783.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr15:32915789 G>A did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr15:30919053 C>T maps to NM_001039841.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:30927751 G>A maps to NM_001039841.1 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr10:32096741 C>T maps to NM_018287.5 E795E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:32197507 C>T maps to NM_018287.5 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr10:32143098 A>T maps to NM_018287.5 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:32120729 T>C did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr2:144461042 C>T maps to NM_018460.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr2:144313999 C>T maps to NM_018460.3 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr2:143986186 C>A maps to NM_018460.3 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:144008162 C>A maps to NM_018460.3 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr2:144276892 G>A maps to NM_018460.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr2:144193180 A>G maps to NM_018460.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr2:144244975 C>T maps to NM_018460.3 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:24971072 A>G maps to NM_001006634.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:129929184 C>A maps to NM_033515.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr6:129905236 C>A maps to NM_033515.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:99025838 G>A maps to NM_032900.4 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr10:99025671 G>A maps to NM_032900.4 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:99003823 C>T maps to NM_032900.4 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr11:110561319 G>A maps to NM_020809.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:110457039 G>A maps to NM_020809.2 R439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:110454328 A>G maps to NM_020809.2 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr10:24909161 T>C maps to NM_020824.3 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:24889826 C>T maps to NM_020824.3 Q960Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr10:24908930 C>T maps to NM_020824.3 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:24909911 G>A maps to NM_020824.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr10:24884679 G>A maps to NM_020824.3 F1226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:24909083 C>T maps to NM_020824.3 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr10:24909163 G>T maps to NM_020824.3 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:24873559 G>A maps to NM_020824.3 T1886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:24909161 T>C maps to NM_020824.3 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr10:24883940 C>A maps to NM_020824.3 E1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr10:49658845 C>T maps to ENST00000417912 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr10:49658836 G>A maps to ENST00000417912 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:86916358 G>T maps to NM_001025616.2 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr4:86844919 G>T maps to NM_001025616.2 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:86916027 T>C maps to NM_001025616.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:69009402 C>T maps to NM_001007231.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:69040532 G>A maps to NM_001007231.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:69002542 G>A maps to NM_001007231.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:69002483 C>T maps to NM_001007231.2 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:68962384 G>A maps to NM_001007231.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:69002473 G>A maps to NM_001007231.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:69045127 T>C did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr2:69045126 G>A did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr2:69045126 G>A did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:142273828 G>A maps to NM_015071.4 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:142393655 G>A maps to NM_015071.4 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:142281546 C>T maps to NM_015071.4 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:43481032 G>A maps to ENST00000428638 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr17:43475329 C>T maps to ENST00000428638 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:43482391 A>G maps to ENST00000428638 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr17:43481983 G>A maps to ENST00000428638 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:43474293 G>A maps to ENST00000428638 R647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:6868207 A>T maps to ENST00000400091 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr18:6882284 C>A maps to ENST00000400091 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr18:6873722 C>T maps to ENST00000400091 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:94640246 A>G maps to NM_004815.3 D988D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:94639931 C>T maps to NM_004815.3 K1093K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:94667364 C>A maps to NM_004815.3 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:94685936 C>A maps to NM_004815.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:94654438 T>C maps to NM_004815.3 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:161022311 G>A maps to NM_001025598.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:161018494 C>T maps to NM_001025598.1 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr1:161018479 T>C maps to NM_001025598.1 Q777Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr1:161021500 T>C maps to NM_001025598.1 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:161019396 C>T maps to NM_001025598.1 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:119120753 C>T maps to NM_020754.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:119134177 C>T maps to NM_020754.2 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:119112314 C>T maps to NM_020754.2 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr3:119128497 G>T maps to NM_020754.2 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr11:128839896 G>A maps to NM_001142685.1 D1723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:128963557 A>G maps to NM_001142685.1 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:128842461 C>T maps to NM_001142685.1 T1299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:128850590 C>T maps to NM_001142685.1 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:128838885 G>T maps to NM_001142685.1 T2060T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:128868313 C>T maps to NM_001142685.1 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:128839182 T>C maps to NM_001142685.1 K1961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:128993397 C>T maps to NM_001142685.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:128993406 A>G maps to NM_001142685.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:128840391 C>T maps to NM_001142685.1 V1558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr11:128839077 G>A maps to NM_001142685.1 N1996N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:128858018 C>T maps to NM_001142685.1 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:36269373 C>A maps to ENST00000007510 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr19:36269255 C>T maps to ENST00000007510 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr19:36273301 G>T maps to ENST00000007510 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr19:36279204 C>T maps to ENST00000007510 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:36278932 C>T maps to ENST00000007510 Q1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:130215817 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:130217763 A>G did not map to a codon.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr23:130215696 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:130217157 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:130219641 C>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:130220385 C>G did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:130215855 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:130217827 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:130218194 G>A did not map to a codon.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr23:130217827 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr23:130217769 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:130220354 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr23:130219683 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:130219642 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:130220559 T>C did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:130220567 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:130220556 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:130215772 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:130220360 C>G did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr23:130222650 C>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:130218649 C>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:130220568 T>C did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:130220568 T>C did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:130218322 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:130218354 C>G did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:130217757 G>A did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:130222715 G>A did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:130220568 T>C did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:130220567 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:145758691 G>A maps to NM_025251.1 N902N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:145759569 C>T maps to NM_025251.1 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:145758565 T>C maps to NM_025251.1 T944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:145773212 C>T maps to NM_025251.1 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr8:145770825 G>A maps to NM_025251.1 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:153185113 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:153178994 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:153187058 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:153178187 C>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:153187087 A>G did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:153175288 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:153184342 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:153184642 T>A did not map to a codon.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr23:153175662 G>A did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:153178221 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:153175377 T>C did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr14:32560562 C>T maps to NM_001030055.1 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr14:32562356 C>T maps to NM_001030055.1 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr14:32561638 C>T maps to NM_001030055.1 H588H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:32561348 G>T maps to NM_001030055.1 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr14:32560546 A>G maps to NM_001030055.1 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:11157272 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:11162245 G>T did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:11162197 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:11196312 A>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:11682941 C>T did not map to a codon.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr23:11682879 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:11174724 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:11682558 G>A did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:11272753 T>C did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:11157235 G>A did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr23:11272753 T>C did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:11272732 T>C did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:11157122 C>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:57870947 A>G maps to ENST00000393797 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr12:57869119 C>T maps to ENST00000393797 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:57872373 G>A maps to ENST00000393797 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:57870188 C>T maps to ENST00000393797 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:57866343 G>A maps to ENST00000393797 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:57871336 G>A maps to ENST00000393797 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr12:57872976 G>A maps to ENST00000393797 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:15095479 C>T maps to NM_001175.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:42398328 C>A maps to NM_199002.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr19:42409944 C>T maps to NM_199002.1 N805N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr19:42410922 G>A maps to NM_199002.1 Q923Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:42402677 C>T maps to NM_199002.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:42410097 C>T maps to NM_199002.1 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr19:42392309 C>A maps to NM_199002.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr8:1808342 C>T maps to ENST00000398564 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr8:1842692 C>T maps to ENST00000398564 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr8:1824808 C>A maps to ENST00000398564 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:1876630 C>T maps to ENST00000398564 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr8:1808261 C>T maps to ENST00000398564 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr8:1905170 A>G maps to ENST00000398564 S1284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:1871946 C>T maps to ENST00000398564 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:1853832 C>A maps to ENST00000398564 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr8:1833836 C>T maps to ENST00000398564 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:1812548 A>G maps to ENST00000398564 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:1905107 C>T maps to ENST00000398564 D1263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr8:1824808 C>A maps to ENST00000398564 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:1857568 C>T maps to ENST00000398564 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr8:1876705 C>T maps to ENST00000398564 Y962Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:17928678 G>A maps to NM_018125.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:17965157 G>A maps to NM_018125.3 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:17928651 A>G maps to NM_018125.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:156907268 G>A maps to NM_198236.1 S1404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:156909519 G>A maps to NM_198236.1 Q1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:156941539 C>T maps to NM_198236.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:156925493 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:156916473 G>A maps to NM_198236.1 R892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:156906686 G>T maps to NM_198236.1 G1517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:156909385 A>G maps to NM_198236.1 D1350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:156950243 G>A maps to NM_198236.1 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:120352053 C>A maps to NM_015313.2 P1441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:120292554 C>T maps to NM_015313.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:120302514 G>A maps to NM_015313.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr11:120350705 T>G maps to NM_015313.2 G1268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:120319002 G>A maps to NM_015313.2 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:120327942 G>T maps to NM_015313.2 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:8219360 C>T maps to NM_173728.3 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:8215467 C>T maps to NM_173728.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:3386004 C>T maps to NM_014448.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:3389758 C>T maps to NM_014448.3 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:3395095 C>T maps to NM_014448.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:73073119 G>A maps to NM_014786.3 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:73078716 T>C maps to NM_014786.3 S2028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:73066618 C>T maps to NM_014786.3 I1165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:73063960 G>A maps to NM_014786.3 E1119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:73067275 G>A maps to NM_014786.3 A1240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:73074306 G>T maps to NM_014786.3 E1685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:7523540 C>T maps to NM_001130955.1 N587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:7504894 C>T maps to NM_001130955.1 D23D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:7504981 C>T maps to NM_001130955.1 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:7505029 G>A maps to NM_001130955.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:16525128 T>A maps to NM_153213.3 K788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:16525125 G>A maps to NM_153213.3 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:155921937 G>A maps to NM_001162383.1 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr1:155934812 T>C maps to NM_001162383.1 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:155921048 C>T maps to NM_001162383.1 Q758Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:56763360 A>T maps to NM_001128615.1 C538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:56992862 C>T maps to NM_001128615.1 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:143885467 A>G maps to NM_001003702.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:106534578 T>C maps to ENST00000420470 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:131796565 C>T maps to NM_015320.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:131799429 C>T maps to NM_015320.2 N460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr2:131704182 C>T maps to NM_015320.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:131798849 C>T maps to NM_015320.2 N384N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:131799020 G>A maps to NM_015320.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr2:131798939 C>A maps to NM_015320.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:131801994 C>T maps to NM_015320.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:131797656 C>T maps to NM_015320.2 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr7:144061069 G>A maps to NM_005435.3 Q436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr7:144075873 C>T maps to NM_005435.3 C1517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:135767978 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:135770111 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:135761807 A>C did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:135757207 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:135750191 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:135764061 T>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:135795498 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:135764084 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:135814275 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:135825806 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:135764962 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:135770099 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:135750295 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:135758844 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:135764063 T>G did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr23:135795514 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr23:135829720 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:135862961 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:135750224 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:111938573 C>T maps to NM_001113511.1 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr13:111932644 A>G maps to NM_001113511.1 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr13:111944570 A>G maps to NM_001113511.1 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr23:62857962 C>T did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:62893976 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:62875543 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:62875562 A>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:62885825 G>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:62898437 C>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:62944422 T>C did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:27105549 C>T maps to NM_006015.4 R1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:27105551 A>G maps to NM_006015.4 R1721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:27105549 C>T maps to NM_006015.4 R1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:27023433 C>T maps to NM_006015.4 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr1:27105552 C>T maps to NM_006015.4 R1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:27100202 G>A maps to NM_006015.4 Q1333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:27057737 G>A maps to NM_006015.4 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:27106860 C>A maps to NM_006015.4 R2158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:27056245 A>G maps to NM_006015.4 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr1:27088696 C>A maps to NM_006015.4 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr1:27057852 C>T maps to NM_006015.4 Q521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:27106718 C>T maps to NM_006015.4 A2110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:27105549 C>T maps to NM_006015.4 R1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:27087502 C>T maps to NM_006015.4 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:27107000 C>G maps to NM_006015.4 A2204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr1:27100206 C>T maps to NM_006015.4 R1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:27106860 C>A maps to NM_006015.4 R2158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:27087960 C>T maps to NM_006015.4 R750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr1:27056188 T>C maps to NM_006015.4 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:27057852 C>T maps to NM_006015.4 Q521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:27059237 A>G maps to NM_006015.4 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr1:27105554 A>G maps to NM_006015.4 R1722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr1:27056245 A>G maps to NM_006015.4 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:27057657 C>T maps to NM_006015.4 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr1:27100918 C>T maps to NM_006015.4 Q1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr1:27057795 C>T maps to NM_006015.4 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr1:27056245 A>G maps to NM_006015.4 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:27056245 A>G maps to NM_006015.4 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr1:27101343 A>G maps to NM_006015.4 E1542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:27105552 C>T maps to NM_006015.4 R1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:27089561 C>T maps to NM_006015.4 Q840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:27058091 G>A maps to NM_006015.4 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:27057978 C>T maps to NM_006015.4 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:157522485 G>A maps to ENST00000367148 T1626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:157150537 C>T maps to ENST00000367148 Q574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:157527947 C>T maps to ENST00000367148 D1931D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr12:46245517 C>T maps to NM_152641.2 S1204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:46287293 G>T maps to NM_152641.2 G1747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:46245857 C>T maps to NM_152641.2 Q1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr12:46244722 T>C maps to NM_152641.2 Y939Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr12:46233178 A>G maps to NM_152641.2 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:46242678 T>C maps to NM_152641.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:46245106 A>G maps to NM_152641.2 K1067K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:46245343 G>A maps to NM_152641.2 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:46287488 C>A maps to NM_152641.2 S1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr12:46233178 A>G maps to NM_152641.2 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:46245967 A>G maps to NM_152641.2 R1354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:46233110 G>A did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr12:46244131 T>C maps to NM_152641.2 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:46233178 A>G maps to NM_152641.2 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:46123920 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:964395 G>A maps to NM_005224.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:74882284 C>A maps to ENST00000395077 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:74882320 C>T maps to ENST00000395077 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:34623620 G>A maps to NM_001017363.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:34622380 G>T maps to NM_001017363.1 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr14:58832237 C>T maps to NM_002892.3 Q1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:58795011 C>T maps to NM_002892.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:58785493 G>A maps to NM_002892.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:58832907 G>A maps to NM_002892.3 P1161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:58820472 C>T maps to NM_002892.3 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr14:58831662 C>T maps to NM_002892.3 I952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr14:58814592 G>A maps to NM_002892.3 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:58768332 C>T maps to NM_002892.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:58832907 G>A maps to NM_002892.3 P1161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr14:58831413 A>T maps to NM_002892.3 I869I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr14:58827641 C>T maps to NM_002892.3 D654D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:235344927 A>G maps to NM_016374.5 N1102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:235344927 A>G maps to NM_016374.5 N1102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:235418987 A>G maps to NM_016374.5 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:235377184 T>C maps to NM_016374.5 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:235345254 A>G maps to NM_016374.5 D993D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:235345424 T>A maps to NM_016374.5 K937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:235345428 C>T maps to NM_016374.5 W935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:235345429 C>T maps to NM_016374.5 W935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr1:235357465 G>T maps to NM_016374.5 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:235345365 C>T maps to NM_016374.5 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:97215074 C>T maps to NM_212481.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr10:63852749 T>G maps to NM_032199.2 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:63817049 C>T maps to NM_032199.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:63852413 C>T maps to NM_032199.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:63662033 T>A maps to NM_032199.2 C46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:63852063 C>T maps to NM_032199.2 R948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:63851102 C>T maps to NM_032199.2 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:63851234 A>G maps to NM_032199.2 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:49017026 G>A maps to NM_006321.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:48965065 A>G maps to NM_006321.2 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:49011194 G>T maps to NM_006321.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:49012254 C>A maps to NM_006321.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr13:50204780 G>A maps to NM_138450.5 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr13:50204798 C>A maps to NM_138450.5 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr13:50204879 G>A maps to NM_138450.5 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr23:100242526 A>G did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:100240832 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:53606276 C>T maps to NM_019087.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:57282554 C>T maps to NM_012106.3 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:104449652 A>T maps to NM_004311.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr10:104459168 T>C maps to NM_004311.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:104465210 T>C maps to NM_004311.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:12728301 A>G maps to NM_005738.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr7:12728421 A>G maps to NM_005738.4 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:235405017 G>A maps to ENST00000339728 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:235404912 C>T maps to ENST00000339728 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:152663434 C>A maps to NM_012097.3 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:97506847 C>T maps to NM_177976.1 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr16:18809332 G>A maps to NM_015161.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:69151131 T>C maps to NM_006407.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:153575539 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:5213836 C>A maps to ENST00000438743 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:102738906 T>C maps to NM_031905.3 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:102738780 C>T maps to NM_031905.3 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:109285495 G>T maps to NM_032131.4 E756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:109274429 G>A maps to NM_032131.4 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:109220942 C>T maps to NM_032131.4 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:109274444 C>T maps to NM_032131.4 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr10:23270544 T>A maps to NM_173081.3 L364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:23297839 C>A maps to NM_173081.3 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:28149709 A>G maps to NM_018076.2 N955N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:28101548 T>C maps to NM_018076.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:28250541 C>T maps to NM_018076.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:28233309 T>C maps to NM_018076.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:28272884 G>A maps to NM_018076.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:28196630 G>A maps to NM_018076.2 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr10:28149640 G>A maps to NM_018076.2 N978N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:28229686 C>T maps to NM_018076.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:28273217 C>A maps to NM_018076.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr10:28284016 C>A maps to NM_018076.2 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr10:28228873 A>G maps to NM_018076.2 N683N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:31475744 A>G maps to ENST00000408912 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:31477858 C>A maps to ENST00000408912 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:31477234 G>A maps to ENST00000408912 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:19162531 C>T maps to ENST00000392336 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:19162516 A>G maps to ENST00000392336 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:19162930 C>T maps to ENST00000392336 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:137963979 G>A maps to ENST00000469044 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:137960737 C>T maps to ENST00000469044 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:137953877 G>A maps to ENST00000469044 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr2:232100063 T>C maps to ENST00000359743 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:232081494 G>T maps to ENST00000359743 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:232143142 C>A maps to ENST00000359743 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:100808226 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:100808327 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:100808095 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:100808095 C>T did not map to a codon.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr23:100808879 C>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:100808968 A>G did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:100808406 C>T did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:100807939 C>T did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:100808983 T>C did not map to a codon.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr23:100808174 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:100808562 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:100809027 A>C did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:100808346 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:100807925 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:100808892 A>G did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:100808742 A>G did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:100808008 C>T did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:100808211 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:100808372 C>T did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:100808008 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:100808890 C>A did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:100911660 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:100911415 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:100911265 T>C did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:100911768 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:100911502 T>C did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:100911659 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:100912396 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:100912348 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:100911660 T>C did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:100880768 T>C did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:100880256 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:100879977 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:100880442 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:100880740 G>T did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:101857747 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:101858098 A>T did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:101858725 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:101857201 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:101857760 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:101857953 G>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:101858099 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:101858349 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:101858098 A>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:100871564 T>A did not map to a codon.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr1:150808900 C>T maps to NM_001668.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:150786601 C>T maps to NM_001668.3 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr1:150788863 A>G maps to NM_001668.3 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:150812018 C>T maps to NM_001668.3 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:80750278 C>T maps to NM_014862.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:80872883 G>T maps to NM_014862.3 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr15:80855553 C>T maps to NM_014862.3 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr15:80762741 C>T maps to NM_014862.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:27543152 A>G maps to NM_020183.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:27540213 C>T maps to NM_020183.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr12:27521310 C>T maps to NM_020183.3 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:27568800 G>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:27533275 G>A maps to NM_020183.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:98957172 T>C maps to NM_006409.3 H265H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CM-6674-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:98931039 C>T maps to ENST00000441989 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:98985758 G>A maps to NM_005720.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:98985794 C>T maps to NM_005720.2 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:98991672 C>T maps to NM_005720.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:98984341 T>C maps to NM_005720.2 H33H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr7:98985759 C>T maps to NM_005720.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:127637391 G>T maps to NM_030978.1 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:169485372 G>A maps to NM_032487.4 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:169485432 A>T maps to NM_032487.4 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr3:169486094 C>A maps to NM_032487.4 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:169485552 A>T maps to NM_032487.4 C262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:52849389 C>T maps to NM_006628.4 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr3:35785413 C>T maps to ENST00000458225 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:35833907 C>T maps to ENST00000458225 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:35748562 G>T maps to ENST00000458225 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr3:35835320 G>A maps to ENST00000458225 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr3:35770909 T>C maps to ENST00000458225 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:69500654 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:69497288 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:69496108 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:69501556 C>T did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:74985211 G>A maps to NM_004041.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:74979999 G>A maps to NM_004041.3 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr11:74985170 G>A maps to NM_004041.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:74994453 C>T maps to NM_004041.3 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr11:74978730 C>T maps to NM_004041.3 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:4619326 A>G maps to ENST00000412477 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:4624306 T>C maps to ENST00000412477 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr9:140508563 T>C maps to NM_152285.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr19:18121519 G>A maps to NM_015683.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:18121108 C>T maps to NM_015683.1 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:18119578 C>T maps to NM_015683.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr5:90678753 T>C maps to NM_020801.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:90670756 G>A maps to NM_020801.2 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:90678753 T>C maps to NM_020801.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:90678711 G>A maps to NM_020801.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr5:90678753 T>C maps to NM_020801.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:98508848 A>G maps to NM_183376.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:98509247 C>T maps to NM_183376.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:98513912 C>A maps to NM_183376.2 C380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:4896696 C>A maps to NM_001080523.1 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr19:4891492 G>A maps to NM_001080523.1 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:4902816 G>A maps to NM_001080523.1 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr22:51065276 C>T maps to ENST00000395624 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:51064630 G>A maps to ENST00000395624 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:78260316 T>C maps to NM_000046.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr5:78135203 G>A maps to NM_000046.3 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr5:78181441 C>T maps to NM_000046.3 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr23:2836232 C>T did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:2833604 C>T did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:2833627 A>C did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:2833630 A>G did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:2833637 C>T did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:2833642 C>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:2843761 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr23:2836210 A>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:2839999 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:2840046 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:2836029 G>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:2864131 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:2873478 C>T did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:2856244 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:2861134 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:2856216 C>T did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:3002504 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:3007573 C>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:3028210 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:3028267 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:3002418 C>T did not map to a codon.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr23:3030422 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr23:3028171 C>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:3030224 T>G did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:3002504 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:3002590 G>A did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:3019220 G>A did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:3019221 A>G did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:3002660 C>T did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr23:3002504 G>T did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr23:3019220 G>T did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:2990190 G>C did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:2990217 T>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:2990118 G>A did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:3019221 A>G did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:3021820 G>C did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:66364730 C>T maps to NM_014960.3 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr17:66391303 G>T maps to NM_014960.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr17:66391273 G>A maps to NM_014960.3 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:66416525 C>T maps to NM_014960.3 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:2945493 G>A did not map to a codon.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr23:2936582 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:2928155 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:2936656 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:2924730 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:2931157 T>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:2928087 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:149681729 G>A maps to NM_001012301.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:149677970 C>T maps to NM_001012301.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:114823951 G>A maps to NM_024590.3 Y426Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:77003374 T>C maps to NM_001130016.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:77018830 T>C did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:77003470 A>G maps to NM_001130016.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr11:3660998 G>A maps to NM_001079536.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:3661225 G>A maps to NM_001079536.1 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:3661420 G>A maps to NM_001079536.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr22:19960284 C>T maps to NM_001670.2 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:25033783 A>C did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:25033762 C>T did not map to a codon.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr23:25033716 G>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:25033812 G>A did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:25033754 C>G did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:25033665 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:104638720 A>C maps to NM_020682.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:17933057 T>C maps to NM_004315.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr10:52504979 A>T maps to NM_001079516.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:122944412 T>G maps to NM_024769.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:122954415 A>G maps to NM_024769.2 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:122944274 A>G maps to NM_024769.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr8:131127885 A>G maps to NM_018482.2 D720D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr8:131179810 T>A maps to NM_018482.2 K294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr8:131073082 T>C maps to NM_018482.2 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr8:131073148 C>T maps to NM_018482.2 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr8:131104264 G>T maps to NM_018482.2 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:131092164 T>C maps to NM_018482.2 G875G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:131127945 G>A maps to NM_018482.2 H700H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr8:131072872 C>T maps to NM_018482.2 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:131127917 G>A maps to NM_018482.2 R710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:131140326 T>C maps to NM_018482.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:131127885 A>G maps to NM_018482.2 D720D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr8:131073205 T>C maps to NM_018482.2 G937G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:9437519 G>A maps to NM_003887.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr2:9496316 T>G maps to NM_003887.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:9540955 G>A maps to NM_003887.2 Q940Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:9514979 C>T maps to NM_003887.2 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:9496398 G>T maps to NM_003887.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:9520873 C>T maps to NM_003887.2 N651N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr2:9514979 C>T maps to NM_003887.2 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:23763782 G>A maps to NM_017707.3 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr2:239355106 G>A maps to NM_001040445.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:239355079 C>T maps to NM_001040445.1 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:15301733 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:15333552 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:15315748 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:15333693 T>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:15315695 G>A did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:63445177 T>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:63445176 A>G did not map to a codon.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr23:63444798 G>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:63445176 A>G did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:63444285 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:63445178 G>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:5694885 G>A maps to NM_024701.3 H57H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr10:5693278 G>A maps to NM_024701.3 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:42248325 C>T maps to NM_080863.4 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr1:76397847 G>A maps to NM_080868.2 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:76397586 T>C maps to NM_080868.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:237172832 G>A maps to NM_212556.2 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:237103537 C>A maps to NM_212556.2 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:94420822 C>T maps to ENST00000434324 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr14:94401049 C>T maps to ENST00000434324 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:94419791 C>T maps to ENST00000434324 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr14:94417474 G>A maps to ENST00000434324 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr14:94405678 G>A maps to ENST00000434324 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:53897666 T>G maps to NM_001164165.1 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:53897735 C>T maps to NM_001164165.1 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr2:53955975 A>C maps to NM_001164165.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:95125352 G>A maps to NM_016116.2 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:95157167 G>A maps to NM_016116.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr7:95125289 C>T maps to NM_016116.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:177138070 C>A maps to NM_080874.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:177146477 G>A maps to NM_080874.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:177190100 C>T maps to NM_080874.3 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:132400452 C>T maps to NM_017873.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:132400184 G>T maps to NM_017873.2 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr15:101169888 G>A maps to NM_198243.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:48545028 C>T maps to NM_024095.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:15287934 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:15272943 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:15268632 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:73887868 C>A maps to NM_001198800.1 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:30218369 G>A maps to NM_032204.3 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr22:30200657 G>T maps to NM_032204.3 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr22:30197020 G>A maps to NM_032204.3 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:30212009 C>T maps to NM_032204.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:101248236 C>A maps to NM_006828.2 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:100957859 G>A maps to NM_006828.2 R2137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:101086480 G>T maps to NM_006828.2 S1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:100965889 T>C maps to NM_006828.2 E1968E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr6:101247330 T>C maps to NM_006828.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:101054824 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:100965889 T>C maps to NM_006828.2 E1968E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:103352462 C>T maps to NM_004316.3 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:103352468 G>A maps to NM_004316.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:103352525 C>T maps to NM_004316.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:8959573 C>T maps to NM_020646.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:108169003 G>A maps to NM_203436.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:7077522 A>G maps to NM_001671.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:155309119 G>A maps to ENST00000368346 R2839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:155385599 G>T maps to ENST00000368346 P1981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr1:155316230 C>A maps to ENST00000368346 V2616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:155327509 G>A maps to ENST00000368346 R2281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:155317515 G>A maps to ENST00000368346 D2583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:155452075 A>G maps to ENST00000368346 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr1:155491264 C>A maps to ENST00000368346 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:155447728 A>G maps to ENST00000368346 L1644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:155452075 A>G maps to ENST00000368346 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:155447914 A>G maps to ENST00000368346 S1582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr1:155491262 T>C maps to ENST00000368346 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:155449531 T>C maps to ENST00000368346 G1043G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:155408815 C>A maps to ENST00000368346 G1710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr1:155317647 T>G maps to ENST00000368346 L2539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:155448574 T>C maps to ENST00000368346 E1362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr8:37986402 A>T maps to NM_004674.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr8:37978663 C>T maps to NM_004674.3 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:37978506 G>A maps to NM_004674.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr8:37964573 T>C maps to NM_004674.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr8:37996371 G>A maps to NM_004674.3 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr8:37964573 T>C maps to NM_004674.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:1761725 T>C did not map to a codon.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr23:1561192 C>T did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:12858228 C>T maps to NM_004317.2 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr7:97482383 G>A maps to NM_183356.3 Y488Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:97488684 C>T maps to NM_183356.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr7:97498309 A>G maps to NM_183356.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:97488687 G>T maps to NM_183356.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr7:97482666 G>A maps to NM_183356.3 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr7:97498309 A>G maps to NM_183356.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr2:190531586 T>C maps to NM_019048.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:190531844 C>T maps to NM_019048.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr19:51015705 C>T maps to NM_001114598.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:62479856 C>T maps to NM_004318.3 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:62550889 C>A maps to NM_004318.3 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:62475356 G>A maps to NM_004318.3 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:62460749 C>T maps to NM_004318.3 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr22:26839162 G>A maps to NM_020437.4 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr22:26830454 C>T maps to NM_020437.4 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr1:197071075 A>G maps to NM_018136.4 I2435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr1:197071075 A>G maps to NM_018136.4 I2435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:197073531 G>A maps to NM_018136.4 R1617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:197073648 G>A maps to NM_018136.4 R1578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:197073532 G>A maps to NM_018136.4 F1616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:197053459 A>C maps to NM_018136.4 P3476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr1:197070067 G>A maps to NM_018136.4 N2771N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:197099173 C>A maps to NM_018136.4 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr1:197059212 C>T maps to NM_018136.4 E3277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:197087004 G>A maps to NM_018136.4 R1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:197098427 G>A maps to NM_018136.4 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:197111557 C>T maps to NM_018136.4 E608E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:197094002 A>G maps to NM_018136.4 F1055F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:197094021 C>T maps to NM_018136.4 W1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr1:197071075 A>G maps to NM_018136.4 I2435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr1:197072416 C>T maps to NM_018136.4 K1988K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:197071075 A>G maps to NM_018136.4 I2435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:197072062 A>G maps to NM_018136.4 G2106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:95228760 A>G maps to NM_017680.4 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr9:95236929 G>T maps to NM_017680.4 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr9:95222774 G>A maps to NM_017680.4 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:95236990 T>C maps to NM_017680.4 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:70187856 C>A maps to NM_152792.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:70188109 C>T maps to NM_152792.2 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:70188013 C>T maps to NM_152792.2 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:70188511 C>T maps to NM_152792.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr17:79952695 G>T did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr17:79941510 C>T maps to ENST00000306729 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:62105604 C>A maps to NM_025080.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:133370290 C>T maps to NM_000050.4 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:133364726 C>T maps to NM_000050.4 Y282Y. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3811-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:130735003 C>A maps to ENST00000514044 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:130743850 G>T maps to ENST00000514044 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:130743084 G>A maps to ENST00000514044 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:96798408 C>T maps to NM_001002036.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:96801136 C>A maps to NM_001002036.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:177133566 G>A maps to ENST00000281881 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr1:176999987 A>T maps to ENST00000281881 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr1:176918355 G>A maps to ENST00000281881 D681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:176903417 C>T maps to ENST00000281881 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:176863877 G>A maps to ENST00000281881 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:176998863 G>A maps to ENST00000281881 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:176853550 G>A maps to ENST00000281881 I1058I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:177001820 G>A maps to ENST00000281881 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr1:176926876 G>A maps to ENST00000281881 N616N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:176863817 G>T maps to ENST00000281881 P948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:119738980 C>A maps to ENST00000313400 G559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:119739056 G>A maps to ENST00000313400 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:119802164 G>A maps to ENST00000313400 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:119976967 G>A maps to ENST00000313400 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:119567972 T>C maps to ENST00000313400 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:119204755 G>A maps to ENST00000313400 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:119582945 C>T maps to ENST00000313400 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:119188282 G>A maps to ENST00000313400 R1289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr9:119582969 A>T maps to ENST00000313400 C711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:119583059 G>T maps to ENST00000313400 C681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:119488176 C>T maps to ENST00000313400 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr9:119976808 G>A maps to ENST00000313400 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr9:119488227 G>T maps to ENST00000313400 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr20:31024699 G>A maps to ENST00000375687 L1395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr20:31021500 C>T maps to ENST00000375687 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:31024196 G>T maps to ENST00000375687 E1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr20:31016149 G>A maps to ENST00000375687 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:31021698 G>A maps to ENST00000375687 E566E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr20:31023407 C>T maps to ENST00000375687 R965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr20:31024480 G>A maps to ENST00000375687 P1322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:30954252 G>T maps to ENST00000375687 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr20:31022999 C>T maps to ENST00000375687 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr20:31024480 G>A maps to ENST00000375687 P1322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr20:31022872 A>G maps to ENST00000375687 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr20:31022923 A>G maps to ENST00000375687 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr20:31022899 C>A maps to ENST00000375687 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr20:31024757 C>T maps to ENST00000375687 R1415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr20:31022591 C>T maps to ENST00000375687 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr20:31022923 A>G maps to ENST00000375687 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr20:31023818 G>T maps to ENST00000375687 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr20:31022288 C>T maps to ENST00000375687 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr20:31021719 G>A maps to ENST00000375687 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr20:31022839 A>G maps to ENST00000375687 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr20:31022872 A>G maps to ENST00000375687 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr20:31022591 C>T maps to ENST00000375687 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr20:31021356 G>A maps to ENST00000375687 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr20:31023472 C>T maps to ENST00000375687 N986N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:31024108 A>G maps to ENST00000375687 G1198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr20:31022923 A>G maps to ENST00000375687 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr20:31023472 C>T maps to ENST00000375687 N986N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr20:31024278 C>A maps to ENST00000375687 S1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:25966229 C>T maps to NM_018263.4 A992A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr2:25976475 G>A maps to NM_018263.4 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:25982467 C>T maps to NM_018263.4 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:25966571 C>T maps to NM_018263.4 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:25982355 G>A maps to NM_018263.4 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:25965212 G>T maps to NM_018263.4 I1331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr18:31325826 T>A maps to NM_030632.1 T2005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:31319968 C>T maps to NM_030632.1 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:31323744 C>A maps to NM_030632.1 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:31325055 G>A maps to NM_030632.1 P1748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:31325871 A>G maps to NM_030632.1 P2020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr18:31318456 C>T maps to NM_030632.1 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr18:31320167 T>C maps to NM_030632.1 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr18:31326507 C>T maps to NM_030632.1 D2232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr18:31319521 G>A maps to NM_030632.1 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:117067424 G>A maps to NM_130768.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:89516600 G>A maps to NM_032810.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr10:89550145 C>T maps to NM_032810.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr10:89514452 A>G maps to NM_032810.2 C359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr8:124346235 C>T maps to NM_014109.3 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:124382178 A>G maps to NM_014109.3 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:124383477 C>A maps to NM_014109.3 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:124359473 G>A maps to NM_014109.3 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:124382181 A>G maps to NM_014109.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr8:124382193 A>G maps to NM_014109.3 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:124369818 G>A maps to NM_014109.3 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:124361553 C>A maps to NM_014109.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:124335285 A>T maps to NM_014109.3 V1341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:124371896 C>A maps to NM_014109.3 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr2:24092543 T>C maps to NM_017552.1 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:23980509 G>A maps to NM_017552.1 Q1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr2:23980759 A>G maps to NM_017552.1 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:24108601 C>A maps to NM_017552.1 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr2:24108625 G>A maps to NM_017552.1 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:24098742 C>T maps to NM_017552.1 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:24103625 C>A did not map to a codon.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:24046383 C>T maps to NM_017552.1 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:24033269 A>G maps to NM_017552.1 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr2:23980759 A>G maps to NM_017552.1 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr2:24092543 T>C maps to NM_017552.1 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr2:24046425 G>A maps to NM_017552.1 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:24092543 T>C maps to NM_017552.1 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:1425969 C>T maps to NM_031921.4 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:1420451 C>T maps to NM_031921.4 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:1425699 T>C maps to NM_031921.4 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:1421182 C>T maps to NM_031921.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:1398006 C>T maps to NM_001039211.2 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:1403786 C>T maps to NM_001039211.2 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr17:29162262 T>C maps to NM_024857.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:29196368 T>C maps to NM_024857.3 T1139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:29161512 C>T maps to NM_024857.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:29170971 G>A maps to NM_024857.3 K761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr17:29219769 T>C maps to NM_024857.3 I1468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr17:29204468 C>T maps to NM_024857.3 Q1274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:29221687 C>T maps to NM_024857.3 R1802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:29221687 C>T maps to NM_024857.3 R1802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr17:29162262 T>C maps to NM_024857.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr17:29161990 G>T maps to NM_024857.3 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr19:3909499 T>C maps to NM_033064.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:3909499 T>C maps to NM_033064.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr19:3907801 G>A maps to NM_033064.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr19:3905636 C>T maps to NM_033064.4 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:3910799 G>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:3908296 C>T maps to NM_033064.4 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:123659395 C>T maps to NM_001001976.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:123600643 G>A maps to NM_001001976.1 Y370Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr12:51213427 C>T maps to NM_005171.4 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:51213429 A>T maps to NM_005171.4 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:51213429 A>G maps to NM_005171.4 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:51213427 C>T maps to NM_005171.4 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr12:51203254 T>C maps to NM_005171.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr12:51203254 T>C maps to NM_005171.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr12:51213427 C>T maps to NM_005171.4 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr12:51213427 C>A maps to NM_005171.4 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:51203254 T>C maps to NM_005171.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:51207886 T>C maps to NM_005171.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:175939456 G>T maps to NM_001880.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr2:175986238 G>A maps to NM_001880.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:212792437 A>G maps to NM_001040619.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr22:39917991 T>C maps to NM_182810.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:50436243 C>T maps to NM_001193646.1 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:50436243 C>T maps to NM_001193646.1 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:161771848 G>A maps to NM_007348.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:161928326 A>G maps to NM_007348.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:161928305 C>T maps to NM_007348.2 I625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr1:161821599 C>T maps to NM_007348.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:32095975 C>T maps to NM_004381.4 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:32087639 G>A maps to NM_004381.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:53910962 C>T maps to NM_001130059.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:14578225 A>G maps to NM_018179.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:14613681 T>C maps to NM_018179.3 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:14650994 C>A maps to NM_018179.3 T1267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:14613516 A>G maps to NM_018179.3 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:14589104 C>T maps to NM_018179.3 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr12:14650919 A>G maps to NM_018179.3 A1242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:14577142 T>C maps to NM_018179.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:10565990 T>A maps to NM_024997.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:10567366 C>T maps to NM_024997.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr16:10532079 T>C maps to NM_024997.2 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:10576084 G>A maps to NM_024997.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:81548427 G>A maps to NM_031482.4 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:81474357 C>A maps to NM_031482.4 C135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:234172708 A>G maps to ENST00000392018 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:234198997 C>T maps to ENST00000392018 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:234198997 C>T maps to ENST00000392018 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr11:64676561 C>T maps to ENST00000421419 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:64669628 C>T maps to ENST00000421419 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:64679721 C>T did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr11:64664002 A>G maps to ENST00000421419 A1788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:64676540 T>C maps to ENST00000421419 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:64665768 G>T maps to ENST00000421419 R1581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:64662681 C>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:64680830 C>T maps to ENST00000421419 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:64668486 C>T maps to ENST00000421419 P1401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr14:96757160 T>C maps to NM_018036.5 L1897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr14:96781570 C>A maps to NM_018036.5 E1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr14:96781802 G>T maps to NM_018036.5 S1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:96782957 A>G maps to NM_018036.5 G1091G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:96791994 C>A maps to NM_018036.5 E810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:96770876 T>C maps to NM_018036.5 G1599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:96777549 C>T maps to NM_018036.5 A1355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:112280339 T>C maps to NM_022488.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:107377623 A>G did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:107377288 T>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:107374573 G>A did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr2:242608057 G>A maps to ENST00000337606 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:242590688 G>A maps to ENST00000337606 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:63284788 G>T maps to NM_032852.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:63300480 C>T maps to NM_032852.2 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:63282306 A>T maps to NM_032852.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:10655786 G>A maps to NM_032885.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:10657767 A>G maps to NM_032885.4 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr3:11389457 G>A maps to NM_006395.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:11356963 G>A maps to NM_006395.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:11389358 C>T maps to NM_006395.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:11354803 T>C maps to NM_006395.2 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:11421483 C>T maps to NM_006395.2 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:11404303 C>A maps to NM_006395.2 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:220088943 G>A maps to NM_024085.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:220085471 G>A maps to NM_024085.3 H837H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr2:220089546 T>C maps to NM_024085.3 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr7:150720190 C>T maps to NM_173681.5 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:150716242 G>A maps to NM_173681.5 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:292613 C>T maps to ENST00000409479 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr2:216203554 T>C maps to NM_004044.6 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:216184442 C>T maps to NM_004044.6 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:216190750 C>T maps to NM_004044.6 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:216203554 T>C maps to NM_004044.6 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr2:216203554 T>C maps to NM_004044.6 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:216203554 T>C maps to NM_004044.6 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr2:216203554 T>C maps to NM_004044.6 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr2:216203554 T>C maps to NM_004044.6 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr14:51087416 C>A maps to ENST00000358385 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr14:51087416 C>A maps to ENST00000358385 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr14:51057727 C>T maps to ENST00000358385 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:38570502 T>C maps to NM_001135673.1 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:38570598 T>C maps to NM_001135673.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:63419960 A>G maps to NM_015459.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr11:63398691 A>C maps to NM_015459.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr11:108224595 T>C maps to NM_000051.3 G2925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr11:108124763 G>T maps to NM_000051.3 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr11:108196252 A>G maps to NM_000051.3 R2263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr11:108106478 A>G maps to NM_000051.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:108115599 C>T maps to NM_000051.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr11:108199845 T>C maps to NM_000051.3 T2396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:108199839 A>G maps to NM_000051.3 S2394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:108106478 A>G maps to NM_000051.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:108138040 C>T maps to NM_000051.3 N870N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:108199926 A>G maps to NM_000051.3 E2423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:108236117 A>G maps to NM_000051.3 K3018K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:108199839 A>G maps to NM_000051.3 S2394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr11:108213986 G>A maps to NM_000051.3 W2769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr11:108173723 G>T maps to NM_000051.3 E1822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:108205710 G>T maps to NM_000051.3 E2676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:108172384 C>T maps to NM_000051.3 R1730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:108115599 C>T maps to NM_000051.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:108168099 G>T maps to NM_000051.3 E1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:108186755 C>T maps to NM_000051.3 H2038H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr11:108188128 T>C maps to NM_000051.3 I2076I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr11:108106478 A>G maps to NM_000051.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr11:108224556 A>G maps to NM_000051.3 R2912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:108199880 C>A maps to NM_000051.3 S2408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:108200956 C>T maps to NM_000051.3 Q2442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr11:108199926 A>G maps to NM_000051.3 E2423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr11:108199839 A>G maps to NM_000051.3 S2394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:108160516 T>A maps to NM_000051.3 Y1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:108199908 G>A maps to NM_000051.3 L2417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:108200946 A>G maps to NM_000051.3 T2438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:108201088 C>T maps to NM_000051.3 R2486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr11:108117784 T>C maps to NM_000051.3 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:108114846 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:108175527 C>T maps to NM_000051.3 R1875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr11:108224595 T>C maps to NM_000051.3 G2925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr11:108236216 A>G maps to NM_000051.3 G3051G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:108192064 G>T maps to NM_000051.3 E2164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr11:108122629 A>G maps to NM_000051.3 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr11:108183200 A>G maps to NM_000051.3 K1994K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr11:108172413 C>T maps to NM_000051.3 N1739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr11:108122665 T>C maps to NM_000051.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr11:108199926 A>G maps to NM_000051.3 E2423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr11:108216627 T>C maps to NM_000051.3 S2859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:108115599 C>T maps to NM_000051.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:108165728 C>T maps to NM_000051.3 R1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr11:108180982 A>G maps to NM_000051.3 T1953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:108106478 A>G maps to NM_000051.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr11:108172506 A>G maps to NM_000051.3 S1770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr11:108235819 T>C maps to NM_000051.3 Y2954Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:108178662 C>A maps to NM_000051.3 S1905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr11:108155172 T>A maps to NM_000051.3 L1322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:108143335 T>C did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:108186611 A>G maps to NM_000051.3 G2023G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr11:108201090 A>G maps to NM_000051.3 R2486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:108155199 G>A maps to NM_000051.3 Q1331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:108199917 C>A maps to NM_000051.3 A2420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr11:108150314 C>T maps to NM_000051.3 Q1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr11:108180982 A>G maps to NM_000051.3 T1953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:108236087 T>C maps to NM_000051.3 R3008R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr11:108153521 G>A maps to NM_000051.3 W1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr11:108155133 A>G maps to NM_000051.3 A1309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr11:108165709 T>C maps to NM_000051.3 L1611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr11:108199845 T>C maps to NM_000051.3 T2396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr11:108181006 T>C maps to NM_000051.3 Y1961Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr11:108126967 G>T maps to NM_000051.3 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr11:108160480 T>C maps to NM_000051.3 F1463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:108098419 A>G maps to NM_000051.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr11:108143456 T>C maps to NM_000051.3 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr11:108216501 T>C maps to NM_000051.3 Y2817Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr11:108199845 T>C maps to NM_000051.3 T2396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr11:108218090 A>G maps to NM_000051.3 L2890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:108224556 A>G maps to NM_000051.3 R2912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr11:108141989 T>C maps to NM_000051.3 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr11:108199845 T>C maps to NM_000051.3 T2396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr11:108172413 C>T maps to NM_000051.3 N1739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:108160498 T>C maps to NM_000051.3 I1469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:108172505 C>A maps to NM_000051.3 S1770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr11:108119823 G>A maps to NM_000051.3 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr11:108199908 G>A maps to NM_000051.3 L2417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr11:108199938 T>A maps to NM_000051.3 L2427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr11:108224607 G>A did not map to a codon.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr11:108129748 C>T maps to NM_000051.3 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:108218090 A>G maps to NM_000051.3 L2890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:108224595 T>C maps to NM_000051.3 G2925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:108186741 C>T maps to NM_000051.3 R2034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:108186599 T>C maps to NM_000051.3 Y2019Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:108199929 A>G maps to NM_000051.3 V2424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:108218090 A>G maps to NM_000051.3 L2890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:108199845 T>C maps to NM_000051.3 T2396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr11:108236117 A>G maps to NM_000051.3 K3018K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr11:108224556 A>G maps to NM_000051.3 R2912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr11:108199782 T>C maps to NM_000051.3 S2375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:108216546 T>G maps to NM_000051.3 R2832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:108129748 C>T maps to NM_000051.3 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:108117799 T>A maps to NM_000051.3 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:108119823 G>T maps to NM_000051.3 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr11:108160480 T>C maps to NM_000051.3 F1463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr11:108200959 C>T maps to NM_000051.3 R2443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr11:108183200 A>G maps to NM_000051.3 K1994K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr11:108199899 A>G maps to NM_000051.3 Q2414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr11:108199917 C>A maps to NM_000051.3 A2420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:108137989 A>G maps to NM_000051.3 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:108186795 G>T maps to NM_000051.3 E2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr11:108199839 A>G maps to NM_000051.3 S2394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr11:108160516 T>A maps to NM_000051.3 Y1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr11:108236081 T>A maps to NM_000051.3 A3006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:108218088 C>T maps to NM_000051.3 L2890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:108236202 C>T maps to NM_000051.3 R3047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr11:108143552 C>A maps to NM_000051.3 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr11:108186611 A>G maps to NM_000051.3 G2023G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:108122629 A>G maps to NM_000051.3 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:108122665 T>C maps to NM_000051.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:108199845 T>C maps to NM_000051.3 T2396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:108138004 T>C maps to NM_000051.3 F858F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:108180946 T>C maps to NM_000051.3 V1941V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:108199782 T>C maps to NM_000051.3 S2375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:81077155 G>A maps to NM_015251.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:7045914 G>A maps to NM_001940.3 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:7045896 G>A maps to NM_001940.3 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:7050699 C>T maps to NM_001940.3 A1174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:7045908 G>A maps to NM_001940.3 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:94750550 G>A maps to NM_005172.1 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr15:25953376 C>T maps to NM_024490.3 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr15:25959160 G>A maps to NM_024490.3 N668N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:25961894 C>T maps to NM_024490.3 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr15:25926203 C>G maps to NM_024490.3 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr15:25981228 G>A maps to NM_024490.3 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr15:25959028 G>A maps to NM_024490.3 C712C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr15:25963436 C>T maps to NM_024490.3 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:25932872 G>A maps to NM_024490.3 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:25958938 G>A maps to NM_024490.3 F742F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:26026210 C>T maps to NM_024490.3 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr15:26026200 T>A maps to NM_024490.3 K207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:25958915 G>T maps to NM_024490.3 S750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:26026360 C>T maps to NM_024490.3 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:25959111 G>A maps to NM_024490.3 Q685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr15:25972361 C>A maps to NM_024490.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr15:25936863 G>A maps to NM_024490.3 Q1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:25963382 G>A maps to NM_024490.3 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr15:25963544 C>T maps to NM_024490.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr15:25969040 C>A maps to NM_024490.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:159996612 G>A maps to NM_025153.2 C1276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:160033838 C>T maps to NM_025153.2 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:159996540 G>A maps to NM_025153.2 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:160114895 G>C maps to NM_025153.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:160059366 T>C maps to NM_025153.2 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr5:160016679 A>G maps to NM_025153.2 D1223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr5:159992750 A>G maps to NM_025153.2 T1365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr5:160016679 A>G maps to NM_025153.2 D1223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:160016679 A>G maps to NM_025153.2 D1223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr4:47537546 C>T maps to NM_020453.3 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:47570889 G>T maps to NM_020453.3 E964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr4:47538042 C>T maps to NM_020453.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr4:47537946 C>T maps to NM_020453.3 N304N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr4:47589067 C>T maps to NM_020453.3 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:113536152 C>T maps to NM_032189.3 D1117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr13:113473679 C>T maps to NM_032189.3 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr13:113487301 G>A maps to NM_032189.3 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:113477718 C>A maps to NM_032189.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr13:113439564 G>A maps to NM_032189.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr13:113496636 C>T maps to NM_032189.3 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:113481129 C>T maps to NM_032189.3 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:113510356 C>T maps to NM_032189.3 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr13:113530176 G>A maps to NM_032189.3 V1083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr3:182584207 G>A maps to NM_014616.1 K532K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:182591671 G>T maps to NM_014616.1 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr3:182602568 T>C maps to NM_014616.1 A846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr23:138844133 A>T did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:138813817 A>G did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:138886723 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:138886724 T>C did not map to a codon.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr23:138886724 T>C did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:138865392 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:138813817 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:138878544 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:138880435 C>A did not map to a codon.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr23:138897072 A>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:138867414 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:138897043 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:138864828 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:138813895 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:138908877 T>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:138865392 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:138845530 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:138850427 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:138856892 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:138850579 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:138865392 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:138871578 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:138886703 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:138908878 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:138856884 A>G did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:138864757 C>T did not map to a codon.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr23:138823226 C>T did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:138832228 T>C did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:138865391 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr23:138850579 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:138864757 C>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:138827939 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:138850532 T>C did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr13:25265210 G>A maps to NM_001185085.1 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr13:25266667 G>A maps to NM_001185085.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:25274945 C>T maps to NM_001185085.1 D595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:25272839 C>T maps to NM_001185085.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:25264761 G>A maps to NM_001185085.1 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr13:25264510 C>T maps to NM_001185085.1 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr13:25281204 G>A maps to NM_001185085.1 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr13:25275026 T>C maps to NM_001185085.1 D622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr13:25280565 C>T maps to NM_001185085.1 Q718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr13:25265129 C>T maps to NM_001185085.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr13:25280565 C>T maps to NM_001185085.1 Q718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr13:25262500 G>A maps to NM_001185085.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr19:19764640 G>A maps to NM_020410.2 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr19:19758406 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:19770790 G>A maps to NM_020410.2 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:19766436 G>A maps to NM_020410.2 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:19758307 G>A maps to NM_020410.2 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:19766158 G>A maps to NM_020410.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr1:17313399 G>A maps to NM_022089.2 Y1045Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:17318989 C>T maps to NM_022089.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:17326987 C>T maps to NM_022089.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:17322518 T>C maps to NM_022089.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:17318280 C>T maps to NM_022089.2 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:194152544 A>G maps to NM_024524.3 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:194175076 C>T maps to NM_024524.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:194152478 C>T maps to NM_024524.3 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr3:194152544 A>G maps to NM_024524.3 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr3:193120533 C>T maps to NM_032279.2 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr3:193210931 C>A maps to NM_032279.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:193125104 G>A maps to NM_032279.2 A1125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:193201723 C>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:193061773 C>T maps to NM_198505.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:192992857 T>C maps to NM_198505.2 T1210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:193039554 G>A maps to NM_198505.2 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr3:193007735 C>T maps to NM_198505.2 V987V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:193039608 G>T maps to NM_198505.2 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:193031886 C>A maps to NM_198505.2 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:192993048 T>G maps to NM_198505.2 R1147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:193016980 G>T maps to NM_198505.2 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:193031886 C>A maps to NM_198505.2 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:193052727 A>C maps to NM_198505.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr3:193019038 G>A maps to NM_198505.2 Y912Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr3:193042661 G>T maps to NM_198505.2 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr3:193019038 G>A maps to NM_198505.2 Y912Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr3:193052738 G>A maps to NM_198505.2 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr3:193019038 G>A maps to NM_198505.2 Y912Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:193081105 A>G maps to NM_198505.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:193019038 G>T maps to NM_198505.2 Y912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:116932064 C>T maps to NM_000701.7 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:116932963 C>A maps to NM_000701.7 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:116943801 C>T maps to NM_000701.7 F923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:116935540 C>T maps to NM_000701.7 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:116932064 C>A maps to NM_000701.7 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:116936292 C>T maps to NM_000701.7 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:116939234 G>T maps to NM_000701.7 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr1:160104401 C>A maps to NM_000702.3 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:160106414 C>T maps to NM_000702.3 N873N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:160105722 C>T maps to NM_000702.3 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:160105027 C>A maps to NM_000702.3 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:160106411 G>A maps to NM_000702.3 E872E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr1:160090718 C>T maps to NM_000702.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:42482425 G>A maps to ENST00000441343 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:42492183 G>A maps to ENST00000441343 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:42489084 C>A maps to ENST00000441343 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr19:42492231 C>T maps to ENST00000441343 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr19:42474548 G>A maps to ENST00000441343 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:42474415 G>T maps to ENST00000441343 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:160151794 C>T maps to NM_144699.3 D981D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:160125025 T>C maps to NM_144699.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:160156152 G>A maps to NM_144699.3 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr1:160147441 C>T maps to NM_144699.3 Y908Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:160124941 C>T maps to NM_144699.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:160144032 C>T maps to NM_144699.3 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr1:160143411 C>A maps to NM_144699.3 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:160144451 C>T maps to NM_144699.3 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:169100585 C>T maps to NM_001677.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr17:7559065 C>A maps to NM_001678.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:7557457 C>T maps to NM_001678.3 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:7559173 C>T maps to NM_001678.3 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:119504980 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:119512554 G>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:119500596 G>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:119504622 A>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:119513480 G>T did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr23:119513444 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:119513373 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:119504597 C>A did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:119512616 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:28892324 C>T maps to NM_173201.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr16:28913311 C>T maps to NM_173201.3 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr16:28906273 G>A maps to NM_173201.3 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr16:28906267 C>A maps to NM_173201.3 C471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr16:28913194 C>T maps to NM_173201.3 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:28913386 C>T maps to NM_173201.3 N768N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:28913392 C>T maps to NM_173201.3 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:110765726 C>T maps to NM_170665.3 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr12:110778759 C>T maps to NM_170665.3 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:110778730 C>T maps to NM_170665.3 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr12:110720596 T>C maps to NM_170665.3 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:3854940 G>A maps to NM_174953.1 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:3839750 C>A maps to NM_174953.1 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:3844423 G>A maps to NM_174953.1 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:3850720 C>T maps to NM_174953.1 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:89984901 T>C maps to ENST00000428670 K1203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:90049657 G>A maps to ENST00000428670 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:89998029 G>A maps to ENST00000428670 R846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:90049524 G>A maps to ENST00000428670 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:90015376 G>T maps to ENST00000428670 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:89992929 G>A maps to ENST00000428670 I1105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:90028930 T>C maps to ENST00000428670 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:10400395 G>A maps to NM_001001331.2 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:10387720 G>A maps to NM_001001331.2 F835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr3:10382254 G>A maps to NM_001001331.2 H1017H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:10387720 G>A maps to NM_001001331.2 F835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:10400557 G>A maps to NM_001001331.2 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:10382368 G>A maps to NM_001001331.2 I979I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr3:10382239 G>A maps to NM_001001331.2 V1022V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:10452383 G>A maps to NM_001001331.2 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:10370596 G>A maps to NM_001001331.2 S1211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:10370647 G>A maps to NM_001001331.2 A1194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:10443964 G>A maps to NM_001001331.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr3:10417221 G>A maps to NM_001001331.2 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:152830535 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:152826152 C>T did not map to a codon.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr23:152825307 G>A did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr23:152845600 C>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:152825308 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:152826335 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:152830476 C>T did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr23:152818542 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:152825302 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr23:152825304 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:152823695 C>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:152821668 C>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:152815703 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:152822431 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr23:152814216 G>A did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr23:152813422 G>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:152823727 G>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:152845476 C>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:152808501 C>T did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:152815645 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:152825298 C>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:152801760 G>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:152815059 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:203683386 G>A maps to NM_001001396.1 A796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:203677150 C>T maps to NM_001001396.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:203677063 C>T maps to NM_001001396.1 C463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr1:203682363 G>A maps to NM_001001396.1 K761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:203677054 C>T maps to NM_001001396.1 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:130718462 G>A maps to NM_001001486.1 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:130656308 T>C did not map to a codon.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:130650983 T>C did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:84456021 C>T maps to ENST00000416219 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:84485696 G>T maps to ENST00000416219 G611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:84432208 G>A maps to ENST00000416219 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:84494379 C>T maps to ENST00000416219 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:36049505 G>A maps to NM_000704.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr19:36050943 G>A maps to NM_000704.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr19:36049520 G>A maps to NM_000704.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:36047955 G>A maps to NM_000704.2 Y576Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr13:114303757 G>A maps to NM_000705.3 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr13:114307229 G>A maps to NM_000705.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:114305994 G>A maps to NM_000705.3 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:114309222 C>T maps to NM_000705.3 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr18:43667150 A>G maps to NM_001001937.1 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:43675040 A>C maps to NM_001001937.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr18:43668216 G>A maps to NM_001001937.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:57033898 T>C maps to NM_001686.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:57038967 C>T maps to NM_001686.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:57036250 G>T maps to NM_001686.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:7838093 C>T maps to NM_001001973.1 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr17:73038646 G>A maps to NM_006356.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr21:27102051 T>C maps to NM_001003701.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:99057761 C>T maps to NM_001198879.1 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:41942367 G>T maps to ENST00000417807 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:153660740 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:153662698 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:153663635 C>T did not map to a codon.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr23:153662731 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:153662684 A>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:153662579 C>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:153657076 G>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:153662579 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:153662579 C>T did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:153662731 T>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:81613992 C>T maps to NM_001017971.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:81614013 G>A maps to NM_001017971.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:81613866 C>T maps to NM_001017971.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:40448332 G>A did not map to a codon.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr23:40448351 G>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:40464995 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:40456787 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:40458932 T>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:40646370 G>A maps to NM_001130020.1 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr17:40647652 G>A maps to NM_001130020.1 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:40622130 T>C maps to NM_001130020.1 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr12:124233130 G>A maps to NM_012463.3 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:124233304 T>C maps to NM_012463.3 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr12:124233130 G>A maps to NM_012463.3 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:124239010 C>T maps to NM_012463.3 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:124209233 G>T maps to NM_012463.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:124241407 C>T maps to NM_012463.3 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:138447110 C>T maps to NM_130840.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr7:138394385 G>A maps to NM_130840.2 H804H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:138434019 G>A maps to NM_130840.2 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr7:138406766 G>A maps to NM_130840.2 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:44442279 T>G maps to NM_004047.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:44441773 G>A maps to NM_004047.3 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:44442761 G>A maps to NM_004047.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr1:44442761 G>A maps to NM_004047.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:44442443 G>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:2569318 C>T maps to NM_001694.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:67477004 G>T maps to NM_004691.4 Y186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:67472490 G>A maps to NM_004691.4 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:87111318 C>T maps to NM_152565.1 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:87151752 G>T maps to NM_152565.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:87111212 C>T maps to NM_152565.1 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:113499924 A>G maps to NM_001690.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:113505161 T>C maps to NM_001690.3 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr3:113497629 C>A maps to NM_001690.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:71187120 G>T maps to NM_001692.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:20068134 C>T maps to NM_001693.3 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:20067894 G>A maps to NM_001693.3 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:10917730 T>A maps to NM_001039362.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:10894130 C>T maps to NM_001039362.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr2:10904520 G>A maps to NM_001039362.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:10904520 G>A maps to NM_001039362.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr14:67814168 A>G maps to NM_015994.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:18096035 T>C maps to NM_001696.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr22:18096035 T>C maps to NM_001696.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr22:18096035 T>C maps to NM_001696.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:46739760 G>A maps to NM_080653.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:46739601 G>A maps to NM_080653.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:46739255 G>A maps to NM_080653.3 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:128505583 C>A maps to ENST00000492758 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:128505571 C>T maps to ENST00000492758 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:198492625 A>G maps to ENST00000489986 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr8:54684640 C>T maps to NM_015941.2 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:54682215 A>G maps to NM_015941.2 N379N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr23:77245431 G>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:77254014 G>A did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr23:77243950 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:77301886 T>C did not map to a codon.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr23:77270224 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:77264679 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:77289306 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:77245176 T>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:77258667 G>T did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:77301995 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:77284786 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:77244073 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:77245263 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:77245407 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:77258636 A>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:52509058 G>T maps to NM_000053.2 R1411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr13:52534301 G>T maps to NM_000053.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:52515217 G>A maps to NM_000053.2 D1185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr13:52524528 C>T maps to NM_000053.2 E818E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:42577653 A>G maps to NM_006095.2 N397N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:42414956 C>T maps to NM_006095.2 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:42580396 G>A maps to NM_006095.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:42526818 C>A maps to NM_006095.2 E590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:42592856 G>T maps to NM_006095.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr4:42580381 T>C maps to NM_006095.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:26148996 T>C did not map to a codon.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr13:26133868 G>T maps to NM_016529.4 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:26156084 G>A maps to NM_016529.4 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr13:26144925 G>T maps to NM_016529.4 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:26104170 C>T maps to NM_016529.4 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:26104697 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:26129151 A>G maps to NM_016529.4 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:26117530 A>G maps to NM_016529.4 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:26343297 C>T maps to NM_016529.4 H833H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr13:26043181 A>C maps to NM_016529.4 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr13:26349042 G>A maps to NM_016529.4 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr13:26411377 C>A maps to NM_016529.4 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:26151249 C>T maps to NM_016529.4 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:55335754 A>G maps to NM_005603.4 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:55328505 G>A maps to NM_005603.4 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:55362762 C>A maps to NM_005603.4 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr18:55355591 C>A maps to NM_005603.4 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:55362762 C>A maps to NM_005603.4 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr18:55328454 G>T maps to NM_005603.4 A886A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D5-6534-01A-21D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr18:55322641 G>A maps to NM_005603.4 H905H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:154304479 A>C maps to NM_020452.3 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:154313509 C>T maps to NM_020452.3 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr1:154316886 C>T maps to NM_020452.3 I717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:154316433 C>T maps to NM_020452.3 Y641Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:154315956 C>T maps to NM_020452.3 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr1:154302929 G>A maps to NM_020452.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:1800384 C>A maps to NM_138813.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr19:1791794 G>C maps to NM_138813.2 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:1802061 C>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr19:1805888 G>A maps to NM_138813.2 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr19:1796743 C>T maps to NM_138813.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr15:50223390 A>G maps to NM_024837.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr15:50264887 C>T maps to NM_024837.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:50209137 C>A maps to NM_024837.2 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:50339640 C>T maps to NM_024837.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr15:50264848 G>A maps to NM_024837.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr15:50223451 G>A maps to NM_024837.2 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr15:50339658 A>G maps to NM_024837.2 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr15:50264940 G>T maps to NM_024837.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr20:50230367 C>A maps to NM_006045.1 G807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:50310567 C>T maps to NM_006045.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr20:50234049 G>T maps to NM_006045.1 C798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:50310600 C>T maps to NM_006045.1 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr20:50273554 G>A maps to NM_006045.1 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:50287684 G>T maps to NM_006045.1 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:50273620 G>A maps to NM_006045.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:50244186 G>A maps to NM_006045.1 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr20:50346471 G>A maps to NM_006045.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr20:50235299 G>A maps to NM_006045.1 Q751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:50244156 C>T maps to NM_006045.1 E609E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr18:77067227 G>A maps to NM_198531.3 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:76973980 C>A maps to NM_198531.3 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:76856575 C>T maps to NM_198531.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr18:77107792 G>A maps to NM_198531.3 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr18:77134018 G>A maps to NM_198531.3 T1064T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:47101585 A>G maps to NM_022745.3 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:142286944 C>T maps to NM_001184.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:142172005 C>T maps to NM_001184.3 A2575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:142266742 C>A maps to NM_001184.3 E1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:142274800 A>G maps to NM_001184.3 C753C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:142284983 C>A maps to NM_001184.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:142168351 T>C maps to NM_001184.3 G2618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:142261539 C>T maps to NM_001184.3 L1139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:142259819 A>G maps to NM_001184.3 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:142261600 T>A did not map to a codon.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr3:142180841 C>A maps to NM_001184.3 E2378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:142266691 C>A maps to NM_001184.3 E1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:142274943 C>A maps to NM_001184.3 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:142255032 G>A maps to NM_001184.3 Q1246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:142180839 T>C maps to NM_001184.3 E2378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr3:142204010 G>A maps to NM_001184.3 L2064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:142241650 T>C maps to NM_001184.3 G1395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr3:48491482 A>G maps to NM_130384.1 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:48501973 G>A maps to NM_130384.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:48506357 C>T maps to NM_130384.1 H728H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr3:48501640 T>G maps to NM_130384.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr3:48502036 G>A maps to NM_130384.1 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr3:48500818 T>C maps to NM_130384.1 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr3:48502012 A>G maps to NM_130384.1 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:48502012 A>G maps to NM_130384.1 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr20:3575195 C>T maps to NM_139321.2 G1131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr20:3527990 C>T maps to NM_139321.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:3619483 C>T maps to NM_139321.2 R1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr20:3578643 C>T maps to NM_139321.2 D1187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:3553392 C>T maps to NM_139321.2 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr20:3578565 T>C maps to NM_139321.2 I1161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:3578565 T>C maps to NM_139321.2 I1161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr10:116931042 C>T maps to NM_207303.2 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr10:116930919 T>C maps to NM_207303.2 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:117486832 G>T maps to NM_207303.2 E1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr10:117154169 T>C maps to NM_207303.2 A1059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:117040935 C>T maps to NM_207303.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr10:117154167 G>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:116931042 C>A maps to NM_207303.2 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:117045868 G>T maps to NM_207303.2 E793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr10:117026309 C>T maps to NM_207303.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr10:117154169 T>C maps to NM_207303.2 A1059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:76937102 A>G did not map to a codon.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr23:76938435 G>A did not map to a codon.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr23:76938026 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:76909631 T>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:76920266 T>G did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:76814234 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:76889175 G>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:76939220 A>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:76875866 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:76937786 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:76890144 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:76938994 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:76939207 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:76939585 T>G did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:76814175 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:76918883 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:76937355 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:76888869 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr23:76874358 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr23:76829805 G>A did not map to a codon.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr23:76912070 T>C did not map to a codon.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr23:76938028 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:76845305 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:76938538 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:76952108 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:76814234 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:76952147 T>G did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:76813057 C>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:76849274 A>G did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr23:76776898 C>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:76814176 T>C did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:76776284 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:76888870 A>G did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:76778749 C>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:76937848 T>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:76938026 T>C did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:76912069 A>G did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:76855977 T>C did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:76888870 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:76855018 T>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:76849280 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:76855977 T>C did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:76939909 A>T did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:76937222 T>C did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:76938312 G>T did not map to a codon.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr23:76776887 G>A did not map to a codon.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr23:76937222 T>C did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:76912070 T>C did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:76939383 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:76937257 C>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:16306991 C>T maps to NM_000332.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:16328058 C>T maps to NM_000332.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:16328274 C>T maps to NM_000332.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr6:16327866 C>T maps to NM_000332.3 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr6:16326657 C>G maps to NM_000332.3 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr22:46239015 C>T maps to NM_013236.3 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr22:46088947 T>C maps to NM_013236.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr12:111948297 A>C maps to NM_002973.3 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:111954042 C>T maps to NM_002973.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:111990213 G>A maps to NM_002973.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:111957768 C>T maps to NM_002973.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr16:28841954 C>T maps to NM_148414.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:28841993 C>T maps to NM_148414.1 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:28836699 G>T maps to NM_148414.1 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:28847719 G>A maps to NM_148414.1 P1071P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:28843821 G>T maps to NM_148414.1 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:28841283 C>T maps to NM_148414.1 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:92548703 C>A maps to ENST00000359819 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr14:92549561 G>A maps to ENST00000359819 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr23:13337511 A>G did not map to a codon.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr23:13337617 T>C did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:13337914 T>C did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:13337698 G>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:13337284 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:13337100 G>A did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:13337343 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:13337504 G>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:13337512 T>C did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:13337467 A>T did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr23:13337512 T>A did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:13337344 G>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:13337118 T>C did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:13337511 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr23:13337119 C>A did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:13337118 T>C did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:13337616 G>T did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:13337616 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:63965618 G>A maps to NM_001177387.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:63973886 C>T maps to NM_001177387.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:63981585 T>C maps to NM_001177387.1 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:63968080 C>T maps to NM_001177387.1 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:63898558 G>A maps to NM_001177387.1 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:63981348 G>A maps to NM_001177387.1 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:63981840 C>T maps to NM_001177387.1 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr7:105516944 C>T maps to NM_020725.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:105264683 G>A maps to NM_020725.1 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:110032749 G>A maps to NM_153340.4 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:110031014 C>T maps to NM_153340.4 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:110033831 G>A maps to NM_153340.4 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:110030319 C>T maps to NM_153340.4 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:110030426 G>A did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:110029638 T>C maps to NM_153340.4 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:42274996 G>A maps to NM_020218.1 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:42272801 G>A maps to NM_020218.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:42272169 G>A maps to NM_020218.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:93983173 G>A maps to NM_001698.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr9:93983251 G>A maps to NM_001698.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:54961463 G>A maps to NM_198437.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:54948570 C>T maps to NM_198437.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr20:54958084 C>A maps to NM_198437.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr20:54948524 C>A maps to NM_198437.1 G265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr20:54958084 C>T maps to NM_198437.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr20:54945232 G>T maps to NM_198437.1 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr20:54945342 T>C maps to NM_198437.1 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr17:8111143 C>A maps to NM_004217.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr19:57743406 C>T maps to NM_001015878.1 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:57746637 A>T maps to NM_001015878.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:57742666 C>T maps to NM_001015878.1 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:57743430 C>T maps to NM_001015878.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr7:70231244 G>A maps to NM_015570.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:70255369 G>A maps to NM_015570.2 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:69364345 A>G maps to NM_015570.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:70255093 G>A maps to NM_015570.2 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:70227971 G>T maps to NM_015570.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:70228048 G>A maps to NM_015570.2 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:69364441 G>A maps to NM_015570.2 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:70231244 G>A maps to NM_015570.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:69755397 T>C maps to NM_001127232.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:34163231 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:58196077 A>G maps to NM_006576.3 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr12:58191763 T>C maps to NM_006576.3 E787E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:58200172 A>G maps to NM_006576.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:32613020 C>T maps to NM_015060.1 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:63541330 G>A maps to NM_000706.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr12:63543875 G>A maps to NM_000706.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:63541221 G>A maps to NM_000706.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:63544064 C>T maps to NM_000706.3 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr12:63544439 C>T maps to NM_000706.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:63544124 C>T maps to NM_000706.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:206225063 C>T maps to NM_000707.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:153172026 A>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:153171031 C>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:153171714 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:153172078 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:153171656 C>A did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:153171564 G>A did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:153172054 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:153171549 C>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:153171550 G>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:69459753 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:69456954 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:69459684 C>T did not map to a codon.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr23:69459615 G>C did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:69459755 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:69457006 C>A did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:69457009 G>A did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:69460018 A>G did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:69459754 T>A did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:69459753 C>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:69459754 T>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:69269695 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:69269718 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:69263345 C>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:69263352 G>T did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:69261769 T>A did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:364604 G>A maps to NM_003502.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:396833 C>T maps to NM_003502.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:338181 G>A maps to NM_003502.3 D843D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:338226 G>A maps to NM_003502.3 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:359971 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:63533584 G>A maps to NM_004655.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:41749521 G>T maps to NM_021913.3 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:41726544 G>A maps to NM_021913.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:41758757 T>C maps to NM_021913.3 C604C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:41726544 G>A maps to NM_021913.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr19:41737136 G>A maps to NM_021913.3 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:41745202 G>A maps to NM_021913.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:41754431 C>T maps to NM_021913.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr7:99565997 G>A maps to NM_001185.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr7:99569606 G>T maps to NM_001185.3 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr7:99569369 G>A maps to NM_001185.3 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr7:99565928 C>T maps to NM_001185.3 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:99565928 C>T maps to NM_001185.3 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:79180996 G>A maps to ENST00000269392 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:79169742 C>T maps to ENST00000269392 E639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:79182759 C>T maps to ENST00000269392 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:28368437 A>G maps to NM_022461.3 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr3:28380073 G>A maps to NM_022461.3 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:103855847 G>A maps to NM_148174.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr15:45003811 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:45007618 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:45007718 G>T maps to NM_004048.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:45008528 C>T maps to NM_004048.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:45007619 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr15:45007618 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr15:45007619 G>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr15:45007711 C>T maps to NM_004048.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:160803675 A>C maps to NM_033168.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:235621957 G>A maps to ENST00000366599 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:235617563 G>A maps to ENST00000366599 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:235643396 C>T maps to ENST00000366599 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:235613550 G>A maps to ENST00000366599 C532C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:168726188 C>A maps to NM_020981.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:168725563 C>A maps to NM_020981.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr1:193149684 A>G maps to NM_003783.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:41032582 G>T maps to NM_033172.1 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr21:41032635 A>C maps to NM_033172.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:31903790 C>T maps to NM_194318.3 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr13:31843392 T>C maps to NM_194318.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr13:31797105 T>C maps to NM_194318.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:31860860 T>C maps to NM_194318.3 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:31891795 C>T maps to NM_194318.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:134253672 C>T maps to NM_054025.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:134254020 C>T maps to NM_054025.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:71571568 G>A maps to NM_080742.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:71665859 G>A maps to NM_080742.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr6:71666057 C>G maps to NM_080742.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:71571553 C>T maps to NM_080742.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:71665958 G>A maps to NM_080742.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:62384187 G>A maps to NM_012200.2 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:62384052 G>T maps to NM_012200.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:62383975 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:62449732 C>G maps to NM_006577.5 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:62449879 G>A maps to NM_006577.5 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:17922426 C>T maps to NM_014256.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:122691469 C>T maps to NM_030765.2 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:122691187 C>T maps to NM_030765.2 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:76751281 C>T maps to ENST00000354301 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:67183467 C>T maps to NM_033309.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:67183701 G>A maps to NM_033309.2 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:81006637 G>A maps to NM_001009905.1 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:80992967 G>A maps to NM_001009905.1 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr17:81006595 T>C maps to NM_001009905.1 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr17:80923623 T>A did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr17:81006595 T>C maps to NM_001009905.1 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr17:80963044 G>A maps to NM_001009905.1 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr17:81006595 T>C maps to NM_001009905.1 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:58024993 G>T maps to NM_001478.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:47241501 C>A maps to NM_153446.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:47246129 G>T maps to NM_153446.2 G455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr17:47246179 C>T maps to NM_153446.2 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr17:47241555 C>T maps to NM_153446.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr12:663017 C>T maps to NM_173593.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:665772 T>G maps to NM_173593.3 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:569685 G>A maps to NM_173593.3 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:372107 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:372874 C>T maps to NM_178537.4 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr11:373027 G>A maps to NM_178537.4 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:33113457 C>T maps to NM_001497.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:44450592 G>A maps to ENST00000309519 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:44456011 C>T maps to ENST00000309519 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:118937519 G>A maps to NM_212543.1 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr20:48260137 A>G maps to NM_004776.3 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:48253963 G>C maps to NM_004776.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr18:29205684 G>A maps to NM_004775.3 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr18:29206286 T>C maps to NM_004775.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:29207070 C>A maps to NM_004775.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr18:29225341 T>C maps to NM_004775.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:177035583 C>T maps to NM_007255.2 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:177031467 C>A maps to NM_007255.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:177034374 C>T maps to NM_007255.2 H162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr17:19246688 C>T maps to NM_015681.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:19250579 A>G did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr9:104130524 G>A maps to NM_001701.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:117161699 G>A maps to NM_012104.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:117161342 C>T maps to NM_012104.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr21:42622777 C>T maps to NM_012105.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr21:42609498 G>A maps to NM_012105.3 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr21:42622779 G>A maps to NM_012105.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr6:90661314 C>T maps to NM_001170794.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:90661335 C>T maps to NM_001170794.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:90642162 A>G maps to NM_001170794.1 C830C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:33255865 A>G maps to NM_004323.5 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:57046916 G>A maps to NM_004282.3 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr6:57046875 G>T maps to NM_004282.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr10:121436595 C>G maps to NM_004281.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:121436433 G>A maps to NM_004281.3 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:38067831 G>T maps to NM_004874.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr21:11097586 A>T maps to NM_182482.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr21:11098731 C>T maps to NM_181704.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr21:11097586 A>T maps to NM_182482.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:79428996 C>T maps to ENST00000436173 S2436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:79409712 C>T maps to ENST00000436173 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:79422358 G>A maps to ENST00000436173 A1504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:79411430 C>T maps to ENST00000436173 F783F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr17:79419841 G>A maps to ENST00000436173 T1470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:79428909 C>T maps to ENST00000436173 S2407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:79425326 C>T maps to ENST00000436173 G1726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:79428888 C>T maps to ENST00000436173 T2400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:143602182 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:143557946 C>T maps to NM_001702.2 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr8:143624774 G>A maps to NM_001702.2 S1475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr8:143607952 C>T maps to NM_001702.2 D1121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:143599548 C>T maps to NM_001702.2 G956G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:32201935 G>A maps to NM_001703.2 Y1062Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr1:32193839 G>A maps to NM_001703.2 H1486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:32206118 C>T maps to NM_001703.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:32205596 C>T maps to NM_001703.2 E699E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:32196523 A>G maps to NM_001703.2 Y1419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:32198144 C>T maps to NM_001703.2 S1231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:69646535 G>T maps to NM_001704.2 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:70037712 T>G maps to NM_001704.2 G989G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr6:69666691 C>T maps to NM_001704.2 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr6:69646474 G>A maps to NM_001704.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr6:69666691 C>T maps to NM_001704.2 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr6:69758141 C>A maps to NM_001704.2 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:69348960 C>T maps to NM_001704.2 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:69640490 A>G maps to NM_001704.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:69666660 G>A maps to NM_001704.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:69703692 C>T maps to NM_001704.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:69349199 G>A maps to NM_001704.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:69785918 T>C maps to NM_001704.2 D823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:69666691 C>T maps to NM_001704.2 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr6:69785914 G>A maps to NM_001704.2 W822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr6:70098767 T>C maps to NM_001704.2 F1518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr6:70040395 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr6:70082296 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:79031741 C>T maps to NM_017451.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:79060364 G>A maps to NM_017451.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr7:97984393 G>A maps to NM_018842.4 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:97939784 C>T maps to NM_018842.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:97939784 C>T maps to NM_018842.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:97939766 A>G maps to NM_018842.4 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr22:38494116 G>A maps to NM_025045.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr22:38481324 T>C maps to NM_025045.4 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:1388917 C>T maps to NM_003933.4 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:33543175 G>A maps to ENST00000360661 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:28970365 C>T maps to NM_012342.2 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:65771230 C>T maps to NM_003860.3 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:102965064 G>T did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr4:102751175 T>C maps to NM_017935.4 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr4:102751175 T>C maps to NM_017935.4 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:102839316 G>T maps to NM_017935.4 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:102751175 T>C maps to NM_017935.4 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr4:102791707 C>T maps to NM_017935.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr4:102783753 A>T maps to NM_017935.4 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:102751181 G>A maps to NM_017935.4 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:102751175 T>C maps to NM_017935.4 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr4:102751175 T>C maps to NM_017935.4 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:88039740 G>A maps to NM_001173543.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:88066772 G>A maps to NM_001173543.1 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr3:52437822 G>A maps to NM_004656.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr3:52443571 C>T maps to NM_004656.2 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:52437234 G>A maps to NM_004656.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr3:52441211 C>T maps to NM_004656.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:52443585 G>A maps to NM_004656.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr3:52436618 T>C maps to NM_004656.2 E685E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:52438565 G>A maps to NM_004656.2 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:52439929 T>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:52439897 G>A maps to NM_004656.2 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:52440916 C>T maps to NM_004656.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:52442075 A>G maps to NM_004656.2 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr3:52439929 T>A did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr3:52442075 A>G maps to NM_004656.2 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr3:52436305 A>G maps to NM_004656.2 *730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:52438536 G>A maps to NM_004656.2 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:52436803 C>T maps to NM_004656.2 K658K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:215593480 C>T maps to NM_000465.2 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr2:215593694 C>T maps to NM_000465.2 W680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr2:215610449 A>G maps to NM_000465.2 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr2:215646108 C>T maps to NM_000465.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:135458513 C>A maps to NM_020064.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:91178099 A>G maps to NM_020063.1 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:91182224 G>A maps to NM_020063.1 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:91182287 C>T maps to NM_020063.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:129321173 G>A maps to NM_003658.4 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr5:17275885 C>T maps to NM_006317.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr6:31498936 G>A maps to ENST00000417556 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:31498580 A>G maps to ENST00000417556 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:31498577 A>G maps to ENST00000417556 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:31603024 A>G maps to NM_080686.2 P1759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:31600383 C>T maps to NM_080686.2 Q1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:31599779 C>T maps to NM_080686.2 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:31593264 G>T maps to NM_080686.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr6:31599191 A>C maps to NM_080686.2 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:31599710 A>G maps to NM_080686.2 T1087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:134349060 G>A maps to NM_013318.3 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:134367632 G>A maps to NM_013318.3 S2153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr9:134353964 C>T maps to NM_013318.3 L1573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:134354636 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:134308064 G>A maps to NM_013318.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:134367590 C>T maps to NM_013318.3 A2139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:134340436 C>T maps to NM_013318.3 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:134350602 C>A maps to NM_013318.3 A1029A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:171548559 G>A maps to ENST00000392078 P2409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:171510544 C>T maps to ENST00000392078 R1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:171492398 T>C maps to ENST00000392078 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:171535909 A>C maps to ENST00000392078 A2162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:171556317 T>C maps to ENST00000392078 I2642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:171510889 C>T maps to ENST00000392078 R1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:171505241 G>A maps to ENST00000392078 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:171553217 C>A maps to ENST00000392078 A2511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr1:171535400 C>T maps to ENST00000392078 L2049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:171553262 A>G maps to ENST00000392078 E2526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:171560805 C>T maps to ENST00000392078 G2839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:171535369 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:171519300 T>C maps to ENST00000392078 F1683F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:31610800 G>T maps to ENST00000404765 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:31615399 G>A maps to ENST00000404765 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:31610162 A>G maps to ENST00000404765 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:31656513 C>T maps to ENST00000375842 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr6:31669880 C>A maps to ENST00000375842 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:31655047 C>A maps to ENST00000375842 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:64757020 C>T maps to NM_138456.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:64756843 G>T maps to NM_138456.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:212860203 G>A maps to NM_018664.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:49458976 G>A maps to NM_138761.3 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:49459502 A>G maps to NM_138761.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr19:49459500 C>A maps to NM_138761.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr14:35234240 G>A maps to NM_013448.2 R1179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:35228013 G>A maps to NM_013448.2 R1428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr14:35331395 T>C maps to NM_013448.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr14:35255127 A>G maps to NM_013448.2 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr14:35331395 T>C maps to NM_013448.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:72891987 C>T maps to NM_032408.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:72892056 C>T maps to NM_032408.3 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:72892311 G>A maps to NM_032408.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:72892668 C>T maps to NM_032408.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:72891743 A>G maps to NM_032408.3 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:72891392 C>A maps to NM_032408.3 E800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr7:72892554 C>G maps to NM_032408.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:72857128 C>T maps to NM_032408.3 R1340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr7:72891393 T>C maps to NM_032408.3 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr7:72877401 A>G maps to NM_032408.3 H1033H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:72903627 G>A maps to NM_032408.3 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr7:72891393 T>C maps to NM_032408.3 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:72884709 G>A maps to NM_032408.3 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr7:72891393 T>C maps to NM_032408.3 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:72891393 T>C maps to NM_032408.3 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:56998976 G>A maps to NM_013449.3 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:57009037 C>A maps to NM_013449.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:56999643 C>T maps to NM_013449.3 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr12:56995455 A>G maps to NM_013449.3 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:160294858 G>T maps to NM_013450.2 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:160240184 G>A maps to NM_013450.2 I1231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:160205344 C>A did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr2:160240191 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:160294819 G>A maps to NM_013450.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:160240192 T>A did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr11:27147227 C>T maps to NM_003986.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:66282146 G>T maps to NM_024649.4 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:66298378 C>T maps to NM_024649.4 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:66298462 C>T maps to NM_024649.4 N524N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:66299486 C>T maps to NM_024649.4 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr12:76740390 T>C maps to NM_024685.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:76740534 A>G maps to NM_024685.3 H410H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:76740197 G>A maps to NM_024685.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:76741365 G>A maps to NM_024685.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr12:76741299 A>G maps to NM_024685.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:76740390 T>C maps to NM_024685.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:123664600 G>A maps to NM_152618.2 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:123664444 C>T maps to NM_152618.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr4:123664600 G>A maps to NM_152618.2 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:123664109 C>T maps to NM_152618.2 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:56539945 C>T maps to NM_031885.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:56519568 A>G maps to NM_031885.3 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:73027523 G>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:122749774 G>A maps to NM_176824.1 Y595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:122775937 G>A maps to NM_176824.1 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:122766817 C>T maps to NM_176824.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr4:122774121 G>A maps to NM_176824.1 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr4:122766831 G>A maps to NM_176824.1 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:33380554 C>T maps to NM_198428.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr7:33397473 G>A maps to NM_198428.2 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:33195288 A>G maps to NM_198428.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr3:107435479 A>T maps to NM_001142568.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:107517460 G>A maps to NM_001142568.1 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:107447704 C>T maps to NM_001142568.1 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:107474458 T>G maps to NM_001142568.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:107492401 G>T maps to NM_001142568.1 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr3:107497277 T>C maps to NM_001142568.1 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr3:107497277 T>C maps to NM_001142568.1 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr19:45315575 C>T maps to NM_005581.3 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:156616845 G>A maps to NM_021948.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr1:156621341 C>T maps to NM_021948.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr1:156621422 C>T maps to NM_021948.3 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr1:156622229 C>G maps to NM_021948.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:156616650 C>T maps to NM_021948.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:156616869 G>A maps to NM_021948.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:107258785 G>A maps to NM_001008405.2 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr7:107258785 G>A maps to NM_001008405.2 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:152969518 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:152981106 C>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:152988990 G>A did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:152988989 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:75268927 G>A maps to NM_001170714.1 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:75263594 G>A maps to NM_001170714.1 R855R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:94054760 G>A maps to NM_003567.2 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:94054873 G>A maps to NM_003567.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:94033330 C>T maps to NM_003567.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:94037298 C>T maps to NM_003567.2 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr20:52612475 A>T maps to NM_003657.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:52645425 G>A maps to NM_003657.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:115118320 C>T maps to NM_005872.2 W103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:59093127 A>G maps to ENST00000407086 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:58824606 C>T maps to ENST00000407086 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr17:59093181 T>C maps to ENST00000407086 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr17:59093181 T>C maps to ENST00000407086 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:59093254 C>T maps to ENST00000407086 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr17:59093181 T>C maps to ENST00000407086 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:58967062 T>C maps to ENST00000407086 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr17:59001766 G>C did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr17:58967062 T>C maps to ENST00000407086 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:49493048 G>A maps to NM_198799.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:25034331 A>T maps to NM_001178093.1 L110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:25047268 G>T maps to NM_001178093.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:49303035 C>A maps to NM_001190.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:127512216 G>T maps to NM_016567.3 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr10:127522352 G>A maps to NM_016567.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:127515177 G>T maps to NM_016567.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:50236840 C>T maps to NM_181708.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:165548101 T>C maps to NM_000055.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:165547543 G>A maps to NM_000055.2 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:165547573 G>T maps to NM_000055.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:165548744 G>T maps to NM_000055.2 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:165547686 G>A maps to NM_000055.2 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:41928240 G>A maps to NM_000709.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:41916564 G>A maps to NM_000709.3 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr6:80982869 C>A maps to NM_183050.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:31120866 C>T maps to NM_005881.2 Y77Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr16:31123555 C>T maps to NM_005881.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:85733593 C>A maps to NM_003921.4 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:85733522 C>T maps to NM_003921.4 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:85733522 C>T maps to NM_003921.4 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:60689437 G>A maps to NM_022893.3 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:60688384 G>A maps to NM_022893.3 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:60695927 A>G maps to NM_022893.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:60687880 C>T maps to NM_022893.3 T722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:60688453 G>A maps to NM_022893.3 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:60687924 C>A maps to NM_022893.3 G708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:99697841 G>T maps to NM_138576.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:99697751 C>T maps to NM_138576.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:99724036 G>T maps to NM_138576.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr14:99724036 G>T maps to NM_138576.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr14:99697697 G>A maps to NM_138576.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:60985878 T>C maps to NM_000633.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:80263050 G>A maps to NM_004049.3 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr20:30309637 A>G maps to NM_138578.1 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:52404728 G>A maps to NM_020396.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr12:12240291 C>T maps to NM_138722.1 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:12232562 G>A maps to NM_138722.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:45262793 C>T maps to NM_005178.4 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr3:187447462 G>T maps to NM_001706.4 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:187444639 C>T maps to NM_001706.4 E529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:187447619 C>T maps to NM_001706.4 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:187444606 G>T maps to NM_001706.4 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:187443313 G>A maps to NM_001706.4 C604C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:6930285 G>A maps to NM_181844.3 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr17:6928517 G>A maps to NM_181844.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:122473265 C>T maps to NM_020993.3 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr12:122468668 G>A maps to NM_020993.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:122492724 C>T maps to NM_020993.3 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:122468668 G>T maps to NM_020993.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:122473295 G>A maps to NM_020993.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:72957940 G>T maps to NM_001707.3 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:147091095 G>T maps to NM_004326.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:147092213 C>T maps to NM_004326.2 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:147094147 T>G maps to NM_004326.2 Y993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:147090653 G>A maps to NM_004326.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:147091128 C>T maps to NM_004326.2 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:147091095 G>T maps to NM_004326.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr1:147087702 G>T did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr1:147091833 C>T maps to NM_004326.2 Q625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:147096423 C>T maps to NM_004326.2 P1315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr11:118772771 G>A maps to NM_182557.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:118770686 G>A maps to NM_182557.2 D1115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:136597296 C>A maps to NM_014739.2 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr6:136594275 C>T maps to NM_014739.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:136597569 C>A maps to NM_014739.2 G365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:136589370 C>A maps to NM_014739.2 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr6:136599280 G>A maps to NM_014739.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:136589343 C>A maps to NM_014739.2 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:136597224 C>A maps to NM_014739.2 E480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:136597486 T>C maps to NM_014739.2 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr6:136597155 C>A maps to NM_014739.2 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:81321000 T>C maps to NM_017429.2 D468D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr16:81314567 G>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr16:81324179 T>C maps to NM_017429.2 *548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:81293314 C>T maps to NM_017429.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:81295824 C>T maps to NM_017429.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:81319148 A>G maps to NM_017429.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:112050079 G>A maps to NM_031938.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:39923759 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:39930914 A>C did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:39923641 T>C did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:39933071 C>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:39932753 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:39914722 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:39932399 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:39933664 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:39933574 G>A did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:39922071 T>C did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:39922071 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:39911589 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr23:39923058 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:39913249 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:39911439 C>T did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr23:39914722 G>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:39916573 C>A did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:39914722 G>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:39932890 C>T did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:39916462 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr23:39922048 G>A did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:39933870 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:39922983 G>A did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:39916572 T>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:39934370 G>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:129148899 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:129148637 C>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:129149241 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:129156933 C>T did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:129148898 C>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:129149486 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:129147016 A>G did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:129149171 G>A did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:129184755 C>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:129162721 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:129146589 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:129171415 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:129149946 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:129149348 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:129149900 G>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:129148241 G>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:129147050 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr23:129150138 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr23:129139261 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:129159221 G>A did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr23:129148487 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:129156933 C>A did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:129149241 G>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:129147137 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:129149724 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:129156933 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:129156933 C>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:129189867 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr22:23596094 G>A maps to NM_004327.3 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr22:23655110 C>T maps to NM_004327.3 D1120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr22:23656756 A>C maps to NM_004327.3 A1194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr3:197273236 T>C maps to NM_203315.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:104012390 G>A maps to NM_020139.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:96730138 G>A maps to NM_000710.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr14:96731068 C>T maps to NM_000710.2 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:96706988 C>T maps to NM_000623.3 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:27679631 C>T maps to NM_001143810.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr11:27679628 G>A maps to NM_001143810.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr11:27695768 A>G maps to NM_001143810.1 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:70754567 T>C maps to NM_018429.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:70818298 C>T maps to NM_018429.2 N1725N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr5:70840880 A>G maps to NM_018429.2 E2193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr5:70757679 C>T maps to NM_018429.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:70798584 G>A maps to NM_018429.2 E736E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:70818638 T>C maps to NM_018429.2 G1750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:70759929 A>C maps to NM_018429.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:70791184 T>G maps to NM_018429.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:70805663 G>A maps to NM_018429.2 T915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:40970590 G>A maps to NM_003766.3 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr14:101005250 C>T maps to NM_020836.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:101005154 C>T maps to NM_020836.3 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:18195738 T>C did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:18234732 A>G did not map to a codon.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr23:18230760 G>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:18230757 A>G did not map to a codon.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr23:18189244 G>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:18238859 C>A did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:18221736 C>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:18213474 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:18222009 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:18189137 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:18213459 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:18230696 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:18234667 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:18221837 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:18198699 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:18221737 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:18195867 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:18195712 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:18194110 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:18183329 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:18192231 G>T did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:18234732 A>G did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:18234732 A>G did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:18234732 A>G did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:18192194 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:18195710 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:18234732 A>G did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:18234732 A>G did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:18209220 G>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:107390102 G>A maps to NM_001080450.2 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:107390027 C>T maps to NM_001080450.2 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr6:107391737 C>T maps to NM_001080450.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:107390756 G>A maps to NM_001080450.2 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:107390786 G>A maps to NM_001080450.2 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr6:107390747 G>A maps to NM_001080450.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr6:107391737 C>T maps to NM_001080450.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:42122161 G>A maps to NM_207406.3 C432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:42145676 G>A maps to NM_207406.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr1:49201983 G>A maps to NM_024603.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr6:56882084 T>G maps to NM_152731.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr6:56883324 T>C maps to NM_152731.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:56880051 G>A maps to NM_152731.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:56846722 G>T maps to NM_152731.2 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:13534850 A>G maps to ENST00000396900 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr10:13481240 C>T maps to ENST00000396900 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:13481285 T>C maps to ENST00000396900 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:13522959 C>T maps to ENST00000396900 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr10:13523022 T>C maps to ENST00000396900 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr10:13522937 G>T maps to ENST00000396900 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:13534829 G>A maps to ENST00000396900 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr10:13541892 C>T maps to ENST00000396900 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:13541892 C>T maps to ENST00000396900 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:61724469 C>T maps to NM_001139443.1 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr11:61725727 C>T maps to NM_001139443.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:12868620 G>A maps to NM_017682.2 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr7:93623625 C>T maps to NM_005868.4 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:205304 C>T maps to NM_001098787.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:102318038 A>G did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr23:102317852 T>C did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:102564880 C>T did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:102564882 C>A did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:102564882 C>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:102564735 G>A did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:102471119 C>T did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:101408939 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:101409124 A>C did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:101409226 A>T did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:101409016 T>C did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:101409015 C>A did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:101409016 T>C did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:101409016 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr16:14738382 A>G maps to NM_016561.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:17492713 C>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:17479550 G>A maps to NM_001195.3 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:17492629 C>T maps to NM_001195.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr3:133191376 C>G maps to NM_003571.2 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:133191307 G>A maps to NM_003571.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:133185679 G>A maps to NM_003571.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:133167354 C>T maps to NM_003571.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:156212346 C>T maps to ENST00000368276 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:152772380 G>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:152772531 G>T did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:152772529 A>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:152771462 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:152772361 C>T did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:152771994 G>A did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:152770135 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:97842121 G>A maps to NM_177455.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:97841962 C>T maps to NM_177455.3 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:102004231 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:102005482 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:102004102 A>G did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr23:102004625 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:102005276 T>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:102004394 G>A did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr23:102004627 C>T did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:102004102 A>G did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:65494195 C>T maps to NM_152414.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:5022089 T>G maps to NM_003670.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr3:5024743 G>A maps to NM_003670.2 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:5024962 C>T maps to NM_003670.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:26276575 A>G maps to NM_030762.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:26277706 G>A maps to NM_030762.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:26277081 C>A maps to NM_030762.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr12:26277465 G>A maps to NM_030762.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr5:78416208 C>A maps to NM_001713.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:78415190 G>A maps to NM_001713.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:78417093 C>T maps to NM_001713.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:78379051 C>T maps to NM_017614.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:78378751 G>T maps to NM_017614.4 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:78379496 C>A maps to NM_017614.4 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr10:60549146 A>G maps to NM_001080512.1 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr10:60588554 G>A maps to NM_001080512.1 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr10:60562920 C>T maps to NM_001080512.1 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:60549146 A>G maps to NM_001080512.1 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:60549098 C>A maps to NM_001080512.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:60549144 A>T maps to NM_001080512.1 K242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:60546780 C>T maps to NM_001080512.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr10:60549146 A>G maps to NM_001080512.1 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:60546760 A>T maps to NM_001080512.1 K156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr12:32481368 C>T maps to NM_001714.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:32530521 C>T maps to NM_001714.2 C963C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:32490520 C>T maps to NM_001714.2 R781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:95482668 G>A maps to NM_001003800.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr22:18232894 G>A maps to NM_197966.1 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:127811492 C>T maps to NM_139343.1 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:127816694 C>T maps to NM_139343.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:51696871 T>C maps to NM_016293.2 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:51685445 T>A maps to NM_016293.2 K482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:51717862 G>A maps to NM_016293.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:51685833 A>G maps to NM_016293.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:51696507 C>A maps to NM_016293.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:22481558 G>A maps to NM_018688.4 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr11:102207518 A>G maps to NM_182962.1 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:102207707 G>T maps to NM_182962.1 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr11:102195607 C>A maps to NM_182962.1 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:76212768 C>T maps to NM_001012271.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr2:32820107 A>G maps to NM_016252.3 K4503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:32820107 A>G maps to NM_016252.3 K4503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:32605321 A>T maps to NM_016252.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:32842944 G>T maps to NM_016252.3 E4850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr2:32658780 C>T maps to NM_016252.3 F1106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:32688376 A>G maps to NM_016252.3 A1623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:32842944 G>T maps to NM_016252.3 E4850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:32703728 G>A maps to NM_016252.3 T2365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:32842944 G>T maps to NM_016252.3 E4850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:32756603 G>T maps to NM_016252.3 E4093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:32724802 C>T maps to NM_016252.3 S2886S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:32654307 A>G maps to NM_016252.3 E989E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:32640461 G>A maps to NM_016252.3 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr2:32820107 A>G maps to NM_016252.3 K4503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:32820107 A>G maps to NM_016252.3 K4503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr2:32820107 A>G maps to NM_016252.3 K4503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:32696193 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:32703800 A>G maps to NM_016252.3 G2389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:32740212 T>C maps to NM_016252.3 H3575H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr2:32770875 T>C maps to NM_016252.3 A4253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:32640419 C>T maps to NM_016252.3 Y687Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr2:32688325 G>A maps to NM_016252.3 S1606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:32824825 G>T maps to NM_016252.3 A4617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:32694520 C>G maps to NM_016252.3 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:32820105 A>T maps to NM_016252.3 K4503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:61870899 G>A maps to NM_139317.1 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:53793269 G>T maps to NM_033341.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:53793537 A>G maps to NM_033341.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:103484011 C>T maps to NM_017693.3 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:103459853 G>A maps to NM_017693.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:103473404 A>C maps to NM_017693.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:103459858 C>A maps to NM_017693.3 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:121986534 G>T maps to NM_001001786.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr8:11400834 C>T maps to ENST00000427279 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:11412976 C>T maps to ENST00000427279 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr8:11407733 C>T maps to ENST00000427279 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr15:91290627 T>A maps to NM_000057.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr15:91292752 G>A maps to NM_000057.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:91326120 A>G maps to NM_000057.2 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:91312367 T>A maps to NM_000057.2 C771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr15:91312750 G>A maps to NM_000057.2 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr15:91312750 G>A maps to NM_000057.2 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr15:91312666 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr15:91337415 T>C maps to NM_000057.2 H1013H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:91306382 G>A maps to NM_000057.2 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr17:28612456 A>G maps to NM_000386.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:28613837 A>G maps to NM_000386.2 N182N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr17:28599595 G>A maps to NM_000386.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:98002497 G>A maps to NM_013314.3 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:97969595 G>A maps to NM_013314.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:43827612 C>T maps to NM_000712.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr7:43846617 A>G maps to NM_000712.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:40964324 G>A maps to NM_000713.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:40953834 G>A maps to NM_000713.2 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr19:40957391 C>A maps to NM_000713.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:169356257 T>C maps to NM_003666.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr15:40398218 C>A maps to NM_001003940.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr8:22031169 A>G maps to NM_006129.4 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:22054769 C>T maps to NM_006129.4 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:22067132 C>T maps to NM_006129.4 C917C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:22069193 C>T maps to NM_006129.4 R972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:22066961 C>T maps to NM_006129.4 C860C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr8:22064409 C>A maps to NM_006129.4 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr2:69093659 G>A maps to NM_014482.1 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:69093515 T>C maps to NM_014482.1 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:69093353 G>A maps to NM_014482.1 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:69092819 G>A maps to NM_014482.1 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:69098271 C>T maps to NM_014482.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:69093515 T>C maps to NM_014482.1 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr2:69093515 T>C maps to NM_014482.1 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:69092849 G>A maps to NM_014482.1 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:50659037 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:50659038 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:50658840 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:50659214 C>A did not map to a codon.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr23:50659424 A>G did not map to a codon.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr23:50653874 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:50653954 A>C did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:50659304 C>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:50658840 G>A did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:50659304 C>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:6759222 C>T maps to NM_001200.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr20:6759342 T>A maps to NM_001200.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr20:6751033 A>G maps to NM_001200.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:79832904 C>A maps to NM_198892.1 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:79833099 G>A maps to NM_198892.1 V1133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:79793866 G>T maps to NM_198892.1 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:79832682 G>A maps to NM_198892.1 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr4:79786722 C>T maps to NM_198892.1 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:81967189 C>A maps to NM_001201.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:81952588 C>T maps to NM_001201.2 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:81952485 C>T maps to NM_001201.2 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:54417139 G>A maps to NM_130850.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr6:55659170 A>G maps to NM_021073.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:55739444 T>C maps to NM_021073.2 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr6:55638912 G>A maps to NM_021073.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr6:7845463 G>A maps to NM_001718.4 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr6:7880315 C>T maps to NM_001718.4 H458H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:7880569 C>T maps to NM_001718.4 C512C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr20:55758859 C>T maps to NM_001719.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr20:55748351 C>T maps to NM_001719.2 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:55758934 C>T maps to NM_001719.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:39991355 G>A maps to NM_181809.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:40226105 G>T maps to NM_001720.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:34006112 C>A maps to NM_133468.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:34094916 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:34094861 C>T maps to NM_133468.3 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr7:34118610 C>T maps to NM_133468.3 N407N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr7:34192857 C>A maps to NM_133468.3 I677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:34091542 C>A maps to NM_133468.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:88683356 C>T maps to NM_004329.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr10:88683436 G>A maps to NM_004329.2 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:96069908 G>T maps to ENST00000440890 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr4:96025667 T>C maps to ENST00000440890 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr4:96052477 C>T maps to ENST00000440890 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:203384808 G>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:203378486 T>A maps to NM_001204.6 L155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:203383559 C>T maps to NM_001204.6 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr2:203420137 C>T maps to NM_001204.6 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:203384917 C>T maps to NM_001204.6 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:203421004 C>T maps to NM_001204.6 R873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:203383768 T>A maps to NM_001204.6 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:203397450 C>T maps to NM_001204.6 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr2:203332318 C>T maps to NM_001204.6 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr2:203383771 C>T maps to NM_001204.6 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr2:203420660 T>A maps to NM_001204.6 L758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr2:203424473 T>C maps to NM_001204.6 R974R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:203383771 C>A maps to NM_001204.6 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:203242223 G>A maps to NM_001204.6 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:203395542 C>T maps to NM_001204.6 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:203383553 C>T maps to NM_001204.6 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:203397346 G>T maps to NM_001204.6 G390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:43315865 C>T maps to NM_014753.3 Y921Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:43292258 G>T maps to NM_014753.3 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr10:43318658 C>T maps to NM_014753.3 R1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr10:43316032 G>A maps to NM_014753.3 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:15568102 T>C did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:15540593 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:15555404 C>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:15527527 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:15568009 T>G did not map to a codon.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr23:15540593 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:15540593 T>C did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:15540603 T>C did not map to a codon.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr23:15540593 T>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:15540593 T>C did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:15540593 T>C did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:15555285 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:83935620 T>C maps to NM_001717.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr15:83936882 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:83926261 G>A maps to NM_001717.3 R973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:83932357 C>A maps to NM_001717.3 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr15:83936885 G>A maps to NM_001717.3 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr15:83932664 C>T maps to NM_001717.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:83932487 A>C maps to NM_001717.3 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:83933378 G>A maps to NM_001717.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr15:83935701 G>T maps to NM_001717.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr15:83935776 C>T maps to NM_001717.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:16436037 A>G maps to NM_017637.5 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr9:16437045 G>T maps to NM_017637.5 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr9:16437027 G>T maps to NM_017637.5 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:16435953 G>A maps to NM_017637.5 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr9:16436763 G>T maps to NM_017637.5 C476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr9:16437045 G>T maps to NM_017637.5 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr9:16419325 C>T maps to NM_017637.5 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:16419421 C>T maps to NM_017637.5 E955E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:16437045 G>T maps to NM_017637.5 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:16437255 G>A maps to NM_017637.5 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:16437045 G>T maps to NM_017637.5 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr9:16437045 G>A maps to NM_017637.5 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr9:16436136 G>T maps to NM_017637.5 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr9:16437045 G>T maps to NM_017637.5 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr9:16419048 G>A maps to NM_017637.5 R1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr9:16436244 G>A maps to NM_017637.5 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:172581347 G>A maps to NM_013979.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:133782051 C>A maps to NM_004052.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr8:26267906 A>G maps to NM_004331.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:151011458 A>T maps to NM_138278.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:112998755 G>A maps to ENST00000273395 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:112992114 C>A maps to ENST00000273395 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:113002345 G>A maps to ENST00000273395 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:112991527 C>T maps to ENST00000273395 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:113002345 G>T maps to ENST00000273395 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:112969451 G>T maps to ENST00000273395 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr3:112997024 C>T maps to ENST00000273395 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:112969453 A>T maps to ENST00000273395 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:173036283 G>A maps to NM_138369.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr5:173036349 T>C maps to NM_138369.2 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:173040252 A>G maps to NM_138369.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:13602931 G>A maps to NM_148894.2 D1864D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr4:13602634 T>C maps to NM_148894.2 S1963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr4:13578550 C>T maps to NM_148894.2 E2983E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:13592028 G>A maps to NM_148894.2 S2730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:13606318 C>T maps to NM_148894.2 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:13604704 T>C maps to NM_148894.2 E1273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:13601500 G>A maps to NM_148894.2 S2341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr4:13601869 G>A maps to NM_148894.2 L2218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:13601836 A>G maps to NM_148894.2 A2229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr4:13601770 G>A maps to NM_148894.2 D2251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:13615148 C>T maps to NM_148894.2 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:13604623 T>C maps to NM_148894.2 V1300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:13617032 A>G maps to NM_148894.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr4:13584321 G>A maps to NM_148894.2 T2824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr4:13604895 G>A maps to NM_148894.2 Q1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr4:13604893 T>C maps to NM_148894.2 Q1210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr4:13584294 T>C maps to NM_148894.2 S2833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:242509579 C>T maps to NM_032515.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:242501865 C>A maps to NM_032515.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:242501817 G>A maps to NM_032515.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:149871842 C>T maps to NM_016074.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:149872004 G>A maps to NM_016074.3 K131K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr2:198631306 G>A maps to NM_197970.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:198631306 G>A maps to NM_197970.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:3137599 C>T maps to NM_004332.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:3129280 G>A maps to NM_004332.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:36939051 G>C maps to NM_001725.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:36954701 C>A maps to NM_001725.2 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr20:36965561 C>T maps to NM_001725.2 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:36936065 G>A maps to NM_001725.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:36936065 G>A maps to NM_001725.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr20:36952309 C>A maps to NM_001725.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr20:36952361 C>T maps to NM_001725.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:36946843 C>A maps to NM_001725.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:31606504 G>A maps to NM_025227.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr20:31606573 G>A maps to NM_025227.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr22:32831696 G>A maps to NM_174932.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:32811961 T>C maps to NM_174932.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:32828359 G>A maps to NM_174932.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr22:32828359 G>A maps to NM_174932.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:31620811 G>A maps to NM_174897.2 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:31623422 T>C maps to NM_174897.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr20:31623425 C>T maps to NM_174897.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:31619501 C>T maps to NM_174897.2 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:31626752 T>C maps to NM_174897.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:31625544 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:220236112 C>A maps to NM_006085.4 G220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:65908823 C>T maps to ENST00000321892 G1734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:65924640 T>C maps to ENST00000321892 A2100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:65971930 A>G maps to ENST00000321892 E2987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:65908496 T>C maps to ENST00000321892 D1625D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:65941552 G>A maps to ENST00000321892 L2369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:65890192 G>T maps to ENST00000321892 E945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:65890282 T>C did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:65928031 C>T maps to ENST00000321892 I2178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:65907728 C>T maps to ENST00000321892 D1369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:65942314 G>A maps to ENST00000321892 V2623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr7:140481382 C>T maps to NM_004333.4 K475K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr7:140453176 T>C maps to NM_004333.4 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr7:140481448 A>G maps to NM_004333.4 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr7:140481400 T>C maps to NM_004333.4 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr7:140481430 C>T maps to NM_004333.4 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:140453122 C>T maps to NM_004333.4 W604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr7:140482871 T>C maps to NM_004333.4 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:140476880 G>A maps to NM_004333.4 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr7:140449172 G>A maps to NM_004333.4 Q636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr7:140453110 A>G maps to NM_004333.4 H608H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:140508767 G>A maps to NM_004333.4 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:140453137 T>C maps to NM_004333.4 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr7:140481409 T>C maps to NM_004333.4 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr7:140481448 A>G maps to NM_004333.4 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr7:140453167 T>C maps to NM_004333.4 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr7:140481429 C>A maps to NM_004333.4 G460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:140453149 A>G maps to NM_004333.4 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:140481441 G>A maps to NM_004333.4 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:140481475 C>A maps to NM_004333.4 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:140453146 A>G maps to NM_004333.4 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr7:140453176 T>C maps to NM_004333.4 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:140453146 A>G maps to NM_004333.4 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr7:140453146 A>G maps to NM_004333.4 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr7:140477854 A>G maps to NM_004333.4 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr7:140481427 T>C maps to NM_004333.4 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr7:140481421 T>C maps to NM_004333.4 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:140453125 T>C maps to NM_004333.4 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:140453140 A>T maps to NM_004333.4 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr7:140453082 A>G maps to NM_004333.4 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr7:140453167 T>C maps to NM_004333.4 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:140453101 T>C maps to NM_004333.4 E611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:140481418 A>G maps to NM_004333.4 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr7:140481487 T>C maps to NM_004333.4 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr7:140481475 C>A maps to NM_004333.4 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr7:140481409 T>C maps to NM_004333.4 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr7:140453152 A>G maps to NM_004333.4 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr7:140481487 T>C maps to NM_004333.4 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr7:140481427 T>C maps to NM_004333.4 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr7:140453146 A>G maps to NM_004333.4 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr7:140453158 T>A maps to NM_004333.4 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:140481403 A>G maps to NM_004333.4 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr7:140481448 A>G maps to NM_004333.4 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:140477846 C>T maps to NM_004333.4 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:140453179 A>G maps to NM_004333.4 H585H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr12:112093422 G>A maps to NM_006768.3 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:112121076 C>T maps to NM_006768.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr17:41246194 T>C maps to ENST00000471181 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr17:41256237 A>G maps to ENST00000471181 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:41234475 A>G maps to ENST00000471181 S1434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:41226408 C>T maps to ENST00000471181 Q1560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:41256237 A>G maps to ENST00000471181 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr17:41256237 A>G maps to ENST00000471181 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:41215924 T>C maps to ENST00000471181 G1728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:41226514 G>T maps to ENST00000471181 S1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:41209067 C>A did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr17:41245273 C>T maps to ENST00000471181 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:41209092 T>C maps to ENST00000471181 R1773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr17:41244520 T>C maps to ENST00000471181 S1009S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr17:41209092 T>C maps to ENST00000471181 R1773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:41258513 C>T maps to ENST00000471181 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr17:41197783 G>A maps to ENST00000471181 R1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr17:41258543 G>A maps to ENST00000471181 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr17:41246254 T>C maps to ENST00000471181 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr17:41245273 C>T maps to ENST00000471181 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr17:41256237 A>G maps to ENST00000471181 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr17:41244316 C>T maps to ENST00000471181 G1077G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr17:41244127 A>G maps to ENST00000471181 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr17:41246194 T>C maps to ENST00000471181 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr17:41244520 T>C maps to ENST00000471181 S1009S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr17:41245275 A>G maps to ENST00000471181 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr17:41256237 A>G maps to ENST00000471181 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr17:41245273 C>T maps to ENST00000471181 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr17:41256237 A>G maps to ENST00000471181 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:41223037 A>G maps to ENST00000471181 S1653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr17:41256231 T>C maps to ENST00000471181 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr17:41197783 G>T maps to ENST00000471181 R1857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr17:41244127 A>G maps to ENST00000471181 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr17:41197781 T>C maps to ENST00000471181 R1857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:41246254 T>C maps to ENST00000471181 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:41256231 T>C maps to ENST00000471181 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr17:41245213 G>T maps to ENST00000471181 G778G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:41276092 G>A maps to ENST00000471181 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr13:32945130 C>T maps to NM_000059.3 R2842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:32932055 G>T maps to NM_000059.3 E2599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:32953498 C>T maps to NM_000059.3 Q2934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:32968853 C>T maps to NM_000059.3 D3095D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:32972720 A>G maps to NM_000059.3 T3357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr13:32910447 T>C maps to NM_000059.3 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:32900640 T>C maps to NM_000059.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr13:32912505 C>T maps to NM_000059.3 G1338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr13:32906625 C>T maps to NM_000059.3 N337N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:32972705 T>G maps to NM_000059.3 L3352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:32953923 T>G maps to NM_000059.3 Y2997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr13:32910624 C>T maps to NM_000059.3 C711C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr13:32911542 C>A maps to NM_000059.3 I1017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:32900677 G>T maps to NM_000059.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr13:32912670 G>A maps to NM_000059.3 A1393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:32906407 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:32912505 C>T maps to NM_000059.3 G1338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr13:32900679 G>A maps to NM_000059.3 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr13:32914503 A>G maps to NM_000059.3 E2004E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:32893434 G>T maps to NM_000059.3 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:32929396 T>G maps to NM_000059.3 T2469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:32912968 G>T maps to NM_000059.3 E1493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr13:32907142 G>T maps to NM_000059.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr13:32914503 A>G maps to NM_000059.3 E2004E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr13:32914503 A>G maps to NM_000059.3 E2004E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr13:32968853 C>T maps to NM_000059.3 D3095D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr13:32968853 C>T maps to NM_000059.3 D3095D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr13:32913537 T>C maps to NM_000059.3 S1682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr13:32911920 A>G maps to NM_000059.3 E1143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr13:32968853 C>T maps to NM_000059.3 D3095D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr13:32971138 G>A maps to NM_000059.3 P3202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr13:32972720 A>T maps to NM_000059.3 T3357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr13:32968853 C>T maps to NM_000059.3 D3095D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr13:32911542 C>A maps to NM_000059.3 I1017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr13:32913270 A>G maps to NM_000059.3 E1593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:32913537 T>C maps to NM_000059.3 S1682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:154348346 G>A did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:154348346 G>A did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:154348346 G>A did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:154345001 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:154299810 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:154301689 G>A did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:154348345 T>C did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr22:50217509 G>A maps to ENST00000342989 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:32948359 G>A maps to ENST00000395289 A792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:136910527 G>A maps to NM_007371.3 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:136913369 C>T maps to NM_007371.3 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr9:136915666 G>A maps to NM_007371.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:136918536 T>G maps to NM_007371.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:15367041 G>T maps to NM_058243.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:15374304 G>A maps to NM_058243.2 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:15367975 G>A maps to NM_058243.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:15374304 G>A maps to NM_058243.2 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr19:15366197 C>A maps to NM_058243.2 E653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr19:15376428 C>A maps to NM_058243.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:50353863 G>A maps to NM_001173984.2 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:50354204 C>T maps to NM_001173984.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:50354258 C>T maps to NM_001173984.2 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr16:50383932 C>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:137486431 A>G did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:137506098 C>A did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:137495847 C>T maps to NM_139199.1 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:137486637 G>A maps to NM_139199.1 C972C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr5:137486574 G>T maps to NM_139199.1 L993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr5:864636 G>A maps to NM_001009877.2 H527H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:878567 C>T maps to NM_001009877.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:876272 G>A maps to NM_001009877.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:92445133 C>T maps to ENST00000347608 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:92441902 G>T maps to ENST00000347608 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:92446933 A>C maps to ENST00000347608 T632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:92430257 G>T maps to ENST00000347608 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr2:28464191 G>T maps to NM_004899.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:28561370 A>G maps to NM_199191.1 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:28117447 C>T maps to NM_004899.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr2:28117449 A>G maps to NM_004899.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:28117447 C>T maps to NM_004899.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr14:105684005 G>A maps to NM_001519.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr14:105684026 C>A maps to NM_001519.2 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:105677555 G>A maps to NM_001519.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr14:105684005 G>T maps to NM_001519.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:37707280 G>A maps to NM_018310.3 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:37702595 G>A maps to NM_018310.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr17:59761056 G>C maps to NM_032043.2 S1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:59934572 G>A maps to NM_032043.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:59878684 C>A maps to NM_032043.2 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr17:59821817 G>A maps to NM_032043.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:59853908 G>A maps to NM_032043.2 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr17:59853800 A>C maps to NM_032043.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:34925004 T>C maps to NM_018321.3 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:167893758 G>A maps to NM_001143674.1 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:9776309 T>C maps to NM_001003694.1 H162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:9785454 G>T maps to NM_001003694.1 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:36168929 C>T maps to NM_015695.2 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:36182125 C>T maps to NM_015695.2 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:36185694 C>T maps to NM_015695.2 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:36178237 C>T maps to NM_015695.2 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:36168278 C>A maps to NM_015695.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:36168860 G>A maps to NM_015695.2 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr23:135574442 C>T did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:135572635 G>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:135572570 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:135572546 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:135572509 C>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:55816953 G>A maps to NM_032430.1 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr19:55805596 G>A maps to NM_032430.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:55800860 G>T maps to NM_032430.1 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:55817760 C>T maps to NM_032430.1 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:55815159 C>T maps to NM_032430.1 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:55805405 G>A maps to NM_032430.1 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:55823417 C>T maps to NM_032430.1 N773N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr19:55815971 C>T maps to NM_032430.1 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr21:40610415 G>A maps to NM_018963.3 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr21:40608627 G>A maps to NM_018963.3 R887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr21:40667674 G>T maps to NM_018963.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:40604126 C>T maps to NM_018963.3 E992E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:40601355 C>A maps to NM_018963.3 E1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr21:40587200 T>C maps to NM_018963.3 S1249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:40578100 G>A maps to NM_018963.3 R1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr23:79988965 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:79952244 A>G did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:79945280 T>C did not map to a codon.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr23:79946597 T>G did not map to a codon.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr23:79965042 G>A did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:79965042 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:79932822 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:79932214 A>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:79932280 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:79932528 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:79932703 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:79942390 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:79978254 T>G did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:79984353 A>G did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:79938012 T>G did not map to a codon.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr23:79932572 G>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:79948463 T>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:79989614 A>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:79964959 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:79936866 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:79942390 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:79936921 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:79971738 C>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:79984404 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:79999705 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr23:79990623 A>G did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr23:79936993 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:79984300 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:79990689 G>A did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:79945493 C>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:79947429 C>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:79973196 A>G did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:79936994 G>A did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:79932400 C>G did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:79985426 G>T did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:79936994 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:79988966 T>C did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:79939574 T>C did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:79979331 G>A did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:79936994 G>A did not map to a codon.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr23:79936993 T>C did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:79938008 C>A did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:79945492 A>T did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:79975051 C>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:79985484 C>T did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:80064519 C>T did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:79999630 G>A did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:80064038 A>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:62458771 G>A maps to NM_001130702.1 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:62459864 C>T maps to NM_001130702.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:62459864 C>T maps to NM_001130702.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr11:62458258 C>A maps to NM_001130702.1 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:62459864 C>T maps to NM_001130702.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:32841890 C>T maps to NM_001143888.1 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:32842127 C>T maps to NM_001143888.1 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:579608 C>T maps to NM_001728.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:581472 C>T maps to NM_001728.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:577879 T>C maps to NM_001728.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr3:49694050 C>T maps to NM_003458.3 F2354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:49700418 C>T maps to NM_003458.3 R3610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:49692355 G>A maps to NM_003458.3 G1789G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:49698823 C>T maps to NM_003458.3 G3182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:49699846 C>T maps to NM_003458.3 P3523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr3:49694548 G>A maps to NM_003458.3 G2520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:49692805 C>T maps to NM_003458.3 S1939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:49699753 G>T maps to NM_003458.3 R3492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr1:55472855 C>T maps to NM_057176.2 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:116130652 G>C maps to NM_017688.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:15709249 T>C maps to ENST00000382346 C159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr4:15733453 A>C maps to ENST00000382346 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:15717389 C>A maps to ENST00000382346 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:17516314 G>A maps to NM_004335.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:17515201 T>C maps to NM_004335.2 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr19:17516282 G>A maps to NM_004335.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr11:122848536 G>A maps to NM_001098169.1 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr11:122848464 G>A maps to NM_001098169.1 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:122850133 C>T maps to NM_001098169.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:93749218 G>A maps to NM_003972.2 T912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr10:93695422 C>T maps to NM_003972.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:93711257 G>T maps to NM_003972.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr10:93778652 T>C maps to NM_003972.2 H1608H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr15:83725176 A>G maps to NM_025238.3 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:13441071 C>A maps to NM_032320.5 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:13443279 G>A maps to NM_032320.5 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:13443228 A>G maps to NM_032320.5 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:108051479 A>G maps to NM_001018072.1 K1100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:108013763 C>T maps to NM_001018072.1 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:108013937 C>T maps to NM_001018072.1 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:108004005 G>T maps to NM_001018072.1 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:108006594 C>T maps to NM_001018072.1 D616D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr12:108012051 C>T maps to NM_001018072.1 C783C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr16:3647604 A>T maps to NM_032444.2 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr16:3647921 G>A maps to NM_032444.2 D414D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:3652147 G>A maps to NM_032444.2 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:3652147 G>A maps to NM_032444.2 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr16:3641121 G>A maps to NM_032444.2 H839H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:3640647 C>T maps to NM_032444.2 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:3639798 G>A maps to NM_032444.2 S1280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:3632465 C>T maps to NM_032444.2 S1794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr16:3639108 C>A maps to NM_032444.2 L1510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:3639042 G>A maps to NM_032444.2 S1532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:3646190 G>A maps to NM_032444.2 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:3632639 G>A maps to NM_032444.2 G1736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:124089045 G>A maps to ENST00000368994 R322R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G4-6588-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:1990030 C>T maps to NM_017797.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:1990740 C>T maps to NM_017797.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr20:11904280 A>G maps to NM_014962.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:11904040 C>T maps to NM_014962.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr20:11900418 T>A maps to NM_014962.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:11899036 C>T maps to NM_014962.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr20:11903653 G>A maps to NM_014962.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr20:11903884 G>A maps to NM_014962.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr20:11904280 A>G maps to NM_014962.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr20:11904280 A>G maps to NM_014962.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:105716162 G>A maps to NM_033271.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:93712260 T>C maps to NM_001002860.2 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:93717890 T>C maps to NM_001002860.2 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:93754984 A>G maps to NM_018167.3 *411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:93714871 G>A maps to NM_001002860.2 R691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:92554374 G>A maps to NM_183242.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr6:38565795 A>G maps to NM_052893.1 H25H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr6:38142790 G>A maps to NM_052893.1 N603N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr6:38565732 A>G maps to NM_052893.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:38565732 A>G maps to NM_052893.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:75681100 G>A maps to NM_001729.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:75695283 A>G maps to NM_001729.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr3:15686682 G>C maps to NM_000060.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:72798353 C>T maps to NM_001037637.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:52530570 A>G maps to NM_152265.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:203276499 C>T maps to NM_006763.2 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:203274820 C>T maps to NM_006763.2 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr21:18981413 G>A maps to NM_001130914.1 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:18977272 G>A maps to NM_001130914.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:111368097 A>G maps to NM_017589.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:100608271 A>C did not map to a codon.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr23:100614311 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:100611130 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:100613398 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:100617222 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:100629611 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:100630267 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:100611046 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:100608282 T>C did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:100617179 G>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:100611133 T>C did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:100612521 T>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:100611137 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:112198535 C>A maps to NM_181780.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:26501896 T>C maps to NM_001732.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:26502085 C>A maps to NM_001732.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:26468344 G>A maps to NM_007049.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:26468275 C>T maps to NM_007049.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:26465446 G>A maps to NM_007049.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:26392753 C>T maps to NM_001197237.1 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:26388403 C>T maps to NM_001197237.1 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:26392717 C>T maps to NM_001197237.1 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:26407962 C>A maps to NM_007048.5 C166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr6:26413703 G>A maps to NM_007048.5 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:26413430 C>A maps to NM_007048.5 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr6:32370751 G>A maps to ENST00000468270 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr6:32363885 G>A maps to ENST00000468270 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:32372926 T>C maps to ENST00000468270 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr5:180432790 G>A maps to NM_197975.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:180338369 G>A maps to NM_001040462.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:180338424 C>A maps to NM_001040462.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:180374639 G>T maps to NM_024850.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:180474990 G>A maps to NM_152547.4 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:180486651 C>T maps to NM_152547.4 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:180472533 G>A maps to NM_152547.4 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:180475149 C>T maps to NM_152547.4 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:180486558 G>A maps to NM_152547.4 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:103296398 G>T maps to NM_033637.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:103291026 C>T maps to NM_033637.2 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr10:103296323 A>G maps to NM_033637.2 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr10:103291059 A>C maps to NM_033637.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:103296369 C>T maps to NM_033637.2 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:111408207 G>A maps to NM_004336.3 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr2:111416092 G>A maps to NM_004336.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:111408267 T>C maps to NM_004336.3 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:111416239 C>T maps to NM_004336.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:111414654 G>T maps to NM_004336.3 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr2:111431893 A>G maps to NM_004336.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:111411068 C>T maps to NM_004336.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:111398960 A>G maps to NM_004336.3 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:40498413 C>T maps to ENST00000412359 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr15:40498413 C>T maps to ENST00000412359 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:40462824 A>G maps to ENST00000412359 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr15:40498413 C>T maps to ENST00000412359 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:116643566 C>T maps to NM_032725.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr7:99008721 A>T maps to NM_003910.3 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr7:99008721 A>T maps to NM_003910.3 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr6:105572451 T>C maps to NM_007073.4 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:105573387 T>C maps to NM_007073.4 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:41897875 C>A maps to NM_004053.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:56400709 G>A maps to NM_004758.2 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr17:56389835 C>T maps to NM_004758.2 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:56400900 C>T maps to NM_004758.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:56403665 C>T maps to NM_004758.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr17:56387923 G>A maps to NM_004758.2 T1216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:56388223 G>A maps to NM_004758.2 H1144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:56389823 G>A maps to NM_004758.2 G786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr17:56386561 A>G maps to NM_004758.2 P1357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:56386555 C>T maps to NM_004758.2 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:56388379 C>T maps to NM_004758.2 P1092P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:56388355 C>T maps to NM_004758.2 A1100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr2:201684818 A>T maps to ENST00000452790 K393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:201683117 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:45472980 C>T maps to NM_007021.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:63520634 A>G maps to NM_173554.2 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:77795767 C>A maps to NM_032024.3 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr10:21435302 A>G maps to NM_001010896.2 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr10:115891830 G>A maps to NM_018017.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:115885785 T>C maps to NM_018017.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:115894802 T>C maps to NM_018017.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:115894802 T>C maps to NM_018017.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr10:115894804 G>A maps to NM_018017.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:121618393 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:121616851 C>A maps to NM_024834.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:121600380 G>A maps to NM_024834.2 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr10:121595177 T>G maps to NM_024834.2 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr10:98742580 G>A maps to NM_015652.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:98744218 C>T maps to NM_015652.2 C1024C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:98744692 G>A maps to NM_015652.2 T1182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:98741900 G>T maps to NM_015652.2 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:98744050 C>T maps to NM_015652.2 P968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:98741467 T>C maps to NM_015652.2 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:124457452 G>A maps to NM_001010912.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:124458004 C>A did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr10:135170493 C>A maps to NM_001098483.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:50373830 C>T maps to ENST00000374148 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr10:50369664 C>T maps to ENST00000374148 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:96954304 C>A maps to NM_207321.2 C21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:127429631 T>C maps to ENST00000356792 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:127438078 C>T maps to ENST00000356792 C1074C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:127426877 C>T maps to ENST00000356792 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:127424343 C>T maps to ENST00000356792 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr10:127436445 C>T maps to ENST00000356792 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr10:127409844 C>T maps to ENST00000356792 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:127429149 C>T maps to ENST00000356792 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:21804681 T>C maps to NM_207371.3 E690E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:21804078 G>A maps to NM_207371.3 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:21804624 G>A maps to NM_207371.3 C709C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr10:21805479 T>C maps to NM_207371.3 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr10:5790756 C>T maps to NM_017782.4 H1791H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:5772916 G>T maps to NM_017782.4 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr10:5772837 C>T maps to NM_017782.4 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:102749488 C>T maps to NM_021830.4 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:102748773 C>T maps to NM_021830.4 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:102748360 C>T maps to NM_021830.4 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr10:102748732 C>T maps to NM_021830.4 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:72541715 C>A maps to NM_152710.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr10:72532279 G>A maps to NM_152710.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:72531152 C>T maps to NM_152710.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:72538314 C>A maps to NM_152710.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:99994205 G>A maps to ENST00000314594 K669K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:99968339 G>T maps to ENST00000314594 G157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:99969616 C>T maps to ENST00000314594 N582N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:99968527 G>A maps to ENST00000314594 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:71391540 C>T maps to ENST00000395055 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:71392598 G>A maps to ENST00000395055 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr10:71392712 G>A maps to ENST00000395055 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr10:11911555 G>A maps to NM_153256.3 P153P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-F4-6570-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:82180342 G>A maps to NM_032333.4 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:99350127 A>G maps to NM_001009997.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr10:23622005 C>T maps to NM_153714.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr10:33000617 A>G maps to ENST00000375025 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr10:33000617 A>G maps to ENST00000375025 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:32974904 T>C maps to ENST00000375025 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:33134819 C>T maps to ENST00000375025 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:33143334 G>A maps to ENST00000375025 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr10:33000615 C>T maps to ENST00000375025 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr10:33000617 A>G maps to ENST00000375025 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr10:33000617 A>G maps to ENST00000375025 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr10:33140741 T>A maps to ENST00000375025 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr10:33135385 G>A maps to ENST00000375025 Q537Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr10:50532656 G>A maps to NM_001135196.1 Q689Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr10:50532104 C>T maps to NM_001135196.1 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:50534657 C>T maps to NM_001135196.1 S1356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr10:50530622 G>A maps to NM_001135196.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:50531117 C>T maps to NM_001135196.1 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:50534576 C>T maps to NM_001135196.1 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:50316029 C>T maps to NM_001031746.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:50285339 G>A maps to NM_001031746.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr10:50255030 C>T maps to NM_001031746.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:50315957 G>A maps to NM_001031746.3 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:103766309 C>T maps to NM_024541.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:103761788 C>T maps to NM_024541.2 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr10:105882816 T>C maps to ENST00000336358 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr10:105952026 T>C maps to ENST00000389588 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr10:105923952 G>A maps to ENST00000389588 R1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:105990459 G>A maps to ENST00000389588 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr10:105990459 G>A maps to ENST00000389588 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:105923958 G>A maps to ENST00000389588 R1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:105921759 C>A maps to ENST00000389588 G1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:105952026 T>C maps to ENST00000389588 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr10:105920863 T>C maps to ENST00000389588 E1158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr10:105920863 T>C maps to ENST00000389588 E1158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:105920863 T>C maps to ENST00000389588 E1158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr10:105990456 G>A maps to ENST00000389588 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr10:105990456 G>A maps to ENST00000389588 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr10:115534018 G>T maps to NM_182601.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:120085725 A>G maps to NM_022063.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr10:120085706 C>A maps to NM_022063.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr10:128192679 A>G maps to NM_001004298.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:128193312 G>A maps to NM_001004298.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr10:128118365 G>A maps to NM_001004298.2 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:128118369 A>G maps to NM_001004298.2 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:128193033 C>T maps to NM_001004298.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:128193312 G>A maps to NM_001004298.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:128193399 C>T maps to NM_001004298.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr10:128192613 T>C maps to NM_001004298.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:118084821 G>A maps to NM_198515.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr10:118116907 A>G maps to NM_198515.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr10:85933675 A>G maps to NM_207373.2 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:111753211 C>T maps to NM_022761.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:61558074 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:61557966 G>A maps to NM_014206.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:8953807 G>A maps to NM_020643.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:64876883 C>T maps to NM_013265.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:64875155 C>T maps to NM_013265.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr11:68030375 G>A maps to NM_022338.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:68030114 C>T maps to NM_022338.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:76183642 C>T maps to ENST00000393457 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr11:76174952 T>C maps to ENST00000393457 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:76224490 A>G maps to ENST00000393457 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:76174988 T>C maps to ENST00000393457 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:76257123 C>A maps to ENST00000393457 S1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:76255440 A>T maps to ENST00000393457 K951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr11:76174958 G>A maps to ENST00000393457 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:556850 G>A maps to NM_173573.2 Y320Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:4598944 T>A maps to NM_144663.1 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:33583250 G>T maps to ENST00000389726 E1059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr11:33573745 G>T maps to ENST00000389726 E981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr11:33640204 C>T maps to ENST00000389726 Y1511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:33566809 C>T maps to ENST00000389726 R800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:33564560 C>T maps to ENST00000389726 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:33564032 T>C maps to ENST00000389726 D11D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:33682407 G>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr11:33604899 G>A maps to ENST00000389726 P1182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:33689543 G>A maps to ENST00000389726 A1804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:33680364 C>T maps to ENST00000389726 H1685H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr11:33581374 C>T maps to ENST00000389726 T1021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr11:33640204 C>T maps to ENST00000389726 Y1511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr11:33564488 C>T maps to ENST00000389726 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:6232256 C>T maps to NM_173525.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:30354450 G>A maps to NM_152316.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:30354450 G>A maps to NM_152316.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:62437485 C>T maps to ENST00000431002 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr11:62435169 G>A maps to ENST00000431002 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr11:47074047 C>T maps to NM_001003677.1 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:111154930 C>A maps to NM_198498.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:93494832 G>A maps to ENST00000354421 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:93494781 A>G maps to ENST00000354421 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr11:71810269 A>G maps to NM_017907.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr11:122774923 G>A maps to NM_024806.2 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:122805606 C>T maps to NM_024806.2 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr11:122817361 G>T maps to NM_024806.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr11:122756743 C>T maps to NM_024806.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:122805408 T>A maps to NM_024806.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:122828072 G>A maps to NM_024806.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr11:122805258 T>A maps to NM_024806.2 C370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr11:122756682 C>A maps to NM_024806.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr11:122795675 C>T maps to NM_024806.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:122828135 A>G maps to NM_024806.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr11:108302547 T>C maps to NM_152587.3 Q33Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr11:108277837 T>C maps to NM_152587.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr11:108277837 T>C maps to NM_152587.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:61253358 C>A maps to NM_145017.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr11:61254634 C>T maps to NM_145017.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:61258017 C>T maps to NM_145017.2 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:61257334 C>T maps to NM_145017.2 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:61252183 C>T maps to NM_145017.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:65685556 G>A maps to NM_001135635.1 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr11:114270957 C>T maps to NM_019021.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:114270819 T>G maps to NM_019021.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:36680607 G>T maps to NM_138787.2 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:36669564 G>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:66555635 C>T maps to ENST00000360962 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:66610329 G>A maps to ENST00000360962 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:82641315 G>A maps to NM_145018.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:82645025 C>T maps to NM_145018.3 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:82643984 G>A maps to NM_145018.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr11:82639884 C>A maps to NM_145018.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr11:62439424 G>T maps to NM_001085372.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr11:62439537 G>A maps to NM_001085372.2 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:63594544 G>A maps to NM_138471.1 W360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:63594589 G>A maps to NM_138471.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:111386777 C>A maps to NM_207430.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:61551355 T>C maps to NM_001127392.1 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:61539199 C>T maps to NM_001127392.1 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:61547321 C>T maps to NM_001127392.1 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:61541492 C>T maps to NM_001127392.1 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr12:27064183 A>G maps to NM_018164.2 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:27064183 A>G maps to NM_018164.2 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:27069005 G>A maps to NM_018164.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr12:27064183 A>G maps to NM_018164.2 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:91348318 C>A maps to NM_152638.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr12:91348042 C>T maps to NM_152638.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr12:91348042 C>T maps to NM_152638.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:91348306 G>A maps to NM_152638.2 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:91348401 G>A maps to NM_152638.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:91347619 C>T maps to NM_152638.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:110927858 G>T maps to NM_013300.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr12:88440655 C>A maps to NM_001009894.2 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:110206975 C>T maps to NM_032829.2 N414N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:32137053 G>A maps to NM_018169.3 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:32134930 C>T maps to NM_018169.3 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:32137006 G>T maps to NM_018169.3 E1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:32136924 G>A maps to NM_018169.3 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:32134465 C>T maps to NM_018169.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:32133918 T>C maps to NM_018169.3 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:4643372 C>A maps to NM_020374.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:4627275 G>A maps to NM_020374.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:4628011 C>A maps to NM_020374.2 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr12:40076823 T>C maps to NM_001031748.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:40076667 G>A maps to NM_001031748.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:40044120 T>C maps to NM_001031748.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr12:40044120 T>C maps to NM_001031748.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:121442024 C>T maps to NM_022895.1 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:102559559 A>G maps to NM_017915.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:102569369 T>C maps to NM_017915.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:117160956 C>T maps to NM_024738.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:4460503 C>T maps to NM_020375.2 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr12:88383073 C>A maps to NM_152589.1 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr12:88380173 C>T maps to NM_152589.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr12:88381684 C>T maps to NM_152589.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:88383073 C>A maps to NM_152589.1 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:88381684 C>T maps to NM_152589.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr12:88391880 G>A maps to NM_152589.1 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:112607394 C>T maps to NM_001109662.2 S3868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:112688089 C>A maps to NM_001109662.2 E1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:112622317 G>A maps to NM_001109662.2 S3312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:112647855 T>C maps to NM_001109662.2 P2438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr12:112622833 C>T maps to NM_001109662.2 R3140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:112642295 G>A maps to NM_001109662.2 R2583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr12:112669381 G>T maps to NM_001109662.2 S1873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:112688089 C>A maps to NM_001109662.2 E1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:112610508 C>T maps to NM_001109662.2 A3745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:112622797 C>T maps to NM_001109662.2 S3152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr12:112638499 G>A maps to NM_001109662.2 R2665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr12:112670866 G>T maps to NM_001109662.2 R1808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:112622026 G>A maps to NM_001109662.2 L3409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:112623067 G>A maps to NM_001109662.2 G3062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:112622917 G>A maps to NM_001109662.2 T3112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr12:112601935 G>A maps to NM_001109662.2 S4054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:112630517 G>T maps to NM_001109662.2 G2874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:113629342 G>A maps to NM_032848.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:48886742 C>A maps to NM_152319.3 C69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:64746707 A>G maps to NM_001170633.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr12:7053753 C>T maps to NM_138425.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr12:10339036 C>T maps to NM_153022.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr12:10342504 G>A maps to NM_153022.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:10339153 C>T maps to NM_153022.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:10342715 C>T maps to NM_153022.2 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:14975901 A>G maps to NM_175874.3 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr12:14976129 T>C maps to NM_175874.3 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr12:14976129 T>C maps to NM_175874.3 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr12:14976540 C>T maps to NM_175874.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr12:14976129 T>C maps to NM_175874.3 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr12:14976540 C>A maps to NM_175874.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:97136254 T>A maps to ENST00000342887 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:80714295 G>A maps to NM_173591.3 A1290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:80658910 C>T maps to NM_173591.3 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:80746082 G>A maps to NM_173591.3 P1749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:80750624 G>T maps to NM_173591.3 E1975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:80665542 C>A maps to NM_173591.3 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:80648306 G>A maps to NM_173591.3 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:80671956 G>A maps to NM_173591.3 E888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:123738487 A>G maps to NM_001143905.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:48578154 C>T maps to NM_001013635.3 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:27234969 G>A maps to ENST00000398815 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:93100550 G>A maps to NM_001037671.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:93100580 C>T maps to NM_001037671.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:93101454 A>G maps to NM_001037671.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:25148934 C>T maps to NM_001101339.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr13:111995177 G>A maps to NM_152324.1 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr13:111980533 T>C maps to NM_152324.1 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:46942915 C>T maps to NM_025113.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:46930591 G>A maps to NM_025113.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr13:46946315 G>A maps to NM_025113.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:39587129 A>T maps to NM_025138.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:39587468 G>A maps to NM_025138.3 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:39596514 C>T maps to NM_025138.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr13:31526880 T>C maps to NM_152325.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr13:31513894 A>G maps to NM_152325.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:103419636 C>A maps to NM_138779.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:103418815 C>A maps to NM_138779.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:103420625 T>C maps to NM_138779.3 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr13:113055410 C>T maps to NM_145248.4 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:113052411 C>T maps to NM_145248.4 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr13:113030744 C>T maps to NM_145248.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr13:113030776 G>A maps to NM_145248.4 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:31495897 G>A maps to NM_032849.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:73320708 G>A maps to ENST00000377815 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:37269535 C>A maps to NM_203451.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr13:103343243 A>G maps to NM_001010977.1 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:57070607 C>A maps to NM_017799.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:57103259 G>T maps to NM_017799.3 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:57114127 G>A maps to NM_017799.3 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr14:90744712 C>T maps to NM_017970.2 P1154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr14:90755318 T>C maps to NM_017970.2 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:90769175 C>T maps to NM_017970.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr14:90783121 A>G maps to NM_017970.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:50094728 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr14:57947442 A>G maps to NM_018168.2 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:45673611 T>C maps to NM_018353.4 P1095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:45711964 G>A maps to NM_018353.4 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:45706855 T>C maps to NM_018353.4 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:45696958 G>A maps to NM_018353.4 H551H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:74823714 C>T maps to NM_018228.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:74824007 G>A maps to NM_018228.2 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr14:74823965 C>T maps to NM_018228.2 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr14:74824469 C>T maps to NM_018228.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr14:74824124 C>T maps to NM_018228.2 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:76662250 T>C maps to NM_017926.2 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:76638220 G>T maps to NM_017926.2 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr14:76638273 T>C maps to NM_017926.2 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr14:76644339 A>G maps to NM_017926.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:76644339 A>G maps to NM_017926.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr14:60581979 T>C maps to ENST00000404681 N386N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:60591288 T>G maps to ENST00000404681 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:60600720 G>T maps to ENST00000404681 E1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr14:60591813 A>T maps to ENST00000404681 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr14:60591813 A>T maps to ENST00000404681 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr14:60591813 A>G maps to ENST00000404681 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:81244279 C>T maps to NM_152446.3 E774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:81302675 T>C maps to NM_152446.3 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:81251879 C>A maps to NM_152446.3 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:77873148 G>A maps to NM_001113475.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr14:77873983 C>T maps to NM_001113475.1 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:77861099 C>T maps to NM_001113475.1 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:59946025 G>A maps to NM_144581.1 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr14:59945956 T>C maps to NM_144581.1 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:78174552 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr14:91642314 C>T maps to NM_001102368.1 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:91636352 C>T maps to NM_001102368.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:91655455 C>T maps to NM_001102368.1 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:91662740 G>A maps to NM_001102368.1 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr14:91633605 C>A maps to NM_001102368.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr14:91666202 C>T maps to NM_001102368.1 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:52471155 C>A maps to NM_016039.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:77327049 C>T maps to NM_194287.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr14:77327037 C>T maps to NM_194287.2 N369N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:73958537 G>A maps to NM_024644.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr14:77845068 C>T maps to NM_001010860.1 N436N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:77845332 C>A maps to NM_001010860.1 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr14:78227394 G>T maps to NM_174943.3 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr14:78236011 C>T maps to NM_174943.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:76542975 C>T maps to NM_052873.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:76488734 G>A maps to NM_052873.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr14:76549619 C>T maps to NM_052873.2 H170H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:105054626 C>T maps to NM_001008404.1 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr14:50472372 G>A maps to NM_001012706.1 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr14:24772966 G>A maps to NM_174913.1 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:24769893 G>A maps to NM_174913.1 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr14:45374590 A>G maps to NM_001017923.1 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:45373675 T>C maps to NM_001017923.1 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:45373729 C>T maps to NM_001017923.1 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:58604897 A>G maps to ENST00000438670 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:58606064 C>T maps to ENST00000438670 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:58605734 A>C maps to ENST00000438670 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr14:58604741 A>C maps to ENST00000438670 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:60938455 C>A maps to NM_174978.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:60936270 C>A maps to NM_174978.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr14:60903691 T>C maps to NM_174978.2 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr14:77492278 G>A maps to NM_024496.2 N619N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr14:77492077 C>T maps to NM_024496.2 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:74203900 G>A maps to NM_001043318.1 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr14:74205709 C>T maps to NM_001043318.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr14:74205904 C>T maps to NM_001043318.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:74205367 G>A maps to NM_001043318.1 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:74186017 T>A maps to NM_001043318.1 K1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:74206243 C>T maps to NM_001043318.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr14:74205745 G>T maps to NM_001043318.1 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:74203709 A>G maps to NM_001043318.1 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr14:74206621 A>G maps to NM_001043318.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:74489848 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr14:95932531 G>A maps to NM_152592.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr14:95921761 C>T maps to NM_152592.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:95923597 C>T maps to NM_152592.3 W235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:95932291 G>T maps to NM_152592.3 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:95910916 G>A maps to NM_152592.3 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:65032132 C>T maps to NM_172365.1 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr14:65054849 A>T maps to NM_172365.1 K307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:103568987 G>T maps to NM_001077594.1 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:103576367 G>A maps to NM_001077594.1 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:103568587 G>A maps to NM_001077594.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr14:105455398 T>A maps to NM_174891.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr14:23456489 T>C maps to NM_021944.2 Q517Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:23467869 A>G maps to NM_021944.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr14:23456441 C>T maps to NM_021944.2 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr15:24923623 A>G maps to NM_018958.2 Q870Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr15:24921460 C>T maps to NM_018958.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr15:24921892 G>A maps to NM_018958.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:24921796 G>A maps to NM_018958.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:24923515 C>T maps to NM_018958.2 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:24923026 C>T maps to NM_018958.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:24922741 T>G maps to NM_018958.2 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr15:24921412 G>A maps to NM_018958.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:24924223 A>C maps to NM_018958.2 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr15:24921511 G>T maps to NM_018958.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr15:24921631 G>T maps to NM_018958.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:24923968 C>T maps to NM_018958.2 A985A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:40685683 G>A maps to NM_033286.3 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:34393916 C>A maps to NM_020154.2 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:81427648 G>A maps to ENST00000458088 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:81440260 T>C maps to ENST00000458088 H247H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr15:81440835 C>T maps to ENST00000458088 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:76467919 C>T maps to NM_152335.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:76467948 C>T maps to NM_152335.2 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:34445259 G>A maps to NM_024713.2 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:49869011 C>A maps to NM_152647.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr15:49867237 G>T maps to NM_152647.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:49833940 C>T maps to NM_152647.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr15:49882083 G>A maps to NM_152647.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:49860533 C>A maps to NM_152647.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:90451515 G>T maps to ENST00000398333 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:90451590 G>A maps to ENST00000398333 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr15:90451569 G>A maps to ENST00000398333 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:75498676 G>A maps to NM_015492.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr15:75500989 G>A maps to NM_015492.4 Q867Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:75499708 C>A maps to NM_015492.4 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:75500893 T>C maps to NM_015492.4 H835H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:75500662 C>T maps to NM_015492.4 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr15:83673688 C>T maps to NM_001160114.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:83679094 T>C maps to NM_144597.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr15:90143883 A>G maps to NM_152259.3 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:90152047 C>T maps to NM_152259.3 R913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:90164724 C>T maps to NM_152259.3 R1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:90168260 C>T maps to NM_152259.3 R1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr15:65899652 G>A maps to ENST00000420799 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:65899652 G>T maps to ENST00000420799 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr15:45723254 T>C maps to NM_197955.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr15:40627526 C>T maps to NM_207380.2 Q479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:40628988 C>T maps to NM_207380.2 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr15:38990623 C>T maps to NM_207444.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:38988822 G>T maps to NM_207444.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr15:34648101 C>T maps to ENST00000438749 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr15:34646713 A>G maps to ENST00000438749 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:34640333 C>T maps to ENST00000438749 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr15:34648734 A>G maps to ENST00000438749 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr15:34646716 T>C maps to ENST00000438749 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:90785067 C>T maps to NM_001013657.2 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:74032350 C>T maps to NM_001039614.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:74032701 C>T maps to NM_001039614.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:74043372 G>A maps to NM_001039614.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:73766190 G>T maps to NM_001042367.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:613722 T>C maps to ENST00000293874 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:90095645 C>T maps to NM_001214.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:1400137 G>A maps to NM_001001410.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:15661869 C>A maps to NM_033201.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr16:81095119 C>T maps to NM_152337.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:81095023 C>T maps to NM_152337.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:4564056 C>T maps to ENST00000359075 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:29755999 G>A maps to NM_175900.3 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:29755753 C>T maps to NM_175900.3 E173E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-F4-6570-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:2512630 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:19702793 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:19663338 G>A maps to NM_020314.5 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:19693611 C>A maps to NM_020314.5 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr16:19648947 C>T maps to NM_020314.5 H645H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:19639972 A>T maps to NM_020314.5 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:8722639 G>T maps to NM_024109.2 G63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:8736009 C>T maps to NM_024109.2 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:8736359 G>A maps to NM_024109.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:89777111 G>A maps to NM_004913.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:89774905 G>A maps to NM_004913.2 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:67165193 C>T maps to NM_025187.3 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr16:67168147 C>T maps to NM_025187.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr16:4787913 C>A maps to NM_139170.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:4797026 G>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:9197093 C>T maps to NM_014117.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr16:9197009 T>C maps to NM_014117.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:9186020 C>T maps to NM_014117.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:9210552 C>T maps to NM_014117.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:1894874 C>A maps to NM_001163560.2 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:1907909 A>G maps to NM_001163560.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr16:1894928 G>A maps to NM_001163560.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr16:11444577 T>C maps to NM_152308.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr16:2259389 C>T maps to NM_182563.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:67701795 G>C maps to NM_001012984.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:46836904 C>A maps to NM_001001436.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:19718371 G>A maps to NM_001012991.2 Q413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:19725514 G>A maps to NM_001012991.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr16:1476346 G>A maps to NM_001010878.1 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:30771608 A>G maps to NM_001014979.2 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:6555529 G>A maps to ENST00000391428 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:80373373 G>A maps to NM_175902.4 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:80373343 G>A maps to NM_175902.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:32904584 C>T maps to NM_207454.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:32906011 G>A maps to NM_207454.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:32904578 T>C maps to NM_207454.2 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:42744752 C>T maps to NM_001145080.2 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:42744748 T>G maps to NM_001145080.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:72955017 G>A maps to NM_030630.2 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:72960586 C>A maps to NM_030630.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr17:72949145 C>T maps to NM_030630.2 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:72948397 G>A maps to NM_030630.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr17:17962244 G>T maps to NM_024052.4 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:17957466 C>T maps to NM_024052.4 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:29226597 A>G maps to NM_024683.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:29231389 C>T maps to NM_024683.3 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:43333056 G>T maps to NM_152343.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:56620914 C>T maps to NM_001038704.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:56621429 G>A maps to NM_001038704.1 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr17:56621448 G>A maps to NM_001038704.1 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:6919951 C>T maps to NM_001142798.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:42225980 G>A maps to NM_024032.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:42225497 C>T maps to NM_024032.3 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:79203195 G>T maps to NM_144679.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:79202955 T>C maps to NM_144679.2 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr17:45438837 T>C maps to NM_152347.4 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:45473245 G>A maps to NM_152347.4 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:45490163 G>A maps to NM_152347.4 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr17:45438837 T>C maps to NM_152347.4 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr17:45447852 C>T maps to NM_152347.4 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr17:45452300 G>T maps to NM_152347.4 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:65989054 G>A maps to NM_181656.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:58506842 C>T maps to NM_181707.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:34182245 G>A maps to NM_152781.2 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:34182333 A>G maps to NM_152781.2 Y482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:34190046 C>T maps to NM_152781.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:34182712 G>T maps to NM_152781.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:8140694 G>A maps to NM_025099.5 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr17:8137862 C>T maps to NM_025099.5 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:8139184 G>A maps to NM_025099.5 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr17:8136230 C>T maps to NM_025099.5 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:8141724 G>A maps to NM_025099.5 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:8134781 T>A maps to NM_025099.5 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr17:8135382 G>T maps to NM_025099.5 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:8141768 G>A maps to NM_025099.5 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:8133970 T>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:8133926 T>C maps to NM_025099.5 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr17:57290746 C>T maps to NM_018149.6 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:57289007 T>C maps to NM_018149.6 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr17:57289007 T>C maps to NM_018149.6 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:7329687 C>T maps to NM_175734.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:7329687 C>T maps to NM_175734.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:7329687 C>T maps to NM_175734.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:16365571 C>T maps to NM_001113567.1 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr17:72588685 G>T maps to NM_152460.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:72588736 G>A maps to NM_152460.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:72588805 C>T maps to NM_152460.2 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:72588587 G>T maps to NM_152460.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr17:35734836 C>T maps to NM_173625.3 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:71231638 C>G maps to NM_017941.4 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:71232496 C>A maps to NM_017941.4 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:71239107 C>T maps to NM_017941.4 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:7162106 G>T maps to NM_203413.1 *280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:59489680 A>G maps to NM_203425.1 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr17:3724561 C>T maps to NM_001114118.1 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr17:5118274 C>T maps to NM_207103.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr17:5114167 T>C maps to NM_207103.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:79632503 G>A maps to NM_001039842.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr18:13438261 C>A maps to NM_181481.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:13645349 G>T maps to NM_181481.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:34378465 G>A maps to NM_015476.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:13681791 A>C maps to NM_152352.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr18:13681656 C>T maps to NM_152352.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr18:77804231 C>T maps to NM_024805.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr18:77806127 C>T maps to NM_024805.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr18:77798510 C>T maps to NM_024805.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:77804286 T>C did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:43820088 C>T maps to NM_145055.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr18:43820103 A>G maps to NM_145055.3 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:52265057 C>T maps to NM_173629.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr18:47009953 C>T maps to NM_001035005.3 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:47009991 C>A maps to NM_001035005.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr18:30554512 G>A maps to NM_001105528.1 Q841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr18:30992028 G>A maps to NM_001105528.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr18:30518019 A>C maps to NM_001105528.1 G853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr18:30806816 A>G maps to NM_001105528.1 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:30672795 C>A maps to NM_001105528.1 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:30804885 G>T maps to NM_001105528.1 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:30795516 A>C maps to NM_001105528.1 L692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:30672795 C>A maps to NM_001105528.1 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr18:30795550 C>A maps to NM_001105528.1 E681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr18:30926283 G>A maps to NM_001105528.1 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:20951383 A>G did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:51888160 G>A maps to ENST00000382911 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:51886974 T>C maps to ENST00000382911 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr18:51900582 G>A did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr18:51889234 T>C maps to ENST00000382911 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr18:73130807 G>A maps to NM_001037331.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr18:21098895 G>A maps to NM_013326.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr18:21098856 C>T maps to NM_013326.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr18:21107819 C>T maps to NM_013326.3 N417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr18:21096297 G>A maps to NM_013326.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:30199251 C>T maps to NM_001031726.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:30199286 G>A maps to NM_001031726.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:30496604 C>T maps to NM_003796.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr19:30477314 C>A maps to NM_003796.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr19:30498384 C>T maps to NM_003796.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:30502083 T>C maps to NM_003796.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr19:30477314 C>A maps to NM_003796.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr19:30477314 C>A maps to NM_003796.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr19:30502056 A>G maps to NM_003796.2 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr19:30477314 C>A maps to NM_003796.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:30502056 A>G maps to NM_003796.2 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:30502056 A>G maps to NM_003796.2 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:518972 C>T maps to NM_033513.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr19:763532 G>A maps to NM_173481.2 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:758238 C>T maps to NM_173481.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:1234626 G>A maps to ENST00000382477 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:1234294 G>A maps to ENST00000382477 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:3546369 C>T maps to NM_021731.2 A359A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3492-01A-01D-1408-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-3697-01A-01D-1719-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-3811-01A-01W-0995-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AD-5900-01A-11D-1650-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AZ-6598-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr19:2278990 C>T maps to NM_198532.2 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr19:11486472 G>A maps to NM_175871.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:16620611 C>T maps to NM_032207.2 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr19:16628106 C>T maps to NM_032207.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:7569037 G>A maps to NM_198534.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:7565731 G>A maps to NM_198534.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr19:36499478 G>A maps to ENST00000455847 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:36496318 G>A maps to ENST00000455847 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:40834430 G>A maps to ENST00000357884 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:40842076 G>A maps to ENST00000357884 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:55670726 G>A maps to ENST00000301249 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:55672043 G>A maps to ENST00000301249 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:13885463 A>G did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:13888897 A>G maps to NM_014047.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:41249970 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr19:36257684 C>T maps to NM_001039887.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr19:14000957 T>G maps to ENST00000454313 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:1012510 C>T maps to NM_001033026.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr19:1014295 G>A maps to NM_001033026.1 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:44249018 A>G maps to NM_019108.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:44235798 A>G maps to NM_019108.2 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:17387339 G>A maps to NM_014173.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:10202909 G>T maps to NM_018381.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:10201987 C>T maps to NM_018381.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:51768821 G>T maps to NM_173635.1 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:50193737 G>A maps to NM_001101340.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:7278336 T>C maps to NM_020156.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr7:7278315 A>G maps to NM_020156.3 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr7:7278210 T>C maps to NM_020156.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr7:7278180 G>A maps to NM_020156.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:119760128 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:119760716 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:119760272 G>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:22965857 C>T maps to NM_015991.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr1:22965614 C>T maps to NM_015991.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:22987548 C>T maps to NM_000491.3 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:22987455 G>A maps to NM_000491.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr17:5341450 G>T maps to NM_001212.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:22974074 C>T maps to NM_172369.3 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:43045029 G>T maps to NM_006688.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:43044900 G>A maps to NM_006688.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:119915203 G>A maps to NM_182528.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:119915746 G>A maps to NM_182528.3 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:119915674 G>A maps to NM_182528.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr2:119915578 C>T maps to NM_182528.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr2:119914434 G>A maps to NM_182528.3 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:119915182 C>T maps to NM_182528.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:119915608 G>A maps to NM_182528.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:16562710 G>A maps to NM_001010908.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:49729783 G>A maps to NM_001008223.1 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:49729921 G>A maps to NM_001008223.1 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:77043758 C>T maps to ENST00000392445 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:159781982 G>T maps to NM_031908.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:159776735 G>A maps to NM_031908.4 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:34020767 G>A maps to NM_181435.4 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:47611522 G>A maps to NM_031909.2 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr11:47612119 C>T maps to NM_031909.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:37578257 G>A maps to NM_182486.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:15444215 C>T maps to NM_001135170.1 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:15444083 C>T maps to NM_001135170.1 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:1143815 G>T maps to NM_207419.3 A148A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-3833-01A-01W-0900-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr13:24465976 C>T maps to NM_001135816.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:7188558 G>A maps to ENST00000290575 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:7252596 G>A maps to NM_016546.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:7249643 G>A maps to NM_016546.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:7249034 C>T maps to NM_016546.2 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr12:7249175 C>T maps to NM_016546.2 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:7177175 G>T maps to NM_001734.3 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr12:7169808 G>A maps to NM_001734.3 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:7169820 G>A maps to NM_001734.3 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:7171658 G>A maps to NM_001734.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:7173876 A>C maps to NM_001734.3 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:7174371 G>A maps to NM_001734.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:244528020 C>T maps to NM_001012970.1 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:244541907 C>T maps to NM_001012970.1 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:244528023 G>T maps to NM_001012970.1 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:244803262 C>T maps to NM_001130957.1 F912F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:244769011 C>T maps to NM_001130957.1 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:244723981 A>T maps to NM_001130957.1 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr1:111490742 T>C maps to NM_018372.3 Q716Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:111493963 A>G maps to NM_018372.3 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:155290982 C>T maps to NM_001039517.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:155290964 C>T maps to NM_001039517.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:210004239 G>A maps to NM_014388.6 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:210016855 G>A maps to NM_014388.6 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:38148796 A>G maps to NM_017850.1 *204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:162825477 G>A maps to NM_178550.4 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:162825016 G>T maps to NM_178550.4 C149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:162829253 C>T maps to NM_178550.4 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:162345134 G>T maps to NM_182581.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:162344380 G>A maps to NM_182581.3 H81H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:169820983 T>G maps to NM_018186.2 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:169770112 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:169822076 G>A maps to NM_018186.2 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:169806192 C>T maps to NM_018186.2 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:36773788 C>T maps to NM_001162530.1 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:36785421 A>G maps to NM_001162530.1 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:36785361 A>G maps to NM_001162530.1 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:36772789 G>A maps to NM_001162530.1 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:36785676 G>A maps to NM_001162530.1 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:169391419 G>T maps to ENST00000367806 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:169391281 C>T maps to ENST00000367806 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:207196481 T>G maps to NM_023938.5 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:207196400 G>T maps to NM_023938.5 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:207200907 G>A maps to NM_023938.5 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:207195830 T>C maps to NM_023938.5 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:231488490 T>G maps to NM_032018.4 L285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:179452331 C>T maps to NM_144696.4 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr1:179478462 T>C maps to NM_144696.4 S807S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:179414184 A>G maps to NM_144696.4 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:179478459 C>T maps to NM_144696.4 C806C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:11008574 G>T maps to NM_001170754.1 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:11008865 C>T maps to NM_001170754.1 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:11007854 G>A maps to NM_001170754.1 Y779Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:11014184 G>A maps to NM_001170754.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:11017711 G>A maps to NM_001170754.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:11015103 A>G maps to NM_001170754.1 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:24112858 C>T maps to NM_020362.4 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:170928699 G>T maps to NM_001163629.1 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:170964585 C>T maps to NM_001163629.1 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:170934392 A>G maps to NM_001163629.1 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:170931074 G>A maps to NM_001163629.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:170955787 C>T maps to NM_001163629.1 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:170955787 C>T maps to NM_001163629.1 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:170993821 A>G maps to NM_001163629.1 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr1:170952656 C>T maps to NM_001163629.1 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:170941022 C>T maps to NM_001163629.1 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:231374776 C>T maps to ENST00000421623 K92K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G4-6628-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:182922178 G>T maps to ENST00000287709 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:67558978 C>T maps to NM_001013674.1 Q304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:67558972 T>C maps to NM_001013674.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr1:67559071 A>G maps to NM_001013674.1 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:92709823 G>T maps to NM_001012425.1 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:92709823 G>T maps to NM_001012425.1 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr1:19949995 T>C maps to ENST00000433528 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr1:169761900 C>G maps to NM_033418.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:169762734 T>C maps to NM_033418.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:12819313 C>T maps to NM_152290.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr1:12820808 G>A maps to NM_152290.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:116675979 G>A maps to NM_152367.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:116670866 C>T maps to NM_152367.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:116670830 G>A maps to NM_152367.2 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:57258368 G>A maps to NM_001004303.4 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:57257912 G>A maps to NM_001004303.4 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:57206383 C>T maps to NM_001004303.4 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:57189323 C>T maps to NM_001004303.4 K637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:57233560 G>T maps to NM_001004303.4 S335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:57254706 G>A maps to NM_001004303.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:27277923 C>T maps to NM_152365.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:27278715 G>A maps to NM_152365.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:75037483 G>A maps to NM_001002912.4 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:75097435 T>C maps to NM_001002912.4 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:75107062 A>G maps to NM_001002912.4 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:75038171 G>A maps to NM_001002912.4 D1074D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:75055748 G>T maps to NM_001002912.4 S581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:75072513 T>C maps to NM_001002912.4 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:75037451 C>T maps to NM_001002912.4 S1314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:75097597 C>T maps to NM_001002912.4 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:75038279 T>C maps to NM_001002912.4 A1038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:75038332 C>A maps to NM_001002912.4 E1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:75072447 T>C maps to NM_001002912.4 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:75072305 G>A maps to NM_001002912.4 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr1:75038384 T>C maps to NM_001002912.4 A1003A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr1:75038996 T>G maps to NM_001002912.4 G799G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:75038282 C>T maps to NM_001002912.4 E1037E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:75038285 A>T maps to NM_001002912.4 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:75038279 T>C maps to NM_001002912.4 A1038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:3807330 G>A maps to NM_207356.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:3809533 C>T maps to NM_207356.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:3807147 G>A maps to NM_207356.2 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:3806622 C>T maps to NM_207356.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:55174702 C>T maps to ENST00000454855 C1257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:55119147 C>T maps to ENST00000454855 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:55119465 C>T maps to ENST00000454855 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:55282732 A>T maps to NM_001110533.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:55277735 C>T maps to NM_001110533.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:156314404 C>T maps to NM_144627.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:112269675 G>A maps to NM_019099.4 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:112270129 G>T maps to NM_019099.4 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:11769473 T>C maps to NM_198545.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:11769500 C>T maps to NM_198545.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:46685759 A>G maps to NM_001013615.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:161335414 G>T maps to NM_001013625.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:109649642 C>T maps to NM_001122961.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr1:230979345 G>A maps to NM_032800.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr1:230979638 G>A maps to NM_032800.2 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:24696291 C>T maps to ENST00000374409 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:24706268 A>G maps to ENST00000374409 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:36181421 C>T maps to NM_152374.1 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:162353142 T>C maps to NM_001135240.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:185125733 C>T maps to NM_030934.4 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr1:185113063 A>G maps to NM_030934.4 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:185108578 C>T maps to NM_030934.4 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr1:185200835 C>T maps to NM_001105518.1 Q813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:185171797 C>T maps to NM_001105518.1 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:185191072 C>A maps to NM_001105518.1 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:185143545 C>T maps to NM_001105518.1 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:186358718 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:186359898 T>G maps to NM_017847.5 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:234510068 C>T maps to ENST00000424237 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:28209184 A>G maps to NM_001105556.1 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr1:28206221 T>C maps to NM_001105556.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:28208515 G>A maps to NM_001105556.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:154185008 C>T maps to NM_001098616.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:43233210 C>T maps to NM_024097.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:43240418 T>C maps to NM_024097.2 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:150256220 G>T maps to NM_144697.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:85724228 T>C maps to NM_198077.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:197875017 G>A maps to NM_001024594.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:150245243 C>A maps to NM_024579.3 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr1:150249033 G>A maps to NM_024579.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:150248180 C>T maps to NM_024579.3 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:151021081 T>C maps to NM_017860.3 C253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:222902083 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:109191495 C>A maps to ENST00000370031 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr1:109197420 A>G maps to ENST00000370031 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:109192988 G>A maps to ENST00000370031 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:25573202 G>A maps to NM_020317.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:16332582 C>T maps to NM_178840.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:16332630 G>T maps to NM_178840.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:223568322 C>T maps to NM_152610.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:223568472 G>A maps to NM_152610.2 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:223567908 G>A maps to NM_152610.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:223567908 G>A maps to NM_152610.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr1:223568253 G>A maps to NM_152610.2 Q479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr1:156704211 C>T maps to NM_015997.3 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:156703835 C>T maps to NM_015997.3 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr1:156706503 C>T maps to NM_015997.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:156702132 C>A maps to NM_015997.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:209956445 G>T maps to NM_152485.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:209956199 C>T maps to NM_152485.2 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:153614769 C>T maps to NM_015607.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:153610872 C>T maps to NM_015607.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr1:153614879 A>G maps to NM_015607.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:43870112 C>T maps to ENST00000310739 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:43870112 C>T maps to ENST00000310739 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:156263207 G>A maps to NM_144580.1 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:156262963 G>A maps to NM_144580.1 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:156263286 G>C maps to NM_144580.1 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr1:2121148 C>T maps to ENST00000378545 *284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:60505654 G>A maps to NM_152377.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:60521103 C>T maps to NM_152377.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr1:60476070 C>T maps to NM_152377.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:60506692 C>T maps to NM_152377.2 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:172538275 G>T maps to ENST00000367723 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:172543040 G>T maps to ENST00000367723 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:172544711 G>A maps to ENST00000367723 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:172522471 G>T maps to NM_014283.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:172579249 C>T maps to ENST00000367723 R1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:156893852 C>T maps to NM_144702.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:156899083 C>T maps to NM_144702.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:156901784 T>C maps to NM_144702.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:156901817 C>T maps to NM_144702.2 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:2520382 T>C maps to NM_001195736.1 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr1:34666596 C>T maps to NM_001134734.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:34677980 G>A maps to NM_001134734.1 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:34663449 A>G maps to NM_001134734.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:34666589 G>A maps to NM_001134734.1 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:34684301 C>T maps to NM_001134734.1 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:226784593 A>G maps to ENST00000366788 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:226784582 C>T maps to ENST00000366788 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr1:229460993 C>T maps to NM_145257.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:229462628 C>T maps to NM_145257.3 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr1:229461146 T>G maps to NM_145257.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:31911466 G>A maps to ENST00000437789 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:31902012 G>A maps to NM_000063.4 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:31895930 G>A maps to ENST00000437789 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:9510316 G>A maps to NM_012261.3 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:55100043 G>A maps to NM_001012971.3 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr20:55111328 C>T maps to NM_001013646.2 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr20:54940255 C>T maps to NM_080821.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:61574893 G>A maps to NM_017896.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:42835588 G>A maps to NM_016470.6 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:42826210 C>T maps to NM_016470.6 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:42826273 C>T maps to NM_016470.6 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr20:31043941 G>A maps to NM_080616.3 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:31040797 C>T maps to NM_080616.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:31873908 C>A maps to NM_033197.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:35443690 G>A maps to NM_080627.2 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:35422830 C>T maps to NM_080627.2 S1218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:35423002 C>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr20:35433263 C>T maps to NM_080627.2 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:35507472 C>A maps to NM_080628.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr20:18396060 C>T maps to NM_001099407.1 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:18414294 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:18396060 C>T maps to NM_001099407.1 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:35776302 G>A maps to ENST00000343811 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:35769597 A>C maps to ENST00000343811 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:62493552 C>T maps to NM_080622.3 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:60991292 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr20:60990843 C>A maps to NM_080833.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:34611606 G>A maps to ENST00000373973 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:34611558 C>T maps to ENST00000373973 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:30616833 C>T maps to ENST00000300415 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:30610515 C>T maps to ENST00000300415 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:58519672 G>A maps to NM_022106.2 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:58519543 C>T maps to NM_022106.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr20:58519282 T>C maps to NM_022106.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:31652620 C>T maps to NM_182658.1 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr20:31652476 C>T maps to NM_182658.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:31657743 C>A maps to NM_182658.1 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr20:31644408 T>C maps to NM_182658.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr20:31644408 T>C maps to NM_182658.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr20:31682937 A>G maps to NM_182519.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:31685511 G>A maps to NM_182519.2 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:31682925 T>C maps to NM_182519.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr20:31677338 C>T maps to NM_182519.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr20:3240164 C>A maps to NM_001009984.1 G1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:3298941 C>A maps to NM_001009984.1 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:3355715 G>A maps to NM_001009984.1 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:3311306 C>T maps to NM_001009984.1 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr20:3240165 G>A maps to NM_001009984.1 S1005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:3355748 C>A maps to NM_001009984.1 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr20:3268300 G>A maps to NM_001009984.1 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr20:62187780 C>T maps to NM_024059.2 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr20:62187702 C>T maps to NM_024059.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:20055877 C>T maps to ENST00000389655 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:20269416 C>T maps to ENST00000389655 Y990Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr20:20269566 A>G maps to ENST00000389655 G1040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:20177282 G>T maps to ENST00000389655 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr20:20269566 A>G maps to ENST00000389655 G1040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:20243712 C>T maps to ENST00000389655 N817N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:3734778 G>A maps to NM_001039140.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:3734788 C>T maps to NM_001039140.1 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:34828458 T>C maps to NM_015511.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:55049751 C>T maps to ENST00000357348 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr20:55088432 C>T maps to ENST00000357348 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:744380 C>T maps to NM_033409.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:745857 G>A maps to NM_033409.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr20:745983 T>C maps to NM_033409.3 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:746382 G>A maps to NM_033409.3 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr20:13773837 A>T maps to NM_024120.4 K114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr20:31760759 C>A maps to NM_080574.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:31813032 C>A maps to NM_178466.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr20:18794791 G>A maps to NM_178483.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr20:56735808 C>T maps to NM_178456.2 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:56726040 C>T maps to NM_178456.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr20:56728623 G>A maps to NM_178456.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:56735790 C>T maps to NM_178456.2 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:10603714 C>T maps to NM_001009608.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:10603807 T>G maps to NM_001009608.1 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr20:270298 G>A maps to NM_153269.1 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr21:46131369 C>T maps to ENST00000443468 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr21:45947183 G>T maps to ENST00000443468 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:45941993 G>A maps to ENST00000443468 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:45947240 G>A maps to ENST00000443468 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr21:45953575 C>T maps to ENST00000443468 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr21:45987779 G>A maps to ENST00000443468 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr21:45950952 G>A maps to ENST00000443468 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr21:45948446 C>T maps to ENST00000443468 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr21:45948446 C>T maps to ENST00000443468 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr21:45564755 C>T maps to NM_004649.6 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr21:33642791 G>A maps to NM_018944.2 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr21:47581448 G>A maps to NM_001142854.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr21:47711309 T>C maps to NM_058181.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:47706980 A>C maps to NM_058181.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr21:47735453 C>T maps to NM_058180.3 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr21:33975569 C>T maps to NM_021254.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr21:33825632 A>G maps to NM_058187.3 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr21:33887379 T>C maps to NM_058187.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr21:30547143 C>T maps to NM_020152.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:38340497 C>A maps to NM_032561.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr22:38341048 G>A maps to NM_032561.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:32330307 C>T maps to NM_015372.1 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr22:32808068 G>A maps to NM_014306.4 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr22:32788262 C>T maps to NM_014306.4 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:32808068 G>T maps to NM_014306.4 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:32788295 A>G maps to NM_014306.4 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr22:32109963 T>C maps to NM_173566.2 V1287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:32109488 C>A maps to NM_173566.2 E1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:32099535 C>T maps to NM_173566.2 E2000E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr22:32113179 G>A maps to NM_173566.2 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:32112333 A>G maps to NM_173566.2 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr22:29454858 C>T maps to NM_015370.1 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:37397961 C>T maps to NM_001163857.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr22:23968210 A>T maps to NM_016449.3 L78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr22:23962790 T>C maps to NM_016449.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr22:45595898 T>G maps to NM_001009880.1 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr22:45593827 G>A maps to NM_001009880.1 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr22:45607957 C>T maps to NM_001009880.1 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr22:45598944 G>A maps to NM_001009880.1 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr21:43327140 C>T maps to NM_015500.1 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr21:43321832 A>G maps to NM_015500.1 D486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr21:43327134 G>A maps to NM_015500.1 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:118981639 G>A maps to NM_014807.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr11:73789394 T>C maps to ENST00000334126 E1456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:73785357 A>G maps to ENST00000334126 L1631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:73785376 C>T maps to ENST00000334126 T1624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:73789295 C>T maps to ENST00000334126 R1489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr11:73748610 C>G maps to ENST00000334126 G1931G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr11:73789394 T>C maps to ENST00000334126 E1456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:73825523 G>A maps to ENST00000334126 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:73834104 C>T maps to ENST00000334126 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr11:73824891 G>A maps to ENST00000334126 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:73789396 C>A maps to ENST00000334126 E1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr2:27802552 C>T maps to NM_032266.3 Y1038Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:27803420 G>T maps to NM_032266.3 G1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:27801362 G>T maps to NM_032266.3 E642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:27801556 A>G maps to NM_032266.3 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:27804853 A>G maps to NM_032266.3 R1805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:27803795 C>T maps to NM_032266.3 R1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:27802819 T>C maps to NM_032266.3 C1127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:27803368 A>G maps to NM_032266.3 T1310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:27799459 C>A maps to NM_032266.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:27001183 C>T maps to NM_017877.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:220039541 C>T maps to NM_015680.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr2:27438210 C>T maps to NM_080592.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:101874415 C>T maps to NM_017546.4 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:75891899 G>A maps to NM_003203.4 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:75933718 T>C maps to NM_003203.4 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr2:75933718 T>C maps to NM_003203.4 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:44999191 G>A maps to NM_024766.3 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:26667778 C>T maps to NM_145038.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:26647235 G>T maps to NM_145038.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:26647286 G>T maps to NM_145038.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:26677529 G>A maps to NM_145038.2 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:24261002 C>T maps to NM_025203.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:24261350 G>A maps to NM_025203.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:24262331 A>G maps to NM_025203.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:24261002 C>T maps to NM_025203.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr2:24261803 A>G maps to NM_025203.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:11273648 C>T maps to NM_182500.2 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:88825963 C>T maps to NM_152670.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:27360639 G>A maps to NM_178553.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:27360978 G>A maps to NM_178553.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:27360063 T>C maps to NM_178553.3 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:241828011 T>C maps to NM_001085437.1 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:241827876 G>A maps to NM_001085437.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:241831031 G>A maps to NM_001085437.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:99414000 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:99412602 G>T maps to NM_207362.2 S910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:99439637 G>A maps to NM_207362.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:99443437 C>T maps to NM_207362.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:99448837 G>A maps to NM_207362.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr2:47378564 G>A maps to NM_001163561.1 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr2:55439839 A>G maps to NM_152385.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:55449541 T>C maps to NM_152385.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:55433494 G>T maps to NM_152385.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:55436805 G>A maps to NM_152385.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:55449430 G>T maps to NM_152385.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:55439839 A>G maps to NM_152385.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:99220597 G>A maps to NM_001008215.1 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:74789441 G>A maps to NM_138804.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:74842228 G>T maps to NM_138804.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:74808924 A>G maps to NM_138804.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr2:197674102 A>G maps to NM_213608.1 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:211018994 G>A maps to NM_152519.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:210888759 G>T maps to NM_152519.2 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:210968947 A>T maps to NM_152519.2 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:73455942 G>A maps to NM_032319.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:29295738 G>T maps to NM_001029883.1 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:29294048 G>A maps to NM_001029883.1 Q1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:29297025 G>A maps to NM_001029883.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:29295480 G>A maps to NM_001029883.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr2:29293872 C>T maps to NM_001029883.1 S1085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:29295789 T>C maps to NM_001029883.1 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:29293602 C>T maps to NM_001029883.1 S1175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:29294445 G>A maps to NM_001029883.1 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr2:29294937 G>A maps to NM_001029883.1 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:120097454 G>A maps to NM_001017927.2 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:170550770 C>A maps to NM_001085447.1 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:74043854 C>A maps to NM_001080474.1 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:74043207 A>T maps to NM_001080474.1 K620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:209036792 G>A maps to NM_001099334.2 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:209045519 T>C maps to NM_001099334.2 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:228476304 G>A maps to NM_020161.3 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr2:24413337 C>T maps to NM_001040710.1 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:24398369 G>A maps to NM_001040710.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:24398435 A>G maps to NM_001040710.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr2:242814285 C>T maps to NM_173821.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr2:242814384 G>A maps to NM_173821.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr2:242814204 C>T maps to NM_173821.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr2:63631604 G>T maps to NM_015910.4 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:63712101 C>T maps to NM_015910.4 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:85051119 G>A maps to ENST00000409520 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr2:85108088 C>T maps to ENST00000409520 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr2:85097693 G>A maps to ENST00000409520 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:6678263 C>T maps to NM_000064.2 T1583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:6710724 C>T maps to NM_000064.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:6677952 T>C maps to NM_000064.2 K1644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:6694610 G>A maps to NM_000064.2 V995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:6680226 G>T maps to NM_000064.2 Y1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:6686913 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:6690654 G>A maps to NM_000064.2 C1158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr19:6697432 G>A maps to NM_000064.2 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:6720531 A>G maps to NM_000064.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:6697435 G>A maps to NM_000064.2 T905T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr19:6720585 T>C maps to NM_000064.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:6718369 G>T maps to NM_000064.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:6709736 G>A maps to NM_000064.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr19:6694613 G>A maps to NM_000064.2 A994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr12:8211767 G>A maps to NM_004054.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:8211565 C>A maps to NM_004054.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr12:8211743 C>A maps to NM_004054.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:119434450 A>G maps to NM_033364.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:119458110 G>T maps to NM_033364.3 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:119463027 C>T maps to NM_033364.3 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:119434528 A>G maps to NM_033364.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr3:119445069 C>T maps to NM_033364.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:112727130 G>A maps to NM_015412.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr3:112732250 C>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:14724255 G>A maps to NM_032137.4 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr3:14770058 G>T maps to NM_032137.4 E602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:14724684 C>T maps to NM_032137.4 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:194790673 G>A maps to NM_152531.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:194877218 G>A maps to NM_152531.4 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:126272179 C>T maps to NM_152533.1 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:44409041 C>T maps to NM_173826.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr3:44438318 G>A maps to NM_173826.3 W293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:10146215 C>T maps to NM_001164839.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:99865848 G>T maps to NM_032359.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:99886633 C>T maps to NM_032359.3 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:118865716 C>T maps to NM_152539.2 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:118865653 T>G maps to NM_152539.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:11885565 C>T maps to ENST00000444133 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:8675540 G>T maps to NM_015931.1 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:196434436 T>C maps to NM_032898.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:128998600 T>A maps to NM_001006109.1 L9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:129007701 A>G maps to NM_001006109.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:88205313 G>A maps to NM_173824.3 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:88205224 G>T maps to NM_173824.3 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:88205682 T>C maps to NM_173824.3 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:43122704 C>T maps to NM_032806.4 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:43122413 G>A maps to NM_032806.4 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr3:43122734 G>A maps to NM_032806.4 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr3:196235126 A>G maps to NM_001077657.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr3:196234794 G>T maps to NM_001077657.1 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:196236518 C>T maps to NM_001077657.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:196235000 T>C maps to NM_001077657.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:196235126 A>G maps to NM_001077657.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr3:196235126 A>G maps to NM_001077657.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:111831891 T>C maps to NM_024616.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:111812208 T>C maps to NM_001171747.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:157289760 C>T maps to NM_001130002.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:143692405 T>C did not map to a codon.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr3:143704491 G>A maps to NM_173552.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr3:192516873 A>G maps to NM_178496.3 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:192635461 C>T maps to NM_178496.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr3:192516447 G>T maps to NM_178496.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:192516714 G>A maps to NM_178496.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:56705635 G>A maps to ENST00000447900 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:56657580 G>A maps to ENST00000447900 N1499N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:56680685 C>T maps to ENST00000447900 K693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:56680903 C>A maps to ENST00000447900 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:56675607 G>A maps to ENST00000447900 A796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr3:56667419 G>A maps to ENST00000447900 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:56680717 C>A maps to ENST00000447900 E683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr3:56667182 T>C maps to ENST00000447900 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:56658671 C>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:56667596 C>T maps to ENST00000447900 V1074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr3:56667184 A>G maps to ENST00000447900 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:58870301 G>A maps to ENST00000482387 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr3:184801097 C>T maps to NM_001025266.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:48955910 C>T maps to NM_001123040.1 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:138669206 C>T maps to NM_001040061.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:207314568 G>A maps to NM_000715.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr1:207317262 T>C maps to NM_000715.3 Y515Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:207297296 T>C maps to NM_000715.3 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:207273168 C>A maps to NM_001017367.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:57829750 G>A maps to NM_032313.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:57829782 G>A maps to NM_032313.2 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr4:57843727 G>A maps to NM_032313.2 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:100463212 G>T maps to NM_032149.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:113538952 C>A maps to NM_018392.4 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:113540066 C>T maps to NM_018392.4 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:113475071 G>A maps to NM_018392.4 D1755D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:113508849 G>T maps to NM_018392.4 T1121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:81791226 G>A maps to ENST00000508675 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:81866026 C>T maps to ENST00000508675 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:8465818 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:76489390 C>A maps to NM_178497.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr4:170663134 G>T maps to NM_017867.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:128930276 C>T maps to ENST00000454347 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:120221585 C>A maps to NM_001170330.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr4:121958186 A>G maps to NM_024574.3 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:71201635 G>T maps to NM_033122.3 G294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr4:98893496 A>G maps to NM_174952.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr4:99027190 A>G maps to NM_174952.2 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:98633878 C>A maps to NM_174952.2 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr4:165878320 G>A maps to NM_153027.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:184618881 G>A maps to NM_021942.4 T915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:184600519 T>C maps to NM_021942.4 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:184628023 C>T maps to NM_021942.4 T1040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr4:184606282 C>T maps to NM_021942.4 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:184628023 C>T maps to NM_021942.4 T1040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:3255095 G>A maps to NM_001042690.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:3251197 C>T maps to NM_001042690.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:3255143 C>T maps to NM_001042690.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:140188115 T>C maps to ENST00000260011 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:5961137 G>A maps to ENST00000324058 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr4:71096919 A>G maps to NM_152997.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:123731376 G>A maps to NM_001735.2 Y1394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:123783947 G>A maps to NM_001735.2 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:123725006 G>T maps to NM_001735.2 L1482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:123739085 G>T maps to NM_001735.2 A1252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr9:123776267 G>A maps to NM_001735.2 R714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:123769200 G>A maps to NM_001735.2 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr9:123751391 C>T maps to NM_001735.2 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr9:123780004 G>A maps to NM_001735.2 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr9:123753468 C>A maps to NM_001735.2 G981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:47823690 G>A maps to ENST00000355085 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:47823603 G>A maps to ENST00000355085 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:47824041 G>A maps to ENST00000355085 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr5:31538630 T>C maps to NM_018356.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:31545773 T>C maps to NM_018356.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:31538630 T>C maps to NM_018356.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:32789529 C>A maps to NM_024563.3 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:32789872 G>T maps to NM_024563.3 *122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:32789863 C>A maps to NM_024563.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:175772201 C>T maps to ENST00000443967 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:175751712 C>T maps to ENST00000443967 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:43446529 A>G maps to NM_022483.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:36226583 A>G maps to NM_001085411.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:36227637 T>A maps to NM_001085411.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:43508740 G>A maps to NM_198566.2 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr5:93856190 A>C maps to ENST00000513200 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:93872758 A>G maps to ENST00000513200 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:93775827 T>C did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:93859772 G>A maps to ENST00000513200 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:93856417 G>A maps to ENST00000513200 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:93798264 G>A maps to ENST00000513200 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:93856333 G>A maps to ENST00000513200 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:93812904 A>G maps to ENST00000513200 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr5:93859771 C>A maps to ENST00000513200 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:93859772 G>A maps to ENST00000513200 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:93798192 A>C maps to ENST00000513200 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:2752864 A>G maps to NM_178569.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr5:43039602 C>T maps to NM_001014279.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:43039617 G>A maps to NM_001014279.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:154202034 A>G maps to NM_032385.3 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:156770202 C>T maps to NM_001001343.3 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:156770019 C>T maps to NM_001001343.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr5:156770535 G>A maps to NM_001001343.3 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr5:172513545 C>T maps to NM_153607.2 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:37198911 A>G maps to NM_023073.3 S1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr5:37198854 T>C maps to NM_023073.3 V1207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:37187587 C>A maps to NM_023073.3 R1336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:37173970 T>C maps to NM_023073.3 Q2019Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:37164387 G>A maps to NM_023073.3 F2525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr5:37170223 G>A maps to NM_023073.3 N2127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:37169588 A>G maps to NM_023073.3 S2179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:37243197 A>G maps to NM_023073.3 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr5:37125381 C>A maps to NM_023073.3 G2920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:37169192 A>G maps to NM_023073.3 I2311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:37157907 A>G maps to NM_023073.3 P2607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr5:37176047 G>A maps to NM_023073.3 Q1981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr5:37185032 T>C maps to NM_023073.3 P1446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:37121879 C>T maps to NM_023073.3 L2954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:37231120 C>T maps to NM_023073.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:179285751 G>A maps to NM_016175.3 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:179267904 C>T maps to NM_016175.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr5:125971836 A>G maps to NM_207408.1 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr5:125968274 C>T maps to NM_207408.1 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:41917124 T>C maps to NM_175921.4 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:41917355 G>A maps to NM_175921.4 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:41917355 G>A maps to NM_175921.4 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:41912199 A>G maps to NM_175921.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:41917355 G>A maps to NM_175921.4 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:41917161 G>T maps to NM_175921.4 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:442847 C>T maps to NM_138464.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:442831 C>A maps to NM_138464.2 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:41181594 C>A maps to NM_001115131.1 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:41154095 C>T maps to NM_001115131.1 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:41154074 C>T maps to NM_001115131.1 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr5:41181493 G>T maps to NM_001115131.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:41176763 C>T maps to NM_001115131.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:41149412 T>C maps to NM_001115131.1 R851R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:41186180 G>A maps to NM_001115131.1 V239V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-A00N-01A-02W-A00E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:32307413 A>G maps to ENST00000447241 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:32317570 C>A maps to ENST00000447241 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:43193500 C>T maps to ENST00000509253 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr6:165715720 G>A maps to NM_144980.3 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr6:165711551 C>T maps to NM_144980.3 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr6:165706920 C>T maps to NM_144980.3 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:33668257 G>A maps to NM_032340.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr6:37452634 C>T maps to NM_138493.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:30610596 C>T maps to ENST00000376485 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr6:47847118 G>A maps to NM_001013732.3 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:47846814 G>A maps to NM_001013732.3 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:47847265 C>T maps to NM_001013732.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr6:47846980 G>A maps to NM_001013732.3 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr6:54095609 A>G maps to ENST00000502396 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:54095669 A>G maps to ENST00000502396 E959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr6:53989518 C>T maps to ENST00000502396 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr6:53989389 A>G maps to ENST00000502396 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr6:3723930 G>A maps to NM_183373.3 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:3727804 G>A maps to NM_183373.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:3751561 G>A maps to NM_183373.3 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:4069070 C>T maps to NM_173563.1 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:4077638 T>G maps to NM_173563.1 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:4070050 G>A maps to NM_173563.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:4069070 C>T maps to NM_173563.1 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:4074895 C>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:31080069 T>C did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:74161691 C>T maps to NM_138441.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:42996964 A>G maps to NM_033112.2 *260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:42995124 C>T maps to NM_033112.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:88049853 C>T maps to NM_020425.4 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:88119611 C>T maps to NM_001031743.2 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:88136248 T>C maps to NM_001031743.2 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr6:88125569 C>T maps to NM_001031743.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:97609895 A>G maps to NM_198468.2 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:97620963 C>T maps to NM_198468.2 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:97676827 G>A maps to NM_198468.2 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr6:97594753 A>T maps to NM_198468.2 Y1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr6:97599696 G>A maps to NM_198468.2 C1144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr6:97720587 G>A maps to NM_198468.2 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:99771428 C>T maps to NM_032511.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:99729264 G>A maps to NM_032511.2 H335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr6:99771497 C>A maps to NM_032511.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr6:121401917 T>C maps to ENST00000275159 *1299W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:121563478 A>G maps to ENST00000275159 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:121655434 C>A maps to ENST00000275159 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr6:121642940 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:121412127 G>A maps to ENST00000275159 C1216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:121577397 C>T maps to ENST00000275159 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:121600270 C>A maps to ENST00000275159 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:121401916 C>A maps to ENST00000275159 *1299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:121624896 C>A maps to ENST00000275159 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr6:121602824 G>A maps to ENST00000275159 Y491Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr6:121401916 C>A maps to ENST00000275159 *1299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr6:121638664 A>G maps to ENST00000275159 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr6:121638679 G>T maps to ENST00000275159 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:127797373 G>A maps to NM_001012279.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr6:127796869 C>A maps to NM_001012279.2 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr6:127796950 C>T maps to NM_001012279.2 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:127797148 C>T maps to NM_001012279.2 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:127836183 G>A maps to NM_001012279.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr6:127796704 G>A maps to NM_001012279.2 A822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:127836754 C>T maps to NM_001012279.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:127797352 G>A maps to NM_001012279.2 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr6:127796767 C>T maps to NM_001012279.2 A801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr6:127796587 G>A maps to NM_001012279.2 D861D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr6:127797387 C>A maps to NM_001012279.2 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:127836183 G>A maps to NM_001012279.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:127836910 G>A maps to NM_001012279.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:127797196 C>T maps to NM_001012279.2 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr6:127796566 G>A maps to NM_001012279.2 H868H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:127836084 G>A maps to NM_001012279.2 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr6:110620307 G>A maps to NM_001123364.1 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr6:130166919 C>A maps to NM_001010876.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:4130373 A>C did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:107361335 T>C maps to NM_001142470.1 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr6:118812935 A>T maps to NM_001042475.2 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:118805005 G>A maps to NM_001042475.2 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:118802969 C>A maps to NM_001042475.2 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr6:118812935 A>G maps to NM_001042475.2 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:118844980 C>A maps to NM_001042475.2 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:118845001 C>A maps to NM_001042475.2 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:151790031 G>A maps to NM_024573.1 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:151789947 T>A maps to NM_024573.1 C343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:151779638 G>A maps to NM_024573.1 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:151775684 C>A maps to NM_024573.1 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:74072908 C>A maps to NM_001017361.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:36291964 C>A maps to NM_001010903.4 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:36298017 G>A maps to NM_001010903.4 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:43970823 C>T maps to NM_153246.4 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:112421941 A>G maps to NM_001033564.1 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr6:31692529 C>T maps to NM_025260.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr6:31736848 T>C maps to NM_025258.2 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:31740845 G>A maps to NM_025258.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:31734089 C>A maps to NM_025258.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:31734293 C>T maps to NM_025258.2 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr6:31734089 C>T maps to NM_025258.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr6:31627261 A>G maps to NM_021184.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:71289256 G>T maps to NM_145267.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:170160769 G>T maps to NM_018341.1 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:170176158 G>A maps to NM_018341.1 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:170169670 T>C maps to NM_018341.1 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr6:170181594 A>T maps to NM_018341.1 K675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:170156840 C>T maps to NM_018341.1 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr6:35715084 G>A maps to NM_145028.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:36882392 G>T maps to NM_152734.3 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:36867325 G>T maps to NM_152734.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr6:36887352 G>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr6:36887352 G>T did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr6:36887352 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:151917658 C>T maps to ENST00000367290 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:151865709 G>A maps to ENST00000367290 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr6:151869500 T>C maps to ENST00000367290 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:151936810 G>A maps to ENST00000367290 K655K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:40955656 T>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:40950022 G>T maps to NM_000587.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:40979970 G>A maps to NM_000587.2 E770E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:40962237 T>C maps to NM_000587.2 C571C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:40945394 G>A maps to NM_000587.2 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:40950022 G>T maps to NM_000587.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:40934492 G>T maps to NM_000587.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr7:40535951 C>A maps to NM_001193311.1 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:40488905 C>T maps to NM_001193311.1 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:40173899 G>T maps to NM_138701.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr7:31735209 G>A maps to NM_006658.4 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr7:31736636 C>A maps to NM_006658.4 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:31735149 A>G maps to NM_006658.4 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr7:42950319 T>C maps to NM_001099858.1 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr7:42950019 A>G maps to NM_001099858.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr7:42949443 T>G maps to NM_001099858.1 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:6634100 G>A maps to NM_024067.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:2594050 G>A maps to NM_152743.3 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr7:2577780 T>C maps to NM_152743.3 E796E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:2584567 G>A maps to NM_152743.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr7:5959525 C>T maps to NM_015622.5 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:23340623 C>T maps to NM_138446.1 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:25207920 C>A maps to NM_138811.3 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:25175650 A>G maps to NM_138811.3 N571N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:148288050 G>T maps to NM_145304.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:142637672 G>A maps to NM_178829.4 *148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:39612280 A>G maps to NM_020192.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:30174814 C>A maps to NM_152793.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:99754736 C>T maps to NM_018275.3 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:43687203 C>T maps to NM_018224.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr7:43684998 C>A did not map to a codon.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr7:100033078 G>A maps to NM_145030.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:100033060 A>G maps to NM_145030.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:134851452 C>T maps to NM_024033.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:1040128 G>A maps to NM_032350.5 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:100086318 G>A maps to ENST00000423930 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:100084701 C>T maps to ENST00000423930 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr7:112127077 A>G maps to NM_182597.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:48092347 T>C maps to ENST00000430738 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:48086155 C>T maps to ENST00000430738 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:48086060 C>A maps to ENST00000430738 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:48092404 C>T maps to ENST00000430738 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr7:120906468 A>G maps to NM_024913.4 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:120629803 C>T maps to NM_024913.4 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:120629708 C>T maps to NM_024913.4 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr7:120655885 G>A maps to NM_024913.4 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:120655724 G>T maps to NM_024913.4 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr7:120655852 C>T maps to NM_024913.4 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:120782098 C>T maps to NM_024913.4 H653H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr7:120767265 A>T maps to NM_024913.4 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr7:120768468 C>T maps to NM_024913.4 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr7:120876862 A>G maps to NM_024913.4 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:112461984 G>A maps to NM_152556.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:112555386 G>A maps to NM_152556.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:112461966 C>T maps to NM_152556.2 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:100054375 T>C maps to ENST00000426357 *289W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr7:89939423 C>T maps to NM_001039706.2 R900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:89917576 C>T maps to NM_001039706.2 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr7:89938626 A>G maps to NM_001039706.2 K867K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr7:89938626 A>G maps to NM_001039706.2 K867K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:92161753 C>T maps to NM_032120.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr7:92164250 A>G maps to NM_032120.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:92164250 A>G maps to NM_032120.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:108524237 C>T maps to NM_001024607.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:108524547 G>T maps to NM_001024607.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr7:108524126 T>C maps to NM_001024607.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:128097426 G>A maps to NM_001098786.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:6370578 C>T maps to NM_001037163.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:6370623 T>C maps to NM_001037163.1 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:6370164 C>T maps to NM_001037163.1 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:57383352 G>A maps to NM_000562.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr1:57333326 G>T maps to NM_000562.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:57399101 C>T maps to NM_000066.2 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:57420417 A>G maps to NM_000066.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:57395223 G>A maps to NM_000066.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:57406581 C>T maps to NM_000066.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:139840434 C>T maps to NM_000606.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:49986796 G>A maps to NM_001007176.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr8:144126109 C>T maps to NM_173687.2 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr8:144130633 C>A maps to NM_173687.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:144126109 C>T maps to NM_173687.2 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:146278776 T>C maps to ENST00000444534 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:69400273 T>C maps to NM_052958.2 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr8:69699761 C>T maps to NM_052958.2 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:69621312 C>T maps to NM_052958.2 F442F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AZ-4315-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:69552611 G>A maps to NM_052958.2 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:69552623 T>C maps to NM_052958.2 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:42401725 C>T maps to NM_001135675.1 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:42403924 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr8:33369537 A>G maps to NM_001102401.1 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:33356729 C>A maps to NM_001102401.1 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr8:33360954 A>C maps to NM_001102401.1 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr8:33367293 T>C maps to NM_001102401.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:442473 G>A maps to NM_175075.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:442413 C>T maps to NM_175075.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr8:67789597 G>T maps to NM_173518.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:67796184 C>T maps to NM_173518.4 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:67422371 C>T maps to NM_152765.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:99101826 T>C maps to NM_173549.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr8:99102198 A>G maps to NM_173549.2 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr8:99105497 T>C maps to NM_173549.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:22458500 T>C maps to ENST00000450780 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:86126810 A>C maps to NM_001099670.1 L94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:10555382 G>A maps to NM_001040032.1 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:10557974 G>A maps to NM_001040032.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:10557956 A>G maps to NM_001040032.1 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:10532212 C>T maps to NM_001040032.1 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr8:124243796 C>T maps to NM_032847.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr8:124232408 T>C maps to NM_032847.1 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:12878673 G>A maps to NM_020844.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:27887826 C>A maps to ENST00000341513 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:27925200 T>A maps to ENST00000341513 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr8:27915780 T>C maps to ENST00000341513 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:27903177 C>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:117950553 G>A maps to NM_001025357.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:39341377 G>A maps to NM_001737.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:39315921 G>A maps to NM_001737.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:39288870 T>C maps to NM_001737.3 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:39342213 G>A maps to NM_001737.3 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:39316095 G>A maps to NM_001737.3 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr9:98683537 C>T maps to NM_001010895.2 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr9:98678016 G>T maps to NM_001010895.2 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:27284879 G>T maps to NM_020641.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr9:27294377 T>A maps to NM_020641.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:130471808 G>A maps to NM_001012502.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:130472914 C>T maps to NM_001012502.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:130471895 C>T maps to NM_001012502.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr9:130475335 C>T maps to NM_001012502.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr9:130473015 G>A maps to NM_001012502.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr9:131050938 C>T maps to NM_001040011.1 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:104238738 G>A maps to NM_032342.1 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:35825362 T>G maps to NM_001012446.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:35818887 G>A maps to NM_001012446.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:96080829 T>C maps to NM_001098808.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr9:35044044 C>T maps to NM_203299.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:35044428 G>A maps to NM_203299.2 K601K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:72472894 T>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:72501768 G>A maps to NM_001010940.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:72521042 G>A maps to NM_001010940.1 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr9:72471493 A>G maps to NM_001010940.1 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:139929356 G>T maps to NM_207511.1 G142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:112963599 T>C maps to NM_001012993.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr9:100672377 A>G maps to NM_016481.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr9:100672809 C>T maps to NM_016481.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr9:100672377 A>C maps to NM_016481.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr9:100678573 C>T maps to NM_016481.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:130925725 C>T maps to NM_024112.3 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:89763653 C>T maps to NM_001001709.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:89763768 G>T maps to NM_001001709.2 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:135285805 C>T maps to NM_207417.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:135357743 C>A maps to NM_207417.1 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:135285726 C>T maps to NM_207417.1 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr9:135418391 C>T maps to NM_207417.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:139738904 C>T maps to NM_001080482.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:139740932 C>T maps to NM_001080482.2 C689C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:140147148 G>A maps to ENST00000388931 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:140146525 G>A maps to ENST00000388931 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:99413722 C>A maps to NM_153698.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:99404097 C>T maps to NM_153698.1 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr9:34611146 G>A maps to NM_148179.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:34611287 C>T maps to NM_148179.1 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:97535436 G>A maps to NM_001193329.1 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr9:103204552 C>T maps to NM_001198812.1 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:103204372 G>A maps to NM_001198812.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:140510480 G>A maps to NM_032937.4 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr9:77631293 G>A maps to NM_152420.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:77632233 C>A maps to NM_152420.1 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:77613612 G>A maps to NM_152420.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr9:77632191 C>A maps to NM_152420.1 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr9:116181393 G>A maps to ENST00000451722 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:116175874 C>T maps to ENST00000451722 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:116183405 G>A maps to ENST00000451722 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:116191561 G>T maps to ENST00000451722 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:116186597 T>C did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:91605991 C>T maps to NM_001001938.3 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr9:111798577 T>C maps to NM_032012.3 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:132381902 C>T maps to NM_199350.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:132381872 C>T maps to NM_199350.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:132382095 C>T maps to NM_199350.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr9:132381872 C>T maps to NM_199350.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:86570382 G>A maps to NM_032307.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:86571106 G>A maps to NM_032307.3 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr9:215364 A>C maps to NM_152569.2 L11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:4617985 G>T maps to ENST00000454239 S311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:4662037 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:4662027 G>A maps to ENST00000454239 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:71152351 A>G maps to NM_153237.1 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:90501447 C>T maps to NM_178828.4 D682D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:90503013 C>T maps to NM_178828.4 G1204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:90500976 C>T maps to NM_178828.4 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr9:90501411 C>T maps to NM_178828.4 D670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:90499848 C>T maps to NM_178828.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:90500931 G>A maps to NM_178828.4 W510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:90502752 G>T maps to NM_178828.4 P1117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:90501417 G>A maps to NM_178828.4 Q672Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:90502974 A>G maps to NM_178828.4 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr9:90501543 G>A maps to NM_178828.4 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr9:26884812 G>C maps to NM_024828.3 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr9:114476801 T>A maps to NM_173521.3 K716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr9:114490174 T>C maps to NM_173521.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr9:114490174 T>C maps to NM_173521.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:114476796 A>C maps to NM_173521.3 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:114453869 C>A maps to NM_173521.3 E1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:114486123 C>T maps to NM_173521.3 E570E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:114489972 G>A maps to NM_173521.3 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:74587676 C>T maps to NM_182505.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:117379513 C>T maps to ENST00000374049 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:117400942 T>C maps to ENST00000374049 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:15744433 T>G maps to NM_173550.2 L738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr9:15695283 G>T maps to NM_173550.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:15846803 G>A maps to NM_173550.2 E1124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:15571670 G>T maps to NM_173550.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:15745612 C>T maps to NM_173550.2 D885D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:15695283 G>T maps to NM_173550.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:15723707 G>A maps to NM_173550.2 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:15744458 C>T maps to NM_173550.2 C746C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:15623360 G>T maps to NM_173550.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:15744419 A>G maps to NM_173550.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:15744353 G>A maps to NM_173550.2 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:136270024 C>A maps to NM_153710.3 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:135601092 C>T maps to NM_152572.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr9:135668079 G>A maps to NM_152572.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:135601176 C>T maps to NM_152572.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr15:63631114 G>A maps to NM_001218.3 C259C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr15:63637684 G>A maps to NM_001218.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:63632561 G>T maps to NM_001218.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr8:86171713 C>T maps to NM_198584.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr8:86163119 C>T maps to NM_198584.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr1:150235537 T>C maps to NM_012113.1 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:86351170 C>T maps to NM_005181.3 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr8:86357401 C>T maps to NM_005181.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:58234798 C>T maps to NM_000717.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:58233927 C>A maps to NM_000717.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:87936072 G>A maps to NM_001739.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:87970044 C>T maps to NM_001739.1 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:87921770 C>T maps to NM_001739.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:15794839 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:15792445 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:9027808 G>A maps to ENST00000413627 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr1:9017331 A>G maps to ENST00000413627 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr8:61178561 G>A maps to NM_004056.4 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr8:61178600 C>T maps to NM_004056.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr8:61178600 C>T maps to NM_004056.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr9:35677794 G>A maps to NM_001216.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:35680801 G>A maps to NM_001216.2 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:35679915 G>A maps to NM_001216.2 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr9:35674150 G>A maps to NM_001216.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr9:35676373 C>A maps to NM_001216.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr2:231624733 G>T maps to NM_001130850.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:231683325 C>T maps to NM_001130850.1 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr13:49951207 G>A maps to NM_001079670.1 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:49951198 T>C maps to NM_001079670.1 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:227172289 C>T maps to NM_020247.4 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr1:227172626 C>T maps to NM_020247.4 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:227170436 G>A maps to NM_020247.4 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:24567725 C>T maps to NM_012295.3 R1935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:24562653 G>A maps to NM_012295.3 R1685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr22:24494132 C>A maps to NM_012295.3 P1365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr22:24530300 C>A maps to NM_012295.3 G1555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:24483551 C>T maps to NM_012295.3 S1137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:24530285 C>T maps to NM_012295.3 R1550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr22:24494153 C>T maps to NM_012295.3 D1372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr18:20774431 C>G maps to NM_001100619.2 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:121098053 C>T maps to NM_001033677.1 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:121098023 C>T maps to NM_001033677.1 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:121098023 C>T maps to NM_001033677.1 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr11:67287602 G>A maps to NM_016366.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:67287273 G>A maps to NM_016366.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:48543976 A>G maps to NM_019855.3 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:21735974 T>C maps to NM_138644.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:21735717 G>T maps to NM_138644.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:21736215 G>T maps to NM_012189.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:65157207 G>A maps to ENST00000371073 A1263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:65129471 C>T maps to ENST00000371073 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:65113556 G>T maps to ENST00000371073 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr1:65141157 G>A maps to ENST00000371073 A934A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:65068575 A>G maps to ENST00000371073 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:65068537 C>T maps to ENST00000371073 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:65145311 C>T maps to ENST00000371073 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:65098410 C>T maps to ENST00000371073 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:65099909 C>T maps to ENST00000371073 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:65147769 A>G maps to ENST00000371073 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr19:13414674 G>A maps to NM_023035.2 N671N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:13410102 G>A maps to NM_023035.2 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr19:13397512 G>A maps to NM_023035.2 A1123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:13365980 G>A maps to NM_023035.2 F1565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr19:13340930 G>A maps to NM_023035.2 Y1835Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:13368283 G>A maps to NM_023035.2 Y1494Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:13418938 G>A maps to NM_023035.2 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:13368241 G>T maps to NM_023035.2 I1508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:13423566 G>T maps to NM_023035.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:13409857 G>A maps to NM_023035.2 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:13410061 G>A maps to NM_023035.2 N799N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:140997237 C>T maps to ENST00000277549 C1767C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:141008881 C>T maps to ENST00000277549 F1864F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:140952581 C>T maps to ENST00000277549 Y1397Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr9:141006958 T>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:140866021 G>A maps to ENST00000277549 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:140948389 G>A maps to ENST00000277549 A1301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:140946600 G>A maps to ENST00000277549 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:140972649 G>A maps to ENST00000277549 E1679E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr9:140968499 C>T maps to ENST00000277549 Y1614Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr9:140991048 C>T maps to ENST00000277549 Y1737Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:140919616 C>T maps to ENST00000277549 V1094V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:140772555 G>A maps to ENST00000277549 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:141016045 G>A maps to ENST00000277549 T2206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr9:140952656 G>A maps to ENST00000277549 E1422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:2743461 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:2595357 C>T maps to NM_199460.2 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:2788860 C>T maps to NM_199460.2 P1829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:2614108 C>T maps to NM_199460.2 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:2717811 C>T maps to NM_199460.2 F1184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr12:2786287 C>T maps to NM_199460.2 Y1667Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:2706655 C>A maps to NM_199460.2 I969I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr12:2566838 C>T maps to NM_199460.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:2675692 G>A maps to NM_199460.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr12:2659199 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr12:2788614 C>T maps to NM_199460.2 A1747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:2622091 C>T maps to NM_199460.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:2797917 C>T maps to NM_199460.2 H2113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:53694271 C>T maps to NM_001128840.1 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr3:53535710 C>T maps to NM_001128840.1 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:53783318 G>A maps to NM_001128840.1 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:53796038 C>T maps to NM_001128840.1 D1267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:53700438 G>A maps to NM_001128840.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:53785873 G>A maps to NM_001128840.1 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:53694271 C>T maps to NM_001128840.1 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:53753779 A>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:53783457 G>T maps to NM_001128840.1 E1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:53531456 C>T maps to NM_001128840.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:53757509 A>C maps to NM_001128840.1 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:53783457 G>T maps to NM_001128840.1 E1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:53845330 T>C maps to NM_001128840.1 Y2128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr3:53810044 C>A maps to NM_001128840.1 I1445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr3:53752753 G>T maps to NM_000720.2 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:53779664 C>T maps to NM_001128840.1 C1007C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:53753779 A>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:181741216 G>A maps to ENST00000357570 E1663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:181686271 C>T maps to ENST00000357570 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:181767783 C>T maps to ENST00000357570 F2252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:181759664 C>T maps to ENST00000357570 D1957D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr1:181701660 G>A maps to ENST00000357570 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:181701630 G>A maps to ENST00000357570 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr1:181727988 C>T maps to ENST00000357570 I1530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:181691011 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:181765885 C>T maps to ENST00000357570 V2097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:181685254 C>T maps to ENST00000357570 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:181724521 G>A maps to ENST00000357570 E1326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:181688957 C>A maps to ENST00000357570 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr1:181480583 C>T maps to ENST00000357570 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:181741276 C>T maps to ENST00000357570 T1683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:181686259 T>C maps to ENST00000357570 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:181690892 G>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:181695253 C>A maps to ENST00000357570 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr1:181690991 G>T maps to ENST00000357570 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:181724380 C>T maps to ENST00000357570 F1279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:181706675 C>A maps to ENST00000357570 C1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr1:181754484 A>C maps to ENST00000357570 A1870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:181701960 G>A maps to ENST00000357570 R913R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:49079017 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:49079430 C>A did not map to a codon.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr23:49063211 C>T did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:49084785 T>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:49083406 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:49072931 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:49081290 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:49082520 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:49066119 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:49066199 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:49076956 C>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:49084576 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:49075888 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:49087679 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:49068716 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:49084875 G>A did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:49075826 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:49088170 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:49071905 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:49079524 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:49084772 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:49087332 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:49069215 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:49074983 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:49075802 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:49069197 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:49061671 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:49072840 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:49079488 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:49067862 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:49084899 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:49067096 G>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:49076226 C>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:49069206 G>A did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:49074941 C>T did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:49066413 G>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:49087679 G>T did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:49075817 C>G did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:49063044 T>C did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:49068717 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:49071545 C>A did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:49083124 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:48653353 C>A maps to NM_018896.3 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:48650028 G>A maps to NM_018896.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr17:48678116 C>T maps to NM_018896.3 R1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:48685339 G>A maps to NM_018896.3 R1555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:48646308 C>T maps to NM_018896.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:48703574 C>T maps to NM_018896.3 G2199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:48696329 C>T maps to NM_018896.3 H1914H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:48649923 C>T maps to NM_018896.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:48646653 C>T maps to NM_018896.3 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:48669392 C>T maps to NM_018896.3 F950F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:48652950 G>A maps to NM_018896.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr16:1256130 C>T maps to NM_021098.2 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:1252153 C>T maps to NM_021098.2 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:1250534 C>T maps to NM_021098.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:1257795 C>T maps to NM_021098.2 D1030D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr16:1262088 G>A maps to NM_021098.2 A1570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:1257081 C>T maps to NM_021098.2 F957F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:1261257 C>T maps to NM_021098.2 C1438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:1265355 C>T maps to NM_021098.2 R1718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr16:1256103 C>T maps to NM_021098.2 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr16:1261242 C>T maps to NM_021098.2 I1433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:1268292 C>T maps to NM_021098.2 F1843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr22:40068311 C>T maps to NM_021096.3 R1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:40075173 G>A maps to NM_021096.3 S1706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:40074067 A>G maps to NM_021096.3 T1670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr22:40036988 C>A maps to NM_021096.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:201012452 G>A maps to NM_000069.2 V1668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:201047119 G>A maps to NM_000069.2 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:201047169 G>A maps to NM_000069.2 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:201018172 A>G maps to NM_000069.2 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr1:201030565 C>T maps to NM_000069.2 A1028A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr1:201017776 G>A maps to NM_000069.2 D1458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:201031160 G>A maps to NM_000069.2 R988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:201061232 G>A maps to NM_000069.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:81599991 C>A maps to NM_000722.2 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr7:81596911 C>T maps to NM_000722.2 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr7:81643756 A>T maps to NM_000722.2 Y394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:81589141 G>T maps to NM_000722.2 I990I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:81591262 G>A maps to NM_000722.2 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr7:81591262 G>A maps to NM_000722.2 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:81667478 A>G maps to NM_000722.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr7:81667452 T>C maps to NM_000722.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr7:81598281 T>C maps to NM_000722.2 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:50417430 C>T maps to ENST00000435965 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:50416967 A>G maps to ENST00000435965 N349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr3:54603874 C>T maps to NM_018398.2 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:54798317 G>A maps to NM_018398.2 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:54661842 C>T maps to NM_018398.2 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:55052284 C>T maps to NM_018398.2 F976F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr3:54786633 C>A maps to NM_018398.2 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:54596956 G>A maps to NM_018398.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:54604067 G>A maps to NM_018398.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr3:54905645 C>T maps to NM_018398.2 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:54914834 G>A maps to NM_018398.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:55021771 C>A maps to NM_018398.2 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:55038840 C>T maps to NM_018398.2 S914S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CM-5348-01A-21D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr3:54604004 G>A maps to NM_018398.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:54880472 G>A maps to NM_018398.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:1902821 C>T maps to NM_172364.4 *1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:1910241 A>G maps to NM_172364.4 S945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:2024073 G>A maps to NM_172364.4 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:1995403 G>A maps to NM_172364.4 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:1992122 G>A maps to NM_172364.4 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:2022200 G>A maps to NM_172364.4 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:2024076 G>A maps to NM_172364.4 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr12:1984445 C>A maps to NM_172364.4 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:37347744 C>T maps to NM_000723.3 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:37340007 C>T maps to NM_000723.3 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr17:37343806 C>G maps to NM_000723.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr17:37340329 G>C maps to NM_000723.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:37347831 G>T maps to NM_000723.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:18827212 T>C maps to NM_201596.2 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:18690957 T>C maps to NM_201596.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:49217483 G>A maps to NM_000725.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:49220594 C>T maps to NM_000725.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:49220216 C>T maps to NM_000725.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:49217504 C>T maps to NM_000725.2 Y70Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:49220273 C>T maps to NM_000725.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:152727062 C>T maps to NM_000726.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:152698422 C>T maps to NM_000726.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:152737388 G>A maps to NM_000726.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:152727062 C>T maps to NM_000726.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:152732944 G>A maps to NM_000726.3 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:152732944 G>A maps to NM_000726.3 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:152698527 C>T maps to NM_000726.3 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:65040805 C>T maps to NM_000727.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:65052173 C>T maps to NM_000727.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr17:65040835 C>T maps to NM_000727.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:36960868 G>A maps to NM_006078.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr22:36983539 G>A maps to NM_006078.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr22:36960730 G>A maps to NM_006078.3 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr22:37098579 G>A maps to NM_006078.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:24372778 C>T maps to NM_006539.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:24372778 C>T maps to NM_006539.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:24372778 C>T maps to NM_006539.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:65026732 C>T maps to NM_014405.3 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:65020983 C>T maps to NM_014405.3 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:64873503 C>T maps to NM_014404.1 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:64881071 C>T maps to NM_014404.1 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:54501526 G>A maps to NM_145814.1 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:54515244 C>T maps to NM_145814.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr19:54496358 C>T maps to NM_145814.1 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr19:54445330 C>T maps to NM_031896.4 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr19:54444844 C>T maps to NM_031896.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:54466539 C>T maps to NM_031895.5 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr19:54466578 C>T maps to NM_031895.5 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:174979136 C>T maps to NM_014412.2 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:174977764 T>C maps to NM_014412.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:27461306 A>G maps to NM_004341.3 L1623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:27445475 G>A maps to NM_004341.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:27454961 C>T maps to NM_004341.3 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:27460680 C>T maps to NM_004341.3 A1553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr2:27456615 C>T maps to NM_004341.3 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:27461345 C>T maps to NM_004341.3 C1636C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:27456892 C>T maps to NM_004341.3 A1139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:27458285 C>T maps to NM_004341.3 G1320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:27449747 T>C maps to NM_004341.3 Y735Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:27460731 C>T maps to NM_004341.3 S1570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:27459688 C>T maps to NM_004341.3 R1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr11:115099866 T>C maps to NM_014333.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:115111099 G>A maps to NM_014333.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:115047274 G>A maps to NM_014333.3 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr11:115099875 C>T maps to NM_014333.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:115049415 G>A maps to NM_014333.3 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:115047286 T>C maps to NM_014333.3 K412K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:115049427 C>T maps to NM_014333.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:86010736 C>T maps to NM_153184.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr1:159166232 C>T maps to NM_021189.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:159163753 G>A maps to NM_021189.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:159163231 C>A maps to NM_021189.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:159163759 C>T maps to NM_021189.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr1:159163753 G>A maps to NM_021189.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:159169586 C>T maps to NM_021189.3 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:159170660 T>C maps to NM_021189.3 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr19:44130984 G>T maps to NM_145296.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:44127514 G>A maps to NM_145296.1 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr3:62459926 G>T maps to ENST00000383709 S1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:62636539 C>T maps to ENST00000383709 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:62636638 G>A maps to ENST00000383709 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:62467399 C>T maps to ENST00000383709 A1057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:62463952 G>A maps to ENST00000383709 I1104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr3:62503857 G>A maps to ENST00000383709 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:62385188 G>A maps to ENST00000383709 I1323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:62556600 G>A maps to ENST00000383709 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:62478007 A>G maps to ENST00000383709 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:121960373 G>A maps to NM_001167940.1 R1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:122033592 G>T maps to NM_001167940.1 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:122221235 T>C maps to NM_001167940.1 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:7373326 G>T maps to NM_001170692.1 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:7374235 G>A maps to NM_001170692.1 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:71411628 C>T maps to NM_001740.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:71418265 C>T maps to NM_001740.4 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:15096317 C>T maps to NM_000728.3 Y18Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr17:46930337 T>C maps to ENST00000448105 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:46937737 G>A maps to ENST00000448105 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:93055879 G>A maps to NM_001164737.1 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:93055724 G>A maps to NM_001164737.1 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:93055898 G>T maps to NM_001164737.1 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr7:93108801 A>G maps to NM_001164737.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:93067574 C>T maps to NM_001164737.1 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr2:188225403 G>C maps to NM_005795.4 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr2:188211084 G>T maps to NM_005795.4 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr2:188217023 A>G maps to NM_005795.4 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:188217023 A>G maps to NM_005795.4 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:134632502 C>T maps to NM_033138.3 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:134617816 C>T maps to NM_033138.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:134644762 G>T maps to NM_033138.3 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr7:134632354 C>T maps to NM_033138.3 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:134625934 G>A maps to NM_033138.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:134613525 C>T maps to NM_033138.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:134625872 G>T maps to NM_033138.3 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:134632502 C>T maps to NM_033138.3 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr7:134618202 T>A maps to NM_033138.3 L228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:105215147 C>T maps to NM_001001412.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:105218276 G>A maps to NM_001001412.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr10:105218007 G>A maps to NM_001001412.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr10:105215357 C>T maps to NM_001001412.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:105209242 G>A maps to NM_015916.4 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:105209500 C>T maps to NM_015916.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:90870302 C>A maps to NM_006888.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:47389780 G>A maps to ENST00000456319 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:47389792 C>A maps to ENST00000456319 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:68489808 C>T maps to NM_033429.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:5541143 G>T maps to NM_017422.4 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:1847965 G>A maps to NM_138705.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:71275423 G>T maps to NM_031468.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:71275474 A>G maps to NM_031468.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:71275405 C>T maps to NM_031468.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:13054433 C>T maps to NM_004343.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:13050365 G>T maps to NM_004343.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:13050930 C>T maps to NM_004343.3 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr19:13051238 C>A maps to NM_004343.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:16589997 T>A maps to NM_145046.3 K367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:16593329 G>A maps to NM_145046.3 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:16606595 C>T maps to NM_145046.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:128394501 C>T maps to ENST00000342367 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr7:128388831 A>C maps to ENST00000342367 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:128407565 C>T maps to ENST00000342367 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr10:135142373 C>T maps to NM_015722.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:9803357 C>T maps to NM_003656.3 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:9803318 G>A maps to NM_003656.3 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:9802433 G>T maps to NM_003656.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:209773345 T>G maps to NM_020439.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:209786204 C>T maps to NM_020439.2 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:209785204 C>T maps to NM_020439.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:149624765 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:149602592 G>A maps to NM_015981.3 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr5:149630364 C>T maps to NM_015981.3 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr5:149636150 C>T maps to NM_015981.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:149629820 G>A maps to NM_015981.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr5:149633043 C>A maps to NM_015981.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:44282197 C>T maps to NM_001220.4 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:44294154 G>A maps to NM_001220.4 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:44259834 G>T maps to NM_001220.4 V609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:75613004 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:75577235 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr10:75585075 T>C maps to ENST00000423381 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:75632759 C>T maps to ENST00000423381 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr10:75583812 A>G maps to ENST00000423381 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:110819770 C>T maps to NM_001744.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:110560201 C>A maps to NM_001744.4 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:110784899 C>T maps to NM_001744.4 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:110819881 C>T maps to NM_001744.4 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:110730456 A>T maps to NM_001744.4 K146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr5:110730458 A>G maps to NM_001744.4 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr5:110730468 G>T maps to NM_001744.4 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:110819728 G>T maps to NM_001744.4 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr5:110730458 A>G maps to NM_001744.4 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:110730458 A>G maps to NM_001744.4 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:110784899 C>T maps to NM_001744.4 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:110560303 G>A maps to NM_001744.4 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:3775864 G>A maps to ENST00000381771 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:121693602 G>A maps to NM_006549.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr12:121707357 G>A maps to NM_006549.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:49897014 A>G maps to NM_024046.3 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:49897113 G>A maps to NM_024046.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr3:49899767 C>T maps to NM_024046.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:49898964 G>T maps to NM_024046.3 Y116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:134077129 G>T maps to NM_001745.2 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr5:134076829 C>T maps to NM_001745.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr3:48265947 C>T maps to NM_004345.3 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:48265908 G>A maps to NM_004345.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:138714244 A>T maps to ENST00000409386 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:138713260 C>T maps to ENST00000409386 T1093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:138713074 C>T maps to ENST00000409386 T1155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:138713659 G>A maps to ENST00000409386 D960D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:138742244 C>A maps to ENST00000409386 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:138713113 C>T maps to ENST00000409386 P1142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr9:138713053 G>A maps to ENST00000409386 D1162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:200817768 C>T maps to ENST00000236925 D635D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:200813969 T>A maps to ENST00000236925 L372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr1:200730072 T>C maps to ENST00000236925 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr1:200817996 C>T maps to ENST00000236925 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:200817161 C>A maps to ENST00000236925 S433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr1:200730072 T>C maps to ENST00000236925 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr1:200819028 G>A maps to ENST00000236925 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:200813968 T>C maps to ENST00000236925 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:7723466 C>A maps to NM_015215.2 S287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:7798517 C>T maps to NM_015215.2 C1386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:7805985 C>T maps to NM_015215.2 F1484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:7797385 G>A maps to NM_015215.2 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:7151392 G>A maps to NM_015215.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:7700551 C>T maps to NM_015215.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:7725174 G>A maps to NM_015215.2 S856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:7723932 C>T maps to NM_015215.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:7806114 T>G maps to NM_015215.2 A1527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:7737695 C>T maps to NM_015215.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr1:7724292 G>A maps to NM_015215.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:7792592 A>G maps to NM_015215.2 K1000K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:4876935 C>T maps to NM_015099.3 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:4875796 C>T maps to NM_015099.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr17:4877765 G>A maps to NM_015099.3 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:4872515 C>T maps to NM_015099.3 Q1133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr3:12858461 C>T maps to NM_001162499.1 D677D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr3:12858014 C>T maps to NM_001162499.1 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:12858209 C>A maps to NM_001162499.1 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:12858668 G>A maps to NM_001162499.1 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:12857987 G>A maps to NM_001162499.1 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:12856685 G>A maps to NM_001162499.1 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:12859301 C>T maps to NM_001162499.1 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr17:76989697 G>A maps to NM_138793.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr17:76989775 G>A maps to NM_138793.3 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:76989889 G>A maps to NM_138793.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr5:179147486 C>T maps to ENST00000415618 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr5:179137001 T>C maps to ENST00000415618 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr5:179132744 T>C maps to ENST00000415618 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:179146761 C>T maps to ENST00000415618 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:40529970 C>A maps to NM_001105530.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:40533226 G>T maps to NM_001105530.1 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr6:17421845 G>A maps to NM_006366.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:85622738 C>T maps to NM_001747.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:85628744 C>T maps to NM_001747.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:64950969 C>T maps to NM_005186.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:64972289 C>T maps to NM_005186.3 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:64977526 C>T maps to NM_005186.3 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:64973986 G>A maps to NM_005186.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:241535791 C>T maps to NM_023083.3 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:44141092 G>A maps to NM_007058.3 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr19:39227906 C>T maps to NM_144691.3 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:31000436 G>A maps to ENST00000295055 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:223934867 G>A did not map to a codon.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr1:223936817 C>T maps to NM_001748.4 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:223934704 C>T maps to NM_001748.4 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr15:42700449 G>A maps to NM_000070.2 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:42694004 C>T maps to NM_000070.2 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr11:76823687 C>T maps to ENST00000360841 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:76826574 C>T maps to ENST00000360841 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:76795940 G>A maps to ENST00000360841 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:110507142 A>G did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr23:110490675 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:110494327 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:110494479 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:110496353 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:110507059 C>A did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:110494230 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:110495618 A>G did not map to a codon.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr23:110494308 G>A did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:110494228 T>C did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:110491985 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:110492220 C>A did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:110489886 T>C did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:110494228 T>C did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:110491920 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:15283695 G>A maps to NM_014296.2 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:15287057 A>G maps to NM_014296.2 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr1:230927673 C>T maps to NM_006615.2 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:230904996 G>A maps to NM_006615.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:230904978 T>C maps to NM_006615.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr1:230927673 C>T maps to NM_006615.2 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:36632071 T>C maps to NM_001749.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:36631951 C>G maps to NM_001749.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr11:34098144 G>A maps to NM_005898.4 W215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:34110996 G>A maps to NM_005898.4 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:34098145 G>A maps to NM_005898.4 W215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:30876190 A>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr12:30877379 A>G maps to NM_001002259.1 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:30869573 C>A maps to NM_001002259.1 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:30876239 C>A maps to NM_001002259.1 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:30869558 C>A maps to NM_001002259.1 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:30887962 C>A maps to NM_001002259.1 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:30906457 C>T maps to NM_001002259.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:30881800 G>A maps to NM_001002259.1 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:30888083 A>G maps to NM_001002259.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:30862937 G>C maps to NM_001002259.1 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:5915320 C>A maps to ENST00000394521 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr12:75687096 G>A maps to NM_032606.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr12:75676115 T>C maps to NM_032606.3 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:35910595 C>A maps to NM_144647.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:35910613 G>A maps to NM_144647.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:35910466 C>A did not map to a codon.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr1:113202385 C>T maps to NM_006135.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:18891663 C>T maps to NM_033328.2 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr12:18891570 C>T maps to NM_033328.2 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:19746199 C>T maps to ENST00000375145 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:19746160 G>A maps to ENST00000375145 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:37903919 C>T maps to NM_014550.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:37891872 G>A maps to NM_014550.3 R733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:2976808 G>A maps to NM_032415.4 D401D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:2987299 C>T maps to NM_032415.4 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:2962888 G>A maps to NM_032415.4 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr7:2951847 G>A maps to NM_032415.4 F1034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:2979514 C>T maps to NM_032415.4 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr7:2979448 A>G maps to NM_032415.4 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:2946385 G>A maps to NM_032415.4 Y1117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr7:2966388 G>A maps to NM_032415.4 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr7:2963931 G>A maps to NM_032415.4 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr7:2956956 C>T maps to NM_032415.4 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:2987281 A>G maps to NM_032415.4 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:2955003 G>A maps to NM_032415.4 F902F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr7:2984028 C>T maps to NM_032415.4 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:2951847 G>A maps to NM_032415.4 F1034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:2984151 G>A maps to NM_032415.4 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr7:2946279 G>A maps to NM_032415.4 Q1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr7:2978351 C>A maps to NM_032415.4 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr7:2968266 G>A maps to NM_032415.4 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:2978408 G>A maps to NM_032415.4 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr17:78176129 C>T maps to NM_024110.2 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr17:78179399 C>T maps to NM_024110.2 S880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:78157985 G>A maps to NM_024110.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr17:78172350 G>A maps to NM_024110.2 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr17:78172296 C>A maps to NM_024110.2 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:104915193 G>A maps to NM_001017534.1 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr5:40853593 T>C maps to NM_032587.3 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr5:40853768 C>T maps to NM_032587.3 R779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr5:40854523 G>A maps to NM_032587.3 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:40853489 A>C maps to NM_032587.3 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:40854208 A>G maps to NM_032587.3 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:40841498 T>C maps to NM_032587.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:48715152 T>C maps to NM_001184900.1 Q476Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:139265517 G>A maps to NM_052813.4 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr9:139265833 C>T maps to NM_052813.4 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:139259008 G>A maps to NM_052813.4 D479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:8949086 G>A maps to NM_014316.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr13:111290684 G>A maps to NM_018210.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr13:111287086 C>A maps to NM_018210.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr13:111290807 G>A maps to NM_018210.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:11027107 C>T maps to NM_199141.1 D291D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AZ-6598-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:3038491 G>T maps to NM_001014437.2 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr11:3069115 G>A maps to NM_001014437.2 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:3038347 G>C maps to NM_001014437.2 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr13:111329325 G>A maps to NM_024537.2 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:25307327 C>T maps to NM_018272.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:25297372 C>A maps to NM_018272.3 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:25297394 G>A maps to NM_018272.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr12:25297570 C>A maps to NM_018272.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:25308339 C>A maps to NM_018272.3 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:25297568 C>T maps to NM_018272.3 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:25297570 C>A maps to NM_018272.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr12:25300038 C>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:38320309 G>T maps to NM_007359.4 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:38318157 C>T maps to NM_007359.4 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:38318157 C>T maps to NM_007359.4 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:38319958 C>T maps to NM_007359.4 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:38323815 C>T maps to NM_007359.4 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:44673002 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:40915755 C>T maps to NM_170589.3 N1124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:40915234 G>T maps to NM_170589.3 E951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr15:40915332 C>A maps to NM_170589.3 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr15:40915332 C>T maps to NM_170589.3 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:40914738 G>A maps to NM_170589.3 E785E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr7:94166882 C>T maps to NM_022900.4 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:94164822 G>A maps to NM_022900.4 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr7:94167157 T>A maps to NM_022900.4 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:41485942 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:41437686 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:41437628 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:41428943 T>C did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:41530768 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:41598676 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:41413142 T>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:41428992 T>C did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr23:41604844 T>C did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:41446232 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:41446231 T>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:41604816 G>A did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:41604844 T>C did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:41604844 T>C did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:41437664 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:41446231 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:41393969 T>C did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:2236984 G>A maps to NM_020764.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:2237386 G>A maps to NM_020764.3 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:2236768 C>T maps to NM_020764.3 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr16:2236771 C>A maps to NM_020764.3 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:73500751 G>A maps to NM_020753.3 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:73499249 G>A maps to NM_020753.3 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr17:73501109 G>A maps to NM_020753.3 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:73499826 G>A maps to NM_020753.3 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr11:104899869 A>G maps to NM_033292.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:104900524 A>G maps to NM_033292.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:104901068 A>G maps to NM_033292.2 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr11:104899869 A>G maps to NM_033292.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:104897047 C>T maps to NM_033292.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:202073907 C>T maps to NM_032977.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:202060634 C>T maps to NM_032977.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:202073853 G>A maps to NM_032977.3 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:15164692 C>T maps to NM_012114.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr19:15166254 C>T maps to NM_012114.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:15166317 G>T maps to NM_012114.2 G200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:142991386 T>C maps to NM_032982.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr7:142988659 T>C maps to NM_032982.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr7:143000970 G>A maps to NM_032982.2 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:185553521 G>A maps to NM_032991.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:185550538 G>A maps to NM_032991.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:104825528 T>C maps to NM_001225.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:104820468 T>C maps to NM_001225.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr11:104819263 C>T maps to NM_001225.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:104820468 T>C maps to NM_001225.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:104825624 C>T maps to NM_001225.3 W37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr11:104820468 T>C maps to NM_001225.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:104820470 T>A maps to NM_001225.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr11:104820291 G>T maps to NM_001225.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:104874035 C>A maps to NM_001136112.1 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:104879558 C>T maps to NM_001136112.1 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr11:104868178 G>A maps to NM_001136112.1 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr11:104868181 G>A maps to NM_001136112.1 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr4:110618908 C>T maps to NM_001226.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:110615797 G>A maps to NM_001226.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:110612141 A>G maps to NM_001226.3 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:110610628 C>A maps to NM_001226.3 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr10:115489259 G>T maps to NM_033338.4 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:115489223 C>T maps to NM_033338.4 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr2:202131232 T>A maps to NM_001080125.1 Y67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:202149632 C>A maps to NM_001080125.1 Y358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:202150029 C>T maps to NM_001080125.1 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:202150029 C>T maps to NM_001080125.1 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:202150014 C>T maps to NM_001080125.1 Q486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:202131301 G>A maps to NM_001080125.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:202149879 G>T maps to NM_001080125.1 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:90576323 T>C maps to NM_012115.3 S1105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr6:90577907 T>G maps to NM_012115.3 A1633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:90573530 A>G maps to NM_012115.3 Q701Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:90573527 A>G maps to NM_012115.3 K700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:90572853 G>T maps to NM_012115.3 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:90564551 C>A maps to NM_012115.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:15844620 T>C maps to NM_001229.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:15844620 T>C maps to NM_001229.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr1:160164822 T>C maps to NM_001231.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:160171123 C>T maps to NM_001231.4 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:160165718 G>A maps to NM_001231.4 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:116245595 C>T maps to NM_001232.3 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:116280875 G>T maps to NM_001232.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:121980928 G>A maps to NM_001178065.1 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr3:121975939 T>C maps to NM_001178065.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr3:121980616 G>A maps to NM_001178065.1 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:122002807 C>T maps to NM_001178065.1 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:122003581 C>T maps to NM_001178065.1 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:122002573 C>T maps to NM_001178065.1 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:122003854 C>T maps to NM_001178065.1 C1028C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:121976179 C>T maps to NM_001178065.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:55012576 G>T maps to NM_020356.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:55012281 C>T maps to NM_020356.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:55027359 C>T maps to NM_020356.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr20:55027485 C>T maps to NM_020356.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:96011268 G>A maps to ENST00000508830 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:96082059 A>G maps to ENST00000508830 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:96075768 G>T maps to ENST00000508830 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:10706325 G>A maps to NM_001079843.1 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:10720465 C>T maps to NM_001079843.1 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:10715762 G>A maps to NM_001079843.1 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:10705132 G>A maps to NM_001079843.1 R1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:10720549 G>A maps to NM_001079843.1 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:10699571 C>T maps to NM_001079843.1 S1569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:10711059 G>A maps to NM_001079843.1 G918G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:10720567 G>A maps to NM_001079843.1 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:10713995 C>T maps to NM_001079843.1 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr1:10713764 T>C maps to NM_001079843.1 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:34489902 C>T maps to NM_001752.3 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:34477598 G>A maps to NM_001752.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr11:34482795 A>G did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:65793394 G>T maps to NM_053054.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:65792842 G>A maps to NM_053054.3 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:65792779 C>T maps to NM_053054.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:43931160 G>A maps to NM_172095.1 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr5:134332021 G>A maps to NM_178019.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:26517890 C>T maps to NM_198137.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:26527937 T>C maps to NM_198137.1 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:26527919 G>T maps to NM_198137.1 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:26524450 G>A maps to NM_198137.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:92159770 T>C maps to NM_024764.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:92174487 G>A maps to NM_024764.2 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr14:92159770 T>C maps to NM_024764.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr14:92159770 T>C maps to NM_024764.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr19:38861335 T>C maps to NM_021185.4 S1128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:38858774 C>T maps to NM_021185.4 I1006I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:38847169 C>T maps to NM_021185.4 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:38855699 G>T did not map to a codon.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr19:38861335 T>C maps to NM_021185.4 S1128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr19:38861335 T>C maps to NM_021185.4 S1128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr3:8787330 G>A maps to NM_001234.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:8775600 C>T maps to NM_001234.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:74311057 T>G maps to NM_006077.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:74183120 G>A maps to NM_006077.3 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:32224503 G>A maps to NM_005093.3 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:32211087 G>A maps to NM_005093.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:88943566 G>T maps to NM_005187.5 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:88951541 G>A maps to NM_005187.5 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr11:119169220 G>A maps to NM_005188.2 W802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:119145630 T>G maps to NM_005188.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:119155972 G>A maps to NM_005188.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:119149290 G>A maps to NM_005188.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr11:119148907 C>T maps to NM_005188.2 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr11:119148880 A>G maps to NM_005188.2 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:119148967 T>C maps to NM_005188.2 C396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr11:119145654 A>G maps to NM_005188.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:119148907 C>T maps to NM_005188.2 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:119148878 C>T maps to NM_005188.2 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr11:119148907 C>T maps to NM_005188.2 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:119149242 T>C maps to NM_005188.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:119149249 C>T maps to NM_005188.2 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:119148874 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:119148922 T>C maps to NM_005188.2 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr11:119149236 C>A maps to NM_005188.2 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr11:119149217 A>G did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr11:119149242 T>C maps to NM_005188.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr3:105389106 G>A maps to NM_170662.3 Q887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr3:105438962 C>T maps to NM_170662.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr7:107394413 T>C maps to NM_024814.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:107398981 C>T maps to NM_024814.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:107393853 A>G did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:49314896 C>T maps to NM_004352.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr18:70209179 C>T maps to NM_182511.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr20:54579011 G>A maps to NM_080617.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:54573711 T>A maps to NM_080617.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr21:37443323 C>T maps to NM_001757.2 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:37510213 G>A maps to NM_001236.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:169931099 G>A maps to NM_032783.4 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr21:44485349 G>A maps to ENST00000398168 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr9:178927 A>G maps to NM_018491.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:77758699 C>T maps to NM_005189.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:77757682 C>T maps to NM_005189.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:77808540 G>A maps to NM_003655.2 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:77808624 G>A maps to NM_003655.2 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:54645899 C>T maps to NM_012117.2 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:39262279 G>A maps to NM_014292.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:39262258 T>C maps to NM_014292.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:39529988 G>T maps to NM_175709.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr22:39530448 C>T maps to NM_175709.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr17:77768526 C>T maps to NM_020649.2 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:77770737 G>A maps to NM_020649.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr17:77768946 G>A maps to NM_020649.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:14024359 G>A maps to NM_017721.4 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:14034582 G>A maps to NM_017721.4 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:14031455 G>A maps to NM_017721.4 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr19:14040411 C>A maps to NM_017721.4 I883I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:52825481 C>T maps to NM_032449.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:52822075 G>A maps to NM_032449.2 G645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:52824767 G>A maps to NM_032449.2 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr1:52822108 G>A maps to NM_032449.2 C634C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:52819262 C>A maps to NM_032449.2 R835R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr4:15575829 C>T maps to NM_001080522.2 R1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:15552444 A>G did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:15517557 C>T maps to NM_001080522.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:15556720 C>A maps to NM_001080522.2 S838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:15504476 C>T maps to NM_001080522.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr10:97772449 T>A maps to NM_001159747.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr10:97791677 A>G maps to NM_001159747.1 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr10:70502275 A>G maps to NM_018237.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:70496663 T>C maps to NM_018237.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:70509296 G>T maps to NM_018237.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr10:70516083 T>C maps to NM_018237.2 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:70509017 C>T maps to NM_018237.2 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:70502218 C>T maps to NM_018237.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:70515218 C>A maps to NM_018237.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr10:70515218 C>T maps to NM_018237.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr10:70502275 A>G maps to NM_018237.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr10:70514548 C>A maps to NM_018237.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr10:70525700 T>C maps to NM_018237.2 Y721Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr10:70547778 T>C maps to NM_018237.2 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr10:70515218 C>A maps to NM_018237.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr18:57122148 T>A maps to NM_133459.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:57147460 G>A maps to NM_133459.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr18:57115281 G>A maps to NM_133459.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:131597817 G>A maps to NM_004059.4 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:89427771 T>C maps to NM_001008661.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr1:89454015 C>T maps to NM_001008661.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:89430625 C>T maps to NM_001008661.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:89427134 C>A maps to NM_001008661.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:42906440 T>A maps to NM_001296.4 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:42906467 G>T maps to NM_001296.4 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:42906980 C>T maps to NM_001296.4 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:28596244 G>A maps to NM_138414.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:28601969 C>T maps to NM_138414.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:28601969 C>T maps to NM_138414.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:66504396 G>T maps to NM_024781.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr18:66564526 A>G maps to NM_024781.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:55750886 G>T maps to ENST00000339012 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr19:15132724 C>T maps to NM_173482.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:15121858 C>T maps to NM_173482.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr19:15121741 G>A maps to NM_173482.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:56162775 C>T maps to NM_013301.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr19:56162760 G>A maps to NM_013301.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:35660865 G>A maps to NM_174923.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:219870795 G>A maps to NM_194302.2 T1623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:219870809 G>A maps to NM_194302.2 R1619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:219894723 G>A maps to NM_194302.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:219890818 C>T maps to NM_194302.2 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr2:219888961 G>A maps to NM_194302.2 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:219888027 C>T maps to NM_194302.2 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:219892614 G>A maps to NM_194302.2 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:219875670 G>C maps to NM_194302.2 V1335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:219888910 C>T maps to NM_194302.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:219869032 A>G maps to NM_194302.2 P1732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:219892422 A>G maps to NM_194302.2 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:219894846 G>A maps to NM_194302.2 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:219886916 G>A maps to NM_194302.2 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:219878726 C>T maps to NM_194302.2 E1214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:219886562 G>T maps to NM_194302.2 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:110581504 A>G maps to NM_017918.4 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:110608687 A>G maps to NM_017918.4 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr4:110581397 T>C maps to NM_017918.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:110606480 T>C maps to NM_017918.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:47777954 C>A maps to NM_145020.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr18:47788427 G>A maps to NM_145020.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr18:47753870 T>C maps to NM_145020.3 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:186379984 C>A maps to NM_152775.3 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:186380032 C>A maps to NM_152775.3 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:185603464 A>G maps to NM_152683.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:185593504 G>A maps to NM_152683.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:185578446 T>C maps to NM_152683.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:114607023 C>T maps to NM_001040440.2 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:114607065 C>T maps to NM_001040440.2 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr5:114620569 A>G maps to NM_001040440.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:114604649 G>A maps to NM_001040440.2 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:114610926 C>A maps to NM_001040440.2 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr19:48800352 G>A maps to NM_144577.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:21990947 G>T maps to NM_152612.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr22:21988735 C>T maps to NM_152612.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr22:21988735 C>T maps to NM_152612.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr22:21988744 G>T maps to NM_152612.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:48920009 G>A did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr23:48924962 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:48924952 C>T did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:48925559 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:48925389 T>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:48924814 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:48925608 G>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:48925014 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:48924773 G>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:27850587 G>A maps to ENST00000435516 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:27851564 T>C maps to ENST00000435516 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr13:44433921 T>C maps to NM_144974.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:33422435 C>A maps to NM_032816.3 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:33457327 C>T maps to NM_032816.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr19:33450806 G>T maps to NM_032816.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:33392242 C>T maps to NM_032816.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:18047300 G>A maps to NM_001136203.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr19:18053491 C>T maps to NM_001136203.1 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:68588153 G>A maps to NM_176816.3 Y320Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr7:23682718 G>A maps to NM_138771.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr7:23682717 C>A maps to NM_138771.3 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:205864 T>C maps to NM_145265.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:206074 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:31594470 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:31683137 G>A maps to NM_194300.2 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr3:42794098 G>A maps to NM_144719.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:42774996 T>A maps to NM_144719.3 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:42781242 G>A maps to NM_144719.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:42787465 C>T maps to NM_144719.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:13869814 C>T maps to NM_030818.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:13869998 G>A maps to NM_030818.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:92940555 T>C maps to NM_017667.2 N609N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:92979197 C>T maps to NM_017667.2 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr22:42206209 G>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:57762411 G>A maps to NM_032269.5 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:57732055 G>A maps to NM_032269.5 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:57736005 G>A maps to NM_032269.5 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr7:128450320 C>T maps to NM_022742.3 H643H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:128441525 C>T maps to NM_022742.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr7:128455930 T>C maps to NM_022742.3 S1103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:128455930 T>C maps to NM_022742.3 S1103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:128434778 C>T maps to NM_022742.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr17:79639682 C>T maps to NM_199287.2 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr17:79638833 G>A maps to NM_199287.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:123634200 C>A maps to NM_022757.4 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:123667597 T>C maps to NM_022757.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:123649958 C>A maps to NM_022757.4 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:179714814 T>C maps to NM_173648.3 E1106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:179702332 C>A maps to NM_173648.3 E1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:179718204 C>T maps to NM_173648.3 R1069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:179701634 C>T maps to NM_173648.3 E1437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr2:179732788 G>T maps to NM_173648.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:179742792 G>T maps to NM_173648.3 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:74708663 T>A maps to ENST00000393965 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr17:16665022 C>T maps to NM_014695.1 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:16612918 G>A maps to NM_014695.1 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr17:16610837 C>A maps to NM_014695.1 C240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:18513520 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:20799141 G>A maps to NM_001004306.1 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr17:20769978 G>A maps to NM_001004306.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:20799102 G>A maps to NM_001004306.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:76866331 T>C maps to NM_020879.2 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:76891534 C>T maps to NM_020879.2 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:76916212 C>T maps to NM_020879.2 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:76908092 G>T maps to NM_020879.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:76916158 C>T maps to NM_020879.2 F731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:76889448 T>C maps to NM_020879.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:106130664 G>T maps to NM_001008723.1 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:106160517 G>A maps to NM_001008723.1 K632K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:106209948 G>T maps to NM_001008723.1 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:106121857 G>T maps to NM_001008723.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:106130712 G>T maps to NM_001008723.1 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:159166001 G>A maps to NM_138803.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:159170267 C>T maps to NM_138803.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:159166106 C>T maps to NM_138803.3 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:159028731 G>A maps to NM_138803.3 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:159170267 C>T maps to NM_138803.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:159035453 C>T maps to NM_138803.3 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:24914474 G>A maps to NM_001130726.2 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr4:24839843 G>A maps to NM_001130726.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:24854798 A>G maps to NM_001130726.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:124857225 G>A maps to NM_025004.2 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:124908477 C>T maps to NM_025004.2 Q855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr11:124847417 A>G maps to NM_025004.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:197530301 A>G maps to NM_001080539.1 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:197523585 T>C did not map to a codon.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr2:197583288 G>A maps to NM_001080539.1 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:197586247 T>C maps to NM_001080539.1 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr2:197597229 A>T maps to NM_001080539.1 K1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:197590777 C>T maps to NM_001080539.1 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:197521395 C>T maps to NM_001080539.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:11534587 G>T maps to NM_145045.4 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:49901373 C>A maps to NM_144688.4 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr19:49920715 T>C maps to NM_144688.4 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:77288484 C>A maps to NM_001042784.1 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr4:77288485 T>C maps to NM_001042784.1 K597K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:77274391 C>A maps to NM_001042784.1 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:77272146 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:11464143 G>A maps to ENST00000427879 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:11464488 G>A maps to ENST00000427879 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:133379643 G>A did not map to a codon.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr23:133379410 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:133379295 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:133379358 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:133379613 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:133379049 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:133379030 T>C did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:133378981 C>A did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:133379030 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:93649648 C>T maps to NM_206886.2 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:93711662 G>T maps to NM_206886.2 E1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:93680444 T>C maps to NM_206886.2 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:93724429 T>G maps to NM_206886.2 A1342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:93712458 T>G maps to NM_206886.2 L1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:93676447 C>A maps to NM_206886.2 C551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:159856409 C>A maps to NM_012337.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:159860276 C>A maps to NM_012337.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:26584708 C>T maps to NM_022778.2 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:26597577 C>T maps to NM_022778.2 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:49105106 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:49103344 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:49105373 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:49098487 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:49099413 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:49099791 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:49103249 A>C did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:49099827 C>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:44461627 C>A maps to NM_152499.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:27614246 G>A maps to NM_018246.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:27614246 G>A maps to NM_018246.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:3680345 G>A maps to NM_152492.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:3670735 C>T maps to NM_152492.2 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:139106368 G>T maps to NM_015439.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:139109508 G>T maps to NM_015439.2 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:13043342 C>T maps to NM_031455.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:13043213 G>T maps to NM_031455.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:43119674 A>G maps to NM_001080850.2 E776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:43011223 C>T maps to NM_001080850.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:43110442 C>T maps to NM_001080850.2 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr15:74573039 G>A maps to ENST00000321288 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr15:74627473 A>T maps to NM_182791.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:74573039 G>A maps to ENST00000321288 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr15:74559106 C>G maps to ENST00000321288 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr15:74625572 G>A maps to ENST00000321288 G853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr11:27362983 T>C maps to NM_030771.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:27379048 T>C maps to NM_030771.1 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:49294517 C>T maps to NM_178173.3 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:49294666 T>C maps to NM_178173.3 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr3:126138985 G>A maps to ENST00000505024 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:126137503 G>A maps to ENST00000505024 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:126152013 C>A maps to ENST00000505024 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:126135211 G>A maps to ENST00000505024 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:126139054 C>T maps to ENST00000505024 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:96275316 G>A maps to NM_182496.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr12:96312692 G>C maps to NM_182496.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:180364956 C>T maps to NM_181426.1 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:180334726 C>A maps to NM_181426.1 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:180372702 T>C maps to NM_181426.1 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:180332708 T>G maps to NM_181426.1 *942Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:180359963 A>C maps to NM_181426.1 L564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:180372578 C>A maps to NM_181426.1 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr3:180361952 G>A maps to NM_181426.1 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:180359821 C>T maps to NM_181426.1 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:180370055 T>C did not map to a codon.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr17:78013678 G>A maps to NM_017950.2 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr17:78058654 C>T maps to NM_017950.2 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr17:78061472 C>T maps to NM_017950.2 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr17:78055491 C>T maps to NM_017950.2 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:94763805 C>A maps to NM_001042399.1 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:94805516 C>A maps to NM_001042399.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:94796989 C>A maps to NM_001042399.1 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:94702609 T>C maps to NM_001042399.1 E695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:8647875 G>A maps to NM_144681.2 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr17:62518976 C>T maps to NM_138363.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:62529285 G>T maps to NM_138363.1 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:62532800 C>T maps to NM_138363.1 R718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:64173133 C>T maps to NM_145036.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr17:63848090 G>C maps to NM_145036.3 S742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:128757672 G>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:128720830 C>T maps to NM_024768.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr3:191107299 C>A maps to NM_178335.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:191093121 G>A maps to NM_178335.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:191098621 C>T maps to NM_178335.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:113225395 C>T maps to NM_144718.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:113187027 C>T maps to NM_144718.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:113187237 C>T maps to NM_144718.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:113225395 C>T maps to NM_144718.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:113187110 C>A maps to NM_144718.3 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr3:107096886 G>A maps to NM_032600.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:107097378 C>T maps to NM_032600.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:107096857 G>T maps to NM_032600.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:107096814 C>T maps to NM_032600.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:28511926 G>A maps to NM_032141.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr17:28443879 C>T maps to NM_032141.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr17:80136986 C>T maps to ENST00000445854 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:80159457 C>T maps to ENST00000445854 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:80115635 G>T maps to ENST00000445854 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:122087020 A>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:61574410 G>A maps to ENST00000395341 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:61566687 G>A maps to ENST00000395341 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:61552773 C>T maps to ENST00000395341 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr10:61574417 A>G maps to ENST00000395341 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:61552751 G>A maps to ENST00000395341 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:119978424 C>T maps to NM_178499.3 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr12:119943007 G>A maps to NM_178499.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr12:119916994 C>T maps to NM_178499.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:46521624 C>T maps to NM_001080402.1 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr12:123276579 A>G maps to NM_201435.3 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:123285841 C>T maps to NM_201435.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr12:123281893 G>A maps to NM_201435.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr12:123265709 G>C did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr12:123262202 C>T maps to NM_201435.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:111317804 C>T maps to NM_152591.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:111345219 C>T maps to NM_152591.1 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:120436389 C>T maps to NM_207311.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr16:3085380 T>C maps to NM_001103175.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:3085305 G>A maps to NM_001103175.1 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:49314774 G>A maps to NM_033124.4 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:49312572 C>T maps to NM_033124.4 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:49298127 G>A maps to NM_033124.4 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr12:49315216 A>G maps to NM_033124.4 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr12:49315216 A>G maps to NM_033124.4 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:56653470 C>T maps to NM_001141947.1 R851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:56650073 G>A maps to NM_001141947.1 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr11:93118641 C>T maps to NM_181645.3 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr18:52604155 G>A maps to NM_025214.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr5:150581210 G>T maps to NM_015621.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr5:150585024 T>C maps to NM_015621.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr5:150581210 G>T maps to NM_015621.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:150585024 T>C maps to NM_015621.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr10:32760002 T>C maps to NM_001026383.1 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:32636380 C>A maps to NM_001008391.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:32635418 C>T maps to NM_001008391.2 E815E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:32635616 A>G maps to NM_001008391.2 C749C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:32657297 C>A maps to NM_001008391.2 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr11:32636147 G>A maps to NM_001008391.2 N572N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:32657369 C>A maps to NM_001008391.2 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr11:32636228 T>A maps to NM_001008391.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:132288158 C>A maps to NM_138770.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr2:132288266 G>A maps to NM_138770.1 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:132289255 C>T maps to NM_138770.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:132285710 C>T maps to NM_138770.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr2:132289303 G>A maps to NM_138770.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr2:130899763 A>G maps to NM_207310.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:37321337 C>T maps to ENST00000379187 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:37317839 A>G maps to ENST00000379187 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:541059 G>A maps to NM_032358.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:542407 C>T maps to NM_032358.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr12:549793 T>C maps to NM_032358.3 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr19:46915158 T>C maps to NM_032040.3 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:112357828 G>A maps to ENST00000447230 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:112324500 G>A maps to ENST00000447230 D883D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:112326061 C>A maps to ENST00000447230 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr3:112356985 A>T maps to ENST00000447230 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:112356985 A>T maps to ENST00000447230 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:112356985 A>T maps to ENST00000447230 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:112348975 G>A maps to ENST00000447230 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr3:112349026 T>C maps to ENST00000447230 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr3:112349026 T>C maps to ENST00000447230 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:86123433 C>A maps to NM_001156474.1 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:86111816 T>C maps to NM_001156474.1 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:86111768 C>A maps to NM_001156474.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:86106446 G>A maps to NM_001156474.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:96117758 A>G maps to NM_024725.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:118882963 G>A maps to NM_198489.1 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr11:118886092 A>G maps to NM_198489.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr11:118886092 A>G maps to NM_198489.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:56599592 C>T maps to NM_001080433.1 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr2:56599585 A>G maps to NM_001080433.1 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:66358683 G>T maps to NM_018219.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:66359586 C>T maps to NM_018219.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:66358883 C>A maps to NM_018219.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:66358341 A>G maps to NM_018219.2 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:66358899 T>C maps to NM_018219.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:55549731 G>A maps to ENST00000436346 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr2:55589524 C>T maps to ENST00000436346 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr2:55562080 G>A maps to ENST00000436346 R626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:55561837 G>A maps to ENST00000436346 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:55522973 C>T maps to ENST00000436346 A1770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:55523591 G>A maps to ENST00000436346 D1631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:55576662 C>T maps to ENST00000436346 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr2:55646037 T>C maps to ENST00000436346 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr2:55555468 G>C maps to ENST00000436346 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr2:55570787 G>A maps to ENST00000436346 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:64108098 G>A maps to NM_032251.5 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:91805659 G>A maps to NM_001080414.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:91776285 C>T maps to NM_001080414.2 E927E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr14:91780017 C>T maps to NM_001080414.2 E714E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:91809954 G>A maps to NM_001080414.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:91770292 G>A maps to NM_001080414.2 S1129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:91770133 C>T maps to NM_001080414.2 S1182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr14:91760647 G>A maps to NM_001080414.2 L1327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr14:91806305 C>T maps to NM_001080414.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:85396651 C>T maps to NM_152723.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:13800602 G>A maps to NM_001031713.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:82996952 T>C maps to NM_021825.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:28515375 A>G maps to NM_018318.3 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:28702031 T>C maps to NM_018318.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr12:28459748 A>G maps to NM_018318.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr12:124428825 G>A maps to NM_025140.1 Y9Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:124421928 G>A maps to NM_025140.1 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:124422024 C>T maps to NM_025140.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:118705740 T>C maps to NM_019044.4 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:118706916 C>A maps to NM_019044.4 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:4262095 C>T maps to NM_018074.4 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:7043264 G>A maps to NM_153376.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:41825581 C>T maps to NM_052848.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr19:41826357 C>T maps to NM_052848.1 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:169025559 T>C maps to NM_017785.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr5:169021195 G>A maps to NM_017785.4 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr5:169015464 G>A maps to NM_017785.4 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:169025523 T>C maps to NM_017785.4 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:169026060 C>T maps to NM_017785.4 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr5:169025559 T>C maps to NM_017785.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:169018167 G>A maps to NM_017785.4 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:169025979 G>T maps to NM_017785.4 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr5:169025559 T>C maps to NM_017785.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr5:169025559 T>C maps to NM_017785.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:31110869 C>T maps to NM_001105564.1 Q787Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr6:31113030 C>T maps to NM_001105564.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr9:36170095 C>T maps to NM_005893.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:42305020 C>T maps to NM_000729.4 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:42305098 G>A maps to NM_000729.4 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:42299700 G>A maps to NM_000729.4 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:26483328 G>A maps to NM_000730.2 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:26490891 G>A maps to NM_000730.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr4:26483454 G>A maps to NM_000730.2 C364C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:6292724 G>A maps to NM_176875.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr11:6291977 C>T maps to NM_176875.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:6292298 C>T maps to NM_176875.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr11:6291426 G>A maps to NM_176875.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:6291429 T>G maps to NM_176875.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:6281298 C>T maps to NM_176875.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:6281293 G>T maps to NM_176875.2 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:6281197 G>T maps to NM_176875.2 G14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:6292763 C>A maps to NM_176875.2 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr11:6292310 C>T maps to NM_176875.2 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr11:6291977 C>T maps to NM_176875.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:6291977 C>T maps to NM_176875.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:34313606 G>A maps to NM_032962.4 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:34325338 G>A maps to NM_032965.4 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr17:34324847 C>A maps to NM_032965.4 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:32583758 C>T maps to NM_002982.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:34709817 G>A maps to NM_002989.2 Y48Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr9:34710048 C>T maps to NM_002989.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:34340328 G>A maps to NM_005064.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr9:34662564 T>C maps to NM_006664.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:34416545 G>A maps to NM_002983.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:34431360 G>A maps to NM_002984.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:34432644 C>T maps to NM_002984.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:34205638 G>T maps to NM_002985.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr17:32597314 A>G maps to ENST00000378569 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:32598769 C>T maps to ENST00000378569 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:32598724 C>A maps to ENST00000378569 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:32647366 A>G maps to ENST00000394620 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr7:45109492 C>T maps to NM_001029835.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr7:45108054 G>T maps to NM_001029835.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr13:37007319 C>T maps to NM_003914.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:37012298 G>T maps to NM_003914.3 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr13:37011833 C>T maps to NM_003914.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr13:37016312 A>G maps to NM_003914.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr13:37011974 C>T maps to NM_003914.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:37006865 G>A maps to NM_003914.3 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr4:122742217 A>G maps to NM_001237.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr14:20781753 A>G maps to NM_182849.1 N168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr14:20784442 C>T maps to NM_182849.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:50051683 T>C did not map to a codon.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr23:50053285 C>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:50051684 C>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:50053800 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:50094336 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:50053058 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:50053872 C>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:50052958 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:50051688 A>C did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:50053781 G>A did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:50053207 T>C did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:50051529 G>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:50052250 C>T did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:50052528 C>T did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:50053207 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:50053207 T>C did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:50053543 C>T did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:50089776 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:69457998 G>A maps to NM_053056.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:69465978 G>T maps to NM_053056.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr12:4409172 T>C maps to NM_001759.3 *290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:4398035 G>A maps to NM_001759.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:4385253 T>G maps to NM_001759.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr15:43482280 C>T maps to NM_012142.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr15:43484939 G>C did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr19:30308147 G>T maps to NM_001238.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr19:30314638 G>A maps to NM_001238.1 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr19:30308145 C>A maps to NM_001238.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:95895099 T>C maps to NM_057749.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:2495546 C>A maps to NM_001761.2 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:2498891 C>T maps to NM_001761.2 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:2493717 C>T maps to NM_001761.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:2503472 G>A maps to NM_001761.2 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr5:162869133 T>C maps to NM_199246.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr5:162869133 T>C maps to NM_199246.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:78085512 T>C maps to NM_004354.2 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr4:78085512 T>C maps to NM_004354.2 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr5:86708550 T>A maps to NM_001239.3 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:86708506 C>A maps to NM_001239.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:86697546 G>A maps to NM_001239.3 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:86700746 C>T maps to NM_001239.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:97816929 G>A maps to NM_001134375.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:159680456 G>A maps to NM_024565.5 C412C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:156867376 T>A maps to NM_020307.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:156870926 G>A maps to NM_020307.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:49087780 G>A maps to NM_001240.2 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:49087825 C>A maps to NM_001240.2 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:49093618 A>G maps to NM_001240.2 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr12:49087469 C>T maps to NM_001240.2 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:49086998 G>T maps to NM_001240.2 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:135712172 C>T maps to NM_058241.2 F716F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:135711656 G>A maps to NM_058241.2 K544K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:135694521 C>T maps to NM_058241.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:135676435 C>T maps to NM_058241.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:135710963 A>G maps to NM_058241.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:135711863 C>T maps to NM_058241.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:135711536 A>G maps to NM_058241.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr2:135711083 A>G maps to NM_058241.2 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr10:35772404 C>T maps to NM_145012.4 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:208576667 G>A maps to ENST00000295414 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:55652509 A>G maps to ENST00000442196 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:55670509 G>A maps to ENST00000442196 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:55670541 C>A maps to ENST00000442196 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:55677899 C>A maps to ENST00000442196 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr3:46245693 C>T maps to NM_001295.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:46244751 G>T maps to NM_001295.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:46245447 G>A maps to NM_001295.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:46399425 C>T maps to NM_001123041.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr3:46399833 C>T maps to NM_001123041.2 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:46399209 C>T maps to NM_001123041.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:46399383 C>T maps to NM_001123041.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:46399938 C>T maps to NM_001123041.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:46307158 C>A maps to NM_178328.1 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:46306816 G>T maps to NM_178328.1 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr3:32995414 C>T maps to NM_005508.4 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:32994925 G>T maps to NM_005508.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:38711920 G>A maps to NM_001838.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:38711920 G>A maps to NM_001838.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:38715177 G>A maps to NM_001838.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:39374871 C>T maps to NM_005201.3 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr3:39374454 C>T maps to NM_005201.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:39373941 C>A maps to NM_005201.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:45943347 G>A maps to NM_031200.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:45943176 C>T maps to NM_031200.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr3:45942891 C>T maps to NM_031200.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:45942447 G>A maps to NM_031200.2 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:45943176 C>T maps to NM_031200.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:45943248 A>G maps to NM_031200.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:45943248 A>G maps to NM_031200.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr3:45943248 A>G maps to NM_031200.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr3:45943248 A>G maps to NM_031200.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:45943062 C>A maps to NM_031200.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:45943248 A>G maps to NM_031200.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr3:132319405 A>G maps to NM_178445.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr3:46449635 C>T maps to NM_001130910.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:46449866 C>T maps to NM_001130910.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:46449635 C>T maps to NM_001130910.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:46449635 C>T maps to NM_001130910.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:139964270 C>T maps to NM_012118.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:139965943 G>A maps to NM_012118.2 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:139966174 C>T maps to NM_012118.2 C281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr4:139964381 G>A maps to NM_012118.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:66373205 C>T maps to NM_005125.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:66373238 C>T maps to NM_005125.1 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr12:69991050 C>T maps to NM_006431.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:156281894 A>G maps to NM_005998.4 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:62100429 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:62115528 A>T maps to NM_006430.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:62106066 T>C maps to NM_006430.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:62099657 C>A maps to NM_006430.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:62110659 T>C maps to NM_006430.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:10262621 C>T maps to NM_012073.3 H403H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:10262705 G>A maps to NM_012073.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:56126353 C>T maps to NM_001762.3 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:73471734 G>A maps to NM_006429.3 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:73477029 G>A maps to NM_006429.3 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr2:73479987 G>A maps to NM_006429.3 *544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr21:30434481 G>A maps to NM_006585.2 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:30441791 C>T maps to NM_006585.2 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:30437423 G>A maps to NM_006585.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:17072246 G>T maps to NM_014406.4 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr22:17072855 G>A maps to NM_014406.4 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:17072753 A>G maps to NM_014406.4 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:17071898 G>A maps to NM_014406.4 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:17072194 C>A maps to NM_014406.4 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr22:17073005 G>T maps to NM_014406.4 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr1:117560814 G>A maps to NM_004258.3 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:117561168 C>T maps to NM_004258.3 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr1:117559853 C>T maps to NM_004258.3 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:117554413 C>T maps to NM_004258.3 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:117568317 G>A maps to NM_004258.3 E872E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:117559724 C>T maps to NM_004258.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr6:74498306 C>T maps to NM_133493.3 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:74516620 T>C maps to NM_133493.3 I1005I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:74472469 G>T maps to NM_133493.3 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:74517807 T>C maps to NM_133493.3 P1064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr6:74407173 G>T maps to NM_133493.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr6:74517957 A>G maps to NM_133493.3 R1114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:74475864 G>A maps to NM_133493.3 E440E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:74493489 T>C maps to NM_133493.3 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr6:74517957 A>G maps to NM_133493.3 R1114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:74524807 A>G maps to NM_133493.3 K1291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:74475744 G>A maps to NM_133493.3 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr6:74517951 T>C maps to NM_133493.3 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:74520782 C>T maps to NM_133493.3 I1205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:74516624 C>T maps to NM_133493.3 Q1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:7649547 G>A maps to NM_004244.4 N320N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:7654008 G>A maps to NM_004244.4 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr12:7651518 T>C maps to NM_004244.4 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:7649628 G>A maps to NM_004244.4 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr12:7639544 C>T maps to NM_004244.4 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:7649458 C>T maps to NM_004244.4 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:7649571 G>A maps to NM_004244.4 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr12:7640084 T>C maps to NM_004244.4 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:7559257 T>C maps to ENST00000416109 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr12:7556227 A>G maps to ENST00000416109 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr12:7528470 G>A maps to ENST00000416109 N847N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:7551109 G>A maps to ENST00000416109 Y503Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:7556299 C>T maps to ENST00000416109 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:7520764 G>T maps to ENST00000416109 I1377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:7527951 G>A maps to ENST00000416109 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr12:7527242 G>A maps to ENST00000416109 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:7531631 T>C maps to ENST00000416109 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr12:7531631 T>C maps to ENST00000416109 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:7548910 G>A maps to ENST00000416109 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:7559281 G>A maps to ENST00000416109 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:7527320 G>A maps to ENST00000416109 D1052D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:7521951 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:7586045 A>G maps to ENST00000416109 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr12:7586045 A>G maps to ENST00000416109 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:7526066 G>A maps to ENST00000416109 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr12:7586045 A>G maps to ENST00000416109 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr12:7527904 A>G maps to ENST00000416109 H1001H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:7586045 A>G maps to ENST00000416109 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:66492382 A>G maps to NM_005582.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr5:66480367 A>G maps to NM_005582.2 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:66478804 C>T maps to NM_005582.2 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:66479671 G>A maps to NM_005582.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr5:66478890 C>A maps to NM_005582.2 E594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:66479776 G>T maps to NM_005582.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr5:66480367 A>G maps to NM_005582.2 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr5:66480367 A>G maps to NM_005582.2 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:28944256 G>A maps to NM_001178098.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:28944304 C>T maps to NM_001178098.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:158224910 C>A maps to NM_001763.2 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr1:158298757 A>G maps to NM_001764.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr1:158298757 A>G maps to NM_001764.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr1:158299825 G>A maps to NM_001764.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:158299819 A>G maps to NM_001764.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr1:158298757 A>G maps to NM_001764.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:158259877 G>A maps to NM_001765.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:158260951 C>A maps to NM_001765.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:158259913 C>T maps to NM_001765.2 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:158263263 T>C maps to NM_001765.2 *334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:158151326 G>A maps to NM_001766.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr1:158151447 C>A maps to NM_001766.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:158152004 G>A maps to NM_001766.3 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:158323828 T>C maps to NM_030893.3 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:117307142 T>C maps to NM_001767.3 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:117307142 T>C maps to NM_001767.3 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:112063893 C>A maps to NM_001004196.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:112648124 G>A maps to NM_138806.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:112647834 C>T maps to NM_138806.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:112648322 T>A maps to NM_138806.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr3:112648322 T>C maps to NM_138806.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:112666766 C>T maps to NM_138806.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr3:112546238 A>G maps to NM_001008784.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr3:112546319 C>T maps to NM_001008784.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:112546238 A>G maps to NM_001008784.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr3:112546238 A>G maps to NM_001008784.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr3:112546238 A>G maps to NM_001008784.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr3:112546238 A>G maps to NM_001008784.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:7809880 G>A maps to NM_021155.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:7808053 A>G maps to NM_021155.3 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:7810923 C>T maps to NM_021155.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:7809009 G>A maps to NM_021155.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:7809880 G>A maps to NM_021155.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr19:35831955 C>T maps to NM_001771.3 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr19:35837104 G>A maps to NM_001771.3 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:35831925 G>A maps to NM_001771.3 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:35836615 C>T maps to NM_001771.3 R774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:35831955 C>T maps to NM_001771.3 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr19:35837098 T>C maps to NM_001771.3 D791D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:35827011 G>A maps to NM_001771.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr19:35828898 G>A maps to NM_001771.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:35827143 C>T maps to NM_001771.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:67563230 C>A maps to NM_006566.2 G145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr18:67562982 G>A maps to NM_006566.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:67563138 G>T maps to NM_006566.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:67614625 A>C maps to NM_006566.2 L6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr18:67563012 C>T maps to NM_006566.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr18:67563117 G>A maps to NM_006566.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:160801145 A>G maps to NM_001166663.1 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr11:66083295 C>T maps to NM_020404.2 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:66082722 C>T maps to NM_020404.2 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:66082431 C>A maps to NM_020404.2 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:66083685 G>A maps to NM_020404.2 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:6559465 G>A maps to NM_001242.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr12:6559345 C>T maps to NM_001242.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:5466800 C>A maps to NM_014143.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:5457398 C>T maps to NM_014143.3 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:5457127 C>T maps to NM_014143.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:73996000 A>G maps to NM_001024736.1 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr15:73996758 C>T maps to NM_001024736.1 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:204591380 G>A maps to NM_006139.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:204599616 C>T maps to NM_006139.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:204599610 C>T maps to NM_006139.2 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:47544820 A>C maps to NM_012120.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:47471131 G>T maps to NM_012120.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr17:72540957 G>A maps to NM_006678.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:72539058 G>T maps to NM_006678.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr17:72613563 A>C maps to ENST00000426295 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr17:72613407 T>C maps to ENST00000426295 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:72522106 G>A maps to NM_174892.2 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:72694550 G>A maps to ENST00000412086 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:72699193 G>A maps to ENST00000412086 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:160628499 T>A maps to NM_001198759.1 A1828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:8369996 G>A maps to NM_016579.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:51728379 G>A maps to NM_001772.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:51738478 C>T maps to NM_001772.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:208062048 C>T maps to NM_001025109.1 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:208062547 G>A maps to NM_001025109.1 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr1:208072345 G>T maps to NM_001025109.1 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:208062048 C>T maps to NM_001025109.1 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:208062879 T>G maps to NM_001025109.1 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:208061148 G>A maps to NM_001025109.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr7:80303417 T>C maps to NM_001127444.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:80276131 C>T maps to NM_001127444.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:80303447 G>A maps to NM_001127444.1 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr7:80300424 T>A maps to NM_001127444.1 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:49841983 C>T maps to NM_001774.2 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:49838987 C>A maps to NM_001774.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:49842066 G>A maps to NM_001774.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:15780174 G>A maps to NM_001775.2 W46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:15780117 C>T maps to NM_001775.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:118209929 G>A maps to NM_000732.4 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:118210568 G>T maps to NM_000732.4 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr11:118186220 G>A maps to NM_000733.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:118183552 G>A maps to NM_000733.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:118220489 G>T maps to NM_000073.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:6909587 C>T maps to NM_000616.4 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:6927641 C>T maps to NM_000616.4 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr20:44751264 C>A maps to NM_001250.4 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr23:135741419 C>A did not map to a codon.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr23:135730557 G>C did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:135732493 G>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:135741494 C>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:135741536 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:135730454 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:135741201 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:135730413 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:135738570 A>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:135730437 C>T did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:135730437 C>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:135741311 T>C did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:135738557 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:135736557 G>A did not map to a codon.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr11:35198188 T>C maps to NM_000610.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:35201841 C>T maps to NM_000610.3 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:35219666 G>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:207956658 A>C maps to NM_172359.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr1:207940367 T>C maps to NM_172359.2 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr1:207933046 C>T maps to NM_172359.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:107799012 G>A maps to NM_001777.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:160651133 C>T maps to NM_001778.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:160654941 G>A maps to NM_001778.2 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr11:60889194 C>T maps to NM_014207.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:60889140 C>T maps to NM_014207.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:60890433 G>A maps to NM_014207.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:111435154 G>A maps to NM_000560.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:111435022 C>T maps to NM_000560.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:111435076 C>T maps to NM_000560.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr1:111434047 G>A maps to NM_000560.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:207495886 G>A maps to NM_001114752.1 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:207500114 G>A maps to NM_001114752.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:117087041 A>T maps to NM_001779.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:117078658 G>A maps to NM_001779.2 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr1:157805847 G>A maps to NM_005894.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr1:157811479 T>A maps to NM_005894.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:157803102 G>A maps to NM_005894.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:157803204 G>A maps to NM_005894.2 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:157805675 C>A maps to NM_005894.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr1:157803128 G>T maps to NM_005894.2 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:157802979 A>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:157803222 G>A maps to NM_005894.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:60785842 G>A maps to NM_006725.3 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:60776195 C>T maps to NM_006725.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:60778606 G>T maps to NM_006725.3 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:60777254 T>C maps to NM_006725.3 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:7484101 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:9908932 G>T maps to NM_001781.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:9907822 G>A maps to NM_001781.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr12:9906145 T>C maps to NM_001781.2 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:6590914 G>A maps to NM_001252.3 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:35612861 C>A maps to NM_001782.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:149786523 C>A did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr19:42384790 G>T maps to NM_001783.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr11:44626695 C>T maps to NM_002231.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:44626656 G>A maps to NM_002231.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr11:44640224 G>A maps to NM_002231.3 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:14131842 C>T maps to NM_004233.3 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr1:160535346 T>A maps to NM_001184879.1 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:160520744 C>A maps to NM_001184879.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:160535428 G>T maps to NM_001184879.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:160523270 G>A maps to NM_001184879.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr1:160535269 T>C maps to NM_001184879.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:121825234 C>T maps to NM_175862.3 Y197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:121825088 G>T maps to NM_175862.3 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr3:121825183 C>T maps to NM_175862.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:6344456 G>A maps to NM_001769.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:23065641 G>A maps to NM_012072.3 C396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:111297944 T>C maps to NM_198196.2 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:111317053 G>T maps to NM_198196.2 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:111263989 C>T maps to NM_198196.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:14501817 C>T maps to NM_078481.2 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr19:14499598 G>A maps to NM_078481.2 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:14513640 C>T maps to NM_078481.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:14517887 G>A maps to NM_078481.2 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:14512310 C>A maps to NM_078481.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:14512561 C>T maps to NM_078481.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:14518739 G>A maps to NM_078481.2 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:14513442 C>T maps to NM_078481.2 N406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr19:14513442 C>T maps to NM_078481.2 N406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:149937530 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:149963716 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:149963934 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:149963725 C>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:149963927 C>A did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:149938797 C>A did not map to a codon.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr23:149999702 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr13:49848469 G>A maps to NM_030911.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:49841912 G>T maps to NM_030911.3 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:43018585 C>T maps to NM_138477.2 R1042R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:43028221 G>T maps to NM_138477.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:12280462 C>T maps to NM_006023.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr10:12291611 A>G maps to NM_006023.2 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:12291611 A>G maps to NM_006023.2 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr1:100856304 A>G maps to NM_033312.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:100963745 G>A maps to NM_033312.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:99285632 T>C maps to NM_033331.2 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr13:115028410 C>T maps to NM_003903.3 N478N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:54439459 C>A maps to NM_001170402.1 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:54420639 C>T maps to NM_001170402.1 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:54420699 C>T maps to NM_001170402.1 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr5:54420693 G>A maps to NM_001170402.1 H384H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:54424445 C>A did not map to a codon.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr5:137542256 C>G maps to NM_004661.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:137528190 A>C did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:137534336 C>T maps to NM_004661.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:48200836 G>A maps to NM_001789.2 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:48209413 G>A maps to NM_001789.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:48219373 G>A maps to NM_001789.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:48219373 G>A maps to NM_001789.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:48200931 T>A maps to NM_001789.2 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr9:116034720 G>A maps to NM_139286.3 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:45249392 A>G maps to NM_001114091.1 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr17:45219254 A>G maps to NM_001114091.1 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:45249351 A>T maps to NM_001114091.1 L61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:45234448 G>A maps to NM_001114091.1 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr17:45234410 G>T maps to NM_001114091.1 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:45201280 C>A maps to NM_001114091.1 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr17:45234628 C>T maps to NM_001114091.1 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr17:45234310 T>C maps to NM_001114091.1 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr17:45234310 T>C maps to NM_001114091.1 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:535880 C>A maps to NM_004359.1 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:10502250 G>A maps to NM_007065.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:4685076 A>G maps to NM_017913.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:110534290 C>T maps to NM_015891.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr1:22405060 G>T maps to NM_001039802.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:227182673 G>A maps to ENST00000366766 S1661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:227381560 T>C maps to ENST00000366766 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:227222378 G>T maps to ENST00000366766 V1151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:227216822 G>A maps to ENST00000366766 R1323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:227259951 G>A maps to ENST00000366766 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:227333285 A>G maps to ENST00000366766 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:227333225 C>T maps to ENST00000366766 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:227333300 A>G maps to ENST00000366766 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:227333300 A>G maps to ENST00000366766 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr1:227261683 C>T maps to ENST00000366766 A872A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr1:227300539 C>T maps to ENST00000366766 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:227335095 C>T maps to ENST00000366766 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr1:227381560 T>C maps to ENST00000366766 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:103406167 G>A maps to NM_006035.3 R1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr14:103420573 C>T maps to NM_006035.3 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr14:103465978 C>T maps to NM_006035.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:103452886 G>A maps to NM_006035.3 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:103449946 C>T maps to NM_006035.3 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr14:103406033 G>T maps to NM_006035.3 S1580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr14:103410690 T>C maps to NM_006035.3 E1315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr14:103433471 A>G maps to NM_006035.3 N794N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr14:103523408 G>A maps to NM_006035.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:103416835 T>C maps to NM_006035.3 R1092R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:64601792 G>T maps to NM_017525.2 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:64606525 G>A maps to NM_017525.2 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:64594593 C>T maps to NM_017525.2 P1439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:64601236 C>T maps to NM_017525.2 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr11:64601971 G>A maps to NM_017525.2 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:64599109 C>T maps to NM_017525.2 W1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:64600378 G>A maps to NM_017525.2 P928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:65088909 C>T maps to NM_006779.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:71281790 A>G maps to NM_012121.4 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:151027509 G>A maps to NM_020239.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:130726771 G>A maps to NM_020240.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr22:19483524 C>T maps to NM_001178010.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:19496118 C>T maps to NM_001178010.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:19470304 C>T maps to NM_001178010.1 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr22:19504123 C>T maps to NM_001178010.1 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:44371686 T>C maps to NM_001253.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:44361249 G>T maps to NM_001253.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:44397571 T>C maps to NM_001253.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:44413559 G>T maps to NM_001253.2 E754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr6:44374092 A>G maps to NM_001253.2 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr6:44387287 C>A maps to NM_001253.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr6:44393898 A>G maps to NM_001253.2 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr17:38457179 A>G maps to NM_001254.3 Q450Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr1:91977174 A>G maps to NM_001134420.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:91977174 A>G maps to NM_001134420.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr1:91977174 A>G maps to NM_001134420.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr1:91977174 A>G maps to NM_001134420.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:91977174 A>G maps to NM_001134420.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr1:193094253 A>G maps to NM_024529.4 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:193094335 C>T maps to NM_024529.4 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:193094335 C>T maps to NM_024529.4 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:193104563 T>C maps to NM_024529.4 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr1:193094253 A>G maps to NM_024529.4 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:193099350 T>C maps to NM_024529.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr1:193091356 A>G maps to NM_024529.4 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:193094253 A>G maps to NM_024529.4 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:193094253 A>G maps to NM_024529.4 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr1:193094335 C>T maps to NM_024529.4 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:193111168 A>G maps to NM_024529.4 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:25364852 C>T maps to ENST00000434814 R892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr8:25343299 C>A maps to ENST00000434814 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:25319669 G>A maps to ENST00000434814 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr8:25364368 T>C maps to ENST00000434814 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:174228616 C>T maps to NM_031942.4 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:174228117 C>T maps to NM_031942.4 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:174228117 C>T maps to NM_031942.4 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:174228616 C>T maps to NM_031942.4 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:21956404 G>A maps to NM_018719.4 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:21942717 G>A maps to NM_018719.4 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:21945183 G>A maps to NM_018719.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr1:38166109 C>T maps to NM_018101.2 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:45130583 C>G maps to NM_022842.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:45132848 G>A maps to NM_022842.3 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:45153707 G>A maps to NM_022842.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:54606840 G>A maps to NM_201546.2 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr16:68849662 G>A did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr16:68844173 T>C maps to NM_004360.3 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr16:68867290 C>T maps to NM_004360.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:68867304 C>A maps to NM_004360.3 S851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr16:68847301 G>A maps to NM_004360.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:68849483 G>T maps to NM_004360.3 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr16:68849662 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr16:68845756 C>T maps to NM_004360.3 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:68855983 C>T maps to NM_004360.3 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:68844125 C>T maps to NM_004360.3 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:68844173 T>C maps to NM_004360.3 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:68853329 T>A did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr16:68844182 C>T maps to NM_004360.3 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr16:68855983 C>T maps to NM_004360.3 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr16:68856104 G>A maps to NM_004360.3 W638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr16:68844191 C>A maps to NM_004360.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr16:68867266 C>T maps to NM_004360.3 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:68772217 C>T maps to NM_004360.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr16:68846035 A>G did not map to a codon.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr16:68835594 T>C maps to NM_004360.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr16:68853329 T>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr16:68845614 A>G maps to NM_004360.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr16:68835582 A>G maps to NM_004360.3 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr16:68849662 G>A did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr16:68835628 C>T maps to NM_004360.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr16:68835628 C>T maps to NM_004360.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr16:68845653 C>A maps to NM_004360.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr16:68849662 G>A did not map to a codon.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr16:68862164 C>T maps to NM_004360.3 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr16:68853329 T>A did not map to a codon.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr16:68846087 G>A maps to NM_004360.3 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:68853293 C>T maps to NM_004360.3 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr16:68853329 T>C did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr16:68844146 A>T maps to NM_004360.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:24488254 T>C maps to NM_006727.3 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:24488245 A>G maps to NM_006727.3 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:24487889 G>T maps to NM_006727.3 S750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr5:24487948 G>A maps to NM_006727.3 Y730Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:24491760 A>T maps to NM_006727.3 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:24498605 G>A maps to NM_006727.3 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:24593440 T>C maps to NM_006727.3 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:24505320 G>T maps to NM_006727.3 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:24511518 G>T maps to NM_006727.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr5:24537495 A>G maps to NM_006727.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:24593557 T>C maps to NM_006727.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr5:24535260 C>A maps to NM_006727.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:24509910 G>A maps to NM_006727.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:24509922 G>A maps to NM_006727.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:65032612 C>T maps to NM_001797.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:65016102 A>C maps to NM_001797.2 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:65016135 C>T maps to NM_001797.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr16:65005890 A>G maps to NM_001797.2 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:64981514 G>A maps to NM_001797.2 D794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr16:65022215 G>A maps to NM_001797.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:64981826 A>G maps to NM_001797.2 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:65006927 A>G maps to NM_001797.2 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:65016003 G>A maps to NM_001797.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:65005848 C>T maps to NM_001797.2 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:64984769 G>A maps to NM_001797.2 N598N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:65032471 G>T maps to NM_001797.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr16:65026937 C>A did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr16:65016135 C>T maps to NM_001797.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:65005890 A>G maps to NM_001797.2 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr16:64981766 T>C maps to NM_001797.2 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr16:65005890 A>G maps to NM_001797.2 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr16:65032678 A>G maps to NM_001797.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr16:64984775 G>A maps to NM_001797.2 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr16:65005518 G>T maps to NM_001797.2 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr16:65005890 A>G maps to NM_001797.2 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:65005560 C>A maps to NM_001797.2 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr16:65005890 A>G maps to NM_001797.2 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:21752337 A>C maps to NM_004061.3 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:21817113 T>C maps to NM_004061.3 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:21802319 G>A maps to NM_004061.3 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:21817148 C>A maps to NM_004061.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:21842390 T>C maps to NM_004061.3 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:21817148 C>A maps to NM_004061.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:21802328 G>T maps to NM_004061.3 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr5:21752319 C>T maps to NM_004061.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:21842401 C>A maps to NM_004061.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:21854885 G>T maps to NM_004061.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr16:83712033 G>A maps to ENST00000268613 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr16:83065759 C>G maps to ENST00000268613 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:83251053 C>T maps to ENST00000268613 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:83378516 G>A maps to ENST00000268613 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:89261423 G>A maps to NM_004933.2 W769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:66947114 G>A maps to NM_004062.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:66949161 G>A maps to NM_004062.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:66946459 C>A maps to NM_004062.2 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:66945941 C>T maps to NM_004062.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:66947091 G>A maps to NM_004062.2 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr16:66950076 G>A maps to NM_004062.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr8:95172297 A>G maps to NM_001144663.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr8:95158219 G>T maps to NM_001144663.1 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr8:95186435 G>T maps to NM_001144663.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr8:95172351 C>T maps to NM_001144663.1 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:95143164 G>A maps to NM_001144663.1 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:95161011 G>A maps to NM_001144663.1 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr8:95164229 C>T maps to NM_001144663.1 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr8:95188823 T>C maps to NM_001144663.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr8:95172297 A>G maps to NM_001144663.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:95160999 A>T maps to NM_001144663.1 Y633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr8:95186435 G>A maps to NM_001144663.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr8:95188823 T>C maps to NM_001144663.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr5:19483619 G>A maps to NM_004934.3 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:19571818 A>G maps to NM_004934.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:19721471 G>A maps to NM_004934.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:19483491 G>A maps to NM_004934.3 C600C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:19838900 T>C maps to NM_004934.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:19747180 A>G maps to NM_004934.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr5:19612576 G>A maps to NM_004934.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:19571761 G>A maps to NM_004934.3 Y393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr5:19591258 G>A maps to NM_004934.3 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:19838996 C>A maps to NM_004934.3 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:19473526 A>G maps to NM_004934.3 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr5:19473718 G>A maps to NM_004934.3 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:19520771 A>T maps to NM_004934.3 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr5:19838996 C>A maps to NM_004934.3 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr18:64178910 A>C maps to NM_021153.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:64202229 T>A maps to NM_021153.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:64172258 G>A maps to NM_021153.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:64172237 C>T maps to NM_021153.2 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr18:64218457 C>A maps to NM_021153.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr18:25563000 T>C maps to NM_001792.3 E752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:25563000 T>C maps to NM_001792.3 E752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:25589701 G>A maps to NM_001792.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:25570149 G>T maps to NM_001792.3 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:25563000 T>C maps to NM_001792.3 E752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:25565636 T>C maps to NM_001792.3 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr18:25573583 C>T maps to NM_001792.3 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr18:25573484 A>G maps to NM_001792.3 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr18:25565036 C>T maps to NM_001792.3 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr18:25532233 C>A maps to NM_001792.3 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr18:25727711 T>A maps to NM_001792.3 K33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr18:59221519 C>T maps to NM_031891.2 D666D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr18:59221531 C>T maps to NM_031891.2 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr18:59157872 G>A maps to NM_031891.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:59217462 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr18:59195429 A>G maps to NM_031891.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr18:59170237 C>T maps to NM_031891.2 Y238Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:44869815 G>A maps to NM_021248.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr20:44869641 G>A maps to NM_021248.1 H170H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:44841666 G>A maps to NM_021248.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:44828152 G>A maps to NM_021248.1 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr20:44856147 G>A maps to NM_021248.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr20:44856237 C>T maps to NM_021248.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:44815560 T>C maps to NM_021248.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:73565968 G>A maps to ENST00000398860 E2708E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr10:73567453 G>A maps to ENST00000398860 Q2835Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:73461951 C>T maps to ENST00000398860 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:73558988 C>T maps to ENST00000398860 I2397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:73567143 C>T maps to ENST00000398860 I2768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:73455224 C>T maps to ENST00000398860 D785D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:73567273 C>T maps to ENST00000398860 A2775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:73326527 C>T maps to ENST00000398860 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:73539106 C>T maps to ENST00000398860 G1762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:73461930 C>A maps to ENST00000398860 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:73537447 C>T maps to ENST00000398860 H1624H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr10:73563152 C>T maps to ENST00000398860 N2621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:73437257 G>A maps to ENST00000398860 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr10:73537989 C>T maps to ENST00000398860 H1709H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:73269848 G>A maps to ENST00000398860 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr10:73558988 C>T maps to ENST00000398860 I2397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr10:73567645 G>C maps to ENST00000398860 V2873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:73498331 C>T maps to ENST00000398860 P1434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:73569712 C>T maps to ENST00000398860 D2958D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:23524561 G>A maps to NM_022478.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr14:23524794 G>A maps to NM_022478.3 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:23523375 G>A maps to NM_022478.3 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:23524046 G>A maps to NM_022478.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:23523754 C>T maps to NM_022478.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:23517530 C>T maps to NM_022478.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr14:23523448 G>A maps to NM_022478.3 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr20:58569314 G>A maps to NM_177980.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:58569359 T>C maps to NM_177980.2 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr20:58564053 G>A maps to NM_177980.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr20:58559833 C>T maps to NM_177980.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr20:58569512 G>A maps to NM_177980.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr20:58570969 A>G maps to NM_177980.2 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr20:58570969 A>G maps to NM_177980.2 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:58569464 G>A maps to NM_177980.2 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr20:58567483 C>T maps to NM_177980.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:68729807 C>T maps to NM_001793.4 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:68721631 C>T maps to NM_001793.4 N596N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr20:60318745 G>A maps to NM_001794.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr20:60470093 C>T maps to NM_001794.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr20:60509208 C>T maps to NM_001794.2 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr20:60419830 G>C maps to NM_001794.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:60503422 C>T maps to NM_001794.2 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr20:60448838 C>T maps to NM_001794.2 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr20:60498687 G>A maps to NM_001794.2 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:60470051 C>A maps to NM_001794.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr20:60348198 C>T maps to NM_001794.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr20:60419726 C>A maps to NM_001794.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr20:60509178 C>T maps to NM_001794.2 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr16:66430009 A>C maps to NM_001795.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr16:66432423 C>T maps to NM_001795.3 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr16:66413332 C>T maps to NM_001795.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr5:31299652 C>T maps to NM_004932.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:31323264 A>G maps to NM_004932.2 E741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr5:31313515 G>T maps to NM_004932.2 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:31323063 C>T maps to NM_004932.2 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr5:31323123 C>T maps to NM_004932.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:31267705 A>G maps to NM_004932.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr5:31323106 C>T maps to NM_004932.2 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr16:62055133 G>T maps to NM_001796.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:61761006 T>C maps to NM_001796.2 K509K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3510-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:61851383 T>G maps to NM_001796.2 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:61689413 G>A maps to NM_001796.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr16:61689413 G>A maps to NM_001796.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:61761045 G>A maps to NM_001796.2 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:61823294 C>A maps to NM_001796.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:61687748 G>A maps to NM_001796.2 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr16:61854973 A>C maps to NM_001796.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:61935149 G>A maps to NM_001796.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr16:61851531 C>T maps to NM_001796.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr16:61854904 G>T maps to NM_001796.2 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:61687934 G>A maps to NM_001796.2 D659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:26988320 C>G maps to NM_016279.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:26906199 C>A maps to NM_016279.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr5:26916011 T>C maps to NM_016279.3 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr5:26906833 C>A maps to NM_016279.3 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:26906066 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:26906149 G>T maps to NM_016279.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:26881589 G>A maps to NM_016279.3 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:26881450 C>A maps to NM_016279.3 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:26886099 C>T maps to NM_016279.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr5:26881622 G>A maps to NM_016279.3 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr5:26886073 C>G did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr5:26915831 C>T maps to NM_016279.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr10:85965586 C>T maps to NM_033100.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr10:85957549 T>C maps to NM_033100.2 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:85974037 G>A maps to NM_033100.2 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:176011588 G>A maps to NM_001171976.1 E769E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr5:176011486 G>A maps to NM_001171976.1 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:176008366 C>T maps to NM_001171976.1 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:176018455 C>T maps to NM_001171976.1 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:105641973 G>A maps to NM_152750.4 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:105660937 A>G maps to NM_152750.4 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:105672842 C>T maps to NM_152750.4 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:105644978 C>T maps to NM_152750.4 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:49836706 G>A maps to NM_001007540.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:49830285 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:49836775 C>T maps to NM_001007540.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr3:49831326 G>A maps to NM_001007540.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr3:49831365 C>A maps to NM_001007540.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:617482 G>A maps to NM_021924.4 D802D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:621657 C>T maps to NM_021924.4 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:619121 G>A maps to NM_021924.4 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:29870554 G>A maps to NM_006319.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:62545454 A>G maps to NM_001786.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:89757905 G>A maps to NM_052988.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:1654193 G>A maps to NM_024011.2 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:1572312 G>T maps to ENST00000401097 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr17:37687086 C>T maps to NM_016507.2 R1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:37686992 C>T maps to NM_016507.2 A1299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:37667817 C>T maps to NM_016507.2 Y901Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:37667784 C>T maps to NM_016507.2 R890R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr17:37665991 C>A maps to NM_016507.2 R882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr7:40037230 A>G maps to NM_003718.4 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:40027800 T>C maps to NM_003718.4 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:40133870 T>C maps to NM_003718.4 Y1277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr7:40037230 A>G maps to NM_003718.4 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:40132765 G>A maps to NM_003718.4 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:90377000 A>T maps to NM_012395.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr7:90613544 C>T maps to NM_012395.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr7:90741854 A>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:90419936 G>T maps to NM_012395.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:90419920 C>A maps to NM_012395.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr7:90741854 A>G did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr7:90546980 C>T maps to NM_012395.2 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:202700460 G>T maps to ENST00000450471 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:202744855 C>T maps to ENST00000450471 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr2:202719628 G>A maps to ENST00000450471 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:47086591 C>T did not map to a codon.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr23:47086433 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:47085210 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:47083884 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:47086410 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:47085737 C>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:47083900 G>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:47082981 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:96688837 T>C maps to NM_002595.4 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:96683009 T>C maps to NM_002595.4 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:96674609 G>A maps to NM_002595.4 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:96707232 C>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:96688845 A>G maps to NM_002595.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:96717777 A>T maps to NM_002595.4 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr12:96676322 G>T maps to NM_002595.4 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr12:96688843 C>T maps to NM_002595.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr1:205498651 G>A maps to NM_212503.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:110948304 C>T maps to NM_015076.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr6:110942498 C>T maps to NM_015076.3 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr6:110942498 C>T maps to NM_015076.3 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr12:56361658 C>T maps to NM_001798.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:90584158 G>A maps to NM_001039803.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:90586163 C>T maps to NM_001039803.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:90585529 G>A maps to NM_001039803.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:123746303 C>T maps to NM_004642.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr11:67274932 G>A maps to NM_005851.3 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:58142346 C>T maps to NM_000075.2 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr7:150754236 T>C maps to NM_004935.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:30814874 G>A maps to NM_003885.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr17:30814874 G>A maps to NM_003885.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:219825321 C>T maps to NM_003936.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:219825120 C>T maps to NM_003936.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr20:31967410 G>A maps to ENST00000357886 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr20:31954679 C>T maps to ENST00000357886 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:31984726 C>T maps to ENST00000357886 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr20:31984678 A>G maps to ENST00000357886 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:123222915 C>T maps to NM_018249.4 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:123210311 C>T maps to NM_018249.4 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:123199657 C>T maps to NM_018249.4 V1290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:123199603 C>T maps to NM_018249.4 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:123220813 G>A maps to NM_018249.4 H763H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:123199786 C>T maps to NM_018249.4 Q1247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:123182102 T>G maps to NM_018249.4 T1380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:123199801 G>A maps to NM_018249.4 Y1242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:123210311 C>T maps to NM_018249.4 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:123165245 G>A maps to NM_018249.4 G1715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:46058858 C>A maps to NM_176096.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:92247412 G>A maps to NM_001145306.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:92244489 C>T maps to NM_001145306.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:68531246 T>C maps to NM_001799.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr13:26956982 T>C maps to NM_001260.1 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr13:26978094 T>C maps to NM_001260.1 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr13:26923303 T>A maps to NM_001260.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr13:26959364 C>T maps to NM_001260.1 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:130551483 C>T maps to ENST00000373265 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:130551701 G>A maps to ENST00000373265 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:20546688 G>A maps to NM_017774.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:50808898 C>T maps to ENST00000356146 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:76507102 T>A maps to ENST00000307465 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:76522174 A>G maps to ENST00000307465 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:133655174 A>G maps to NM_001113575.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:133643920 G>A maps to NM_001113575.1 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:133644136 C>T maps to NM_001113575.1 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:39440538 A>G did not map to a codon.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr23:18646617 G>A did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:18598026 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:18671645 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:18606105 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:18622374 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:18598041 A>G did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:18622114 C>T did not map to a codon.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr23:18664177 G>A did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:18646534 G>A did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:18643279 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:18622878 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:18622327 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:18646616 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:18671564 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:18622165 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:18668672 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:18622079 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:18627682 T>G did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:18668700 C>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:18622765 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:18606220 G>T did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:18622163 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:18671622 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:18622165 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:18622764 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:18664126 A>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:36651985 G>A maps to ENST00000448526 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:36652019 C>T maps to ENST00000448526 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:12870940 C>T maps to NM_004064.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr9:21968242 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:21971057 G>A maps to NM_001195132.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:21974676 C>T maps to NM_001195132.1 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:21970901 T>C maps to NM_001195132.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:184368295 G>T maps to NM_017632.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:184368309 G>A maps to NM_017632.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:22006165 A>G maps to NM_004936.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:22008919 C>T maps to NM_004936.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:51439701 G>A maps to NM_078626.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:125831787 G>A maps to ENST00000392693 H1154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr11:125875869 A>G maps to ENST00000392693 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:125871641 T>C maps to ENST00000392693 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr11:125875869 A>G maps to ENST00000392693 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:125888243 G>T maps to ENST00000392693 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:125853839 G>A maps to ENST00000392693 G974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:125891224 G>T maps to ENST00000392693 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr11:125885328 A>C maps to ENST00000392693 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:125893316 G>A maps to ENST00000392693 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:125853857 G>A maps to ENST00000392693 I968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr11:125864215 A>G maps to ENST00000392693 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:125867171 G>A maps to ENST00000392693 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:125831706 T>C maps to ENST00000392693 E1181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:125851075 G>A maps to ENST00000392693 H1048H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr11:125875869 A>G maps to ENST00000392693 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:125875869 A>G maps to ENST00000392693 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr11:125888243 G>T maps to ENST00000392693 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:139866269 G>A did not map to a codon.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr23:139865860 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:139866079 C>T did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:139866512 C>T did not map to a codon.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr23:139866080 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:22358878 G>A maps to NM_001802.1 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:22358875 G>A maps to NM_001802.1 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:22358840 T>C maps to NM_001802.1 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:15510988 G>A maps to ENST00000455584 Y701Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:15516053 G>A maps to ENST00000455584 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:15501876 G>A maps to ENST00000455584 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:15492513 A>G maps to ENST00000261644 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:85540672 C>A maps to NM_001263.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:85566479 T>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:5157301 C>T maps to NM_003818.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr20:5157343 C>A maps to NM_003818.2 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:31084944 T>G maps to NM_001264.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:31085253 C>T maps to NM_001264.4 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr6:31084857 G>C maps to NM_001264.4 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:31083918 A>G maps to NM_001264.4 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:88870972 C>T maps to NM_030928.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:88873828 G>A maps to NM_030928.3 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr16:88874616 C>T maps to NM_030928.3 D524D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:88871991 C>T maps to NM_030928.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:133302863 C>T maps to NM_017548.4 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:72667324 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:72667220 C>T did not map to a codon.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr23:72667232 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:72673465 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:72667220 C>T did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:72667133 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:4943785 C>T maps to ENST00000328908 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:4937796 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:4943785 C>T maps to ENST00000328908 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:4935845 C>T maps to ENST00000328908 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:4943785 C>T maps to ENST00000328908 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:4937866 C>T maps to ENST00000328908 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:4891978 A>G maps to ENST00000328908 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr16:80654787 G>A maps to NM_152342.2 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:80638386 G>A maps to NM_152342.2 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:80718936 C>T maps to NM_152342.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:43031244 G>T maps to NM_001712.4 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:43015752 C>T maps to NM_001712.4 E468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:43013353 C>T maps to NM_001712.4 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:51986277 C>T maps to NM_001080405.1 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:45175934 G>A maps to NM_020219.3 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:45182196 G>A maps to NM_020219.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr19:45028151 G>T maps to NM_001102597.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr19:45021082 G>A maps to NM_001102597.1 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:45024580 C>T maps to NM_001102597.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:45024751 G>A maps to NM_001102597.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:45028151 G>A maps to NM_001102597.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:45029257 C>T maps to NM_001102597.1 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr19:42083747 C>T maps to NM_001098506.1 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:42090698 G>A did not map to a codon.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr19:42083573 C>T maps to NM_001098506.1 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr19:42301734 C>T maps to NM_001815.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:42132143 G>A maps to NM_001817.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:42225007 G>A maps to NM_004363.2 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:42260619 C>A maps to NM_002483.4 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:42265289 G>A maps to NM_002483.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr19:42265289 G>T maps to NM_002483.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr19:42265289 G>T maps to NM_002483.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr19:42187882 C>T maps to NM_006890.3 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:42191096 G>A maps to NM_006890.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:42187989 C>T maps to NM_006890.3 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:42190844 G>A maps to NM_006890.3 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:43092953 T>G maps to NM_001816.3 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:43093086 A>G maps to NM_001816.3 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:43093011 G>A maps to NM_001816.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:33792420 G>A maps to NM_004364.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr19:33792315 C>T maps to NM_004364.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:33792315 C>T maps to NM_004364.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr19:33792303 C>T maps to NM_004364.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:33792348 C>T maps to NM_004364.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr19:33792389 G>A maps to NM_004364.3 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr14:23586812 G>A maps to NM_001805.2 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr14:23586740 A>G maps to NM_001805.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:33870312 G>A maps to NM_001806.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:37441042 C>A maps to NM_005760.2 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:37455759 A>G maps to NM_005760.2 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:37455501 G>A maps to NM_005760.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:37455986 C>A maps to NM_005760.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:37456065 A>G maps to NM_005760.2 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr2:37455764 C>A maps to NM_005760.2 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr22:17662735 G>T maps to NM_017424.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:17662828 A>G maps to NM_017424.2 D441D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr22:18020201 C>T maps to ENST00000400579 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr22:18021604 G>A maps to ENST00000400579 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr22:18031733 C>T maps to ENST00000400579 V1411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr22:18028279 G>A maps to ENST00000400579 P1080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:18020201 C>T maps to ENST00000400579 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:18022246 C>T maps to ENST00000400579 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr22:18020243 C>T maps to ENST00000400579 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr22:18022117 G>A maps to ENST00000400579 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr22:18022120 C>T maps to ENST00000400579 Y742Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:17619024 G>A maps to NM_033070.2 H386H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:135939795 C>T maps to NM_001807.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:135945949 C>T maps to NM_001807.3 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:135940526 C>A maps to NM_001807.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr9:135940592 G>A maps to NM_001807.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:51723533 G>A maps to NM_001971.5 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr1:15789902 C>T maps to ENST00000375924 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:15809839 C>T maps to ENST00000442979 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr1:15812541 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:22333866 C>T maps to NM_005747.4 T167T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DM-A1HB-01A-21D-A183-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:22329496 C>A maps to NM_005747.4 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:22313061 T>C maps to NM_007352.2 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:47496957 C>T maps to NM_001172639.1 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:47494745 G>A maps to NM_001172639.1 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:11370997 C>T maps to NM_006561.3 N516N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr10:11299734 A>T maps to NM_006561.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:151678721 T>C maps to NM_007185.4 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:151678724 C>T maps to NM_007185.4 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:151678724 C>T maps to NM_007185.4 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr1:151679199 G>A maps to NM_007185.4 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr18:34853093 T>A maps to NM_020180.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr18:35145328 G>T maps to NM_020180.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:34833779 C>T maps to NM_020180.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:34854408 C>T maps to NM_020180.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr18:35145331 T>G maps to NM_020180.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr18:34853003 C>T maps to NM_020180.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr18:35145541 G>A maps to NM_020180.3 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:3224847 C>T maps to NM_021938.3 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:3281333 C>T maps to NM_021938.3 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:3224835 G>T maps to NM_021938.3 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr15:72582588 T>C maps to NM_052840.4 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr22:46793715 G>A maps to NM_014246.1 N1852N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:46793724 C>A maps to NM_014246.1 T1849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:46787146 G>A maps to NM_014246.1 G2062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr22:46835147 C>T maps to NM_014246.1 P1448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:46859958 C>T maps to NM_014246.1 P1276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:46768912 G>A maps to NM_014246.1 Y2542Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:46765642 C>T maps to NM_014246.1 S2606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:46760035 C>T maps to NM_014246.1 S2964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr22:46930670 A>G maps to NM_014246.1 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr22:46761130 T>A maps to NM_014246.1 K2851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr22:46931999 C>T maps to NM_014246.1 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr22:46794519 G>A maps to NM_014246.1 I1809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:109793684 G>A maps to NM_001408.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:109813094 C>A maps to NM_001408.2 C2452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr1:109814913 C>G maps to NM_001408.2 P2647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr1:109814916 C>T maps to NM_001408.2 S2648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:109793996 C>T maps to NM_001408.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:109812411 C>T maps to NM_001408.2 F2359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:109794173 G>A maps to NM_001408.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:109810582 C>T maps to NM_001408.2 D2073D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:109801219 G>A maps to NM_001408.2 T1159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:109793264 C>A maps to NM_001408.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr3:48680242 G>A maps to NM_001407.2 T2827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:48689336 G>A maps to NM_001407.2 Q1966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:48696658 C>A maps to NM_001407.2 E1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr3:48699137 C>T maps to NM_001407.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:48697376 C>A maps to NM_001407.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr3:48696842 C>A maps to NM_001407.2 R1075R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:48699631 C>A maps to NM_001407.2 G146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:48697376 C>T maps to NM_001407.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr3:48696382 G>A maps to NM_001407.2 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:48698249 T>C maps to NM_001407.2 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:48698738 G>A maps to NM_001407.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:27015670 G>A maps to NM_001809.3 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr2:27015024 C>A maps to NM_001809.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr2:27014999 C>T maps to NM_001809.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:27015629 G>T maps to NM_001809.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:3765579 C>T maps to NM_001810.5 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr4:68385062 C>T maps to NM_001812.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr4:68385110 T>C maps to NM_001812.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:68358707 G>A maps to NM_001812.2 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr4:68358652 C>A maps to NM_001812.2 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:104070140 C>A maps to NM_001813.2 E1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:104068800 G>A maps to NM_001813.2 I1282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr4:104055001 G>A maps to NM_001813.2 S2190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:104067111 T>C maps to NM_001813.2 R1429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:104072447 G>A maps to NM_001813.2 A1108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:104070123 A>G maps to NM_001813.2 A1240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr4:104065687 A>G maps to NM_001813.2 L1649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:104055001 G>A maps to NM_001813.2 S2190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:104041483 G>A maps to NM_001813.2 R2384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:104061149 T>C maps to NM_001813.2 E2000E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr4:104067111 T>C maps to NM_001813.2 R1429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr4:104055001 G>A maps to NM_001813.2 S2190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:104030095 T>C maps to NM_001813.2 Q2625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:214814930 G>T maps to NM_016343.3 E1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:214813303 A>G maps to NM_016343.3 Q541Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:214794050 G>A maps to NM_016343.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr1:214816318 G>A maps to NM_016343.3 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:214828672 G>A maps to NM_016343.3 Q2804Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:214815490 A>G maps to NM_016343.3 E1270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:214818798 G>A maps to NM_016343.3 Q1962Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:214795473 A>G maps to NM_016343.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:214795473 A>G maps to NM_016343.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr1:214815523 A>G maps to NM_016343.3 T1281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr1:214795473 A>G maps to NM_016343.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr1:214795473 A>G maps to NM_016343.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr1:214795473 A>G maps to NM_016343.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr1:214818879 A>G maps to NM_016343.3 Q1989Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:214787153 A>G maps to NM_016343.3 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:214814720 T>C maps to NM_016343.3 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:214820016 C>A maps to NM_016343.3 T2368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:100402773 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:100356189 A>C did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:100395662 G>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:100364524 C>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:100387396 T>C did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:100364956 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:100364542 C>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:100387395 T>C did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:25473684 C>A maps to NM_018451.3 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr13:25481071 T>C maps to NM_018451.3 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:25463525 G>A maps to NM_018451.3 R1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:25463525 G>A maps to NM_018451.3 R1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:25458546 G>A maps to NM_018451.3 R1178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:25480957 A>C maps to NM_018451.3 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr13:25479880 G>A maps to NM_018451.3 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr13:25484158 C>A maps to NM_018451.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:25478061 A>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:64825023 G>A maps to NM_022145.3 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:64817342 C>A maps to NM_022145.3 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:81060180 C>T maps to NM_001100624.1 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:81053802 C>T maps to NM_001100624.1 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:25022671 C>T maps to NM_024322.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:25037307 T>C maps to NM_024322.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:95094496 G>A maps to NM_001012267.1 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr6:49448716 T>A maps to NM_018132.3 L134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr6:49448716 T>A maps to NM_018132.3 L134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr16:67862685 G>A maps to NM_025082.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:123877462 T>C maps to NM_007018.4 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr9:123904530 C>T maps to NM_007018.4 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:123932024 T>C maps to NM_007018.4 A2069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:123914933 G>T maps to NM_007018.4 E1379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:123888120 T>C maps to NM_007018.4 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:123921146 G>A maps to NM_007018.4 Q1593Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr9:123877462 T>A maps to NM_007018.4 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:123930414 C>T maps to NM_007018.4 S1962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr9:123877468 A>G maps to NM_007018.4 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr9:123877468 A>G maps to NM_007018.4 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:123927346 C>T maps to NM_007018.4 N1850N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:123933804 G>A maps to NM_007018.4 E2132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr5:122754174 A>C maps to NM_153223.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr5:122724241 T>C maps to NM_153223.3 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr5:122685639 G>A maps to NM_153223.3 N908N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr5:122682347 A>G maps to NM_153223.3 D942D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:56837449 C>T maps to NM_025009.3 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:56837449 C>T maps to NM_025009.3 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:56840967 C>T maps to NM_025009.3 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr4:56878120 A>G maps to NM_025009.3 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:56837449 C>A maps to NM_025009.3 C375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr4:56858233 A>T maps to NM_025009.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:56878112 C>T maps to NM_025009.3 R922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:56878120 A>G maps to NM_025009.3 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:49090224 A>G maps to NM_001194998.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:49073394 G>T maps to NM_001194998.1 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr15:49081138 C>T maps to NM_001194998.1 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr15:49061212 A>G maps to NM_001194998.1 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr11:117232585 T>C maps to NM_014956.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr11:117280454 G>A maps to NM_014956.4 P1290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:117266343 G>T maps to NM_014956.4 E999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:117257954 C>A maps to NM_014956.4 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:117282543 G>A maps to NM_014956.4 S1399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr11:117232585 T>C maps to NM_014956.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr1:243327981 T>G maps to NM_014812.2 R1094R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr18:13068878 G>A maps to NM_032142.3 S1617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:13008508 C>A maps to NM_032142.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:12999435 C>T maps to NM_032142.3 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr18:13049589 C>T maps to NM_032142.3 Q934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr18:13116475 C>T maps to NM_032142.3 R2464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr18:13056462 G>T maps to NM_032142.3 G1292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr18:13029786 G>A maps to NM_032142.3 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr18:13114130 C>T maps to NM_032142.3 S2390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr20:34087876 G>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:34065922 T>C maps to NM_007186.3 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:34091174 C>T maps to NM_007186.3 L1660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:34054846 G>A maps to NM_007186.3 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr20:34099218 T>C maps to NM_007186.3 L2365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:34055176 G>A maps to NM_007186.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:34092154 G>A maps to NM_007186.3 E1986E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:34084469 C>T maps to NM_007186.3 R1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr20:34085703 C>T maps to NM_007186.3 R1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:34064420 G>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:34085610 C>T maps to NM_007186.3 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr20:34090453 G>A maps to NM_007186.3 L1419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr20:34053621 C>T maps to NM_007186.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:88487612 T>C maps to NM_025114.3 E1081E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:88513912 A>G maps to NM_025114.3 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:88514773 C>T maps to NM_025114.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:88476829 C>A maps to NM_025114.3 E1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:88500574 C>T maps to NM_025114.3 R898R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:88533328 C>A maps to NM_025114.3 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:88500852 C>A maps to NM_025114.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:88465690 C>A maps to NM_025114.3 E1908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:88500648 C>A maps to NM_025114.3 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:88524074 A>G maps to NM_025114.3 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr1:180006124 C>T maps to NM_014810.4 N1337N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:180044214 C>T maps to NM_014810.4 L1876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:179965889 C>T maps to NM_014810.4 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:180056744 C>T maps to NM_014810.4 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:179965889 C>T maps to NM_014810.4 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:180063225 T>G maps to NM_014810.4 S2662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:179965889 C>T maps to NM_014810.4 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:179983104 C>A maps to NM_014810.4 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:180056747 G>A maps to NM_014810.4 E2107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:95262964 C>A maps to NM_018131.4 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:95561023 T>G maps to NM_014679.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:95532500 C>T maps to NM_014679.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:134214197 G>A maps to NM_025180.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr3:134256013 G>A maps to NM_025180.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr2:65305045 T>C maps to NM_015147.2 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:138256128 G>A maps to NM_024491.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr18:12686425 T>G maps to NM_024899.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:12701087 C>A maps to NM_024899.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:80854978 G>A maps to NM_001098802.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:80866876 G>T maps to NM_001098802.1 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:80880365 T>G maps to NM_001098802.1 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:101484238 C>T maps to ENST00000327230 D840D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:101476616 G>A maps to ENST00000327230 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:101476574 G>A maps to ENST00000327230 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:111702096 T>C maps to NM_001007794.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:14720297 G>A maps to NM_005454.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:14722232 C>T maps to NM_005454.2 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr9:131193518 G>A maps to NM_016174.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:131190695 A>G maps to NM_016174.4 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:131186484 A>G maps to NM_016174.4 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:131196730 C>A maps to NM_016174.4 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr22:47116880 G>A maps to NM_022766.5 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:182402939 C>A maps to NM_001030311.2 G550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr2:182423356 C>A maps to NM_001030311.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:55855433 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:55862719 T>C maps to NM_001025195.1 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:55862761 C>G maps to NM_001025195.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr16:66976105 G>A maps to NM_003869.5 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:66973260 G>T maps to NM_003869.5 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:66997154 C>T maps to NM_024922.5 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:67005175 C>T maps to NM_024922.5 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr16:66997109 C>T maps to NM_024922.5 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:55880741 C>T maps to NM_001143685.1 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:55897346 G>T maps to NM_001143685.1 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:55880593 C>T maps to NM_001143685.1 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:67038039 T>G maps to ENST00000326686 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr18:580536 C>T maps to NM_004066.1 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr18:580536 C>T maps to NM_004066.1 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr18:580554 C>T maps to NM_004066.1 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:151996467 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:151996461 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:57003555 C>T maps to NM_000078.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:57003555 C>T maps to NM_000078.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:57003369 C>T maps to NM_000078.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:57012037 C>T maps to NM_000078.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:57003564 C>A maps to NM_000078.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:31915758 A>G maps to ENST00000437789 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:131356220 C>A maps to NM_032545.2 G81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:75338934 G>A maps to NM_006324.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:196715080 C>T maps to NM_000186.3 R1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:196648758 C>A maps to NM_000186.3 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:196712741 A>G maps to NM_000186.3 E1098E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr1:196695660 G>A maps to NM_000186.3 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:196648783 T>C maps to NM_000186.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr1:196694260 C>T maps to NM_000186.3 C569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:196648918 T>C maps to NM_000186.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:196706041 A>G maps to NM_000186.3 K834K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:196648751 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:196621305 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:196716253 A>T maps to NM_000186.3 I1169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:196715100 A>G maps to NM_000186.3 G1155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:196695951 C>T maps to NM_000186.3 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:196682938 G>T maps to NM_000186.3 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:196654200 A>G maps to NM_000186.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:196794721 T>C maps to NM_002113.2 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:196796061 A>G maps to NM_002113.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr1:196796112 C>T maps to NM_002113.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:196918732 C>A maps to ENST00000367421 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:196920057 A>G maps to ENST00000367421 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:196920135 T>C maps to ENST00000367421 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:196918666 A>G maps to ENST00000367421 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:196762466 G>T maps to NM_021023.5 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:196762636 C>T maps to NM_021023.5 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:196757354 C>G maps to NM_021023.5 S147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:196883715 C>T maps to NM_006684.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:196953190 C>T maps to ENST00000367414 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr1:196964886 T>C maps to ENST00000367414 N240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:196977765 C>T maps to ENST00000367414 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:196977765 C>T maps to ENST00000367414 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:196953103 T>C maps to ENST00000367414 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr1:196973806 T>C maps to ENST00000367414 C473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:110670420 T>C maps to ENST00000394635 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:110667383 C>A maps to ENST00000394635 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:110682703 G>A maps to ENST00000394635 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:110662060 C>T maps to ENST00000394635 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr4:110663683 G>A maps to ENST00000394635 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr4:110685745 G>A maps to ENST00000394635 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:110663746 G>A maps to ENST00000394635 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:110670692 G>A maps to ENST00000394635 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:65623542 G>A maps to NM_005507.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:65623713 C>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:47489070 A>G did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:47486557 C>T did not map to a codon.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr23:47487605 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:47489068 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:47489215 G>A did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:47487627 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:117282580 C>T maps to NM_000492.3 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr7:117232510 C>T maps to NM_000492.3 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:117307065 C>A maps to NM_000492.3 L1449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:117243762 G>A maps to NM_000492.3 S945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:117235043 C>T maps to NM_000492.3 R851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:117267715 C>T maps to NM_000492.3 I1203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr7:117232392 C>T maps to NM_000492.3 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:117251804 G>T maps to NM_000492.3 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:117232199 C>A maps to NM_000492.3 S660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:117292915 A>G maps to NM_000492.3 G1298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr19:49539503 C>T maps to ENST00000391869 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:88105119 G>A maps to NM_001195308.1 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:151506581 C>T maps to NM_020770.2 D958D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:151502561 C>T maps to NM_020770.2 R762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr1:151508327 G>T maps to NM_020770.2 E1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:57810601 A>G maps to NM_032866.3 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr15:57810599 C>T maps to NM_032866.3 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:57743714 T>C maps to NM_032866.3 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr15:57730452 C>T maps to NM_032866.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr15:57816919 C>T maps to NM_032866.3 R1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr15:57809045 G>A maps to NM_032866.3 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:57809129 C>T maps to NM_032866.3 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr15:57730904 C>T maps to NM_032866.3 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr15:57745949 A>T maps to NM_032866.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:57730400 G>A maps to NM_032866.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:57731034 C>T maps to NM_032866.3 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:27324339 G>A maps to ENST00000404694 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:54997722 G>A maps to NM_006568.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr14:54997668 T>C maps to NM_006568.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:90966905 G>A maps to NM_003956.3 Y48Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:53995088 C>T maps to NM_001008708.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:48545405 C>A maps to NM_001267.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr17:48545964 C>T maps to NM_001267.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:4433466 G>A maps to NM_005483.2 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr19:4428854 C>T maps to NM_005483.2 H524H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr21:37785220 C>T maps to NM_005441.2 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr21:37785463 C>T maps to NM_005441.2 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:50856569 C>T maps to NM_020549.4 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:50827940 G>A maps to NM_020549.4 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr10:50854614 G>A maps to NM_020549.4 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr10:50856590 C>T maps to NM_020549.4 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:50824638 T>C maps to NM_020549.4 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr10:50863173 C>T maps to NM_020549.4 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr22:24108330 C>T maps to ENST00000401675 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:132709303 A>G did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:132570460 A>G maps to ENST00000448878 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:113343679 C>A maps to ENST00000409719 C44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:113343556 G>A maps to ENST00000409719 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:98235401 A>G maps to NM_001270.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:98230369 C>T maps to NM_001270.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:98192176 A>G maps to NM_001270.2 D1680D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:98192176 A>G maps to NM_001270.2 D1680D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:146736082 C>T maps to NM_004284.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:146756066 G>A maps to NM_004284.3 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr1:146751865 T>G did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:146751820 C>A maps to NM_004284.3 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:93567631 C>T maps to NM_001271.3 S1728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:93482925 C>T maps to NM_001271.3 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr15:93486196 C>A maps to NM_001271.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:7793076 C>T maps to NM_001005271.2 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:7796732 G>A maps to NM_001005271.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr17:7810507 A>G maps to NM_001005271.2 E1636E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AZ-6601-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr17:7814169 C>A maps to NM_001005271.2 Y1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:7806729 G>A maps to NM_001005271.2 G1271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:6707537 C>T maps to ENST00000309577 Q512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:6709723 G>A maps to ENST00000309577 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:6710554 C>T maps to ENST00000309577 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:6702752 G>A maps to ENST00000309577 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:6701668 C>T maps to ENST00000309577 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:6687280 A>G maps to ENST00000309577 N1742N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:6696606 A>G maps to ENST00000309577 N1274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr12:6705224 C>T maps to ENST00000309577 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr1:6228281 C>T maps to NM_015557.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr1:6209102 G>A maps to NM_015557.2 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:6203924 C>T maps to NM_015557.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr1:6188195 G>A maps to NM_015557.2 D1271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:6181216 C>T maps to NM_015557.2 E1620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr1:6188946 G>A maps to NM_015557.2 D1190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:6184143 G>A maps to NM_015557.2 N1521N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:6171833 C>T did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr1:6184071 C>T maps to NM_015557.2 S1545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr1:6203924 C>T maps to NM_015557.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:6204193 C>T maps to NM_015557.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr1:6209102 G>A maps to NM_015557.2 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:6188946 G>A maps to NM_015557.2 D1190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:6202355 C>T maps to NM_015557.2 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr20:40141529 A>G maps to NM_032221.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:40033232 C>A maps to NM_032221.3 *2716Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr20:40084601 T>C maps to NM_032221.3 K949K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:40161759 C>T maps to NM_032221.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:40141630 G>A maps to NM_032221.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr20:40050300 T>C maps to NM_032221.3 E1658E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:40112129 G>A maps to NM_032221.3 R763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr20:40045272 T>C maps to NM_032221.3 E2147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:40161693 C>T maps to NM_032221.3 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr20:40044083 T>C maps to NM_032221.3 P2227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:40050468 G>A maps to NM_032221.3 N1602N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr20:40054020 G>A maps to NM_032221.3 S1381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr20:40050300 T>C maps to NM_032221.3 E1658E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr20:40050300 T>C maps to NM_032221.3 E1658E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr20:40081483 G>A maps to NM_032221.3 S1073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr20:40033916 T>C maps to NM_032221.3 P2488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr20:40120390 G>A maps to NM_032221.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr20:40141529 A>G maps to NM_032221.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr20:40141529 A>G maps to NM_032221.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr20:40034130 T>C did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr20:40112057 A>G maps to NM_032221.3 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr8:61750654 A>G maps to NM_017780.2 K1458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:61655556 C>T maps to NM_017780.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:61767018 C>T maps to NM_017780.2 D2291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:61763049 A>C did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr8:61655121 C>T maps to NM_017780.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr8:61655105 C>A maps to NM_017780.2 S372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr8:61655610 C>A maps to NM_017780.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:61735062 C>T maps to NM_017780.2 R987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:61655505 G>A maps to NM_017780.2 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr8:61750654 A>G maps to NM_017780.2 K1458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr8:61754291 T>C maps to NM_017780.2 D1541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr8:61750654 A>G maps to NM_017780.2 K1458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:61732564 G>A did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr8:61750654 A>G maps to NM_017780.2 K1458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr8:61655058 C>T maps to NM_017780.2 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr8:61654491 G>A maps to NM_017780.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr8:61765976 T>C maps to NM_017780.2 S2231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:61729018 C>T maps to NM_017780.2 R858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr14:21870223 T>C maps to NM_001170629.1 E1318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr14:21868667 G>A maps to NM_001170629.1 L1492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr14:21896410 A>G maps to NM_001170629.1 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:21896332 T>C maps to NM_001170629.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr14:21870530 A>T maps to NM_001170629.1 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr14:21871753 G>A maps to NM_001170629.1 Q1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr14:21870223 T>C maps to NM_001170629.1 E1318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr14:21870223 T>C maps to NM_001170629.1 E1318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr14:21876695 A>G maps to NM_001170629.1 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:21868712 G>A maps to NM_001170629.1 R1477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:53276847 C>T maps to ENST00000219084 R992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:53261309 G>A maps to ENST00000219084 E682E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:53308164 G>T maps to ENST00000219084 E1640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr16:53283785 C>T maps to ENST00000219084 Y1223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr16:53272300 C>T maps to ENST00000219084 Q894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr16:53301836 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:53358449 T>C maps to ENST00000219084 T2779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:53851887 T>C maps to NM_018397.4 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr3:53857750 C>A maps to NM_018397.4 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:53857399 C>T maps to NM_018397.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:125525191 A>T maps to NM_001274.4 K470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr11:125503112 T>C maps to NM_001274.4 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr22:29092945 A>G maps to NM_001005735.1 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr22:29091780 C>A maps to NM_001005735.1 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr22:29092945 A>G maps to NM_001005735.1 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:16643557 G>A maps to NM_006387.5 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:16638926 G>A maps to NM_006387.5 D423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:16646424 C>T maps to NM_006387.5 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr19:16643944 C>T maps to NM_006387.5 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:16641461 G>A maps to NM_006387.5 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:133430077 G>A maps to NM_001161344.1 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:93398721 G>A maps to NM_001275.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr14:93397925 G>A maps to NM_001275.3 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr20:5903380 T>C maps to NM_001819.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr20:5897521 C>T maps to NM_001819.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:5904742 C>T maps to NM_001819.2 D651D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:5897512 G>A maps to NM_001819.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:203149762 G>A maps to NM_001276.2 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:203151977 T>C maps to NM_001276.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:111773481 C>T maps to NM_004000.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:111781397 T>C maps to NM_004000.2 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:111781433 C>A maps to NM_004000.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:72783404 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:72900806 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:72804305 A>C did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:72899158 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:904729 G>A maps to NM_001142676.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:203186052 C>T maps to NM_003465.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:203186949 C>T maps to NM_003465.2 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:67837722 C>A maps to NM_001277.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:51017684 C>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:51020755 G>A maps to NM_005198.4 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:391203 C>T maps to NM_006614.2 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:424338 G>T maps to NM_006614.2 E721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:432639 A>C maps to NM_006614.2 I863I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr3:424220 C>A maps to NM_006614.2 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:439979 G>A maps to NM_006614.2 P1055P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:439919 C>A maps to NM_006614.2 I1035I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:433472 T>C maps to NM_006614.2 Y969Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:402096 T>C maps to NM_006614.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:431044 G>A maps to NM_006614.2 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:386386 A>G maps to NM_006614.2 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:391167 C>T maps to NM_006614.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:85236775 A>G did not map to a codon.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr23:85236775 A>G did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:85302516 G>A did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:85236775 A>G did not map to a codon.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr1:241797526 A>G maps to NM_001821.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr1:241797526 A>G maps to NM_001821.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:241798756 G>A maps to NM_001821.3 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:241797526 A>G maps to NM_001821.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr1:241798261 C>T maps to NM_001821.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr1:241797184 A>G maps to NM_001821.3 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr1:241797526 A>G maps to NM_001821.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:241798042 T>C maps to NM_001821.3 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr1:241797184 A>G maps to NM_001821.3 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr1:241797526 A>G maps to NM_001821.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:241797526 A>G maps to NM_001821.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr19:59065486 G>A maps to NM_014453.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:87294926 C>T maps to NM_014043.3 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr3:87294928 A>G maps to NM_014043.3 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:87302593 C>T maps to NM_014043.3 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr14:24680706 C>T maps to NM_014169.3 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr14:24679118 T>C maps to NM_014169.3 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr14:24679118 T>C maps to NM_014169.3 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:32438838 G>A maps to NM_176812.4 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr20:32436294 T>A maps to NM_176812.4 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr8:82667602 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr8:82667603 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:33267861 G>A maps to NM_016410.5 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:78970841 C>T maps to NM_024591.4 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:175665002 G>A maps to NM_001822.4 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:175809627 G>T maps to NM_001822.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:29535644 G>T maps to NM_004067.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr7:29519893 G>A maps to NM_001039936.1 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr7:29546871 T>C maps to NM_004067.2 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr21:19638303 T>C maps to NM_024944.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr21:19635156 C>T maps to NM_024944.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr21:19632556 A>T maps to NM_024944.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr21:19628896 C>T maps to NM_024944.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:89944397 C>A maps to NM_012124.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:89948398 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:220405769 C>T maps to NM_024536.5 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:150934602 C>A maps to NM_019015.1 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:150932388 C>T maps to NM_019015.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:150935229 C>T maps to NM_019015.1 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr12:102091872 G>A maps to NM_020244.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:102091869 C>A maps to NM_020244.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:184106749 C>T maps to NM_003741.2 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr23:110002960 G>A did not map to a codon.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr23:109919584 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:109919532 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:109919545 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:110006013 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:109931855 T>C did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:109943894 G>A did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr23:109937494 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:74415609 G>A maps to NM_015424.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:74429833 G>A maps to NM_015424.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:74417543 C>T maps to NM_015424.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:74421965 G>A maps to NM_015424.3 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr11:74417543 C>T maps to NM_015424.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:74407599 A>G maps to NM_015424.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:74413953 C>T maps to NM_015424.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:30659719 G>A maps to NM_139320.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:30664536 G>A maps to NM_139320.1 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr11:62677984 G>C maps to NM_000738.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:62677423 G>T maps to NM_000738.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr7:136700562 T>C maps to NM_001006628.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:136699791 C>A maps to NM_001006628.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:136700565 G>A maps to NM_001006628.1 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:136700116 A>C maps to NM_001006628.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr7:136700424 T>C maps to NM_001006628.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr7:136699767 C>A maps to NM_001006628.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:240071647 C>T maps to NM_000740.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:240071377 C>A maps to NM_000740.2 Y209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:240071263 G>A maps to NM_000740.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:240071911 C>T maps to NM_000740.2 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr1:240071632 A>G maps to NM_000740.2 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr1:240072214 A>G maps to NM_000740.2 K488K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:46407882 C>T maps to NM_000741.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:34355952 T>G maps to NM_012125.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr15:34355343 T>C maps to NM_012125.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr15:34355343 T>A maps to NM_012125.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:175618345 G>T maps to NM_001039523.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:175613343 G>A maps to NM_001039523.2 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:175618366 G>A maps to NM_001039523.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr2:175619027 G>T maps to NM_001039523.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr11:3687609 G>A maps to NM_020402.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:27320981 C>T maps to NM_000742.3 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr8:27320962 G>A maps to NM_000742.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:27321404 G>A maps to NM_000742.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:27321035 G>A maps to NM_000742.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:27321002 C>T maps to NM_000742.3 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:27320975 G>A maps to NM_000742.3 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:78893596 C>A maps to NM_000743.4 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr15:78894482 C>T maps to NM_000743.4 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr15:78893930 G>T maps to NM_000743.4 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:61981544 C>T maps to NM_000744.5 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr20:61982030 G>C maps to NM_000744.5 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:61981868 G>T maps to NM_000744.5 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:61987737 G>A maps to NM_000744.5 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:61982081 G>A maps to NM_000744.5 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr15:78882284 T>C maps to NM_000745.3 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:78880726 A>C maps to NM_000745.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr8:42611522 C>T maps to NM_004198.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:42611558 G>T maps to NM_004198.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:42623558 C>T maps to NM_004198.3 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:32455436 C>T maps to NM_001190455.1 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr4:40356407 C>T maps to NM_017581.2 D437D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:40351147 C>T maps to NM_017581.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:40350913 T>G maps to NM_017581.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr4:40351168 G>A maps to NM_017581.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:7350400 C>T maps to NM_000747.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:7358652 C>T maps to NM_000747.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:7348649 C>T maps to NM_000747.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:7349402 G>T maps to NM_000747.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:7358670 G>T maps to NM_000747.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:7350195 C>T maps to NM_000747.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr17:7358670 G>A maps to NM_000747.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:154543991 C>T maps to NM_000748.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:154544282 G>A maps to NM_000748.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:154544000 G>A maps to NM_000748.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:154543670 C>T maps to NM_000748.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:154543739 G>A maps to NM_000748.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr1:154544273 G>A maps to NM_000748.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr8:42586824 C>T maps to NM_000749.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr8:42587258 C>A maps to NM_000749.3 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:233398973 C>A maps to NM_000751.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:233393336 C>T maps to NM_000751.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:233393270 C>T maps to NM_000751.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:233393216 C>T maps to NM_000751.1 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:4805560 G>A maps to NM_000080.3 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:4804387 C>T maps to NM_000080.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:4805382 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:4804128 C>T maps to NM_000080.3 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:233406137 C>T maps to NM_005199.4 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:233407186 C>T maps to NM_005199.4 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:45672014 G>A maps to NM_003654.4 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr11:45671651 C>T maps to NM_003654.4 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr11:45672136 G>T maps to NM_003654.4 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:45672317 G>T maps to NM_003654.4 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr11:45671645 G>A maps to NM_003654.4 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:101012005 C>T maps to NM_004854.3 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:101014520 G>A maps to NM_004854.3 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr12:105151190 C>T maps to NM_018413.5 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:105150989 C>T maps to NM_018413.5 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:105151088 C>T maps to NM_018413.5 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:105151346 C>T maps to NM_018413.5 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr12:105150995 C>T maps to NM_018413.5 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr7:2472882 G>A maps to NM_018641.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:2473275 C>T maps to NM_018641.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:2472369 G>A maps to NM_018641.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:126260703 C>T maps to NM_152889.1 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:126261393 C>T maps to NM_152889.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:125805554 G>A maps to NM_015892.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr10:125805629 C>T maps to NM_015892.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:125780804 G>A maps to NM_015892.3 C438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:125805395 G>A maps to NM_015892.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:125771978 C>T maps to NM_015892.3 G455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:142840470 C>T maps to NM_004267.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:142841088 G>A maps to NM_004267.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr3:142840374 C>T maps to NM_004267.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:142840875 G>A maps to NM_004267.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:73767766 C>T maps to NM_004273.4 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:73768120 C>T maps to NM_004273.4 C444C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:71571005 A>G maps to NM_001166395.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:71571272 G>A maps to NM_001166395.1 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:71571150 C>T maps to NM_001166395.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:71571458 C>T maps to NM_001166395.1 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:75512724 G>T maps to NM_021615.4 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:34263070 G>A maps to NM_022467.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:34263625 C>T maps to NM_022467.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr18:24496306 A>G maps to NM_031422.4 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:24496846 T>A maps to NM_031422.4 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr15:101718591 G>A maps to NM_014918.4 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr15:101775529 G>A maps to NM_014918.4 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr15:101717888 G>A maps to NM_014918.4 R705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:101775583 G>A maps to NM_014918.4 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:101718210 G>A maps to NM_014918.4 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:101717849 G>A maps to NM_014918.4 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:101775430 G>A maps to NM_014918.4 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:129243878 T>C maps to NM_175856.4 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr5:129244010 C>T maps to NM_175856.4 C348C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:129520719 G>T maps to NM_175856.4 G629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:129521408 C>T maps to NM_175856.4 F858F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr5:129521387 A>G maps to NM_175856.4 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:129521386 T>A maps to NM_175856.4 L851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:129521385 T>C maps to NM_175856.4 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:841900 C>T maps to ENST00000317063 H580H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:840569 T>C maps to ENST00000317063 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:101982693 C>A maps to NM_001278.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:101967041 A>G maps to NM_001278.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr10:101961843 C>T did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr10:101966985 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:96936923 G>A maps to NM_004804.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:57466419 G>A maps to NM_020313.2 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:57474720 G>A maps to NM_020313.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:90775480 G>A maps to NM_006384.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:78398175 G>A maps to NM_006383.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:78403504 A>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:16275686 C>A maps to NM_054113.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr19:42791863 C>T maps to NM_015125.3 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:42795130 C>A maps to NM_015125.3 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:42795708 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:42797189 C>T maps to NM_015125.3 I1184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr19:42797277 C>T maps to NM_015125.3 R1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:42791818 C>T maps to NM_015125.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:42794804 C>T maps to NM_015125.3 Q629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:42794789 G>T maps to NM_015125.3 G624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr18:12277217 A>G maps to ENST00000342845 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr18:12274237 C>T maps to ENST00000342845 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:24775268 G>A maps to NM_014430.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr14:24776696 C>T maps to NM_014430.2 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:11001394 C>T maps to NM_000246.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:11001149 C>A maps to NM_000246.3 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr16:10995943 C>T maps to NM_000246.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr16:11001349 G>A maps to NM_000246.3 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:11001451 C>T maps to NM_000246.3 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:10996513 G>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:11016290 C>T maps to NM_000246.3 A1087A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr15:65490721 T>C maps to NM_003613.3 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr15:65489347 G>A maps to NM_003613.3 L1092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:65489950 C>T maps to NM_003613.3 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:19654601 C>T maps to NM_153221.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:19655093 C>T maps to NM_153221.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:19654874 C>T maps to NM_153221.2 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:19654649 C>T maps to NM_153221.2 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:19655507 C>T maps to NM_153221.2 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:19656443 C>T maps to NM_153221.2 Y1030Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:175213352 G>A maps to NM_004882.3 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:175213289 T>A maps to NM_004882.3 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr2:175213551 C>T maps to NM_004882.3 E342E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:69167421 C>T maps to NM_032830.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:69184453 C>T maps to NM_032830.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:120168425 G>A maps to ENST00000392521 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:120168377 C>T maps to ENST00000392521 K1136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:120172008 G>A maps to ENST00000392521 R1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:120139748 T>C maps to ENST00000392521 S1773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:120135612 C>T maps to ENST00000392521 P1911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:120156209 G>T maps to ENST00000392521 A1336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:120172993 G>A maps to ENST00000392521 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:120263121 C>T maps to ENST00000392521 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:120173111 A>G maps to ENST00000392521 A1003A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:120156060 G>T maps to ENST00000392521 S1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:71521713 G>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr9:130941072 C>T maps to NM_012127.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:130931779 G>A maps to NM_012127.2 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:130941027 G>A maps to NM_012127.2 C486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr9:130931405 G>A maps to NM_012127.2 F740F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:130941072 C>T maps to NM_012127.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:130928628 G>A maps to NM_012127.2 C848C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:53049245 C>T maps to NM_001098525.1 C674C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr13:53049041 G>A maps to NM_001098525.1 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:53047982 T>G maps to NM_001098525.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:113514136 C>A maps to NM_152515.3 G271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:106633422 C>T maps to NM_006825.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:46829613 G>A maps to ENST00000415402 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:46818454 G>A maps to ENST00000415402 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:46799748 C>T maps to ENST00000415402 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:103986540 C>T maps to NM_001823.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:45818753 C>T maps to NM_001824.3 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:45818834 A>G maps to NM_001824.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:80553566 G>A maps to NM_001825.2 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:80550933 C>T maps to NM_001825.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:80555015 G>A maps to NM_001825.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:122215333 C>T did not map to a codon.
Alternatively spliced codon TCGA-AA-3845-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:122125290 C>T maps to NM_015282.2 P1253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:122120866 G>A maps to NM_015282.2 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:122106150 G>A maps to NM_015282.2 V1450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:122363376 G>T maps to NM_015282.2 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:122227525 G>A maps to NM_015282.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:122104658 G>A maps to NM_015282.2 I1495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:122205894 C>T maps to NM_015282.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:122106125 G>A maps to NM_015282.2 L1459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:33617753 C>T maps to ENST00000359576 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:33644563 G>A maps to ENST00000359576 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:33592746 C>T maps to ENST00000359576 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:33648168 A>G maps to ENST00000359576 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:33725897 T>C maps to ENST00000359576 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:33725897 T>C maps to ENST00000359576 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:33725897 T>C maps to ENST00000359576 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:40224963 C>A maps to NM_001828.4 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:86942143 C>G maps to NM_001285.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:86965353 C>A maps to NM_001285.3 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:86959937 G>A maps to NM_001285.3 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:86939147 C>T maps to NM_001285.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:86959125 G>A maps to NM_001285.3 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:86959134 C>T maps to NM_001285.3 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr1:86904725 G>A maps to NM_006536.5 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr1:86890004 A>G maps to NM_006536.5 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:86907189 C>A maps to NM_006536.5 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:86919104 C>T maps to NM_006536.5 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:86906007 G>T maps to NM_006536.5 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:86919157 A>G maps to NM_006536.5 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:86889956 T>G maps to NM_006536.5 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:86909467 A>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:86896605 T>C maps to NM_006536.5 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:87033231 C>T maps to ENST00000263723 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:87045799 C>T maps to ENST00000263723 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:87025690 T>G maps to ENST00000263723 L79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:109482714 G>T maps to NM_001048210.1 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr1:109479935 C>T maps to NM_001048210.1 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:109482711 A>G maps to NM_001048210.1 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr7:143018910 C>G maps to NM_000083.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:143036629 G>T maps to NM_000083.2 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr7:143036694 T>C maps to NM_000083.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:143048991 C>T maps to NM_000083.2 A967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:143027959 C>T maps to NM_000083.2 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr7:143028356 C>T maps to NM_000083.2 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:184076072 C>T maps to NM_004366.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:170634338 C>T maps to NM_173872.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:170641110 C>T maps to NM_173872.2 D832D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr4:170608810 C>T maps to NM_173872.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:10166059 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:10153201 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:10181807 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:10181920 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:10153086 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:10176181 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:10176426 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr23:10188914 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:10153088 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:10155556 C>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:10165983 C>T did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:10153170 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:10181921 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:10181909 A>G did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:10176319 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:10166076 T>C did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:49851178 A>G did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:49834583 G>T did not map to a codon.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr23:49855334 C>T did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr23:49855381 G>A did not map to a codon.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr23:49855021 T>G did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:49855486 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:49855518 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:49834627 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:49851136 C>T did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:49851064 C>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:49856789 T>C did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:49851177 G>A did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:49851178 A>G did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:49851178 A>G did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr23:49845318 C>T did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:49854897 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:49851436 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:11875968 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:11898405 G>A maps to ENST00000376496 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr1:11898420 C>T maps to ENST00000376496 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:11894382 C>T maps to ENST00000376496 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:1498421 G>A maps to ENST00000382745 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:16356550 C>T maps to NM_004070.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:16353270 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:16355652 C>T maps to NM_004070.3 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:16359705 C>T maps to NM_004070.3 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr3:190026191 A>G maps to NM_021101.4 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr3:190026191 A>G maps to NM_021101.4 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr3:190026191 A>G maps to NM_021101.4 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr13:96086239 C>T maps to NM_182848.3 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr13:96086272 A>G maps to NM_182848.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr13:96086270 C>T maps to NM_182848.3 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr13:96205228 T>C did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:170141077 G>A maps to NM_005602.5 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:170141026 T>C maps to NM_005602.5 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:170137081 T>C did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:170141026 T>C maps to NM_005602.5 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr3:170141026 T>C maps to NM_005602.5 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:90042334 C>A maps to NM_001185072.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:90042043 C>T maps to NM_001185072.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr3:190126232 T>C maps to NM_006580.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:190126223 C>T maps to NM_006580.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr3:190126232 T>C maps to NM_006580.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr21:31538884 G>A maps to NM_012131.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr21:31538769 G>A maps to NM_012131.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr21:31538356 T>C maps to NM_012131.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr21:31538769 G>A maps to NM_012131.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr3:137742516 C>T maps to NM_016369.3 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:137742518 A>G maps to NM_016369.3 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:43205542 G>A maps to NM_148960.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:106172005 T>A did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:106171623 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:184240786 A>C maps to NM_001111319.1 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:8560090 C>T maps to NM_194284.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr21:31587808 G>T maps to NM_199328.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:31587592 G>A maps to NM_199328.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr21:31588177 C>A maps to NM_199328.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr21:31588018 C>T maps to NM_199328.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:31587853 G>A maps to NM_199328.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr19:51870762 G>A maps to NM_152353.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr17:6978411 G>A maps to NM_182906.2 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:51227301 C>T maps to NM_002975.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr19:51228699 C>A maps to NM_002975.2 Y316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:10165459 G>A maps to NM_001129998.1 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:38724258 G>A maps to NM_175060.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr14:38724588 A>G maps to NM_175060.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr14:38724648 G>A maps to NM_175060.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:38723829 G>A maps to NM_175060.1 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:38724798 G>A maps to NM_175060.1 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:38724741 G>A maps to NM_175060.1 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:38724075 A>C maps to NM_175060.1 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:38724540 G>A maps to NM_175060.1 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr14:38724945 G>A maps to NM_175060.1 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr14:38725218 C>T maps to NM_175060.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:11118701 C>T maps to ENST00000409790 H487H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr16:11056398 G>A maps to ENST00000409790 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:11217663 G>A maps to ENST00000409790 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:11272258 G>T maps to ENST00000409790 T958T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:11217624 C>T maps to ENST00000409790 D765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:11154757 G>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr16:11073214 G>A maps to ENST00000409790 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr16:74444803 G>A maps to NM_001011880.2 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:70219799 C>T maps to NM_173619.2 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:70211280 G>A maps to NM_173619.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr12:10233935 G>T maps to NM_016511.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:10233935 G>T maps to NM_016511.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:10150920 G>A maps to NM_016509.3 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr12:10005898 T>G maps to NM_005127.2 *150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:10010171 G>A maps to NM_005127.2 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:9847445 T>C maps to NM_013269.4 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:45077289 C>T maps to NM_003278.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:45077262 C>T maps to NM_003278.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:8276482 G>A maps to NM_016184.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr12:7894076 G>A maps to NM_130441.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:8670799 A>T maps to NM_080387.4 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr12:8687239 A>G maps to NM_014358.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:71036483 T>C maps to NM_173535.2 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:71044223 C>A maps to NM_173535.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:71044211 G>A maps to NM_173535.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:71036485 T>A maps to NM_173535.2 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:7794925 G>A maps to NM_198492.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:7830500 A>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:7830086 C>T maps to NM_014257.4 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:7831626 C>T maps to NM_014257.4 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:7830569 C>T maps to NM_014257.4 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:141645174 G>A maps to NM_013252.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:8608721 G>A maps to NM_001007033.1 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:10277931 G>T maps to NM_197947.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:10277931 G>T maps to NM_197947.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr12:10218212 G>A maps to NM_207345.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr12:10206913 G>T maps to NM_207345.2 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:141321544 G>A maps to NM_004362.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:141321658 T>C maps to NM_004362.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr4:141321658 T>C maps to NM_004362.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr4:141321658 T>C maps to NM_004362.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr4:141311796 A>T maps to NM_004362.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr4:141321658 T>C maps to NM_004362.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:141315039 T>C maps to NM_004362.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:141321658 T>C maps to NM_004362.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:154508601 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:154507218 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:154507218 G>A did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:154507271 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:154507271 G>C did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr23:154507269 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:154528178 G>A did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:154507271 G>A did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:154507332 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:139889216 C>T maps to NM_004669.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:139890989 C>T maps to NM_004669.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:25140617 G>A maps to NM_013943.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:25167302 G>T maps to NM_013943.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:45870986 C>T maps to NM_001114086.1 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:46047838 A>G maps to NM_001114086.1 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:45917075 C>T maps to NM_001114086.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr21:36079612 G>A maps to ENST00000360731 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr21:36080253 C>T maps to ENST00000360731 D517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr21:36079612 G>A maps to ENST00000360731 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:36042631 C>T maps to ENST00000360731 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:157214830 T>C maps to NM_001195555.1 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:122763670 G>A maps to ENST00000302528 D1223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr12:122812505 G>A maps to ENST00000302528 A1079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr12:122821268 C>T maps to ENST00000302528 Q826Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:122862148 C>T maps to ENST00000302528 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:122801299 C>A maps to ENST00000302528 E1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr12:122864918 C>T maps to ENST00000302528 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:122825727 C>A maps to ENST00000302528 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr12:122862273 G>T maps to ENST00000302528 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:73752919 C>T maps to NM_003388.4 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:73790404 G>A maps to NM_003388.4 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:73770751 C>T maps to NM_003388.4 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:73770772 C>T maps to NM_003388.4 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:73795176 G>A maps to NM_003388.4 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:36517491 C>T maps to NM_015526.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:29386761 C>T maps to ENST00000379543 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:29356671 G>A maps to ENST00000379543 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:29386761 C>T maps to ENST00000379543 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:201726142 G>A maps to NM_001162407.1 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr2:201722694 C>G did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:155239278 C>T maps to ENST00000368361 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:155233077 A>C maps to ENST00000368361 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:74911639 C>T maps to NM_001130028.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr15:74914534 C>T maps to NM_001130028.1 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:178050266 C>A maps to NM_020666.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:178045724 G>A maps to NM_020666.2 Y72Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:92818614 T>C maps to NM_001025233.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:92821891 C>A maps to NM_001025232.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:95669363 G>A maps to NM_024734.3 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:95679560 C>T maps to NM_024734.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:95677179 C>T maps to NM_024734.3 W215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr14:95670422 C>T maps to NM_024734.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:28495333 C>T maps to NM_000086.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr16:28488848 G>T maps to NM_000086.2 C435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:77569309 C>T maps to NM_006493.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:77570182 C>T maps to NM_006493.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr15:68506660 G>T maps to NM_017882.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr8:1719231 G>A maps to NM_018941.3 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:10567678 C>T maps to NM_052964.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:10542209 C>T maps to NM_052964.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:10567678 C>T maps to NM_052964.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:10509651 C>T maps to NM_052964.2 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:77336028 C>A maps to NM_001293.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr11:77340940 G>A maps to NM_001293.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:56344993 G>A maps to NM_004898.2 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:56325369 C>T maps to NM_004898.2 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:57427142 T>A maps to NM_006831.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr11:57427502 G>A maps to NM_006831.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:57427373 C>T maps to NM_006831.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:57427284 C>T maps to NM_006831.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:57427451 C>T maps to NM_006831.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr11:57427142 T>C maps to NM_006831.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:57427284 C>T maps to NM_006831.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:72005086 G>A maps to NM_030813.3 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:6364547 C>T maps to NM_006012.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:6361601 T>A maps to NM_006012.2 L6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:45495924 C>T maps to NM_001294.2 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:65472540 A>G maps to NM_006660.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:65445959 A>T maps to NM_006660.3 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr15:65451078 C>T maps to NM_006660.3 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:65445919 G>A maps to NM_006660.3 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:150645836 G>A maps to NM_001195794.1 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:150645761 G>A maps to NM_001195794.1 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:150690294 G>A maps to NM_001195794.1 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:17528581 C>T maps to NM_001079827.2 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:17528461 C>T maps to NM_001079827.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:17528581 C>T maps to NM_001079827.2 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:129676640 C>T maps to NM_152311.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr1:36226050 G>T maps to NM_022111.3 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:36226200 C>A maps to NM_022111.3 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr1:36230087 G>A maps to NM_022111.3 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:36204751 G>A maps to NM_022111.3 R1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr1:36226697 T>A maps to NM_022111.3 K335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr1:36226155 G>A maps to NM_022111.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr1:36202123 T>A maps to NM_022111.3 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:36202123 T>C maps to NM_022111.3 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr1:36202125 G>T maps to NM_022111.3 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr1:9809561 G>A maps to NM_001009566.1 C314C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:9791437 G>A maps to NM_001009566.1 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:9791918 G>A maps to NM_001009566.1 H821H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:9796070 G>A maps to NM_001009566.1 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:9833432 C>T maps to NM_001009566.1 W37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:140282007 T>C maps to NM_022131.2 H815H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr3:140281148 C>T maps to NM_022131.2 Y737Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:140284986 C>T maps to NM_022131.2 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:140167445 C>T maps to NM_022131.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr3:140275464 G>A maps to NM_022131.2 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:140140114 A>G maps to NM_022131.2 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr3:140281017 T>C maps to NM_022131.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr3:140281949 C>G maps to NM_022131.2 S796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:140122615 C>A maps to NM_022131.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr12:7295516 C>T maps to NM_014718.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:7295477 G>A maps to NM_014718.3 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr12:7289473 C>T maps to NM_014718.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:7285728 G>A maps to NM_014718.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:7310121 C>T maps to NM_014718.3 C855C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:7295790 C>T maps to NM_014718.3 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:57759016 G>T maps to NM_004859.3 E1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:57759750 G>T maps to NM_004859.3 E1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:57771128 C>T maps to NM_004859.3 A1648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:19241745 C>T maps to NM_007098.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:19241681 C>A maps to NM_007098.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:27457476 G>A maps to NM_001831.2 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:27462567 C>T maps to NM_001831.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr8:27468058 C>T maps to NM_001831.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr8:27462576 G>C maps to NM_001831.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:27462567 C>T maps to NM_001831.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:3573214 C>T maps to NM_015041.1 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:3586165 C>T maps to NM_015041.1 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:3586165 C>T maps to NM_015041.1 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:3554745 G>T maps to NM_015041.1 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr18:618059 C>T maps to NM_199167.1 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:625016 C>A maps to NM_199167.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:618036 C>T maps to NM_199167.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr18:644983 T>C maps to NM_199167.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr18:644983 T>C maps to NM_199167.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr18:644983 T>C maps to NM_199167.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:62366811 T>C did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr6:123369831 G>C maps to NM_001010852.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:123319161 G>A maps to NM_001010852.2 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr14:24975713 A>C maps to NM_001836.2 Y102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:22218238 A>G maps to NM_018686.3 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:10282398 G>A maps to NM_138809.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:10290709 C>T maps to NM_138809.3 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:28304851 G>A maps to NM_182523.1 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:28304842 C>A maps to NM_182523.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:28357879 G>T maps to NM_182523.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:81737545 C>T maps to NM_198390.2 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:81703764 C>T maps to NM_198390.2 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr12:108686028 T>G maps to NM_001142344.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:108686130 C>T maps to NM_001142344.1 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:108685815 G>A maps to NM_001142344.1 N308N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr12:108685923 G>T maps to NM_001142344.1 C272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:47840642 G>A maps to NM_016308.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:47834242 G>T maps to NM_016308.2 G92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:47840866 A>G did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr16:66620968 C>T maps to NM_144673.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr16:66620925 T>C maps to NM_144673.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr16:66670373 G>A maps to NM_178818.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr16:66670388 C>T maps to NM_178818.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr14:23847589 G>A maps to ENST00000339180 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:23847619 G>A maps to ENST00000339180 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:32495739 C>T maps to NM_138410.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:79030635 T>C maps to NM_153610.3 S2016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:79089265 G>A maps to NM_153610.3 P3932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:79031887 C>T maps to NM_153610.3 Q2434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:79030575 A>G maps to NM_153610.3 L1996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:79028223 T>C maps to NM_153610.3 D1212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:79034571 C>T maps to NM_153610.3 D3328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr5:79033164 C>T maps to NM_153610.3 S2859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:79030692 T>C maps to NM_153610.3 D2035D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:79054674 C>A maps to NM_153610.3 S3737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr5:79035025 G>T maps to NM_153610.3 E3480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:79028706 C>T maps to NM_153610.3 I1373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:79028018 C>A maps to NM_153610.3 S1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:79048549 G>A maps to NM_153610.3 A3681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:79034790 C>T maps to NM_153610.3 I3401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr5:79031241 T>C maps to NM_153610.3 D2218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:79027414 G>T maps to NM_153610.3 G943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:79026351 T>G maps to NM_153610.3 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:79029378 G>A maps to NM_153610.3 E1597E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:79030901 C>A maps to NM_153610.3 S2105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:79031640 C>T maps to NM_153610.3 I2351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:79025121 C>T maps to NM_153610.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:79033074 C>T maps to NM_153610.3 N2829N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:79027038 T>C maps to NM_153610.3 N817N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:79029480 G>A maps to NM_153610.3 P1631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:79032747 T>G maps to NM_153610.3 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:79089358 C>A maps to NM_153610.3 S3963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr8:88249246 G>A maps to NM_173538.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:87878803 T>C maps to NM_173538.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:88296958 G>A maps to NM_173538.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:88296958 G>A maps to NM_173538.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:88365928 C>T maps to NM_173538.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr8:87878809 A>T maps to NM_173538.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr18:72226559 G>A maps to NM_032649.5 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr18:72247373 A>G maps to NM_032649.5 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:72244254 C>T maps to NM_032649.5 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:72223646 G>A maps to NM_032649.5 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr18:72173169 C>T maps to NM_018235.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr18:72179720 C>T maps to NM_018235.2 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr18:72168607 G>A maps to NM_018235.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:47954624 G>A maps to NM_001142564.1 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr4:47953377 T>A maps to NM_001142564.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:47953470 A>G maps to NM_001142564.1 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr4:47945298 T>C maps to NM_001142564.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr4:47945298 T>C maps to NM_001142564.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr4:47945298 T>C maps to NM_001142564.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:150908120 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:150906983 G>A did not map to a codon.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr23:150906961 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:150911725 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:150909268 G>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:150907321 C>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:150912169 C>T did not map to a codon.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr23:150912868 C>T did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:150911599 A>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:150912169 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:150908041 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:150912063 C>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:99013246 C>T maps to NM_001298.2 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:99012373 G>A maps to NM_001298.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:99006147 C>T maps to NM_001298.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:99013441 G>A maps to NM_001298.2 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:99012778 C>T maps to NM_001298.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:98996736 C>T maps to NM_001298.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr2:99013219 G>T maps to NM_001298.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:99013477 G>A maps to NM_001298.2 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:98994254 G>T maps to NM_001298.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:6261461 C>T maps to NM_001037329.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:6261770 C>T maps to NM_001037329.2 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:6261476 C>T maps to NM_001037329.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:6265402 C>T maps to NM_001037329.2 R498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:6261722 C>T maps to NM_001037329.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr11:6261854 G>A maps to NM_001037329.2 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr11:6261905 C>T maps to NM_001037329.2 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr16:57921800 G>A maps to NM_001297.4 A1140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:57954315 G>T maps to NM_001297.4 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:57991250 G>A maps to NM_001297.4 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr16:57935473 G>A maps to NM_001297.4 I950I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr16:57996883 C>T maps to NM_001297.4 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr8:87755807 C>T maps to NM_019098.4 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:87641194 G>A maps to NM_019098.4 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:87656031 T>C maps to NM_019098.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:87590933 G>A maps to NM_019098.4 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:87641171 A>C maps to NM_019098.4 Y485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:87679218 G>A maps to NM_019098.4 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr8:87683310 C>T maps to NM_019098.4 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr8:87683256 C>A maps to NM_019098.4 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:87680361 G>A maps to NM_019098.4 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr8:87623851 G>A maps to NM_019098.4 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr8:87641194 G>A maps to NM_019098.4 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:66045977 C>T maps to NM_182553.1 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:66050235 C>T maps to NM_182553.1 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:26510563 G>A maps to ENST00000374253 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:26509851 C>T maps to ENST00000374253 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:21627653 G>A did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr23:21393035 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:21534628 G>A did not map to a codon.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr23:21549996 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:21581499 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr23:21627196 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:21624993 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:21627605 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:21450737 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:21613499 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:21450749 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:21627417 C>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:21519701 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:21609137 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:21627404 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:154762476 C>T maps to NM_173515.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:154743696 A>G maps to NM_173515.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr6:154727529 G>T maps to NM_173515.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr6:154743696 A>G maps to NM_173515.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:154754626 C>T maps to NM_173515.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr6:154743696 A>G maps to NM_173515.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr6:154743696 A>G maps to NM_173515.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3517-01A-01W-0831-10 chr19:11660429 C>T maps to NM_001299.4 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr19:11651940 C>T maps to NM_001299.4 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:11657702 C>T maps to NM_001299.4 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:11660519 C>T maps to NM_001299.4 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:95367748 G>A maps to NM_001839.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:101148017 G>A maps to NM_020348.2 Q878Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:101147722 C>T maps to NM_020348.2 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:101147584 G>A maps to NM_020348.2 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr10:101120664 G>A maps to NM_020348.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:104836840 C>T maps to NM_017649.3 D844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:104835903 C>T maps to NM_017649.3 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr10:104687136 T>C maps to NM_199077.1 *553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:97493855 C>T maps to NM_017623.4 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:97492678 G>A maps to NM_017623.4 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:58585540 C>T maps to NM_016284.3 T1051T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:58573745 G>A maps to NM_016284.3 R1640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:58621722 C>T maps to NM_016284.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:58559182 C>T maps to NM_016284.3 A2228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:58608604 G>A maps to NM_016284.3 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr16:58576376 A>G maps to NM_016284.3 T1510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:58583771 C>A maps to NM_016284.3 E1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:58621755 C>T maps to NM_016284.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:58616771 A>G maps to NM_016284.3 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr16:58576376 A>G maps to NM_016284.3 T1510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:58579270 A>G maps to NM_016284.3 N1377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:32769187 T>C maps to NM_015442.1 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:32769196 A>G maps to NM_015442.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:32778971 G>T maps to NM_015442.1 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:32769187 T>C maps to NM_015442.1 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:32806234 G>A maps to NM_015442.1 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:70732479 G>A maps to NM_014515.5 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:70737927 C>T maps to NM_014515.5 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:70724189 G>A maps to NM_014515.5 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:54651971 G>A maps to NM_014516.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr19:54649748 C>G maps to NM_014516.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr19:54657463 C>T maps to NM_014516.3 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:54656702 C>T maps to NM_014516.3 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:135099951 A>G maps to NM_001190850.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:135047843 G>A maps to NM_001190850.1 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:135079000 C>T maps to NM_001190850.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr7:135047876 C>T maps to NM_001190850.1 W634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:179992871 G>A maps to NM_015455.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:179992943 C>A maps to NM_015455.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:179992865 G>A maps to NM_015455.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:78652580 G>A maps to ENST00000512485 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr8:17094734 C>T maps to NM_013354.5 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr8:17094763 C>A maps to NM_013354.5 G144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:17092329 G>A maps to NM_013354.5 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:154250218 A>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:154244778 C>T maps to NM_004779.4 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:154252120 T>C maps to NM_004779.4 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:40120696 C>T maps to NM_033133.4 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr17:40125569 C>T maps to NM_033133.4 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr17:40120327 G>A maps to NM_033133.4 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:155301672 G>A maps to NM_001103176.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:155299712 A>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:56704347 A>G maps to NM_014255.5 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr6:88854285 C>T maps to NM_016083.4 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:88853780 G>A maps to NM_016083.4 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr6:88853706 C>T maps to NM_016083.4 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:88854384 G>A maps to NM_016083.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr6:88854903 G>A maps to NM_016083.4 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:68544327 C>T maps to NM_015463.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:68544333 G>A maps to NM_015463.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:68546436 G>A maps to NM_015463.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:246754875 C>T maps to NM_152609.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:246811113 C>T maps to NM_152609.2 D537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:40951108 A>G maps to NM_173478.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:40732509 C>T maps to NM_024877.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:58390314 C>T maps to NM_000614.3 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:58391871 G>A maps to NM_000614.3 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:34564677 C>A maps to NM_147164.1 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:34557566 C>A maps to NM_147164.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:17366695 T>C maps to NM_017738.2 C656C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr9:17273795 T>C maps to NM_017738.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:17394950 G>A maps to NM_017738.2 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:41327519 G>A maps to NM_001843.2 W275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:41327514 C>T maps to NM_001843.2 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:41337803 G>A maps to NM_001843.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr12:41337804 C>T maps to NM_001843.2 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:41312457 G>T maps to NM_001843.2 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr12:41374735 G>T maps to NM_001843.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:41386997 C>T maps to NM_001843.2 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr12:41410680 T>C maps to NM_001843.2 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:41333233 G>A maps to NM_001843.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr12:41352942 C>T maps to NM_001843.2 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr12:41410680 T>C maps to NM_001843.2 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:41327657 T>C maps to NM_001843.2 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:41352950 G>A maps to NM_001843.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:205031671 C>T maps to NM_005076.3 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:205033577 G>T maps to NM_005076.3 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:205034948 C>T maps to NM_005076.3 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:205034383 T>G maps to NM_005076.3 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:205041112 G>A maps to NM_005076.3 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr1:205036253 C>T maps to NM_005076.3 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:205028275 C>T maps to NM_005076.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:205042317 C>T maps to NM_005076.3 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:74474053 C>T maps to NM_020872.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:74315782 G>A maps to NM_020872.1 S945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:74548921 G>A maps to NM_020872.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:74474038 G>A maps to NM_020872.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:74413624 T>C maps to NM_020872.1 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:74316518 C>T maps to NM_020872.1 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:74334558 C>A maps to NM_020872.1 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr3:2967364 A>G maps to NM_175607.1 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:3095579 T>C maps to NM_175607.1 D967D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:3030055 C>A maps to NM_175607.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:3030070 T>C maps to NM_175607.1 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:2861263 A>G maps to NM_175607.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:2942486 C>T maps to NM_175607.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:2928807 T>A maps to NM_175607.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:3085369 G>A maps to NM_175607.1 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:2944640 G>T maps to NM_175607.1 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:2944660 C>A maps to NM_175607.1 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:3080688 T>G did not map to a codon.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr3:3080617 C>G maps to NM_175607.1 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:2967364 A>G maps to NM_175607.1 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:100226884 T>A maps to NM_014361.2 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:99941214 C>T maps to NM_014361.2 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:100141896 T>C maps to NM_014361.2 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:100211265 C>T maps to NM_014361.2 F934F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:100064253 A>C maps to NM_014361.2 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr11:100126627 G>T maps to NM_014361.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr11:99715587 T>C maps to NM_014361.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:99945011 T>C maps to NM_014361.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:100061875 C>T maps to NM_014361.2 D533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:99715587 T>C maps to NM_014361.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:1269508 C>T maps to NM_014461.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:1371595 G>A maps to NM_014461.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:1444106 A>C maps to NM_014461.2 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:1414607 T>C maps to NM_014461.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:1424798 G>T maps to NM_014461.2 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr3:1425049 T>C maps to NM_014461.2 A825A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr3:1414073 C>A maps to NM_014461.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:40839012 C>T maps to NM_003632.2 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr17:40836222 G>A maps to NM_003632.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:40839805 C>T maps to NM_003632.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr17:40840484 C>T maps to NM_003632.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:40843524 C>T maps to NM_003632.2 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:40845417 T>C maps to NM_003632.2 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:40840915 A>T maps to NM_003632.2 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:40837367 C>A maps to NM_003632.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr7:147600792 C>T maps to NM_014141.5 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:147914605 C>G maps to NM_014141.5 V1079V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:146825924 T>C maps to NM_014141.5 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:148106516 C>T maps to NM_014141.5 G1250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:146741066 C>A maps to NM_014141.5 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:146829380 C>T maps to NM_014141.5 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:146805320 C>A maps to NM_014141.5 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:148106555 C>A maps to NM_014141.5 I1263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:147815225 C>T maps to NM_014141.5 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:146997278 C>G maps to NM_014141.5 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:147600655 G>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:146818107 A>G maps to NM_014141.5 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr7:147914437 A>G maps to NM_014141.5 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:147092737 C>T maps to NM_014141.5 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:147259320 G>A maps to NM_014141.5 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:147092860 G>T maps to NM_014141.5 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr7:147844668 C>T maps to NM_014141.5 Q881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:147869553 A>G maps to NM_014141.5 G998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr7:146818098 C>T maps to NM_014141.5 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:147844725 C>A maps to NM_014141.5 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr7:146829389 C>T maps to NM_014141.5 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr7:148112575 C>T maps to NM_014141.5 R1288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:148080918 G>A maps to NM_014141.5 P1218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:39140579 A>C maps to NM_033655.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr16:76486527 C>T maps to NM_033401.3 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr16:76569541 A>G maps to NM_033401.3 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:76569604 G>A maps to NM_033401.3 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:76513346 G>A maps to NM_033401.3 K597K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr16:76523610 C>T maps to NM_033401.3 N636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:76555104 G>T maps to NM_033401.3 E811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:76482092 C>A maps to NM_033401.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:125669090 C>T maps to NM_130773.2 R1234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:125504941 C>T maps to NM_130773.2 C737C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:125281883 C>T maps to NM_130773.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:125281922 C>T maps to NM_130773.2 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:125175106 C>T maps to NM_130773.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:124783253 C>T maps to NM_130773.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:125660582 G>A maps to NM_130773.2 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr2:125547593 C>A maps to NM_130773.2 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:125262113 C>T maps to NM_130773.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:125547596 C>T maps to NM_130773.2 C956C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:125192059 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:125367381 C>A maps to NM_130773.2 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:125367498 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr2:125175106 C>T maps to NM_130773.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr2:125521566 C>T maps to NM_130773.2 N791N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:7849086 C>G maps to NM_001037144.4 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr17:7849071 C>T maps to NM_001037144.4 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:40717717 C>T maps to NM_001042532.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:51258565 G>A maps to ENST00000395542 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:51096640 G>A maps to ENST00000395542 R800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:51203959 C>T maps to ENST00000395542 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:51111351 C>T maps to ENST00000395542 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:51095858 C>A maps to ENST00000395542 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr7:51095858 C>T maps to ENST00000395542 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr7:51095858 C>T maps to ENST00000395542 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:51095750 G>A maps to ENST00000395542 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:51111183 T>C maps to ENST00000395542 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:165578722 C>T maps to ENST00000392717 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:165561492 C>T maps to ENST00000392717 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:140166584 G>A maps to NM_015456.3 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:140150858 C>T maps to NM_015456.3 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:140166982 G>A maps to NM_015456.3 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:140166957 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:31355237 C>A maps to NM_004086.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr14:31354666 C>T maps to NM_004086.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:71193533 C>T maps to NM_018714.2 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:71197687 C>T maps to NM_018714.2 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:71197999 C>T maps to NM_018714.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:71189282 T>C maps to NM_018714.2 H25H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:230805277 C>T maps to NM_007357.2 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:230795217 C>T maps to NM_007357.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:230798931 C>T maps to NM_007357.2 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:230827252 C>T maps to NM_007357.2 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:230798924 T>C maps to NM_007357.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:46056514 G>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:46056550 C>T maps to NM_031431.2 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr13:46090288 T>C maps to NM_031431.2 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr16:70524288 G>A maps to NM_015386.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:70514999 C>T maps to NM_015386.2 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:70542316 G>A maps to NM_015386.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:107053072 A>G maps to NM_006348.3 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:107204356 G>A maps to NM_006348.3 N26N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:107167687 C>A maps to NM_006348.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:106851032 G>A maps to NM_006348.3 H802H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:106924101 G>A maps to NM_006348.3 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:106964888 T>C maps to NM_006348.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr13:40325091 C>A maps to ENST00000255468 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:40297471 C>T maps to ENST00000255468 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr13:40293401 A>G maps to ENST00000255468 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:40261742 G>T maps to ENST00000255468 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:40297567 A>G maps to ENST00000255468 K594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:23456398 G>A maps to NM_153603.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr16:23415032 C>T maps to NM_153603.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:23430122 C>T maps to NM_153603.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:69369011 G>A maps to NM_032382.4 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:69370541 C>A maps to NM_032382.4 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:55027342 C>T maps to NM_004645.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:103354141 A>T maps to NM_080629.2 P1545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:103354290 G>A maps to NM_080629.2 N1526N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:103488405 G>A maps to NM_080629.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:103491078 C>A maps to NM_080629.2 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:103470214 A>G maps to NM_080629.2 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:103343613 C>T maps to NM_080629.2 K1806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:103488536 C>A maps to NM_080629.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr1:103470187 A>G maps to NM_080629.2 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr1:103470187 A>G maps to NM_080629.2 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:103471637 C>A maps to NM_080629.2 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:103491410 G>T maps to NM_080629.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:103405990 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:103364505 T>C maps to NM_080629.2 K1389K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr1:103347318 T>C maps to NM_080629.2 V1670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:33133707 C>T maps to NM_080680.2 P1494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:33154445 T>C maps to NM_080680.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr6:33146854 G>A maps to NM_080680.2 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:33142330 A>G maps to NM_080680.2 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:33146104 G>A maps to NM_080680.2 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:33132063 C>A maps to NM_080680.2 E1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr6:33146120 G>A maps to NM_080680.2 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:33154550 G>T maps to NM_080680.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr6:75834064 C>A maps to ENST00000322507 L2210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:75858075 C>A maps to ENST00000322507 E1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:75865478 C>A maps to ENST00000322507 V1114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:75855892 C>T maps to ENST00000322507 Q1495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:75834956 C>A maps to ENST00000322507 E2165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:75799985 C>T maps to ENST00000322507 L2927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:75833082 T>C maps to ENST00000322507 T2303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr6:75892994 T>C maps to ENST00000322507 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr6:75828852 G>T maps to ENST00000322507 G2420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr6:75831095 G>A maps to ENST00000322507 D2336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:75840607 C>T maps to ENST00000322507 S2009S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr6:75855877 A>G maps to ENST00000322507 A1500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr6:75861640 G>A maps to ENST00000322507 D1314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:75839857 C>T maps to ENST00000322507 Q2053Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:71690280 A>G maps to ENST00000356340 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:121262943 G>A maps to NM_021110.1 V897V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr8:121354668 C>T maps to NM_021110.1 C1624C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr8:121322276 C>T maps to NM_021110.1 G1477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr8:121220532 T>C maps to NM_021110.1 Y418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr8:121302004 G>A maps to NM_021110.1 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr8:121344381 C>A maps to NM_021110.1 G1554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:121354656 G>A maps to NM_021110.1 A1620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr8:121354668 C>T maps to NM_021110.1 C1624C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr8:121211758 A>G maps to NM_021110.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:121239470 G>T maps to NM_021110.1 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:121243716 G>T maps to NM_021110.1 G737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:121211758 A>G maps to NM_021110.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr8:121237331 A>G maps to NM_021110.1 E581E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr8:121237331 A>G maps to NM_021110.1 E581E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:121292321 C>T maps to NM_021110.1 C1210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr9:101777748 G>T maps to NM_001855.3 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:101747904 G>A maps to NM_001855.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:101810281 G>A maps to NM_001855.3 Q931Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:101832014 C>A maps to NM_001855.3 Y1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:101785682 C>T maps to NM_001855.3 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr9:101817635 C>T maps to NM_001855.3 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:101814692 T>C maps to NM_001855.3 S976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr9:101759340 C>T maps to NM_001855.3 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:101749650 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:32137215 G>A maps to NM_001856.3 I1050I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:32151694 C>T maps to NM_001856.3 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr1:32120950 C>T maps to NM_001856.3 S1418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:32149745 C>T maps to NM_001856.3 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:32165424 G>T maps to NM_001856.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:32127272 G>T maps to NM_001856.3 L1238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:32163524 C>T maps to NM_001856.3 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:32119501 G>A maps to NM_001856.3 G1500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:32149556 G>A maps to NM_001856.3 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr10:105795126 A>G maps to NM_000494.3 S1171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:105799230 A>T maps to NM_000494.3 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:105831819 G>A maps to NM_000494.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr10:105823550 C>T maps to NM_000494.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:105797436 G>A maps to NM_000494.3 F1055F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr10:105819889 G>T maps to NM_000494.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr10:105819889 G>C maps to NM_000494.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr10:105819889 G>A maps to NM_000494.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr21:46925160 G>A maps to ENST00000359759 G1409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr21:46888355 G>T maps to ENST00000359759 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr21:46888601 A>C maps to ENST00000359759 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr21:46907402 C>T maps to ENST00000359759 R1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:46876319 C>T maps to ENST00000359759 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:46930090 C>T maps to ENST00000359759 R1618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr21:46888516 C>T maps to ENST00000359759 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr21:46911228 G>A did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr21:46876211 C>T maps to ENST00000359759 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr21:46909410 C>T maps to ENST00000359759 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr21:46929358 G>A maps to ENST00000359759 A1528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr21:46876475 C>T maps to ENST00000359759 C344C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr21:46876301 G>A maps to ENST00000359759 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr21:46916424 C>T maps to ENST00000359759 G1255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr21:46913455 C>T maps to ENST00000359759 G1188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr21:46888393 G>A maps to ENST00000359759 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr21:46914822 A>G maps to ENST00000359759 G1224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:70608849 C>T maps to NM_001858.4 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr6:70840102 G>T maps to NM_001858.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr6:70866059 A>G maps to NM_001858.4 K707K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:70639565 C>T maps to NM_001858.4 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:70890208 A>G maps to NM_001858.4 K891K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr6:70733533 A>T maps to NM_001858.4 K348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:48268237 G>A maps to NM_000088.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr17:48267939 G>A maps to NM_000088.3 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:48268237 G>A maps to NM_000088.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:48263203 C>A maps to NM_000088.3 E1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr17:48268237 G>A maps to NM_000088.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:48275321 C>T maps to NM_000088.3 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:48272128 G>A maps to NM_000088.3 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:48269226 G>A maps to NM_000088.3 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:48264184 G>A maps to NM_000088.3 H1210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:94039063 C>T maps to NM_000089.3 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:94041936 A>C maps to NM_000089.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr7:94056577 C>T maps to NM_000089.3 R1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:94050337 C>T maps to NM_000089.3 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr7:94054935 C>T maps to NM_000089.3 N932N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr7:94049719 C>T maps to NM_000089.3 V717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr7:94052381 C>T maps to NM_000089.3 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:94055838 C>T maps to NM_000089.3 I1034I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr7:94054953 C>T maps to NM_000089.3 R938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:94041432 C>T maps to NM_000089.3 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:94049935 C>T maps to NM_000089.3 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:94056982 C>T maps to NM_000089.3 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr7:94048860 C>A maps to NM_000089.3 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:94049914 C>T maps to NM_000089.3 N750N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr7:94051254 A>G maps to NM_000089.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:94054953 C>T maps to NM_000089.3 R938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr20:61950884 C>T maps to ENST00000326996 A958A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:61951494 C>T maps to ENST00000326996 F1014F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:61929320 G>T maps to ENST00000326996 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr20:61958145 C>T maps to ENST00000326996 R1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:56047327 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:55925565 G>A maps to NM_030820.3 R794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr6:56032960 G>T maps to NM_030820.3 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:56033092 C>T maps to NM_030820.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:56044910 C>T maps to NM_030820.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:56032924 A>C maps to NM_030820.3 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:56021690 A>G maps to NM_030820.3 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:56031762 G>A maps to NM_030820.3 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:139833569 G>A maps to NM_152888.1 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr8:139833474 C>T maps to NM_152888.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:139833645 G>T maps to NM_152888.1 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:139727974 C>A maps to NM_152888.1 E823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr8:139611015 A>G maps to NM_152888.1 N1437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:139601537 G>A maps to NM_152888.1 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:139658921 C>A maps to NM_152888.1 E1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr8:139734290 C>A maps to NM_152888.1 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:139833396 G>A maps to NM_152888.1 Y409Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:139603696 G>A maps to NM_152888.1 R1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:139705906 A>G maps to NM_152888.1 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr8:139890116 G>A maps to NM_152888.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr8:139703107 C>A maps to NM_152888.1 G922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:139825208 C>T maps to NM_152888.1 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:139772491 T>C maps to NM_152888.1 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:139838990 G>A maps to NM_152888.1 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr8:139618623 C>A maps to NM_152888.1 P1368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr8:139890386 C>T maps to NM_152888.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:177715338 G>A maps to ENST00000390654 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr5:177684569 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:177675216 C>T maps to ENST00000390654 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr5:177715324 C>T maps to ENST00000390654 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:86361538 A>G did not map to a codon.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr1:86210493 A>T maps to NM_152890.5 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:86590584 T>C maps to NM_152890.5 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:86210514 G>A maps to NM_152890.5 S1502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:86590761 G>A maps to NM_152890.5 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:86334488 A>G maps to NM_152890.5 G1056G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:86426946 T>C maps to NM_152890.5 G849G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:86512509 G>A maps to NM_152890.5 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:86590782 G>A maps to NM_152890.5 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr4:109839332 G>A maps to ENST00000333642 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:109769917 C>T maps to ENST00000333642 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:109780850 C>T maps to ENST00000333642 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:109740473 G>A maps to ENST00000333642 G619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:110223139 G>C maps to ENST00000333642 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:116931352 G>T maps to NM_032888.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:117027229 G>A maps to NM_032888.2 P1092P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr9:116956724 C>T maps to NM_032888.2 H686H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:116931298 C>A maps to NM_032888.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr9:117020835 C>T maps to NM_032888.2 R1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr9:117053103 C>T maps to NM_032888.2 D1461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:117071592 C>T maps to NM_032888.2 S1757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:117052592 C>T maps to NM_032888.2 D1450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:117069994 C>T maps to NM_032888.2 I1718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:116930887 G>T maps to NM_032888.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:116930995 T>C maps to NM_032888.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr9:116958293 T>C did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr9:117070033 T>C maps to NM_032888.2 C1731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr9:117008171 G>A maps to NM_032888.2 P987P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr9:117066928 C>T maps to NM_032888.2 D1638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:117027362 A>G maps to NM_032888.2 R1104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:117072872 C>A maps to NM_032888.2 T1827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:7493093 C>A maps to NM_001037763.2 G473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:7495686 A>G maps to NM_001037763.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:48367303 G>A maps to NM_001844.4 I1450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr12:48368604 G>A maps to NM_001844.4 D1309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:48380199 A>G maps to NM_001844.4 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:189871108 C>T maps to NM_000090.3 G1044G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr2:189868485 T>C maps to NM_000090.3 R878R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr2:189875582 A>G maps to NM_000090.3 K1407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr2:189856933 C>T maps to NM_000090.3 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:189859786 C>T maps to NM_000090.3 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr2:189861914 C>A maps to NM_000090.3 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:189873846 T>C maps to NM_000090.3 V1241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr2:189856239 G>T maps to NM_000090.3 G294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:189875381 C>T maps to NM_000090.3 Y1340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr2:189870101 C>T maps to NM_000090.3 N986N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:189861174 C>T maps to NM_000090.3 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr2:189873732 T>C maps to NM_000090.3 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr2:189873708 T>G maps to NM_000090.3 P1195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:189873732 T>C maps to NM_000090.3 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:110830243 G>A maps to NM_001845.4 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:110847451 T>C maps to NM_001845.4 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr13:110838881 C>A maps to NM_001845.4 G583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr13:110830408 A>C did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr13:110839556 G>A maps to NM_001845.4 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:110845182 C>A maps to NM_001845.4 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:110864823 T>G maps to NM_001845.4 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:110818588 C>T maps to NM_001845.4 P1337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr13:110835438 G>A maps to NM_001845.4 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr13:110804733 G>A maps to NM_001845.4 Y1625Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr13:110804811 C>T maps to NM_001845.4 A1599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:110862350 C>T maps to NM_001845.4 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:110802748 C>T maps to NM_001845.4 T1657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr13:111160288 G>T maps to NM_001846.2 A1534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr13:111098225 C>T maps to NM_001846.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:111077154 A>G maps to NM_001846.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:111134959 C>T maps to NM_001846.2 F952F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr13:111158798 T>C maps to NM_001846.2 G1480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:111111208 C>T maps to NM_001846.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:111111151 C>T maps to NM_001846.2 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:111117927 C>T maps to NM_001846.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:228137805 G>T maps to NM_000091.4 G634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:228116060 G>T maps to NM_000091.4 G207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:228153869 C>T maps to NM_000091.4 F962F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr2:228137792 G>A maps to NM_000091.4 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:228153864 G>T did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr2:228169765 G>T maps to NM_000091.4 E1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:228131169 C>T maps to NM_000091.4 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:74675209 G>A maps to NM_001130105.1 Y740Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:74681745 G>A maps to NM_001130105.1 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:74681787 G>A maps to NM_001130105.1 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:74801890 A>G maps to NM_001130105.1 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:74676951 T>C maps to NM_001130105.1 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:227942699 C>A maps to ENST00000396625 G633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:227924241 A>G maps to ENST00000396625 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:227915821 G>A maps to ENST00000396625 Y1007Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:227927270 G>A maps to ENST00000396625 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:227979358 G>T maps to ENST00000396625 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:227872202 C>T maps to ENST00000396625 R1637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr2:227924262 G>A maps to ENST00000396625 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:227958978 C>A maps to ENST00000396625 G411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr2:227919390 C>A maps to ENST00000396625 G927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:227958985 C>T maps to ENST00000396625 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:227924139 C>T maps to ENST00000396625 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:227898180 A>G maps to ENST00000396625 P1174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr2:227895189 A>G maps to ENST00000396625 F1314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:227924241 A>G maps to ENST00000396625 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr2:227924241 A>G maps to ENST00000396625 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr2:227924930 A>G maps to ENST00000396625 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr23:107924166 G>A did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:107936000 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:107834293 C>A did not map to a codon.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr23:107827718 A>C did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:107938583 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:107807150 A>T did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:107898596 G>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:107834310 G>T did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:107863579 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:107834377 C>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:107936121 T>C did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:107938566 G>A did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:107816824 A>G did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:107929331 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:107826126 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:107865095 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:107841965 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:107829916 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:107869541 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:107911688 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:107834846 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:107911575 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:107842065 T>C did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:107920862 G>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:107911659 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:107911671 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:107840797 T>C did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:107911705 T>G did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr23:107930810 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:107868947 C>T did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:107939570 G>A did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:107846219 G>T did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:107838749 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:107829918 A>C did not map to a codon.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr23:107683416 G>A did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:107683416 G>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:107939569 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:107457455 G>A did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:107420196 C>A did not map to a codon.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr23:107408626 C>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:107431841 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:107438316 G>A did not map to a codon.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr23:107464600 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:107402893 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:107419004 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:107422581 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:107431199 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr23:107408222 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:107431199 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr23:107434697 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:107418968 A>C did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:107403777 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr23:107462934 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:107400240 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:107454944 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:107457428 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:107418398 A>G did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:107464522 C>T did not map to a codon.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr23:107403864 G>C did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:107420194 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:107403858 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:107420158 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr23:107412825 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:107431871 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:107464600 G>A did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:107406237 T>C did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:107406237 T>C did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:107554055 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:107431774 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:107406139 C>T did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:107417731 C>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:137706665 G>A maps to NM_000093.3 E1310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr9:137716639 G>A maps to NM_000093.3 T1631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:137642462 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:137622200 G>A maps to NM_000093.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:137710578 G>A maps to NM_000093.3 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:137704335 C>T maps to NM_000093.3 D1244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:137721845 G>T maps to NM_000093.3 E1698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr9:137716564 C>T maps to NM_000093.3 D1606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:137658316 C>T maps to NM_000093.3 D702D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:137623972 G>A maps to NM_000093.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:137717743 C>T maps to NM_000093.3 S1687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr9:137660299 C>T maps to NM_000093.3 D759D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:137623481 G>A maps to NM_000093.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr9:137646132 G>A maps to NM_000093.3 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr9:137710509 C>T maps to NM_000093.3 A1413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:137657580 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:137619110 G>T did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr9:137710728 C>T maps to NM_000093.3 D1458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr9:137620568 C>T maps to NM_000093.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:189901446 A>G maps to NM_000393.3 C1336C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:189943794 A>G maps to NM_000393.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:189904244 A>G maps to NM_000393.3 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:189904058 C>T maps to NM_000393.3 S1288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:189925497 A>G maps to NM_000393.3 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:189951475 T>G maps to NM_000393.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:189898828 G>A maps to NM_000393.3 F1489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr2:189933586 C>T maps to NM_000393.3 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:189929780 A>C maps to NM_000393.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:189903995 A>G did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr19:10071545 G>A maps to NM_015719.3 D1624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr19:10088091 C>T maps to NM_015719.3 G1061G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr19:10087907 G>A maps to NM_015719.3 D1095D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:10071134 C>T maps to NM_015719.3 T1730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:10112452 C>T maps to NM_015719.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr21:47410290 G>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr21:47421227 G>A maps to NM_001848.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr21:47419071 C>T maps to NM_001848.2 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr21:47406925 C>G maps to NM_001848.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr21:47402614 C>T maps to NM_001848.2 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr21:47552252 C>T maps to NM_001849.3 D949D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr21:47532439 C>T maps to NM_001849.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr21:47549155 G>A maps to NM_058174.2 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr21:47538571 C>T maps to NM_001849.3 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:238267890 G>A maps to NM_004369.3 G2104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:238285511 C>T maps to NM_004369.3 A991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:238249680 G>A maps to NM_004369.3 S2626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:238275762 G>A maps to NM_004369.3 D1689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:238253456 C>A maps to NM_004369.3 E2402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:238277371 G>A maps to NM_004369.3 I1578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr2:238303524 G>A maps to NM_004369.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:238275389 C>A maps to NM_004369.3 E1814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:238277491 G>A maps to NM_004369.3 D1538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:238280870 G>A maps to NM_004369.3 D1263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:238289831 G>A maps to NM_004369.3 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:238268787 C>T maps to NM_004369.3 P2075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:238275480 C>T maps to NM_004369.3 S1783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr2:238283277 G>A maps to NM_004369.3 S1152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:238249593 G>A maps to NM_004369.3 P2655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:238273011 A>G maps to NM_004369.3 S1966S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:238275564 C>T maps to NM_004369.3 S1755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr2:238270390 G>A maps to NM_004369.3 I2049I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr2:238243428 G>A maps to NM_004369.3 T3023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr2:238303596 T>C maps to NM_004369.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr2:238285676 G>A maps to NM_004369.3 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:238250705 A>G did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:238285463 T>C maps to NM_004369.3 P1007P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr2:238253304 G>A maps to NM_004369.3 N2452N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr2:238287636 T>C maps to NM_004369.3 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:238303260 A>C maps to NM_004369.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:238303587 C>T maps to NM_004369.3 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr2:238283187 C>T maps to NM_004369.3 P1182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:238285892 A>G maps to NM_004369.3 D864D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:130162393 C>T maps to ENST00000312481 Q2188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:130114018 T>C maps to ENST00000312481 N1093N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr3:130098804 T>G maps to ENST00000312481 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:130116893 C>T maps to ENST00000312481 D1310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:130174371 G>T maps to ENST00000312481 E2218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:130174353 G>T maps to ENST00000312481 E2212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr3:130159293 C>T maps to ENST00000312481 Q2038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:130103663 G>T maps to ENST00000312481 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:130128893 C>T maps to ENST00000312481 G1528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:130140032 C>T maps to ENST00000312481 R1663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:130107628 G>T maps to ENST00000312481 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:130124490 G>A maps to ENST00000312481 A1447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr3:130150711 G>A maps to ENST00000312481 T1884T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr3:130113898 C>T maps to ENST00000312481 Y1053Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr3:130120686 C>T maps to ENST00000312481 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr3:130159661 G>A maps to ENST00000312481 S2160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:130159446 G>T maps to ENST00000312481 E2089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:130282317 C>T maps to NM_001102608.1 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:130285810 C>T maps to NM_001102608.1 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:130345355 G>T maps to NM_001102608.1 G1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:130283847 C>T maps to NM_001102608.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:130285972 C>T maps to NM_001102608.1 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr3:130311939 C>T maps to NM_001102608.1 N1469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:130290055 G>T maps to NM_001102608.1 T932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:130285921 C>A maps to NM_001102608.1 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:130311927 T>C maps to NM_001102608.1 I1465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:130279231 C>T maps to NM_001102608.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:130292806 A>G maps to NM_001102608.1 E995E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:130292933 C>T maps to NM_001102608.1 R1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:130287017 T>C maps to NM_001102608.1 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:130282383 G>A maps to NM_001102608.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr3:130290055 G>T maps to NM_001102608.1 T932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr3:130340711 A>G maps to NM_001102608.1 G1621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:130380901 C>T maps to NM_001102608.1 V2084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:130305377 G>T maps to NM_001102608.1 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:130285810 C>T maps to NM_001102608.1 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:130285930 T>A maps to NM_001102608.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr3:48629184 C>A maps to NM_000094.3 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr3:48623671 A>G maps to NM_000094.3 N1186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:48630586 G>A maps to NM_000094.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr3:48613109 C>T maps to NM_000094.3 R1976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:48609450 C>A maps to NM_000094.3 G2351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:48628153 G>A maps to NM_000094.3 R578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:48628205 G>A maps to NM_000094.3 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr3:48629184 C>T maps to NM_000094.3 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr3:48607194 T>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:99514796 C>A maps to ENST00000429802 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr3:99513282 G>T maps to ENST00000429802 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:36563292 G>A maps to NM_005202.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:36563424 G>A maps to NM_005202.2 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:70991095 G>A maps to NM_001851.4 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:71003929 A>G maps to NM_001851.4 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr6:70961872 G>A maps to NM_001851.4 Q608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:71009858 C>T maps to NM_001851.4 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:70950405 C>A maps to NM_001851.4 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:71004055 C>T maps to NM_001851.4 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:70942385 G>A maps to NM_001851.4 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:71004055 C>T maps to NM_001851.4 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr6:71003929 A>G maps to NM_001851.4 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr6:70965038 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:70990574 A>T maps to NM_001851.4 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:40770063 C>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:40777742 G>A maps to NM_001852.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:40777741 G>A maps to NM_001852.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr20:61450602 G>A maps to NM_001853.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:61460144 C>T maps to NM_001853.3 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:61461753 C>T maps to NM_001853.3 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:120118081 C>T maps to NM_006438.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:120118249 A>G maps to NM_006438.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:3691599 C>A maps to ENST00000418971 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr2:3660952 C>T maps to ENST00000418971 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:3660934 C>T maps to ENST00000418971 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr18:347141 G>A maps to NM_130386.2 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:346820 C>T maps to NM_130386.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr18:346825 G>A maps to NM_130386.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:333083 C>A maps to NM_130386.2 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:15497517 A>G maps to NM_005677.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:15529766 C>T maps to NM_005677.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:15520859 T>C maps to NM_005677.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:15497436 G>A maps to NM_005677.3 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:15540055 G>T maps to NM_080538.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:15563060 C>T maps to NM_005677.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:22608896 G>A maps to NM_012071.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:75632088 C>T maps to NM_017828.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:146076507 C>T maps to NM_001081003.1 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:146076708 C>A maps to NM_001081003.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:36310926 G>A maps to NM_014186.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr11:36296244 C>T maps to NM_014186.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:18897443 G>A maps to NM_000095.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr19:18895073 G>A maps to NM_000095.2 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:18899119 G>A maps to NM_000095.2 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr10:76993889 T>G maps to NM_144589.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:160267379 G>A maps to NM_001098398.1 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:160268939 G>T maps to NM_001098398.1 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:160268939 G>A maps to NM_001098398.1 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:160309763 G>A maps to NM_001098398.1 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr1:160268939 G>A maps to NM_001098398.1 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:14487846 T>C maps to NM_001144061.1 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:14501221 A>T maps to NM_001144061.1 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:14512225 C>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr3:139077101 C>T maps to NM_004766.2 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:19011222 G>A maps to NM_007263.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:19015630 G>A maps to NM_007263.3 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:128994049 T>C maps to NM_016128.3 N803N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:128987452 G>A maps to NM_016128.3 E588E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:128984486 C>T maps to NM_016128.3 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:128987437 G>A maps to NM_016128.3 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:130146534 G>T maps to NM_012133.4 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:49420278 G>A maps to NM_001143887.1 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr15:49426008 C>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:49431798 G>T maps to NM_001143887.1 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr4:83996451 C>T maps to ENST00000503682 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:83970410 G>T maps to ENST00000503682 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr8:67963525 A>T maps to NM_006837.2 L237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:99688873 G>T maps to NM_006833.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:99686654 C>T maps to NM_006833.4 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:99688710 G>A maps to NM_006833.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:6838558 C>T maps to NM_001164093.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr12:6839872 A>G maps to NM_001164093.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:46111265 G>A maps to NM_016429.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr12:56661667 A>G maps to NM_144576.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:131087428 C>T maps to NM_016035.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:131087516 C>T maps to NM_016035.3 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:120954400 C>T maps to NM_032314.3 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr14:74428208 C>A maps to NM_182476.1 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr14:74428051 C>T maps to NM_182476.1 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:19085310 G>A maps to NM_016138.4 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:57485090 T>C maps to NM_020312.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:47647098 G>A maps to NM_006587.2 C652C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:47682239 G>A maps to NM_006587.2 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:47788925 G>A maps to NM_006587.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr4:47628471 G>A maps to NM_006587.2 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr4:47605477 C>T maps to NM_006587.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr4:47655568 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:47628536 C>A maps to NM_006587.2 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:47625682 C>T maps to NM_006587.2 W815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr16:30196691 C>T maps to NM_007074.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:67207811 G>A maps to NM_020441.2 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr11:67208980 G>A maps to NM_020441.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr9:100887057 A>T maps to NM_052820.3 *526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:100897159 C>T maps to NM_052820.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:100888860 G>A maps to NM_052820.3 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:68937659 C>T maps to NM_006091.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr15:68987576 G>A maps to NM_006091.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:69006920 C>T maps to NM_006091.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:69006340 C>A maps to NM_006091.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:69006920 C>T maps to NM_006091.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:69006920 C>T maps to NM_006091.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:27943991 G>A maps to ENST00000345068 Y345Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:27945837 G>T maps to ENST00000345068 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:27948316 G>A maps to ENST00000345068 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr17:27943781 C>T maps to ENST00000345068 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:4457526 G>A maps to NM_024535.3 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:4412703 C>T maps to NM_024535.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:4438578 G>T maps to NM_024535.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:4455500 C>T maps to NM_024535.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:84651118 G>A maps to NM_021149.2 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:14110262 C>T maps to NM_001303.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr17:53045802 G>A maps to NM_004375.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr10:101487247 C>T maps to NM_078470.4 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:73935225 A>T maps to NM_173827.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:73923971 G>A maps to NM_173827.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr20:30227793 C>T maps to NM_032609.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr20:30226831 A>G maps to NM_032609.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:85814049 G>A maps to NM_006067.4 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:75221511 A>G maps to NM_004255.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr16:31439160 G>A maps to NM_005205.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:36642415 G>A maps to ENST00000437291 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr6:75947667 G>T maps to NM_001865.3 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:63742267 T>C did not map to a codon.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr3:148904316 A>C maps to NM_000096.3 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr3:148939522 C>T maps to NM_000096.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr3:148930322 A>G maps to NM_000096.3 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:19548037 C>T maps to NM_014711.4 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:19547449 A>G maps to NM_014711.4 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:130023568 C>T maps to NM_001868.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr7:130021518 C>T maps to NM_001868.2 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr7:130023269 C>T maps to NM_001868.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:130023625 G>A maps to NM_001868.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:130021986 G>A maps to NM_001868.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr7:130025026 C>T maps to NM_001868.2 H276H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:130020942 C>T maps to NM_001868.2 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr7:130024453 C>T maps to NM_001868.2 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:148583292 A>G maps to NM_001870.2 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:148596230 C>A maps to NM_001870.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:129948156 G>A maps to NM_016352.3 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:129948166 G>A maps to NM_016352.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:129989835 A>G maps to NM_080385.4 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:130008323 G>T maps to NM_080385.4 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr7:130007796 C>T maps to NM_080385.4 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr7:130002338 G>T maps to NM_080385.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:130003312 C>G maps to NM_080385.4 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:130007748 C>T maps to NM_080385.4 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:68658283 C>T maps to NM_020361.4 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr19:17007057 G>A maps to ENST00000443236 D1842D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:17032725 C>T maps to ENST00000443236 S1263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:17081795 C>T maps to ENST00000443236 R763R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:17036129 C>T maps to ENST00000443236 P1198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:17062784 G>A maps to ENST00000443236 C891C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:17025595 G>A maps to ENST00000443236 F1276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:17132957 G>A maps to ENST00000443236 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:17008586 G>A maps to ENST00000443236 N1717N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:17038858 G>A maps to ENST00000443236 G1167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr19:17025493 C>A maps to ENST00000443236 V1310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:17104273 C>T maps to ENST00000443236 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:17013580 C>T maps to ENST00000443236 P1578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:46658367 G>A maps to NM_001872.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr17:28791681 G>A maps to NM_001304.4 K1331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:28749973 A>T maps to NM_001304.4 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr4:166405607 C>T maps to NM_001873.2 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:166300669 C>T maps to NM_001873.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:166414351 A>G maps to NM_001873.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:83296033 G>A maps to ENST00000261723 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:83218321 G>A maps to ENST00000261723 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:83218321 G>A maps to ENST00000261723 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr4:15067884 C>T maps to NM_001177382.1 Q996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:15054165 C>T maps to NM_001177382.1 R777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:15060809 G>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:15067829 C>T maps to NM_001177382.1 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr10:93812115 C>T maps to NM_014912.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr10:93812148 G>T maps to NM_014912.4 C639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:93999101 C>A did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr10:93952354 C>T maps to NM_014912.4 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:173317560 G>A maps to NM_030627.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr5:175306957 C>A maps to NM_001008220.1 C105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:75122505 T>C maps to NM_001030005.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:75122511 C>T maps to NM_001030005.2 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:56985655 T>C maps to NM_181654.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:69264028 G>A maps to NM_001874.4 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr10:101823464 G>A maps to NM_001308.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr10:101823428 G>A maps to NM_001308.2 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr10:101816847 G>A maps to NM_001308.2 C311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:194062252 G>A maps to NM_001080513.2 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:194063266 G>T maps to NM_001080513.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:194063119 G>T maps to NM_001080513.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:194062028 C>T maps to NM_001080513.2 W468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:194062381 C>T maps to NM_001080513.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:34220486 C>T maps to NM_003915.5 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr20:34214665 A>T maps to NM_003915.5 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:57159797 C>T maps to NM_152727.5 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:57147336 C>T maps to NM_152727.5 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:57147357 G>A maps to NM_152727.5 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:57180208 C>T maps to NM_152727.5 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:57180025 C>T maps to NM_152727.5 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:87559982 T>C maps to NM_003909.3 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:87570619 G>A maps to NM_003909.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr8:87560533 A>G maps to NM_003909.3 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:131624257 G>A maps to ENST00000502818 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:131268790 C>T maps to ENST00000502818 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr6:36714184 G>A maps to NM_020939.1 H396H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:36789931 G>A maps to NM_020939.1 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:36767802 G>A maps to NM_020939.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:36767802 G>A maps to NM_020939.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:24545602 C>T maps to NM_006032.2 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:24542859 C>T maps to NM_006032.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:89657452 C>T maps to NM_014427.4 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:89651906 C>A maps to NM_014427.4 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:89651231 C>T maps to NM_014427.4 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr16:89662989 T>C maps to NM_014427.4 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:89650175 C>T maps to NM_014427.4 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr12:39124111 T>C maps to NM_153634.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:39079420 T>C did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:39087459 A>T maps to NM_153634.2 L381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr12:39064566 G>T maps to NM_153634.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr3:9760229 C>T maps to ENST00000383832 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:207804353 T>C maps to NM_173077.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:207804355 G>A maps to NM_173077.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:98299541 C>T maps to NM_000097.5 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:12798553 G>A maps to NM_018340.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr16:12875117 G>A maps to NM_018340.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:211476995 G>A maps to NM_001122633.1 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:211460264 G>T maps to NM_001122633.1 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:211507286 G>T maps to NM_001122633.1 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:211521298 G>T maps to NM_001122633.1 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr2:211459245 C>A maps to NM_001122633.1 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:211459299 G>A maps to NM_001122633.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr2:211471608 C>A maps to NM_001122633.1 I718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:145623949 C>A maps to NM_013291.2 G573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:145625082 G>A maps to NM_013291.2 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:145619759 C>T maps to NM_013291.2 W1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr8:145621890 G>A maps to NM_013291.2 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr8:145624541 G>A maps to NM_013291.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:92622915 T>C maps to NM_017437.1 D512D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr14:92621484 T>C maps to NM_017437.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:9572804 C>T maps to NM_016207.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:9611522 C>T maps to NM_016207.2 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:9613143 T>A maps to NM_016207.2 *685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr2:9613144 G>A maps to NM_016207.2 *685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:9570053 C>T maps to NM_016207.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:9572810 C>T maps to NM_016207.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:1247976 C>T maps to NM_017871.4 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:1247976 C>T maps to NM_017871.4 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr7:99051617 G>A maps to NM_006693.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:99054059 C>T maps to NM_006693.2 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr7:99051689 C>T maps to NM_006693.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr12:69652697 G>A maps to ENST00000266679 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:69652683 C>T maps to ENST00000266679 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:68529156 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:68529026 A>C maps to NM_001876.3 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:68549420 G>A maps to NM_001876.3 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:68566685 G>A maps to NM_001876.3 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:68566811 C>T maps to NM_001876.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:68542897 G>A maps to NM_001876.3 Y487Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr22:51014507 G>A maps to NM_152245.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr22:51007810 G>A maps to NM_152245.2 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:50195539 C>T maps to NM_152359.2 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:50216708 C>T maps to NM_152359.2 D753D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr19:50216033 T>C maps to NM_152359.2 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr7:29111386 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:29070249 G>T maps to NM_031311.3 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr7:29160539 G>C maps to NM_031311.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr7:29111386 A>G did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:88008449 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:88009004 G>T did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:88008813 A>G did not map to a codon.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr23:88009169 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:88008448 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:88008710 A>C did not map to a codon.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr23:88008647 A>T did not map to a codon.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr23:88009031 G>A did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr23:88008567 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:88009125 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:88009084 A>G did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr23:88009032 T>C did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:88009030 C>T did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:88008921 T>C did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:88008655 C>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:88008992 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:88009043 A>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:88008746 G>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr20:2775069 G>A maps to NM_019609.4 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:2778919 G>A maps to NM_019609.4 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:2779112 G>T maps to NM_019609.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:2779512 G>A maps to NM_019609.4 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr10:125521472 G>A maps to NM_198148.2 D564D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:125651013 G>A maps to NM_198148.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:125557510 G>T maps to NM_198148.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr4:8608523 C>T maps to NM_001014447.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr4:8609142 C>T maps to NM_001014447.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:207718749 C>T maps to NM_000651.4 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:207741172 C>A maps to NM_000651.4 I1319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:207697016 G>A maps to NM_000651.4 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:207790016 C>T maps to NM_000651.4 C2253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:207790064 C>T maps to NM_000651.4 S2269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:207679265 G>T maps to NM_000651.4 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:207751318 C>T maps to NM_000651.4 D1569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:207741238 C>A maps to NM_000651.4 P1341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:207669701 T>C maps to NM_000651.4 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:207867926 G>A maps to NM_175710.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:207851609 C>T maps to NM_175710.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:207890888 G>T maps to NM_175710.1 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:207867845 C>T maps to NM_175710.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr1:207872578 A>G maps to NM_175710.1 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr1:207646450 T>C maps to NM_001006658.2 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:207644348 G>A maps to NM_001006658.2 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:207646369 A>G maps to NM_001006658.2 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr1:207643265 G>A maps to NM_001006658.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:207648362 C>T maps to NM_001006658.2 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:207651374 G>A maps to NM_001006658.2 S1016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr15:78633454 C>T maps to NM_004378.2 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:156670447 G>A maps to NM_001878.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:94243965 G>A maps to NM_003805.3 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr12:94072615 G>T maps to NM_003805.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:94072615 G>A maps to NM_003805.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:1716534 G>A maps to NM_020825.3 T990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:1706200 C>T maps to NM_020825.3 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:131870305 G>A maps to NM_000755.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:197390427 C>T maps to NM_201253.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:197390220 C>T maps to NM_201253.2 C421C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:197297927 C>T maps to NM_201253.2 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:197390427 C>T maps to NM_201253.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:197390427 C>T maps to NM_201253.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:197390652 A>T maps to NM_201253.2 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:197396761 C>T maps to NM_201253.2 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:197390706 C>T maps to NM_201253.2 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:197396749 C>T maps to NM_201253.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:197411382 C>T maps to NM_201253.2 L1322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:197390427 C>T maps to NM_201253.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:197446927 C>T maps to NM_201253.2 S1380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr1:197390643 C>A maps to NM_201253.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr1:197396761 C>T maps to NM_201253.2 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr1:197390931 C>A maps to NM_201253.2 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:197390289 C>T maps to NM_201253.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr1:197411331 G>A maps to NM_201253.2 P1305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:197390427 C>T maps to NM_201253.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:126128583 C>A maps to NM_173689.5 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:126133394 C>T maps to NM_173689.5 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:6465574 T>C maps to NM_174881.2 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:3216858 C>T maps to NM_016302.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:208461636 G>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:35733036 G>A maps to NM_006368.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:35735144 C>T maps to NM_006368.4 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr9:35736222 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:46332691 G>A maps to ENST00000288400 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:46333874 G>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:46342258 A>G did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:46339027 G>A maps to ENST00000288400 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:137567348 G>A maps to NM_194071.2 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr19:4171821 G>A maps to NM_032607.1 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:153941407 C>T maps to NM_130898.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr1:153946390 T>C maps to NM_130898.2 N346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:153941144 A>G maps to NM_130898.2 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:28610020 G>A maps to NM_182898.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:28843919 G>A maps to NM_182898.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:28547291 C>T maps to NM_182898.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr16:3790454 G>T maps to NM_004380.2 R1360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:3900429 A>G maps to NM_004380.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr16:3786075 C>T maps to NM_004380.2 R1563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr16:3808955 A>G maps to NM_004380.2 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:3807899 T>C maps to NM_004380.2 R1173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr16:3794916 T>C maps to NM_004380.2 K1320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:3778975 C>T maps to NM_004380.2 A2024A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr16:3807901 G>T maps to NM_004380.2 R1173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr16:3790454 G>T maps to NM_004380.2 R1360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr16:3824674 G>A maps to NM_004380.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr16:3779623 G>T maps to NM_004380.2 C1808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:3828174 A>C maps to NM_004380.2 Y650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr16:3808862 C>A maps to NM_004380.2 G1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:3900825 G>A maps to NM_004380.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr16:3781471 G>T maps to NM_004380.2 V1631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:3779533 G>A maps to NM_004380.2 C1838C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr16:3790511 G>A maps to NM_004380.2 R1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr16:3794916 T>C maps to NM_004380.2 K1320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr16:3786712 G>A maps to NM_004380.2 Q1500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:3788651 C>A maps to NM_004380.2 L1434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr16:3779386 T>C maps to NM_004380.2 S1887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:3807901 G>T maps to NM_004380.2 R1173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr16:3820639 C>T maps to NM_004380.2 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr16:3817811 A>G maps to NM_004380.2 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr16:3781300 C>T maps to NM_004380.2 T1688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr16:3807911 G>A maps to NM_004380.2 R1169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr16:3801785 A>G maps to NM_004380.2 C1240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr16:3832856 G>T maps to NM_004380.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr16:3807901 G>A maps to NM_004380.2 R1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr16:3779387 G>T maps to NM_004380.2 S1887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr16:3786704 C>T maps to NM_004380.2 W1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr16:3790518 C>T maps to NM_004380.2 L1338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr16:3900696 C>G maps to NM_004380.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr16:3779765 G>T maps to NM_004380.2 S1761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr16:3777940 G>A maps to NM_004380.2 P2369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr16:3801785 A>G maps to NM_004380.2 C1240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:3790520 A>G maps to NM_004380.2 L1338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:3786075 C>T maps to NM_004380.2 R1563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:3786764 G>A maps to NM_004380.2 Y1482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:3790511 G>T maps to NM_004380.2 R1341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:3795309 G>A maps to NM_004380.2 C1294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:3828183 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:85375577 C>T maps to NM_001039618.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:85375835 A>C maps to NM_001039618.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr11:85375253 T>C maps to NM_001039618.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:85375255 G>T maps to NM_001039618.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr11:85375255 G>T maps to NM_001039618.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:101971818 G>A maps to NM_153836.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:101967420 C>T maps to NM_153836.3 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:9976244 T>C maps to NM_001077415.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr10:35500602 C>T maps to ENST00000429130 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:76249983 C>T maps to NM_001882.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:43907808 C>T maps to NM_001145146.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:43906606 C>T maps to NM_001145146.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr17:43898766 C>T maps to NM_001145146.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:30705195 G>A maps to ENST00000348438 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr7:30693146 G>T maps to ENST00000348438 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:30695598 G>A maps to ENST00000348438 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:30721530 G>T maps to ENST00000348438 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:30694687 G>A maps to ENST00000348438 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:36744683 A>G maps to NM_016441.2 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:36706763 C>T maps to NM_016441.2 C433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:36706685 C>T maps to NM_016441.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:36691679 C>T maps to NM_016441.2 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr2:36669755 A>G did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr6:43276070 G>A maps to ENST00000449267 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:43275613 G>A maps to ENST00000449267 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr4:1389480 C>T maps to NM_175918.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:1389045 C>T maps to NM_175918.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:1389039 G>A maps to NM_175918.3 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:49819809 G>A maps to NM_001131.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr6:49819809 G>A maps to NM_001131.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr6:49676894 C>T maps to ENST00000211238 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:49676894 C>T maps to ENST00000211238 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr6:49665619 G>T maps to ENST00000211238 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:49704214 G>A maps to NM_001190986.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:49701517 G>A maps to NM_001190986.1 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:49704178 C>T maps to NM_001190986.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr6:49698882 T>C maps to NM_001190986.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr8:75941647 A>G maps to NM_031461.5 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:75924704 G>A maps to NM_031461.5 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr8:75928926 C>T maps to NM_031461.5 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr8:75929155 C>T maps to NM_031461.5 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:84900530 G>A maps to NM_031476.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:84888422 T>C maps to NM_031476.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:1340132 G>A maps to NM_016823.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:18710393 G>A maps to NM_004750.4 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:29111326 G>A maps to NM_015986.3 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:29130940 A>G maps to NM_015986.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr4:5862864 G>A maps to NM_001014809.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr4:5862768 G>A maps to NM_001014809.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:5830263 C>T maps to NM_001014809.1 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr4:5830296 G>A maps to NM_001014809.1 N574N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:5823525 C>G maps to NM_001014809.1 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr4:5857975 G>A maps to NM_001014809.1 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr4:5827219 C>T did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr4:5838494 C>T maps to NM_001014809.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:5862837 C>T maps to NM_001014809.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr4:5862882 G>A maps to NM_001014809.1 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr4:5862882 G>A maps to NM_001014809.1 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:5868444 G>A maps to NM_001014809.1 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:20023133 C>T maps to NM_016652.4 W494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:20020342 G>A maps to NM_016652.4 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:20016970 G>T maps to NM_016652.4 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:20018070 G>A maps to NM_016652.4 R759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:20023103 G>A maps to NM_016652.4 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:20030018 G>A maps to NM_016652.4 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:20030018 G>A maps to NM_016652.4 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:20033184 G>A maps to NM_016652.4 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr20:20028490 A>G maps to NM_016652.4 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr20:20031248 C>A maps to NM_016652.4 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:152382291 T>C maps to NM_016190.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:152382217 G>T maps to NM_016190.2 S447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:17257856 G>A maps to NM_014675.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:17292586 C>T maps to NM_014675.3 Q1557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:17264165 T>C maps to NM_014675.3 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:17250887 G>T maps to NM_014675.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:17285238 G>A maps to NM_014675.3 R1342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:17250943 C>T maps to NM_014675.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr1:17272037 C>T maps to NM_014675.3 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr1:17263308 G>A maps to NM_014675.3 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:17250934 C>T maps to NM_014675.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:17256492 G>A maps to NM_014675.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:87011833 C>T maps to NM_001143935.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr7:87022263 C>T maps to NM_001143935.1 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:87011451 A>G maps to NM_001143935.1 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:159683632 C>T maps to NM_000567.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr1:159683617 G>A maps to NM_000567.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr10:99677377 G>A maps to NM_018058.4 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:99664497 G>A maps to NM_018058.4 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:99667845 G>A maps to NM_018058.4 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:99696032 G>A maps to NM_018058.4 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:122724706 G>T maps to NM_019604.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:122738115 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:122735371 G>A maps to NM_019604.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:18860638 G>A maps to NM_001098482.1 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr1:153924883 G>A maps to NM_181715.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:153923903 G>A maps to NM_181715.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:91147676 C>T maps to NM_022769.3 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:48337720 G>A maps to NM_000554.4 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:48343112 C>T maps to NM_000554.4 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:48337708 G>A maps to NM_000554.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr12:107386773 G>A maps to NM_004075.3 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr12:107398957 A>G maps to NM_004075.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr12:107393836 T>C maps to NM_004075.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:107395138 A>G maps to NM_004075.3 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:107395057 T>C maps to NM_004075.3 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:107395057 T>C maps to NM_004075.3 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:45892055 C>T maps to NM_021117.3 Q529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:45882545 C>T maps to NM_021117.3 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr21:44592188 C>T maps to NM_000394.2 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr17:27581240 T>C maps to NM_005208.4 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:219855691 G>A maps to NM_057094.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:219856937 G>A maps to NM_057094.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr22:27019223 C>T maps to NM_001886.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr22:27021496 C>T maps to NM_001886.2 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr22:26997910 G>A maps to NM_001887.3 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr22:25598690 G>A maps to NM_004076.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:97634534 C>T maps to ENST00000182096 C784C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr2:209028059 G>A maps to NM_014617.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:209010605 G>A maps to NM_005210.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr7:151135318 A>T maps to NM_144727.1 Y11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:186256577 C>T maps to NM_017541.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:21278989 C>T maps to NM_001888.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:21278911 C>T maps to NM_001888.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:75188918 G>A maps to NM_001889.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:56669949 G>A maps to NM_004077.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr12:53553934 G>T maps to NM_015989.4 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:151909158 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:151909177 G>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:151908808 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:151908812 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:151908815 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:151909157 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:10854629 C>A maps to NM_003651.4 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:41970778 C>A maps to NM_014460.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:115262216 A>G maps to NM_001130523.1 C748C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:115275229 C>A maps to NM_001130523.1 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:115268949 G>A maps to NM_001130523.1 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr20:47682764 C>T maps to NM_001316.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:47689136 A>C maps to NM_001316.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr20:47710754 T>C maps to NM_001316.2 C842C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr20:47710754 T>C maps to NM_001316.2 C842C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr5:149449812 A>C maps to NM_005211.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr5:149435643 C>T maps to NM_005211.3 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:149457737 G>A maps to NM_005211.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:149457757 G>A maps to NM_005211.3 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:149460417 G>A maps to NM_005211.3 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr5:149439315 G>A maps to NM_005211.3 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr23:1407700 G>A did not map to a codon.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr23:1428407 G>A did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr23:1407700 G>A did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr22:37325715 C>A maps to ENST00000262825 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:38172757 C>T maps to NM_000759.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:38172790 G>A maps to NM_000759.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:36937166 G>A maps to NM_156039.3 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:36935286 T>C maps to NM_156039.3 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:36939483 A>G maps to NM_156039.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:36933706 G>T maps to NM_156039.3 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:36931759 G>T maps to NM_172313.2 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:36935331 C>A maps to NM_156039.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr1:36935286 T>C maps to NM_156039.3 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr8:19363276 G>A maps to NM_018371.4 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:19362991 G>A maps to NM_018371.4 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr8:19276169 C>T maps to NM_018371.4 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:19363108 G>A maps to NM_018371.4 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr8:19316085 G>A maps to NM_018371.4 H234H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:19363219 C>T maps to NM_018371.4 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:19315955 G>A maps to NM_018371.4 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:43651125 C>T maps to NM_018590.3 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr17:61987256 G>A maps to NM_022579.1 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr17:61987644 C>T maps to NM_022579.1 S116S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DM-A1D6-01A-21D-A152-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr8:3855603 G>A maps to NM_033225.5 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr8:3047482 G>A maps to NM_033225.5 S1783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:2910157 C>A maps to NM_033225.5 G2496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr8:2813207 C>T maps to NM_033225.5 V3299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:3072025 G>T maps to NM_033225.5 S1620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:3141804 C>A maps to NM_033225.5 P1338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:2836196 C>A maps to NM_033225.5 G2835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:3205573 G>A maps to NM_033225.5 A1138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:2836158 C>T maps to NM_033225.5 W2847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:3059170 C>T maps to NM_033225.5 Q1687Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:2876119 C>T maps to NM_033225.5 T2636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:2855670 C>A maps to NM_033225.5 G2747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr8:2887033 C>T maps to NM_033225.5 P2554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr8:2832111 G>A maps to NM_033225.5 N2867N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr8:2832078 G>A maps to NM_033225.5 G2878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr8:3019722 G>A maps to NM_033225.5 N1934N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:3226890 A>T maps to NM_033225.5 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:3072097 A>G maps to NM_033225.5 I1596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:3265739 A>G maps to NM_033225.5 C584C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:3019743 G>A maps to NM_033225.5 I1927I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:3141849 G>A maps to NM_033225.5 F1323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr8:3351197 G>T maps to NM_033225.5 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:2886843 G>A maps to NM_033225.5 R2618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:3081267 G>A maps to NM_033225.5 I1489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:2808749 C>A maps to NM_033225.5 E3363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:2820885 C>T maps to NM_033225.5 Q3104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:2964053 A>G maps to NM_033225.5 C2315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:3611472 C>A maps to NM_033225.5 G304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:2808660 G>A maps to NM_033225.5 A3392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr8:3141810 G>A maps to NM_033225.5 D1336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:3253833 G>A maps to NM_033225.5 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:2796225 C>A maps to NM_033225.5 E3526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:3057245 G>A maps to NM_033225.5 F1728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr8:3009018 C>A maps to NM_033225.5 T1977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:2796247 T>C maps to NM_033225.5 Q3518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:3224578 G>A maps to NM_033225.5 Y1030Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:4851878 G>A maps to NM_033225.5 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr8:3253767 C>T maps to NM_033225.5 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:2807761 T>G maps to NM_033225.5 L3435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:2820048 T>G maps to NM_033225.5 G3189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:2965246 G>A maps to NM_033225.5 F2276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:3205653 C>A maps to NM_033225.5 E1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:2813222 G>A maps to NM_033225.5 F3294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:3165341 C>T maps to NM_033225.5 A1275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr8:4494898 G>A maps to NM_033225.5 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr8:3000086 C>T maps to NM_033225.5 T2047T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr8:2796247 T>C maps to NM_033225.5 Q3518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr8:3855462 A>G maps to NM_033225.5 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr8:2910134 G>A maps to NM_033225.5 N2503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr8:3047473 G>A maps to NM_033225.5 N1786N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr8:2966164 G>A maps to NM_033225.5 S2238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:3263588 G>A maps to NM_033225.5 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr8:3855576 C>T maps to NM_033225.5 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:3326276 C>T maps to NM_033225.5 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:33987144 C>T maps to ENST00000373381 S3465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr1:34038175 G>A maps to ENST00000373381 G2524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:34123627 G>A maps to ENST00000373381 Y1415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr1:34033331 G>A maps to ENST00000373381 N2707N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:34035121 A>G maps to ENST00000373381 I2621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:34254219 T>C maps to ENST00000373381 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr1:34002690 C>T maps to ENST00000373381 P3230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr1:34401391 G>A maps to ENST00000373381 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:34128600 G>A maps to ENST00000373381 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:34090741 G>A maps to ENST00000373381 S1763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:34128631 C>T maps to ENST00000373381 G1331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:34070948 G>A maps to ENST00000373381 G2115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:33987078 G>A maps to ENST00000373381 F3487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:34112311 G>A maps to ENST00000373381 S1530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:34033232 C>T maps to ENST00000373381 Q2740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:34180304 G>A maps to ENST00000373381 G1056G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr1:34554714 G>A maps to ENST00000373381 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:34208950 G>A maps to ENST00000373381 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:34276441 G>A maps to ENST00000373381 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:34035124 C>T maps to ENST00000373381 P2620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:34554599 G>A maps to ENST00000373381 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr1:34164524 A>G maps to ENST00000373381 C1211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr1:34006146 G>A maps to ENST00000373381 T3163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:34011754 G>A maps to ENST00000373381 S2954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:34190219 C>T maps to ENST00000373381 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr8:113317004 G>A maps to NM_198123.1 I2737I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:113988156 A>G maps to NM_198123.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:113326670 A>G maps to NM_198123.1 L2512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr8:113988231 C>T maps to NM_198123.1 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:113323290 G>A maps to NM_198123.1 R2601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:113420639 C>A maps to NM_198123.1 E1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr8:114449031 C>A maps to NM_198123.1 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr8:113317110 A>T maps to NM_198123.1 L2702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr8:114031386 T>C maps to NM_198123.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:114186071 G>A maps to NM_198123.1 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr8:113326670 A>G maps to NM_198123.1 L2512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr8:113347627 A>G maps to NM_198123.1 T2365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:113421169 A>T maps to NM_198123.1 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr8:113518999 A>G maps to NM_198123.1 P1605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr8:113702220 G>A maps to NM_198123.1 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr8:113841955 G>A maps to NM_198123.1 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:113568989 A>G did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:113697830 A>C maps to NM_198123.1 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:113318263 G>A maps to NM_198123.1 S2681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:113347672 G>A maps to NM_198123.1 I2350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:113349921 G>A maps to NM_198123.1 R2231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:114111091 G>T maps to NM_198123.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr8:113504826 G>T maps to NM_198123.1 V1723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr8:113649130 C>T maps to NM_198123.1 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:113318304 C>A maps to NM_198123.1 E2668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:113697734 A>C maps to NM_198123.1 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:113988125 T>G maps to NM_198123.1 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:114186077 G>A maps to NM_198123.1 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr8:113237017 C>T maps to NM_198123.1 T3702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:113299308 C>T maps to NM_198123.1 R3105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:113585787 C>T maps to NM_198123.1 W1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr8:113569151 G>A maps to NM_198123.1 G1358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:113304831 G>A maps to NM_198123.1 Q2908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr8:113841952 A>G maps to NM_198123.1 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr8:113392623 T>C maps to NM_198123.1 S2031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:113988219 C>T maps to NM_198123.1 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:113253955 C>T maps to NM_198123.1 K3487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:113353771 C>A maps to NM_198123.1 E2196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:114326989 C>A maps to NM_198123.1 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:113702186 C>A maps to NM_198123.1 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr8:114290887 A>T maps to NM_198123.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr8:113299449 A>G maps to NM_198123.1 D3058D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr8:113266555 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:113516099 C>A maps to NM_198123.1 E1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:113266490 G>A maps to NM_198123.1 F3367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:113392623 T>C maps to NM_198123.1 S2031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr8:113657413 G>T maps to NM_198123.1 I1078I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr8:113326670 A>G maps to NM_198123.1 L2512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:113316981 C>T maps to NM_198123.1 W2745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:113349921 G>A maps to NM_198123.1 R2231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr8:113256680 T>C maps to NM_198123.1 T3448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr8:113326787 T>C maps to NM_198123.1 G2473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr8:113326670 A>G maps to NM_198123.1 L2512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr8:113504880 G>T maps to NM_198123.1 G1705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr8:113266514 C>A maps to NM_198123.1 R3359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:113364764 T>C did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr8:113275877 C>T maps to NM_198123.1 P3284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:113267534 G>T maps to NM_198123.1 T3328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr8:114326852 G>A maps to NM_198123.1 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr8:113316980 C>T maps to NM_198123.1 W2745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr8:113316953 G>A maps to NM_198123.1 C2754C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr8:113418906 T>C maps to NM_198123.1 R1885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr8:113299386 A>G maps to NM_198123.1 R3079R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr8:113256694 A>G maps to NM_198123.1 L3444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:113529281 G>A maps to NM_198123.1 P1579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:113694760 C>A maps to NM_198123.1 G863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr8:114448939 G>A maps to NM_198123.1 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:70798318 A>C maps to NM_001890.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr4:70802198 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:70823399 C>A maps to NM_001891.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:70823462 G>A maps to NM_001891.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:70823462 G>A maps to NM_001891.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr4:71114806 C>T maps to NM_005212.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:71114915 C>T maps to NM_005212.2 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:148929651 G>A maps to NM_001025105.1 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr13:37679160 C>T maps to NM_145203.5 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:37678625 G>A maps to NM_145203.5 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:37679039 G>A maps to NM_145203.5 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:37679378 G>A maps to NM_145203.5 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:37678625 G>A maps to NM_145203.5 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr13:37679378 G>A maps to NM_145203.5 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr13:37678436 G>A maps to NM_145203.5 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr13:37679330 C>T maps to NM_145203.5 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:80210919 G>A maps to NM_001893.3 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:38695924 G>A maps to NM_001894.4 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:64499736 G>A maps to NM_022048.3 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:64508897 G>A maps to NM_022048.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:1978631 G>A maps to NM_001319.6 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:1979776 C>T maps to NM_001319.6 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:1978323 G>T maps to NM_001319.6 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr19:1978712 C>T maps to NM_001319.6 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:122881405 C>T maps to NM_001044723.1 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:122923798 T>C maps to NM_001044723.1 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:122881413 T>C maps to NM_001044723.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr16:58201151 G>T maps to NM_001896.2 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr6:31637259 A>T maps to ENST00000375885 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:75970134 C>T maps to NM_001897.4 P1681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr15:75979814 A>G maps to NM_001897.4 V1197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:75982100 G>A maps to NM_001897.4 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr15:75980078 G>A maps to NM_001897.4 D1109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr15:75982631 G>T maps to NM_001897.4 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr15:75975361 C>T maps to NM_001897.4 A1490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr15:75980474 G>A maps to NM_001897.4 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:75967905 G>A maps to NM_001897.4 G2318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:47618885 G>A maps to ENST00000383738 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:47618504 G>A maps to ENST00000383738 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr3:47618906 C>T maps to ENST00000383738 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:47618363 G>A maps to ENST00000383738 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:47618972 G>A maps to ENST00000383738 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:47618885 G>A maps to ENST00000383738 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:68024217 C>T maps to ENST00000389042 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:68066341 G>T maps to ENST00000389042 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:67986476 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:68024220 G>T maps to ENST00000389042 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr8:68102915 A>G maps to ENST00000389042 E1114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:39185876 G>A maps to NM_033027.3 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:51457702 G>A maps to NM_030809.1 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:51461616 G>A maps to NM_030809.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:166535948 C>T maps to ENST00000409420 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:166514325 T>C maps to ENST00000409420 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:166535443 C>T maps to ENST00000409420 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:166533084 G>A maps to ENST00000409420 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr2:166532934 A>G maps to ENST00000409420 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:166536166 A>G maps to ENST00000409420 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:201454410 C>A maps to NM_001193572.1 G169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:201459356 G>A maps to NM_001193572.1 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr12:77252743 A>G maps to NM_001321.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:77252743 A>G maps to NM_001321.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:77252743 A>G maps to NM_001321.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr20:18165252 C>T maps to NM_020536.4 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:19207813 A>C maps to NM_003476.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:19213931 C>A maps to NM_003476.3 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr11:19209750 G>A maps to NM_003476.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:19209822 C>T maps to NM_003476.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr20:23731338 A>T maps to NM_001898.2 Y55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:23731353 G>A maps to NM_001898.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:23432485 C>T maps to NM_130794.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:23433316 C>T maps to NM_130794.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:23807207 G>A maps to NM_001322.2 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:23805879 G>T maps to NM_001322.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:23614558 G>A maps to NM_000099.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:23667835 G>C maps to NM_001899.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:23669429 G>A maps to NM_001899.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr20:23667793 G>A maps to NM_001899.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:23858212 G>A maps to NM_001900.4 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:65779733 C>T maps to NM_001323.2 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr20:23586351 T>C maps to NM_001008693.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:122060380 C>T maps to NM_005213.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:54972701 C>A maps to NM_001033522.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:100077308 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:100093246 T>C did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:100088306 C>T did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr10:53458364 A>C maps to NM_015235.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr10:53459246 C>T maps to NM_015235.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:53457713 G>A maps to NM_015235.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:53458330 G>A maps to NM_015235.2 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:33123753 A>G maps to NM_001326.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:33120280 A>G maps to NM_001326.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:134947965 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:134947908 C>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:134948045 A>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:134947915 G>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:134947942 A>G did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:134948033 A>G did not map to a codon.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr23:120008830 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:120008789 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:120009206 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:120009263 G>A did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr23:120009263 G>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:120008997 C>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:120008997 C>G did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:120008763 G>A did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:120008857 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:153881577 G>A did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:153881590 C>T did not map to a codon.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr18:19997411 C>T maps to NM_172241.2 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr18:19995710 G>A maps to NM_172241.2 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr14:39771400 T>C maps to ENST00000396158 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:39782627 A>G maps to ENST00000396158 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:39796221 G>A maps to ENST00000396158 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:39815180 T>C maps to ENST00000396158 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:39790183 A>G maps to ENST00000396158 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:39819362 C>T maps to ENST00000396158 F775F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr4:1206093 G>A maps to NM_001328.2 H419H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr10:126715929 G>A maps to NM_022802.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr10:126714882 C>T maps to NM_022802.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr10:126681867 C>T maps to NM_022802.2 P854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:126691538 G>A maps to NM_022802.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:126715518 G>A maps to NM_022802.2 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:126691556 G>A maps to NM_022802.2 N650N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr16:67645512 A>T maps to NM_006565.3 K260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr16:67645942 G>T maps to NM_006565.3 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:56090776 C>T maps to ENST00000423479 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr20:56090865 G>T maps to ENST00000423479 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr20:56090860 G>T maps to ENST00000423479 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr20:56090865 G>A maps to ENST00000423479 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:77488927 G>A maps to NM_004715.3 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:77474530 G>A maps to NM_004715.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr18:77473100 G>A maps to NM_004715.3 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:77488915 G>A maps to NM_004715.3 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:219267780 C>T maps to NM_021198.1 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:58223305 G>A maps to NM_005730.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr12:58223296 A>G maps to NM_005730.3 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr12:58223296 A>G maps to NM_005730.3 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:38022270 G>A maps to NM_001008392.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:30910811 G>A maps to NM_001330.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:132270532 G>A maps to NM_001901.2 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:70896078 T>C did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr8:104390424 A>G maps to NM_138455.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:104394813 G>T maps to NM_138455.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr8:104390424 A>G maps to NM_138455.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:204735456 G>A maps to NM_005214.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:204736137 G>A maps to NM_005214.3 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr5:138240091 C>T maps to ENST00000355078 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:138240091 C>T maps to ENST00000355078 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:138160286 G>A maps to ENST00000355078 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:138261053 T>C maps to ENST00000355078 Y619Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:138266582 G>T maps to ENST00000355078 G753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:138163268 T>C maps to ENST00000355078 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr2:80874951 G>A maps to ENST00000402739 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:80831216 A>G maps to ENST00000402739 K736K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr2:80782905 C>A maps to ENST00000402739 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:80835325 T>C maps to ENST00000402739 C771C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:80782864 G>T maps to ENST00000402739 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:80646681 G>T maps to ENST00000402739 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr2:80101323 G>A maps to ENST00000402739 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:80874922 C>T maps to ENST00000402739 R930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr2:80646723 G>T maps to ENST00000402739 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:80085217 G>A maps to ENST00000402739 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:68940232 G>A maps to NM_013266.2 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr10:69299302 C>T maps to NM_013266.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:68040272 G>T maps to NM_013266.2 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:68940073 C>T did not map to a codon.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr10:68535222 C>T maps to NM_013266.2 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr10:67680162 G>A maps to NM_013266.2 V871V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr10:68940274 A>G maps to NM_013266.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:68979454 T>G maps to NM_013266.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:68940274 A>G maps to NM_013266.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:68979364 C>T maps to NM_013266.2 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:111727687 C>A maps to NM_003798.2 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:111741713 C>T maps to NM_003798.2 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:111761422 T>C maps to NM_003798.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:111761527 C>T maps to NM_003798.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:111746668 T>C maps to NM_003798.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr9:111739268 A>G maps to NM_003798.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr3:41266877 T>C maps to NM_001904.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:41266143 T>C maps to NM_001904.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:41266152 C>A maps to NM_001904.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:41266077 G>A maps to NM_001904.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:41266128 A>G maps to NM_001904.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:41266137 T>C maps to NM_001904.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr3:41266143 T>C maps to NM_001904.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr3:41266110 T>C maps to NM_001904.3 H36H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr3:41277949 T>C maps to NM_001904.3 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:41266137 T>C maps to NM_001904.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:41266077 G>A maps to NM_001904.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:41278079 G>A maps to NM_001904.3 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:41266017 T>C maps to NM_001904.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:41266047 A>G maps to NM_001904.3 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:41268766 A>G maps to NM_001904.3 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr3:41266089 T>C maps to NM_001904.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr3:41266116 T>C maps to NM_001904.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:41266071 T>C maps to NM_001904.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:41266922 T>C maps to NM_001904.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:41266113 T>C maps to NM_001904.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr3:41266104 A>G maps to NM_001904.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr3:41266110 T>C maps to NM_001904.3 H36H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr3:41266158 T>C maps to NM_001904.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr3:41266017 T>C maps to NM_001904.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr3:41266134 T>C maps to NM_001904.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:41266071 T>C maps to NM_001904.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr3:41266101 T>C maps to NM_001904.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr3:41266922 T>C maps to NM_001904.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:41266083 A>G maps to NM_001904.3 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:41266104 A>G maps to NM_001904.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:41266125 C>T maps to NM_001904.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:41266131 T>C maps to NM_001904.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr3:41267276 C>T maps to NM_001904.3 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr3:41266065 T>C maps to NM_001904.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:41266149 A>G maps to NM_001904.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr3:41268766 A>G maps to NM_001904.3 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr3:41266203 A>G maps to NM_001904.3 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr3:41266877 T>C maps to NM_001904.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr3:41277949 T>C maps to NM_001904.3 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr3:41278076 A>C did not map to a codon.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr3:41266164 A>G maps to NM_001904.3 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr3:41266200 G>A maps to NM_001904.3 W66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr3:41266122 T>A maps to NM_001904.3 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:41266116 T>C maps to NM_001904.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:41266227 T>C maps to NM_001904.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr3:41277949 T>C maps to NM_001904.3 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:41266149 A>G maps to NM_001904.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr20:36407704 C>T maps to NM_030877.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr20:36365802 A>G maps to NM_030877.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr20:36488708 A>G maps to NM_030877.3 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr20:36470758 T>C maps to NM_030877.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr20:36488708 A>G maps to NM_030877.3 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:36488706 C>T maps to NM_030877.3 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:57564285 C>T maps to NM_001085458.1 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:57563942 G>A maps to NM_001085458.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:57571169 G>T maps to NM_001085458.1 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:57576002 G>T maps to NM_001085458.1 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:57561543 C>T maps to NM_001085458.1 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr11:57564065 C>T maps to NM_001085458.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:57569202 A>G did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr11:57573403 C>T maps to NM_001085458.1 H591H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr11:57569528 A>G maps to NM_001085458.1 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:11117618 C>T maps to NM_001332.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:11111044 G>A maps to NM_001332.2 G796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr5:11111129 A>T maps to NM_001332.2 L768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr5:11023011 C>T maps to NM_001332.2 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:11117635 C>A maps to NM_001332.2 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:11159845 G>A maps to NM_001332.2 C667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:11117570 G>A maps to NM_001332.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:11022927 G>A maps to NM_001332.2 A984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:11346719 G>A maps to NM_001332.2 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr5:11364841 C>T maps to NM_001332.2 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:11732265 G>A maps to NM_001332.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:11117570 G>A maps to NM_001332.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:11117570 G>A maps to NM_001332.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:11082865 G>A maps to NM_001332.2 C910C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr5:11364898 G>A maps to NM_001332.2 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr5:11397304 C>A maps to NM_001332.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr5:11732304 G>A maps to NM_001332.2 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr5:10973765 T>C maps to NM_001332.2 P1159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:11082850 C>T maps to NM_001332.2 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr5:11397247 C>T maps to NM_001332.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr5:10973726 G>A maps to NM_001332.2 F1172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:10973588 C>T maps to NM_001332.2 P1218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:11384885 G>A maps to NM_001332.2 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:11411723 G>A maps to NM_001332.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:3543515 C>T maps to NM_001031681.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:41466759 C>T maps to NM_001905.2 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:41473203 G>A maps to NM_001905.2 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr23:16707626 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:16657319 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:16717045 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:16721005 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:16635369 C>T did not map to a codon.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr11:10786264 T>A maps to NM_014633.3 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:75238124 C>T maps to NM_001025200.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:15769940 A>G maps to NM_007272.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:67963905 G>A maps to NM_001907.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr16:67964428 G>A maps to NM_001907.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:44522701 C>T maps to NM_000308.2 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr20:44520335 G>A maps to NM_000308.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:44520356 C>A maps to NM_000308.2 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr20:44521413 G>A maps to NM_000308.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:11703218 T>C maps to NM_147783.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:88068131 A>G maps to NM_001814.4 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:88033706 G>A maps to NM_001814.4 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:88045715 C>A maps to NM_001814.4 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr11:88027272 G>T maps to NM_001814.4 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr11:88033788 A>G maps to NM_001814.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:1774843 C>T maps to NM_001909.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:206318412 C>T maps to ENST00000361052 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:206325371 A>G maps to ENST00000361052 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:206325317 T>C maps to ENST00000361052 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:206328778 A>G maps to ENST00000361052 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr1:206328778 A>G maps to ENST00000361052 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr1:206328778 A>G maps to ENST00000361052 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:206328751 C>T maps to ENST00000361052 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:66334965 G>A maps to NM_003793.3 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:66333833 G>A maps to NM_003793.3 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:66331415 C>T maps to NM_003793.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:66333181 G>A maps to NM_003793.3 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr11:66333181 G>A maps to NM_003793.3 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:25043680 G>A maps to NM_001911.2 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:25042962 G>A maps to NM_001911.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr9:90343298 T>G maps to NM_145918.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr9:90342607 C>A maps to NM_145918.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:90345359 C>T maps to NM_145918.2 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr9:99795260 G>A maps to NM_001333.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:99797894 C>T maps to NM_001333.2 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:99797123 G>A maps to NM_001333.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:99800313 C>T maps to NM_001333.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr4:156858569 G>A maps to NM_001334.2 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:156860678 G>T maps to NM_001334.2 C132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr4:156860676 C>T maps to NM_001334.2 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:150722509 A>G maps to NM_004079.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:65648878 G>A maps to NM_001335.3 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:70281195 C>T maps to NM_001184740.1 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:70263206 G>A maps to NM_001184740.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:70253450 C>T maps to NM_001184740.1 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:70277322 G>A maps to NM_001184740.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:70281207 C>T maps to NM_001184740.1 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:117432148 G>A maps to NM_033427.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr7:117432607 G>T maps to NM_033427.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:117432607 G>T maps to NM_033427.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:117375137 T>C maps to NM_033427.2 E1235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:117432265 T>A maps to NM_033427.2 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:117431902 T>C maps to NM_033427.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:117417798 G>A maps to NM_033427.2 H848H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:117432607 G>T maps to NM_033427.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr7:117365286 G>A maps to NM_033427.2 G1360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:117398013 C>T maps to NM_033427.2 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:112991592 A>G maps to NM_018704.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:112999946 T>C maps to NM_018704.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr1:112958849 G>A maps to NM_018704.2 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:112998998 C>T maps to NM_018704.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:112999601 C>T maps to NM_018704.2 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:112999502 C>T maps to NM_018704.2 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:112997072 G>A maps to NM_018704.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:112998845 C>A maps to NM_018704.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:51602385 G>A maps to NM_145232.3 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:88780173 C>A maps to ENST00000378384 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr16:88778717 C>A maps to ENST00000378384 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:88779061 C>A maps to ENST00000378384 C233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr10:17113928 G>A maps to NM_001081.3 N781N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:16980979 G>A maps to NM_001081.3 C1905C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr10:16911791 G>A maps to NM_001081.3 Y3099Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr10:17127689 C>T maps to NM_001081.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:17089540 A>G maps to NM_001081.3 N1067N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr10:16970252 G>T maps to NM_001081.3 I2058I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr10:16996514 G>A maps to NM_001081.3 R1576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:17026158 G>A maps to NM_001081.3 T1490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr10:16990477 C>T maps to NM_001081.3 S1736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:16992051 T>C maps to NM_001081.3 A1676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:16957157 G>T maps to NM_001081.3 G2408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:17146543 C>A maps to NM_001081.3 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:16960756 C>T maps to NM_001081.3 S2288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:16996541 G>A maps to NM_001081.3 Y1567Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr10:16883019 C>T maps to NM_001081.3 A3230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:17130201 G>A maps to NM_001081.3 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:16981012 G>T maps to NM_001081.3 I1894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:17127754 G>A maps to NM_001081.3 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:17157583 T>C maps to NM_001081.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:16982061 G>A maps to NM_001081.3 S1839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr10:16980961 C>T maps to NM_001081.3 R1911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr10:16916443 G>A maps to NM_001081.3 Y3055Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr10:17126269 C>T maps to NM_001081.3 E767E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr10:16911749 G>A maps to NM_001081.3 C3113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr10:17085892 G>A maps to NM_001081.3 S1254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:17142217 A>G maps to NM_001081.3 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:16992048 A>G maps to NM_001081.3 R1677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:55948674 G>A maps to NM_017949.1 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:55950972 G>T maps to NM_017949.1 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:148494914 G>A maps to NM_003592.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:148497632 C>T maps to NM_003592.2 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:148487508 C>A maps to NM_003592.2 C594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:148457555 C>T maps to NM_003592.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr7:148464823 G>T maps to NM_003592.2 G356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr10:35327979 G>A maps to NM_001198778.1 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:35322102 C>T maps to NM_001198778.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:35327979 G>A maps to NM_001198778.1 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:35317782 T>A maps to NM_001198778.1 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:35328010 C>A did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr10:35349818 A>T maps to NM_001198778.1 Y119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:35327979 G>A maps to NM_001198778.1 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:225339012 T>C maps to NM_003590.3 E752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:225400346 A>G maps to NM_003590.3 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:225343023 C>A maps to NM_003590.3 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:225422489 A>G maps to NM_003590.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr13:113893822 C>T maps to NM_001008895.1 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:113917886 C>T maps to NM_001008895.1 Y757Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr13:113909021 C>T maps to NM_001008895.1 Q590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:119674339 C>A did not map to a codon.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr23:119670834 T>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:119666281 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:119666281 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:119678366 C>T did not map to a codon.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr23:119681024 C>G did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:119668390 C>A did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:119694437 T>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:119678360 A>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:119694089 T>C did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:119666398 T>C did not map to a codon.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr11:107925383 T>C maps to NM_003478.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:107916999 T>C maps to NM_003478.3 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr11:107920750 C>T maps to NM_003478.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:107923518 G>T maps to NM_003478.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:107925479 G>A maps to NM_003478.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:107925383 T>C maps to NM_003478.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:107959387 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr11:107925383 T>C maps to NM_003478.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr11:107925383 T>C maps to NM_003478.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr11:107925383 T>C maps to NM_003478.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:43013765 G>A maps to NM_001168370.1 C992C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:43018058 A>G maps to NM_001168370.1 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:43015992 T>C did not map to a codon.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr6:43190321 G>A maps to ENST00000354495 P2325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr6:43166413 G>T maps to ENST00000354495 G957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr6:43153282 C>T maps to ENST00000354495 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:43188318 G>A maps to ENST00000354495 S2135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:43154737 G>A maps to ENST00000354495 W431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:43155479 C>A maps to ENST00000354495 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:43166399 C>T maps to ENST00000354495 R953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:43154153 C>T maps to ENST00000354495 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:43152503 C>T maps to ENST00000354495 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:43188603 C>T maps to ENST00000354495 C2181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:43191032 C>A maps to ENST00000354495 A2395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr6:43164380 A>G did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:43171201 G>A maps to ENST00000354495 K1299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:101502946 A>G maps to NM_015960.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:101514389 C>T maps to NM_015960.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr10:101515474 C>T maps to NM_015960.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:101844796 C>A maps to ENST00000360264 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr7:101845270 C>T maps to ENST00000360264 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:101459360 A>G maps to ENST00000360264 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:101758535 T>C maps to ENST00000360264 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:101813826 C>T maps to ENST00000360264 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:101842124 G>A maps to ENST00000360264 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:101842124 G>A maps to ENST00000360264 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:101916706 C>T maps to NM_001913.2 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:101882762 G>A maps to ENST00000360264 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:101845321 G>A maps to ENST00000360264 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:101848403 C>T maps to ENST00000360264 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:101844883 A>G maps to ENST00000360264 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr7:101844796 C>T maps to ENST00000360264 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:101821834 C>T maps to ENST00000360264 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr7:101559405 T>C maps to ENST00000360264 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:111760253 C>T maps to NM_015267.3 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:111652083 C>T maps to NM_015267.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr12:111750003 C>T maps to NM_015267.3 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr12:111748482 C>T maps to NM_015267.3 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr12:111748091 C>T maps to NM_015267.3 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr12:111779830 C>T maps to NM_015267.3 T1211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:124597029 T>A maps to NM_022034.4 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:124593208 G>A maps to NM_022034.4 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:124597053 G>A maps to NM_022034.4 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:124598698 G>A maps to NM_022034.4 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:124596428 G>A maps to NM_022034.4 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:124598704 G>T maps to NM_022034.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:124598560 G>A maps to NM_022034.4 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:124593236 G>A maps to NM_022034.4 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:124598659 G>T maps to NM_022034.4 C107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:124596380 G>T maps to NM_022034.4 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:124598686 G>A maps to NM_022034.4 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:180815275 G>A maps to NM_020943.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:180829281 A>G maps to NM_020943.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:180837940 C>T maps to NM_020943.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:180809948 T>C maps to NM_020943.2 R878R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:180838419 C>A maps to NM_020943.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:36958984 C>T maps to NM_017748.3 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:64100102 T>C maps to NM_005869.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:64267620 A>G maps to NM_005869.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:102016153 T>C maps to NM_018294.4 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:102003463 G>A maps to NM_018294.4 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:107325240 C>A maps to NM_152434.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:107326465 C>A maps to NM_152434.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:107286999 G>A maps to NM_152434.2 Q518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:49034675 C>T maps to NM_025087.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:57413555 C>T maps to NM_002996.3 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:39307550 G>A maps to NM_001171174.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:39307972 C>A maps to NM_001171174.1 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:39307286 G>A maps to NM_001171174.1 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:39307447 C>A maps to NM_001171174.1 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr3:39307073 C>G maps to NM_001171174.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr21:18933708 C>T maps to NM_001338.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr21:18919505 C>T maps to NM_001338.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:18924065 G>T did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr21:18924200 T>C maps to NM_001338.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr10:44874128 C>T maps to NM_001178134.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:78528950 C>A maps to NM_006419.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:4638399 C>T maps to NM_001100812.1 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:4642628 T>C maps to NM_001100812.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:42937143 G>C maps to NM_198477.1 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr4:74903850 T>C maps to NM_002090.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:74702708 G>A maps to NM_002993.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr4:76924816 T>C maps to NM_002416.1 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr4:76924816 T>C maps to NM_002416.1 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr4:76925960 C>A did not map to a codon.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr2:219029889 T>C maps to NM_000634.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:70836821 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:70837301 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:70837192 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:70837156 G>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:70836820 G>A did not map to a codon.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:136872552 G>A maps to NM_001008540.1 H319H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:136873119 G>A maps to NM_001008540.1 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr2:136872497 G>A maps to NM_001008540.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:136872987 G>A maps to NM_001008540.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:136873029 G>T maps to NM_001008540.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:118764549 G>A maps to NM_001716.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:118764534 C>T maps to NM_001716.3 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:118765254 G>A maps to NM_001716.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr3:45988068 C>T maps to NM_006564.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:237490019 G>A maps to NM_020311.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:237489830 G>A maps to NM_020311.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:237489152 G>A maps to NM_020311.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:237489152 G>A maps to NM_020311.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:47811602 C>T maps to NM_001101654.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr18:47809046 G>A maps to NM_001101654.1 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:105412122 G>A maps to NM_025212.1 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:139060341 G>A maps to NM_016463.7 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:144909346 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:144909517 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:30578256 C>T did not map to a codon.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr23:30577651 C>T did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:30578014 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:35985887 T>C did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:35944220 G>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:35959476 C>A did not map to a codon.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr23:35984784 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:36007540 C>T did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr23:35970072 A>G did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr23:35971835 A>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:35944212 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:35969990 A>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:35993923 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:36007493 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:36007609 A>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:35974223 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:35989735 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:35985834 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:35988990 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:35944222 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:35988901 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:36007538 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:35937928 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:35988929 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:35989994 G>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:35944222 A>G did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:35944222 A>G did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:35944220 G>A did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:35988902 T>C did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:35944221 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:35989795 G>T did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:19968957 T>C did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:19953994 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:19983601 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:19984318 T>G did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr23:19971167 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr23:19983233 G>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:19971159 A>T did not map to a codon.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr23:75397737 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:75396781 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:75397515 T>C did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:75397618 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:37850382 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:45051018 G>A did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:45060033 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:45011147 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr23:45010953 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:45013347 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:45017101 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:40498287 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:40496389 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:40495838 C>A did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:40496388 T>C did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:40496388 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:40495956 G>A did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:148627362 A>G did not map to a codon.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr23:148628483 G>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:148627258 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:106466041 T>G did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:106456244 C>A did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:134292130 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:118678359 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:118678409 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:118678357 C>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:118678441 C>T did not map to a codon.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr23:105876479 C>A did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:105883844 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:105876238 G>A did not map to a codon.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr23:105855879 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:105855703 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:105855825 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:105882828 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:105891592 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:105876480 A>G did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:105879792 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:105855865 A>C did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:105881009 A>G did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:105868477 C>A did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr23:105868477 C>T did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr23:105868374 C>T did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:105912496 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:105876478 C>A did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:105855398 C>T did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:105868477 C>A did not map to a codon.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr23:23934410 T>C did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:23953326 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:23956724 T>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:23928503 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr23:23956733 C>T did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:23956757 A>G did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:23945382 G>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:23953369 C>T did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:36091448 C>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:36122792 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:36090061 A>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:36103514 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr23:36103477 A>T did not map to a codon.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr23:36156548 C>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:36103601 A>C did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:36103602 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:36117880 C>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:36122628 C>A did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:36091445 A>G did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:36091445 A>G did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:36091445 A>G did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:36122631 G>A did not map to a codon.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr23:115593069 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:115592986 T>C did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:115593060 A>G did not map to a codon.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr23:70326215 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:70325891 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:70324158 C>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:139038062 T>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:139038494 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:139038784 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:139040315 A>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:139040285 A>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:110038713 C>T maps to NM_001134400.1 L197L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3977-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:50388900 C>A maps to NM_007022.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:4053287 T>C maps to NM_144611.3 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr17:4047069 T>C maps to NM_144611.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:7694035 C>T maps to NM_016229.3 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:84634287 C>A maps to NM_016230.3 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:84603244 C>T maps to NM_016230.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr6:84646000 G>A maps to NM_016230.3 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:88713176 G>A maps to NM_000101.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:61121435 C>T maps to NM_001161454.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:37655301 C>T did not map to a codon.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr23:37653049 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:37655331 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:37664264 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:37652918 G>A did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr23:37663349 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:37655342 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:37660571 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:172398197 C>T maps to NM_024843.3 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr8:145152211 G>C maps to NM_001916.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr15:22955183 G>A maps to NM_014608.2 E526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:22954271 C>T maps to NM_014608.2 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:22993151 C>T maps to NM_014608.2 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr15:22956343 G>A maps to NM_001033028.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:22945080 C>T maps to NM_014608.2 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:22955234 C>T maps to NM_014608.2 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:22998433 A>G maps to NM_014608.2 R1042R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:22947019 C>T maps to NM_014608.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:22956211 C>T maps to NM_001033028.1 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:156712445 G>A maps to ENST00000442283 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:156752607 G>A maps to ENST00000442283 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:156752563 C>T maps to ENST00000442283 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:156747678 C>T maps to ENST00000442283 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:156747708 C>T maps to ENST00000442283 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr5:156768140 G>A maps to ENST00000442283 Q908Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:145677760 G>A maps to NM_138496.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:145676013 G>A maps to NM_138496.1 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:83129027 A>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:83128183 T>G did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:83128698 A>G did not map to a codon.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr23:83128902 A>G did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:83128981 A>G did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr23:83128981 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:83141589 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:83128278 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:83129489 G>A did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr23:83128478 G>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:83128900 C>A did not map to a codon.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr23:83128418 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:83128378 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:83128545 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:83128242 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:83127911 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:83128540 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:83128644 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:83129163 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:83129181 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:83128697 A>G did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:83128901 A>G did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr23:83128418 T>C did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:83129586 T>A did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:83128980 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:83128923 T>G did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:83128903 G>T did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:83128902 A>G did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:83128418 T>C did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr23:83128507 G>C did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:83128418 T>C did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:83128980 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:83128362 C>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:105765521 C>T maps to NM_001340.3 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:105767459 G>T maps to NM_001340.3 G183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr9:105767797 C>T maps to NM_001340.3 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr9:105767413 T>C maps to NM_001340.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr16:50816344 C>A maps to ENST00000311559 Y598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:50815179 G>A maps to ENST00000311559 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:50825537 C>T maps to ENST00000311559 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:50815179 G>A maps to ENST00000311559 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr16:50828127 C>T maps to ENST00000311559 H825H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr16:50811850 A>G maps to ENST00000311559 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:50783687 G>T maps to ENST00000311559 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:50816263 A>G maps to ENST00000311559 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:50815320 A>G maps to ENST00000311559 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr16:50816344 C>T maps to ENST00000311559 Y598Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr16:50830353 C>T maps to ENST00000311559 R936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:50811850 A>G maps to ENST00000311559 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:50828192 G>A maps to ENST00000311559 W847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr16:50785684 C>T maps to ENST00000311559 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr16:50811826 A>G maps to ENST00000311559 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:50788264 T>C maps to ENST00000311559 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr16:50815320 A>G maps to ENST00000311559 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:50826584 G>A maps to ENST00000311559 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:50816344 C>T maps to ENST00000311559 Y598Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:74636322 G>A maps to NM_000781.2 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr15:74630944 G>A maps to NM_000781.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr15:74640281 G>T maps to NM_000781.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:74630360 G>T maps to NM_000781.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:74637571 G>T maps to NM_000781.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:143958577 G>A maps to ENST00000377675 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr8:143957130 A>T maps to ENST00000377675 L444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr8:143956504 G>T maps to ENST00000377675 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr8:143957131 A>G maps to ENST00000377675 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr8:143961127 T>C maps to ENST00000377675 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr8:143994113 C>T maps to NM_000498.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr10:104597007 C>A maps to NM_000102.3 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr10:104592809 G>A maps to NM_000102.3 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:104592821 G>T maps to NM_000102.3 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:104595062 C>T maps to NM_000102.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:104591368 C>T did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr10:104595062 C>T maps to NM_000102.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr15:51503033 T>A maps to NM_031226.2 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:51535007 A>G maps to NM_031226.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:51503099 T>A maps to NM_031226.2 K473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:51503250 A>G maps to NM_031226.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr15:75014964 G>A maps to NM_000499.3 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr15:75045578 C>A maps to NM_000761.3 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:75045572 C>T maps to NM_000761.3 C405C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:38297952 G>T maps to NM_000104.3 S515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:38301820 C>T maps to NM_000104.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:38301838 G>A maps to NM_000104.3 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:38298076 C>A maps to NM_000104.3 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:204154518 C>T maps to ENST00000429815 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr6:32006321 G>A maps to NM_000500.5 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:52779387 G>A maps to NM_000782.4 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:52773732 C>T maps to NM_000782.4 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:52789986 G>A maps to NM_000782.4 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:52773732 C>T maps to NM_000782.4 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:94836742 G>A maps to NM_000783.3 W392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:94837059 G>T maps to NM_000783.3 *498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:94834925 C>A maps to NM_000783.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:94834558 C>T maps to NM_000783.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr10:94835659 T>A maps to NM_000783.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:72371228 G>A maps to NM_019885.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:94821085 G>A maps to NM_183374.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:219679737 G>A maps to NM_000784.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:219647123 C>T maps to NM_000784.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:219677130 C>A maps to NM_000784.3 Y211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:219677091 G>A maps to NM_000784.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:127956957 G>A maps to NM_001001665.3 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:41594440 C>A maps to NM_000766.3 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:41601773 C>T maps to NM_000766.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr19:41596012 A>G maps to NM_000766.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:41354651 G>A maps to NM_000762.5 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:41351887 G>A maps to NM_000762.5 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:41354282 G>A maps to NM_000762.5 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:41384721 C>T maps to NM_000764.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:41386462 G>A maps to NM_000764.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:41386462 G>A maps to NM_000764.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:41384771 G>A maps to NM_000764.2 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr19:41386474 G>T maps to NM_000764.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:41383820 G>A maps to NM_000764.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr19:41387539 G>A maps to NM_000764.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr19:41387535 G>A maps to NM_000764.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:41516002 C>T maps to NM_000767.4 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:96454743 T>C maps to NM_000772.2 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:96493118 G>A maps to NM_000772.2 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr10:96447996 C>T maps to NM_000772.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:96602621 C>A maps to NM_000769.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:96612592 G>A maps to NM_000769.1 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr10:96535288 A>G maps to NM_000769.1 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:96824625 A>G maps to NM_000770.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr10:96824642 G>A maps to NM_000770.3 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr10:96701685 T>C maps to NM_000771.3 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr10:96731977 C>T maps to NM_000771.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:42524348 G>A maps to NM_000106.4 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:42522620 G>A maps to NM_000106.4 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr10:135347294 C>T maps to NM_000773.3 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:135346209 T>C maps to NM_000773.3 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:41626274 C>T maps to NM_000774.3 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:60370605 G>A maps to NM_000775.2 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:14902248 G>A maps to NM_024514.4 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:41703756 C>T maps to ENST00000301173 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:41699339 C>T maps to ENST00000301173 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:108866750 C>T maps to NM_183075.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:1024815 C>T maps to NM_017781.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:46518150 G>A maps to NM_016593.3 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:99355764 A>G maps to NM_017460.3 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:99359827 C>T maps to NM_017460.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:99441778 C>T maps to NM_022820.3 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:99453256 C>T maps to NM_022820.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr7:99246002 C>T maps to NM_000777.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:99264261 C>T maps to NM_000777.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:99308386 G>A maps to ENST00000292414 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:99313528 G>A maps to ENST00000292414 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:99317964 C>A maps to ENST00000292414 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:99319949 C>A maps to ENST00000292414 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr7:99314836 G>T maps to ENST00000292414 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr7:99317953 A>G maps to ENST00000292414 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:100166405 G>A maps to NM_006668.1 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr14:100182531 T>C maps to NM_006668.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:47403013 C>T maps to ENST00000371904 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:47406991 G>A maps to ENST00000371904 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:47407036 G>T maps to ENST00000371904 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:47395795 G>A maps to ENST00000371904 D518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:47400684 G>A maps to ENST00000371904 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:47608984 C>A maps to NM_001010969.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:47280903 C>T maps to NM_001099772.1 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:47283664 C>T maps to NM_001099772.1 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:47279203 C>T maps to NM_001099772.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:47264933 G>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:16045212 C>T maps to NM_021187.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:16045053 C>T maps to NM_021187.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:15789168 C>T maps to NM_023944.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:15789138 G>T maps to NM_023944.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:16003139 A>G maps to NM_001082.3 N168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:15996843 A>G maps to NM_001082.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:15654982 G>A maps to NM_173483.3 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:15654985 C>A maps to NM_173483.3 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:15651470 G>A maps to NM_173483.3 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:15662182 C>T maps to NM_173483.3 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:15648199 C>T maps to NM_173483.3 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:15756569 G>T maps to NM_000896.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr19:15756569 G>T maps to NM_000896.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:15760810 C>T maps to NM_000896.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:15756539 G>A maps to NM_000896.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:15730530 C>T maps to NM_007253.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr19:15739611 G>A maps to NM_007253.3 K451K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:15739189 C>T maps to NM_007253.3 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:187122435 C>T maps to NM_207352.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr4:187122354 T>C maps to NM_207352.3 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr4:187130154 T>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:187130277 C>T maps to ENST00000511608 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:47499003 C>T maps to NM_178033.1 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr1:47515117 C>T maps to NM_178033.1 Q433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:47548004 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:91753093 C>A maps to NM_000786.3 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr7:91755715 G>C maps to NM_000786.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr7:91752622 C>T maps to NM_000786.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:59404206 A>G maps to NM_000780.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr8:65527679 G>A maps to NM_004820.3 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:42915952 G>T maps to NM_004391.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:42916312 A>G maps to NM_004391.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:42916537 G>A maps to NM_004391.2 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:86047741 G>T maps to NM_001554.4 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:77528367 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:77528546 C>A did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:77528367 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:77528979 A>C did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:77528507 A>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:77528367 A>G did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:77529108 G>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:77528355 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:77529089 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:77528651 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:77528519 A>C did not map to a codon.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr23:77528367 A>G did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:77528367 A>T did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:77528367 A>G did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:77528367 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:77528367 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:49281768 G>A maps to NM_020377.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:49281067 G>T maps to NM_020377.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:49281252 A>G maps to NM_020377.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr13:49281252 A>G maps to NM_020377.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr17:76672211 T>C maps to NM_004762.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:48973758 T>C did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:6230099 C>A maps to ENST00000396741 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:6205414 G>T maps to ENST00000396741 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:6210908 C>T maps to ENST00000396741 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:6204983 G>A maps to ENST00000396741 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr7:6204983 G>A maps to ENST00000396741 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr7:6210532 G>T maps to ENST00000396741 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr22:37708119 C>T maps to NM_013385.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:158272491 A>G maps to NM_004288.4 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:158300366 G>A maps to NM_004288.4 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:158272227 G>A maps to NM_004288.4 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:5018685 G>T maps to NM_018659.2 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr22:24717467 C>T maps to NM_015330.2 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr22:24718634 G>T maps to NM_015330.2 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:24720263 T>G maps to NM_015330.2 L672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr17:20109065 C>T maps to NM_001033553.1 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr17:20107754 A>G maps to NM_001033553.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr21:27840930 G>A maps to ENST00000435845 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr21:27852645 C>T maps to ENST00000435845 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr14:59782008 A>G maps to NM_014992.1 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:59798093 T>C maps to NM_014992.1 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:59826193 C>T maps to NM_014992.1 R879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr14:59819299 C>T maps to NM_014992.1 H749H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:39836619 C>T maps to ENST00000398904 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:39855320 G>T maps to ENST00000398904 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:39839296 C>T maps to ENST00000398904 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:39864965 C>T maps to ENST00000398904 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr6:39869689 G>A maps to ENST00000398904 S1028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:39869725 A>G maps to ENST00000398904 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr6:39824227 C>T maps to ENST00000398904 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:39835393 C>T maps to ENST00000398904 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr1:57476832 G>A maps to ENST00000371231 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:57611010 G>A maps to ENST00000371231 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:57602311 G>A maps to ENST00000371231 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:57602299 G>A maps to ENST00000371231 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:57602244 C>A maps to ENST00000371231 G93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:57538000 C>T maps to ENST00000371231 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:57476943 A>G maps to ENST00000371231 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr1:57491652 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:39376884 C>T maps to NM_001343.2 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:39383253 C>T maps to NM_001343.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr5:39383089 G>T maps to NM_001343.2 S324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr5:39383079 C>T maps to NM_001343.2 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr5:39393448 A>G maps to NM_001343.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:39382914 A>G maps to NM_001343.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:39382914 A>G maps to NM_001343.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr5:39382914 A>G maps to NM_001343.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:124525920 C>T maps to ENST00000408936 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr9:124544626 G>A maps to ENST00000408936 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:124536618 C>T maps to ENST00000408936 D1016D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:124528832 C>T maps to ENST00000408936 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:124461653 G>A maps to ENST00000408936 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:124535420 C>T maps to ENST00000408936 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:124521256 A>G maps to ENST00000408936 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:72053444 G>A maps to ENST00000359684 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr13:72440148 C>T maps to ENST00000359684 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:72204823 A>G maps to ENST00000359684 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr13:72063260 T>C maps to ENST00000359684 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:85769291 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:85403789 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:85969557 T>C did not map to a codon.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr23:86069767 C>T did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr23:85950140 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:86069718 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:86069767 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:85403877 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:85950049 G>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:85404019 C>T did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:85950138 T>C did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:85950138 T>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:85994759 C>T did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:85994759 C>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:85403795 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:86069719 A>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:85631834 G>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr14:59112891 C>T maps to NM_016651.5 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr14:59112483 G>T maps to NM_016651.5 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:59113386 G>A maps to NM_016651.5 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr14:59113155 G>A maps to NM_016651.5 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:59112604 G>T maps to NM_016651.5 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:59112483 G>A maps to NM_016651.5 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:59112078 C>A maps to NM_016651.5 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr14:59107479 T>C maps to NM_016651.5 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:59112483 G>A maps to NM_016651.5 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:49548245 C>A maps to NM_004393.4 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:49568495 G>A maps to NM_004393.4 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:49569500 G>A maps to NM_004393.4 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:49569278 G>A maps to NM_004393.4 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr3:49569284 C>A maps to NM_004393.4 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr3:49568627 G>A maps to NM_004393.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:61488149 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:61504706 G>A maps to NM_006133.2 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:61505206 G>A maps to NM_006133.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr11:61511876 G>A maps to NM_006133.2 A1015A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr11:61511711 C>T maps to NM_006133.2 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:6487395 C>A maps to NM_139179.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:6464409 G>A maps to NM_139179.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:6449512 G>A maps to NM_139179.3 C658C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:6449614 C>T maps to NM_139179.3 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr7:6487434 G>A maps to NM_139179.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:61111617 G>A maps to NM_015533.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:61109939 C>T maps to NM_015533.3 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:49055171 C>A maps to NM_001009996.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr12:109283295 G>T maps to NM_001917.4 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr12:109284019 A>G maps to NM_001917.4 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:106124953 C>T maps to NM_172370.3 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:10748351 T>C maps to ENST00000432074 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:155701736 T>C maps to NM_004632.3 H302H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:155707990 C>T maps to NM_004632.3 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr9:90296536 C>T maps to NM_004938.2 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr9:90321078 C>T maps to NM_004938.2 D1031D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr9:90264999 C>T maps to NM_004938.2 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr9:90264906 C>T maps to NM_004938.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:90296515 T>A maps to NM_004938.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:90321348 C>T maps to NM_004938.2 D1121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:90321474 C>T maps to NM_004938.2 G1163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:90321663 G>A maps to NM_004938.2 T1226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:90262263 C>T maps to NM_004938.2 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:90264931 C>A maps to NM_004938.2 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:90266521 C>T maps to NM_004938.2 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:90321849 C>T maps to NM_004938.2 H1288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:90301592 G>A maps to NM_004938.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:90321474 C>T maps to NM_004938.2 G1163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr9:90264850 C>T maps to NM_004938.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:64275874 C>T maps to NM_014326.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:64231443 C>T maps to NM_014326.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:64204324 A>G maps to NM_014326.3 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:3964715 C>T maps to NM_001348.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:3964715 C>T maps to NM_001348.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr19:3964715 C>T maps to NM_001348.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr19:3964299 C>T maps to NM_001348.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr19:3964715 C>T maps to NM_001348.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:159651926 G>T maps to NM_001017920.2 G15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr4:100738168 G>A maps to NM_014395.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:159176072 C>T maps to NM_001122951.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:159175675 C>T maps to NM_001122951.2 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:173794476 C>A maps to NM_018122.4 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:33286558 G>A maps to NM_001350.4 C728C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:33288636 G>T maps to NM_001350.4 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:33289660 G>A maps to NM_001350.4 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr6:33289558 T>C maps to NM_001350.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:33288636 G>T maps to NM_001350.4 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:33289567 A>G maps to NM_001350.4 H45H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr6:33289558 T>C maps to NM_001350.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:33289693 G>A maps to NM_001350.4 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:33286920 G>A maps to NM_001350.4 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:1434802 C>A maps to NM_018959.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:16638304 A>C maps to NM_001190811.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr9:121929511 C>T maps to NM_014618.2 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:121929910 G>A maps to NM_014618.2 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:121929631 T>A maps to NM_014618.2 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr9:121929961 G>T maps to NM_014618.2 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:122004330 T>C maps to NM_014618.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr9:121971106 C>T maps to NM_014618.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:121976433 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:121929880 C>T maps to NM_014618.2 K589K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:122011319 G>A maps to NM_014618.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:121929427 G>A maps to NM_014618.2 H740H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr9:122011319 G>A maps to NM_014618.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr7:87536838 T>A maps to NM_006716.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:42807310 C>T maps to NM_145663.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:42818778 C>A maps to NM_145663.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr17:42825822 C>T maps to NM_145663.2 C393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:42807326 G>T maps to NM_145663.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:136508596 C>T maps to NM_000787.3 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr9:136507456 G>A maps to NM_000787.3 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr9:136507369 G>A maps to NM_000787.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:136508638 C>T maps to NM_000787.3 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:136508680 C>T maps to NM_000787.3 H297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr9:136501744 C>T maps to NM_000787.3 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:136507564 C>T maps to NM_000787.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:136507381 G>A maps to NM_000787.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr9:136513025 C>T maps to NM_000787.3 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr9:136505113 A>G maps to NM_000787.3 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:120125861 T>C maps to NM_001178017.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:176893955 G>A maps to ENST00000393565 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:176885118 C>T maps to ENST00000393565 E618E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:176884463 T>C maps to ENST00000393565 E686E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:90075267 G>A maps to ENST00000392973 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr20:44038605 G>A maps to NM_001048225.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr7:44096435 A>G maps to NM_001122956.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:44100496 C>T maps to NM_001122956.1 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:49136712 C>T maps to NM_001352.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr3:137882198 C>A maps to NM_016216.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:137893514 C>T maps to NM_016216.3 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr1:100680396 G>C maps to NM_001918.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:100680434 C>A maps to NM_001918.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:20177984 G>A maps to ENST00000227256 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:20180779 G>A maps to ENST00000227256 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:20178707 G>A maps to ENST00000227256 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr12:45417618 G>T maps to NM_001004329.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:45410346 C>A maps to NM_001004329.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr9:37842160 C>T maps to NM_024345.3 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:24586587 C>T maps to NM_025230.4 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr14:24588996 T>C maps to NM_025230.4 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:34088425 C>T maps to NM_015397.3 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:34098320 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:34107503 C>T maps to NM_015397.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:125686182 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:125685946 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:125685910 G>A did not map to a codon.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr23:125685312 A>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:125685699 G>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:125686196 C>T did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:125685438 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:125685784 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:125686236 T>C did not map to a codon.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr23:125686559 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:125685628 G>A did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:125686039 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:125685531 G>A did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:125685952 G>A did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:125685750 A>G did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:125686353 C>A did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:125685346 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:125298774 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:125299781 C>A did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:125299761 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:125298906 G>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:125298898 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:125299019 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:125299603 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:125299407 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:125298539 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:125299858 C>T did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:125298588 T>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:125299119 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:125299439 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:125299313 G>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:125299440 T>C did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:125298735 A>G did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:125299440 T>C did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:125299407 C>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:125299282 C>T did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:125298735 A>G did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr8:104427571 T>C maps to NM_015420.6 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:104427265 C>T maps to NM_015420.6 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:14070283 G>A maps to NM_138353.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:17805170 A>G maps to NM_017741.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:17805170 A>G maps to NM_017741.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr4:17805170 A>G maps to NM_017741.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr14:73406560 C>T maps to NM_015604.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr4:41984615 T>C maps to NM_001029955.3 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:41984708 G>A maps to NM_001029955.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:41984873 G>A maps to NM_001029955.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr4:41984543 C>T maps to NM_001029955.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr4:41984147 C>T maps to NM_001029955.3 H113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:41984924 C>T maps to NM_001029955.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:88885083 G>A maps to NM_152418.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr8:88886021 G>A maps to NM_152418.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr8:88885116 G>A maps to NM_152418.3 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:88886082 G>A maps to NM_152418.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr8:88885353 G>T maps to NM_152418.3 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr8:88885716 C>T maps to NM_152418.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:88886073 A>T maps to NM_152418.3 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:88885200 G>A maps to NM_152418.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr8:88885962 C>T maps to NM_152418.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr8:88885653 G>T maps to NM_152418.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr14:69520612 A>G maps to NM_003861.2 D930D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr14:69521029 C>T maps to NM_003861.2 E791E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr14:69522262 G>A maps to NM_003861.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:167935896 G>T maps to ENST00000367840 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:167973228 T>C did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:168013866 G>T maps to ENST00000367840 G630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:168034883 C>T maps to ENST00000367840 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:61657247 C>T maps to NM_005828.3 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:61655937 C>T maps to NM_005828.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:61661047 C>T maps to NM_005828.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:160201109 C>T maps to NM_015726.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:160209744 G>A maps to NM_015726.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr23:27998166 T>C did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:27998263 A>G did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:27999213 C>T did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr23:27997961 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:27998165 T>C did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:27998989 G>T did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:27998644 T>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:27998573 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:27997864 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:27997801 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:27998053 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr23:27998124 C>G did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:27998386 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:27998149 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:27997671 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:27998445 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:27999099 G>A did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:27998264 A>G did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:27998165 T>C did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:27998667 C>G did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:27998263 A>G did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:27998264 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:27765446 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:27766244 C>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:27766230 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:27765749 C>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:27765897 C>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:27766392 A>G did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:27765562 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:43101857 G>A maps to NM_001128631.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:43111603 G>A maps to NM_001128631.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:117840977 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:117860424 G>A maps to ENST00000338728 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:117841039 C>T maps to ENST00000338728 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:98538220 C>T maps to ENST00000326857 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr3:98518264 G>C maps to ENST00000326857 S774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr3:98518662 T>C maps to ENST00000326857 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr18:50741918 G>T maps to NM_005215.3 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr18:50976897 G>A maps to NM_005215.3 P1086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:49867231 G>A maps to NM_005215.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:51025695 A>G maps to NM_005215.3 Q1309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:50848501 A>G maps to NM_005215.3 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr18:50994336 G>A maps to NM_005215.3 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr18:50923745 G>A maps to NM_005215.3 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:50432439 G>T maps to NM_005215.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr18:50734110 T>C maps to NM_005215.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr18:50683846 T>C maps to NM_005215.3 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:50589678 G>A maps to NM_005215.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:50923700 T>C maps to NM_005215.3 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:50936927 T>C maps to NM_005215.3 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:51025777 C>T maps to NM_005215.3 R1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr18:50734110 T>C maps to NM_005215.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr18:50976948 G>T maps to NM_005215.3 V1103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr18:50832018 A>G maps to NM_005215.3 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr18:51013218 A>T maps to NM_005215.3 G1263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr18:50731649 T>C maps to NM_005215.3 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr18:50683846 T>C maps to NM_005215.3 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:55038966 G>A maps to NM_053283.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr11:31327275 G>A maps to NM_181807.2 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:31327323 G>A maps to NM_181807.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr11:31327258 G>A maps to NM_181807.2 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr11:31327886 C>T maps to NM_181807.2 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:24278357 C>A maps to NM_016356.3 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:32678162 C>T maps to NM_001099434.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:32674835 C>T maps to NM_001099434.1 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr11:6653960 G>T maps to NM_003737.2 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:6651377 C>T maps to NM_003737.2 P1549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:6650999 C>T maps to NM_003737.2 A1646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:6662658 G>A maps to NM_003737.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:6662496 G>T maps to NM_003737.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:6649972 G>T maps to NM_003737.2 T1750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:6651053 C>T maps to NM_003737.2 P1628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:6652617 C>T maps to NM_003737.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:6661149 G>A maps to NM_003737.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:6644440 C>T maps to NM_003737.2 V2822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:6651347 C>T maps to NM_003737.2 P1559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:155241810 A>G maps to NM_017639.3 I1125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:155411925 C>T maps to NM_001142552.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:155411277 C>T maps to NM_001142552.1 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:155254100 A>G maps to NM_017639.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:155244398 G>A maps to NM_001142552.1 I1367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:155312428 C>T maps to NM_017639.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:155256152 G>A maps to NM_017639.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr4:155254419 G>T maps to NM_017639.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:155252804 T>C maps to NM_017639.3 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:155156383 G>A maps to NM_017639.3 D2685D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:155219696 A>C maps to NM_017639.3 V1468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:155219657 A>C maps to NM_017639.3 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:155156017 C>T maps to NM_017639.3 L2807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:155157657 C>A maps to NM_017639.3 E2261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:155237035 C>T maps to NM_017639.3 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:155156524 G>A maps to NM_017639.3 G2638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:155250755 C>T maps to NM_017639.3 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr4:155237074 C>T maps to NM_017639.3 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:155249245 T>A maps to NM_017639.3 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:155156632 G>A maps to NM_017639.3 D2602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:155244398 G>T maps to NM_001142552.1 I1367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:155410589 C>A maps to NM_001142552.1 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:155219635 C>A maps to NM_017639.3 E1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:155156853 C>A maps to NM_017639.3 G2529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:155412195 C>T maps to NM_001142552.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:155410935 C>T maps to NM_001142552.1 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr4:155411001 G>A maps to NM_001142552.1 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr4:155219027 C>T maps to NM_017639.3 G1691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr4:155242047 T>C maps to NM_017639.3 E1046E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr4:155157577 A>C maps to NM_017639.3 A2287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr4:155312423 G>T maps to NM_017639.3 S9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr4:155158081 G>A maps to NM_017639.3 I2119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:155157523 C>T maps to NM_017639.3 L2305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr4:155155779 A>G maps to NM_017639.3 L2887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr4:155411805 C>T maps to NM_001142552.1 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:155225917 A>G maps to NM_017639.3 I1381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:2294450 G>A maps to NM_001919.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:2290102 C>T maps to NM_001919.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:2290113 G>A maps to NM_001919.3 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:2293146 C>T maps to NM_001919.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:71892390 C>T maps to ENST00000504952 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr4:71888091 A>G maps to ENST00000504952 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr4:71888091 A>G maps to ENST00000504952 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr13:36367571 T>C maps to NM_004734.4 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:36686116 C>T maps to NM_004734.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:36367607 G>A maps to NM_004734.4 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr13:36428680 C>T maps to NM_004734.4 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr13:36686116 C>T maps to NM_004734.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr13:36700030 G>A maps to NM_004734.4 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:36367592 T>C maps to NM_004734.4 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:36699997 G>T maps to NM_004734.4 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr13:36699917 G>A maps to NM_004734.4 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr13:36686116 C>T maps to NM_004734.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:36700118 G>A maps to NM_004734.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr13:36686199 G>A maps to NM_004734.4 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr13:36413286 C>T maps to NM_004734.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr13:36700190 G>A maps to NM_004734.4 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr13:36699997 G>T maps to NM_004734.4 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:151153865 G>A maps to NM_001040261.4 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:151168814 G>A maps to NM_001040261.4 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr4:151114364 C>T maps to NM_001040261.4 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr3:36763045 G>A maps to NM_033403.1 Y519Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr3:36759633 G>A maps to NM_033403.1 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:36759585 A>G maps to NM_033403.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr3:36778710 C>T maps to NM_033403.1 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr3:36778800 C>T maps to NM_033403.1 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:36779784 C>T maps to NM_033403.1 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:36778884 T>C maps to NM_033403.1 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:115609915 C>T maps to NM_014881.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:115609398 A>G maps to NM_014881.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:14970118 G>T maps to NM_001033855.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:14977460 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:14950588 C>A maps to NM_001033855.1 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:14976405 G>T maps to NM_001033855.1 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr10:14978592 C>A did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr12:91552211 T>C maps to NM_133503.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr12:91552211 T>C maps to NM_133503.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:53326308 G>A maps to ENST00000480258 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr3:53321639 G>A maps to ENST00000480258 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:53353456 G>A maps to ENST00000480258 H116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:2102454 A>G maps to NM_152640.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr12:2102454 A>G maps to NM_152640.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr12:2102454 A>G maps to NM_152640.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr12:2102454 A>G maps to NM_152640.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr12:2058461 C>T maps to NM_152640.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr5:112343732 T>C maps to NM_152624.4 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:112321633 G>A maps to NM_152624.4 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:112343633 G>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr11:126208230 C>T maps to NM_014026.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:155020272 C>T maps to NM_152494.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:154999150 G>A maps to NM_144622.2 Y461Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:155002939 G>A maps to NM_144622.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:155005606 G>A maps to NM_144622.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr13:95131314 T>C maps to NM_001129889.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr13:95112365 G>A maps to NM_001129889.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:95121179 C>A maps to NM_001129889.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr13:95114391 A>G maps to NM_001129889.1 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr13:95121165 G>A maps to NM_001129889.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:183836079 C>T maps to NM_001012732.1 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:183814254 A>G maps to NM_001012732.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr2:74594924 G>A maps to NM_004082.4 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:74592214 A>G maps to NM_004082.4 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:74594188 G>A maps to NM_004082.4 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:74593454 T>C maps to NM_004082.4 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:57939810 C>T maps to ENST00000434715 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:34618748 G>A maps to NM_007234.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:23678399 C>T maps to NM_032486.3 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr16:30435598 C>A maps to NM_024096.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:182683523 C>T maps to NM_020640.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr16:20873512 A>G maps to NM_173475.2 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:20873698 G>A maps to NM_173475.2 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:20873512 A>G maps to NM_173475.2 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr4:52779713 G>A maps to ENST00000451288 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr11:102937289 G>A maps to NM_032299.3 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr23:110653382 C>T did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:110644349 A>G did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:110555902 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:110555911 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:110653538 T>C did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:110555903 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:110653527 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:110654059 T>C did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:110555911 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:110544916 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:110644302 A>C did not map to a codon.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr23:110555902 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr23:110653438 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:110653360 C>T did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:110644349 A>G did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:110653536 A>G did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:110644349 A>G did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:110653538 T>A did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:110644351 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr23:110653459 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:110574187 C>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:110555913 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:17425178 C>T maps to NM_024050.5 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:85790563 G>T maps to NM_012137.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:85816214 G>A maps to NM_012137.3 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:61070138 G>A maps to NM_001923.3 H1009H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:61081928 A>C maps to NM_001923.3 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:61070069 C>T maps to NM_001923.3 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:61099101 G>A maps to NM_001923.3 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:61081666 T>C maps to NM_001923.3 E535E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:61079462 T>C maps to NM_001923.3 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:61090530 A>G maps to NM_001923.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr11:47254444 A>T maps to NM_000107.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:50566899 G>A maps to NM_000790.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr14:53529889 A>G maps to NM_001160148.1 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:103907675 C>T maps to NM_001001711.2 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:103907741 C>T maps to NM_001001711.2 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr11:103907570 C>T maps to NM_001001711.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:103907978 C>T maps to NM_001001711.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr11:103907585 C>T maps to NM_001001711.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr12:57911084 C>A maps to NM_001195056.1 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:101109121 C>T maps to NM_145244.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr4:101108905 G>A maps to NM_145244.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:49391488 A>G maps to NM_015086.1 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr6:110714040 G>A maps to NM_003649.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:110714028 C>T maps to NM_003649.2 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:20987792 C>A maps to NM_005216.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:20981982 T>A maps to NM_005216.4 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:20978910 G>A maps to NM_005216.4 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:20979148 G>T maps to NM_005216.4 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:20978955 G>A maps to NM_005216.4 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:30863239 C>T maps to NM_013994.2 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:30864638 G>T maps to NM_013994.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:30857110 C>T maps to NM_013994.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:30867042 C>T maps to NM_013994.2 F910F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr6:30866045 C>T maps to NM_013994.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:30866780 C>T maps to NM_013994.2 N862N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr6:30861112 C>T maps to NM_013994.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr6:30859814 T>C maps to NM_013994.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr6:30866783 G>A maps to NM_013994.2 A863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:162741859 G>A maps to NM_006182.2 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr1:162725488 C>T maps to NM_006182.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:162748467 T>C maps to NM_006182.2 D794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:162745516 T>C maps to NM_006182.2 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:162737017 G>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:162740171 C>A maps to NM_006182.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr1:162729633 C>T maps to NM_006182.2 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:162722918 C>A maps to NM_006182.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:3175975 G>A maps to NM_023935.1 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:3183996 G>A maps to NM_023935.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr2:15742717 A>G maps to NM_004939.1 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:15742715 G>T maps to NM_004939.1 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr2:15760411 T>C maps to NM_004939.1 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr2:15742717 A>G maps to NM_004939.1 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr2:15769811 C>T maps to NM_004939.1 N654N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:108546425 T>C maps to NM_004398.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr11:108811026 C>T maps to NM_004398.2 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:108559728 T>C maps to NM_004398.2 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:108564255 G>A maps to NM_004398.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr11:108593921 C>T maps to NM_004398.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:108593921 C>T maps to NM_004398.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:31245823 C>T maps to NM_030653.3 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr12:31242359 G>A maps to NM_030653.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr12:31237904 G>A maps to NM_030653.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr22:38883887 G>A maps to NM_001098504.1 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr22:38883896 G>A maps to NM_001098504.1 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr22:38895404 G>A maps to NM_001098504.1 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:38881996 C>T maps to NM_001098504.1 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr2:118575056 A>G maps to NM_006773.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:118579519 C>T maps to NM_006773.3 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:118588271 C>A maps to NM_006773.3 S662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr2:118575056 A>G maps to NM_006773.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:70399017 C>T maps to NM_018332.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:70405299 C>T maps to NM_018332.3 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:70398466 G>A maps to NM_018332.3 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:70359578 C>T maps to NM_007242.4 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr16:70359578 C>T maps to NM_007242.4 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr16:70359526 G>A maps to NM_007242.4 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:112305327 G>T maps to NM_007204.4 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:112305321 G>A maps to NM_007204.4 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:112308653 G>C maps to NM_007204.4 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr1:112308651 C>T maps to NM_007204.4 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr10:70721881 C>T maps to NM_004728.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:70742432 C>T maps to NM_004728.2 D739D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr10:70741330 A>G maps to NM_004728.2 E692E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr10:70728774 C>T maps to NM_004728.2 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:49225072 T>C maps to NM_004818.2 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr12:49227239 G>A maps to NM_004818.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr12:49226266 G>A maps to NM_004818.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr14:94519454 G>A maps to NM_020414.3 R733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr14:94545482 C>T maps to NM_020414.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr14:94527392 C>T maps to NM_020414.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:125780329 C>T maps to NM_013264.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:134713924 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:134713719 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:134711278 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:134679421 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:134690146 T>G did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:134706757 C>T did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:134654949 C>T did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:134683607 G>A did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:134680761 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr23:134683645 A>G did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr20:47841699 G>A maps to NM_017895.7 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:47845261 C>T maps to NM_017895.7 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:47838068 T>C maps to NM_017895.7 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:47843001 G>A maps to NM_017895.7 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:47849866 G>A maps to NM_017895.7 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr20:47860195 C>A maps to NM_017895.7 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr20:47838083 G>A maps to NM_017895.7 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr20:47838089 T>C maps to NM_017895.7 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:47841522 G>T maps to NM_017895.7 G201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:47859171 G>T maps to NM_017895.7 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr9:135505702 A>G maps to NM_022779.7 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:135522320 G>A maps to NM_022779.7 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:14523891 C>T maps to ENST00000451994 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:14520445 G>A maps to ENST00000451994 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:41201824 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:41206138 G>T did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:41203508 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:41204755 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:41201774 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:41206160 T>G did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:41205799 A>G did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:41206138 G>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:41203508 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:41201799 A>G did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:41206137 A>G did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:41206138 G>T did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr23:41203508 A>G did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:41206138 G>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr24:15027676 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr24:15027057 G>A did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr5:55083693 T>A maps to NM_024415.2 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:55056043 T>G maps to NM_024415.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr5:55056043 T>C maps to NM_024415.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:55075871 G>T maps to NM_024415.2 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:55088467 G>T did not map to a codon.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:55056086 C>A maps to NM_024415.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:55056043 T>C maps to NM_024415.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:55056043 T>C maps to NM_024415.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:176940032 G>A maps to NM_016222.2 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:176938920 G>A maps to NM_016222.2 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:61864594 T>C maps to NM_203499.1 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:74111579 A>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:74123490 C>T maps to NM_018665.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:74104867 C>T maps to NM_018665.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr6:74104867 C>A maps to NM_018665.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr6:74118978 T>C maps to NM_018665.2 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:134109504 C>T maps to ENST00000452510 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:134106622 G>T maps to ENST00000452510 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:12980303 C>T maps to NM_016355.3 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:12978977 C>T maps to NM_016355.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:19038784 G>A maps to NM_019070.4 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:19039079 G>A maps to NM_019070.4 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr10:70670878 T>C maps to NM_024045.1 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:70696697 G>A maps to NM_024045.1 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:132624212 C>T maps to NM_175066.3 E647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:132624315 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:35981445 T>C maps to NM_007010.3 Q449Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:35981513 C>A maps to NM_007010.3 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:35986095 G>A maps to NM_007010.3 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:36002148 C>A maps to NM_007010.3 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr23:23019695 C>A did not map to a codon.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr23:23018420 C>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:23019628 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:23018962 A>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:23019467 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:23018962 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:23019946 G>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:113600801 G>A maps to NM_001111322.1 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:113614727 C>T maps to NM_001111322.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr12:113614667 G>A maps to NM_001111322.1 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:113607629 C>T maps to NM_001111322.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr12:113612844 C>T maps to NM_001111322.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:124104093 G>A maps to NM_020936.1 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:124102328 C>T maps to NM_020936.1 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:124104178 A>T maps to NM_020936.1 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr12:124090657 C>A maps to NM_020936.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr12:124104148 C>T maps to NM_020936.1 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr12:124090657 C>A maps to NM_020936.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:44609492 G>A maps to NM_019082.2 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:32485254 C>A maps to NM_014314.3 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr9:32480267 G>A maps to NM_014314.3 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:32480253 G>A maps to NM_014314.3 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:200635637 G>T maps to NM_001031725.4 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:200613606 C>T maps to NM_001031725.4 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:200635637 G>T maps to NM_001031725.4 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:200635637 G>T maps to NM_001031725.4 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:200635637 G>T maps to NM_001031725.4 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:200635637 G>T maps to NM_001031725.4 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:118650340 C>T maps to NM_004397.4 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:118656863 C>A maps to NM_004397.4 G33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:118627888 T>C maps to NM_004397.4 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr4:169204653 C>T maps to NM_017631.5 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr4:169146818 A>G maps to NM_017631.5 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:169189109 G>T maps to NM_017631.5 Y937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:169197321 C>T maps to NM_017631.5 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:169172257 C>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:169197285 C>T maps to NM_017631.5 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:169189073 G>A maps to NM_017631.5 T949T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:169196507 G>A maps to NM_017631.5 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:169317133 A>G maps to NM_001012967.1 T1211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:169341456 G>A maps to NM_001012967.1 C823C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:678760 G>T maps to NM_021008.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:678760 G>A maps to NM_021008.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:674718 C>T maps to NM_021008.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr11:686859 G>A maps to NM_021008.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr9:118163578 A>G maps to NM_017418.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:91031160 C>T maps to NM_001359.1 T99T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A6-3810-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr16:460273 C>T maps to NM_020664.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:461020 C>T maps to NM_020664.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:42703607 G>A maps to NM_133328.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr6:35287450 C>T maps to NM_022047.3 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:35287673 G>A maps to NM_022047.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr16:90020686 T>C maps to NM_207514.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:49976859 G>A maps to NM_001037728.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr6:50016292 T>G maps to NM_001037498.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:49936506 C>T maps to NM_001037729.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr20:29845534 T>A maps to NM_001037730.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:29992829 T>G maps to NM_001011878.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr20:30053371 C>T maps to NM_001037500.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr20:76997 T>C maps to NM_153325.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr20:76997 T>C maps to NM_153325.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr20:168601 A>G maps to NM_001037732.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr20:168610 C>T maps to NM_001037732.1 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:210033 A>G maps to NM_080831.3 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr20:210246 C>T maps to NM_080831.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:238440 T>C maps to NM_207469.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr8:11839852 G>A maps to NM_001033017.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:11831510 G>A maps to NM_001033018.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:11831601 T>G maps to NM_001033018.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:11831607 A>G maps to NM_001033018.2 N25N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:18250061 C>T maps to NM_003472.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:18236732 G>A maps to NM_003472.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:18258231 G>A maps to NM_003472.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:40980887 C>A maps to NM_022774.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr9:126319857 T>C maps to NM_020946.1 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:126146017 C>T maps to NM_020946.1 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:126345477 G>A maps to NM_020946.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:126144826 G>T maps to NM_020946.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr9:126146014 C>T maps to NM_020946.1 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:197614825 G>A maps to NM_001195215.1 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:197586838 C>T maps to NM_001195215.1 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:197515895 C>T maps to NM_001195215.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr1:197643248 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:197616226 A>G maps to NM_001195215.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:6471450 G>A maps to NM_024898.2 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr19:6467793 C>T maps to NM_024898.2 E709E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr7:140219441 C>T maps to NM_015689.3 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:140301726 G>T maps to NM_015689.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:140246730 A>G maps to NM_015689.3 D682D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:140302089 T>C maps to NM_015689.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:140266969 G>A maps to NM_015689.3 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr7:140302089 T>C maps to NM_015689.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:115168238 C>A maps to ENST00000393274 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:115147640 G>A maps to ENST00000393274 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:115168050 G>A maps to ENST00000393274 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:111737330 C>T maps to NM_024901.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:111739806 C>T maps to NM_024901.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr8:142160982 C>T maps to NM_014957.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr8:142178145 C>T maps to NM_014957.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:142178484 G>A maps to NM_014957.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:142175325 G>A maps to NM_014957.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:142195253 C>T maps to NM_014957.2 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:65959825 T>G maps to ENST00000443035 G1734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:65983310 G>A maps to ENST00000443035 V1207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:65994167 G>A maps to ENST00000443035 R831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:66048661 C>A maps to ENST00000443035 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:66031085 A>T maps to ENST00000443035 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr15:66044893 G>A maps to ENST00000443035 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr15:66010131 A>G maps to ENST00000443035 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:19346378 A>G maps to NM_017925.4 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:19341078 G>T maps to NM_017925.4 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:19346105 G>A maps to NM_017925.4 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr9:19305498 T>C maps to NM_017925.4 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr9:19341044 A>G maps to NM_017925.4 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr9:19296226 T>C maps to NM_017925.4 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:19358080 C>T maps to NM_017925.4 Q1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:9168574 A>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:31605051 A>T maps to NM_144973.3 L484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:31600697 G>T maps to NM_144973.3 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:31545312 G>A maps to NM_144973.3 T1118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:31648767 A>G maps to NM_144973.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr12:31605206 T>C maps to NM_144973.3 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:31604951 G>A maps to NM_144973.3 Y517Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:68944889 A>G maps to NM_001114120.1 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:68948449 G>A maps to NM_001114120.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr5:59982910 G>A maps to NM_018369.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:59943361 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:59899282 G>A maps to NM_018369.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:59982921 G>A maps to NM_018369.2 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:100649854 C>A maps to ENST00000422147 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:100656044 C>A maps to ENST00000422147 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:100657284 C>A maps to ENST00000422147 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr12:100660808 A>G maps to ENST00000422147 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr22:32301982 C>T maps to NM_001136029.1 Q1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr22:32162609 C>T maps to NM_001136029.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:120940718 G>T maps to NM_022783.2 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:121061894 G>A maps to NM_022783.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:16135308 G>A maps to NM_015954.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr8:124054245 G>A maps to NM_024295.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr8:124035969 A>G maps to NM_024295.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:5389430 G>A maps to NM_016041.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:220286105 T>C maps to NM_001927.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:220285632 G>A maps to NM_001927.3 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:220284877 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:89060107 G>A maps to NM_017996.3 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:89060017 T>C maps to NM_017996.3 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:89074629 C>A maps to NM_017996.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:10532401 G>A maps to NM_004401.2 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr1:3782463 G>A maps to ENST00000430539 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:24784284 C>T maps to NM_001127453.1 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:24756912 G>A maps to NM_001127453.1 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:117165210 G>A maps to NM_015404.3 G849G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr9:117266598 C>T maps to NM_015404.3 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:117169016 G>T maps to NM_015404.3 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr9:117240982 G>A maps to NM_015404.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:179323340 G>C maps to NM_001042702.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr8:145542151 C>G maps to NM_012079.4 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:75511495 C>T maps to NM_032564.3 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr11:75509331 C>T maps to NM_032564.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:69424949 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:69421803 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:69424252 T>C did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:69420251 G>T did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:69397503 C>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr22:19124886 A>G maps to NM_022719.2 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr22:19130245 C>T maps to NM_022719.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr22:19026485 G>A maps to NM_005137.2 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:19026632 G>A maps to NM_005137.2 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr22:18898435 G>A maps to NM_005675.4 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr22:18897697 G>A maps to NM_005675.4 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr22:20073953 T>C maps to NM_022720.6 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:20094183 C>T maps to NM_022720.6 Y653Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr22:20093737 C>T maps to NM_022720.6 Y609Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:56345563 C>T maps to NM_201554.1 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:56346660 A>G maps to NM_201554.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:56345817 G>T did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr12:56346681 C>T maps to NM_201554.1 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr7:14647096 A>G maps to NM_004080.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr7:14517820 G>T maps to NM_004080.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr7:14797282 T>C maps to NM_004080.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:14880849 C>T maps to NM_004080.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr7:14188818 C>T maps to NM_004080.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:14733797 C>A maps to NM_004080.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:14188829 G>A maps to NM_004080.2 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:14378223 G>A maps to NM_004080.2 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:14775792 T>C maps to NM_004080.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:14647096 A>G maps to NM_004080.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr7:14217693 A>G maps to NM_004080.2 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr7:14613878 T>C maps to NM_004080.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr7:14797282 T>C maps to NM_004080.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr7:14613905 A>T maps to NM_004080.2 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:14724956 G>A maps to NM_004080.2 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:14733743 C>A maps to NM_004080.2 G223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr7:14384940 T>C maps to NM_004080.2 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr7:14384940 T>C maps to NM_004080.2 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr2:234377150 C>T maps to NM_152879.2 H1169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:234359622 T>C maps to NM_152879.2 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr2:234296985 A>G maps to NM_152879.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:54939213 C>T maps to NM_003647.2 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:54939585 C>T maps to NM_003647.2 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr3:185906066 G>A maps to NM_001346.2 N673N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:185906027 A>G maps to NM_001346.2 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr3:185990067 G>A maps to NM_001346.2 Y325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:185985530 G>A maps to NM_001346.2 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:185882786 C>A maps to NM_001346.2 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:42764563 C>G maps to NM_178009.2 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr13:42783189 G>A maps to NM_178009.2 Q899Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr13:42703749 T>C maps to NM_178009.2 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:42769147 C>T maps to NM_178009.2 C721C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr13:42793919 T>C maps to NM_178009.2 S1144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:42803248 G>A maps to NM_178009.2 P1196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr7:137206666 G>A maps to NM_004717.2 I731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:137304602 C>T maps to NM_004717.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:137266593 A>G did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr7:137266623 A>G maps to NM_004717.2 H538H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:50122710 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:50213306 T>G did not map to a codon.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr23:50121587 A>G did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:50146543 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:50213352 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:50121097 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:50123028 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:50130603 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:50146547 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:50213047 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:50167349 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:50129559 T>C did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:50131531 C>T did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:50122710 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:50213443 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:50127252 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:959035 C>T maps to NM_001347.2 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:46389604 G>A maps to NM_001105540.1 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:46395756 C>T maps to NM_001105540.1 H647H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:46393056 C>T maps to NM_001105540.1 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:46393068 G>A maps to NM_001105540.1 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:71148914 G>A maps to NM_001360.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:71155212 G>A maps to NM_001360.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:71155233 G>A maps to NM_001360.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:26764696 C>T maps to NM_024887.2 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:26774085 T>C maps to NM_024887.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr1:26774085 T>C maps to NM_024887.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:49439355 C>T maps to NM_014475.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr19:49442818 C>T maps to NM_014475.3 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:49442935 C>T maps to NM_014475.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:49447675 G>A maps to NM_014475.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr10:99359883 G>T maps to NM_138413.3 G222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:79945214 C>A maps to NM_000791.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr3:93780295 G>A maps to NM_001195643.1 N20N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:49488259 G>A maps to NM_021044.2 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:49485013 G>A maps to NM_021044.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:72057107 C>T maps to NM_001361.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr16:72057065 G>A maps to NM_001361.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:72057062 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:12786944 G>A maps to NM_001930.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:12790514 C>T maps to NM_001930.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr19:12786913 C>A maps to NM_001930.2 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr19:12792463 A>G maps to NM_001930.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr19:12792376 G>A maps to NM_001930.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr14:24766023 G>A maps to NM_001136050.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr14:24760345 G>A maps to NM_001136050.2 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:24761911 G>A maps to NM_001136050.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr13:52345966 G>A maps to NM_001031719.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr14:24113712 C>T maps to NM_182908.4 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr14:24108168 C>T maps to NM_182908.4 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr1:12639323 G>A maps to NM_004753.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:12639428 G>T maps to NM_004753.4 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:24437992 C>T maps to NM_021004.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:24506954 C>T maps to NM_001082488.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr14:24459519 T>C maps to NM_198083.3 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr14:24459528 T>C maps to NM_198083.3 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr14:24459528 T>C maps to NM_198083.3 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:60611704 G>T maps to NM_016029.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:9684870 C>T maps to ENST00000330255 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:169948416 G>A maps to NM_001142271.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:169939875 C>T maps to NM_001142271.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:2139237 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:12129586 C>T maps to NM_018706.5 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:12150011 C>T maps to NM_018706.5 Q718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:12160844 C>T maps to NM_018706.5 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:12131175 C>T maps to NM_018706.5 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:12129619 C>T maps to NM_018706.5 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:24544571 C>T maps to NM_001358.2 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:24529609 T>C maps to NM_001358.2 E775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:24556418 G>A maps to NM_001358.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:24578021 C>T maps to NM_001358.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr4:24541845 T>C maps to NM_001358.2 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:24557945 A>G maps to NM_001358.2 H263H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr6:30624194 G>A maps to NM_003587.4 A801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:30632916 C>T maps to NM_003587.4 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:30640498 G>T maps to NM_003587.4 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:30632927 G>A maps to NM_003587.4 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:54563593 T>C maps to NM_019030.2 R1117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr5:54567970 A>G maps to NM_019030.2 G936G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:54565414 A>G maps to NM_019030.2 P1040P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:54566409 C>A maps to NM_019030.2 E997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:54570515 G>T maps to NM_019030.2 I872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:54579345 T>C maps to NM_019030.2 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:54579408 C>T maps to NM_019030.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr5:54579408 C>A maps to NM_019030.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr5:54579408 C>A maps to NM_019030.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:54581180 A>G maps to NM_019030.2 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:54581630 A>C maps to NM_019030.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:54579408 C>A maps to NM_019030.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr5:54579408 C>T maps to NM_019030.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:54581180 A>G maps to NM_019030.2 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:54579408 C>T maps to NM_019030.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:54593112 C>T maps to NM_019030.2 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:47889960 G>A maps to NM_138615.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:47883152 C>T maps to NM_138615.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:47887956 G>A maps to NM_138615.2 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:47868903 C>T maps to NM_138615.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:47888804 C>T maps to NM_138615.2 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:47887890 C>T maps to NM_138615.2 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr10:127548393 T>C maps to NM_018180.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:127548393 T>C maps to NM_018180.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:127569240 A>G maps to NM_018180.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:127548393 T>C maps to NM_018180.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:5364414 T>A maps to ENST00000457531 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:5364366 G>A maps to ENST00000457531 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:5347638 C>T maps to ENST00000457531 E729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:5352215 C>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:47870383 A>G maps to NM_014681.5 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr19:47876902 G>C maps to NM_014681.5 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr19:47858432 C>A maps to NM_014681.5 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr19:47863313 C>T maps to NM_014681.5 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:47884191 C>A maps to NM_014681.5 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:37634880 C>T maps to NM_021931.3 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr20:37650574 C>T maps to NM_021931.3 H530H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:37650496 T>C maps to NM_021931.3 C504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr20:37612385 A>G maps to NM_021931.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr20:37630404 C>T maps to NM_021931.3 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:37653985 C>T maps to NM_021931.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr20:37657079 G>T maps to NM_021931.3 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:154010356 T>C maps to NM_020865.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:153993960 C>T maps to NM_020865.2 *1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:154006722 G>A maps to NM_020865.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:154013084 A>G maps to NM_020865.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:125451398 C>T maps to NM_032656.3 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:125460011 G>A maps to NM_032656.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:125470679 G>A maps to NM_032656.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:72137512 C>T maps to NM_014003.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:72130239 C>T maps to NM_014003.3 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:72143342 C>T maps to NM_014003.3 D1137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:72135073 G>A maps to NM_014003.3 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:72131654 C>A maps to NM_014003.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr17:57644003 G>A maps to NM_024612.4 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:57652818 A>C maps to NM_024612.4 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr17:57644021 T>C maps to NM_024612.4 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:39050304 G>A maps to NM_198963.1 R1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:39033742 G>A maps to NM_198963.1 N1258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:39081277 G>A maps to NM_198963.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:40263416 G>T maps to NM_024119.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr17:41584438 C>T maps to NM_004941.1 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:41570860 T>C maps to NM_004941.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:41570100 C>T maps to NM_004941.1 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:41576320 T>C maps to NM_004941.1 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr17:41582111 T>A maps to NM_004941.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr17:41570100 C>A maps to NM_004941.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:182856343 C>T maps to NM_001357.4 S1196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:182827933 C>T maps to NM_001357.4 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:182835665 C>T maps to NM_001357.4 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:182845279 C>T maps to NM_001357.4 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:140953601 A>G maps to ENST00000398557 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr23:96171542 C>A did not map to a codon.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr23:96136641 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:96173572 C>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:96330186 G>A did not map to a codon.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr23:95993740 G>C did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:96194317 C>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:96212915 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:96502786 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:95993591 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:96167487 A>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:96192337 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:96203955 G>A did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr23:96192328 A>G did not map to a codon.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr23:95993590 C>T did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr23:96502830 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:96171574 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:96204002 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:96327970 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:96603242 C>A did not map to a codon.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr23:96502830 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:96396767 G>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:95993675 A>G did not map to a codon.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr23:95993675 A>G did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:96212915 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:96396766 T>C did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:95993675 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:96200544 G>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:96212915 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:96212915 G>A did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:96502830 A>G did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr23:96502830 A>G did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr13:60407276 A>G maps to NM_001042517.1 F997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr13:60435634 C>T maps to NM_001042517.1 T881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:60413505 G>T maps to NM_001042517.1 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr13:60407276 A>G maps to NM_001042517.1 F997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr13:60545099 G>A maps to NM_001042517.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:60348329 A>G maps to NM_001042517.1 C1104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr14:95583961 T>C maps to NM_177438.2 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr14:95590692 G>A maps to NM_177438.2 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr14:95595890 C>A maps to NM_177438.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:95582971 C>A maps to NM_177438.2 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:95577680 C>T maps to NM_177438.2 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:95557624 C>T maps to NM_177438.2 S1814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:95590926 C>A maps to NM_177438.2 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr14:95583961 T>C maps to NM_177438.2 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr14:95583961 T>C maps to NM_177438.2 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr14:95572541 C>T maps to NM_177438.2 Q941Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr20:61511928 T>C maps to NM_033081.2 R1793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:61542331 G>A maps to NM_033081.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:61522459 G>A maps to NM_033081.2 V1131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr20:61523413 T>G maps to NM_033081.2 T1090T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:61526424 C>T maps to NM_033081.2 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr20:61512783 C>T maps to NM_033081.2 G1508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr20:61526170 C>A maps to NM_033081.2 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr20:61510680 G>A maps to NM_033081.2 R2209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr20:61511241 G>A maps to NM_033081.2 G2022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:61511655 G>A maps to NM_033081.2 G1884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:61513680 G>A maps to NM_033081.2 D1209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:61694693 T>C maps to NM_014473.2 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:61688000 A>G maps to NM_014473.2 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:61699168 G>T maps to NM_014473.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:54375617 T>G maps to NM_000792.5 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:54370372 T>C maps to NM_000792.5 C124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:54360101 C>T maps to NM_000792.5 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr14:80677722 G>T maps to NM_001007023.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr14:102028510 C>T maps to NM_001362.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:102028507 G>A maps to NM_001362.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr14:102028079 G>T maps to NM_001362.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr14:102028185 G>A maps to NM_001362.3 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:102028529 C>T maps to NM_001362.3 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr21:47974165 C>T maps to ENST00000318711 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr21:47977644 C>T maps to ENST00000318711 G1260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr21:47931411 C>T maps to ENST00000318711 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr21:47929287 A>G maps to ENST00000318711 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr12:51112571 C>T maps to NM_173602.2 Q978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr12:51074521 A>G maps to NM_173602.2 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr12:51097920 A>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr12:51069110 G>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr12:51097920 A>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:51108258 G>T maps to NM_173602.2 G911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:51125253 T>G maps to NM_173602.2 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:51084857 A>G maps to NM_173602.2 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:51092137 A>G maps to NM_173602.2 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr12:51097920 A>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr12:51092137 A>G maps to NM_173602.2 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:51097920 A>T did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr12:51080371 A>G maps to NM_173602.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:51092137 A>G maps to NM_173602.2 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr12:51019780 T>C maps to NM_173602.2 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr12:51097920 A>G did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr12:51074521 A>G maps to NM_173602.2 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr12:51097920 A>G did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr12:51097920 A>T did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr12:51097920 A>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:51079614 G>T did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:51097920 A>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:415506 C>T maps to NM_014974.2 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:429999 G>A maps to NM_014974.2 R615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:459991 G>A maps to NM_014974.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr10:327144 C>A maps to NM_014974.2 T1471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:428684 G>A maps to NM_014974.2 C631C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr10:429976 G>A maps to NM_014974.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr10:375465 G>C maps to NM_014974.2 A1220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:410450 G>A maps to NM_014974.2 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:390981 C>T maps to NM_014974.2 A1100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr10:430084 T>C maps to NM_014974.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:436202 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:93375575 G>A maps to NM_017594.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:189599497 A>C maps to NM_052952.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:122591310 C>T maps to NM_032839.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:122545724 G>A maps to NM_032839.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr13:73349357 T>C maps to NM_014953.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr13:73346019 A>T maps to NM_014953.3 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:73346887 A>G maps to NM_014953.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:66615041 A>G maps to NM_001143688.1 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr15:66604060 G>C did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:66612994 C>T maps to NM_001143688.1 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:66618288 A>G maps to NM_001143688.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr15:66607521 G>A maps to NM_001143688.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:232952348 C>T maps to NM_152383.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:233128131 C>T maps to NM_152383.4 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:232880269 T>G maps to NM_152383.4 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:233199190 C>T maps to NM_152383.4 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:233199396 C>T maps to NM_152383.4 F782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr1:231954190 A>T maps to NM_001164537.1 K669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:231931027 G>T maps to NM_001164537.1 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:223176178 C>T maps to NM_032890.2 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:223176565 C>T maps to NM_032890.2 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:223178728 G>A maps to NM_032890.2 T1330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:223176481 G>A maps to NM_032890.2 W581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:223177198 C>T maps to NM_032890.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:223179181 A>G maps to NM_032890.2 Q1481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:223176856 C>T maps to NM_032890.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:223177420 C>A maps to NM_032890.2 I894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr1:223177474 G>A maps to NM_032890.2 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:223116176 C>T maps to NM_032890.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:223178518 C>T maps to NM_032890.2 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:40662408 C>T maps to NM_033510.1 R1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr11:111856023 T>C maps to NM_001037954.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr11:111866862 T>C maps to NM_001037954.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:111835322 G>A maps to NM_001037954.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr11:111856023 T>C maps to NM_001037954.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:153996698 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:154004515 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:153994219 A>G did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:153994225 T>C did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:154003526 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:154003543 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:153993211 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:54076459 G>T maps to NM_012242.2 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:54074810 C>T maps to NM_012242.2 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr10:54076386 C>T maps to NM_012242.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr4:107845720 A>T maps to NM_014421.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:107847034 C>A maps to NM_014421.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:107845712 G>T maps to NM_014421.2 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr4:107845849 A>G maps to NM_014421.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr4:107845224 A>G maps to NM_014421.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr4:107845849 A>G maps to NM_014421.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:107845266 G>T maps to NM_014421.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr4:107845720 A>T maps to NM_014421.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr4:107845224 A>G maps to NM_014421.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:12020302 T>C maps to ENST00000450094 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr11:12020291 G>T maps to ENST00000450094 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr8:42231698 A>G maps to NM_014420.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr8:42231698 A>G maps to NM_014420.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr19:49869072 G>A maps to NM_014419.3 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:111916595 C>T maps to NM_001931.4 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr8:12960304 C>A maps to NM_182643.2 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr8:13259110 T>C maps to NM_182643.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:13357145 G>T maps to NM_182643.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr8:13259110 T>C maps to NM_182643.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:12960304 C>A maps to NM_182643.2 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:12952632 G>A maps to NM_182643.2 Q1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:12957109 G>A maps to NM_182643.2 H912H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:12957934 G>A maps to NM_182643.2 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:12957877 G>A maps to NM_182643.2 H656H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:12958129 C>T maps to NM_182643.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:12952623 G>A maps to NM_182643.2 R1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:13162734 T>C maps to NM_024767.3 *464W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:13357487 A>G maps to NM_182643.2 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:13356742 G>A maps to NM_182643.2 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:13356869 T>C maps to NM_182643.2 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr8:13259110 T>A maps to NM_182643.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr8:13259110 T>C maps to NM_182643.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:107545822 A>C maps to NM_000108.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:107558487 A>G maps to NM_000108.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr7:107558487 A>G maps to NM_000108.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:38151607 C>A maps to NM_007335.2 G1093G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:38080790 G>A maps to NM_007335.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:38080950 C>T maps to NM_007335.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:38153806 C>T maps to NM_007335.2 G1207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:38127849 G>A maps to NM_007335.2 W518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:38163909 G>A maps to NM_007337.2 P1717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:38139094 G>T maps to NM_007335.2 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:38103774 C>T maps to NM_007335.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:38125713 G>A maps to NM_007335.2 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:38134345 C>T maps to NM_007335.2 C577C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:38101314 T>C maps to NM_007335.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:38125713 G>A maps to NM_007335.2 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:196807933 C>T maps to NM_004087.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:196807971 G>A maps to NM_004087.2 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:196876612 C>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr11:83182723 C>T maps to NM_001142699.1 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr11:83809964 C>G did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:84996338 G>A maps to NM_001142699.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:83676424 A>G maps to NM_001142699.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr11:83180387 C>T maps to NM_001142699.1 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr11:84865602 T>C maps to NM_001142699.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:83195170 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:84996400 C>A maps to NM_001142699.1 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:83770408 G>A maps to NM_001142699.1 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr11:83344363 G>A maps to NM_001142699.1 Y610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr11:83182723 C>A maps to NM_001142699.1 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:69670125 C>T did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:69712424 G>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:69669234 C>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:69719038 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:69670125 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:69668795 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:69719830 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:69712392 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:69699034 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:69673620 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:69670625 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr23:69719848 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:69672497 C>T did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:7099861 A>G maps to NM_001365.3 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:7111531 C>T maps to NM_001365.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:7111525 A>G maps to NM_001365.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr17:7111525 A>G maps to NM_001365.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr10:79553802 C>T maps to NM_004747.3 A1873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr10:79576423 G>A maps to NM_004747.3 Q1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:79581844 G>A maps to NM_004747.3 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:79565549 C>T maps to NM_004747.3 T1679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr18:3582067 G>T maps to NM_004746.2 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr18:3729201 G>A maps to NM_004746.2 C508C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:3582184 C>T maps to NM_004746.2 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr18:3879555 G>A maps to NM_004746.2 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr18:3879597 C>T maps to NM_004746.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr18:3582067 G>A maps to NM_004746.2 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:3879897 G>A maps to NM_004746.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr18:3534240 C>T maps to NM_004746.2 W810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr8:1626769 G>A maps to ENST00000357934 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr8:1497557 C>T maps to ENST00000357934 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr8:1497422 C>T maps to ENST00000357934 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:1497407 G>A maps to ENST00000357934 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr8:1626697 G>A maps to ENST00000357934 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr8:1626778 C>T maps to ENST00000357934 N838N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:1497659 C>T maps to ENST00000357934 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:1626538 C>T maps to ENST00000357934 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr8:1626718 C>T maps to ENST00000357934 H818H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr8:1497833 G>A maps to ENST00000357934 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:1616625 C>T maps to ENST00000357934 Q590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr8:1581003 G>A maps to ENST00000357934 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr8:1497821 C>T maps to ENST00000357934 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:35370774 C>T maps to NM_001080418.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:35370318 G>T maps to NM_001080418.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:35370972 G>T maps to NM_001080418.1 Y4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:35334230 C>T maps to NM_001080418.1 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:35060230 G>A maps to ENST00000339266 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:35155373 A>G maps to ENST00000339266 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:35060359 C>T maps to ENST00000339266 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr14:55637435 C>T maps to NM_014750.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:55625285 G>A maps to NM_014750.4 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr14:55636164 C>T maps to NM_014750.4 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr14:55621513 G>A maps to NM_014750.4 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr14:55642642 A>G maps to NM_014750.4 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr14:55642642 A>G maps to NM_014750.4 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:55621399 G>A maps to NM_014750.4 A666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:101198457 C>A maps to NM_003836.5 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:101198421 C>A maps to NM_003836.5 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr14:101200644 T>C maps to NM_003836.5 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr6:170592117 G>A maps to NM_005618.3 Y708Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:170592332 C>T maps to NM_005618.3 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr6:170594356 G>A maps to NM_005618.3 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:170592908 C>T maps to NM_005618.3 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:39994894 C>T maps to NM_016941.3 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:39998231 G>A maps to NM_016941.3 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr19:39995966 C>T maps to NM_016941.3 N323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:39994769 C>T maps to NM_016941.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr19:39995966 C>T maps to NM_016941.3 N323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:39998562 G>A maps to NM_016941.3 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr15:41229720 G>A maps to NM_019074.3 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:75349301 C>T maps to NM_001933.4 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:75348659 C>T maps to NM_001933.4 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr14:75359669 G>A maps to NM_001933.4 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:172951505 G>A maps to NM_178120.4 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:172965543 C>A maps to NM_004405.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr2:172966864 A>T did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr2:172965279 C>T maps to NM_004405.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:48069045 C>T maps to NM_005220.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:48046987 C>T maps to NM_138281.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr7:96650098 C>T maps to NM_005221.5 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:96650251 C>T maps to NM_005221.5 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:96653683 G>A maps to NM_005221.5 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:96653770 C>T maps to NM_005221.5 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:96639244 C>T maps to NM_005222.3 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:96635627 C>T maps to NM_005222.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr7:96639148 A>G maps to NM_005222.3 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:44684828 G>A maps to NM_019100.4 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:124340397 G>A maps to ENST00000368915 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr10:124402772 G>A maps to ENST00000368915 A2496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:124390573 T>C maps to ENST00000368915 D2041D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr10:124358296 A>G maps to ENST00000368915 E988E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:124331830 T>C maps to ENST00000368915 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:124339143 C>T maps to ENST00000368915 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr10:124336020 C>T maps to ENST00000368915 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr10:124358362 C>G maps to ENST00000368915 Y1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:124330427 G>A maps to ENST00000368915 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:124331836 G>A maps to ENST00000368915 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:124399572 C>T maps to ENST00000368915 I2320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr10:124340397 G>A maps to ENST00000368915 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:124358581 C>T maps to ENST00000368915 G1083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr10:124379787 C>T maps to ENST00000368915 N1755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr10:124351842 C>T maps to ENST00000368915 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:46977934 C>T maps to NM_147192.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:46977841 G>A maps to NM_147192.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:46972717 C>T maps to NM_147192.2 H12H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:46977889 G>A maps to NM_147192.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr1:46972810 G>A maps to NM_147192.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr1:46976776 C>T maps to NM_147192.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr22:38945946 A>G maps to NM_007068.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:38964209 C>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr22:38934386 G>A maps to NM_007068.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:38934545 A>G maps to NM_007068.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr22:38934387 A>G maps to NM_007068.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:32429960 A>C did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:31152240 G>T did not map to a codon.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr23:31950217 T>A did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:32456429 G>A did not map to a codon.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr23:32834616 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:32360239 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:33357374 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:31227761 T>C did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:31525419 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:31224763 C>T did not map to a codon.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr23:32482737 A>T did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr23:32235178 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:31854922 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:31224763 C>T did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:31224773 C>A did not map to a codon.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr23:31747810 C>T did not map to a codon.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr23:32380917 A>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:31222120 C>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:31144782 A>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:31792123 T>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:32466597 A>G did not map to a codon.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr23:32486646 C>G did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:31514961 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:32583901 T>C did not map to a codon.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr23:32404542 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:32398653 A>C did not map to a codon.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr23:32716112 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:32407651 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:32466752 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:32472918 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:31697634 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:31947810 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:32456467 T>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:31496379 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:31514978 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:32398751 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:32717375 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:32536244 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:32834688 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr23:32381046 C>T did not map to a codon.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr23:31986470 G>C did not map to a codon.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr23:31496309 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:31676261 C>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:32613994 T>C did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:31497167 T>A did not map to a codon.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr23:32398667 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:31165530 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:31196869 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:31227747 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:31241216 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:32361360 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:32482767 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:32613953 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:32481639 C>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:31224778 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:31462742 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:32834721 C>A did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:31838156 C>T did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:32509485 G>T did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:32360389 G>T did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:32408249 T>A did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:31496248 G>C did not map to a codon.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr23:32486637 T>C did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr23:31496266 C>T did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:32490292 G>A did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:31497168 C>T did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:31497168 C>A did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:31165490 A>G did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:32456488 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:31165490 A>G did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:31497167 T>C did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:31165497 A>G did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr23:31165490 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:31198487 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:32490324 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:32459412 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:32509515 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:32663097 G>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:32834668 C>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:78322348 G>A maps to NM_013391.2 D696D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:78359597 T>C maps to NM_013391.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:78338268 G>A maps to NM_013391.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:78328589 C>T maps to NM_013391.2 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:78294039 T>C maps to NM_013391.2 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:78322348 G>A maps to NM_013391.2 D696D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr5:78359471 C>T maps to NM_013391.2 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:36003575 T>C maps to NM_033317.4 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:35990907 C>T maps to NM_033317.4 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:36004068 G>T maps to NM_033317.4 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:36003532 C>A maps to NM_033317.4 G196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:88580620 A>G maps to NM_004407.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr4:88583221 G>T maps to NM_004407.3 G98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr4:88584261 C>T maps to NM_004407.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr4:88583969 C>A maps to NM_004407.3 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:46281417 G>A maps to NM_004409.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr19:46281815 C>T maps to NM_004409.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:46280656 G>A maps to NM_004409.3 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr19:46283071 C>T maps to NM_004409.3 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr19:46274622 C>T maps to NM_004409.3 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:46281767 C>T maps to NM_004409.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr9:846982 C>A maps to NM_021951.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr9:1053756 C>T maps to NM_181872.4 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:990941 C>T maps to NM_021240.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr9:990716 G>A maps to NM_021240.2 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:977210 G>A maps to NM_021240.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:990728 G>A maps to NM_021240.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:990554 C>A maps to NM_021240.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:22451143 C>A maps to NM_022160.2 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:50884381 G>A maps to NM_032110.1 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:50884471 G>A maps to NM_032110.1 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:53930455 G>A maps to NM_033067.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr1:53925161 G>A maps to NM_033067.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:53930455 G>A maps to NM_033067.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr1:53925257 C>T maps to NM_033067.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr7:86811621 G>A maps to NM_021145.3 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr7:86811624 C>T maps to NM_021145.3 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:86811588 G>A maps to NM_021145.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:46289742 G>A maps to NM_004943.1 D337D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr5:118469796 C>T maps to NM_005509.4 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:118574736 C>T maps to NM_005509.4 S2850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:118485122 C>T maps to NM_005509.4 R1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:118454521 T>C maps to NM_005509.4 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:118433744 T>G maps to NM_005509.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr15:51834581 A>G maps to NM_001174116.1 H351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr15:51791394 A>G maps to NM_001174116.1 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:51783888 C>A maps to NM_001174116.1 L1613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:51766615 G>A maps to NM_001174116.1 R2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:51792125 C>A maps to NM_001174116.1 E1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:51747413 C>T maps to NM_001174116.1 A2825A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr15:51827949 A>G maps to NM_001174116.1 F782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr15:51829846 T>C maps to NM_001174116.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr15:51829846 T>C maps to NM_001174116.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr15:51749620 A>G maps to NM_001174116.1 Y2726Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:70182050 A>G maps to NM_001080449.1 Y962Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:70179640 C>T maps to NM_001080449.1 A988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:70202678 C>T maps to NM_001080449.1 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:70191702 C>T maps to NM_001080449.1 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:70192158 C>T maps to NM_001080449.1 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:52380621 C>T maps to ENST00000273600 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:52378586 C>T maps to ENST00000273600 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:52422838 G>T maps to ENST00000273600 S3191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:52428587 G>A maps to ENST00000273600 S3642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:52422904 C>T maps to ENST00000273600 G3213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:52396495 G>A maps to ENST00000273600 T1691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:52417881 C>T maps to ENST00000273600 I2719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:52427416 C>T maps to ENST00000273600 C3578C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:52395206 G>T maps to ENST00000273600 L1571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:52420213 G>A maps to ENST00000273600 V2888V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr12:124297772 G>A maps to NM_207437.3 E951E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr12:124272389 C>T maps to NM_207437.3 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:124298174 T>C maps to NM_207437.3 H1085H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr12:124377792 G>A maps to NM_207437.3 A2885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr12:124330338 C>T maps to NM_207437.3 N1733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr12:124419925 C>T maps to NM_207437.3 N4438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:124265682 C>T maps to NM_207437.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:124413886 C>T maps to NM_207437.3 H4006H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:124414242 G>A maps to NM_207437.3 T4065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:124265752 G>T maps to NM_207437.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:124323148 C>T maps to NM_207437.3 F1565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:124341664 T>C maps to NM_207437.3 V2049V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:124352640 T>G maps to NM_207437.3 V2380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:124408311 C>T maps to NM_207437.3 L3719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr12:124330607 G>A maps to NM_207437.3 T1789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:124415972 G>A maps to NM_207437.3 A4172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr12:124274526 G>A maps to NM_207437.3 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:124270426 C>T maps to NM_207437.3 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:124284788 G>A maps to NM_207437.3 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:124343719 C>T maps to NM_207437.3 F2100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:124383341 C>T maps to NM_207437.3 I3089I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:124401140 C>A maps to NM_207437.3 V3502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:124330658 C>A maps to NM_207437.3 V1806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:124393877 G>T maps to NM_207437.3 E3178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:124401222 C>T maps to NM_207437.3 L3530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr12:124352075 A>C maps to NM_207437.3 I2292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr12:124315102 G>T maps to NM_207437.3 E1350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr12:124352060 T>C maps to NM_207437.3 Y2287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:21675536 G>T maps to NM_003777.3 E1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:21640728 C>T maps to NM_003777.3 S1119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:21675536 G>T maps to NM_003777.3 E1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:21906111 C>T maps to NM_003777.3 R3848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr7:21813559 C>T maps to NM_003777.3 S3100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:21646114 T>C maps to NM_003777.3 H1240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr7:21901499 C>T maps to NM_003777.3 I3751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr7:21747334 C>T maps to NM_003777.3 R2196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:21657370 G>A maps to NM_003777.3 W1415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr7:21721231 C>T maps to NM_003777.3 I1804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:21631113 C>A maps to NM_003777.3 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:21599383 G>T maps to NM_003777.3 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:21627705 C>T maps to NM_003777.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:21611486 G>T maps to NM_003777.3 G497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:21640752 G>A maps to NM_003777.3 W1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:21730461 C>T maps to NM_003777.3 R2009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:21611525 G>T maps to NM_003777.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:21640503 G>T maps to NM_003777.3 E1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:21940793 C>A maps to NM_003777.3 I4498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:21654868 G>A maps to NM_003777.3 W1330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:21840786 T>G maps to NM_003777.3 A3360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:21678593 G>T maps to NM_003777.3 E1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:21751401 T>C maps to NM_003777.3 L2310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:21813535 G>A maps to NM_003777.3 L3092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:21882248 G>A maps to NM_003777.3 K3600K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr7:21639472 C>T maps to NM_003777.3 D912D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr7:21730397 G>T maps to NM_003777.3 G1987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr7:21639562 G>A maps to NM_003777.3 P942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr7:21813559 C>T maps to NM_003777.3 S3100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:21939034 C>T maps to NM_003777.3 S4384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:21932149 A>G maps to NM_003777.3 A4212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr7:21641131 C>T maps to NM_003777.3 R1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:21659596 C>A maps to NM_003777.3 T1472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr3:57509541 A>G maps to NM_178504.4 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:57457260 C>A maps to NM_178504.4 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:57330448 A>G maps to NM_178504.4 D2981D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:57431826 C>T maps to NM_178504.4 P1347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:57419491 C>T maps to NM_178504.4 T1550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:57488145 C>A maps to NM_178504.4 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:57391409 G>T maps to NM_178504.4 I2163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:57329621 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:57357040 A>C maps to NM_178504.4 S2591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:57475245 C>A maps to NM_178504.4 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:57488127 A>G maps to NM_178504.4 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:57344965 C>A maps to NM_178504.4 E2691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:57431826 C>T maps to NM_178504.4 P1347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr3:57509541 A>G maps to NM_178504.4 D80D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A6-6781-01A-22D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:76445501 C>T maps to ENST00000389840 T3721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:76492000 G>A maps to ENST00000389840 Y1939Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:76498976 G>A maps to ENST00000389840 Y1687Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:76450615 C>A maps to ENST00000389840 G3434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr17:76497279 G>T maps to ENST00000389840 T1809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:76498708 G>T maps to ENST00000389840 G1707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr17:76420103 A>G maps to ENST00000389840 C4447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:76533479 T>A maps to ENST00000389840 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr17:76567098 G>A maps to ENST00000389840 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:76495092 C>A maps to ENST00000389840 V1900V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr17:76422537 C>T maps to ENST00000389840 R4328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:76539983 G>A maps to ENST00000389840 Y829Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:76563140 G>T maps to ENST00000389840 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:76451809 G>A maps to ENST00000389840 F3348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:76455906 G>A maps to ENST00000389840 F3190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:76535956 G>A maps to ENST00000389840 N846N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr17:76503605 G>A maps to ENST00000389840 S1502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:76498762 G>T maps to NM_173628.3 T1700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:76490758 G>A maps to ENST00000389840 D2048D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr17:76445582 G>A maps to ENST00000389840 D3694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr17:76523068 C>A maps to ENST00000389840 E1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:76454681 G>A maps to ENST00000389840 A3300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:76440870 C>T maps to ENST00000389840 S3767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr17:7721316 C>T maps to NM_020877.2 H3430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:7720678 A>G maps to NM_020877.2 G3322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:7721316 C>T maps to NM_020877.2 H3430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:7660450 G>A maps to NM_020877.2 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:7637852 G>T maps to NM_020877.2 G269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr17:7662787 G>T maps to NM_020877.2 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:7669763 C>T maps to NM_020877.2 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:7662915 A>T maps to NM_020877.2 G875G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr17:7668734 C>T maps to NM_020877.2 N1121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr17:7678611 C>T maps to NM_020877.2 G1591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:7640485 G>A maps to NM_020877.2 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:7689468 C>T maps to NM_020877.2 R2053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:7699852 G>A maps to NM_020877.2 K2582K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:7667449 G>A maps to NM_020877.2 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:7681675 C>T maps to NM_020877.2 T1810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:7699900 C>T maps to NM_020877.2 T2598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr17:7689991 G>C maps to NM_020877.2 R2151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:7695252 G>T maps to NM_020877.2 E2307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:7623079 C>T maps to NM_020877.2 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:7643238 G>A maps to NM_020877.2 W453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:7680850 G>T maps to NM_020877.2 E1716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:7700555 G>T maps to NM_020877.2 R2642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:7637570 G>A maps to NM_020877.2 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr17:7736209 C>T maps to NM_020877.2 S4314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:20974699 T>C maps to NM_017539.1 E3502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:20986634 C>A maps to NM_017539.1 E2727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:20999095 C>T maps to NM_017539.1 S2267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:21061268 C>A maps to NM_017539.1 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr16:21136678 G>C maps to NM_017539.1 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:20974744 C>T maps to NM_017539.1 A3487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:21093009 T>C maps to NM_017539.1 E972E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:21073942 G>A maps to NM_017539.1 R1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:20975350 C>T maps to NM_017539.1 T3285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:21093000 G>A maps to NM_017539.1 C975C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:20974858 G>T maps to NM_017539.1 I3449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:20986718 C>A maps to NM_017539.1 E2699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:21151885 C>A maps to NM_017539.1 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:21011657 G>A maps to NM_017539.1 F2103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:21147735 C>T maps to NM_017539.1 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr16:20975824 A>G maps to NM_017539.1 I3127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr16:21128624 A>G maps to NM_017539.1 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:21051213 C>A maps to NM_017539.1 E1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:21108811 A>G maps to NM_017539.1 N843N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:21115868 C>T maps to NM_017539.1 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:21151885 C>A maps to NM_017539.1 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:20996656 C>T maps to NM_017539.1 W2469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr16:21093009 T>C maps to NM_017539.1 E972E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:20975596 A>G maps to NM_017539.1 D3203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:21156622 G>A maps to NM_017539.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr16:20975410 G>A maps to NM_017539.1 S3265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:20990738 C>T maps to NM_017539.1 T2663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr16:21049208 A>G maps to NM_017539.1 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:21049208 A>G maps to NM_017539.1 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:21053387 G>A maps to NM_017539.1 P1533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr16:21080894 A>G maps to NM_017539.1 I1074I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:20996451 C>A maps to NM_017539.1 G2538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:21008662 C>T maps to NM_017539.1 V2181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:21086883 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:21117954 C>A maps to NM_017539.1 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:20986718 C>A maps to NM_017539.1 E2699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:21109981 A>C maps to NM_017539.1 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:21011678 G>C maps to NM_017539.1 Y2096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr16:21031085 C>T maps to NM_017539.1 W1961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr16:21080894 A>G maps to NM_017539.1 I1074I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:21031085 C>T maps to NM_017539.1 W1961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr16:21049208 A>G maps to NM_017539.1 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:20944793 G>A maps to NM_017539.1 P4011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr16:21049208 A>G maps to NM_017539.1 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr16:21049208 A>G maps to NM_017539.1 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr16:21073985 G>A maps to NM_017539.1 N1179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr16:21098244 G>A maps to NM_017539.1 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr16:21053408 A>G maps to NM_017539.1 A1526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:13776685 G>A maps to NM_001369.2 R3079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr5:13769115 G>A maps to NM_001369.2 L3284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:13931305 C>T maps to NM_001369.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:13920645 A>G maps to NM_001369.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:13865949 C>T maps to NM_001369.2 L1394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr5:13701413 T>C maps to NM_001369.2 G4490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr5:13839484 T>C maps to NM_001369.2 V1954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr5:13923451 C>T maps to NM_001369.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr5:13769230 C>T maps to NM_001369.2 V3245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr5:13714519 G>T maps to NM_001369.2 P4373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr5:13692193 G>A maps to NM_001369.2 R4592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:13916492 A>G maps to NM_001369.2 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:13770874 C>T maps to NM_001369.2 V3196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:13717564 C>G maps to NM_001369.2 V4188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:13721258 C>T maps to NM_001369.2 T4043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:13777309 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:13919296 C>T maps to NM_001369.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:13864712 C>T maps to NM_001369.2 W1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:13894779 C>A maps to NM_001369.2 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr5:13737541 C>T maps to NM_001369.2 K3758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:13820542 C>T maps to NM_001369.2 T2251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:13862814 T>C maps to NM_001369.2 Q1546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:13864622 C>T maps to NM_001369.2 E1493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:13876926 C>A did not map to a codon.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr5:13919390 C>T maps to NM_001369.2 W290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:13807738 A>G maps to NM_001369.2 S2616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:13776574 G>A maps to NM_001369.2 R3116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr5:13807738 A>G maps to NM_001369.2 S2616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:13737535 T>G maps to NM_001369.2 L3760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:13770907 A>G maps to NM_001369.2 Y3185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:13900415 C>A maps to NM_001369.2 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr5:13766222 C>A maps to NM_001369.2 R3321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr5:13864741 G>A maps to NM_001369.2 R1454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr5:13901591 A>G maps to NM_001369.2 Y607Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr5:13754366 T>C maps to NM_001369.2 K3500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:13700866 G>A maps to NM_001369.2 V4535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:13807738 A>G maps to NM_001369.2 S2616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:13868011 C>T maps to NM_001369.2 K1308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr5:13807738 A>G maps to NM_001369.2 S2616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr5:13839570 C>A maps to NM_001369.2 E1926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:85012833 G>A maps to NM_001370.1 W3685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:84945498 G>A maps to NM_001370.1 Q3261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:84832697 C>T maps to NM_001370.1 G1052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:85032862 A>G maps to NM_001370.1 K3852K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:84844107 T>C did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:84864452 G>A maps to NM_001370.1 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:84897487 G>T maps to NM_001370.1 E2115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:196889163 G>T maps to NM_018897.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr2:196759936 C>T maps to NM_018897.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:196786881 G>A maps to NM_018897.2 R1289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:196799503 A>T maps to NM_018897.2 P1094P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:196729034 C>T maps to NM_018897.2 K2448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:196726484 G>A maps to NM_018897.2 L2564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:196729429 G>A maps to NM_018897.2 R2317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:196825552 G>A maps to NM_018897.2 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:196749475 G>A maps to NM_018897.2 R1866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:196912109 C>A maps to NM_018897.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:196723326 A>G maps to NM_018897.2 A2646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr2:196756456 G>A maps to NM_018897.2 Y1656Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:196771667 G>T maps to NM_018897.2 L1390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:196737141 G>T maps to NM_018897.2 G2155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr2:196756381 T>G maps to NM_018897.2 S1681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:196756381 T>C maps to NM_018897.2 S1681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr6:38998066 C>T maps to ENST00000327475 R4663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:38793987 C>T maps to ENST00000327475 R1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr6:38818163 G>A maps to ENST00000327475 L1767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr6:38885109 A>G maps to ENST00000327475 Q3400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr6:38854739 T>C maps to ENST00000327475 N2799N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr6:38952064 A>G maps to ENST00000327475 L4333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:38917232 T>A maps to ENST00000327475 S4033S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:38729518 T>C maps to ENST00000327475 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:38867574 G>A maps to ENST00000327475 S3017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:38813384 C>T maps to ENST00000327475 I1615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:38702335 G>T maps to ENST00000327475 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:38834642 T>A maps to ENST00000327475 L2216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr6:38919129 A>G maps to ENST00000327475 R4083R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr6:38821011 T>C maps to ENST00000327475 D1862D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:38794013 G>A maps to ENST00000327475 K1298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:38941565 C>T maps to ENST00000327475 R4207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr6:38851758 T>C maps to ENST00000327475 N2736N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr6:38834431 T>C maps to ENST00000327475 A2176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:38747775 G>T maps to ENST00000327475 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:38941487 G>T maps to ENST00000327475 E4181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:38950162 C>T maps to ENST00000327475 Y4280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:38754598 C>T maps to ENST00000327475 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:38758150 T>G maps to ENST00000327475 V905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:38773315 G>T maps to ENST00000327475 E1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:38790624 G>T maps to ENST00000327475 E1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:38810147 G>T maps to ENST00000327475 E1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:38890847 C>T maps to ENST00000327475 D3547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:38997981 A>G maps to ENST00000327475 L4634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:38821002 G>A maps to ENST00000327475 W1859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr6:38759416 T>A maps to ENST00000327475 A944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:38830058 C>A maps to ENST00000327475 C2033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:11687750 C>T maps to NM_001372.3 I2652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:11840814 A>G maps to NM_001372.3 G4212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:11666871 G>T maps to NM_001372.3 E2371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:11568193 G>A maps to NM_001372.3 W880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr17:11583112 C>T maps to NM_001372.3 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:11784618 G>A maps to NM_001372.3 E3565E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:11650928 C>T maps to NM_001372.3 G2152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:11865428 G>T maps to NM_001372.3 T4363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:11790239 C>T maps to NM_001372.3 N3690N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:11556084 C>T maps to NM_001372.3 C787C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:11584041 G>A maps to NM_001372.3 E1193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:11687705 C>T maps to NM_001372.3 L2637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:11865311 C>A maps to NM_001372.3 L4324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:11738128 C>T maps to NM_001372.3 Q3141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:11554403 G>T maps to NM_001372.3 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:11671787 G>T maps to NM_001372.3 E2397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:11701104 C>T maps to NM_001372.3 R2805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:11797741 C>T maps to NM_001372.3 R3779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr17:11845720 T>C maps to NM_001372.3 V4254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:11778336 G>A maps to NM_001372.3 W3438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr17:11786997 C>T maps to NM_001372.3 F3634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:11572853 G>A maps to NM_001372.3 G1032G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:11659958 G>A maps to NM_001372.3 L2271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:11790161 T>C maps to NM_001372.3 T3664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr17:11840811 C>T maps to NM_001372.3 D4211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr17:11872817 G>T maps to NM_001372.3 G4479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:11837304 C>T maps to NM_001372.3 R4136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:11573025 C>T maps to NM_001372.3 R1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:11511583 C>T maps to NM_001372.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr17:11790161 T>C maps to NM_001372.3 T3664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:11783393 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr17:11808980 T>C maps to NM_001372.3 D3868D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr17:11687753 T>C maps to NM_001372.3 D2653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:11772521 G>A maps to NM_001372.3 Q3335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:11778483 G>A maps to NM_001372.3 T3487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:34514691 G>A maps to NM_012144.2 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:34491515 T>C maps to NM_012144.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:34514691 G>A maps to NM_012144.2 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr9:34514718 A>C maps to NM_012144.2 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:72306208 C>T maps to NM_023036.4 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:72277997 C>T maps to NM_023036.4 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:72278078 C>T maps to NM_023036.4 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr17:72297183 G>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:33036610 C>T maps to NM_001539.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:46991039 T>C maps to NM_005880.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:4498738 C>T maps to NM_005147.4 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:78562927 A>G maps to NM_018602.3 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:78562927 A>G maps to NM_018602.3 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:14627325 C>T maps to NM_006145.1 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:186299798 A>G maps to NM_016306.4 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:186289884 C>T maps to NM_016306.4 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr3:186299798 A>G maps to NM_016306.4 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:186299796 G>T maps to NM_016306.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr3:186299798 A>G maps to NM_016306.4 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr3:186299798 A>G maps to NM_016306.4 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr3:186299798 A>G maps to NM_016306.4 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr3:186299798 A>G maps to NM_016306.4 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:74104787 G>A maps to NM_017626.4 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:73681023 G>A maps to NM_153614.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:73676079 G>A maps to NM_153614.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr2:220146760 A>G maps to NM_006736.5 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr2:234652343 C>T maps to NM_001001394.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:234652388 G>A maps to NM_001001394.3 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr22:41257497 G>T maps to NM_145174.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr3:128181992 G>A maps to NM_153330.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:128181605 G>A maps to NM_153330.2 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:128181557 C>T maps to NM_153330.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:108212224 G>T maps to NM_012328.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:108213392 G>T maps to NM_012328.2 G90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:22048329 C>T maps to NM_022365.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:183621114 C>T maps to NM_018981.1 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:183616839 A>G maps to NM_018981.1 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:183619755 A>G maps to NM_018981.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:183593607 G>T maps to NM_018981.1 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:6704652 G>A maps to NM_018198.3 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:6740974 A>C maps to NM_018198.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:6761815 A>G maps to NM_018198.3 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:6705925 G>A maps to NM_018198.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:6727782 G>A maps to NM_018198.3 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:6727836 G>A maps to NM_018198.3 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:132226082 T>C maps to NM_015268.3 G1667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:132179197 T>C maps to NM_015268.3 H518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:132179152 G>A maps to NM_015268.3 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:132222113 G>A maps to NM_015268.3 G1591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:132247166 T>C maps to NM_015268.3 Y2172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr3:132244500 C>T maps to NM_015268.3 S2036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:132172320 A>T maps to NM_015268.3 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:132207143 A>G maps to NM_015268.3 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:132230065 A>G maps to NM_015268.3 R1757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:132244491 T>C maps to NM_015268.3 C2033C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr12:56222376 G>A maps to NM_032364.5 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:56215817 G>T maps to NM_032364.5 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr13:43659902 G>A did not map to a codon.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr1:15893647 C>G maps to NM_015291.2 Y611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr5:138760696 A>G maps to NM_152686.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:102956229 C>T maps to NM_014377.1 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr7:102985030 G>A maps to NM_014377.1 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:102953081 G>A maps to NM_014377.1 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:102957290 A>G maps to NM_014377.1 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr5:34937648 G>A maps to NM_194283.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:34937607 C>T maps to NM_194283.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:34954773 C>T maps to NM_194283.3 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:31392363 T>C maps to NM_181706.4 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:114411899 G>A maps to NM_001015882.2 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr2:25180729 A>G maps to NM_016544.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:25186306 G>T maps to NM_016544.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:25190146 G>A maps to NM_016544.2 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr21:34861028 T>A maps to NM_001040192.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:34861247 C>T maps to NM_001040192.1 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:34861391 G>T maps to NM_001040192.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:34860655 C>A maps to NM_001040192.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:34861549 C>A maps to NM_001040192.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:34861072 C>A maps to NM_001040192.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:64000193 C>T maps to NM_005528.3 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr8:66988978 C>T maps to NM_033105.4 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:67012233 G>T maps to NM_033105.4 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr8:66963844 C>T maps to NM_033105.4 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:65855251 T>G maps to ENST00000371069 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:65864496 T>C maps to ENST00000371069 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:65851460 A>G maps to ENST00000371069 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:65858501 C>T maps to ENST00000371069 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:65855050 G>T maps to ENST00000371069 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr1:65855052 A>G maps to ENST00000371069 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:65845170 G>A maps to ENST00000371069 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:40152566 T>C maps to NM_003315.3 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:28534914 G>A maps to NM_014280.2 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:28555495 C>T maps to NM_014280.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:28555495 C>T maps to NM_014280.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr10:75003606 G>T maps to NM_015190.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:38027224 C>T maps to NM_003462.3 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:38027213 C>T maps to NM_003462.3 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:38024978 T>C maps to NM_003462.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:3706637 G>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr16:3707075 C>T maps to NM_005223.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:3707075 C>T maps to NM_005223.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:58191287 C>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:230341946 C>T maps to NM_139072.3 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:230253059 A>G maps to NM_139072.3 H592H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:230253101 G>A maps to NM_139072.3 C578C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:230341868 G>A maps to NM_139072.3 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:230377559 C>T maps to NM_139072.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr2:230450598 G>A maps to NM_139072.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr2:230456520 G>C maps to NM_139072.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:6579215 C>T maps to NM_144666.2 R2897R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:6589898 G>A maps to NM_144666.2 V4222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:6588670 C>T maps to NM_144666.2 R3978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:6566656 C>T maps to NM_144666.2 V1496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:6592139 C>T maps to NM_144666.2 S4466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:6567859 C>T maps to NM_144666.2 C1897C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:6560488 G>A maps to NM_144666.2 T1122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:6578492 C>T maps to NM_144666.2 C2656C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr9:131010866 C>T maps to ENST00000372923 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr9:130981326 G>C did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:131004548 C>T maps to ENST00000372923 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:130982592 G>A maps to ENST00000372923 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:131012469 C>A maps to ENST00000372923 S718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr9:130996370 C>T maps to ENST00000372923 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:131008710 C>A maps to ENST00000372923 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr9:130986607 C>A maps to ENST00000372923 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:32891218 G>T maps to ENST00000381000 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:32893060 G>T maps to ENST00000381000 G604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:32861116 G>T maps to ENST00000381000 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:10829035 C>T maps to NM_001005361.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:10939773 C>T maps to NM_001005361.2 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr19:10897346 C>T maps to NM_001005361.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr19:10940994 G>A maps to NM_001005361.2 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr19:10941716 C>T maps to NM_001005361.2 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:10934545 C>T maps to NM_001005361.2 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:10893642 T>C maps to NM_001005361.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr19:10923031 G>A maps to NM_001005361.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:172017854 G>T maps to ENST00000359070 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:172222795 C>T maps to ENST00000359070 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:172061969 G>A maps to ENST00000359070 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:101715376 C>T maps to ENST00000342239 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:101716419 G>T maps to ENST00000342239 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr10:101716729 C>T maps to ENST00000342239 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:101648643 G>T maps to ENST00000342239 R1099R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:101668829 C>T maps to ENST00000342239 E778E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:101716438 G>A maps to ENST00000342239 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr10:101646214 G>T maps to ENST00000342239 R1178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:101639726 C>T maps to ENST00000342239 P1487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:101716081 C>T maps to ENST00000342239 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr10:101659758 A>G maps to ENST00000342239 H873H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr10:101639942 A>G maps to ENST00000342239 A1415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr10:101716492 G>C maps to ENST00000342239 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:10277309 G>A maps to NM_001130823.1 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr19:10259678 G>A maps to NM_001130823.1 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:10252727 G>A maps to NM_001130823.1 G1095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:10259657 G>A maps to NM_001130823.1 D874D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:10283798 C>T maps to NM_001130823.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:10259612 G>A maps to NM_001130823.1 Y889Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr19:10273345 T>C maps to NM_001130823.1 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:10248606 C>T maps to NM_001130823.1 S1398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:25457173 G>A maps to NM_175629.1 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:25469588 A>G maps to NM_175629.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:25536838 G>A maps to NM_175629.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:25457240 G>T maps to NM_175629.1 R882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:25470561 G>A maps to NM_175629.1 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr20:31375142 G>A maps to NM_006892.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr20:31390201 G>T maps to NM_006892.3 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:31388079 C>T maps to NM_006892.3 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr20:31375163 C>A maps to NM_006892.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr20:31383225 C>T maps to NM_006892.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:31388675 C>T maps to NM_006892.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:31374310 C>T maps to NM_006892.3 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:31381376 A>C maps to NM_006892.3 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:31372592 T>C maps to NM_006892.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr20:31372577 T>C maps to NM_006892.3 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:31389201 C>T maps to NM_006892.3 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr21:45681136 C>T maps to NM_013369.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:220246091 G>A maps to NM_012100.2 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:98088545 G>T maps to NM_004088.3 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:98079059 G>A maps to NM_004088.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:98078204 G>A maps to NM_004088.3 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr10:98064310 G>A maps to NM_004088.3 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:98082467 C>T maps to NM_004088.3 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:94342200 C>T maps to NM_014597.4 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr1:94337666 G>T maps to NM_014597.4 Y676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:94342647 G>A maps to NM_014597.4 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr16:30017746 G>T maps to NM_003586.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:30020816 A>G maps to NM_003586.2 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:30017982 A>G maps to NM_003586.2 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:128835995 G>A maps to ENST00000398025 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr10:128821506 T>C maps to ENST00000398025 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:128821471 C>T maps to ENST00000398025 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:129207383 C>T maps to ENST00000398025 A1447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:129245727 C>T maps to ENST00000398025 S1873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:129202677 C>T maps to ENST00000398025 F1414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:128830432 G>A maps to ENST00000398025 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr10:128797686 A>G maps to ENST00000398025 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:129216756 C>T maps to ENST00000398025 N1593N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:225761070 C>T maps to NM_014689.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:225739400 T>C maps to NM_014689.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:225639730 G>A maps to NM_014689.2 F1968F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:225672641 G>A maps to NM_014689.2 R1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:225668854 G>A maps to NM_014689.2 C1414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:225639697 G>A maps to NM_014689.2 F1979F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr2:225672459 G>A maps to NM_014689.2 Y1209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:225639744 G>T maps to NM_014689.2 R1964R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:225796310 A>G maps to NM_014689.2 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:117758579 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:117815703 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:117695459 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:117707829 C>T did not map to a codon.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr23:117758568 G>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:117796704 G>A did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:117707960 C>G did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:117712533 C>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:117699981 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:117718781 A>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:117744374 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:117786001 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:117680024 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:117777479 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:117796731 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:117814642 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:117695425 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:117702068 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:117727210 A>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:117742268 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:117742038 C>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:117815193 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:117742089 A>G did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr5:169129307 G>A maps to NM_004946.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:169468130 C>T maps to NM_004946.2 L1246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:169230161 C>T maps to NM_004946.2 C885C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:169116271 C>T maps to NM_004946.2 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:169472852 C>T maps to NM_004946.2 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:169111324 C>A maps to NM_004946.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:169174415 G>T maps to NM_004946.2 E762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr5:169507234 G>A maps to NM_004946.2 A1745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:169186767 G>A maps to NM_004946.2 A812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:169186716 T>G maps to NM_004946.2 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:169472839 T>C maps to NM_004946.2 S1299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:169145741 G>A maps to NM_004946.2 K738K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:169188630 T>C did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:169230068 G>T maps to NM_004946.2 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:169139121 A>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:169494543 G>T maps to NM_004946.2 E1500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr5:169141180 C>T maps to NM_004946.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:169098090 G>A maps to NM_004946.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:169098124 G>T maps to NM_004946.2 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr5:169483729 G>A maps to NM_004946.2 R1446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:169116271 C>T maps to NM_004946.2 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:169507216 G>A maps to NM_004946.2 A1739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr5:169116271 C>T maps to NM_004946.2 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:169122917 C>T maps to NM_004946.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr5:169435499 G>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:51367651 A>G maps to NM_004947.4 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:51352549 C>T maps to NM_004947.4 N1131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:51392443 C>T maps to NM_004947.4 C1413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:51413216 C>T maps to NM_004947.4 V1817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:51127716 C>T maps to NM_004947.4 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:51265437 C>A maps to NM_004947.4 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:51273834 C>T maps to NM_004947.4 Y659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:51315166 G>A maps to NM_004947.4 Q935Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:51315088 C>T maps to NM_004947.4 D909D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:51400016 G>A maps to NM_004947.4 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:111508078 C>T maps to ENST00000428084 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:111368515 G>T maps to ENST00000428084 V1914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:111449457 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:111368569 G>A maps to ENST00000428084 Y1896Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr7:111629110 G>A maps to ENST00000428084 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr7:111517167 C>T maps to ENST00000428084 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr7:111503488 C>T maps to ENST00000428084 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:111368368 C>T maps to ENST00000428084 P1963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:111381185 C>T maps to ENST00000428084 G1668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:111423965 G>A maps to ENST00000428084 G1157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr8:25154058 T>C maps to NM_024940.6 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:25232160 G>A maps to NM_024940.6 E1269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:25220615 C>A maps to NM_024940.6 V1001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:25209257 G>A maps to NM_024940.6 A922A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:25222156 T>G maps to NM_024940.6 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr8:25261237 T>C maps to NM_024940.6 D1697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr8:25101273 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:25249426 T>C maps to NM_024940.6 N1457N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:11348158 C>T maps to ENST00000319867 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:11347513 G>A maps to ENST00000319867 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:11363598 A>G maps to ENST00000319867 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr19:11312771 C>T maps to ENST00000319867 P1829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:11353960 C>T maps to ENST00000319867 T453T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D5-6930-01A-11D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:11348925 G>A maps to ENST00000252453 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr19:11333409 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr19:11338138 C>T maps to ENST00000319867 A943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:11328011 G>A maps to ENST00000319867 G1202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:62940944 C>T maps to ENST00000371140 Q2013Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:62979247 G>A maps to ENST00000371140 S1383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:63009371 C>T maps to ENST00000371140 T968T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:62995044 C>T maps to ENST00000371140 R1228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:62961292 T>C maps to ENST00000371140 E1661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:62941520 G>A maps to ENST00000371140 R1940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:62943429 C>A maps to ENST00000371140 E1859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr1:63119430 T>C maps to ENST00000371140 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:62970432 T>C maps to ENST00000371140 E1544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:63113774 A>G did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:63119430 T>C maps to ENST00000371140 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:63096923 T>C maps to ENST00000371140 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr9:463546 T>C maps to NM_203447.3 R2033R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr9:376990 G>A maps to NM_203447.3 E740E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr9:396804 C>T maps to NM_203447.3 H997H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr9:420429 G>A maps to NM_203447.3 A1290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:311982 C>T maps to NM_203447.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:414883 C>T maps to NM_203447.3 I1211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:418119 A>G maps to NM_203447.3 G1251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr9:332450 G>A maps to NM_203447.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr9:463546 T>C maps to NM_203447.3 R2033R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:463546 T>C maps to NM_203447.3 R2033R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr9:463546 T>C maps to NM_203447.3 R2033R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr9:328143 G>A maps to NM_203447.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:289508 G>T did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr9:406979 C>T maps to NM_203447.3 F1147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:463546 T>C maps to NM_203447.3 R2033R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:336696 C>T maps to NM_203447.3 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:99575594 A>G maps to ENST00000428223 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:99532812 G>A maps to ENST00000428223 N953N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:99549791 G>A maps to ENST00000428223 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr13:99452622 C>T maps to ENST00000428223 A1959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:99505746 G>A maps to ENST00000428223 S1287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:99575567 G>A maps to ENST00000428223 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr13:99534153 G>A maps to ENST00000428223 N889N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:3496575 T>C maps to NM_001145165.1 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:21768225 G>A maps to NM_003974.2 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:57507648 C>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr16:57507842 C>T maps to NM_018110.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr20:53205042 A>T maps to NM_018431.3 K66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:67365727 C>A maps to NM_152721.5 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr18:67345063 C>T maps to NM_152721.5 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr18:67266711 G>A maps to NM_152721.5 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr4:3478222 C>T maps to ENST00000389653 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:3494582 G>A maps to ENST00000389653 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr9:131708487 T>C maps to NM_014908.3 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:31938743 C>T maps to NM_005510.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr21:34956930 A>G maps to NM_017613.2 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:34953637 A>C maps to NM_017613.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:34958405 G>A maps to NM_017613.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr21:34950613 C>T maps to NM_017613.2 *567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:34954535 C>T maps to NM_017613.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:83819942 A>G maps to NM_015018.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:83877654 C>T maps to NM_015018.2 T2389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:83848495 C>T maps to NM_015018.2 Q1579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr6:83855343 T>G maps to NM_015018.2 V1881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:83847870 C>T maps to NM_015018.2 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:83839059 C>A maps to NM_015018.2 S725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:83847732 C>T maps to NM_015018.2 F1324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:83861379 T>G did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr6:83863931 T>C maps to NM_015018.2 H2141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr6:83842023 C>T maps to NM_015018.2 Q916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr21:37665616 G>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr21:37649352 C>T maps to NM_005128.2 S1889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr21:37626107 C>T maps to NM_005128.2 V1720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr21:37610993 T>C maps to NM_005128.2 F957F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr21:37617518 C>T maps to NM_005128.2 R1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr21:37623527 G>A maps to NM_005128.2 A1689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr21:37571453 G>A maps to NM_005128.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:37665827 G>T maps to NM_005128.2 E2286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:37602869 G>A maps to NM_005128.2 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:2206737 C>T maps to ENST00000221482 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:2199921 C>T maps to ENST00000221482 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr19:2210822 C>T maps to ENST00000221482 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:2225434 G>A maps to ENST00000221482 P1215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:118971499 G>A maps to NM_001382.3 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:30917125 G>A maps to NM_080870.3 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:68024016 G>A maps to NM_022355.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr16:68011672 G>A maps to NM_022357.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr16:68010088 C>T maps to NM_022357.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:68011239 G>A maps to NM_022357.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:38707023 G>T maps to NM_001135155.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:65116379 G>A maps to NM_006268.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:65111481 C>T maps to NM_006268.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr11:65113742 C>T maps to NM_006268.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:65108492 C>T maps to NM_006268.3 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:73140966 G>A maps to NM_012074.3 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:73181137 G>T maps to NM_012074.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:1939862 C>T maps to NM_001383.3 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr1:44438183 C>T maps to NM_001384.4 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:44437735 T>C maps to NM_001384.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:16305670 A>T maps to NM_206831.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr20:49575036 A>G maps to ENST00000449701 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:155112710 C>T maps to NM_018973.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:116503696 T>G maps to NM_020868.3 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:116283472 G>A did not map to a codon.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr2:116497468 G>A maps to NM_020868.3 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:116572516 C>A maps to NM_020868.3 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:116447264 T>C maps to NM_020868.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:116257176 T>G maps to NM_020868.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr2:116510800 A>T maps to NM_020868.3 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:116598396 C>T maps to NM_020868.3 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:116593755 A>G maps to NM_020868.3 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:66249817 G>A maps to NM_005700.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:162903492 C>A maps to NM_001935.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:162851861 T>C maps to NM_001935.3 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:162875263 C>T maps to NM_001935.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:162875263 C>T maps to NM_001935.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:162865132 C>T maps to NM_001935.3 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:154429559 C>T maps to NM_130797.2 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:154593063 G>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr7:154593072 A>G maps to NM_130797.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:154645511 G>T maps to NM_130797.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:154667714 C>T maps to NM_130797.2 D661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:154667714 C>T maps to NM_130797.2 D661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr7:154585833 C>T maps to NM_130797.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr7:154593072 A>G maps to NM_130797.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr7:154561190 C>T maps to NM_130797.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:154002620 G>A maps to NM_001936.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:65772601 C>T maps to NM_197960.2 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:65782574 C>A maps to NM_197960.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:65780043 G>A maps to NM_197960.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:4704160 G>A maps to ENST00000357909 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:4714183 C>T maps to ENST00000357909 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:109023515 G>A maps to NM_138815.3 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:109047734 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:109050879 T>C did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:74063573 A>G did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:63954369 G>A maps to NM_173812.4 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:64061999 C>T maps to NM_173812.4 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:64057542 C>A maps to NM_173812.4 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:64041054 C>A maps to NM_173812.4 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:63954303 T>C maps to NM_173812.4 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:32949391 C>T maps to NM_001172774.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:32973073 C>T maps to NM_001172774.1 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:32927472 G>A maps to NM_001172774.1 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:32971456 C>T maps to NM_001172774.1 N661N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr19:32955671 G>A maps to NM_001172774.1 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr19:32955671 G>T maps to NM_001172774.1 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr8:95792594 T>C maps to NM_181787.2 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr2:32264519 C>T maps to ENST00000452582 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:98039505 T>C maps to NM_000110.3 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:98187098 A>G maps to NM_000110.3 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:97700455 A>G maps to NM_000110.3 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:97981340 G>A maps to NM_000110.3 R561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:98060693 G>T maps to NM_000110.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:98187158 A>G maps to NM_000110.3 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:98039522 C>A maps to NM_000110.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:97839161 A>G maps to NM_000110.3 C671C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:97839161 A>G maps to NM_000110.3 C671C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr1:98015253 T>C maps to NM_000110.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr1:98157278 A>G maps to NM_000110.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:105405212 G>T maps to NM_001385.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr8:105459695 T>C maps to NM_001385.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr8:105459695 T>C maps to NM_001385.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr8:26509933 T>C maps to NM_001197293.1 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr8:26509933 T>C maps to NM_001197293.1 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:146785257 A>G maps to NM_001197294.1 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:146773642 G>A maps to NM_001197294.1 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:146773618 A>G maps to NM_001197294.1 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:134017315 C>T maps to NM_006426.2 H504H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:134015478 C>T maps to NM_006426.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:134012446 C>T maps to NM_006426.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:27165476 C>T maps to NM_020134.3 H433H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:27167549 C>T maps to NM_020134.3 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:27150300 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:74750463 G>T maps to NM_133637.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:74746318 G>A maps to NM_133637.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr1:93819492 C>T maps to NM_001938.2 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:102315001 C>A maps to NM_018370.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:102302085 G>A maps to NM_018370.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:102302022 C>T maps to NM_018370.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:102302022 C>T maps to NM_018370.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:102315001 C>A maps to NM_018370.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:102315001 C>A maps to NM_018370.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:102315001 C>A maps to NM_018370.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr1:111667438 G>T maps to NM_178454.4 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr11:65688884 C>T maps to ENST00000376991 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:65688884 C>T maps to ENST00000376991 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:174869982 C>A maps to NM_000794.3 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:174869970 G>A maps to NM_000794.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:113295178 C>T maps to ENST00000355319 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:113288813 G>A maps to ENST00000355319 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:113281529 G>T maps to ENST00000355319 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:113850075 G>A maps to NM_000796.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:113850075 G>A maps to NM_000796.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:113858436 G>T maps to NM_000796.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:113847661 C>T maps to NM_000796.3 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr3:113850208 A>G maps to NM_000796.3 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:9785071 G>A maps to NM_000798.4 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:9783985 G>A maps to NM_000798.4 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:9784675 C>T maps to NM_000798.4 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr22:31819348 T>C maps to NM_004147.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:31819348 T>C maps to NM_004147.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:17997274 C>A maps to NM_001388.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:18009787 C>T maps to NM_001388.3 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr17:18003748 G>A maps to NM_001388.3 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr17:18005257 C>T maps to NM_001388.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr17:18003880 A>G did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr10:50574409 A>G maps to NM_001080520.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:100505426 T>C did not map to a codon.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr23:100492658 T>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:100496719 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:100490967 G>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:100503521 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:100492712 G>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:100492714 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:100513417 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:100490891 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:100492740 C>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:100492762 C>T did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:100506063 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:28710635 A>G maps to NM_024421.2 H842H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:28720059 C>A maps to NM_024421.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr18:28736049 A>G maps to NM_024421.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr18:28714697 G>A maps to NM_024421.2 N571N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr18:28734801 C>A maps to NM_024421.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr18:28671092 A>G maps to ENST00000438199 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr18:28666670 T>C maps to ENST00000438199 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr18:28666670 T>C maps to ENST00000438199 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:28669412 C>A maps to ENST00000438199 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr18:28598068 C>A maps to NM_001941.3 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:28609588 C>T maps to NM_001941.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr18:28609534 T>C maps to NM_001941.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr18:28588039 C>T maps to NM_001941.3 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr18:28605881 C>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr21:41741044 G>A maps to NM_001389.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr21:41684089 C>T maps to NM_001389.3 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr21:41711085 C>T maps to NM_001389.3 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr21:41459185 C>T maps to NM_001389.3 G1293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr21:42080431 T>A maps to NM_001389.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr21:41424020 C>T maps to NM_001389.3 T1683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr21:41725662 C>T maps to NM_001389.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr21:41516639 G>A maps to NM_001389.3 Q1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr21:41385140 G>A maps to NM_001389.3 S1953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr21:41719795 C>T maps to NM_001389.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:41648130 G>T maps to NM_001389.3 S750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:42064769 G>T maps to NM_001389.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:41427664 C>T maps to NM_001389.3 T1674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:41416203 T>C did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr21:41505829 T>C maps to NM_001389.3 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr21:41684180 C>T maps to NM_001389.3 W630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr21:42080551 G>A maps to NM_001389.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr21:41561121 C>T maps to NM_001389.3 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr11:117303113 C>T maps to NM_020693.2 Q1771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:117389358 G>A maps to NM_020693.2 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:117395706 C>T maps to NM_020693.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:117307880 G>A maps to NM_020693.2 C1619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:117307883 G>T maps to NM_020693.2 G1618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:117308734 G>A maps to NM_020693.2 S1496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:117351209 G>A maps to NM_020693.2 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:117329509 G>A maps to NM_020693.2 G1236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:117352737 G>A maps to NM_020693.2 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:117395556 G>A maps to NM_020693.2 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr11:117310620 G>A maps to NM_020693.2 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:117301615 G>T maps to NM_020693.2 I1896I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:117303143 G>A maps to NM_020693.2 G1761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:117308794 G>A maps to NM_020693.2 F1476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:117375711 G>A maps to NM_020693.2 Y763Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:117321270 G>A maps to NM_020693.2 G1294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:117391991 G>A maps to NM_020693.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr21:38604719 C>G maps to NM_006052.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr21:39493331 C>T maps to ENST00000398948 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr21:39426981 C>T maps to NM_005867.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr21:39426981 C>T maps to NM_005867.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:116757958 C>T maps to NM_013352.2 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:116757214 A>G maps to NM_013352.2 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:116747769 G>A maps to NM_013352.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr18:65180216 G>T maps to NM_032160.2 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:65179473 C>T maps to NM_032160.2 W801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr18:65179441 G>A maps to NM_032160.2 R812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr18:65180918 C>T maps to NM_032160.2 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:65180402 T>C maps to NM_032160.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:65181271 G>A maps to NM_032160.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr18:65180276 C>T maps to NM_032160.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr18:65180813 T>C maps to NM_032160.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:65179583 T>G maps to NM_032160.2 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:65181065 C>T maps to NM_032160.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:65179271 G>T maps to NM_032160.2 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr18:65180417 A>C maps to NM_032160.2 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:28934327 C>T maps to NM_001942.2 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:28934867 T>G maps to NM_001942.2 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:28908231 C>A maps to NM_001942.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr18:28913634 C>T maps to NM_001942.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr18:28934291 A>G maps to NM_001942.2 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr18:29126219 G>A maps to NM_001943.3 Q957Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:29126054 A>C maps to NM_001943.3 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr18:29116354 T>C maps to NM_001943.3 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr18:29126513 C>T maps to NM_001943.3 S1055S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:29049247 G>A maps to NM_001944.2 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:29044208 G>T maps to NM_001944.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:29045373 T>G maps to NM_001944.2 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr18:29052370 C>A maps to NM_001944.2 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr18:29055844 T>A maps to NM_001944.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr18:29055970 C>T maps to NM_001944.2 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr18:28991110 C>T maps to NM_001134453.1 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr18:28966730 C>T maps to NM_001134453.1 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:28956897 C>T maps to NM_001134453.1 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr18:28993380 G>A maps to NM_001134453.1 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr18:28986046 G>A maps to NM_001134453.1 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:28986205 G>T maps to NM_001134453.1 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr18:28991122 C>T maps to NM_001134453.1 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr18:28986205 G>A maps to NM_001134453.1 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr18:28993335 A>G maps to NM_001134453.1 R986R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr20:35396410 T>C maps to NM_001145315.1 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:7579569 G>A maps to NM_004415.2 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:7556049 G>A maps to NM_004415.2 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:7580157 A>G maps to NM_004415.2 E1245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:7585651 G>A maps to NM_004415.2 P2719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:7581030 A>G maps to NM_004415.2 T1536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:7581471 G>A maps to NM_004415.2 E1683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:7583581 C>T maps to NM_004415.2 Y2029Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:7584977 G>T maps to NM_004415.2 E2495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr6:7581030 A>G maps to NM_004415.2 T1536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:7565620 G>A maps to NM_004415.2 L269L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A6-5657-01A-01D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:88534081 G>A maps to NM_014208.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:88533778 A>G maps to NM_014208.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:88536450 C>T maps to NM_014208.3 S879S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3977-01A-01W-0995-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-3984-01A-02W-0995-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-3984-01A-02W-0995-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-A01X-01A-21W-A096-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AZ-4315-01A-01D-1408-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CA-6718-01A-11D-1835-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CA-6718-01A-11D-1835-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CM-5861-01A-01D-1650-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D5-6928-01A-11D-1924-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DM-A1D4-01A-21D-A152-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr4:88535232 C>A maps to NM_014208.3 G473G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DM-A28H-01A-11D-A16V-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-F4-6570-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:88533664 G>A maps to NM_014208.3 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:88536360 C>T maps to NM_014208.3 D849D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G4-6628-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr6:56392377 C>T maps to ENST00000361203 W5734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:56504743 C>A maps to ENST00000361203 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr6:56505249 A>G maps to ENST00000361203 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:56496106 T>C maps to ENST00000361203 A1137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:56506871 G>A maps to ENST00000361203 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:56481862 C>T maps to ENST00000281662 T2698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr6:56399961 C>G maps to ENST00000361203 S5422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:56485438 A>G maps to ENST00000281662 L1695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:56374626 G>A maps to ENST00000361203 I6064I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:56354332 G>A maps to ENST00000361203 I6733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:56417415 G>A maps to ENST00000361203 R5181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:56425200 C>T maps to ENST00000361203 K4566K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:56463284 C>A maps to ENST00000361203 E3762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:56483460 C>A maps to ENST00000281662 E2355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:56484237 C>A maps to ENST00000281662 E2096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr6:56498938 A>G maps to ENST00000361203 N993N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:56485141 G>A maps to ENST00000281662 A1794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:56417103 C>A maps to ENST00000361203 E5285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:56417395 G>A maps to ENST00000361203 F5187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:56376095 G>A maps to ENST00000361203 Q6016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:56373329 T>C maps to ENST00000361203 A6201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:56462686 C>A maps to ENST00000361203 E3805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:56483455 A>G maps to ENST00000281662 N2356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:56504148 C>A maps to ENST00000361203 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr6:56497778 A>G maps to ENST00000361203 R1015R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr6:56357222 G>A maps to ENST00000361203 A6642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr6:56422284 T>A maps to ENST00000361203 T4613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr6:56481342 G>A maps to ENST00000281662 R2872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:56481862 C>T maps to ENST00000281662 T2698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr6:56417686 C>T maps to ENST00000361203 S5090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:56490034 G>T maps to ENST00000361203 R1373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr6:56496106 T>C maps to ENST00000361203 A1137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr6:56483971 A>G maps to ENST00000281662 G2184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:56335021 G>A maps to ENST00000361203 G7222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr6:56399961 C>T maps to ENST00000361203 S5422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr6:56483971 A>G maps to ENST00000281662 G2184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:56505287 G>A maps to ENST00000361203 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:17587709 A>G maps to NM_006870.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:17581460 G>T maps to NM_006870.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:17587709 A>G maps to NM_006870.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr20:17587707 G>T maps to NM_006870.3 G139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:205116853 A>G maps to NM_015375.2 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr1:205116853 A>G maps to NM_015375.2 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr20:18724807 C>G maps to NM_080820.4 S181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:18576814 G>A maps to NM_080820.4 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:212218014 A>G maps to NM_016448.2 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:212273744 C>A maps to NM_016448.2 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:212273603 G>A maps to NM_016448.2 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:212218051 C>T maps to NM_016448.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:212274107 T>G maps to NM_016448.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr18:32409010 C>T maps to NM_001392.4 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:32431838 C>T maps to NM_001390.4 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:25611181 G>T maps to NM_021907.3 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:25830126 T>C maps to NM_021907.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:15615616 C>T maps to NM_032122.4 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:15533513 C>T maps to NM_032122.4 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:15533473 G>A maps to NM_032122.4 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr15:49935669 C>A maps to NM_001144955.1 Y270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr5:118280283 G>A maps to NM_173666.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:118264383 A>G maps to NM_173666.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr5:118324136 G>A maps to NM_173666.2 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr5:118264230 C>A did not map to a codon.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr12:113515277 G>A maps to NM_004416.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:113515343 C>A maps to NM_004416.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:113515331 C>T maps to NM_004416.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:113533197 C>A maps to NM_004416.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:76134773 C>T maps to NM_020892.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:58001350 C>T maps to NM_178502.2 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:122288681 C>T maps to NM_138287.3 C582C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:45435472 G>A maps to NM_175940.1 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr15:45427458 C>T maps to NM_175940.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:45444490 C>A maps to NM_175940.1 A1067A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:45456987 C>T maps to NM_175940.1 I1515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr15:45443356 C>T maps to NM_175940.1 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:45454071 G>A maps to NM_175940.1 T1331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:45405185 A>G maps to NM_014080.4 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:45404916 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:45398320 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:45386382 G>A maps to NM_014080.4 R1538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:45401049 C>T maps to NM_014080.4 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:45410262 G>A maps to NM_144565.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:45408412 C>T maps to NM_207581.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:45410088 T>C maps to NM_207581.3 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:76797818 G>A maps to NM_001003892.1 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr16:68083442 A>G maps to NM_017803.3 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:68087528 A>C maps to NM_017803.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:107215740 T>G maps to NM_181581.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:107217818 C>T maps to NM_181581.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:107214230 G>A maps to NM_181581.1 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:172195877 G>A maps to NM_004417.3 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:221913065 G>A maps to NM_007207.3 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr1:221879788 C>T maps to NM_007207.3 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:221913053 T>C maps to NM_007207.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:74002126 C>T maps to NM_003584.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:161719722 G>A maps to NM_007240.1 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:161721523 C>A maps to NM_007240.1 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr10:76865506 G>A maps to NM_001007271.1 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:76868903 G>T maps to NM_001007272.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr10:76861701 G>A maps to ENST00000356369 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr10:76861662 C>T maps to ENST00000356369 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:76867858 G>A maps to NM_001007271.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:35872649 C>A maps to NM_007026.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:35872742 C>T maps to NM_007026.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr17:35872742 C>T maps to NM_007026.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:12673992 T>G maps to NM_030640.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr12:12630317 G>A maps to NM_030640.2 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr12:12630317 G>A maps to NM_030640.2 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:12630638 G>A maps to NM_030640.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr12:12630632 G>A maps to NM_030640.2 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:31059603 G>A maps to NM_152511.3 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:183943747 G>A maps to NM_080876.3 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr2:183960271 G>A maps to NM_080876.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:183960223 C>T maps to NM_080876.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr2:183960271 G>A maps to NM_080876.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:183960265 T>C maps to NM_080876.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr2:183960265 T>C maps to NM_080876.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr2:96809714 A>T maps to NM_004418.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:44703737 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:44703473 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:44703734 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:44703878 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:44703876 C>T did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:44703876 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:348818 A>G maps to ENST00000457386 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr6:348204 A>G maps to ENST00000457386 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr6:348180 C>T maps to ENST00000457386 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr6:311893 G>T maps to ENST00000457386 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr1:159752031 A>G maps to NM_017823.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr8:33449665 G>A maps to NM_024025.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:33449620 G>T maps to NM_024025.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr8:33451123 C>T maps to NM_024025.1 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:167096068 C>T maps to NM_001080426.1 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:167064176 C>T maps to NM_001080426.1 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr1:167095997 C>T maps to NM_001080426.1 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:167095771 A>T maps to NM_001080426.1 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:167095771 A>G maps to NM_001080426.1 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr1:167096377 C>T maps to NM_001080426.1 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:41847024 G>T maps to NM_004090.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:41847039 G>A maps to NM_004090.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:29202958 G>A maps to NM_057158.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr10:112266748 C>G maps to NM_004419.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:112266760 C>T maps to NM_004419.3 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr12:89744460 C>A maps to NM_001946.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:89745468 C>T maps to NM_001946.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr3:52084932 C>T maps to NM_001947.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:52084902 C>T maps to NM_001947.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr11:1585168 C>G maps to NM_004420.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr23:152915581 A>G did not map to a codon.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr23:152915599 A>G did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:152915581 A>G did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:152914853 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:152915600 C>T did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:152915707 C>A did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:152914840 C>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:152913444 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:152915582 C>T did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:152915581 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:152914787 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:57670630 G>A maps to NM_001012729.1 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:1274016 C>T maps to ENST00000378888 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:1275636 C>T maps to ENST00000378888 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:1273498 C>T maps to ENST00000378888 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:1275468 G>A maps to ENST00000378888 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:7130507 G>A maps to NM_004422.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:7129812 C>T maps to NM_004422.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:7129800 G>T maps to NM_004422.2 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr17:7132718 G>A maps to NM_004422.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr3:183884283 A>G maps to NM_004423.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:183882623 A>G maps to NM_004423.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr3:183882623 A>G maps to NM_004423.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:82102056 C>A maps to NM_138812.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr10:82122273 G>T maps to ENST00000372198 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:46645262 G>A maps to NM_017653.3 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:46906062 C>A maps to NM_017653.3 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:46645262 G>A maps to NM_017653.3 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:46798597 A>G maps to NM_017653.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:46860146 C>A maps to NM_017653.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr14:102494375 G>A maps to NM_001376.4 V3122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:102471464 C>T maps to NM_001376.4 A1775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:102483447 T>C maps to NM_001376.4 S2624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr14:102461366 G>A maps to NM_001376.4 E1126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:102505810 C>T maps to NM_001376.4 Y3841Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:102516127 C>A maps to NM_001376.4 A4531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:102515816 C>T maps to NM_001376.4 A4471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:102516184 C>T maps to NM_001376.4 G4550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr14:102483188 C>T maps to NM_001376.4 V2567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr14:102516208 C>T maps to NM_001376.4 F4558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:102466396 C>T maps to NM_001376.4 D1292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:102466730 C>T maps to NM_001376.4 R1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr14:102453860 C>T maps to NM_001376.4 D870D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:102483492 C>T maps to NM_001376.4 C2639C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:102463571 C>T maps to NM_001376.4 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:102478788 C>T maps to NM_001376.4 R2332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr14:102507986 C>T maps to NM_001376.4 H4006H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:102508807 C>T maps to NM_001376.4 C4121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:102510967 C>T maps to NM_001376.4 P4313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:102468920 C>A maps to NM_001376.4 I1530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:102514298 G>A maps to NM_001376.4 A4384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr14:102499760 C>T maps to NM_001376.4 Y3451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr14:102461588 T>C maps to NM_001376.4 Y1172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr14:102500437 C>T maps to NM_001376.4 F3513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr14:102461588 T>C maps to NM_001376.4 Y1172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr14:102461588 T>C maps to NM_001376.4 Y1172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:102463448 C>T maps to NM_001376.4 I1214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr7:95616428 A>T maps to NM_004411.4 K286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:95657560 T>A maps to NM_004411.4 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:95442583 G>A maps to NM_004411.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:95668609 C>A maps to NM_004411.4 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:95668609 C>A maps to NM_004411.4 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:95668609 C>A maps to NM_004411.4 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr7:95705505 C>A maps to NM_004411.4 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr7:95705505 C>A maps to NM_004411.4 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr2:172569285 T>C maps to NM_001378.1 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr2:172563855 C>T maps to NM_001378.1 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:172604354 C>T maps to NM_001378.1 R625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:172584386 T>C maps to NM_001378.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:32576105 C>A maps to NM_016141.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:32570046 C>T maps to NM_016141.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr16:66759827 C>T maps to NM_006141.2 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:66770061 G>A maps to NM_006141.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:103044892 C>T maps to NM_001080463.1 Q1890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr11:103027439 C>T maps to NM_001080463.1 F1356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:103055758 A>G maps to NM_001080463.1 S2204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:103068689 G>T maps to NM_001080463.1 R2579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr11:103041638 C>T maps to NM_001080463.1 R1726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:103041638 C>T maps to NM_001080463.1 R1726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:102999734 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:103048491 G>T maps to NM_001080463.1 E2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:103068660 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:103102061 G>T maps to NM_001080463.1 E3143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:103130679 G>T maps to NM_001080463.1 E3564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:103158278 G>A maps to NM_001080463.1 A3687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:103349821 G>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:103349845 G>A maps to NM_001080463.1 P4270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:102987391 G>T maps to NM_001080463.1 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:103086512 G>T maps to NM_001080463.1 E2920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:102986000 G>T maps to NM_001080463.1 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:103102070 G>T maps to NM_001080463.1 E3146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:103029526 G>T maps to NM_001080463.1 E1417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:103070168 A>G maps to NM_001080463.1 G2684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:103040917 G>T maps to NM_001080463.1 G1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr11:103070166 G>T maps to NM_001080463.1 G2684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr11:103182692 A>G maps to NM_001080463.1 R3867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:103270419 T>C maps to NM_001080463.1 P4069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:44028782 C>A maps to NM_001193464.1 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:33128421 C>T maps to ENST00000374846 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:80583507 T>C maps to NM_130897.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:159057873 G>A maps to NM_006519.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:37699853 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr21:38862660 C>T maps to NM_001396.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr21:38862660 C>A maps to NM_001396.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr21:38853088 C>T maps to NM_001396.3 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr21:38877654 C>T maps to NM_001396.3 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:40318963 G>A maps to NM_004714.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:40321104 G>A maps to NM_004714.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:40320568 C>T maps to NM_004714.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr19:40316723 G>A maps to NM_004714.1 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr19:40319077 G>A maps to NM_004714.1 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:40318017 G>A maps to NM_004714.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:40322447 C>T maps to NM_004714.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:68051109 G>A maps to NM_006482.2 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr12:68051841 G>A maps to NM_006482.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:68051019 T>C maps to NM_006482.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:68051772 C>T maps to NM_006482.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr12:68051037 G>A maps to NM_006482.2 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:68051739 C>T maps to NM_006482.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr12:68051280 C>A maps to NM_006482.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:68051679 G>T maps to NM_006482.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:68050890 C>T maps to NM_006482.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr12:68051679 G>T maps to NM_006482.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr12:68051679 G>T maps to NM_006482.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr12:68051877 C>T maps to NM_006482.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:206821004 C>A maps to NM_003582.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr1:206821217 G>A maps to NM_003582.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr1:206822150 G>A maps to NM_003582.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:4700453 G>A maps to NM_003845.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:71796967 C>T maps to NM_001130987.1 D961D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:71780967 C>T maps to NM_001130987.1 N672N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:71766359 G>T maps to NM_001130987.1 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr2:71908180 G>A maps to NM_001130987.1 E2038E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:71795468 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr2:71797369 G>A maps to NM_001130987.1 K997K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:71801332 G>A maps to NM_001130987.1 R1078R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:71816796 G>T maps to NM_001130987.1 T1159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:71838445 C>A maps to NM_001130987.1 I1343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr2:71886114 C>A maps to NM_001130987.1 I1621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr2:71797360 C>T maps to NM_001130987.1 N994N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:207527789 G>A maps to NM_001093730.1 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:55727167 A>G maps to NM_130810.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:96251624 C>A maps to NM_198968.2 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr13:96277053 C>A maps to NM_198968.2 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:96234558 C>A maps to NM_198968.2 E845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:96242539 G>A maps to NM_198968.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:96251639 C>A maps to NM_198968.2 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr13:96277050 A>G maps to NM_198968.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:96239823 G>A maps to NM_198968.2 I729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr13:96237101 T>C maps to NM_198968.2 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr13:96242592 G>T maps to NM_198968.2 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr13:96264406 G>A maps to NM_198968.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr3:137811362 C>T maps to NM_173543.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:137787060 G>T maps to NM_173543.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:137811254 A>G maps to NM_173543.2 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr3:137787060 G>A maps to NM_173543.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr3:108363341 G>A maps to NM_014648.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:108380749 C>T maps to NM_014648.3 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:108406944 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:108363416 T>A maps to NM_014648.3 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:32264597 G>A maps to NM_005225.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr1:23847465 G>A maps to NM_004091.3 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:23848381 C>A maps to NM_004091.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr1:23836581 C>T maps to NM_004091.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr1:23836448 G>A maps to NM_004091.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:20490525 G>A maps to NM_001949.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr6:20481482 T>C maps to NM_001949.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:67227028 G>A maps to NM_001950.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr8:86121613 C>T maps to ENST00000256117 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:86124413 C>A maps to ENST00000256117 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr8:86115472 C>T maps to ENST00000256117 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:11587882 G>A maps to NM_198256.2 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:77417803 G>A maps to NM_203394.2 G909G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:77427678 T>A maps to NM_203394.2 K423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr12:77436970 G>A maps to NM_203394.2 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:77419659 A>T maps to NM_203394.2 L748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:77427635 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:77423673 C>T maps to NM_203394.2 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:77419685 C>T maps to NM_203394.2 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr12:77421831 G>A maps to NM_203394.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:19252270 G>A maps to NM_024680.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:19253832 G>A maps to NM_024680.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:19247124 A>C maps to NM_024680.2 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:19256509 G>A maps to NM_024680.2 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:19258974 G>A maps to NM_024680.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:19247043 G>A maps to NM_024680.2 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:19259574 G>A maps to NM_024680.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:19256450 G>A maps to NM_024680.2 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:2284932 G>A maps to NM_004424.3 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:2282274 C>T maps to NM_004424.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:2283132 C>T maps to NM_004424.3 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:15478047 G>A maps to NM_033083.6 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:121575995 C>T maps to NM_018456.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:121575995 C>T maps to NM_018456.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:34998568 T>C maps to NM_018453.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:23555929 C>T maps to NM_001083614.1 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:110573134 C>A maps to ENST00000276658 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:158139315 T>C maps to NM_024007.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr5:158522657 G>A maps to NM_024007.3 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr5:158139237 G>A maps to NM_024007.3 Y491Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:158139300 G>A maps to NM_024007.3 Y470Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr5:158139237 G>A maps to NM_024007.3 Y491Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:158250202 C>T maps to NM_024007.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr5:158526372 G>A maps to NM_024007.3 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:25718857 C>A maps to NM_022659.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:25716003 T>C maps to NM_022659.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:131639294 G>A maps to ENST00000355311 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr10:131671827 G>T maps to ENST00000355311 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:131639233 G>A maps to ENST00000355311 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:131760447 G>T maps to ENST00000355311 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr10:131757262 G>T maps to ENST00000355311 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr10:131639150 C>T maps to ENST00000355311 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr19:4231296 C>T maps to NM_005755.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:73111474 G>A maps to NM_018029.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr3:73111420 C>T maps to NM_018029.3 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr1:43637774 C>T maps to NM_001159936.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:48382376 G>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:48386764 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:48386662 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:48382419 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:48382320 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:48386650 C>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:48382319 C>T did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:48382320 G>T did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr23:48382320 G>T did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:48382320 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:74897788 A>C maps to NM_001135752.1 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:74899179 G>A maps to NM_001135752.1 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:74908162 C>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:21546459 G>A maps to NM_001397.2 C767C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:21554506 G>A maps to NM_001397.2 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:21573784 G>A maps to NM_001397.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:184009983 C>T maps to NM_014693.3 V870V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:184009211 C>T maps to NM_014693.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:183994687 C>T maps to NM_014693.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:184009860 G>A maps to NM_014693.3 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:233349765 C>T maps to NM_004826.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:233347168 C>T maps to NM_004826.2 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:233349744 G>A maps to NM_004826.2 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr19:39307980 G>A maps to NM_001398.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:53363123 C>T maps to ENST00000371522 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:53370362 G>A maps to ENST00000371522 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:11789353 C>T maps to NM_024693.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr10:135178160 C>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:135178223 C>A maps to NM_004092.3 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:135184163 G>A maps to NM_004092.3 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:150483605 G>T maps to ENST00000369049 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:150485807 C>A maps to ENST00000369049 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:150484216 A>G maps to ENST00000369049 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:95264792 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:95267972 C>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:95272251 A>T maps to NM_001393.3 L412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr9:95277255 C>T maps to NM_001393.3 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr9:95277071 G>A maps to NM_001393.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:95277071 G>A maps to NM_001393.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr9:95277071 G>A maps to NM_001393.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:95263105 C>A maps to NM_001393.3 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:95277071 G>A maps to NM_001393.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr9:95277069 T>C maps to NM_001393.3 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:172477987 C>T maps to ENST00000392692 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:172533395 G>A maps to ENST00000392692 E801E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:172478054 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr3:172533491 T>C maps to ENST00000392692 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr3:172533491 T>C maps to ENST00000392692 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr6:139135629 C>A maps to NM_001195037.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:139135715 T>A maps to NM_001195037.2 L52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:139170452 A>G maps to NM_001195037.2 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:139202242 G>A maps to NM_001195037.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:69253249 C>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:69247797 T>A did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:68836337 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:69176937 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:65819340 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:65824926 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:65835784 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr23:65824340 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:65819381 C>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:65825034 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:65819502 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:236631571 T>A maps to NM_145861.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:236645642 C>T maps to NM_145861.2 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:236645870 C>T maps to NM_145861.2 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr15:74927837 C>A maps to NM_025083.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:74964111 T>A maps to NM_025083.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:74963985 A>G maps to NM_025083.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:74964032 C>A maps to NM_025083.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:74963940 G>A maps to NM_025083.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr16:67916399 G>A maps to NM_014329.3 R1115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:67911504 C>T maps to NM_014329.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:67915671 T>C maps to NM_014329.3 C976C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:67916426 G>T maps to NM_014329.3 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr16:67915024 C>T maps to NM_014329.3 R860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:21215910 G>T maps to NM_006683.4 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr14:21238386 A>G maps to NM_022360.4 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr14:21238386 A>G maps to NM_022360.4 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr14:21238386 A>G maps to NM_022360.4 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr20:33722564 C>T maps to NM_018217.2 W226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr20:33703610 G>A maps to NM_018217.2 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr1:184686098 T>C maps to NM_025191.3 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:184681638 G>T maps to NM_025191.3 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:184706785 G>A maps to NM_025191.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:184671947 G>A maps to NM_025191.3 R796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:184680915 A>G maps to NM_025191.3 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:83476214 C>T maps to NM_005711.3 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:83360552 A>C maps to NM_005711.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:83239339 G>A maps to NM_005711.3 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:83356121 T>C maps to NM_005711.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:41946787 C>A maps to NM_001956.3 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:41946776 G>T maps to NM_001956.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:148441085 G>T maps to NM_001957.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr4:148407240 C>A maps to NM_001957.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr4:148407112 G>T maps to NM_001957.3 G94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr4:148460971 C>T maps to NM_001957.3 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr4:148463715 C>T maps to NM_001957.3 H410H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr4:148407240 C>A maps to NM_001957.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr13:78492537 A>G maps to ENST00000377211 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr13:78492519 C>T maps to ENST00000377211 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr13:78492582 G>A maps to ENST00000377211 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:78475212 A>G maps to ENST00000377211 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:78492699 C>T maps to ENST00000377211 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr13:78492288 G>A maps to ENST00000377211 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:78477334 G>A maps to ENST00000377211 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr13:78474741 G>C maps to ENST00000377211 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr13:78492441 C>T maps to ENST00000377211 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr13:78492594 C>T maps to ENST00000377211 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr13:78492519 C>T maps to ENST00000377211 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:78492426 G>A maps to ENST00000377211 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr12:93213182 T>C maps to NM_003566.3 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:93251204 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:93245997 C>A maps to NM_003566.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:93171425 C>A maps to NM_003566.3 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:93247689 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:93202826 C>A maps to NM_003566.3 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:93285428 G>A maps to NM_003566.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:93172965 C>T maps to NM_003566.3 Q1193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:85988173 G>A maps to ENST00000351625 W398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:85963251 A>G maps to ENST00000351625 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:74228921 A>G maps to NM_001402.5 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:62119734 G>A maps to NM_001958.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:144672047 G>T maps to NM_032378.4 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:144672137 G>A maps to NM_032378.4 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr19:3984135 T>A maps to NM_001961.3 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:3977915 G>A maps to NM_001961.3 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:22285032 G>A maps to NM_013302.3 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:22269945 C>T maps to NM_013302.3 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr3:128060107 C>T maps to NM_021937.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:128060395 C>T maps to NM_021937.3 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:128060155 C>T maps to NM_021937.3 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:36336701 G>A maps to NM_030636.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:36194487 C>A maps to NM_030636.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:245246986 G>T maps to ENST00000421886 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:60451198 C>A maps to NM_001144933.1 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:60460393 A>G maps to NM_001144933.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:60493511 G>A maps to NM_001144933.1 W432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr17:60460351 A>T maps to NM_001144933.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:829537 C>T maps to NM_173584.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr11:830024 C>T maps to NM_173584.3 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr12:3768783 G>T maps to NM_001144958.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:28326991 G>T maps to NM_198529.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:28380823 C>T maps to NM_198529.3 R618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:28386703 G>T maps to NM_198529.3 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:28378219 C>T maps to NM_198529.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:28417477 T>C maps to NM_198529.3 V1241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:28419057 T>G maps to NM_198529.3 S1369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:28434912 G>A maps to NM_198529.3 W1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr17:28417567 C>T maps to NM_198529.3 G1271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr17:28434975 G>A maps to NM_198529.3 P1482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr22:44028089 A>G maps to NM_022785.3 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:43924792 G>A maps to NM_022785.3 Y1482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:43950772 G>A maps to NM_022785.3 R1208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:44074009 G>A maps to NM_022785.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr22:44028056 G>A maps to NM_022785.3 Y720Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr22:44011708 A>G maps to NM_022785.3 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:43972308 T>C maps to NM_022785.3 Q1096Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:44074009 G>A maps to NM_022785.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:44151702 C>T maps to NM_022785.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:44004465 G>A maps to NM_022785.3 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:44067869 C>T maps to NM_022785.3 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr22:44027991 G>T maps to NM_022785.3 S742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr22:44064846 G>A maps to NM_022785.3 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:63999207 T>C maps to NM_032437.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:63997631 C>A maps to NM_032437.2 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:64027453 C>T maps to NM_032437.2 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:56104884 G>A maps to NM_001039349.1 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr2:56149515 G>A maps to NM_001039349.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr2:56145145 A>T maps to NM_001039349.1 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr2:56144916 G>A maps to NM_001039349.1 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:56098223 C>T maps to NM_001039349.1 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:56149536 C>T maps to NM_001039349.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:56108764 G>A maps to NM_001039349.1 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:56145351 A>G did not map to a codon.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr2:56108764 G>A maps to NM_001039349.1 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr2:56145351 A>G did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:56103830 G>A maps to NM_001039349.1 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:65638703 C>T maps to NM_016938.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:65637622 G>A maps to NM_016938.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr11:65638688 G>A maps to NM_016938.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr13:22084179 T>G maps to NM_152726.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:22113510 G>A maps to NM_152726.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:16955968 A>G maps to NM_181723.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:16935351 C>T maps to NM_181723.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:16961931 T>C maps to NM_181723.2 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:16935338 A>G maps to NM_181723.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:19921202 C>A maps to NM_144715.3 E808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:19956848 C>A maps to NM_144715.3 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:19975021 G>A maps to NM_144715.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:19975375 C>T maps to NM_144715.3 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:19959748 C>T maps to NM_144715.3 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr6:52288835 C>T maps to NM_018100.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:52317601 T>C maps to NM_018100.3 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:44101460 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:44120517 T>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:44101533 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:44088924 T>G did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:44120478 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:44091782 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:44023209 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:44108119 G>A did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:44037780 T>C did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:44037781 T>C did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:44120528 C>T did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:44101519 A>G did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:44101519 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:44101519 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:1295723 C>T maps to NM_001405.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:68058541 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:68058542 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:68059877 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:68060375 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:107145543 G>A maps to NM_004093.2 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:107145555 G>A maps to NM_004093.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr13:107145495 G>A maps to NM_004093.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr13:107145606 C>T maps to NM_004093.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:107165141 T>C maps to NM_004093.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr17:7611832 C>T maps to NM_001406.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:7612767 T>C maps to NM_001406.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:133014007 T>C maps to NM_015137.3 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr8:132999908 T>C maps to NM_015137.3 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:133008660 C>T maps to NM_015137.3 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:132982783 C>T maps to NM_015137.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:132968035 T>G maps to NM_015137.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr14:23828090 C>T maps to NM_005864.2 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:82444298 C>T maps to NM_024580.5 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:82512019 T>C maps to NM_024580.5 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:82444222 C>A maps to NM_024580.5 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:42932290 C>T maps to NM_004247.3 W709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr4:110901994 C>T maps to NM_001963.4 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:110862126 C>A maps to NM_001963.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:110880561 C>T maps to NM_001963.4 Y345Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:13626556 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:13618204 C>T did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:13618130 A>G did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:13636105 G>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:13607687 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:13626534 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:13612988 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:13637363 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:13635877 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:13607759 A>G did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:13588046 G>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:13651159 C>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:38427309 C>T maps to ENST00000354891 H670H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:38463033 C>T maps to ENST00000354891 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:38412740 C>T maps to ENST00000354891 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:38425120 C>A maps to ENST00000354891 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:38370554 C>A maps to ENST00000354891 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr5:38427309 C>T maps to ENST00000354891 H670H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:38406312 C>T maps to ENST00000354891 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:38438391 C>T maps to ENST00000354891 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:38438519 C>T maps to ENST00000354891 D809D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:38418257 C>T maps to ENST00000354891 R529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:55221774 C>T maps to NM_005228.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:55224337 G>A maps to NM_005228.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:55241705 G>A maps to NM_005228.3 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:55242473 A>G maps to NM_005228.3 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:55224337 G>A maps to NM_005228.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr7:55223619 C>T maps to NM_005228.3 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:55260523 C>A maps to NM_005228.3 V897V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:55249062 G>A maps to NM_005228.3 Q787Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr7:55241648 C>T maps to NM_005228.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:55249113 A>G maps to NM_005228.3 E804E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr7:55242458 T>C maps to NM_005228.3 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:55249008 G>A maps to NM_005228.3 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr7:55211164 C>T maps to NM_005228.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr7:55241675 G>A maps to NM_005228.3 K708K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:55242431 A>G maps to NM_005228.3 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:55210009 G>A maps to NM_005228.3 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr7:55211164 C>T maps to NM_005228.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr7:55242458 T>C maps to NM_005228.3 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:55218987 C>T maps to NM_005228.3 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:55249143 G>A maps to NM_005228.3 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:55266470 C>T maps to NM_005228.3 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr7:55260484 A>G maps to NM_005228.3 E884E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr7:55241636 T>C maps to NM_005228.3 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr7:55241705 G>A maps to NM_005228.3 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:55242503 A>G maps to NM_005228.3 E758E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr7:55211029 T>C maps to NM_005228.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr7:55221732 G>C maps to NM_005228.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr7:55242428 A>G maps to NM_005228.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr7:55233040 A>G maps to NM_005228.3 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:55233041 G>T maps to NM_005228.3 G598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr7:55241661 T>C maps to NM_005228.3 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr7:55242488 G>A maps to NM_005228.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr7:55249056 C>T maps to NM_005228.3 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:55272979 C>T maps to NM_005228.3 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr7:55241648 C>A maps to NM_005228.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr7:55241642 A>G maps to NM_005228.3 E697E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr7:55241657 T>C maps to NM_005228.3 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr7:55242485 T>C maps to NM_005228.3 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr7:55233040 A>G maps to NM_005228.3 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr7:55242479 A>G maps to NM_005228.3 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr7:55273166 C>T maps to NM_005228.3 Q1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr7:55233055 A>G maps to NM_005228.3 E602E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr7:55211080 A>G maps to NM_005228.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr7:55249056 C>T maps to NM_005228.3 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr7:55242469 T>A maps to NM_005228.3 L747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr7:55241671 T>A maps to NM_005228.3 L707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr7:55233040 A>G maps to NM_005228.3 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:231557529 G>A maps to NM_022051.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr19:41307052 C>T maps to NM_053046.2 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr19:41306809 C>T maps to NM_053046.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:41307139 C>T maps to NM_053046.2 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr5:137803577 G>A maps to NM_001964.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:137802587 G>A maps to NM_001964.2 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:137803763 T>C maps to NM_001964.2 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr5:137803365 G>T maps to NM_001964.2 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr10:64573520 G>T maps to NM_001136178.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr10:64574106 G>T maps to NM_001136178.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr10:64575759 G>A maps to NM_001136178.1 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr10:64575654 T>C maps to NM_001136178.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr10:64573218 G>A maps to NM_001136178.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:22548546 G>A maps to NM_004430.2 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:22548771 C>T maps to NM_004430.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr8:22548882 G>A maps to NM_004430.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:73518830 C>T maps to NM_001965.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:73518743 G>A maps to NM_001965.3 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr2:73519364 G>A maps to NM_001965.3 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:63206337 C>T maps to NM_015252.3 R861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:63101663 T>C maps to NM_015252.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr11:65348581 C>T maps to NM_001099409.1 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:65347810 C>T maps to NM_001099409.1 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr11:65348755 C>T maps to NM_001099409.1 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr11:65350167 A>G maps to NM_001099409.1 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:48229327 C>T maps to NM_014601.3 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:48244550 C>T maps to NM_014601.3 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:48244376 C>T maps to NM_014601.3 D440D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:48244616 C>T maps to NM_014601.3 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:48220120 C>T maps to NM_014601.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:31489203 C>T maps to NM_014600.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr2:31457627 G>A maps to NM_014600.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:31483634 C>T maps to NM_014600.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:31467289 C>T maps to NM_014600.2 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:31489065 T>C maps to NM_014600.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:31483649 C>A maps to NM_014600.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:31457645 C>T maps to NM_014600.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:31483460 C>T maps to NM_014600.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:31483727 G>T maps to NM_014600.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:31484536 C>T maps to NM_014600.2 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr15:42192953 C>T maps to NM_139265.3 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr15:42192995 G>A maps to NM_139265.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:184910745 C>T maps to NM_001966.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:140648627 G>A maps to NM_024757.4 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:140638478 G>A maps to NM_024757.4 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:140672432 G>A maps to NM_024757.4 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:140728802 C>T maps to NM_024757.4 D1181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:140611120 A>G maps to NM_024757.4 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr11:125452298 G>A maps to ENST00000278903 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:125447464 C>T maps to ENST00000278903 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:40030437 G>A maps to NM_153232.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:20156741 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:40353487 A>T maps to NM_005875.2 K109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:150285987 C>T maps to NM_032025.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:150290154 T>C maps to NM_032025.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr7:6084195 G>A maps to NM_014413.3 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:6085725 A>G maps to NM_014413.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr7:6085760 G>A maps to NM_014413.3 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr7:6089587 T>C maps to NM_014413.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr7:6082570 C>A maps to NM_014413.3 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:37368715 C>T maps to NM_001135651.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:88874881 C>A maps to NM_004836.5 E707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:88890437 T>C maps to NM_004836.5 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:88874765 T>C maps to NM_004836.5 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr2:88890439 C>A maps to NM_004836.5 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr2:88857409 T>C maps to NM_004836.5 R1065R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:88890494 G>A maps to NM_004836.5 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:40318188 C>T maps to NM_001013703.2 F1467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr15:40321615 C>T maps to NM_001013703.2 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:40259876 C>T maps to NM_001013703.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:40259645 C>T maps to NM_001013703.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:40241470 T>C did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:124111633 G>A maps to NM_001414.3 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:124110994 A>T maps to NM_001414.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr1:45363049 G>A maps to NM_020365.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:27587404 G>A maps to NM_172195.3 N498N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:27587422 C>T maps to NM_172195.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr3:183861951 G>A maps to NM_003907.2 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:183857921 C>T maps to NM_003907.2 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:183860378 C>T maps to NM_003907.2 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr3:183860606 T>C maps to NM_003907.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr3:183860567 A>G maps to NM_003907.2 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:36381013 G>A maps to NM_012199.2 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:36367133 G>A maps to NM_012199.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:36381110 C>T maps to NM_012199.2 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:36354151 C>T maps to NM_012199.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:141569614 C>T maps to NM_012154.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:141572580 G>A maps to NM_012154.3 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:141542516 G>A maps to NM_012154.3 D823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:141545599 G>A maps to NM_012154.3 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:141595387 C>G maps to NM_012154.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:141567304 C>T maps to NM_012154.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:36509115 C>T maps to NM_024852.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:36437666 C>T maps to NM_024852.2 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:36505911 T>G maps to NM_024852.2 L681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:36282547 C>T maps to NM_017629.2 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:36291530 T>C maps to NM_017629.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:36291650 A>G maps to NM_017629.2 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:67848322 T>G maps to NM_004094.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:32693248 C>A maps to NM_003908.3 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:24086127 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:24091213 A>G did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr10:120824933 G>A maps to NM_003750.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr10:120801575 A>G maps to NM_003750.2 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:120795657 C>A maps to NM_003750.2 E1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:120809333 G>A maps to NM_003750.2 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr10:120796667 G>A maps to NM_003750.2 D1294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:2419092 C>T maps to ENST00000314800 F802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr22:36907709 T>C maps to NM_003753.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr22:36915529 C>T maps to NM_003753.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:36919317 G>A maps to NM_003753.3 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:36920659 G>A maps to NM_003753.3 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:36912816 G>A maps to NM_003753.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr8:109240602 A>G maps to NM_001568.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr8:109240602 A>G maps to NM_001568.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:109240602 A>G maps to NM_001568.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr8:109240602 A>G maps to NM_001568.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:109252218 A>G maps to NM_001568.2 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:8016556 C>T maps to ENST00000449102 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:10226440 G>A maps to NM_003755.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:10226449 C>T maps to NM_003755.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:117658785 C>T maps to ENST00000411422 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:117658824 C>T maps to ENST00000411422 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:38273691 G>A maps to ENST00000262832 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:32610203 A>G maps to NM_006360.3 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:78113918 G>A maps to NM_014740.3 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:78117975 G>A maps to NM_014740.3 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr17:78115123 G>A maps to NM_014740.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:78112878 G>A maps to NM_014740.3 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:78120592 G>A maps to NM_014740.3 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:99806158 G>A maps to NM_001130679.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr4:99823100 T>C maps to NM_001130679.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:233428955 G>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:71759631 G>T maps to NM_001134651.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:71748774 G>A maps to NM_001134651.1 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:71733850 A>G maps to NM_001134651.1 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:71748774 G>A maps to NM_001134651.1 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr22:31845415 T>C maps to NM_019843.3 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:184045001 A>G did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:184038426 C>T maps to NM_001194947.1 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:184045634 G>A maps to NM_001194947.1 V1273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:184049133 T>C maps to NM_001194947.1 G1421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:184044739 G>T maps to NM_001194947.1 E1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:184041988 C>T maps to NM_001194947.1 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:10827529 G>A maps to ENST00000429377 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:10823751 G>A maps to ENST00000429377 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:10822511 T>C maps to ENST00000429377 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr11:10821214 T>C maps to ENST00000429377 E809E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr11:10821214 T>C maps to ENST00000429377 E809E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:21137324 C>T maps to NM_001198801.1 P1530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr1:21268152 C>T maps to NM_001198801.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:21268014 T>C maps to NM_001198801.1 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:21180096 C>T maps to NM_001198801.1 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:21155644 A>G maps to NM_001198801.1 L1374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:21205994 G>A maps to NM_001198801.1 R795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:21151619 T>C maps to NM_001198801.1 E1427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:73604021 C>T maps to NM_022170.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:103803129 G>T maps to NM_183004.3 G91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:170612118 C>A maps to NM_020390.5 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:99995516 C>T maps to NM_015904.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr2:99978206 A>G maps to NM_015904.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:99977706 G>T maps to NM_015904.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:99978107 G>A maps to NM_015904.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:100010994 A>C maps to NM_015904.3 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:100006710 T>C maps to NM_015904.3 N811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr2:100007117 C>T maps to NM_015904.3 Q900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr2:100007119 G>A maps to NM_015904.3 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr20:33867744 C>T maps to NM_002212.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:48513364 A>G maps to NM_018696.2 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:48513401 G>T maps to NM_018696.2 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:12909099 G>A maps to NM_018127.6 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:12899971 A>G maps to NM_018127.6 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:12903542 C>T maps to NM_018127.6 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:12896296 G>A maps to NM_018127.6 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:12897078 G>A maps to NM_018127.6 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:12896260 C>A maps to NM_018127.6 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:12897036 G>A maps to NM_018127.6 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr19:8028660 G>A maps to ENST00000351593 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:8032483 G>A maps to ENST00000351593 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:8028648 G>A maps to ENST00000351593 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:8032528 G>A maps to ENST00000351593 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:23701563 G>A maps to ENST00000359598 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:23704919 G>A maps to ENST00000359598 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr9:23692596 T>C maps to ENST00000359598 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr9:23762154 C>T maps to ENST00000359598 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr9:23692566 C>A maps to ENST00000359598 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr9:23692566 C>T maps to ENST00000359598 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:11565373 G>T maps to NM_001420.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr19:11568958 C>T maps to NM_001420.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:11577525 G>A maps to NM_001420.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:11565499 G>T maps to NM_001420.3 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:11568949 C>T maps to NM_001420.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:11569315 G>A maps to NM_001420.3 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr19:11569360 G>A maps to NM_001420.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:50610724 C>T maps to NM_021952.3 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr1:50663130 C>T maps to NM_021952.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr1:50666630 C>T maps to NM_021952.3 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:50666479 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:50659453 G>A maps to NM_021952.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:41507961 G>A maps to NM_172373.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:41556166 G>A maps to NM_172373.3 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr4:139983020 C>T maps to ENST00000379550 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:139980634 C>T maps to ENST00000379550 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:139994704 G>A maps to ENST00000379550 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr4:139980193 T>C maps to ENST00000379550 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr4:139980193 T>C maps to ENST00000379550 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:139980193 T>C maps to ENST00000379550 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:129205017 A>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:129201150 T>C did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:129203476 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:129205058 T>C did not map to a codon.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr23:129205115 T>C did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:129201446 C>A did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:129208064 T>A did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:129203383 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr22:37770596 C>T maps to NM_052906.3 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr22:37770539 G>A maps to NM_052906.3 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:37771292 G>A maps to NM_052906.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr22:37771001 G>A maps to NM_052906.3 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr22:37770898 G>A maps to NM_052906.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr22:37770065 G>T maps to NM_052906.3 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr22:37770755 C>T maps to NM_052906.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr22:37771073 G>A maps to NM_052906.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:47496420 G>A did not map to a codon.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr23:47498499 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:47498480 G>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:47498651 C>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:47496451 C>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:47496441 C>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr12:96640794 T>C maps to NM_005230.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:96641121 G>A maps to NM_005230.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:205589081 C>T maps to NM_021795.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:18557586 C>T maps to NM_006532.3 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:18555591 G>A maps to NM_006532.3 Y612Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:18572546 G>A maps to NM_006532.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:18572449 G>A maps to NM_006532.3 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr19:18572546 G>A maps to NM_006532.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:18555660 G>A maps to NM_006532.3 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:95255132 G>A maps to NM_012081.5 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:95234229 G>A maps to NM_012081.5 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:44066402 G>T maps to NM_025165.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr15:44066457 A>G maps to NM_025165.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:44068277 G>A maps to NM_025165.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:44065391 G>A maps to NM_025165.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:44066457 A>G maps to NM_025165.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr15:44066457 A>G maps to NM_025165.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr15:44066551 C>G did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:37052996 G>A maps to NM_014800.9 H448H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr7:37354498 A>G maps to NM_014800.9 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:36934499 G>A maps to NM_014800.9 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:37251016 G>A maps to NM_014800.9 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr7:37283994 G>A maps to NM_014800.9 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:37053011 C>T maps to NM_014800.9 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr7:37354506 C>A maps to NM_014800.9 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:45016003 G>A maps to ENST00000439931 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr20:45014806 T>A maps to ENST00000439931 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:67237692 C>T maps to NM_024712.3 N745N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:67233132 A>G maps to NM_024712.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:107501244 C>A maps to NM_018712.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr11:107502334 C>T maps to NM_018712.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:85617348 C>T maps to NM_001135023.1 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:85598650 T>C maps to NM_001135023.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:85598240 G>A maps to NM_001135023.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:73450915 T>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:73481087 T>C maps to ENST00000358929 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:73457478 G>T maps to ENST00000358929 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:73462884 C>T maps to ENST00000358929 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:73455552 A>G maps to ENST00000358929 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:73469100 T>C did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:43829588 A>G maps to NM_022821.2 *280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr6:10984132 G>A maps to NM_017770.3 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:103988930 C>A maps to NM_152310.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:103986385 G>A maps to NM_152310.1 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr6:80634668 C>T maps to NM_022726.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr6:80626570 C>T maps to NM_022726.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:80626332 C>A maps to NM_022726.3 G313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:60067888 G>T maps to NM_024930.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:60053404 T>A maps to NM_024930.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr18:33754459 A>G maps to ENST00000442325 T844T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr18:33726310 G>A maps to ENST00000442325 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr18:33716273 T>C maps to ENST00000442325 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:33740918 T>C maps to ENST00000442325 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr18:33718821 G>A maps to ENST00000442325 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr8:27957422 T>A maps to NM_018091.5 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:27987171 C>T maps to NM_018091.5 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:31805010 C>T maps to ENST00000265650 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr11:31561278 G>A maps to ENST00000395934 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr11:31671663 A>G maps to ENST00000395934 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr11:31671663 A>G maps to ENST00000395934 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:48519240 C>T maps to NM_022142.4 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:79383321 A>G maps to NM_022159.3 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:79383651 G>T maps to NM_022159.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:79358808 T>C maps to NM_022159.3 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr1:79385972 G>A maps to NM_022159.3 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr1:79357298 G>A maps to NM_022159.3 H640H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:49695704 C>T maps to NM_198449.2 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:101344550 T>C maps to NM_016242.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:153609453 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:153609452 C>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:153609401 C>A did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr17:48457756 A>G maps to NM_001166131.1 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:48453344 G>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr17:48457702 C>T maps to NM_001166131.1 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:1824265 T>C maps to NM_001010865.1 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:1824305 C>T maps to NM_001010865.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:7084461 G>A maps to ENST00000261406 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr22:29654923 G>A maps to NM_133455.2 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:29628374 C>T maps to NM_133455.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr22:29627579 A>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:101200761 G>A maps to ENST00000397927 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr7:101183244 G>A maps to ENST00000397927 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:27305470 G>A maps to NM_007046.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:27305761 T>G maps to NM_007046.3 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:27305479 C>A maps to NM_007046.3 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr2:27302088 A>G maps to NM_007046.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:2891478 G>T maps to NM_032048.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:2891537 T>C maps to NM_032048.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr20:39990777 G>A maps to NM_052846.1 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:39992389 C>T maps to NM_052846.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr14:100380550 C>T maps to NM_001008707.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:100404166 C>A maps to NM_001008707.1 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr14:100341314 C>A maps to NM_001008707.1 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr14:100364625 C>A maps to NM_001008707.1 S314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:100363559 C>T maps to NM_001008707.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr14:100364626 G>T maps to NM_001008707.1 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:46124887 G>A maps to NM_001193268.1 N484N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:46128061 C>T maps to NM_001193268.1 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:46116891 G>A maps to NM_001193268.1 N778N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:46124821 G>A maps to NM_001193268.1 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:46117887 A>C maps to NM_001193268.1 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:46133253 G>T maps to NM_001193268.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:46128025 G>A maps to NM_001193268.1 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:46137677 G>A maps to NM_001193268.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:42510010 G>A maps to NM_019063.3 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:42483683 C>A maps to NM_019063.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:42557058 C>A maps to NM_019063.3 V886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:42483730 C>A maps to NM_019063.3 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:89123738 C>A maps to ENST00000380664 E1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:89172768 C>T maps to ENST00000380664 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr14:89206859 C>T maps to ENST00000380664 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:89082532 A>G maps to ENST00000380664 F1950F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:89124645 A>C maps to ENST00000380664 V1254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:89178613 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:10626893 G>A maps to NM_001424.4 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:10626896 A>G maps to NM_001424.4 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:6924732 C>T maps to ENST00000381407 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:6916350 T>C maps to ENST00000381407 C466C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:6901985 C>T maps to ENST00000381407 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:6916285 G>T maps to ENST00000381407 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:6896481 C>T maps to ENST00000381407 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr19:6913692 T>G maps to ENST00000381407 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:6919601 G>A maps to ENST00000381407 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:6904059 C>T maps to ENST00000381407 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:6919736 C>A maps to ENST00000381407 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr19:6924769 C>T maps to ENST00000381407 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:6919601 G>T maps to ENST00000381407 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr19:6926552 G>A maps to ENST00000381407 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:6926552 G>A maps to ENST00000381407 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:14854577 C>T maps to NM_013447.2 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:14866534 G>T maps to NM_013447.2 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:14862303 A>G maps to NM_013447.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:14748917 G>A maps to NM_032571.3 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:14772865 G>A maps to NM_032571.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:14772865 G>A maps to NM_032571.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:14765791 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:14772865 G>A maps to NM_032571.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr19:14765800 A>G maps to NM_032571.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:14755063 G>T maps to NM_032571.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:14761984 G>A maps to NM_032571.3 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr19:14748917 G>A maps to NM_032571.3 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:14758091 A>G maps to NM_032571.3 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr10:119303089 G>A maps to NM_004098.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:119307646 G>A maps to NM_004098.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:119600756 G>A maps to NM_001426.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:71509042 G>T maps to NM_031889.2 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:71509878 C>T maps to NM_031889.2 D912D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:71509245 C>A maps to NM_031889.2 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr4:71509314 G>A maps to NM_031889.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr4:71509966 C>T maps to NM_031889.2 Q942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:73930774 G>A maps to NM_003633.2 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:73930594 C>T maps to NM_003633.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:94862742 A>C maps to NM_015036.2 *501Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:131584867 C>A maps to NM_004435.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr12:48105513 G>A maps to NM_001172439.1 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:48110671 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:130580413 G>A maps to NM_001114753.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:77076358 G>A maps to NM_001042573.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr9:34521489 A>G maps to NM_198573.2 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr10:25288438 G>A maps to NM_145010.2 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:8924017 G>A maps to NM_001428.2 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:8927232 G>T maps to NM_001428.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:8927256 A>T maps to NM_001428.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:8928071 G>A maps to NM_001428.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:8928071 G>A maps to NM_001428.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr17:4858386 C>T maps to NM_053013.3 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr17:4860151 G>T maps to NM_053013.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:83375976 C>T maps to NM_021204.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr18:706500 A>T maps to ENST00000319815 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:690629 C>T maps to ENST00000319815 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr18:690584 G>A maps to ENST00000319815 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr18:706545 G>A maps to ENST00000319815 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr13:43872543 C>A maps to NM_001127615.1 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:43896529 G>A maps to NM_001127615.1 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:43935430 A>C maps to NM_001127615.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr13:43810853 A>G maps to NM_001127615.1 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr13:43934080 G>A maps to NM_001127615.1 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:43930079 G>A maps to NM_001127615.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr23:129801664 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:129799651 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:129813618 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:129799651 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:129804009 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:129790662 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr23:129804165 C>T did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:129771384 C>T did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:129813702 G>T did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:111469409 G>A maps to NM_001977.3 Q693Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr4:111474531 C>T maps to NM_001977.3 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr4:111398160 C>T maps to NM_001977.3 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:111398028 C>T maps to NM_001977.3 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:111397716 C>T maps to NM_001977.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr4:111398004 G>A maps to NM_001977.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr4:111480820 A>G maps to NM_001977.3 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:111480820 A>G maps to NM_001977.3 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:132201029 T>C maps to NM_006208.2 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:132168929 T>C maps to NM_006208.2 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:132190589 C>T maps to NM_006208.2 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:132206137 C>T maps to NM_006208.2 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:132171148 C>T maps to NM_006208.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr8:120575153 A>G maps to NM_006209.3 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr8:120596273 A>G maps to NM_006209.3 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:120613689 G>A maps to NM_006209.3 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr8:120596273 A>G maps to NM_006209.3 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr8:120575153 A>G maps to NM_006209.3 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr8:120575111 G>A maps to NM_006209.3 N854N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr8:120581595 G>A maps to NM_006209.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:131995407 G>A maps to NM_005021.3 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:131995407 G>A maps to NM_005021.3 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr6:132047337 T>C maps to NM_005021.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:131958550 G>A maps to NM_005021.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:46107331 A>G maps to NM_014936.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:46135993 A>G maps to NM_021572.4 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:46135861 A>G maps to NM_021572.4 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:185138759 C>T maps to NM_153343.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr4:185038146 C>T maps to NM_153343.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr4:185038989 G>A maps to NM_153343.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr17:77709212 C>T maps to NM_178543.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:77708969 C>T maps to NM_178543.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:77709044 G>A maps to NM_178543.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:150600052 C>A maps to NM_207042.1 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:40161537 G>T maps to NM_152512.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:40217021 C>A maps to NM_152512.3 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr22:40283569 G>C maps to NM_152512.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:97583000 C>T maps to NM_001098175.1 N15N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:97605148 C>T maps to NM_001098175.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr10:97599542 A>G maps to NM_001098175.1 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:139946782 G>A maps to NM_203468.1 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:139944351 T>C maps to NM_203468.1 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:139945764 G>A maps to NM_203468.1 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:40457428 A>G maps to NM_001248.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:40453411 C>T maps to NM_001248.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:23294494 T>C maps to NM_004901.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:23299141 G>A maps to NM_004901.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:23306282 G>A maps to NM_004901.3 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr8:23306282 G>A maps to NM_004901.3 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:23306297 G>A maps to NM_004901.3 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:74439680 T>C maps to NM_001249.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:74449812 G>A maps to NM_001249.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr14:74449768 T>C maps to NM_001249.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr20:25203486 C>T maps to NM_001247.2 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr20:25206148 T>C maps to NM_001247.2 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr10:101462397 C>T maps to NM_020354.3 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr8:110351620 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:27761749 G>A maps to ENST00000449599 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:27761749 G>A maps to ENST00000449599 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:27758889 G>A maps to ENST00000449599 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:27758782 T>C maps to ENST00000449599 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr3:27758620 C>T maps to ENST00000449599 E686E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:27758620 C>T maps to ENST00000449599 E686E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:27763047 G>A maps to ENST00000449599 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:27758697 G>A maps to ENST00000449599 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr22:41569718 A>G maps to NM_001429.3 K1570K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr22:41525930 C>T maps to NM_001429.3 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:41513539 G>A maps to NM_001429.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:41569718 A>G maps to NM_001429.3 K1570K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr22:41574533 T>G maps to NM_001429.3 V2273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:41513674 C>T maps to NM_001429.3 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:41574486 C>T maps to NM_001429.3 Q2258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr22:41527629 C>T maps to NM_001429.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr22:41564588 A>T maps to NM_001429.3 P1337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:41548250 A>G maps to NM_001429.3 E1013E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:41572907 C>T maps to NM_001429.3 R1731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:41573045 C>T maps to NM_001429.3 G1777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr22:41568567 T>C maps to NM_001429.3 G1506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr22:41569718 A>G maps to NM_001429.3 K1570K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr22:41527629 C>T maps to NM_001429.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr22:41566478 T>C maps to NM_001429.3 P1452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr22:41574683 C>T maps to NM_001429.3 P2323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr22:41560054 A>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr22:41548250 A>G maps to NM_001429.3 E1013E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:41536152 C>T maps to NM_001429.3 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr22:41573354 C>A maps to NM_001429.3 P1880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:41547863 G>T maps to NM_001429.3 G949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:41573576 C>T maps to NM_001429.3 H1954H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:132446292 C>T maps to ENST00000333577 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr12:132539740 T>C maps to ENST00000333577 P2660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:132530095 G>A maps to ENST00000333577 A2375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:132547125 G>A maps to ENST00000333577 Q2774Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:132551941 C>T maps to ENST00000333577 Q2965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr12:132446292 C>T maps to ENST00000333577 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr12:132508376 C>T maps to ENST00000333577 R1618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:132554104 C>A maps to ENST00000333577 A3016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:132446240 G>A maps to ENST00000333577 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:132547164 G>A maps to ENST00000333577 T2787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:132522523 T>G maps to ENST00000333577 V2066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:132537748 C>T maps to ENST00000333577 R2521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr12:132549334 G>A maps to ENST00000333577 P2855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr12:132530373 C>T maps to ENST00000333577 R2413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:132510278 C>T maps to ENST00000333577 G1684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:132551398 G>A maps to ENST00000333577 A2914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr12:132445309 C>A maps to ENST00000333577 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:132446393 T>C maps to ENST00000333577 H410H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr12:132466935 T>C maps to ENST00000333577 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr12:132446292 C>T maps to ENST00000333577 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:132529373 C>T maps to ENST00000333577 D2256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:132551422 G>A maps to ENST00000333577 P2922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:46588037 G>A maps to NM_001430.4 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:46574156 C>T maps to NM_001430.4 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:46608857 C>T maps to NM_001430.4 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:46611750 G>A maps to NM_001430.4 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:29359621 T>C maps to NM_001166005.1 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:29379625 C>T maps to NM_001166005.1 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:29386997 T>C did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:29365837 G>A maps to NM_001166005.1 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr1:29323782 G>A maps to NM_001166005.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr20:34773185 C>T maps to NM_012156.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:34783253 G>T maps to NM_012156.2 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr20:34797462 G>C maps to NM_012156.2 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:34761860 G>A maps to NM_012156.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:131191035 G>T maps to NM_001431.3 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:131190882 T>C maps to NM_001431.3 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr6:131190882 T>C maps to NM_001431.3 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr18:5416005 C>T maps to NM_012307.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:5398136 C>T maps to NM_012307.2 K785K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:5406868 C>T maps to NM_012307.2 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr18:5406796 G>A maps to NM_012307.2 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:5434097 G>A maps to NM_012307.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr18:5394741 T>C maps to NM_012307.2 S1068S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:5397203 C>T maps to NM_012307.2 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr18:5416020 C>T maps to NM_012307.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:5397140 T>C maps to NM_012307.2 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:5395106 G>A maps to NM_012307.2 R1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr18:5445237 G>A maps to NM_012307.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr18:5397140 T>C maps to NM_012307.2 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:111504762 C>T maps to NM_022140.3 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:111504471 C>T maps to NM_022140.3 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:111541194 C>T maps to NM_022140.3 K395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:111615966 A>G did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr5:111504699 C>A maps to NM_022140.3 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr5:111504699 C>T maps to NM_022140.3 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr5:111504699 C>A maps to NM_022140.3 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:111615972 G>T maps to NM_022140.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:111598211 G>A maps to NM_022140.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr5:111504699 C>T maps to NM_022140.3 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:111945077 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:111965989 C>T maps to NM_019114.3 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:112018738 C>T maps to NM_019114.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:112015789 G>A maps to NM_019114.3 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr2:120776785 C>A maps to NM_020909.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:120889269 C>T maps to NM_020909.3 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:120831701 C>T maps to NM_020909.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:120848066 C>T maps to NM_020909.3 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:43501559 G>A maps to NM_000119.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:43494121 C>T maps to NM_000119.2 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:43498612 A>G maps to NM_000119.2 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:21926528 C>A maps to ENST00000265800 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr8:21927828 G>A maps to ENST00000265800 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr8:21925111 C>T maps to ENST00000265800 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr10:32581545 G>A maps to NM_025209.2 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr10:32562138 T>C maps to NM_025209.2 Q605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:32581511 G>A maps to NM_025209.2 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:149519493 G>A maps to NM_015630.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:149520245 T>C maps to NM_015630.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:149539288 C>A maps to NM_015630.3 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:149543882 C>T maps to NM_015630.3 H787H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:47612345 T>C maps to ENST00000426238 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:37988588 C>T maps to NM_017549.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:37989952 C>T maps to NM_017549.3 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr7:143095838 C>T maps to NM_005232.4 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:143091978 A>G maps to NM_005232.4 N758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:143098542 G>A maps to NM_005232.4 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:143092576 G>A maps to NM_005232.4 R640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr7:143088819 A>G maps to NM_005232.4 Y915Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:143096354 G>A maps to NM_005232.4 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr7:143088786 G>A maps to NM_005232.4 R926R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:38187398 G>T maps to NM_001099439.1 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:38197212 C>T maps to NM_001099439.1 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr1:38227575 G>A maps to NM_001099439.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr1:38188839 T>C did not map to a codon.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr1:38187425 G>A maps to NM_001099439.1 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:38185580 G>A maps to NM_001099439.1 D854D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:16462194 C>T maps to NM_004431.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:16458756 G>A maps to NM_004431.3 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:16474933 C>T maps to NM_004431.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr1:16477402 C>T maps to NM_004431.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:16464827 G>A maps to NM_004431.3 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:89259539 G>T maps to NM_005233.5 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr3:89498445 T>C maps to NM_005233.5 D806D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr3:89391217 C>T maps to NM_005233.5 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:89390123 G>A maps to NM_005233.5 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:89259476 G>A maps to NM_005233.5 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr3:89498445 T>C maps to NM_005233.5 D806D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr3:89259542 T>C maps to NM_005233.5 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:89391214 G>A maps to NM_005233.5 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:89445005 G>A maps to NM_005233.5 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:89468454 G>A maps to NM_005233.5 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:89445026 C>T maps to NM_005233.5 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:89391112 G>T maps to NM_005233.5 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr3:89456515 T>C maps to NM_005233.5 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:89259476 G>A maps to NM_005233.5 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:89480346 A>T maps to NM_005233.5 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr3:89448562 C>A maps to NM_005233.5 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr3:89480346 A>G maps to NM_005233.5 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr3:89445026 C>A maps to NM_005233.5 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:89480346 A>G maps to NM_005233.5 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr3:89391112 G>A maps to NM_005233.5 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr3:89259500 G>A maps to NM_005233.5 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:89259542 T>C maps to NM_005233.5 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:89468499 C>T maps to NM_005233.5 D678D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:89259626 T>A maps to NM_005233.5 C257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr3:89480460 A>G maps to NM_005233.5 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:89391086 C>T maps to NM_005233.5 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:89462312 T>G maps to NM_005233.5 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr3:89259500 G>A maps to NM_005233.5 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:89480458 G>T maps to NM_005233.5 G766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:89445026 C>T maps to NM_005233.5 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:89259542 T>C maps to NM_005233.5 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:89391238 T>C maps to NM_005233.5 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:89448465 A>G did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:89391112 G>T maps to NM_005233.5 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:89448465 A>G did not map to a codon.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:222428511 C>T maps to NM_004438.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr2:222291218 A>G maps to NM_004438.3 Y937Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:222294688 C>T maps to NM_004438.3 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:222294688 C>T maps to NM_004438.3 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:222347279 T>C maps to NM_004438.3 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:222347369 G>A maps to NM_004438.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:66231650 T>C maps to NM_004439.5 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3517-01A-01W-0831-10 chr4:66356224 G>A maps to NM_004439.5 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr4:66189897 C>T maps to NM_004439.5 Q1016Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:66467911 G>T maps to NM_004439.5 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:66217127 G>T maps to NM_004439.5 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:66356134 G>T maps to NM_004439.5 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:66231667 C>A maps to NM_004439.5 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:66233078 C>G maps to NM_004439.5 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:66361118 T>C maps to NM_004439.5 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:66230869 C>A maps to NM_004439.5 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:66213861 A>G maps to NM_004439.5 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:66270108 G>A maps to NM_004439.5 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr4:66356245 C>T maps to NM_004439.5 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:66280140 C>T maps to NM_004439.5 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:66509106 C>A maps to NM_004439.5 G74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:66242744 C>A maps to NM_004439.5 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:66242741 G>A maps to NM_004439.5 C610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr4:66467434 G>A maps to NM_004439.5 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:66356247 G>T maps to NM_004439.5 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:66270108 G>A maps to NM_004439.5 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:96533722 G>T maps to NM_001080448.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:97467473 C>T maps to NM_001080448.2 R1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:97356752 G>T maps to NM_001080448.2 G871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:96706199 A>G maps to NM_001080448.2 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:97194218 G>T maps to NM_001080448.2 G640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:97356862 A>G maps to NM_001080448.2 K907K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:97124057 G>A maps to NM_001080448.2 W557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:97251320 G>T maps to NM_001080448.2 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr3:96706661 T>C maps to NM_001080448.2 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr3:97251229 T>C maps to NM_001080448.2 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:97454941 C>T maps to NM_001080448.2 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:97367128 G>T did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr3:96706661 T>C maps to NM_001080448.2 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:97454803 A>G maps to NM_001080448.2 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:96533580 C>T maps to NM_001080448.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:96945171 C>T maps to NM_001080448.2 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:94120753 A>G maps to NM_004440.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:93969171 G>A maps to NM_004440.3 Y608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr6:94066482 G>A maps to NM_004440.3 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr6:93956552 G>A maps to NM_004440.3 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr6:93953251 C>A maps to NM_004440.3 V963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:94066572 C>A maps to NM_004440.3 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:94066662 T>G maps to NM_004440.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:94066684 C>T maps to NM_004440.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:94120687 T>C maps to NM_004440.3 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:93953227 A>G maps to NM_004440.3 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr6:93979368 C>A maps to NM_004440.3 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr6:93979276 A>G maps to NM_004440.3 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:93955109 C>A maps to NM_004440.3 E930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:94120726 A>G maps to NM_004440.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr6:93956526 G>A maps to NM_004440.3 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr6:93979276 A>G maps to NM_004440.3 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:93964481 G>A maps to NM_004440.3 P805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:22895824 G>A maps to NM_020526.3 W46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:22903329 C>T maps to NM_020526.3 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:22903143 C>T maps to NM_020526.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:22927431 C>A maps to NM_020526.3 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:22903329 C>T maps to NM_020526.3 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:22903218 G>A maps to NM_020526.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:22903080 C>T maps to NM_020526.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:22902828 C>T maps to NM_020526.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr1:22927431 C>T maps to NM_020526.3 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr3:134911427 A>G maps to NM_004441.4 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr3:134670232 C>T maps to NM_004441.4 Y48Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:134851811 C>A maps to NM_004441.4 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr3:134967276 G>A maps to NM_004441.4 A872A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:134898813 C>A maps to NM_004441.4 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:134670616 T>C maps to NM_004441.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:134851763 C>T maps to NM_004441.4 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr3:134851556 C>T maps to NM_004441.4 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:134851763 C>T maps to NM_004441.4 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr3:134911655 T>C maps to NM_004441.4 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr3:134920467 C>A maps to NM_004441.4 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr3:134911523 G>A maps to NM_004441.4 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:134885844 C>T maps to NM_004441.4 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr3:134644715 G>A maps to NM_004441.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:23233410 C>T maps to ENST00000400191 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:23232531 C>T maps to ENST00000400191 N606N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:23111063 C>T maps to ENST00000400191 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:23233236 G>A maps to ENST00000400191 K641K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:23232594 C>T maps to ENST00000400191 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:23222972 T>C did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:23191379 C>T maps to ENST00000400191 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:184298941 C>T maps to NM_004443.3 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr3:184290593 C>T maps to NM_004443.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr3:184297565 C>T maps to NM_004443.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:184297301 C>T maps to NM_004443.3 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:184298227 C>T maps to NM_004443.3 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:100410497 G>A maps to NM_004444.4 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:100421316 C>T maps to NM_004444.4 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr7:100402933 G>A maps to NM_004444.4 H896H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:142568281 G>T did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr7:142564818 T>A maps to NM_004445.3 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:142563772 A>G maps to NM_004445.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:142566074 C>T maps to NM_004445.3 V665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr1:226027014 G>A maps to NM_001136018.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:226016612 C>T maps to NM_001136018.2 H61H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:226019508 T>C maps to NM_001136018.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:226032993 G>A maps to NM_001136018.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:15341893 C>T maps to NM_001142886.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:145956465 G>T maps to NM_005670.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr6:145948826 G>T maps to NM_005670.3 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr6:145948725 G>A maps to NM_005670.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:37033488 C>T maps to NM_014805.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:37034066 G>A maps to NM_014805.3 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:37032990 C>G maps to NM_014805.3 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:37033704 G>A maps to NM_014805.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:37033488 C>T maps to NM_014805.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:37033625 G>A maps to NM_014805.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:56204052 T>C maps to NM_001130071.1 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr19:56204055 G>A maps to NM_001130071.1 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:56206239 G>A maps to NM_001130071.1 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:56201264 G>A maps to NM_001130071.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:56204124 A>G maps to NM_001130071.1 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:56204363 C>A maps to NM_001130071.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:19237473 A>G maps to NM_014964.4 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:48614045 C>T maps to NM_017957.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:11489154 T>C maps to NM_000121.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr8:144940980 G>A maps to NM_031308.1 T2147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:144946611 G>A maps to NM_031308.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:220203771 C>T maps to NM_004446.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr1:51866590 G>A maps to NM_001981.2 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:51875221 A>C maps to NM_001981.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:16528905 G>A maps to ENST00000455140 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:16497039 G>A maps to ENST00000455140 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:16536022 G>A maps to ENST00000455140 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:15784421 G>A maps to NM_004447.5 G666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:55591174 C>T maps to NM_133180.2 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:55593910 C>T maps to NM_133180.2 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:721569 C>T maps to NM_022772.3 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:722483 C>T maps to NM_022772.3 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:110294673 G>A maps to NM_139053.1 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:110300470 G>A maps to NM_139053.1 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:43469204 A>G maps to NM_001002264.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr13:43462619 C>T maps to NM_001002264.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr13:43462588 C>A maps to NM_001002264.1 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:43462544 G>A maps to NM_001002264.1 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr17:56276416 G>A maps to NM_000502.4 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:56271341 G>A maps to NM_000502.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:56274481 G>A maps to NM_000502.4 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr17:56280665 C>A maps to NM_000502.4 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr17:27182093 G>C maps to NM_005702.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:96139230 C>T maps to NM_016442.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:96121493 G>C maps to NM_016442.3 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr5:96244817 C>A maps to NM_001130140.1 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:96253290 G>A maps to NM_001130140.1 W955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:48687822 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:37883768 C>T maps to NM_004448.2 Y1127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:37881620 G>A maps to NM_004448.2 R897R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr17:37883786 C>T maps to NM_004448.2 C1133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:37883087 C>A maps to NM_004448.2 A997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:37864665 G>A maps to NM_004448.2 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr5:65340059 A>G maps to ENST00000506030 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:65350254 C>T maps to ENST00000506030 R1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:65349674 T>C maps to ENST00000506030 C843C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr5:65340059 A>G maps to ENST00000506030 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr5:65342359 T>A maps to ENST00000506030 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:65317213 G>T did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:65350484 G>T maps to ENST00000506030 A1113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:65350571 T>C maps to ENST00000506030 P1142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:65290591 G>A maps to ENST00000506030 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:65340059 A>G maps to ENST00000506030 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr12:56481367 C>A maps to NM_001982.2 P185P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-A022-01A-21W-A096-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:56478897 C>T maps to NM_001982.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:56493965 C>T maps to NM_001982.2 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr12:56477658 A>G maps to NM_001982.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr12:56482345 A>G maps to NM_001982.2 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:56493770 C>A maps to NM_001982.2 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr12:56478795 A>G maps to NM_001982.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr12:56481923 A>G maps to NM_001982.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:212248375 C>T maps to NM_005235.2 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr2:212812155 T>C maps to NM_005235.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:212615424 T>G maps to NM_005235.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:212812155 T>C maps to NM_005235.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:212530133 A>G maps to NM_005235.2 D595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:213403194 G>A maps to NM_005235.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:212578347 A>G maps to NM_005235.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr2:212566740 T>A maps to NM_005235.2 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr2:212248518 G>T maps to NM_005235.2 R1250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr2:212615364 A>T maps to NM_005235.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr2:212812226 A>G maps to NM_005235.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:212251740 G>T maps to NM_005235.2 C1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:212295792 A>C maps to NM_005235.2 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:212288963 C>A maps to NM_005235.2 E928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:212578347 A>G maps to NM_005235.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr2:212589809 T>C maps to NM_005235.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:212812155 T>C maps to NM_005235.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr2:212576854 C>T maps to NM_005235.2 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr2:212589809 T>C maps to NM_005235.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr2:212288940 T>C maps to NM_005235.2 K935K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr2:212566830 C>A maps to NM_005235.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr2:212812155 T>C maps to NM_005235.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr12:1137344 C>T maps to NM_178040.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr12:1599350 C>T maps to NM_178040.2 P1102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:1299072 C>T maps to NM_178040.2 R736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr12:1289716 T>C maps to NM_178040.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr12:1346028 C>T maps to NM_178040.2 R816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:56207482 G>A maps to ENST00000460849 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:56468440 C>A maps to ENST00000460849 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:56026215 G>A maps to ENST00000460849 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:55922480 C>A maps to ENST00000460849 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:56468947 G>A maps to ENST00000460849 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:45924591 C>T maps to NM_202001.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:45926584 C>T maps to NM_202001.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:45922412 C>T maps to NM_202001.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:45860928 G>A maps to NM_000400.3 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:45860791 G>A maps to NM_000400.3 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:45860907 G>C maps to NM_000400.3 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:128044399 A>G maps to NM_000122.1 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:128030524 G>A maps to NM_000122.1 Y581Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:128036929 C>A maps to NM_000122.1 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:128018920 C>A maps to NM_000122.1 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:14026057 C>T maps to NM_005236.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:14041621 C>T maps to NM_005236.2 C723C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr16:14041798 T>C maps to NM_005236.2 N782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr16:14041792 C>T maps to NM_005236.2 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:14026057 C>T maps to NM_005236.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:14041666 C>T maps to NM_005236.2 N738N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:103524700 G>A maps to NM_000123.2 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr13:103518110 G>A maps to NM_000123.2 E683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr13:103528096 A>G maps to NM_000123.2 E1135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr13:103518239 T>C maps to NM_000123.2 H726H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:103510723 G>T maps to NM_000123.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:103515359 C>T maps to NM_000123.2 Q621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr13:103518188 C>T maps to NM_000123.2 D709D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr13:103515359 C>T maps to NM_000123.2 Q621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr10:50678650 C>A maps to NM_000124.2 E1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:50708698 G>A maps to NM_000124.2 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:50667139 C>T maps to NM_000124.2 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:50690777 G>A maps to NM_000124.2 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:50701210 C>T maps to NM_000124.2 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:50679167 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr10:50679165 T>C maps to NM_000124.2 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:71427423 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:71425314 T>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:71425174 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:71427620 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:71426490 T>G did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:71424880 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:71425604 A>G did not map to a codon.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr23:71426421 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:71425981 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:71427102 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:71425496 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:71426419 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:71426756 A>G did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:71426274 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:71426550 T>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:71425091 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:71426274 G>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:71426273 G>T did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:71424878 T>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:60214196 G>A maps to NM_000082.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr4:75250453 C>A maps to NM_001432.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:75245222 A>T maps to NM_001432.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:75250453 C>T maps to NM_001432.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr4:75245220 G>T maps to NM_001432.2 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:42753819 C>T maps to NM_006494.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:42752772 A>G maps to NM_006494.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr21:39755654 A>G maps to NM_001136154.1 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr21:39764301 C>T maps to NM_001136154.1 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr21:39817370 G>A maps to NM_001136154.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr21:39755836 G>A maps to NM_001136154.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr21:39775574 C>A maps to NM_001136154.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr21:39755798 C>A maps to NM_001136154.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr21:39755654 A>G maps to NM_001136154.1 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr21:39755654 A>G maps to NM_001136154.1 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:172351072 G>A maps to NM_001031711.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr5:172324046 C>A maps to NM_001031711.2 S42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr5:172324047 G>A maps to NM_001031711.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:29494109 A>C maps to NM_016570.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr12:29510632 C>T maps to NM_016570.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:29494088 T>C maps to NM_016570.2 *378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr20:34130259 A>G did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr20:34144754 A>G maps to ENST00000447986 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr14:69847299 C>T maps to NM_004450.2 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:20811302 C>A maps to NM_001142725.1 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:44818549 G>A maps to NM_024066.1 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:44804758 C>T maps to NM_024066.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:665933 C>T maps to NM_207332.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:618760 G>T maps to NM_207332.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:623400 G>A maps to NM_207332.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:623516 C>A maps to NM_207332.1 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:54036355 C>T maps to NM_015701.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:101923793 C>A maps to NM_001100626.1 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr10:101915905 G>T maps to NM_001100626.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr10:101935816 G>A maps to NM_001100626.1 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:37610974 A>G maps to NM_007175.6 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:158178084 C>A maps to NM_001009959.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr9:5801199 C>T maps to NM_024896.2 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:5810163 A>G maps to NM_024896.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:5787161 G>A maps to NM_024896.2 Y899Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:5825109 A>G maps to NM_024896.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:5810076 C>T maps to NM_024896.2 L494L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DM-A28F-01A-11D-A16V-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr9:5787593 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:62144227 G>A maps to NM_001433.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:62125337 G>T maps to NM_001433.3 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:62133185 G>A maps to NM_001433.3 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:62157057 C>T maps to NM_001433.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:62121356 G>A maps to NM_001433.3 D975D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:62130319 T>C maps to NM_001433.3 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr16:23707285 G>A maps to NM_033266.3 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:23717678 C>T maps to NM_033266.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:23706579 C>A maps to NM_033266.3 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:23702650 G>A maps to NM_033266.3 H872H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:23702322 T>C maps to NM_033266.3 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr14:53120022 T>C maps to NM_014584.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr14:53133178 C>T maps to NM_014584.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:236389776 C>A maps to NM_019891.3 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:236389776 C>A maps to NM_019891.3 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:236399098 C>T maps to NM_019891.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:15090957 C>T maps to NM_152321.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr12:112457579 C>T maps to NM_006817.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:8074070 A>G maps to NM_018948.3 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr6:11105006 A>G maps to NM_207582.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr6:11105462 T>C maps to NM_207582.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:11104367 A>G maps to NM_207582.2 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:11104868 C>T maps to NM_207582.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:11104868 C>T maps to NM_207582.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:11104271 C>T maps to NM_207582.2 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:11105006 A>G maps to NM_207582.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:11105006 A>G maps to NM_207582.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr6:11105006 A>G maps to NM_207582.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr6:11105321 A>G maps to NM_207582.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr6:11105462 T>C maps to NM_207582.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:124624597 G>A maps to NM_138961.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:124623826 G>T maps to NM_138961.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr11:124626446 G>A maps to NM_138961.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr11:124626560 C>G maps to NM_138961.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr18:19153435 C>A maps to NM_052911.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr18:19154336 T>C maps to NM_052911.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:19153792 C>A maps to NM_052911.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:27634628 G>A maps to NM_001017420.2 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:27650199 G>T maps to NM_001017420.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:27650199 G>T maps to NM_001017420.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:27650249 A>G maps to NM_001017420.2 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr8:27650249 A>G maps to NM_001017420.2 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:27634475 T>C maps to NM_001017420.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr13:47361168 C>T maps to NM_001984.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr20:13763609 G>T maps to NM_016649.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr20:13753201 T>C maps to NM_016649.3 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:13756818 G>A maps to NM_016649.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr20:13753201 T>C maps to NM_016649.3 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr5:54277951 C>T maps to NM_007036.4 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:53671708 C>T maps to NM_012291.4 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:53668785 A>G maps to NM_012291.4 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr12:53682997 G>A maps to NM_012291.4 R1611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:53663625 G>A maps to NM_012291.4 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:53677018 G>A maps to NM_012291.4 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr12:53670436 G>A maps to NM_012291.4 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr1:6504668 T>C maps to NM_031475.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:6520127 G>A maps to NM_031475.2 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:6511708 G>A maps to NM_031475.2 E654E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:239038948 C>A maps to NM_194312.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:239039001 G>A maps to NM_194312.2 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:152265431 G>A maps to NM_001122741.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr6:152201826 C>A maps to NM_001122741.1 C227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr6:152163747 C>T maps to NM_001122741.1 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:152265533 C>A maps to NM_001122741.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:152265569 G>A maps to NM_001122741.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr6:152419947 C>T maps to NM_001122741.1 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr6:152265568 C>A maps to NM_001122741.1 S341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:64746819 A>G maps to NM_001437.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr14:64727346 G>A maps to NM_001437.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:64699872 C>T maps to NM_001437.2 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:64749622 G>A maps to NM_001437.2 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:95686534 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr8:95704958 C>T maps to NM_017697.3 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr16:68265576 G>A maps to NM_024939.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:68264754 G>T maps to NM_024939.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr16:68264170 A>C maps to NM_024939.2 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:68264868 C>T maps to NM_024939.2 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr11:64082665 A>G maps to NM_004451.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:76949059 C>T maps to NM_004452.3 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:76928918 C>T maps to NM_004452.3 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:76964569 C>T maps to NM_004452.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr14:76905905 C>G maps to NM_004452.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr14:76964734 C>T maps to NM_004452.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:76948425 C>T maps to NM_004452.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:216737573 C>T maps to NM_001438.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:216741440 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:216850805 A>G maps to NM_001438.2 D28D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:216692641 G>A maps to NM_001438.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr1:216850580 G>A maps to NM_001438.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:216850766 C>A maps to NM_001438.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:216692626 G>A maps to NM_001438.2 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:216850766 C>A maps to NM_001438.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr23:103499211 G>A did not map to a codon.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr23:103499519 A>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:103498866 G>A did not map to a codon.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr23:103499141 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:103495446 G>A did not map to a codon.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr23:103494958 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:103499516 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:103498989 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:103498866 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:103497498 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:103499198 G>A did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:103495037 C>A did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:103499516 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:103494938 G>T did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr12:56531356 G>A maps to NM_001184796.1 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:56522339 T>C maps to NM_001184796.1 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr12:56528163 G>A maps to NM_001184796.1 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr12:56522339 T>C maps to NM_001184796.1 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:56532787 A>G maps to NM_001184796.1 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:56527916 C>A maps to NM_001184796.1 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:56524642 G>A maps to NM_001184796.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:158531715 G>A maps to NM_020728.2 C782C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:158540967 G>A maps to NM_020728.2 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:158560359 C>T maps to NM_020728.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:158528250 G>A maps to NM_020728.2 D843D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr3:138193180 C>T maps to NM_031913.3 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:138179499 G>A maps to NM_031913.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:138195298 A>G maps to NM_031913.3 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:67637094 A>G maps to NM_019002.3 R902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:67630381 G>T maps to NM_019002.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:67632348 T>G maps to NM_019002.3 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:67631304 T>C maps to NM_019002.3 C497C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr2:67637094 A>G maps to NM_019002.3 R902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:137847194 G>A maps to NM_004730.2 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:137853275 A>G maps to NM_004730.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:137844391 C>T maps to NM_004730.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr4:159606316 C>T maps to NM_004453.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr4:159629519 T>C maps to NM_004453.2 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:159611543 C>T maps to NM_004453.2 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr12:22837881 T>C maps to NM_018638.4 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr12:22796861 C>T maps to NM_018638.4 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:204115878 C>A maps to NM_018208.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr1:204115783 G>A maps to NM_018208.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:128332363 C>T maps to NM_001143820.1 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr11:128354814 T>C maps to NM_001143820.1 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr11:128354730 C>A maps to NM_001143820.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr11:128354816 G>T maps to NM_001143820.1 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr21:40194761 G>A maps to NM_005239.4 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:13946170 G>A maps to NM_004956.4 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr7:14017050 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:13978746 A>G maps to NM_004956.4 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr7:13971232 G>A maps to NM_004956.4 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:13975487 C>T maps to NM_004956.4 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr7:13978836 T>C maps to NM_004956.4 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:13975457 C>T maps to NM_004956.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr7:13975475 G>C maps to NM_004956.4 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:14017049 A>G did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:157094740 C>T maps to NM_001145312.1 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:157095748 T>C maps to NM_001145312.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:41607484 G>A maps to NM_001079675.1 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr17:41613827 A>G maps to NM_001079675.1 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:41607294 T>C maps to NM_001079675.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:41606972 G>A maps to NM_001079675.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:185766604 A>G maps to NM_004454.2 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:185766541 G>A maps to NM_004454.2 C473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:185766625 G>A maps to NM_004454.2 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:185774979 G>A maps to NM_004454.2 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr3:185769817 C>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:185783692 A>G maps to NM_004454.2 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr3:185766625 G>A maps to NM_004454.2 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:185797640 C>T maps to NM_004454.2 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:185797865 C>T maps to NM_004454.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr12:11905442 G>A maps to NM_001987.4 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:12022874 G>A maps to NM_001987.4 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:36343776 G>A maps to NM_016135.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:5795411 C>T maps to NM_153717.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:5721018 G>A maps to NM_153717.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:5750008 C>T maps to NM_153717.2 C358C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:5749975 G>A maps to NM_153717.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:5785316 C>T maps to NM_153717.2 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:5803747 G>A maps to NM_153717.2 A792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:5795435 C>T maps to NM_153717.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:5800440 C>T maps to NM_153717.2 C742C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr4:5806511 G>A maps to NM_153717.2 S835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:5687095 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:5690973 G>A maps to NM_147127.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:5586478 G>T maps to NM_147127.4 S976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr4:5667361 G>A maps to NM_147127.4 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:5620243 G>A maps to NM_147127.4 F889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:5586352 G>A maps to NM_147127.4 S1018S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:5627574 G>T maps to NM_147127.4 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr4:5624667 C>G maps to NM_147127.4 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:5586426 A>G maps to NM_147127.4 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:5570322 G>A maps to NM_147127.4 P1135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:5696100 C>T maps to NM_147127.4 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:5633609 G>T maps to NM_147127.4 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:5667328 G>A maps to NM_147127.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr4:5627631 T>C maps to NM_147127.4 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr4:5682986 C>T maps to NM_147127.4 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr4:5564751 G>A maps to NM_147127.4 G1250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr4:5624288 G>A maps to NM_147127.4 R826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr4:5586391 C>A maps to NM_147127.4 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:29645542 G>T maps to NM_001003927.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:92979404 A>G maps to NM_005665.4 D747D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:93091380 C>T maps to NM_005665.4 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:93142744 C>T maps to NM_005665.4 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:93091445 C>A maps to NM_005665.4 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr1:93163455 T>C maps to NM_005665.4 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr1:92979335 G>T maps to NM_005665.4 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:93163457 C>A maps to NM_005665.4 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:7927329 G>A maps to NM_001159944.1 Q619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:7920935 G>A maps to NM_001159944.1 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:7926876 G>A maps to NM_001159944.1 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr14:100594937 C>T maps to NM_016337.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:74003873 C>T maps to NM_001988.2 P1804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr17:74004773 G>T maps to NM_001988.2 V1504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:74017799 G>A maps to NM_001988.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:74018562 G>A maps to NM_001988.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:74005451 G>A maps to NM_001988.2 N1278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr17:74005493 G>A maps to NM_001988.2 P1264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:74011616 G>A maps to NM_001988.2 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr17:74004254 C>T maps to NM_001988.2 T1677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:18284721 G>A maps to NM_001145127.1 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr2:176946935 C>A maps to NM_001080458.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:176948450 G>A maps to NM_001080458.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:29694787 G>T maps to NM_013986.3 G500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:29695766 G>T maps to NM_013986.3 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:29695661 C>T maps to NM_013986.3 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:29688150 T>G maps to NM_013986.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr22:29684652 A>G maps to NM_013986.3 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:29682980 G>A maps to NM_013986.3 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr22:29674163 T>C maps to NM_013986.3 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr22:29695769 G>C maps to NM_013986.3 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr15:41476617 T>C maps to NM_152596.2 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr15:41476617 T>C maps to NM_152596.2 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:41483662 C>A maps to NM_152596.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr15:41476617 T>C maps to NM_152596.2 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:41476617 T>C maps to NM_152596.2 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:69707762 C>T maps to NM_001193363.1 N604N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr14:69701635 C>T maps to NM_001193363.1 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr14:69703250 C>T maps to NM_001193363.1 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:140247217 C>T maps to NM_017820.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:242048758 G>A maps to NM_006027.4 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:242030148 T>C maps to NM_006027.4 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr1:242035397 A>G maps to NM_006027.4 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:242042272 G>A maps to NM_006027.4 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:56766034 T>C maps to NM_018261.3 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr4:56766034 T>C maps to NM_018261.3 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:556549 T>C maps to NM_018303.4 E622E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr6:564657 G>A maps to NM_018303.4 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:564561 G>A maps to NM_018303.4 H550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:532499 A>C maps to NM_018303.4 Y783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr6:532565 T>C maps to NM_018303.4 E761E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:454127 C>T maps to ENST00000315013 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr5:446325 G>A maps to ENST00000315013 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:67218686 C>T maps to NM_178516.3 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr16:67222774 C>T maps to NM_178516.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr19:45735071 G>A maps to NM_138568.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:45731010 G>A maps to NM_138568.3 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:132973728 G>A maps to NM_021807.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:133622822 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:133580413 A>G maps to NM_021807.3 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr7:133602392 T>C maps to NM_021807.3 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:132937874 T>C maps to NM_021807.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr7:132937874 T>C maps to NM_021807.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr14:57710939 G>A maps to ENST00000340918 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr14:57704080 A>G maps to ENST00000340918 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:94712092 G>T maps to NM_019053.4 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr10:94818034 C>T maps to NM_019053.4 R780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:94654775 T>C maps to NM_019053.4 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:94695597 C>T maps to NM_019053.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:94688172 G>A maps to NM_019053.4 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:94818042 A>G maps to NM_019053.4 K782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:94712092 G>T maps to NM_019053.4 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:94688160 G>A maps to NM_019053.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:94714498 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:94608328 G>A maps to NM_019053.4 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:73052975 G>A maps to NM_015189.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:72968431 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:72740313 C>A maps to NM_015189.1 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:74087314 C>T maps to NM_001145297.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:74083753 G>A maps to NM_001145297.2 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:74097829 G>A maps to NM_001145297.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:74084188 C>T maps to NM_001145297.2 K489K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:99205604 C>A did not map to a codon.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr1:11158080 G>A maps to NM_001001998.1 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr1:11142797 G>C maps to NM_001001998.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr1:11134370 C>A maps to NM_001001998.1 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:11147552 A>G maps to NM_001001998.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr1:11137496 A>G maps to NM_001001998.1 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:11151151 G>A maps to NM_001001998.1 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:11150669 G>A maps to NM_001001998.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr9:133570878 G>T maps to NM_014285.5 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr9:37784014 T>A maps to NM_016042.2 K124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr8:145134898 A>G maps to NM_019037.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:45052749 A>G maps to NM_015004.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:45048961 G>A maps to NM_015004.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr13:37583364 C>T maps to NM_181503.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr4:122731148 A>G maps to NM_001034194.1 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:108385464 C>A maps to NM_015065.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:108381958 A>T maps to NM_015065.2 S1425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr11:108383881 C>T maps to NM_015065.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:108383469 C>A maps to NM_015065.2 E922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:108385507 G>A maps to NM_015065.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:108384916 G>A maps to NM_015065.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:108383197 A>C maps to NM_015065.2 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr8:119122871 G>A maps to NM_000127.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:118819568 C>T maps to NM_000127.2 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:118825128 C>A maps to NM_000127.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr8:119122832 C>T maps to NM_000127.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr8:118825128 C>A maps to NM_000127.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:44129681 T>C maps to NM_000401.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:44129711 C>A maps to NM_000401.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:26355722 C>T maps to NM_004455.2 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:26349802 C>T maps to NM_004455.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:26349754 G>A maps to NM_004455.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:26361745 T>C maps to NM_004455.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr8:28574277 C>T maps to NM_001440.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:28573839 G>A maps to NM_001440.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr8:28573944 C>T maps to NM_001440.2 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:28574952 C>T maps to NM_001440.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:28575123 G>A maps to NM_001440.2 W516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr8:28574883 C>T maps to NM_001440.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:72128996 C>T maps to NM_000503.4 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:72181992 G>A maps to NM_000503.4 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr8:72184070 A>G maps to NM_000503.4 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:72156885 T>C maps to NM_000503.4 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:72211363 C>T maps to NM_000503.4 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr8:72156894 T>C maps to NM_000503.4 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr8:72234050 T>C maps to NM_000503.4 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr8:72156894 T>C maps to NM_000503.4 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:72184069 G>A maps to NM_000503.4 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr8:72156896 G>T maps to NM_000503.4 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr8:72127862 C>A maps to NM_000503.4 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:72127880 C>T maps to NM_000503.4 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:45801429 C>T maps to ENST00000360649 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:45771705 G>A maps to ENST00000360649 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:45801423 C>T maps to ENST00000360649 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:45801432 C>T maps to ENST00000360649 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:28365414 A>G maps to NM_001990.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr1:28326512 A>G maps to NM_001990.2 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:133789801 T>C maps to ENST00000452339 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:133783855 C>T maps to ENST00000452339 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr6:133789801 T>C maps to ENST00000452339 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr6:133777721 C>A maps to ENST00000452339 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr6:64498962 C>T maps to ENST00000370616 E2522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr6:65523430 G>A maps to ENST00000370616 Q1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr6:66204813 G>A maps to ENST00000370616 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:66045005 C>A maps to ENST00000370616 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr6:66205164 C>A maps to ENST00000370616 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:66200487 T>C maps to ENST00000370616 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:64498061 A>G maps to ENST00000370616 G2553G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:65300635 G>A maps to ENST00000370616 G1708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:65301639 G>A maps to ENST00000370616 R1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:66115177 A>C maps to ENST00000370616 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:64436463 G>A maps to ENST00000370616 L2748L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D5-6533-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr6:64488016 C>A maps to ENST00000370616 G2594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:65300221 C>T maps to ENST00000370616 V1846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr6:65149245 C>T did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr6:65301178 C>T maps to ENST00000370616 Q1527Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:66205224 G>A maps to ENST00000370616 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:40870595 A>G maps to ENST00000264646 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:40854914 T>C maps to ENST00000264646 E724E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr7:148525835 T>C maps to NM_004456.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:148525904 A>G maps to NM_004456.3 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:148543623 G>A maps to NM_004456.3 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr7:148508752 C>T maps to NM_004456.3 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:148506453 A>G maps to NM_004456.3 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:148514987 A>G maps to NM_004456.3 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr7:148506164 G>A maps to NM_004456.3 Y731Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr7:148507485 A>G maps to NM_004456.3 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr7:148525837 G>T maps to NM_004456.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:148523648 A>G maps to NM_004456.3 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr7:148508791 A>C maps to NM_004456.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:148506432 A>G maps to NM_004456.3 N693N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr7:148506164 G>A maps to NM_004456.3 Y731Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr7:148507431 C>T maps to NM_004456.3 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:148512618 T>A maps to NM_004456.3 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:148544315 T>A maps to NM_004456.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr7:148525837 G>T maps to NM_004456.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr7:148525837 G>T maps to NM_004456.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:148525837 G>T maps to NM_004456.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:148526859 T>C maps to NM_004456.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr7:148506432 A>G maps to NM_004456.3 N693N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr7:148525837 G>T maps to NM_004456.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr7:148525880 A>G maps to NM_004456.3 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr7:148523705 T>C maps to NM_004456.3 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr7:148516735 T>C maps to NM_004456.3 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr7:148526868 G>A maps to NM_004456.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr13:113803353 C>A maps to NM_000504.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:113793761 C>T maps to NM_000504.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:113803515 C>T maps to NM_000504.3 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:187201234 T>G maps to NM_000128.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:160969965 G>T maps to NM_016946.4 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:160971099 A>G maps to NM_016946.4 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr5:176829442 C>T maps to NM_000505.3 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr5:176829691 C>T maps to NM_000505.3 E513E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:176831326 C>T maps to NM_000505.3 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:176832771 G>A maps to NM_000505.3 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:6251103 G>A maps to NM_000129.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr6:6222387 T>C maps to NM_000129.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr6:6197480 G>A maps to NM_000129.3 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr6:6266845 T>C maps to NM_000129.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:197036304 C>A maps to NM_001994.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:197021803 G>A maps to NM_001994.2 C505C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:46747646 C>T maps to NM_000506.3 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:46747421 C>A maps to NM_000506.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr11:46747679 C>T maps to NM_000506.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:46745003 G>T maps to NM_000506.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:46744958 C>T maps to NM_000506.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr5:76028928 C>T maps to NM_001992.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:76029027 C>T maps to NM_001992.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr5:76028928 C>A maps to NM_001992.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr5:76028928 C>T maps to NM_001992.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr5:76028814 T>C maps to NM_001992.3 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:76129239 C>T maps to NM_005242.4 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:76129502 C>T maps to NM_005242.4 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:76128857 T>A maps to NM_005242.4 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:76129361 T>C maps to NM_005242.4 H310H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:76129514 C>T maps to NM_005242.4 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr5:76129109 T>C maps to NM_005242.4 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr1:94998693 C>T maps to NM_001993.4 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:169529960 G>A maps to ENST00000367796 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:169529960 G>A maps to ENST00000367796 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:169512109 G>A maps to ENST00000367796 R745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr1:169525984 G>C maps to ENST00000367796 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:169555600 G>A maps to ENST00000367796 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:169511555 C>T maps to ENST00000367796 W929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:169509824 A>C maps to ENST00000367796 T1506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:169512035 G>A maps to ENST00000367796 F769F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:169519080 A>G maps to ENST00000367796 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:113770001 C>T maps to NM_000131.3 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:154185254 A>G did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:154159514 C>A did not map to a codon.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr23:154159624 G>A did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:154090094 T>C did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:154157915 G>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:154159806 T>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:154091434 C>T did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr23:154088760 G>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:154158386 C>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:154159623 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:154250807 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:154158524 T>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:154221251 A>G did not map to a codon.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr23:154157326 G>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:154159274 A>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:154159881 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:154213061 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:154132581 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:154213005 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:154225368 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:154132792 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:154159624 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:154175986 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:154088800 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:154158673 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:154159624 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:154215560 C>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:154090099 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:154133283 A>G did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:154194814 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:154194730 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:154157125 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:154157706 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr23:154185252 A>G did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr23:154157727 C>T did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr23:154133086 A>G did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr23:154159622 T>C did not map to a codon.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr23:154227759 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:154124356 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:154157081 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:154158675 C>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:154133085 C>T did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:154133085 C>T did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:154090094 T>C did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:154157081 G>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:154156919 T>C did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:154156919 T>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:154090094 T>C did not map to a codon.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr23:154227757 C>T did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:154156919 T>C did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:154159622 T>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:154158526 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr23:154227758 C>T did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:154090034 A>G did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:154158815 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:154156919 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:154176134 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:154182176 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:154227758 C>T did not map to a codon.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr23:138642944 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:138633279 A>G did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:138630597 C>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:138612968 A>G did not map to a codon.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr23:138643724 G>A did not map to a codon.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr23:138633257 T>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:138644028 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:138643705 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:138643993 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:138643993 C>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:138642940 T>C did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:138643812 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:138630595 T>C did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr23:138630595 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:138619264 G>T did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:138612929 C>T did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:138623281 A>G did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:138643849 A>C did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:138643812 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:138623282 A>G did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:138623282 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:138643985 C>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:138619244 T>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:138643913 G>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr16:74750359 G>A maps to NM_024306.4 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:46874246 G>T maps to NM_001441.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:46871415 C>A maps to NM_001441.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:57515326 A>G did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr23:57473465 T>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:57337093 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr23:57358062 C>T did not map to a codon.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr23:57313370 C>G did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:57473465 T>C did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:57319014 T>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:57473467 C>A did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr23:57358059 C>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:57473465 T>C did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:57475048 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr8:82437316 G>A maps to NM_001105281.1 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:120240753 T>C maps to NM_000134.3 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:120241934 C>A maps to NM_000134.3 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:120241938 T>C maps to NM_000134.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:120241908 T>C maps to NM_000134.3 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:159656584 C>T maps to NM_001040442.1 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:159659147 C>T maps to NM_001040442.1 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:61584179 C>T maps to NM_013402.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr11:61605260 C>T maps to NM_004265.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:61646028 G>A maps to NM_021727.3 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:72889675 G>C maps to ENST00000310226 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr17:72875596 C>T maps to ENST00000310226 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:51049376 G>A maps to NM_007051.2 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:51253771 T>C maps to NM_007051.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr5:175913450 C>T maps to NM_014613.2 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr5:175933766 A>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:80473418 G>A maps to NM_000137.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:80467416 C>A maps to NM_000137.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr16:1877697 C>G maps to NM_001018104.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:1877634 G>A maps to NM_001018104.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr16:1877265 C>T maps to NM_001018104.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:96076721 C>T maps to NM_016044.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr2:97749738 T>C maps to NM_199336.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:97751571 G>A maps to NM_199336.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:138341121 C>T maps to NM_001033030.1 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr12:50283293 G>C maps to NM_012306.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:50291786 G>A maps to NM_012306.2 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:207086358 T>C maps to NM_005449.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr12:124798800 C>T maps to ENST00000389727 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr17:293239 G>A maps to NM_182705.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr1:109154825 A>G maps to NM_001010883.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr1:109154825 A>G maps to NM_001010883.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:71228232 G>C maps to NM_001098832.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:55170216 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:55172593 G>C did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:14681685 G>A maps to NM_138348.4 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:14673796 G>T maps to NM_138348.4 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:14693135 G>A maps to NM_138348.4 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:14563960 T>C maps to NM_031453.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr10:14563960 T>C maps to NM_031453.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:81046693 G>T maps to NM_021214.1 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:42473902 G>A maps to NM_001002034.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr20:826247 C>T maps to NM_031424.4 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:59058938 C>T maps to NM_147189.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr8:59059310 G>A maps to NM_147189.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:59059391 G>A maps to NM_147189.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:59059511 C>T maps to NM_147189.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr8:59059718 C>T maps to NM_147189.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:59059601 C>T maps to NM_147189.2 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr8:59058938 C>T maps to NM_147189.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:59059118 C>T maps to NM_147189.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr8:59059442 T>C maps to NM_147189.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr11:58920139 G>A maps to NM_198847.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr11:58920334 T>C maps to NM_198847.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr11:58920847 T>A maps to NM_198847.2 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:58920847 T>C maps to NM_198847.2 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:58892778 G>A maps to NM_198947.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr11:58893361 C>T maps to NM_198947.3 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:58892778 G>A maps to NM_198947.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:58893273 A>G maps to NM_198947.3 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr20:2816820 C>T maps to NM_022760.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr12:47629949 C>T maps to NM_138371.1 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:47629953 G>T maps to NM_138371.1 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:47628896 C>T maps to NM_138371.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:47629949 C>T maps to NM_138371.1 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:47629839 C>A maps to NM_138371.1 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:47629949 C>T maps to NM_138371.1 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:47629949 C>T maps to NM_138371.1 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:47629931 A>G maps to NM_138371.1 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:38924480 G>T maps to NM_138389.2 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr4:38907143 T>G maps to NM_138389.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr3:57647251 A>C maps to NM_152678.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:50756339 C>T maps to NM_001001794.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:50755781 G>A maps to NM_001001794.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr22:50752263 C>T maps to NM_001001794.3 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr17:47809954 A>C maps to NM_030802.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:47788772 G>T maps to NM_030802.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr17:47799881 G>T maps to NM_030802.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr2:203622018 G>A maps to NM_173511.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:203620334 C>T maps to NM_173511.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:45723844 C>T maps to NM_017911.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:45728571 C>A maps to NM_017911.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr11:126124303 C>T maps to NM_024556.3 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:126104958 C>T maps to NM_024556.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:208488952 C>T maps to ENST00000272839 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:58174254 G>A maps to NM_015433.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr12:58166629 C>A maps to NM_015433.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:58174351 C>T maps to NM_015433.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:96320200 G>A maps to ENST00000333936 P887P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A6-5659-01A-01D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:96233499 G>A maps to ENST00000333936 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:96291777 C>T maps to ENST00000333936 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:96324499 G>T maps to ENST00000333936 G1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:96312930 G>A maps to ENST00000333936 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:96291813 G>A maps to ENST00000333936 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:96318707 C>T maps to ENST00000333936 F801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr6:170626691 C>T maps to NM_032448.1 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:170626849 G>A maps to NM_032448.1 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:170626531 T>C maps to NM_032448.1 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:54160245 C>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:54160249 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:54099658 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:54186046 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:54143102 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr23:54185962 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:54099547 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:54159139 G>A did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:54185988 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:54161424 G>T did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:54185986 G>A did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:54185988 A>G did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:54112317 C>T did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:54185988 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:133915874 G>A did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:133988177 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:133988127 C>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:133948835 G>T did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr13:25744368 C>T maps to NM_152704.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:25744146 C>T maps to NM_152704.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr23:63411317 C>A did not map to a codon.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr23:63411677 G>A did not map to a codon.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr23:63412094 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:63412032 A>G did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:63411533 A>G did not map to a codon.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr23:63410485 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:63412217 T>C did not map to a codon.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr23:63412001 C>A did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:63412094 G>A did not map to a codon.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr23:63411782 C>A did not map to a codon.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr23:63412094 G>A did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:63411062 C>A did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:63411410 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:63412381 A>G did not map to a codon.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr23:63411677 G>A did not map to a codon.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr23:63411677 G>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:63411228 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:63412871 G>T did not map to a codon.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr23:63411365 G>A did not map to a codon.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr23:63412109 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:63410596 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:63412640 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:63411761 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:63412693 T>G did not map to a codon.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr23:63411365 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:63412523 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:63413033 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:63410342 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:63411187 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:63412094 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:63413079 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:63411677 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:63410341 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:63412019 C>A did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:63413033 A>G did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:63412545 G>A did not map to a codon.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr23:63411677 G>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:63412108 C>A did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:63411365 G>A did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:63411302 C>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:63412108 C>T did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr23:63411575 G>A did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:63413031 G>T did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr23:63412094 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:63411936 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:63412693 T>G did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:63412870 A>G did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:63412165 T>C did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:63411409 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:131520406 C>T maps to NM_001105195.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:131520568 G>A maps to NM_001105195.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:131522197 C>A maps to NM_001105195.1 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:131521411 A>C maps to NM_001105195.1 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:131521423 C>T maps to NM_001105195.1 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr13:51854659 T>A maps to NM_145019.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr13:51825734 C>T maps to NM_145019.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr13:51855295 C>T maps to NM_145019.2 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:51825658 C>T maps to NM_145019.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:51825973 G>A maps to NM_145019.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr13:51826045 C>T maps to NM_145019.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr13:51825760 G>A maps to NM_145019.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr13:51825913 C>T maps to NM_145019.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:17534315 C>T maps to NM_138401.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:129157881 C>T maps to NM_033446.1 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:129184163 C>T maps to NM_033446.1 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:129148858 T>C maps to NM_033446.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:22985252 A>G maps to NM_032581.3 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr7:22985294 G>A maps to NM_032581.3 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:23018049 A>G maps to NM_032581.3 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr7:22985294 G>A maps to NM_032581.3 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr7:22985294 G>A maps to NM_032581.3 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:201876150 A>G maps to NM_173822.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:201846223 A>G maps to NM_173822.3 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr2:201846544 T>A maps to NM_173822.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:134166696 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:134166741 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:134185927 G>A did not map to a codon.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr23:134186120 C>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:134185866 A>G did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:134186082 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:134186122 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:134185996 T>A did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:134185376 C>T did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:134156394 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:130948057 C>T maps to ENST00000409255 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr1:184765070 C>T maps to NM_052966.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:184853785 G>A maps to NM_052966.2 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:184777212 G>A maps to NM_052966.2 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr1:184777333 G>A maps to NM_052966.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:184801064 T>C maps to NM_052966.2 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:184764467 G>A maps to NM_052966.2 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:184764560 C>T maps to NM_052966.2 E779E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr1:184767258 G>C maps to NM_052966.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:130270407 C>T maps to NM_022833.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:130279253 C>T maps to NM_022833.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:17643166 C>T maps to ENST00000335393 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:17657583 C>T maps to ENST00000335393 C579C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:17664281 C>T maps to ENST00000335393 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr19:17654208 G>A maps to ENST00000335393 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:184062487 C>T maps to NM_144635.4 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:184060592 C>T maps to NM_144635.4 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:143056109 T>C maps to NM_001031690.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:16386472 G>A maps to NM_182623.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr1:16384985 G>T maps to NM_182623.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:16385072 C>T maps to NM_182623.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:1178488 G>A maps to NM_001014980.1 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:92964737 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:92964616 G>A did not map to a codon.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr23:92964756 T>C did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:92964457 A>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:92965088 A>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:92964799 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:92964520 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:92964644 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:92964552 G>T did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:92964578 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:92207635 T>C maps to NM_152789.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:220047260 G>A maps to NM_024293.4 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr2:220046154 C>T maps to NM_024293.4 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:220045400 C>T maps to NM_024293.4 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr2:220044832 G>T maps to NM_024293.4 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:220047077 T>C maps to NM_024293.4 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:220046948 G>A maps to NM_024293.4 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:16479052 A>G maps to NM_001034850.1 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:16478971 T>C maps to NM_001034850.1 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:16478971 T>C maps to NM_001034850.1 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:16478971 T>C maps to NM_001034850.1 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr17:40733872 C>A maps to NM_178126.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:71162192 A>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:71235075 C>A maps to NM_001162529.1 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:71266529 G>T maps to NM_001162529.1 E1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr6:71190627 T>C maps to NM_001162529.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr8:139163684 C>A maps to NM_015912.3 G1011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:139151336 A>G maps to NM_015912.3 L1265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:139323149 G>A maps to NM_015912.3 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr8:139164284 A>C maps to NM_015912.3 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:139180249 C>A maps to NM_015912.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr8:139209857 G>A maps to NM_015912.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:139163789 C>A maps to NM_015912.3 P976P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:139165459 C>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr8:139163522 G>A maps to NM_015912.3 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:139164569 C>T maps to NM_015912.3 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr8:139165262 A>G maps to NM_015912.3 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:139268933 C>T maps to NM_015912.3 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr8:139163846 G>A maps to NM_015912.3 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:70528091 G>A maps to ENST00000430566 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr2:70524510 A>G maps to ENST00000430566 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:89649709 T>A maps to NM_014883.2 R1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:89670992 G>A maps to NM_014883.2 R670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:89709082 T>C maps to NM_014883.2 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:89702485 C>A maps to NM_014883.2 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:89702495 A>G maps to NM_014883.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:89859292 A>G maps to NM_014883.2 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr4:89671056 C>A maps to NM_014883.2 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr4:89702447 A>G maps to NM_014883.2 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:137281635 C>T maps to NM_016603.2 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:137278591 G>A maps to NM_016603.2 R832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:137292229 C>T maps to NM_001101801.1 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:61112137 C>T maps to ENST00000442566 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:61112203 G>A maps to ENST00000442566 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:61012599 T>C maps to ENST00000442566 K540K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:61043168 C>T maps to ENST00000442566 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:61043168 C>T maps to ENST00000442566 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr10:61083758 T>C maps to ENST00000442566 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:61011368 C>A maps to ENST00000442566 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:61011368 C>A maps to ENST00000442566 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:61083758 T>C maps to ENST00000442566 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr4:187086506 C>T maps to ENST00000356371 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr4:187088178 C>T maps to ENST00000356371 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr4:187088243 G>A maps to ENST00000356371 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr4:187084078 T>C maps to ENST00000356371 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:187078827 C>T maps to ENST00000356371 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:283161 G>A maps to NM_001002919.2 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:55075480 G>A maps to NM_176782.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:55085576 G>A maps to NM_176782.2 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr1:55077375 C>T maps to NM_176782.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:79817894 C>T maps to NM_205548.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:79809444 T>C maps to NM_205548.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:177166114 G>A maps to ENST00000425383 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr5:175528080 A>G maps to NM_001079529.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr9:18928983 G>C maps to NM_153707.2 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr9:18941665 G>A maps to NM_153707.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:18928208 A>C maps to NM_153707.2 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr15:82563946 G>A maps to NM_001008226.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr15:82574763 T>C maps to NM_001008226.1 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:82575114 G>A maps to NM_001008226.1 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:108518818 C>T maps to NM_001080396.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:68725721 C>T did not map to a codon.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr23:68749442 G>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:68748880 C>A did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:68725684 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:68749003 A>G did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:68725684 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:68725685 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:68749690 T>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:68749598 C>G did not map to a codon.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr11:6239971 G>A maps to NM_032127.3 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:6239291 C>T maps to NM_032127.3 Q522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:6239986 A>G maps to NM_032127.3 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:6245412 A>G maps to NM_032127.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:6245046 C>T maps to NM_032127.3 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:116593028 G>A maps to NM_020940.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:21953935 G>A maps to NM_022749.5 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:21959323 C>T maps to NM_022749.5 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:62067343 T>C maps to ENST00000404929 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:62067078 G>A maps to ENST00000404929 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:62067127 G>A maps to ENST00000404929 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:62053618 C>A maps to ENST00000404929 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:62067430 A>G maps to ENST00000404929 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:62067078 G>A maps to ENST00000404929 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:62069405 A>C maps to ENST00000404929 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr2:62067124 C>A maps to ENST00000404929 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:62067124 C>A maps to ENST00000404929 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:62067126 G>T maps to ENST00000404929 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr14:74409101 G>T maps to NM_152445.1 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:74411251 G>A maps to NM_152445.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:117083172 G>A maps to NM_001085480.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr6:117073807 A>T maps to NM_001085480.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr8:79609697 T>G maps to NM_016010.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr8:79598805 C>T maps to NM_016010.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:75537839 G>T maps to NM_024643.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:75538331 G>A maps to NM_024643.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:75538140 G>T maps to NM_024643.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:75537301 C>G maps to NM_024643.2 S9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:140138223 G>A maps to NM_001001710.1 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:11301686 C>T maps to NM_053279.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:11282070 T>C maps to NM_053279.2 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:11301713 C>T maps to NM_053279.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr1:32713084 G>A maps to NM_032648.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr1:32713084 G>A maps to NM_032648.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:131840164 C>A maps to NM_001009993.2 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:131812929 C>A maps to NM_001009993.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr5:74134801 C>T maps to NM_015566.1 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:74078860 A>G maps to NM_015566.1 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:74078920 G>A maps to NM_015566.1 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr5:74137455 A>G maps to NM_015566.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr15:98984356 A>G maps to NM_182562.2 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:118970051 G>A maps to ENST00000420106 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr10:15290671 G>T maps to NM_001010924.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:15256374 C>T maps to NM_001010924.1 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr10:15296786 C>T maps to NM_001010924.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:15256371 G>A maps to NM_001010924.1 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:15296783 G>A maps to NM_001010924.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:187626640 T>C maps to NM_177454.3 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:187615925 G>T maps to NM_177454.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:187627228 C>T maps to NM_177454.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr2:187627030 A>T maps to NM_177454.3 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:187627366 A>G maps to NM_177454.3 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr2:187627429 A>G maps to NM_177454.3 E787E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:187627366 A>G maps to NM_177454.3 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:93159892 G>A maps to NM_032042.5 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:93300219 C>T maps to NM_032042.5 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:84391525 G>A maps to NM_139076.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:84391407 C>A maps to NM_139076.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:84390195 T>C maps to NM_139076.2 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr4:84406192 C>T maps to NM_139076.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:84383921 G>A maps to NM_139076.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:84383729 A>C maps to NM_139076.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr4:84384667 C>A maps to NM_139076.2 G259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:126517436 G>T maps to NM_032182.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr10:126495443 C>T maps to NM_032182.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr2:75720574 G>A maps to NM_032181.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:75745236 C>T maps to NM_032181.2 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:75720613 C>T maps to NM_032181.2 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:75720541 G>A maps to NM_032181.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:102676522 T>C maps to NM_001136123.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr10:102677047 G>T maps to NM_001136123.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:102698382 G>A maps to NM_001136123.1 W848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:102684005 C>T maps to NM_001136123.1 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:97595043 G>A maps to ENST00000417561 H512H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:97587282 G>A maps to ENST00000417561 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:29245039 G>A maps to NM_199280.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:29237417 C>T maps to NM_199280.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:29247231 G>A maps to NM_199280.2 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:29222087 G>T maps to NM_199280.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:29249828 T>A maps to NM_199280.2 L655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:29245126 G>A maps to NM_199280.2 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:29249827 T>C maps to NM_199280.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr14:45432818 C>T maps to ENST00000361462 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:45497492 C>T maps to ENST00000361462 R1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr14:45475442 C>T maps to ENST00000361462 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr14:45468647 T>C maps to ENST00000361462 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:45432313 T>G maps to ENST00000361462 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:135421849 G>A maps to NM_205855.3 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr7:135419013 G>A maps to NM_205855.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:94394669 C>T maps to NM_138344.3 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:94394669 C>T maps to NM_138344.3 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:94394798 G>A maps to NM_138344.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr14:94395291 C>T maps to NM_138344.3 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:94395248 C>T maps to NM_138344.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:82443568 G>A maps to NM_175885.3 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:82443559 A>C maps to NM_175885.3 Y404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr11:82443493 G>A maps to NM_175885.3 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:82443868 C>T maps to NM_175885.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:43613663 C>T maps to NM_001101376.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr6:119301434 C>T maps to NM_024581.4 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:119324730 T>C maps to NM_024581.4 E624E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:119341145 C>T maps to NM_024581.4 E443E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:119301413 C>T maps to NM_024581.4 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr6:119324730 T>C maps to NM_024581.4 E624E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr6:119324732 C>A maps to NM_024581.4 E624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:119301421 G>T maps to NM_024581.4 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:49993729 G>A maps to NM_032130.2 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr12:49997064 T>C maps to NM_032130.2 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:49993310 C>T maps to NM_032130.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr12:49997064 T>C maps to NM_032130.2 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:35718874 C>A maps to NM_152481.1 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr19:35718938 G>A maps to NM_152481.1 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:35719256 G>A maps to NM_152481.1 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr7:30868342 C>T maps to NM_032222.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:30818125 C>T maps to NM_032222.2 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:30825421 G>A maps to NM_032222.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:71992393 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:71990690 G>T maps to NM_001127608.1 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:72003279 G>T maps to NM_001127608.1 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:155223415 C>A maps to ENST00000368370 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:155224235 G>A maps to ENST00000368370 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr16:10867232 G>A maps to NM_001079512.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr17:18707458 T>A maps to NM_016078.4 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr4:91229527 T>C maps to NM_001145065.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:91549283 A>G maps to NM_001145065.1 E611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:91549202 C>T maps to NM_001145065.1 D584D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:91229440 G>A maps to NM_001145065.1 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:91389458 G>T maps to NM_001145065.1 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr4:91549283 A>G maps to NM_001145065.1 E611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:91645096 G>A maps to NM_001145065.1 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:92520060 G>A maps to NM_001145065.1 T852T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:91844586 C>T maps to NM_001145065.1 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr4:91549235 C>T maps to NM_001145065.1 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr4:91549283 A>G maps to NM_001145065.1 E611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:86131209 T>C maps to ENST00000372088 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:86132007 G>A maps to ENST00000372088 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:86131903 G>T maps to ENST00000372088 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:86185538 G>A maps to ENST00000372088 Q586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:86131680 T>C maps to ENST00000372088 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:86273215 A>G maps to ENST00000372088 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:57188276 G>A maps to NM_024946.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:2696714 C>T maps to ENST00000324666 Y754Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:2702137 A>T maps to ENST00000324666 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr4:2696741 G>A maps to ENST00000324666 E763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:176951591 T>C maps to ENST00000442143 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:176963387 C>T maps to ENST00000442143 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr5:176965929 C>T maps to ENST00000442143 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:176959575 G>A maps to ENST00000442143 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:150421592 C>T maps to NM_152394.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr3:150421442 G>C maps to NM_152394.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr3:150398687 C>T maps to NM_152394.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:150377750 G>A maps to NM_152394.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:150421507 A>G maps to NM_152394.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:150377686 C>A maps to NM_152394.3 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:150387167 C>A maps to NM_152394.3 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:150416626 T>C maps to NM_152394.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:697879 G>A maps to NM_138418.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:128973675 C>T maps to NM_001039762.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:159091792 A>C maps to NM_001128424.1 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:159048639 G>A maps to NM_001128424.1 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr23:103434423 G>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:103411570 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:103430794 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:103434384 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:103411634 G>A did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:103434384 T>C did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:103434292 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:103420328 A>C did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:103432803 C>G did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:103430888 A>C did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:103434384 T>C did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:68588009 C>T maps to NM_213609.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:62148731 T>C maps to NM_178539.3 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr12:62148731 T>C maps to NM_178539.3 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:62148707 G>T maps to NM_178539.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:99145470 A>C maps to NM_145111.3 L187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:66539854 G>A maps to NM_017565.3 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:66537038 G>A maps to NM_017565.3 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:179013108 C>T maps to NM_014864.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr1:179013242 C>A maps to NM_014864.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:51829308 A>G maps to NM_001005751.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:51829357 G>T maps to NM_001005751.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:47945944 G>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:46222941 G>A maps to ENST00000399588 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:46246264 C>T maps to ENST00000399588 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:46280017 C>T maps to ENST00000399588 C828C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:88992642 C>T maps to NM_001099338.1 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:97081277 T>C maps to NM_017561.1 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr10:124672467 T>C maps to NM_001029888.1 *106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr10:124672469 A>C maps to NM_001029888.1 *106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr10:124609947 G>A maps to NM_152644.2 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:116833254 G>A maps to NM_153711.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:116784661 G>T maps to NM_001010919.1 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:16296327 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:88930233 G>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:88911950 C>T maps to ENST00000298786 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr18:10696187 C>A maps to NM_022068.2 V2245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr18:10680293 A>C maps to NM_022068.2 S2505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:10671630 G>A maps to NM_022068.2 R2718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:153741210 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:153735597 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr21:42694868 C>T maps to ENST00000398652 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr21:42719015 C>T maps to ENST00000398652 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:58622080 G>A maps to NM_138805.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:58639467 C>A maps to NM_138805.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:58631255 A>G maps to NM_138805.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:110584362 G>A maps to NM_033088.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:110590169 G>T maps to NM_033088.2 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:110582020 G>A maps to NM_033088.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:110587642 G>A maps to NM_033088.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:110587642 G>A maps to NM_033088.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:129098163 C>T maps to ENST00000450266 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:194408250 C>T maps to NM_153690.4 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:20879492 C>T maps to NM_207334.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:20879558 G>A maps to NM_207334.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:120892036 A>G maps to NM_207009.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr10:120892036 A>G maps to NM_207009.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr6:82459453 C>T maps to ENST00000369756 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:82459453 C>T maps to ENST00000369756 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:82460061 C>A maps to ENST00000369756 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:82461726 A>G maps to ENST00000369756 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:27332719 G>A maps to NM_052943.3 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:79698223 A>G did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:79698595 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:79698523 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:79698515 A>C did not map to a codon.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr23:79699150 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:79698409 T>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:79698341 G>T did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:79698223 A>G did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:79699151 G>A did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:79698380 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:34148613 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:34149419 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:34148346 C>T did not map to a codon.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr23:34148353 G>A did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:34150178 G>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:34148347 G>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:34149315 G>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:34149317 A>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:34148140 C>T did not map to a codon.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr23:34149810 C>T did not map to a codon.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr23:34148352 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:34148309 C>A did not map to a codon.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr23:34148327 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:34148154 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:34150305 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00W-01A-01W-A005-10 chr23:34150043 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:34148861 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:34148900 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:34149359 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:34148838 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:34148347 G>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:34148896 C>T did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr23:34148955 C>T did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr23:34148988 C>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:34149358 C>T did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:34150285 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:34148764 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:34149946 A>C did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:34148893 G>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:34149317 A>G did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:34148257 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:34148967 G>T did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:34148348 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:34148346 C>A did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:34148591 T>C did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:34150173 G>A did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:34148876 C>G did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:34148256 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:34150179 G>A did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:34961023 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:34961002 C>T did not map to a codon.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr23:34961266 C>A did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr23:34962763 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:34962306 T>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:34961295 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:34962801 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:34961478 C>T did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:34962338 G>A did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:34962024 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:34961103 G>T did not map to a codon.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr23:34962222 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:34961037 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:34962306 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:34962029 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:34961690 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:34961216 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:34962816 T>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:34961690 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:34962304 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:34961453 G>A did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:34962304 T>C did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:34961021 C>T did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:34962304 T>C did not map to a codon.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr23:34962358 G>C did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:34962056 C>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:34961602 C>T did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:34961122 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:34961480 A>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:37027910 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:37027352 C>T did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:37028157 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:37028255 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:37028108 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:37029324 G>T did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:37027866 C>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:37028305 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:37028279 C>A did not map to a codon.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr23:37027669 A>G did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:37028539 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:37028226 C>A did not map to a codon.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr23:37026685 C>T did not map to a codon.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr23:37029365 G>C did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:37027581 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:37029563 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:37027063 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:37028718 C>T did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:37028942 A>G did not map to a codon.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr23:37027956 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:37028733 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:37029486 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:37028495 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:37603970 C>T maps to NM_001014286.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:37622721 T>C maps to NM_001014286.2 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:37618303 G>A maps to NM_001014286.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:24381366 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:24382419 G>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:24381515 T>C did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr23:24330011 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:24329793 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:24330592 C>T did not map to a codon.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr23:24329854 G>A did not map to a codon.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr23:24331424 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:16743284 G>A maps to NM_030797.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:16734205 A>G maps to NM_030797.3 *324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:130874493 G>A maps to NM_016623.3 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:130864484 G>A maps to NM_016623.3 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr8:130866568 C>T maps to NM_016623.3 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:130861608 G>A maps to NM_016623.3 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:130861515 T>C maps to NM_016623.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:130874511 G>A maps to NM_016623.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:153677293 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:153674895 A>G did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:153676897 G>A did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr6:3850629 G>A maps to NM_012135.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr6:3850152 C>T maps to NM_012135.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:3850443 G>A maps to NM_012135.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:126370820 G>A maps to NM_014661.3 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:137682515 C>A maps to NM_001135647.1 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:137680835 G>T maps to NM_001135647.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:137682560 G>A maps to NM_001135647.1 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:137680934 C>T maps to NM_001135647.1 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:137680986 C>T maps to NM_001135647.1 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:137682560 G>A maps to NM_001135647.1 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:136564054 A>C maps to NM_138419.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:26153282 C>T maps to NM_001099626.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:26156237 C>T maps to NM_001099626.1 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:114401267 T>G maps to ENST00000424269 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:114577567 G>A maps to NM_182495.5 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:114569422 T>C maps to NM_182495.5 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:101540611 C>T maps to NM_145037.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:101520683 G>A maps to NM_145037.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:101540680 C>T maps to NM_145037.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr11:114451016 T>C maps to NM_001077639.1 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:114453614 G>T maps to NM_001077639.1 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:114452462 A>G maps to NM_001077639.1 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:114453221 G>A maps to NM_001077639.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr11:114451016 T>A maps to NM_001077639.1 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr16:30040787 G>A maps to NM_031478.4 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:152861534 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:152858112 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:152860069 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:200182832 C>T maps to NM_001105517.1 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:200183335 C>T maps to NM_001105517.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:200182993 C>T maps to NM_001105517.1 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr18:29848666 G>A maps to ENST00000269209 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr18:29868112 A>G maps to ENST00000269209 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr18:29867125 A>G maps to ENST00000269209 C478C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:177250327 T>G maps to NM_021165.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr1:177249793 G>A maps to NM_021165.2 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:177226447 C>T maps to NM_021165.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr1:177249694 C>T maps to NM_021165.2 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:177199269 C>T maps to NM_021165.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:177250435 T>C maps to NM_021165.2 Y708Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:177245421 C>T maps to NM_021165.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:177249820 T>C maps to NM_021165.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:177245346 G>A maps to NM_021165.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:177250621 G>A maps to NM_021165.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:190068146 G>A maps to NM_199051.1 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr1:190067270 G>A maps to NM_199051.1 C726C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr1:190068113 G>A maps to NM_199051.1 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:190067180 T>C maps to NM_199051.1 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:190067180 T>C maps to NM_199051.1 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr1:190250768 A>G maps to NM_199051.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:190067324 G>A maps to NM_199051.1 D708D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:190250768 A>G maps to NM_199051.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr1:190250768 A>G maps to NM_199051.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:31440632 T>G maps to NM_001135812.1 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:150970608 A>G maps to NM_001163258.1 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:67575618 C>A maps to NM_001193523.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:67576719 C>T maps to NM_001193523.1 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr16:67580317 C>T maps to NM_001193523.1 A1224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr16:67576566 C>A maps to NM_001193523.1 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:67573990 G>A maps to NM_001193523.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:24806639 G>A maps to NM_014722.2 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:24843134 A>G maps to NM_014722.2 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:24843179 C>T maps to NM_014722.2 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:24843614 C>T maps to NM_014722.2 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:49225212 G>A maps to NM_080829.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr20:49218613 G>A maps to NM_080829.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr20:49221289 G>A maps to NM_080829.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:49218764 G>A maps to NM_080829.2 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:139612126 G>A maps to NM_152421.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:119410882 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:119445131 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:119410800 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr23:119445137 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:119394779 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:119419525 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:119425123 G>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:119410880 C>T did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:119410882 C>A did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:119410882 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:212798647 C>T maps to NM_153606.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:212798350 G>A maps to NM_153606.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr5:156590099 T>C maps to NM_130899.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:156589466 T>C maps to NM_130899.2 K603K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:156589817 G>A maps to NM_130899.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:156590054 G>C maps to NM_130899.2 Y407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:156590504 A>G maps to NM_130899.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:156593131 A>C maps to NM_130899.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:156590504 A>G maps to NM_130899.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr5:156590099 T>C maps to NM_130899.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:156590150 C>T maps to NM_130899.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:100041975 G>A maps to NM_153364.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr12:100042383 G>A maps to NM_153364.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:100042239 C>T maps to NM_153364.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr12:100042095 C>T maps to NM_153364.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr12:100042056 C>T maps to NM_153364.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:67671481 C>T maps to NM_173526.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:50979134 G>A maps to ENST00000391816 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr19:50971049 G>A maps to ENST00000391816 H192H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:128315871 C>A maps to NM_001012454.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:120854555 A>G maps to NM_001100910.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:78325043 A>G maps to NM_198549.2 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr1:78338708 C>G maps to NM_198549.2 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:78329637 A>G maps to NM_198549.2 E478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:78309041 C>T maps to NM_198549.2 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:131804642 C>T maps to NM_032809.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:131812136 G>A maps to NM_032809.2 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:40704209 C>T maps to NM_001083124.1 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:43630672 A>C maps to NM_001145196.1 L10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:90535520 G>A maps to NM_001145124.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:134151557 A>G maps to NM_033387.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr9:134151299 G>A maps to NM_033387.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr1:166039924 A>T maps to NM_001017961.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:166039834 G>A maps to NM_001017961.3 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:166135352 T>A maps to NM_001017961.3 K45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr15:59752197 C>T maps to NM_152450.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:94756011 C>T maps to NM_152548.2 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:94784151 G>A maps to NM_152548.2 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:94764393 C>T maps to NM_152548.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:38202381 C>T maps to NM_144713.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr2:38179074 C>T maps to NM_144713.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:38179074 C>A maps to NM_144713.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr15:41044217 G>A maps to NM_018145.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:41046903 G>A maps to NM_018145.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:87500862 C>A maps to NM_016033.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:87492519 G>A maps to NM_016033.2 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr8:87498712 C>T maps to NM_016033.2 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr8:124219412 G>T maps to NM_032899.4 G264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:54804566 T>C maps to NM_001010872.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:54805295 G>A maps to NM_001010872.1 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr6:54804566 T>C maps to NM_001010872.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr6:54806537 T>A maps to NM_001010872.1 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:54804566 T>C maps to NM_001010872.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:54805115 G>A maps to NM_001010872.1 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:54804566 T>C maps to NM_001010872.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr20:33879792 G>C maps to NM_178468.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr20:33875144 C>T maps to NM_178468.4 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr20:37580955 A>G maps to NM_030919.2 E547E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:37580838 C>A maps to NM_030919.2 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr20:37580832 G>A maps to NM_030919.2 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr20:37580955 A>G maps to NM_030919.2 E547E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:49107101 G>A maps to NM_017708.3 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:49113188 G>T maps to NM_017708.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr19:49116437 A>G maps to NM_017708.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:18874869 G>A maps to NM_001039999.2 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:18881469 G>A maps to NM_001039999.2 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:18891616 G>A maps to NM_001039999.2 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:144812307 G>A maps to NM_198488.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:144808303 C>T maps to NM_198488.3 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr8:144810283 G>A maps to NM_198488.3 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:144808600 C>A maps to NM_198488.3 T1010T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr8:144808164 C>A maps to NM_198488.3 E1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:14774954 C>T maps to NM_145175.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:127569487 C>T maps to NM_174911.4 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:5140530 C>T maps to NM_201400.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:17602825 G>T maps to NM_016255.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr12:8377371 G>T maps to NM_018088.3 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr12:8375281 G>T maps to NM_018088.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:124789509 T>C maps to NM_144963.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:124817527 G>T maps to NM_144963.2 G611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr8:124811839 A>G maps to NM_144963.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:94740444 C>T maps to ENST00000452913 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr8:94713616 G>A maps to ENST00000452913 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:85143978 C>T maps to ENST00000393246 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr16:85141692 C>A maps to ENST00000393246 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr15:64373323 G>A maps to NM_032231.4 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:33810163 G>A maps to ENST00000395190 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:33810415 G>A maps to ENST00000395190 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:33810009 G>A maps to ENST00000395190 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr2:33810436 C>T maps to ENST00000395190 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr15:38776832 T>A maps to NM_173611.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:38776700 A>T maps to NM_173611.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:38896166 G>A maps to NM_174905.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:8766515 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:8768147 G>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:8761779 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:8764366 C>T did not map to a codon.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr23:8997445 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:8998382 C>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:9000412 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:9000468 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:9000418 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:8995963 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:13058907 T>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:89833629 T>C maps to NM_000135.2 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:89813021 C>T maps to NM_000135.2 T1161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:89845228 C>T maps to NM_000135.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:14863357 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:14862650 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:14882985 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:14861942 C>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:14861870 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:14882735 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:14883282 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:14863104 T>C did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:14862791 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:97864099 G>T maps to NM_000136.2 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr3:10128850 A>G maps to NM_033084.3 Q1123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:10133903 C>T maps to NM_033084.3 R1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr3:10076914 C>T maps to NM_033084.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:10084750 G>A maps to NM_033084.3 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:10106039 G>T maps to NM_033084.3 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr3:10128850 A>G maps to NM_033084.3 Q1123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:35423685 G>A maps to NM_021922.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:22646549 C>T maps to NM_022725.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:35075291 A>G maps to NM_004629.1 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr9:35076547 C>T maps to NM_004629.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:35074491 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:35074152 G>T maps to NM_004629.1 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:58392928 G>A maps to NM_001114636.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr2:58388662 T>C maps to NM_001114636.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:45645388 C>T maps to NM_020937.2 F1144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr14:45636335 C>T maps to NM_020937.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr14:45644953 G>A maps to NM_020937.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr14:45618122 T>G maps to NM_020937.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr14:45658222 A>G maps to NM_020937.2 R1666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:45605590 T>C maps to NM_020937.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:45633644 T>G maps to NM_020937.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:127697109 G>A maps to ENST00000368692 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr10:127697034 G>A maps to ENST00000368692 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:127697034 G>A maps to ENST00000368692 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:127697109 G>A maps to ENST00000368692 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:127697034 G>T maps to ENST00000368692 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:163027569 G>A maps to NM_004460.2 H734H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr2:163074522 A>G maps to NM_004460.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:163074537 G>A maps to NM_004460.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:163074522 A>G maps to NM_004460.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:163072472 G>A maps to NM_004460.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:13749137 A>G maps to NM_032228.5 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:29450070 G>A maps to NM_018099.3 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr13:99038037 C>T maps to NM_005766.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr13:99061769 C>T maps to NM_005766.2 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:99040701 C>A maps to NM_005766.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:99087924 T>C maps to NM_005766.2 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:99064273 A>G maps to NM_005766.2 Q604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:99100529 C>T maps to NM_005766.2 R1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:242415308 A>G maps to NM_014808.2 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:242343250 C>T maps to NM_014808.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:242380759 A>G maps to NM_014808.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:242430474 G>C did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:5613418 G>A maps to NM_006567.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:5431350 G>T maps to NM_006567.3 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr19:13039174 G>A maps to NM_004461.2 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:223513509 G>A maps to NM_005687.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr2:223464782 G>C maps to NM_005687.3 Y494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:172628517 G>A maps to NM_000639.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr1:172628391 C>T maps to NM_000639.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:172628520 G>A maps to NM_000639.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:80048266 G>A maps to NM_004104.4 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:80044375 G>A maps to NM_004104.4 P1162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:80039072 G>A maps to NM_004104.4 Q2188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:80042476 G>A maps to NM_004104.4 G1560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:80043275 G>A maps to NM_004104.4 D1375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr7:150774113 C>T maps to NM_006712.3 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr2:170428266 A>G maps to NM_024622.3 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:170394535 T>C maps to NM_024622.3 Q687Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:170394537 G>A maps to NM_024622.3 Q687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:170428479 A>C maps to NM_024622.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:170387168 A>G maps to NM_024622.3 N790N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr2:170394535 T>C maps to NM_024622.3 Q687Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:207652688 T>C maps to NM_014929.3 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:7861311 C>A maps to NM_024091.3 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:7867230 G>A maps to NM_024091.3 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr5:7867782 A>G maps to NM_024091.3 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr5:7867092 A>G maps to NM_024091.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr5:7867782 A>G maps to NM_024091.3 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:3128516 G>A maps to NM_021826.4 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:187540140 A>G maps to ENST00000260147 N2536N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:187628614 G>T maps to ENST00000260147 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:187524651 G>A maps to ENST00000260147 N3679N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:187540872 C>T maps to ENST00000260147 A2292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:187630711 G>A maps to ENST00000260147 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:187534319 C>A maps to ENST00000260147 E3139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr4:187518842 C>A maps to ENST00000260147 G4124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:187517919 C>T maps to ENST00000260147 P4261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:187542150 C>T maps to ENST00000260147 A1866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:187540602 G>A maps to ENST00000260147 D2382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:187522485 G>A maps to ENST00000260147 L3862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:187517778 C>T maps to ENST00000260147 A4308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:187518852 C>T maps to ENST00000260147 S4120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:187627927 A>G maps to ENST00000260147 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:187628365 G>A maps to ENST00000260147 S872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr4:187540227 G>A maps to ENST00000260147 N2507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr4:187629913 A>C maps to ENST00000260147 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:187518258 C>T maps to ENST00000260147 T4148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:187518018 C>T maps to ENST00000260147 T4228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:187525662 G>A maps to ENST00000260147 N3475N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:187539012 G>A maps to ENST00000260147 T2912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr5:150945611 G>A maps to NM_001447.2 R961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:150914045 G>A maps to NM_001447.2 H3117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:150891828 G>A maps to NM_001447.2 G3934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00W-01A-01W-A005-10 chr5:150948444 C>T maps to NM_001447.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:150946746 C>T maps to NM_001447.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:150933922 C>T maps to NM_001447.2 T1315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:150924143 C>A maps to NM_001447.2 E2182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:150922788 G>T maps to NM_001447.2 V2633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:150925629 G>A maps to NM_001447.2 S1686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:150920313 G>T maps to NM_001447.2 P2951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:150947892 G>A maps to NM_001447.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:150925425 A>G maps to NM_001447.2 N1754N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:150947828 G>A maps to NM_001447.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr5:150933922 C>T maps to NM_001447.2 T1315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:150923088 G>T maps to NM_001447.2 P2533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:150945558 T>G maps to NM_001447.2 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr5:150945378 C>T maps to NM_001447.2 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:150911529 G>A maps to NM_001447.2 G3143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr5:150947718 C>T maps to NM_001447.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr11:92531026 C>A maps to ENST00000298047 I1616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:92577515 C>T maps to ENST00000298047 F3661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:92087551 T>C maps to ENST00000298047 N758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:92088176 C>T maps to ENST00000298047 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:92600166 G>A maps to ENST00000298047 T3973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:92086870 T>C maps to ENST00000298047 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr11:92624170 C>T maps to ENST00000298047 G4554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:92615948 C>T maps to ENST00000298047 N4109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr11:92564830 T>A maps to ENST00000298047 G3175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr11:92565031 G>A maps to ENST00000298047 L3242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:92533004 C>T maps to ENST00000298047 L2276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:92534137 C>T maps to ENST00000298047 I2653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:92534392 C>A maps to ENST00000298047 V2738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:92531137 T>G maps to ENST00000298047 A1653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:92087596 C>A maps to ENST00000298047 C773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:92534101 C>T maps to ENST00000298047 S2641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:92577197 A>G maps to ENST00000298047 E3555E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:92565106 A>G maps to ENST00000298047 T3267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr11:92087131 A>T maps to ENST00000298047 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr11:92590392 G>A maps to ENST00000298047 P3793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:92577818 C>T maps to ENST00000298047 H3762H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:92086087 T>A maps to ENST00000298047 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:92531590 C>T maps to ENST00000298047 D1804D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:92430581 C>T maps to ENST00000298047 R1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:92577515 C>T maps to ENST00000298047 F3661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:92592425 C>T maps to ENST00000298047 R3866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:92535040 C>T maps to ENST00000298047 S2954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr11:92534641 C>A maps to ENST00000298047 T2821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:92533039 C>T maps to ENST00000298047 F2287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:92087648 C>T maps to ENST00000298047 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr11:92534269 C>T maps to ENST00000298047 H2697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr11:92615972 C>T maps to ENST00000298047 F4117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr11:92623744 G>A maps to ENST00000298047 G4412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:92086159 G>A maps to ENST00000298047 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:92534287 G>A maps to ENST00000298047 T2703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:92577314 C>T maps to ENST00000298047 S3594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:92086993 C>T maps to ENST00000298047 N572N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:92534953 G>A maps to ENST00000298047 A2925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr4:126242618 C>T maps to NM_024582.4 R1685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr4:126241924 T>C maps to NM_024582.4 G1453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr4:126240716 C>T maps to NM_024582.4 Q1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr4:126373381 C>T maps to NM_024582.4 A3737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr4:126242249 G>T maps to NM_024582.4 E1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:126398384 A>G maps to NM_024582.4 G4123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:126238576 C>T maps to NM_024582.4 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:126373625 C>T maps to NM_024582.4 R3819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:126240481 T>C maps to NM_024582.4 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:126240310 C>A maps to NM_024582.4 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr4:126372658 A>G maps to NM_024582.4 L3496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:126238927 G>A maps to NM_024582.4 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:126238393 C>T maps to NM_024582.4 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:126239173 C>A maps to NM_024582.4 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:126373339 G>A maps to NM_024582.4 K3723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:126372820 C>T maps to NM_024582.4 S3550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:126372541 G>A maps to NM_024582.4 P3457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:126336756 C>T maps to NM_024582.4 V2213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:126370340 G>T maps to NM_024582.4 E2724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:126371437 C>T maps to NM_024582.4 F3089F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr4:126400913 C>T maps to NM_024582.4 G4164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr4:126412604 T>C maps to NM_024582.4 S4876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:126239890 C>T maps to NM_024582.4 N775N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:126238663 G>A maps to NM_024582.4 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:126239623 C>T maps to NM_024582.4 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:126355484 G>A maps to NM_024582.4 A2368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:126241852 T>A maps to NM_024582.4 I1429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr4:126238573 C>T maps to NM_024582.4 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:126242081 G>T maps to NM_024582.4 E1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:126242398 G>A maps to NM_024582.4 R1611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:126336448 G>T maps to NM_024582.4 E2111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:126369631 G>A maps to NM_024582.4 A2487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:126370700 C>T maps to NM_024582.4 R2844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:126336507 T>C maps to NM_024582.4 G2130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr4:126373165 T>C maps to NM_024582.4 T3665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr4:126241924 T>C maps to NM_024582.4 G1453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr4:126329632 T>C maps to NM_024582.4 D1868D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr4:126239152 C>T maps to NM_024582.4 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr4:126238414 G>A maps to NM_024582.4 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr4:126238561 C>T maps to NM_024582.4 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:126241852 T>A maps to NM_024582.4 I1429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr4:126328106 G>T maps to NM_024582.4 G1794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr4:126240976 T>C maps to NM_024582.4 Y1137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr4:126411630 G>T maps to NM_024582.4 E4552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr4:126389778 G>A maps to NM_024582.4 T4004T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr4:126373472 C>T maps to NM_024582.4 R3768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr4:126241852 T>A maps to NM_024582.4 I1429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:126238483 G>A maps to NM_024582.4 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr23:150890398 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:150891180 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:150889902 T>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:150890397 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:150884672 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:73933671 T>C maps to ENST00000389570 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:40329740 A>G maps to NM_001436.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:40325321 G>A maps to NM_001436.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:40331394 G>A maps to NM_001436.3 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr19:40331398 G>A maps to NM_001436.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:16101279 C>T maps to NM_017556.2 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr1:16111113 C>T maps to NM_017556.2 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr22:45938047 C>T maps to ENST00000348697 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr22:45944505 C>T maps to ENST00000348697 C485C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:13663398 G>A maps to NM_001165035.1 A760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:13660437 G>A maps to NM_001165035.1 E658E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:13679214 C>T maps to NM_001165035.1 I1164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:13677981 C>T maps to NM_001165035.1 S1084S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:13670438 T>C maps to NM_001165035.1 C868C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:92347724 G>A maps to ENST00000267620 N397N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:92349412 G>A maps to ENST00000267620 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:92347649 C>T maps to ENST00000267620 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr14:92403370 G>T maps to ENST00000267620 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr2:112942838 C>T maps to NM_153214.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:112944905 C>T maps to NM_153214.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:112940488 C>T maps to NM_153214.2 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr15:48766464 G>A maps to NM_000138.4 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:48725168 G>A maps to NM_000138.4 A2211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:48703476 G>A maps to NM_000138.4 R2776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:48829904 G>A maps to NM_000138.4 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:48755377 C>A maps to NM_000138.4 E1709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr15:48719917 G>A maps to NM_000138.4 I2350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr15:48748873 T>C maps to NM_000138.4 P1794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr15:48729200 G>A maps to NM_000138.4 C2151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr15:48766553 C>A maps to NM_000138.4 G1370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr15:48788315 A>G maps to NM_000138.4 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:48788294 A>G did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:48787771 G>A maps to NM_000138.4 C811C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr15:48718035 G>A maps to NM_000138.4 H2410H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:48713848 G>A maps to NM_000138.4 C2535C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr15:48718025 G>A maps to NM_000138.4 R2414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr15:48707932 G>A maps to NM_000138.4 C2617C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:48812925 G>T maps to NM_000138.4 C359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr5:127645047 A>G maps to NM_001999.3 T1748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:127641314 G>A maps to NM_001999.3 C1854C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:127673806 G>A maps to NM_001999.3 D1160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:127685159 A>C maps to NM_001999.3 V956V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:127713525 G>A maps to NM_001999.3 R590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr5:127680194 A>G maps to NM_001999.3 N1075N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr5:127700374 C>G maps to NM_001999.3 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr5:127728858 G>A maps to NM_001999.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:127610259 G>A maps to NM_001999.3 I2570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr5:127599223 G>A maps to NM_001999.3 D2695D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:127712496 G>T maps to NM_001999.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:127637113 G>A maps to NM_001999.3 N2002N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:127654613 G>A maps to NM_001999.3 C1517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:127611838 G>A maps to NM_001999.3 C2495C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:127641611 G>A maps to NM_001999.3 G1817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:127595386 A>G maps to NM_001999.3 R2833R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:127686611 G>A maps to NM_001999.3 C920C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:127599169 C>T maps to NM_001999.3 T2713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:127728870 G>A maps to NM_001999.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr5:127595386 A>G maps to NM_001999.3 R2833R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:127697482 C>A maps to NM_001999.3 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr5:127595386 A>G maps to NM_001999.3 R2833R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:8150343 C>A maps to NM_032447.3 R2330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:8176044 G>A maps to NM_032447.3 N1369N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr19:8161800 G>A maps to NM_032447.3 R1793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:8176568 G>A maps to NM_032447.3 C1349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:8140179 G>A maps to NM_032447.3 G2523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:8152974 G>T maps to NM_032447.3 G2155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:8175807 G>A maps to NM_032447.3 S1418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:8196609 C>T maps to NM_032447.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:8154983 G>A maps to NM_032447.3 S2061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:8152018 G>A maps to NM_032447.3 F2232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr19:8191394 G>T maps to NM_032447.3 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:8174599 G>A maps to NM_032447.3 N1457N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr9:97349726 G>A maps to NM_003837.2 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:97333872 A>G maps to NM_003837.2 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr9:97355957 G>A maps to NM_003837.2 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:102566733 G>A maps to NM_145032.3 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:102553634 A>G maps to NM_145032.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:102669145 T>A maps to NM_145032.3 K40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr7:102566785 C>T maps to NM_145032.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:104182674 G>A maps to NM_024326.3 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:746985 C>T maps to NM_153350.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr7:5540276 C>A maps to ENST00000312577 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:5541407 G>A maps to ENST00000312577 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr16:30939831 C>T maps to NM_001099784.2 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:30938630 C>T maps to NM_001099784.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:33415147 G>A maps to NM_012157.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:33416889 T>C maps to NM_012157.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:33427045 G>A maps to NM_012157.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:33406148 C>T maps to NM_012157.3 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:37420534 G>A maps to NM_032875.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr17:37431305 C>T maps to NM_032875.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:37455309 G>A maps to NM_032875.2 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:135276972 C>T maps to NM_012159.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:135276972 C>T maps to NM_012159.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr5:135276349 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:77589589 T>G maps to NM_012158.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:99374513 C>T maps to NM_012160.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr6:99374411 G>A maps to NM_012160.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:99365357 G>T maps to NM_012160.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:15638153 C>T maps to NM_012161.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr8:145579963 A>G maps to NM_012162.1 C407C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr8:145579966 T>C maps to NM_012162.1 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:145579782 G>A maps to NM_012162.1 C439C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:145579772 G>A maps to NM_012162.1 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr8:145580512 C>T maps to NM_012162.1 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr5:15928350 G>T maps to NM_012304.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:15616143 G>A maps to NM_012304.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr5:15936658 G>A maps to NM_012304.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr5:15936994 C>T maps to NM_012304.3 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:15937066 C>T maps to NM_012304.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr5:15936964 C>T maps to NM_012304.3 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:15936859 G>A maps to NM_012304.3 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr5:15936616 C>T maps to NM_012304.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:15937267 C>T maps to NM_012304.3 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr5:15937087 G>A maps to NM_012304.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:67197170 G>A maps to NM_018378.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:37516058 C>T maps to NM_012166.2 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr9:37537814 G>A maps to NM_012166.2 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:37518346 G>T maps to NM_012166.2 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:37521629 G>A maps to NM_012166.2 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:37518142 C>T maps to NM_012166.2 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:37522870 C>A maps to NM_012166.2 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:48063015 G>A maps to NM_001190274.1 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:48066029 G>T maps to NM_001190274.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:48066864 A>G maps to NM_001190274.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:48045928 C>A maps to NM_001190274.1 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr18:71740833 G>A maps to NM_001142958.1 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr18:71740791 C>T maps to NM_001142958.1 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:71797880 G>A maps to NM_001142958.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr18:71740791 C>T maps to NM_001142958.1 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:39435737 G>A maps to ENST00000448145 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:5960395 C>T maps to NM_032807.3 N736N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:5948408 T>C maps to NM_032807.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:5963483 C>T maps to NM_032807.3 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr10:5963426 C>T maps to NM_032807.3 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:5965658 C>T maps to NM_032807.3 Q851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:5959450 G>A maps to NM_032807.3 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:5978483 G>A maps to NM_032807.3 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:11710105 C>T maps to NM_012168.4 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:117615421 G>A maps to NM_033624.2 Y165Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:117615421 G>A maps to NM_033624.2 Y165Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr15:76222307 C>T maps to NM_147188.2 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:100198306 C>T maps to NM_012172.4 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:100192162 A>G maps to NM_012172.4 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr7:100198500 G>T maps to NM_012172.4 G612G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr7:100190452 C>T maps to NM_012172.4 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr7:100190452 C>T maps to NM_012172.4 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:39521868 C>T maps to NM_178820.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr19:39517629 G>A maps to NM_178820.3 H196H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr19:39521862 G>A maps to NM_178820.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:39516071 G>A maps to NM_178820.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:39517629 G>A maps to NM_178820.3 H196H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr1:224345375 T>C maps to NM_015176.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr1:224345354 C>T maps to NM_015176.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:146126917 G>A maps to NM_032145.4 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:146125579 A>G maps to NM_032145.4 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr6:146125579 A>G maps to NM_032145.4 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:87368969 G>A maps to NM_024735.3 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:87369858 C>T maps to NM_024735.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:87365025 G>A maps to NM_024735.3 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr14:39870629 T>C maps to NM_203301.3 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:55818103 C>A maps to NM_152231.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:55818418 A>G maps to NM_152231.1 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr14:55818418 A>G maps to NM_152231.1 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:230875524 C>A maps to NM_174899.4 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:147806801 C>T maps to NM_205836.1 R649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:147806801 C>T maps to NM_205836.1 R649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:147820772 C>T maps to NM_205836.1 R1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:147795557 T>C maps to NM_205836.1 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:147806821 T>C maps to NM_205836.1 H655H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:147795507 C>T maps to NM_205836.1 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr5:147795557 T>C maps to NM_205836.1 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr17:6683780 C>G maps to NM_153230.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:6683786 C>T maps to NM_153230.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:6684107 G>A maps to NM_153230.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:6683399 T>C maps to NM_153230.2 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:6690669 C>T maps to NM_153230.2 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:41939552 G>A maps to NM_012176.2 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr5:41941370 G>A maps to NM_012176.2 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:121340971 A>C maps to NM_016298.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:121340692 A>G maps to NM_016298.3 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr3:121341409 G>T maps to NM_016298.3 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:121340509 C>T maps to NM_016298.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:121345660 G>A maps to NM_016298.3 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:121341803 C>T maps to NM_016298.3 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:121345660 G>A maps to NM_016298.3 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:73496005 C>T maps to ENST00000295133 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:16580146 G>T maps to NM_018994.1 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:101154373 C>T maps to NM_001029860.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:101154207 C>A maps to NM_001029860.3 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr8:101153575 C>T maps to NM_001029860.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:101146523 A>G maps to NM_001029860.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr8:101153749 T>C maps to NM_001029860.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:46216543 A>G maps to NM_001080469.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:46216447 G>T maps to NM_001080469.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:46216045 C>T maps to NM_001080469.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:46215283 C>T maps to NM_001080469.1 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr19:46216375 G>A maps to NM_001080469.1 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:46215736 C>T maps to NM_001080469.1 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:68692130 C>T maps to NM_001024680.1 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:68692186 G>A maps to NM_001024680.1 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr6:153293472 T>C maps to NM_012177.3 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:153296115 G>A maps to NM_012177.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:153292420 C>T maps to NM_012177.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:153296744 C>A maps to NM_012177.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:32880053 T>C maps to NM_012179.3 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr4:175184039 G>A maps to NM_012180.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:175184057 C>T maps to NM_012180.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr4:175162327 C>T maps to NM_012180.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr4:175158715 T>A maps to NM_012180.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:52935851 C>T maps to NM_012347.4 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:52945765 C>T maps to NM_012347.4 Y146Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DM-A1D9-01A-11D-A152-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:18668093 C>T maps to ENST00000395665 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:18681918 C>T maps to ENST00000395665 Q823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr17:18653078 A>C maps to ENST00000395665 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:18682092 C>T maps to ENST00000395665 R881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:171327012 C>T maps to NM_012300.2 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:171326005 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:48414290 C>T maps to NM_207102.2 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:48423199 C>T maps to NM_207102.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:48414290 C>T maps to NM_207102.2 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:48423199 C>T maps to NM_207102.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:123538406 C>A maps to NM_012164.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr10:103371382 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:103371149 C>T maps to ENST00000331272 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:103371429 G>A maps to ENST00000331272 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr10:103372098 G>A maps to ENST00000331272 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:103432677 C>T maps to ENST00000331272 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:139835460 G>A maps to NM_018998.2 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr9:139837323 G>T maps to NM_018998.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:153247366 G>A maps to NM_033632.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:153332916 T>C maps to NM_033632.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:153247364 T>C maps to NM_033632.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr4:153244077 T>C maps to NM_033632.2 E693E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr4:153247366 G>A maps to NM_033632.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:153244089 C>T maps to NM_033632.2 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr4:153249456 G>T maps to NM_033632.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr4:153244209 C>T maps to NM_033632.2 W649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr4:153332661 T>C maps to NM_033632.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr4:153332918 G>A maps to NM_033632.2 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:153253823 T>C maps to NM_033632.2 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr4:153332916 T>C maps to NM_033632.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr4:153251906 G>A maps to NM_033632.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr4:153251906 G>A maps to NM_033632.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr4:153251990 T>A maps to NM_033632.2 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr4:153253787 A>G maps to NM_033632.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:153332523 C>T maps to NM_033632.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:153245449 G>A maps to NM_033632.2 Q581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr4:153251894 T>A maps to NM_033632.2 K371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:153303406 A>G maps to NM_001013415.1 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:153332678 C>A maps to NM_033632.2 G93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr4:153244205 A>G maps to NM_033632.2 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:153253787 A>G maps to NM_033632.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr4:153245342 T>A maps to NM_033632.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:153249382 A>G maps to NM_033632.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr4:153245402 A>T maps to NM_033632.2 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr4:153251906 G>A maps to NM_033632.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr4:153244140 C>T maps to NM_033632.2 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr4:153253796 T>C maps to NM_033632.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:153244077 T>C maps to NM_033632.2 E693E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr4:153332463 T>C maps to NM_033632.2 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr4:153271205 G>C maps to NM_033632.2 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr4:153253787 A>G maps to NM_033632.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr4:153258969 G>T maps to NM_033632.2 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:153244203 C>T maps to NM_033632.2 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr4:153249382 A>G maps to NM_033632.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr4:153247172 T>C maps to NM_033632.2 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr4:153332916 T>C maps to NM_033632.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr4:153247166 A>G maps to NM_033632.2 Y545Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr4:153247166 A>G maps to NM_033632.2 Y545Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr4:153253823 T>C maps to NM_033632.2 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr4:153258980 T>C maps to NM_033632.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr4:153249508 T>A maps to NM_033632.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr4:153332661 T>C maps to NM_033632.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr4:153247220 A>G maps to NM_033632.2 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr4:153332915 G>A maps to NM_033632.2 R14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr4:153268147 T>C maps to NM_033632.2 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr4:153244077 T>C maps to NM_033632.2 E693E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr4:153249517 A>G maps to NM_033632.2 H420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr4:153251904 T>C maps to NM_033632.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr4:153249439 C>T maps to NM_033632.2 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr4:153245445 G>T maps to NM_033632.2 S582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr4:153268147 T>C maps to NM_033632.2 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr4:153249440 C>T maps to NM_033632.2 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr4:153249439 C>T maps to NM_033632.2 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr4:153258980 T>C maps to NM_033632.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr4:153259022 T>C maps to NM_033632.2 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr4:153332922 T>C maps to NM_033632.2 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr4:153253871 C>T did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr4:153253871 C>A did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr4:153249508 T>C maps to NM_033632.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:153249456 G>T maps to NM_033632.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr4:153253838 G>A maps to NM_033632.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:117423200 G>A maps to NM_153348.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr19:12800595 G>A maps to ENST00000380339 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:12805672 G>A maps to ENST00000380339 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:207140972 T>C maps to NM_001170631.1 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:207135702 A>G maps to NM_001170631.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:207131861 C>T maps to NM_001170631.1 *578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:207135630 G>A maps to NM_001170631.1 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:55396899 A>G maps to NM_002000.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:55396743 C>A maps to NM_002000.2 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr19:7755055 G>A maps to NM_002002.4 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr14:75200825 A>G maps to NM_015962.4 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr14:75200825 A>G maps to NM_015962.4 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:40433200 G>A maps to NM_003890.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:40433041 G>A maps to NM_003890.2 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:40392670 G>A maps to NM_003890.2 G2611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:40421415 G>A maps to NM_003890.2 C835C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:40433092 C>T maps to NM_003890.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:40366556 G>A maps to NM_003890.2 F4559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:40382676 C>T maps to NM_003890.2 A3403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:40421292 G>A maps to NM_003890.2 D876D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:40366424 C>A maps to NM_003890.2 A4603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:40430340 G>A maps to NM_003890.2 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:40433200 G>A maps to NM_003890.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr19:40366142 G>A maps to NM_003890.2 D4697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:40424315 C>T maps to NM_003890.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:40364355 G>A maps to NM_003890.2 P4762P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr19:40408314 G>A maps to NM_003890.2 Y1508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr19:40433542 C>T maps to NM_003890.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:40367822 G>A maps to NM_003890.2 A4379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:40411889 G>T maps to NM_003890.2 A1246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:40366457 A>G maps to NM_003890.2 D4592D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:40424192 G>A maps to NM_003890.2 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:40424419 G>A maps to NM_003890.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr1:161479631 T>C maps to NM_001136219.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr1:161487913 C>T maps to NM_001136219.1 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:161641410 C>T maps to NM_004001.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:161641284 C>T maps to NM_004001.4 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:161559502 G>A maps to NM_201563.4 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr1:161569496 C>T maps to NM_201563.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:161559541 C>T maps to NM_201563.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:161559487 C>A maps to NM_201563.4 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:161512912 A>C maps to NM_000569.6 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:161599760 A>G maps to ENST00000367964 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:17893963 C>T maps to NM_015122.2 N692N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:17877510 C>A maps to NM_015122.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:72286422 G>T maps to NM_138782.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:72313047 G>T maps to NM_138782.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:72377613 C>A maps to NM_138782.2 S662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:72377620 T>C maps to NM_138782.2 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr5:72286676 A>C maps to NM_138782.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:141027588 A>C maps to ENST00000354789 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:141026178 A>G maps to ENST00000354789 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:141027072 C>T maps to ENST00000354789 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:141026259 G>A maps to ENST00000354789 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:72552499 G>A maps to ENST00000409314 N709N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:72549835 T>C maps to ENST00000409314 *765W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr11:72553806 A>G maps to ENST00000409314 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:72600903 A>C maps to ENST00000409314 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:72560904 G>A maps to ENST00000409314 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:72712058 G>A maps to ENST00000409314 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:72554253 C>T maps to ENST00000409314 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:72554352 T>C maps to ENST00000409314 Q540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:72579047 G>A maps to ENST00000409314 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:137804915 G>A maps to NM_002003.3 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:137801784 G>A maps to NM_002003.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:137804392 G>A maps to NM_002003.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:137775172 T>C maps to NM_004108.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:27695921 G>A maps to NM_003665.2 D235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr1:27695731 G>A maps to NM_003665.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:27699707 G>A maps to NM_003665.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:157772380 G>A maps to NM_052938.4 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:157771885 A>G maps to NM_052938.4 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr1:157737147 C>T maps to NM_030764.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:157740379 G>A maps to NM_030764.3 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:157737186 G>A maps to NM_030764.3 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:157738450 G>C maps to NM_030764.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:157739893 G>A maps to NM_030764.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr1:157665980 T>C maps to NM_052939.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr1:157666076 G>A maps to NM_052939.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:157648556 T>C maps to NM_052939.3 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:157650855 C>T maps to NM_052939.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr1:157667155 G>T maps to NM_052939.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr1:157667560 G>T maps to NM_052939.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr1:157659609 G>A maps to NM_052939.3 Y596Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:157665980 T>C maps to NM_052939.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr1:157665980 T>C maps to NM_052939.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr1:157557883 A>C maps to NM_031282.2 Y111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:157559003 G>T maps to NM_031282.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:157557186 C>T maps to NM_031282.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:157557705 C>A maps to NM_031282.2 G171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:157559003 G>T maps to NM_031282.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr1:157559003 G>T maps to NM_031282.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr1:157557703 T>C maps to NM_031282.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:157512685 G>A maps to NM_031281.2 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:157490846 G>A maps to NM_031281.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:157494198 G>T maps to NM_031281.2 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr1:157514277 T>C maps to NM_031281.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:159785377 C>A maps to NM_001004310.2 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:159785345 G>A maps to NM_001004310.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr1:161681928 C>T maps to NM_001184866.1 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:161681259 C>T maps to NM_001184866.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:161697382 G>A maps to NM_001002901.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:161695809 G>A maps to NM_001002901.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:161693353 C>T maps to NM_001002901.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:161697217 G>A maps to NM_001002901.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:161696643 G>A maps to NM_001002901.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr8:11683555 G>A maps to NM_004462.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:155282170 C>T maps to NM_001135821.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:155279944 G>A maps to NM_001135821.1 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:10421250 G>A maps to NM_001031734.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:10426119 A>G maps to NM_001031734.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:111746626 T>G maps to NM_138378.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:111746122 A>G maps to NM_138378.1 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:111745738 G>T maps to NM_138378.1 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:72861038 C>T maps to ENST00000442102 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:72861007 G>A maps to ENST00000442102 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr18:55247405 A>G maps to NM_001012515.2 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:4792954 G>A maps to NM_018708.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:4793794 G>A maps to NM_018708.2 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:4793680 C>A maps to NM_018708.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:4793719 C>T maps to NM_018708.2 Y618Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:68582431 C>A maps to NM_015322.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr15:68583558 A>G maps to NM_015322.3 E621E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:114860604 G>A maps to NM_020177.2 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:114878875 A>G maps to NM_020177.2 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:61563117 C>T maps to NM_004111.4 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:108171462 G>T maps to NM_005246.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:108521973 T>C maps to NM_005246.2 C759C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr5:108516582 A>G maps to NM_005246.2 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:108219162 T>G maps to NM_005246.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:108294939 C>T maps to NM_005246.2 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:108233524 A>G maps to NM_005246.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr5:108233524 A>G maps to NM_005246.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr5:108516582 A>G maps to NM_005246.2 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr5:108290478 G>A maps to NM_005246.2 W460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:108516582 A>G maps to NM_005246.2 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr5:108233524 A>G maps to NM_005246.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:108290479 G>A maps to NM_005246.2 W460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:97327430 C>T maps to NM_001113382.1 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:97368968 C>T maps to NM_001113382.1 A1895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:97370065 A>G maps to NM_001113382.1 A2008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:97370410 T>C maps to NM_001113382.1 L2088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:97356309 C>T maps to NM_001113382.1 H904H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:97370296 C>T maps to NM_001113382.1 N2050N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:97355401 C>A maps to NM_001113382.1 I844I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr2:97357240 C>T maps to NM_001113382.1 H982H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:97368450 G>A maps to NM_001113382.1 A1826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr8:125061885 T>C maps to NM_001039112.2 P921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:125052132 T>C maps to NM_001039112.2 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:125058030 G>A maps to NM_001039112.2 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:125074121 G>A maps to NM_001039112.2 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:125082839 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:125076738 C>T maps to NM_001039112.2 V1160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:124978466 G>A maps to NM_001039112.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:125035778 C>T maps to NM_001039112.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:125080047 G>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:125015515 G>T maps to NM_001039112.2 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:125074136 C>T maps to NM_001039112.2 C1064C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:19184517 G>A maps to NM_152898.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:19184934 G>A maps to NM_152898.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:19184784 G>A maps to NM_152898.2 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:19184595 C>T maps to NM_152898.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr7:19184586 G>A maps to NM_152898.2 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr14:53339538 T>C maps to NM_001134999.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:53326296 G>T maps to NM_001134999.1 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:53326362 G>A maps to NM_001134999.1 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr11:63990889 C>A maps to NM_178443.2 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:63979203 C>T maps to NM_178443.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:63979146 G>A maps to NM_178443.2 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:91436970 G>A maps to NM_002005.3 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:91433078 A>G maps to NM_002005.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:91430229 C>T maps to NM_002005.3 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:91430279 C>T maps to NM_002005.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:186358278 C>A maps to NM_014375.2 C10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:186358444 C>T maps to NM_014375.2 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr3:186370380 G>A maps to NM_014375.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:186364078 G>T maps to NM_014375.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:186370174 G>T maps to NM_014375.2 G302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr3:186362642 G>A maps to NM_014375.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:62355880 G>A maps to NM_018008.3 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:62356970 C>T maps to NM_018008.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr3:62356970 C>T maps to NM_018008.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:62357264 G>A maps to NM_018008.3 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:62357907 C>A maps to NM_018008.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr3:62355871 G>A maps to NM_018008.3 C422C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr19:35842981 G>A maps to NM_005303.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr19:35842807 G>T maps to NM_005303.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:35842729 C>A maps to NM_005303.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:35940828 G>A maps to NM_005306.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:35850517 C>T maps to NM_005304.3 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:35850251 G>T maps to NM_005304.3 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:35849965 C>T maps to NM_005304.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:155507374 G>A maps to NM_000508.3 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:155507278 G>T maps to NM_000508.3 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:155508048 G>A maps to NM_000508.3 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:155507815 C>T maps to NM_000508.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:155505371 A>C maps to NM_000508.3 Y835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:155507479 G>A maps to NM_000508.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:155510669 G>A maps to NM_000508.3 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:155506885 A>G maps to NM_000508.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr4:155506885 A>G maps to NM_000508.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:155491795 G>A maps to NM_005141.4 Q490Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:155487063 T>C maps to NM_005141.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:155487036 G>A maps to NM_005141.4 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr4:155491582 T>C maps to NM_005141.4 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr4:155491582 T>C maps to NM_005141.4 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:54496802 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:54482723 G>A did not map to a codon.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr23:54476182 G>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:54496516 C>T did not map to a codon.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr23:54496517 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:54491901 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:54496798 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr23:54492162 G>T did not map to a codon.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr23:54491964 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:54496651 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:54476148 A>G did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:54521657 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:54473767 C>T did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:54482153 G>A did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:54496727 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:54472705 G>A did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:54497901 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:36983626 C>T maps to NM_173558.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:36981421 C>T maps to NM_173558.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr6:36976711 C>T maps to NM_173558.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:36995228 C>T maps to NM_173558.3 Q544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:95792187 A>G maps to NM_033086.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr9:95796860 C>T maps to NM_033086.2 C608C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr9:95778077 C>T maps to NM_033086.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:32735175 G>A maps to NM_139241.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:14974113 C>T maps to NM_152536.3 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:14861027 C>T maps to NM_152536.3 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:14963934 G>T maps to NM_152536.3 G1229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:14862491 C>T maps to NM_152536.3 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:14905700 G>A maps to NM_152536.3 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr3:14905694 T>G maps to NM_152536.3 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:14862326 C>A maps to NM_152536.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:14939526 C>T maps to NM_152536.3 F997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr3:14860760 C>T maps to NM_152536.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:14939574 G>A maps to NM_152536.3 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:95604774 A>G maps to NM_018351.3 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:95501352 G>A maps to NM_018351.3 R1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:95531377 C>A maps to NM_018351.3 E972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:95566507 G>T maps to NM_018351.3 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:95604225 C>T maps to NM_018351.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr12:95478361 C>A maps to NM_018351.3 E1390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr12:95604951 A>G maps to NM_018351.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:44305290 C>A maps to NM_004465.1 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:44310603 G>A maps to NM_004465.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:7345914 G>A maps to NM_004112.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:191861899 T>C maps to NM_021032.4 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr3:192125853 G>T maps to NM_021032.4 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr3:192125880 G>A maps to NM_021032.4 H44H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:192078253 A>G maps to NM_021032.4 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:192078232 G>A maps to NM_021032.4 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:191888385 G>T maps to NM_021032.4 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:192125844 G>A maps to NM_021032.4 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr3:192125813 C>A maps to NM_021032.4 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:137715118 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:137717644 C>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:137793060 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:137715098 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:137793009 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:137717698 T>C did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:137793141 C>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:137939678 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:137793110 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:137715083 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:102379129 C>A maps to NM_175929.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:102568809 C>T maps to NM_004115.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr13:102379043 T>C maps to NM_175929.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr13:103053896 C>T maps to NM_175929.2 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr13:103053896 C>T maps to NM_175929.2 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:76709672 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:76711815 T>G did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:76711769 G>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:69518097 G>A maps to NM_005117.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:123813398 C>T maps to NM_002006.4 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr4:123813547 C>T maps to NM_002006.4 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr19:49261362 C>T maps to NM_019113.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr19:49259639 C>T maps to NM_019113.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:4479940 G>A maps to NM_020638.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr12:4553334 G>A maps to NM_020996.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:4553375 G>A maps to NM_020996.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:4554550 G>A maps to NM_020996.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:49716707 C>T maps to NM_002009.3 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr13:22275486 G>A maps to NM_002010.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:22255224 C>T maps to NM_002010.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:15938000 G>A maps to NM_005130.3 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr10:93668129 G>C maps to NM_152429.4 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:38314904 G>A maps to NM_001174067.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:38273561 G>A maps to NM_001174067.1 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr8:38279324 G>A maps to NM_001174067.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr8:38282206 A>G maps to NM_001174067.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr8:38279450 T>C maps to NM_001174067.1 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr8:38287278 G>A maps to NM_001174067.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr8:38285888 T>C maps to NM_001174067.1 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr8:38285936 C>T maps to NM_001174067.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr8:38285888 T>C maps to NM_001174067.1 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:167417769 C>T maps to NM_007045.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:167435985 A>G maps to NM_007045.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr6:167438362 T>C maps to NM_007045.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:27110624 C>T maps to NM_015633.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr12:27110639 G>A maps to NM_015633.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr10:123256186 T>C maps to ENST00000351936 E594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr10:123247546 G>A maps to ENST00000351936 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:123310911 G>A maps to ENST00000351936 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr10:123258090 A>G maps to ENST00000351936 D550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr10:123298196 T>C maps to ENST00000351936 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:123274777 A>T maps to ENST00000351936 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:123325096 C>T maps to ENST00000351936 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr10:123310947 T>C maps to ENST00000351936 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr10:123310818 G>A maps to ENST00000351936 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:123298219 G>A maps to ENST00000351936 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:123310947 T>C maps to ENST00000351936 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:123324982 A>G maps to ENST00000351936 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr10:123263321 C>T maps to ENST00000351936 W494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:123310947 T>C maps to ENST00000351936 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr10:123274628 T>C did not map to a codon.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr10:123247582 T>C maps to ENST00000351936 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr10:123247582 T>C maps to ENST00000351936 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr10:123279680 G>A maps to ENST00000351936 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:123279680 G>A maps to ENST00000351936 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr10:123247582 T>C maps to ENST00000351936 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr10:123247582 T>C maps to ENST00000351936 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:123298109 A>G maps to ENST00000351936 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:1805486 C>T maps to NM_000142.4 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:1808308 G>A maps to NM_000142.4 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:1804705 C>T maps to NM_001163213.1 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr4:1803568 C>T maps to NM_000142.4 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr4:1805451 G>T maps to NM_000142.4 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr5:176522552 G>A maps to NM_213647.1 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:176518720 C>T maps to NM_213647.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:176522552 G>A maps to NM_213647.1 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:176516659 C>A maps to NM_213647.1 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:176522552 G>A maps to NM_213647.1 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:1016228 C>T maps to NM_021923.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr4:155530901 A>G maps to ENST00000407946 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:155527860 G>A maps to ENST00000407946 Y383Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr4:155529760 T>C maps to ENST00000407946 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:155529625 G>T maps to ENST00000407946 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:155530817 G>A maps to ENST00000407946 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr1:60139780 C>T maps to NM_001113411.1 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:17726235 G>A maps to NM_201552.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:76826110 G>A maps to NM_006682.2 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:27950394 C>T maps to NM_005248.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:241680541 G>A maps to NM_000143.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr1:241663821 C>A maps to NM_000143.3 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:241663800 T>C maps to NM_000143.3 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:153896980 C>T maps to NM_033393.2 G846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:59737978 G>A maps to NM_002012.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr23:135288683 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:135289216 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:135278978 C>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:105977775 G>A maps to ENST00000344213 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr6:97063626 C>T maps to NM_020482.4 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:67264296 G>T maps to NM_013241.2 R991R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr16:67271602 T>C maps to NM_013241.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:67270569 G>A maps to NM_013241.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:67264013 G>A maps to NM_013241.2 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr16:67270581 C>T maps to NM_013241.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:67268080 G>A maps to NM_013241.2 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:67268095 G>A maps to NM_013241.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr18:34205640 G>A maps to NM_025135.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:34297975 T>C maps to NM_025135.2 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:34205487 C>T maps to NM_025135.2 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr18:34298570 C>T maps to NM_025135.2 R929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr18:34340638 C>T maps to NM_025135.2 D1323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:34205616 G>A maps to NM_025135.2 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:34297963 G>A maps to NM_025135.2 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:34289209 G>T maps to NM_025135.2 E622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr9:133779696 C>T maps to NM_001145106.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr9:133780705 G>A maps to NM_001145106.1 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:133805190 G>A maps to NM_001145106.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr9:133779537 G>A maps to NM_001145106.1 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr9:133787221 C>T maps to NM_001145106.1 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:65652459 G>A maps to NM_198897.1 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:65651921 G>A maps to NM_198897.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:108912202 C>T maps to NM_007076.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:108910973 C>T maps to NM_007076.2 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:108913101 C>T maps to NM_007076.2 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:108912981 C>T maps to NM_007076.2 N369N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:108912291 C>T maps to NM_007076.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:110081502 T>G maps to NM_014845.5 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr23:15371235 T>C did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:15365349 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:15376160 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:15381327 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:15381293 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:15364381 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:164467708 C>T maps to NM_018086.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:164467863 C>A maps to NM_018086.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr2:164466934 G>A maps to NM_018086.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr2:164466484 C>T maps to NM_018086.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:164466778 G>A maps to NM_018086.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:50513026 A>G maps to NM_022116.3 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:50513665 A>G maps to NM_022116.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:50513418 C>A maps to NM_022116.3 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr6:76022882 G>A maps to NM_015687.2 R889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:76072564 G>A maps to NM_015687.2 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:76023009 G>A maps to NM_015687.2 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr6:76018472 A>G maps to NM_015687.2 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:76022913 G>A maps to NM_015687.2 N878N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:76023899 C>A maps to NM_015687.2 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr6:76018423 C>A maps to NM_015687.2 G1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr6:76023534 C>T maps to NM_015687.2 Q671Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr3:99567696 C>T maps to NM_001042459.1 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:99648747 C>T maps to NM_001042459.1 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:99567714 C>A maps to NM_001042459.1 V935V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:99643224 C>A maps to NM_001042459.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr3:99568980 T>C maps to NM_001042459.1 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:99567750 G>A maps to NM_001042459.1 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:99567938 G>A maps to NM_001042459.1 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr4:54256784 G>A maps to NM_030917.3 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr14:24601980 C>T maps to NM_203402.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:24600786 G>A maps to NM_203402.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:24602022 G>A maps to NM_203402.2 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:56103965 G>A maps to NM_032836.2 C447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:56104859 C>T maps to NM_032836.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:56103965 G>A maps to NM_032836.2 C447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:35641182 G>A maps to NM_014344.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:39978651 G>T maps to NM_021939.3 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr7:30054362 G>A maps to NM_017946.2 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:115959229 G>A maps to ENST00000446284 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:115948553 C>T maps to ENST00000446284 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:115935730 A>G did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr14:45590786 C>A maps to NM_002013.3 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:2907921 C>T maps to NM_002014.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:2907024 G>A maps to NM_002014.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:35604902 C>T maps to NM_001145775.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:35554887 C>A maps to NM_001145775.1 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:72755319 C>T maps to NM_003602.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:72744228 G>A maps to NM_003602.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:72755319 C>T maps to NM_003602.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:72744175 C>T maps to NM_003602.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:18649179 G>A maps to NM_012181.3 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:18650471 C>T maps to NM_012181.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr19:18649131 G>A maps to NM_012181.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr7:33042438 C>T maps to NM_007270.3 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr7:33014893 C>T maps to NM_007270.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr7:33028238 C>T maps to NM_007270.3 H338H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:33014914 C>A maps to NM_007270.3 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr7:33014327 T>C maps to NM_007270.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:32096893 G>A maps to NM_022110.3 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:32096893 G>A maps to NM_022110.3 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:32096902 C>A maps to NM_022110.3 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:47259948 C>T maps to NM_024301.4 H414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:108397343 G>A maps to NM_006731.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:108370217 C>T maps to NM_006731.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:108377632 G>T maps to NM_006731.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:154960825 A>G maps to NM_025207.4 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:17125837 C>T maps to NM_144997.5 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr17:17119703 C>T maps to NM_144997.5 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:17131373 G>A maps to NM_144997.5 H26H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:152285795 T>C maps to NM_002016.1 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr1:152281307 T>C maps to NM_002016.1 R2018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:152281790 C>T maps to NM_002016.1 G1857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:152284649 G>A maps to NM_002016.1 D904D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr1:152275268 A>G maps to NM_002016.1 Y4031Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:152275898 G>A maps to NM_002016.1 D3821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:152281466 G>A maps to NM_002016.1 A1965A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr1:152279765 C>T maps to NM_002016.1 S2532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr1:152281307 T>C maps to NM_002016.1 R2018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr1:152276881 G>A maps to NM_002016.1 Q3494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:152279039 G>T maps to NM_002016.1 S2774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:152281307 T>C maps to NM_002016.1 R2018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr1:152279963 C>T maps to NM_002016.1 P2466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr1:152284999 G>A maps to NM_002016.1 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr1:152281307 T>C maps to NM_002016.1 R2018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:152284999 G>A maps to NM_002016.1 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr1:152281307 T>C maps to NM_002016.1 R2018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr1:152284126 C>A maps to NM_002016.1 E1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr1:152286134 G>A maps to NM_002016.1 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:152281307 T>C maps to NM_002016.1 R2018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr1:152285795 T>C maps to NM_002016.1 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:152282522 C>A maps to NM_002016.1 S1613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:152282522 C>T maps to NM_002016.1 S1613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:152286914 C>T maps to NM_002016.1 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr1:152281307 T>C maps to NM_002016.1 R2018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:152280425 A>G maps to NM_002016.1 G2312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:152281307 T>C maps to NM_002016.1 R2018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:152327348 G>T maps to NM_001014342.2 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:152326088 A>G maps to NM_001014342.2 T1391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:152328590 G>A maps to NM_001014342.2 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:152324038 G>A maps to NM_001014342.2 Q2075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:152324129 G>A maps to NM_001014342.2 H2044H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr1:152326459 G>A maps to NM_001014342.2 R1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:152324420 T>A maps to NM_001014342.2 T1947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:152326082 T>C maps to NM_001014342.2 G1393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr1:152329513 C>A maps to NM_001014342.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr1:152328179 G>T maps to NM_001014342.2 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:152325478 G>A maps to NM_001014342.2 R1595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:152328872 G>T maps to NM_001014342.2 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:152329483 C>A maps to NM_001014342.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr1:152328935 G>A maps to NM_001014342.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:152327873 T>C maps to NM_001014342.2 Q796Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr1:152327066 T>C maps to NM_001014342.2 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr1:152328935 G>A maps to NM_001014342.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr1:152328935 G>A maps to NM_001014342.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:152328590 G>A maps to NM_001014342.2 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr1:152323673 A>G maps to NM_001014342.2 H2196H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:152328239 G>A maps to NM_001014342.2 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:128675297 C>T maps to NM_002017.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:128642752 C>T maps to NM_002017.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:128680399 C>T maps to NM_002017.3 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:128680519 C>T maps to NM_002017.3 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:128628029 C>T maps to NM_002017.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:128628056 G>A maps to NM_002017.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:18151247 G>T maps to NM_002018.2 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:18150605 C>T maps to NM_002018.2 E851E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:18160255 G>A maps to NM_002018.2 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr14:21546385 G>T maps to NM_018071.3 R695R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:21543849 G>A maps to NM_018071.3 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr14:21542824 C>T maps to NM_018071.3 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:78389020 G>A maps to NM_173627.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:142487537 A>G maps to NM_207414.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:142477591 G>A maps to NM_207414.2 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr8:142446114 C>T maps to NM_207414.2 A1151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:142476660 A>C maps to NM_207414.2 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:142481201 G>A maps to NM_207414.2 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:142487543 C>T maps to NM_207414.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:142459746 G>A maps to NM_207414.2 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:142487995 G>A maps to NM_207414.2 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr8:142500349 C>T maps to NM_207414.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:71379769 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:71379911 T>C did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:71379768 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:71379903 C>T did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:84608468 T>C maps to NM_001001670.2 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr9:84608057 A>G maps to NM_001001670.2 E891E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr9:84603885 G>A maps to NM_001001670.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:84608004 C>T maps to NM_001001670.2 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:84607985 C>A maps to NM_001001670.2 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr9:84607217 C>T maps to NM_001001670.2 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:84605879 G>A maps to NM_001001670.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr9:84606694 C>A maps to NM_001001670.2 S437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr9:84606233 G>A maps to NM_001001670.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:153588809 C>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:153581768 T>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:153592417 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:153590649 G>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:153585843 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:153593018 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:153588785 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:153577381 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:153587973 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:153586904 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:153590862 C>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:153578197 C>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:153592467 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:153594510 C>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:153593613 G>A did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr23:153594578 G>A did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:153577743 T>C did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:153587692 G>A did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:153592919 C>T did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:153583340 G>A did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:153592919 C>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:153586915 C>T did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:153580715 C>T did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:153581375 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr23:153585913 G>A did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:153596278 T>C did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:153587481 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:153587720 T>C did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:153593209 C>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:153577335 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:153599543 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:153583055 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:153588825 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:57994509 C>A maps to NM_001164317.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:58116576 G>A maps to NM_001164317.1 T1444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:58067393 C>T maps to NM_001164317.1 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:58092500 C>T maps to NM_001164317.1 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr3:58124153 T>C maps to NM_001164317.1 D1700D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:58109235 T>C maps to NM_001164317.1 S1181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:58092500 C>T maps to NM_001164317.1 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:58067370 G>T maps to NM_001164317.1 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:58145285 G>A maps to NM_001164317.1 S2329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:58145333 C>T maps to NM_001164317.1 G2345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr3:58135721 C>T maps to NM_001164317.1 H2110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:58139195 C>T maps to NM_001164317.1 C2185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:58134514 C>T maps to NM_001164317.1 G2040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:58092527 C>T maps to NM_001164317.1 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:58139270 C>T maps to NM_001164317.1 S2210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:128482672 C>T maps to NM_001458.4 Y770Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr7:128498527 G>A maps to NM_001458.4 W2710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:128485076 G>A maps to NM_001458.4 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:128477522 C>T maps to NM_001458.4 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:128488728 C>T maps to NM_001458.4 D1565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr7:128492762 C>T maps to NM_001458.4 N1987N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:128486892 G>T maps to NM_001458.4 E1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:128487757 G>A maps to NM_001458.4 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:128477802 C>T maps to NM_001458.4 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr7:128484289 G>A maps to NM_001458.4 V1054V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:128493532 C>A maps to NM_001458.4 G2073G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:128486119 G>A maps to NM_001458.4 T1289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr7:128498546 T>A maps to NM_001458.4 P2716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr7:128486397 C>T maps to NM_001458.4 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:128478789 T>C maps to NM_001458.4 H448H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr7:128487757 G>A maps to NM_001458.4 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:128484983 G>A maps to NM_001458.4 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:30698299 G>A maps to NM_005803.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:63885616 G>A maps to NM_013280.4 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr14:86089444 T>C maps to NM_013231.4 H529H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr14:86089195 C>T maps to NM_013231.4 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:86089252 C>T maps to NM_013231.4 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr14:86089456 G>A maps to NM_013231.4 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:86088493 C>T maps to NM_013231.4 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr14:86088445 C>T maps to NM_013231.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:86089366 G>A maps to NM_013231.4 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr14:86089048 T>A maps to NM_013231.4 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:86089837 G>A maps to NM_013231.4 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr14:86087995 T>C maps to NM_013231.4 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:86088862 G>A maps to NM_013231.4 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr14:86089684 C>T maps to NM_013231.4 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr14:86089456 G>A maps to NM_013231.4 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr14:86088635 C>T maps to NM_013231.4 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:86089045 G>A maps to NM_013231.4 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr14:86089195 C>A maps to NM_013231.4 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr14:86089195 C>T maps to NM_013231.4 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr20:14306460 T>C maps to NM_198391.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:14306877 G>T maps to NM_198391.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:14306418 A>G maps to NM_198391.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr13:29004197 C>T maps to NM_002019.4 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr13:28877333 C>T maps to NM_002019.4 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr13:28931757 A>G maps to NM_002019.4 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr13:28979916 C>T maps to NM_002019.4 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr13:28885758 C>T maps to NM_002019.4 P1201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:28903854 C>T maps to NM_002019.4 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:28959070 C>T maps to NM_002019.4 E689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:28877351 C>T maps to NM_002019.4 P1323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:28942783 C>T maps to NM_001160030.1 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr13:28919595 G>T maps to NM_002019.4 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:29007957 C>A maps to NM_002019.4 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr13:29008333 A>G maps to NM_002019.4 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr13:28919595 G>T maps to NM_002019.4 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:28919595 G>T maps to NM_002019.4 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr13:29001900 G>A maps to NM_002019.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:28931757 A>G maps to NM_002019.4 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr13:28636173 C>T maps to NM_004119.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr13:28608279 A>G maps to NM_004119.2 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr13:28626794 T>C maps to NM_004119.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:28623777 G>A maps to NM_004119.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:28626713 C>T maps to NM_004119.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:28608054 G>T maps to NM_004119.2 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr13:28644699 A>G maps to NM_004119.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr13:28592636 G>T maps to NM_004119.2 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr13:28597615 T>C did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr13:28589291 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr13:28608084 T>C maps to NM_004119.2 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr13:28592642 T>C maps to NM_004119.2 R834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:28608084 T>A maps to NM_004119.2 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:49978962 C>T maps to NM_001459.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:49983639 A>G maps to NM_001459.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:180052867 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr5:180057642 G>A maps to NM_182925.4 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr5:180046292 G>A maps to NM_182925.4 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr5:180050982 G>A maps to NM_182925.4 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:180048758 C>T maps to NM_182925.4 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:213062508 T>C maps to NM_014053.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr14:76105697 G>A maps to NM_017791.2 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:76045428 C>T maps to NM_017791.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:76045428 C>T maps to NM_017791.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:2983437 C>T maps to ENST00000399667 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr16:2979913 C>T maps to ENST00000399667 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:2949089 T>C maps to NM_138439.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:33091137 G>A maps to NM_001103184.2 R1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:33358894 C>T maps to NM_001103184.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr1:240371327 G>A maps to ENST00000406993 A1215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:240370268 C>T maps to ENST00000406993 G862G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:240371066 C>T maps to ENST00000406993 G1128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:240370358 G>A maps to ENST00000406993 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:240370367 C>T maps to ENST00000406993 G895G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr1:240370670 T>A maps to ENST00000406993 C996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:240371369 C>A maps to ENST00000406993 P1229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:240286626 G>A maps to ENST00000406993 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:240351519 T>C maps to ENST00000406993 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:240256587 G>T maps to ENST00000406993 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr1:240370940 T>C maps to ENST00000406993 P1086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr1:240371453 C>T maps to ENST00000406993 P1257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:240371057 C>T maps to ENST00000406993 P1125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:43313574 C>T maps to NM_005892.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr17:43317919 G>A maps to NM_005892.3 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:43318930 C>T maps to NM_005892.3 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:43307969 G>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:153476080 T>A maps to NM_052905.3 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:153378468 C>T maps to NM_052905.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr2:153437544 A>G maps to NM_052905.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:153417546 G>T maps to NM_052905.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr1:171250068 C>T maps to NM_002021.1 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:171165936 G>A maps to NM_001460.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:171177992 C>T maps to NM_001460.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:171076899 G>T maps to NM_006894.5 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:171083374 A>G maps to NM_006894.5 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:171303753 C>G maps to NM_002022.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:171303753 C>A maps to NM_002022.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:171300906 C>T maps to NM_002022.1 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:146684067 G>A maps to NM_001461.2 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:146673055 A>G maps to NM_001461.2 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:203317218 C>T maps to NM_002023.3 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:203317017 A>G maps to NM_002023.3 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:203317071 A>G maps to NM_002023.3 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:147024824 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:147030312 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:147024666 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:147018983 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:147030280 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:147010267 C>T did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr23:147024700 A>G did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:147024748 A>G did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:147014000 A>T did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:147003489 G>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:147024700 A>G did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr23:147009911 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:147024698 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:147014109 G>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:147024700 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:147030281 G>A did not map to a codon.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr23:147062931 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:147084786 C>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:147084777 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:147090170 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:147088296 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:147063029 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr23:147106455 G>A did not map to a codon.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr23:147090191 T>C did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:147063000 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:147090212 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:147063035 C>T did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr2:216262559 T>C maps to NM_212482.1 R1120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:216262520 T>A maps to NM_212482.1 S1133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr2:216248138 C>A maps to NM_212482.1 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr2:216262559 T>C maps to NM_212482.1 R1120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:216251522 G>T maps to NM_212482.1 R1501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:216248845 G>A maps to NM_212482.1 S1597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:216235113 G>A maps to NM_212482.1 G2252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:216243984 G>A maps to NM_212482.1 S1830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr2:216230255 G>A maps to NM_212482.1 N2372N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:216288914 C>T maps to NM_212482.1 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:216251679 A>G maps to NM_212482.1 G1448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:216226753 C>A maps to NM_212482.1 E2434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:216272024 C>T maps to NM_212482.1 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:216226298 G>A maps to NM_212482.1 D2471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:216274707 C>A maps to NM_212482.1 E691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:216249661 C>T maps to NM_212482.1 A1550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr2:216269175 G>A maps to NM_212482.1 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:216272030 G>A maps to NM_212482.1 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr2:216232730 T>C maps to NM_212482.1 Q2291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr2:216289964 C>T maps to NM_212482.1 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:216235107 G>T maps to NM_212482.1 T2254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr2:216274397 G>A maps to NM_212482.1 T729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr2:216262559 T>C maps to NM_212482.1 R1120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr17:80708378 C>T maps to NM_022158.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:132740884 C>T maps to NM_015033.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:132671200 T>C maps to NM_015033.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:132687263 A>C maps to NM_015033.2 L321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr9:132740859 G>A maps to NM_015033.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:93965032 C>T maps to ENST00000370253 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:94012482 G>A maps to ENST00000370253 E448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:93988961 C>T maps to ENST00000370253 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:47744731 T>C maps to NM_015308.2 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:47755639 G>A maps to NM_015308.2 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:47746214 G>T maps to NM_015308.2 P708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:47746315 C>A maps to NM_015308.2 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr6:159650862 C>T maps to NM_032532.2 Y399Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:159653394 G>A maps to NM_032532.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:159672346 G>A maps to NM_032532.2 T1616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr6:159655176 C>T maps to NM_032532.2 G1211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr6:159677631 T>C maps to NM_032532.2 L1715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:159653280 C>T maps to NM_032532.2 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:159670155 C>T maps to NM_032532.2 G1592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:159654304 C>A maps to NM_032532.2 R921R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:159653364 G>A maps to NM_032532.2 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:159682220 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:159657304 G>A maps to NM_032532.2 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:159657307 T>C maps to NM_032532.2 N1343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr6:159677631 T>C maps to NM_032532.2 L1715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr6:159677631 T>C maps to NM_032532.2 L1715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr6:159653589 C>T maps to NM_032532.2 R682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:159660604 C>T maps to NM_032532.2 R1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr6:159652959 C>T maps to NM_032532.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:159660765 G>A maps to NM_032532.2 P1466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr6:159677631 T>C maps to NM_032532.2 L1715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:49760215 A>G maps to NM_001079673.1 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr13:49781443 C>T maps to NM_001079673.1 D1170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr13:49765243 C>T maps to NM_001079673.1 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr13:49649453 A>G maps to NM_001079673.1 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:49781443 C>T maps to NM_001079673.1 D1170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr13:49765415 G>T maps to NM_001079673.1 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:49772149 T>C maps to NM_001079673.1 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr13:49772149 T>C maps to NM_001079673.1 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:172046818 A>G maps to NM_022763.3 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:109270670 C>A maps to NM_001144937.1 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:109261507 C>T maps to NM_001144937.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:109284420 G>T maps to NM_001144937.1 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:109265161 A>G maps to NM_001144937.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:109271320 A>G maps to NM_001144937.1 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:109265110 C>T maps to NM_001144937.1 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:33454354 G>A maps to NM_017559.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:33456442 T>A maps to NM_017559.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:159789758 A>G maps to ENST00000379346 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:159789395 C>G maps to ENST00000379346 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr14:65499348 C>G maps to ENST00000448390 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:49195002 G>A maps to NM_004476.1 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:49190745 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:49221833 G>T maps to NM_004476.1 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:49229879 G>A maps to NM_004476.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:49190810 C>T did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr11:89409337 T>C did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr11:71906953 C>T maps to NM_016729.2 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr11:71906690 C>T maps to NM_016729.2 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr11:71932637 C>T maps to NM_001113536.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:71929684 C>T maps to NM_001113536.1 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:71932685 C>T maps to NM_001113536.1 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:71929672 A>G maps to NM_001113536.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:71850485 C>A maps to ENST00000442948 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:94040692 C>T maps to NM_001080486.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr11:94040407 C>T maps to NM_001080486.1 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:28634796 G>T maps to NM_005253.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:28635191 C>T maps to NM_005253.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:38061736 G>A maps to NM_004496.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr20:22563344 G>A maps to NM_021784.4 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr20:22563747 G>A maps to NM_021784.4 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:46367740 C>T maps to NM_004497.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:79634680 C>T maps to NM_001013735.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr6:1611192 G>A maps to NM_001453.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr16:86601000 C>T maps to NM_005251.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:86602437 G>A maps to NM_005251.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:72744052 C>T maps to NM_004472.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:118008 G>A maps to NM_207305.3 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:117018 C>T maps to NM_207305.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:117624 G>A maps to NM_207305.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:116919 C>T maps to NM_207305.3 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:114257165 G>A maps to NM_012184.4 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:114257060 C>T maps to NM_012184.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:114256841 G>A maps to NM_012184.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:114257043 C>T maps to NM_012184.4 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr2:114257297 C>T maps to NM_012184.4 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr9:100616549 C>T maps to NM_004473.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:86544489 C>T maps to NM_001451.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:86546651 G>A maps to NM_001451.2 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:86546555 G>T maps to NM_001451.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr16:86544264 G>A maps to NM_001451.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:29237768 G>A maps to NM_005249.3 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:29237714 C>T maps to NM_005249.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr14:29237819 G>A maps to NM_005249.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:29237012 C>T maps to NM_005249.3 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr14:29237213 G>A maps to NM_005249.3 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:29237045 C>T maps to NM_005249.3 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:29237858 C>A maps to NM_005249.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:29237711 G>A maps to NM_005249.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:145700587 C>T maps to NM_003923.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:145699944 G>A maps to NM_003923.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:169533080 C>T maps to NM_012188.4 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr5:169535059 G>T maps to NM_012188.4 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:169532984 G>A maps to NM_012188.4 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:169533470 C>T maps to NM_012188.4 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:169535539 C>T maps to NM_012188.4 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:129537174 C>T maps to NM_207426.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr1:42647651 C>T maps to NM_001198850.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:42671456 C>A maps to NM_001198850.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:42647654 T>G maps to NM_001198850.1 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:4798729 C>T maps to ENST00000450194 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:4800737 G>A maps to ENST00000450194 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:4798840 C>T maps to ENST00000450194 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:4794893 C>T maps to ENST00000450194 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:4801929 G>A maps to NM_001037165.1 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:4800920 T>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:80540696 G>A maps to NM_004514.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:80543972 G>A maps to NM_004514.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:80540615 G>T did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr17:80545125 G>A maps to NM_004514.3 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:80521310 G>A maps to NM_004514.3 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr16:86613216 G>A maps to NM_005250.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:2977833 G>A maps to NM_202002.1 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:2968559 T>C maps to NM_202002.1 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:2981353 G>A maps to NM_202002.1 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:2983164 G>A maps to NM_202002.1 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:26851049 C>T maps to NM_003593.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:48573833 C>T maps to NM_002158.3 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr14:89629042 G>A maps to NM_001085471.1 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr12:109719494 C>T maps to NM_213596.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:109723256 G>A maps to NM_213596.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:41134253 C>T maps to NM_002015.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr13:41133680 T>C maps to NM_002015.3 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr13:41134889 G>A maps to NM_002015.3 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:108985661 C>T maps to NM_001455.3 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:108984983 C>T maps to NM_001455.3 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr6:108985142 G>T maps to NM_001455.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:70316682 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:70316649 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:70316384 C>G did not map to a codon.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr23:70320752 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:70321422 C>A did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:70320685 C>A did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:70321040 C>T did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:70316624 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:70316669 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:70321109 T>C did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:71064749 G>A maps to NM_032682.4 C308C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:71015120 C>A maps to NM_032682.4 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr3:71050154 G>A maps to NM_032682.4 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:71247445 G>A maps to NM_032682.4 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:71026982 C>T maps to NM_032682.4 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:71101767 G>A maps to NM_032682.4 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:114302154 T>C maps to NM_148898.3 C586C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:114271743 C>T maps to NM_148898.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr7:114302154 T>C maps to NM_148898.3 C586C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr7:114302154 T>C maps to NM_148898.3 C586C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:114304492 T>C did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr7:114302154 T>C maps to NM_148898.3 C586C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:49113303 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:49107805 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:49110401 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:49107800 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:41566580 C>T maps to NM_001012426.1 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr6:41565520 C>T maps to NM_001012426.1 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:118851223 G>A maps to NM_181721.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:55650172 T>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:55650464 T>G did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr23:55650796 T>C did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:55650795 A>G did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:55650886 A>G did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr22:36894069 G>A maps to NM_001102371.1 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr20:30432646 G>A maps to NM_004118.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr20:30432766 T>C maps to NM_004118.3 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:30433165 G>A maps to NM_004118.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:130570895 C>T maps to NM_004957.4 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:130570889 G>A maps to NM_004957.4 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:74670225 C>A maps to NM_003838.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:74670891 T>C maps to NM_003838.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:74670324 G>A maps to NM_003838.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:52249433 A>G maps to NM_002029.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:52249899 G>A maps to NM_002029.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:52249509 G>A maps to NM_002029.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:52272915 G>A maps to NM_001005738.1 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:52272396 C>A maps to NM_001005738.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:52327672 C>T maps to NM_002030.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:52327441 G>A maps to NM_002030.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:95459845 G>A maps to NM_145246.4 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr10:95452419 G>A maps to NM_145246.4 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr4:79207631 G>T maps to NM_025074.6 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:79403069 C>T maps to NM_025074.6 Y2852Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:79371455 C>T maps to NM_025074.6 G2142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:79236859 C>A maps to NM_025074.6 Y597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:79321943 G>A maps to NM_025074.6 G1344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:79284766 C>T maps to NM_025074.6 H841H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr4:79188076 G>A maps to NM_025074.6 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:79428587 C>A maps to NM_025074.6 I3110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:79173679 C>T maps to NM_025074.6 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:79437038 C>T maps to NM_025074.6 R3421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:79461920 G>A maps to NM_025074.6 A3894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:79334175 C>T maps to NM_025074.6 I1454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:79368026 T>C maps to NM_025074.6 P2001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:79296908 C>T maps to NM_025074.6 C1056C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:79410137 G>A maps to NM_025074.6 R2954R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:79284778 C>T maps to NM_025074.6 D845D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:79321997 T>C maps to NM_025074.6 A1362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:79308549 G>T maps to NM_025074.6 E1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:79400645 G>A maps to NM_025074.6 A2739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:79434659 C>T maps to NM_025074.6 H3376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:79366859 C>T maps to NM_025074.6 T1950T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:14784561 C>T maps to ENST00000380880 T1419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr9:14819248 G>C maps to ENST00000380880 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr9:14806685 C>A maps to ENST00000380880 E1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:14776170 C>T maps to ENST00000380880 E1494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:14841510 G>T maps to ENST00000380880 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:14848726 A>G maps to ENST00000380880 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:14776044 G>A maps to ENST00000380880 T1536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:14759847 G>T maps to ENST00000380880 V1755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:14868804 G>T maps to ENST00000380880 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:14748563 C>T maps to ENST00000380880 L1880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:14750215 A>G maps to ENST00000380880 D1825D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr9:14797512 T>C maps to ENST00000380880 E1277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr13:39262686 T>C maps to NM_207361.4 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:39264072 C>A maps to NM_207361.4 I864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:39358826 T>C maps to NM_207361.4 D1967D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:39265300 G>T maps to NM_207361.4 E1274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr13:39424214 C>T maps to NM_207361.4 S2140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr13:39432169 A>C maps to NM_207361.4 T2405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr13:39266574 T>C maps to NM_207361.4 F1698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:39265332 G>A maps to NM_207361.4 G1284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr13:39266577 C>T maps to NM_207361.4 I1699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:39271910 A>G maps to NM_207361.4 A1750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:39265419 A>G maps to NM_207361.4 E1313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:39425865 A>G maps to NM_207361.4 E2262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:39430305 C>T maps to NM_207361.4 I2323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:39438676 C>T maps to NM_207361.4 F2639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:39425171 A>G maps to NM_207361.4 Q2223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr13:39430278 A>G maps to NM_207361.4 E2314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:39358814 A>T maps to NM_207361.4 I1963I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:39433572 C>T maps to NM_207361.4 F2455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:39446934 C>T maps to NM_207361.4 Y2680Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr13:39263268 G>T maps to NM_207361.4 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr13:39262882 T>C maps to NM_207361.4 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr13:39425847 C>T maps to NM_207361.4 T2256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:39262155 C>T maps to NM_207361.4 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:39263844 C>A maps to NM_207361.4 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:39265956 C>A maps to NM_207361.4 I1492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr6:116263642 A>G maps to NM_002031.2 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr6:116325070 A>G maps to NM_002031.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr6:116263642 A>G maps to NM_002031.2 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:116381180 G>A maps to NM_002031.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:168464402 G>T maps to NM_024919.3 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr6:168461534 G>A maps to NM_024919.3 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:168467484 G>A maps to NM_024919.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:168464427 G>A maps to NM_024919.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr6:168467433 C>A did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr6:168465577 G>A maps to NM_024919.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:168457899 G>A maps to NM_024919.3 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:13698867 C>T maps to NM_018027.3 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr10:13716985 C>T maps to NM_018027.3 K392K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:13749073 C>A maps to NM_018027.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:13735925 G>A maps to NM_018027.3 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:13698806 G>A maps to NM_018027.3 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr3:69351554 G>A maps to NM_015123.1 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:69267493 A>G maps to NM_015123.1 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:69230097 G>A maps to NM_015123.1 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:52171625 C>T maps to ENST00000344768 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr14:52171562 A>G maps to ENST00000344768 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:52171625 C>T maps to ENST00000344768 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr14:52194515 T>C maps to ENST00000344768 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:131212511 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:131212640 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:131212511 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:131218573 G>A did not map to a codon.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr23:131212597 A>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:131212607 G>A did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr11:65156931 C>T maps to NM_031904.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:65178743 C>T maps to NM_031904.3 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:37740348 C>A maps to NM_014907.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr9:37744837 C>T maps to NM_014907.2 R937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr9:37729786 C>A maps to NM_014907.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr9:37744545 G>A maps to NM_014907.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr9:37733587 C>T maps to NM_014907.2 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr10:49450380 G>A maps to NM_001018071.3 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:49371501 T>A maps to NM_001018071.3 T1250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:49400805 C>A maps to NM_001018071.3 G696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr10:49446129 C>T maps to NM_001018071.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:49450320 C>T maps to NM_001018071.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr10:49452862 G>T maps to NM_001018071.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr10:49393640 C>A maps to NM_001018071.3 E772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:49420065 A>G maps to NM_001018071.3 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:12735868 C>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:12725721 C>T did not map to a codon.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr23:12712556 A>G did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:12736503 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:12736599 G>A did not map to a codon.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr23:12736334 A>G did not map to a codon.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr23:12157128 G>A did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:12735822 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:12632964 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:12708398 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:12734433 A>C did not map to a codon.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr23:12734225 G>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:12701705 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:12734639 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:12712555 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:12708364 T>C did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:12701705 G>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:12701705 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:12736267 A>G did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:12720086 T>C did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:12734594 A>G did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:12735797 C>T did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:12734594 A>G did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr23:12701705 G>A did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:12734594 A>G did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:12701705 G>A did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:12720003 T>C did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:12712495 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:12516899 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:12701705 G>A did not map to a codon.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr23:12736749 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:12516898 C>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:12725010 C>T did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:12735217 C>T did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:12734595 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:12736251 G>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:100212942 C>T maps to NM_001013660.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:100174630 T>A maps to NM_001013660.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:69965896 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:69968141 C>T maps to NM_006654.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:41743344 T>C did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:41738950 C>T maps to NM_006653.3 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr13:32798429 G>A maps to NM_023037.2 P1608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:32735335 C>T maps to NM_023037.2 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr13:32821470 G>A maps to NM_023037.2 W2280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:32828497 C>T maps to NM_023037.2 F2461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:32811932 C>T maps to NM_023037.2 L2076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:32805399 A>G maps to NM_023037.2 L1830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:32776158 C>T maps to NM_023037.2 I1276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:32814018 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:32768338 A>C maps to NM_023037.2 I1217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr13:32835793 T>C maps to NM_023037.2 R2486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr4:48501624 G>A maps to NM_015030.1 F2952F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:48559609 G>A maps to NM_015030.1 R1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:48514650 C>T maps to NM_015030.1 P2664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr4:48636382 A>G maps to NM_015030.1 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr4:48548247 A>C maps to NM_015030.1 P1705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr4:48503732 T>C maps to NM_015030.1 R2833R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:48608582 C>A maps to NM_015030.1 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr4:48559609 G>T maps to NM_015030.1 R1329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:48584669 C>T maps to NM_015030.1 W610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr2:183703156 A>G maps to NM_001463.3 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr2:183703156 A>G maps to NM_001463.3 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr14:44973865 C>T maps to NM_032135.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:44974875 C>A maps to NM_032135.3 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:44976156 C>A maps to NM_032135.3 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr14:44973866 G>T maps to NM_032135.3 S775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr14:44973866 G>T maps to NM_032135.3 S775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr14:44973865 C>T maps to NM_032135.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:5645020 C>T maps to ENST00000340250 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:5643159 T>C maps to ENST00000340250 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:79495601 C>T maps to NM_001077182.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:127238545 C>T maps to NM_020369.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr7:127235722 C>T maps to NM_020369.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:127235419 C>T maps to NM_020369.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:127235395 A>G maps to NM_020369.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr7:127235722 C>T maps to NM_020369.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:4318364 G>T maps to NM_024333.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:4311845 C>T maps to NM_024333.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr19:4323175 C>A maps to NM_024333.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:83434012 G>T maps to NM_001007122.2 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:83456037 G>T maps to NM_001007122.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:83437636 T>C maps to NM_001007122.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr11:30255299 C>T maps to NM_001018080.1 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr11:30255217 T>C maps to NM_001018080.1 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:30255217 T>C maps to NM_001018080.1 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr11:30253520 C>A maps to NM_001018080.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:30253520 C>A maps to NM_001018080.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:49210241 A>G maps to NM_000145.3 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:49189990 C>A maps to NM_000145.3 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr2:49247268 C>A maps to NM_000145.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:49190966 A>G maps to NM_000145.3 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr2:49190069 G>C maps to NM_000145.3 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr15:39910269 T>C maps to NM_152597.4 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:40057929 C>A maps to NM_152597.4 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr15:40056112 A>G maps to NM_152597.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr15:40056112 A>G maps to NM_152597.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:186670980 C>T maps to NM_173651.2 R5739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:186671207 G>A maps to NM_173651.2 S5814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:186671135 G>A maps to NM_173651.2 S5790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr2:186673508 C>A maps to NM_173651.2 A6581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:186672479 C>A maps to NM_173651.2 I6238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:186678472 G>T maps to NM_173651.2 E6766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:186671355 C>A maps to NM_173651.2 R5864R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:186670149 G>T maps to NM_173651.2 E5462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:52776662 G>C maps to NM_013409.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:120130700 C>A maps to NM_007085.4 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:120118750 G>T maps to NM_007085.4 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr3:120130737 T>C maps to NM_007085.4 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:120130737 T>C maps to NM_007085.4 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:132585212 G>A maps to NM_015082.1 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:132535224 G>A maps to NM_015082.1 D697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:132553051 T>G maps to NM_015082.1 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:132561461 T>C maps to NM_015082.1 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:132535489 C>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr4:162697122 G>A maps to NM_020116.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:162307429 T>C maps to NM_020116.3 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr4:163032430 G>A maps to NM_020116.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:162306946 G>T maps to NM_020116.3 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:162431555 C>A maps to NM_020116.3 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:162307318 G>A maps to NM_020116.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:162402285 A>G maps to NM_020116.3 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr4:162307171 G>A maps to NM_020116.3 Y757Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:162680653 A>G maps to NM_020116.3 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:162680653 A>G maps to NM_020116.3 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr21:47557170 G>A maps to ENST00000397748 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr21:47571844 C>T maps to ENST00000397748 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:31090041 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:31089871 C>T did not map to a codon.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr23:31089556 C>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:121188110 C>T maps to NM_177478.1 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:53907765 C>T maps to NM_001080432.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:53913778 T>C maps to NM_001080432.2 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr16:53860209 C>T maps to NM_001080432.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr16:53859805 C>T maps to NM_001080432.2 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:48340876 C>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:48340993 G>A did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:48340101 C>A did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr7:2279193 G>T maps to NM_013393.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:61901767 C>T maps to NM_017647.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:61902632 A>G maps to NM_017647.3 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:61898985 G>A maps to NM_017647.3 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:71318025 G>A maps to NM_018348.5 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:71317966 A>G maps to NM_018348.5 D619D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:71318914 A>G maps to NM_018348.5 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr16:71318527 T>C maps to NM_018348.5 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:71318569 C>T maps to NM_018348.5 W418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr6:37426524 T>C maps to NM_015050.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:37430661 C>T maps to NM_015050.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:37440241 G>A maps to NM_015050.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:37440241 G>A maps to NM_015050.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr6:37426440 C>T maps to NM_015050.2 C277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:37430703 C>T maps to NM_015050.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:37426521 C>G maps to NM_015050.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:37426575 A>G maps to NM_015050.2 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr1:78428484 A>G maps to ENST00000436586 Y459Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:78426048 T>A maps to ENST00000436586 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr1:78430839 C>T maps to ENST00000436586 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:78414845 T>G maps to ENST00000436586 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:133491781 C>T maps to NM_003934.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:133491781 C>T maps to NM_003934.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:133506175 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:143828533 C>T maps to NM_032020.4 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr6:143825324 C>T maps to NM_032020.4 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:143823205 G>T maps to NM_032020.4 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:70500792 G>A maps to NM_145059.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:70504971 G>A maps to NM_145059.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr16:70505101 C>T maps to NM_145059.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:70503206 C>T maps to NM_145059.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr16:70508131 C>T maps to NM_145059.2 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:44401265 A>C did not map to a codon.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr23:44386550 T>C did not map to a codon.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr23:154261806 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:154261690 A>C did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:91422702 G>A maps to NM_002569.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:91424618 C>T maps to NM_002569.2 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:91424645 C>T maps to NM_002569.2 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr15:91419721 C>T maps to NM_002569.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr15:91425098 C>T maps to NM_002569.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr15:91423935 C>T maps to NM_002569.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr15:91424199 C>G maps to NM_002569.2 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:31193941 C>A maps to NM_004960.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:31202389 T>C maps to NM_004960.3 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr16:31193861 C>T maps to NM_004960.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr19:49253899 G>A maps to NM_000148.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr19:49253950 C>T maps to NM_000148.3 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:49254343 G>A maps to NM_000148.3 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr19:49254085 C>T maps to NM_000148.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr19:49253668 C>T maps to NM_000148.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr8:33246992 G>A maps to ENST00000380081 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr8:33318898 G>A maps to ENST00000380081 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:33310836 C>T maps to ENST00000380081 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:33246972 G>A maps to ENST00000380081 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr10:75533459 C>A maps to NM_173540.2 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:49207082 G>A maps to NM_001097638.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr19:49206461 C>T maps to NM_001097638.2 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:49207128 C>T maps to NM_001097638.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:5866956 G>A maps to NM_002034.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:5831552 T>C maps to NM_001040701.1 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:139925311 G>A maps to NM_004479.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr14:66136172 T>C maps to NM_178155.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr14:66136172 T>G maps to NM_178155.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr14:66136172 T>C maps to NM_178155.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:66083892 A>C maps to NM_004480.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:66209074 C>T maps to NM_178155.1 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr14:66188637 G>A maps to NM_178155.1 W327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr6:96651361 C>T maps to NM_006581.3 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:96651663 A>G maps to NM_006581.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:50310454 G>A maps to NM_025129.4 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr19:50316276 G>A maps to NM_025129.4 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr19:50315909 G>T maps to NM_025129.4 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:180667023 G>T maps to NM_005087.3 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr3:180680718 C>T maps to NM_005087.3 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:7499183 A>G maps to NM_004860.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:7499266 G>A maps to NM_004860.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:35631516 C>T maps to NM_005031.3 H26H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:35648345 G>A maps to NM_001164605.1 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:35655083 G>A maps to NM_001164605.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr11:117712536 G>A maps to NM_001164831.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr5:39202246 G>T maps to ENST00000263405 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:39126230 T>C maps to ENST00000263405 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr5:39126220 G>A maps to ENST00000263405 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:45972742 G>A maps to NM_024513.2 I1357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr3:46016732 G>A maps to NM_024513.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:112025267 G>A maps to NM_153047.1 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:112017651 C>T maps to NM_153047.1 W287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:112041194 G>A maps to NM_153047.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:112025267 G>A maps to NM_153047.1 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr6:112041226 C>A maps to NM_153047.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr6:112020829 C>T maps to NM_153047.1 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:112015620 T>C maps to NM_153047.1 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr6:112017478 C>T did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr6:112017478 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:197503819 G>T maps to NM_032288.6 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:90895133 C>T maps to NM_003505.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:90895349 C>T maps to NM_003505.1 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:90895664 C>T maps to NM_003505.1 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:90894893 C>T maps to NM_003505.1 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:130648620 C>T maps to NM_007197.3 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:130648176 G>A maps to NM_007197.3 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:130648971 C>T maps to NM_007197.3 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr12:130647573 G>T maps to NM_007197.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:130648149 C>T maps to NM_007197.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:42636600 G>A maps to NM_001466.3 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:42636588 G>A maps to NM_001466.3 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:42635328 C>T maps to NM_001466.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:42636354 C>T maps to NM_001466.3 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr17:42636600 G>A maps to NM_001466.3 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:42635259 C>T maps to NM_001466.3 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:28385131 C>A maps to NM_017412.3 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr8:28385221 T>C maps to NM_017412.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:104336726 G>A maps to NM_003506.3 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:104340563 C>T maps to NM_003506.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:104330965 T>G maps to NM_003506.3 L109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:202900170 G>A maps to NM_003507.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:202900080 C>T maps to NM_003507.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:202900842 C>T maps to NM_003507.1 Y491Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr2:202900752 C>T maps to NM_003507.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr2:202900248 G>A maps to NM_003507.1 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr2:202900539 C>T maps to NM_003507.1 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:35928803 G>A maps to NM_031866.2 D518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:35929112 C>T maps to NM_031866.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:35929055 G>A maps to NM_031866.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:35930279 C>A maps to NM_031866.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:35928665 C>T maps to NM_031866.2 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:72849236 G>A maps to NM_003508.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:72849197 C>T maps to NM_003508.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:72849809 C>T maps to NM_003508.2 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr7:72850055 C>T maps to NM_003508.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr1:209849220 G>A maps to NM_015714.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:31071310 T>C maps to NM_017769.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr14:31081492 C>T maps to NM_017769.3 L527L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A6-2672-01A-01W-0833-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:151169955 C>T maps to NM_198395.1 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:151179561 G>A did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr4:76570760 G>T maps to NM_203505.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:42152694 C>T maps to NM_138387.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr17:42152399 G>A maps to NM_138387.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:42152339 C>A maps to NM_138387.3 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr17:42152706 C>T maps to NM_138387.3 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr17:42151629 T>C maps to NM_138387.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:153762658 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:153762269 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:153762675 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:153763387 G>T did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:153762328 C>T did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:153761270 C>T did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:153761843 C>T did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:153774344 C>T did not map to a codon.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr23:153760228 G>T did not map to a codon.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr23:153760890 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr23:153760227 G>T did not map to a codon.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr23:153764231 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:153760227 G>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:78078777 C>T maps to NM_001079804.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr4:144336805 C>T maps to NM_207123.2 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr4:144361030 T>C maps to NM_207123.2 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:144359746 C>T maps to NM_207123.2 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:144361276 C>T maps to NM_207123.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr4:144361441 A>C maps to NM_207123.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:144387341 C>A maps to NM_207123.2 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:77932743 G>A maps to NM_080491.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr11:77937886 G>A maps to NM_080491.2 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr11:77930446 G>A maps to NM_080491.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr11:77933206 G>A maps to NM_080491.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:77937862 G>A maps to NM_080491.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:153928300 T>A did not map to a codon.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr23:153927571 T>A did not map to a codon.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr23:153928303 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:153940640 C>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:153924240 A>C did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:153928304 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:153908448 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:153944339 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:153944423 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:153924197 G>A did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:153906482 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:153906479 G>A did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:153906455 C>G did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr22:17468905 T>C maps to NM_001037814.1 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr22:17445745 G>T maps to NM_001037814.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:17468926 C>T maps to NM_001037814.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr6:29576386 G>A maps to NM_001470.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:29572333 G>A maps to NM_001470.2 N883N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr6:29599362 T>A maps to NM_001470.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:29581253 C>T maps to NM_001470.2 Q444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr6:29574953 G>A maps to NM_001470.2 Y678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:29598264 G>A maps to NM_001470.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:29574953 G>A maps to NM_001470.2 Y678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:29591191 G>A maps to NM_001470.2 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:101304193 G>A maps to NM_005458.7 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr9:101168384 G>T maps to NM_005458.7 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:101073403 G>A maps to NM_005458.7 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:101216492 G>A maps to NM_005458.7 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:101068537 G>A maps to NM_005458.7 N698N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr21:27136931 C>T maps to NM_002040.3 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr21:27136963 C>T maps to NM_002040.3 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr21:27113930 G>T maps to NM_002040.3 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr21:27121412 C>T maps to NM_002040.3 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr21:27134676 G>A did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr15:50601902 G>T maps to NM_005254.5 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:151079543 C>T maps to NM_144618.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:151079639 A>G maps to NM_144618.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:151070419 G>A maps to NM_144618.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr5:161300148 T>C maps to NM_001127648.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr5:161302589 G>A maps to NM_001127648.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr5:161300148 T>C maps to NM_001127648.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:161300148 T>C maps to NM_001127648.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:161322741 T>C maps to NM_001127648.1 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:46334646 G>A maps to ENST00000507069 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:46314654 G>A maps to ENST00000507069 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:46388183 C>A maps to ENST00000507069 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr23:151336815 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:151376585 G>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:151532942 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:151514066 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:151533038 T>C did not map to a codon.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr23:151514096 C>T did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:151336918 A>G did not map to a codon.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr4:46930281 A>C maps to NM_000809.2 L542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:46966985 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:46976284 G>A maps to NM_000809.2 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:27128355 C>T maps to NM_000810.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:27182353 C>T maps to NM_000810.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr15:27185150 C>T maps to NM_000810.3 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr15:27128507 C>T maps to NM_000810.3 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:27128355 C>T maps to NM_000810.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:27193301 C>T maps to NM_000810.3 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:27128517 G>A maps to NM_000810.3 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr15:27128677 C>T maps to NM_000810.3 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr15:27160015 T>G maps to NM_000810.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:27182398 G>A maps to NM_000810.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:161128724 C>T maps to NM_000811.2 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:161119082 C>T maps to NM_000811.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:161128571 C>T maps to NM_000811.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:161119103 C>A maps to NM_000811.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr5:161117307 C>T maps to NM_000811.2 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr5:161128736 T>C maps to NM_000811.2 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr5:161128736 T>C maps to NM_000811.2 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr5:161128619 T>C maps to NM_000811.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:161128640 G>A maps to NM_000811.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr4:47427753 G>T maps to NM_000812.3 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:47163448 C>T maps to NM_000812.3 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:47033679 A>G maps to NM_000812.3 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr4:47427959 C>T maps to NM_000812.3 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:26812788 C>T maps to NM_021912.4 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:26825535 T>C maps to NM_021912.4 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:26825508 G>A maps to NM_021912.4 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:26806110 T>A maps to NM_021912.4 K350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:26806116 T>A maps to NM_021912.4 K348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:26812788 C>T maps to NM_021912.4 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:27017587 G>A maps to NM_021912.4 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr15:26866522 T>G maps to NM_021912.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:27018810 G>T maps to NM_021912.4 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:1961426 C>T maps to NM_000815.4 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:1960601 C>T maps to NM_000815.4 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:1957036 T>C maps to NM_000815.4 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:151129760 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:151138712 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:151123497 C>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:151123279 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:151129802 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:151123950 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:151123900 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:151130965 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:151129758 A>G did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:151129759 G>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:151123994 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr4:46067523 A>G maps to NM_173536.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr4:46043241 A>G maps to NM_173536.3 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr4:46099353 T>A maps to NM_173536.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr4:46043241 A>G maps to NM_173536.3 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr4:46053581 C>T maps to NM_173536.3 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr5:161576231 C>T maps to NM_198903.2 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:161569245 C>A maps to NM_198903.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr5:161530998 A>C maps to NM_198903.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr5:161580199 C>T maps to NM_198903.2 D458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr5:161524810 C>T maps to NM_198903.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:161576234 T>C maps to NM_198903.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr15:27572152 C>T maps to NM_033223.4 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:27772648 C>T maps to NM_033223.4 Y312Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:27725864 C>A maps to NM_033223.4 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr15:27574003 C>T maps to NM_033223.4 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr15:27772702 G>A maps to NM_033223.4 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr5:170235673 C>T maps to NM_014211.2 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:151821311 T>C did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:151815620 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:151814043 G>T did not map to a codon.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr23:151820207 G>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:151815615 C>T did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:151820174 G>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:151820153 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:151821370 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:151818998 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:151818225 T>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:151821309 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:151820076 C>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:151806749 T>C did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:151821310 A>G did not map to a codon.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr23:151815583 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:151821310 A>G did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr23:151821311 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:151817770 G>T did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:151821285 G>A did not map to a codon.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr6:89890187 G>T maps to NM_002042.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr6:89907749 G>T maps to NM_002042.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:89890169 C>G maps to NM_002042.3 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr6:89888634 C>A maps to NM_002042.3 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr6:89978954 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:89967671 G>T maps to NM_002043.2 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr3:97705721 T>G maps to NM_001105580.1 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:97726746 T>A maps to NM_001105580.1 *205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:97753721 G>T maps to NM_001105580.1 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:97726614 G>A maps to NM_001105580.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr2:171716382 G>A maps to NM_000817.2 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:171678624 T>C maps to NM_000817.2 H37H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:171700553 G>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:171702521 G>A maps to NM_000817.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:26518594 C>T maps to NM_001134366.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:26507981 G>A maps to NM_001134366.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr10:26506539 G>A maps to NM_001134366.1 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:13065201 G>T maps to NM_052850.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:49173763 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:49161348 G>A did not map to a codon.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr23:49179754 G>A did not map to a codon.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr23:49179716 A>G did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:843472 C>T maps to NM_005255.2 R1308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:845592 C>T maps to NM_005255.2 S1151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:887730 G>A maps to NM_005255.2 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:877201 G>A maps to NM_005255.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:860942 G>A maps to NM_005255.2 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr22:30951317 G>A maps to NM_004861.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:30951872 A>G maps to NM_004861.1 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:242743475 C>T maps to NM_022134.2 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:242742809 C>T maps to NM_022134.2 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:242741318 C>T maps to NM_022134.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:99758174 G>A maps to NM_024637.4 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr7:99758054 G>A maps to NM_024637.4 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:99764277 C>T maps to NM_024637.4 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:88401183 C>T maps to NM_000153.2 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:24125439 G>A maps to NM_001008216.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:24123058 C>T maps to NM_001008216.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:24123369 G>T maps to NM_001008216.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:24124705 C>T maps to NM_001008216.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:73754427 C>A maps to ENST00000437911 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:73759467 C>T maps to ENST00000437911 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:73760038 C>T maps to ENST00000437911 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:49509453 T>C maps to NM_002044.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:49493397 A>T maps to NM_002044.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr15:49574269 A>G maps to NM_002044.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:38908516 G>A maps to NM_138801.2 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr16:88901660 C>T maps to NM_000512.4 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:88901651 G>A maps to NM_000512.4 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr16:88898411 T>C maps to NM_000512.4 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:33289704 C>T maps to NM_020474.3 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:33257665 C>T maps to NM_020474.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr5:153789138 C>T maps to NM_198321.3 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:153765980 C>T maps to NM_198321.3 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:153760080 C>T maps to NM_198321.3 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:153677534 C>T maps to NM_198321.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:151797896 G>T maps to NM_022087.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:151791542 C>T maps to NM_022087.2 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:151805264 C>T maps to NM_022087.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:151810422 C>A maps to NM_022087.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:101606463 C>T maps to NM_024642.3 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:101594116 C>T maps to NM_024642.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr9:101585624 T>C maps to NM_024642.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr2:154801132 T>C maps to NM_052917.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr2:155306960 C>T maps to NM_052917.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:155102454 G>T maps to NM_052917.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:155157938 C>T maps to NM_052917.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr2:155295172 G>T maps to NM_052917.2 G489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:155306934 C>A maps to NM_052917.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:155306934 C>T maps to NM_052917.2 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:155252596 C>T maps to NM_052917.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:155306936 A>G maps to NM_052917.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr2:31215852 G>A maps to NM_024572.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr2:31133823 G>C maps to NM_024572.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr2:31168724 C>A maps to NM_024572.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr2:31133844 G>A maps to NM_024572.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:31133826 G>A maps to NM_024572.2 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:31165142 G>A maps to NM_024572.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr2:31215852 G>A maps to NM_024572.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:31133838 G>A maps to NM_024572.2 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:31360902 C>T maps to NM_024572.2 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:230338889 A>G maps to NM_004481.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:230401051 T>A maps to NM_004481.3 L460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:230372443 C>T maps to NM_004481.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:230372104 T>C maps to NM_004481.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr2:166621442 A>G maps to NM_004482.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:166613619 C>T maps to NM_004482.3 W443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:166605290 T>G maps to NM_004482.3 *634Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr2:166621442 A>G maps to NM_004482.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr2:166626715 T>C maps to NM_004482.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr2:166621442 A>G maps to NM_004482.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:166606308 A>G maps to NM_004482.3 C574C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:166626715 T>C maps to NM_004482.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:89917753 G>A maps to NM_003774.4 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:158115028 C>T maps to NM_014568.1 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr2:158114818 A>G maps to NM_014568.1 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr2:158156137 T>C maps to NM_014568.1 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr2:158140859 A>G maps to NM_014568.1 E507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr2:158156137 T>C maps to NM_014568.1 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr2:158156137 T>C maps to NM_014568.1 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:51754612 C>T maps to NM_007210.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:51753077 G>A maps to NM_007210.3 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:51758059 G>A maps to NM_007210.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:51754522 G>A maps to NM_007210.3 N383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:51758029 G>A maps to NM_007210.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr12:51748225 G>A maps to NM_007210.3 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:51751153 G>A maps to NM_007210.3 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:174223218 A>G maps to NM_017423.2 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:174219283 G>A maps to NM_017423.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr4:174235210 C>T maps to NM_017423.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:174216608 C>T maps to NM_017423.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr4:174219442 G>A maps to NM_017423.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:4835956 G>A maps to NM_017417.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:4855381 A>T maps to NM_017417.1 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:4870215 C>T maps to NM_017417.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:132685782 G>A maps to NM_001122636.1 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:132683760 G>A maps to NM_001122636.1 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:69800216 G>A maps to NM_020692.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:16264159 C>T maps to NM_054110.4 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr3:16254134 C>T maps to NM_054110.4 Y419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:16268973 T>A maps to NM_054110.4 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr3:16217077 C>T maps to NM_054110.4 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr11:11454219 C>T maps to NM_198516.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:11314602 C>T maps to NM_198516.2 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:11400659 G>T maps to NM_198516.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr7:151699835 G>T maps to NM_145292.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:151705005 G>T maps to NM_145292.3 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr7:151711778 A>G maps to NM_145292.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr7:151716756 T>C maps to NM_145292.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:151716756 T>C maps to NM_145292.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr7:151711778 A>G maps to NM_145292.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr7:151711778 A>G maps to NM_145292.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr7:151711778 A>G maps to NM_145292.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr4:173269751 A>T maps to NM_001034845.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:173232774 A>G maps to NM_001034845.2 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr4:173269782 C>T maps to NM_001034845.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:74963023 C>T maps to NM_001480.3 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:74962605 C>T maps to NM_001480.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr18:74980779 A>G maps to NM_001480.3 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr18:74962644 T>C maps to NM_001480.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr19:1399019 G>A maps to NM_138924.1 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:81388170 C>T maps to NM_022041.3 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:81391439 C>T maps to NM_022041.3 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:81391439 C>T maps to NM_022041.3 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:81397412 C>T maps to NM_022041.3 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:81397493 C>T maps to NM_022041.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:81388060 C>T maps to NM_022041.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:62406564 C>T maps to NM_198335.2 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:62393906 C>A maps to NM_198335.2 G864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr11:62407100 G>T maps to NM_198335.2 C47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:42630585 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:42618581 G>A maps to NM_198141.2 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr15:42614112 G>A maps to NM_198141.2 W396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:36033441 G>A maps to NM_014364.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:128064535 C>T maps to NM_015635.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr9:128070038 T>C maps to NM_015635.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr9:128099545 G>A maps to NM_015635.2 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:128099687 C>T maps to NM_015635.2 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:128111711 C>T maps to NM_015635.2 D1098D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:128099734 T>C maps to NM_015635.2 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:128092495 A>G maps to NM_015635.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr9:128083728 T>C maps to NM_015635.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:128070106 T>C maps to NM_015635.2 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr9:128103502 A>G maps to NM_015635.2 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:128118025 G>A maps to NM_015635.2 A1314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr9:130095308 A>G maps to NM_032293.4 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:130098438 C>T maps to NM_032293.4 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:130117613 G>T maps to NM_032293.4 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:130098492 C>T maps to NM_032293.4 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:130119577 G>A maps to NM_032293.4 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:30671086 T>C maps to NM_002047.2 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:30656824 G>A maps to NM_002047.2 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:30673439 G>T maps to NM_002047.2 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:30649217 G>A maps to NM_002047.2 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:30668180 G>T maps to NM_002047.2 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:34889727 G>A maps to NM_001136006.1 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:34894555 G>A maps to NM_001136006.1 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:34876520 A>G maps to NM_001136006.1 H981H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr21:34911477 G>A maps to NM_001136006.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr21:34876493 C>A maps to NM_001136006.1 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:22696537 C>A maps to NM_005256.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr11:22759269 A>G maps to NM_005256.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:22696507 T>G maps to NM_005256.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr22:29708417 G>A maps to NM_152236.1 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:34073168 C>A maps to NM_139285.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:34079749 C>T maps to NM_139285.2 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr17:34074204 G>T maps to NM_139285.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:34073378 G>A maps to NM_139285.2 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:101017791 A>G maps to NM_174942.1 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr12:101016161 T>G did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:9862568 G>A maps to NM_201433.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:9923133 C>T maps to NM_201433.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:9862536 G>A maps to NM_201433.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr17:9830077 G>A maps to NM_201433.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr17:9850237 G>A maps to NM_201433.1 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:90094048 G>A maps to NM_001481.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr23:48649605 A>G did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:48650311 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:48649737 T>C did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:48649602 A>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:48652358 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:48650386 G>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:48650809 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:48652310 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:48650389 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:48650853 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:48650478 C>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:48649688 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:48649564 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:48649603 T>C did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:48649702 T>C did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:48649669 A>G did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:48649553 A>G did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:48649670 C>T did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:48649733 C>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:48649565 A>G did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:48649593 C>A did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:128202737 G>A maps to NM_032638.4 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:128200119 A>C maps to NM_032638.4 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr3:128200729 A>G maps to NM_032638.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:128204678 C>T maps to NM_032638.4 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:8100469 G>A maps to NM_001002295.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:8100643 C>T maps to NM_001002295.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:11607621 C>T maps to NM_002052.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:11615947 C>A maps to NM_002052.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:11614477 C>T maps to NM_002052.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr7:92080016 C>T maps to NM_021167.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:153800732 G>A maps to NM_020699.2 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:153800715 C>A maps to NM_020699.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr1:153784506 C>T maps to NM_020699.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:45654351 G>A maps to ENST00000432007 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:30684751 T>G maps to ENST00000330168 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr22:30683541 G>A maps to ENST00000434291 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr22:30682268 A>G maps to NM_001037666.2 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:155207350 A>G maps to NM_001005742.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:155207998 C>T maps to NM_001005742.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:155209727 G>A maps to NM_001005742.2 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:35737803 G>A maps to NM_020944.2 Q816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:35739366 G>T maps to NM_020944.2 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:22820386 G>A maps to NM_020973.3 W417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:22820530 T>G maps to NM_020973.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:22749192 G>A maps to NM_020973.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:22749268 C>T maps to NM_020973.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:22820362 C>A maps to NM_020973.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:22749049 G>T maps to NM_020973.3 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:81640217 C>T maps to ENST00000264326 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr3:81699051 G>A maps to ENST00000264326 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:81630324 G>A maps to ENST00000264326 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:104126942 A>G maps to NM_004193.2 K844K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:104018767 C>T maps to NM_004193.2 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:104139293 C>T maps to NM_004193.2 C1553C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:104125323 C>T maps to NM_004193.2 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr10:104128552 C>T maps to NM_004193.2 I978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:136029050 G>C maps to NM_021996.4 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:89519109 G>A maps to NM_002053.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:89523681 G>A maps to NM_002053.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr1:89522644 G>T maps to NM_002053.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:89524575 T>C maps to NM_002053.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:89528848 C>T maps to NM_002053.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:89524695 T>C maps to NM_002053.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:89522548 T>C maps to NM_002053.2 Q381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:89579785 C>T maps to NM_004120.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:89477537 G>T maps to NM_018284.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:89477603 T>G maps to NM_018284.2 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:89486335 C>T maps to NM_018284.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr1:89481074 C>A maps to NM_018284.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:89659056 A>G maps to NM_052941.4 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:89655890 G>A maps to NM_052941.4 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:89735133 C>T maps to NM_052942.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:89729562 C>T maps to NM_052942.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:89734519 C>T maps to NM_052942.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:89730611 G>A maps to NM_052942.3 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:89834125 A>T maps to NM_198460.2 K6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:89835207 C>A maps to NM_198460.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:89845978 C>A maps to NM_198460.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:89616099 G>A maps to NM_207398.2 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:89615229 G>A maps to NM_207398.2 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:89615133 G>T maps to NM_207398.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:150845833 G>A maps to NM_001098834.1 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:237074711 G>A maps to NM_001485.2 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:72623782 G>T maps to ENST00000504199 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr4:72618246 G>A maps to ENST00000504199 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:163215667 G>A did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr22:38211182 C>T maps to NM_001171690.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr7:127222790 C>A maps to NM_024523.5 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr7:127222949 T>C maps to NM_024523.5 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:127225212 G>A maps to NM_024523.5 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:127222288 G>A maps to NM_024523.5 Q703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:109087545 A>G maps to NM_181453.3 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:109092067 G>T maps to NM_181453.3 E980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:109098744 T>C maps to NM_181453.3 C1061C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr2:109087641 G>A maps to NM_181453.3 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr2:109088073 T>G maps to NM_181453.3 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr21:34132275 A>G maps to NM_016631.3 N335N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr21:34134571 G>A maps to NM_016631.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:34142145 C>A maps to NM_016631.3 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr21:34123488 G>A maps to NM_016631.3 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:34109596 G>A maps to NM_016631.3 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr21:34133367 A>G did not map to a codon.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr21:34134413 C>T maps to NM_016631.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr21:34132230 G>A maps to NM_016631.3 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr2:163003972 G>A maps to ENST00000233604 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:163003890 G>A maps to ENST00000233604 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:163003900 T>C maps to ENST00000233604 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr15:41059450 C>A maps to NM_005258.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:44189612 C>T maps to NM_000162.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr7:44189377 G>A maps to NM_000162.3 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:44189603 G>A maps to NM_000162.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr7:44189371 G>A maps to NM_000162.3 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:44187319 G>A maps to NM_000162.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:44184879 C>A did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr7:44190668 G>A maps to NM_000162.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:44185127 G>A maps to NM_000162.3 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr7:44187277 G>A maps to NM_000162.3 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:27745343 C>T maps to NM_001486.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:27730117 T>C maps to NM_001486.3 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:27730117 T>C maps to NM_001486.3 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:27722271 C>T maps to NM_001486.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:27731051 C>A maps to NM_001486.3 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:27722271 C>A maps to NM_001486.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr2:27722271 C>T maps to NM_001486.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:27745334 T>C maps to NM_001486.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr6:53379055 C>T maps to NM_001498.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:53363685 A>G maps to NM_001498.3 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:52993609 G>A maps to NM_003643.3 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr6:10874875 A>G maps to NM_004752.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr6:10876689 C>T maps to NM_004752.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:10875153 G>A maps to NM_004752.3 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:10877553 C>T maps to NM_004752.3 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:10874512 C>T maps to NM_004752.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:10874449 C>T maps to NM_004752.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr6:10875151 T>C maps to NM_004752.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr6:10874797 G>A maps to NM_004752.3 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr6:10874449 C>A maps to NM_004752.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:10875151 T>C maps to NM_004752.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:10874875 A>G maps to NM_004752.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:10875151 T>C maps to NM_004752.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:10874827 C>T maps to NM_004752.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:120611962 G>A maps to NM_006836.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:120597761 G>T maps to NM_006836.1 G872G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:120621397 G>A maps to NM_006836.1 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:120565670 G>A maps to NM_006836.1 D2666D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:120574454 A>G maps to NM_006836.1 L2287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:120611466 G>T maps to NM_006836.1 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:120596336 C>T maps to NM_006836.1 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:120611631 T>G did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:120567151 G>A maps to NM_006836.1 T2606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:120621461 G>A maps to NM_006836.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:120574413 C>T maps to NM_006836.1 R2300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:120589063 G>C maps to NM_006836.1 A1398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:120591142 A>G maps to NM_006836.1 Y1312Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:120582537 G>T maps to NM_006836.1 R1753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr9:79118163 C>T maps to NM_001097636.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:79118163 C>T maps to NM_001097636.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:79118112 C>T maps to NM_001097636.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:10621674 C>T maps to NM_145649.4 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:10557072 G>A maps to NM_001491.2 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:10529449 C>T maps to NM_145649.4 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr6:10557282 A>G maps to NM_001491.2 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr6:10529440 C>T maps to NM_145649.4 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:59911394 G>T maps to NM_004751.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:74324605 G>T maps to NM_016591.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:74325791 C>T maps to NM_016591.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:57929906 G>A maps to NM_001018090.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr15:57913813 C>T maps to NM_001018090.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:74860097 A>G maps to ENST00000238018 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:74840687 T>G maps to ENST00000238018 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr9:74860097 A>G maps to ENST00000238018 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr9:74834403 A>G maps to ENST00000238018 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:75276556 T>C maps to NM_018972.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:42887116 C>T maps to NM_024034.3 H139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:42907861 C>T maps to NM_024034.3 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:118424459 G>A maps to NM_017686.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr16:19516279 G>C maps to NM_016641.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr16:19528412 A>G maps to NM_016641.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:48428730 G>A maps to NM_004962.2 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:48428829 C>T maps to NM_004962.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:18499510 G>A maps to NM_004864.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:48413859 G>A maps to NM_016204.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:48413583 G>A maps to NM_016204.1 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:48413613 G>A maps to NM_016204.1 Y418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr10:48413904 G>A maps to NM_016204.1 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:7848240 G>T maps to NM_020634.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:7848318 A>G maps to NM_020634.1 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr20:34025225 C>T maps to NM_000557.2 P161P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AU-6004-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:34022108 G>A maps to ENST00000374375 T51T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AZ-4315-01A-01D-1408-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AZ-6598-01A-11D-1771-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CM-6677-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr20:34021706 C>A maps to NM_000557.2 *502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr8:97172827 G>A maps to NM_001001557.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr8:97172647 G>A maps to NM_001001557.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr8:97157669 G>A maps to NM_001001557.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr8:97156940 C>T maps to NM_001001557.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:20870224 C>T maps to NM_182828.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:132200008 G>A maps to NM_005260.3 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:132197469 A>G maps to NM_005260.3 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:132200087 A>G maps to NM_005260.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:132197319 C>T maps to NM_005260.3 E442E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:153670882 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:5838765 G>A maps to NM_001494.3 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:37834847 C>T maps to NM_001190468.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:37816031 G>T maps to NM_001190468.1 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:37815920 G>A maps to NM_001190468.1 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr17:57348305 A>G maps to NM_182569.3 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:57322786 C>T maps to NM_182569.3 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:69647187 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:69652283 C>T did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr23:69647196 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:69652906 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:69652245 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:69646847 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:69649806 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:69646529 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:76982357 T>C maps to ENST00000376217 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:76944067 A>G did not map to a codon.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr11:75168749 G>A maps to NM_030792.6 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:75152761 G>A maps to NM_030792.6 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:75160998 C>T maps to NM_030792.6 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:75150997 G>A maps to NM_030792.6 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:58009347 C>T maps to NM_001111270.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:58006809 C>T maps to NM_001111270.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:58009470 A>C maps to NM_001111270.1 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:58006740 G>A maps to NM_001111270.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:58009320 C>A maps to NM_001111270.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:95262609 G>T maps to NM_181702.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:95264345 G>A maps to NM_181702.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:95264364 G>A maps to NM_181702.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:95262747 G>A maps to NM_181702.2 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:648243 C>T maps to NM_015721.2 E1013E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:650076 G>T maps to NM_015721.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:649335 G>A maps to NM_015721.2 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:650283 G>A maps to NM_015721.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr17:650373 G>T maps to NM_015721.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:154297546 G>A maps to NM_015465.3 H539H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:154282718 C>T maps to NM_015465.3 V883V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:154287275 G>T maps to NM_015465.3 S757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:154271207 C>T maps to NM_015465.3 L1285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:154287274 C>T maps to NM_015465.3 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:154272091 G>A maps to NM_015465.3 C1205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:45593512 T>C maps to NM_024707.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr23:14027261 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:14027141 C>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:14038484 G>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:17962591 G>T maps to NM_001130009.1 E705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:17954544 A>G maps to NM_001130009.1 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr17:42991125 C>T maps to NM_002055.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:42985452 G>A maps to NM_002055.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:92941603 C>T maps to NM_005263.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr1:92944145 A>G maps to NM_005263.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr1:92944145 A>G maps to NM_005263.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr9:135862798 G>A maps to NM_004188.4 P77P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A6-5656-01A-21D-1835-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-3655-01A-02D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:158409189 C>T maps to ENST00000264263 D749D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AD-6548-01A-11D-1835-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AY-6196-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:158371185 T>C maps to ENST00000264263 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:158376716 C>T maps to ENST00000264263 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr3:158371187 A>G maps to ENST00000264263 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr3:158363503 T>C maps to ENST00000264263 D56D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-F4-6807-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:74018215 T>C maps to NM_032380.3 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr5:74026211 A>G maps to NM_032380.3 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:13365112 G>A maps to NM_018988.2 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr5:179729554 G>A maps to NM_005110.2 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:179739523 G>T maps to NM_005110.2 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr5:179743365 G>A maps to NM_005110.2 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:179739487 G>A maps to NM_005110.2 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:179744023 G>A maps to NM_005110.2 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:117856199 G>A maps to NM_005264.4 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:117884970 C>T maps to NM_005264.4 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr10:117856226 A>T maps to NM_005264.4 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr10:117884825 G>A maps to NM_005264.4 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:117849266 C>T maps to NM_005264.4 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr10:117884823 T>A maps to NM_005264.4 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr10:117884823 T>C maps to NM_005264.4 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr10:117884823 T>C maps to NM_005264.4 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:137593479 G>A maps to NM_001496.3 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:3641211 C>A maps to NM_145762.2 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr20:3641212 G>A maps to NM_145762.2 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:55223856 T>C maps to NM_207410.2 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:55216049 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:55266626 G>A maps to NM_207410.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:55223886 A>G maps to NM_207410.2 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr22:38026099 C>T maps to ENST00000381756 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:23507061 C>T maps to NM_015044.4 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:23494256 G>A maps to NM_015044.4 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:23503027 G>A maps to NM_015044.4 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:23498052 A>C maps to NM_015044.4 L213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:23504779 C>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:73237109 C>T maps to NM_138619.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr17:73236435 C>T maps to NM_138619.2 W417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:85777723 G>A maps to NM_000821.4 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr2:85785624 G>A maps to NM_000821.4 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:85782631 G>T maps to NM_000821.4 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:63936644 G>A maps to NM_003878.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:38876296 C>T maps to NM_152657.3 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:38877739 G>A maps to NM_152657.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr19:38877643 A>C maps to NM_152657.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:38877250 G>A maps to NM_152657.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr19:38876167 G>A maps to NM_152657.3 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:38877091 G>C maps to NM_152657.3 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:34923616 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:34937863 G>T maps to NM_024835.3 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr22:25010757 C>T maps to NM_005265.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr22:24622661 C>T maps to NM_001099781.1 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:4462997 C>T maps to ENST00000414312 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:33437794 C>T maps to NM_178026.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:33447365 C>T maps to NM_178026.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:23966809 G>A maps to NM_178311.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:23967200 G>A maps to NM_178311.2 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr20:23966528 C>A maps to NM_178311.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr17:61995179 A>C maps to NM_000515.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:61995469 C>T maps to NM_000515.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr17:61995188 G>A maps to NM_000515.3 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr17:61958170 G>A maps to NM_002059.3 H139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr17:61958119 T>C maps to NM_022557.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:61958040 G>A maps to NM_022557.2 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:40344926 C>T maps to NM_032484.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:40344980 A>G maps to NM_032484.4 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr10:85903784 G>A maps to ENST00000436406 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:85903761 G>T maps to ENST00000436406 G84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr10:85901369 G>A maps to ENST00000436406 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr5:42718973 A>G maps to NM_000163.2 K455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:42719396 C>T maps to NM_000163.2 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr5:42711412 C>T maps to NM_000163.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr5:42718688 A>G maps to NM_000163.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr5:42718688 A>G maps to NM_000163.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:42689022 C>T maps to NM_000163.2 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:31008525 A>G maps to NM_000823.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr3:172165930 G>A maps to NM_198407.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:172166122 G>A maps to NM_198407.2 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:172165456 C>A maps to NM_198407.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr3:172165639 G>A maps to NM_198407.2 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:172166071 C>T maps to NM_198407.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:59610012 C>T maps to NM_005142.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr11:59597016 C>A maps to NM_005142.2 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:100285137 C>T maps to NM_022574.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr7:100279775 C>T maps to NM_022574.4 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:100281713 C>T maps to NM_022574.4 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:233681730 C>T maps to ENST00000373566 R809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:233712211 G>A maps to ENST00000373566 Q1227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr2:233684544 T>C maps to ENST00000373566 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:233721554 G>A maps to ENST00000373566 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr2:233626111 C>T maps to ENST00000373566 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:233613720 G>T maps to ENST00000373566 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:233613720 G>T maps to ENST00000373566 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:233710456 G>C maps to ENST00000373566 V1129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:233620983 C>T maps to ENST00000373566 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:233677151 A>G maps to ENST00000373566 P708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr2:233659581 T>C maps to ENST00000373566 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:233708805 A>G maps to ENST00000373566 Q1002Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr2:233620971 C>T maps to ENST00000373566 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:233659581 T>C maps to ENST00000373566 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr2:233656088 G>A maps to ENST00000373566 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:233652023 C>T maps to ENST00000373566 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:150417541 C>A maps to NM_130759.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:150389905 C>T maps to NM_015660.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:150389676 G>C maps to NM_015660.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr7:150269274 C>T maps to ENST00000430830 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:150269439 G>A maps to ENST00000430830 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:150269274 C>A maps to ENST00000430830 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr7:150269274 C>T maps to ENST00000430830 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr7:150440144 C>A maps to ENST00000447239 Y342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:150439956 C>T maps to ENST00000447239 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:150439742 C>T maps to ENST00000447239 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:150324836 G>A maps to ENST00000438845 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:150325094 G>A maps to ENST00000438845 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:150325355 G>A maps to ENST00000438845 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:150217752 G>T maps to NM_153236.3 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr7:150217394 C>T maps to NM_153236.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:150217529 C>T maps to NM_153236.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr7:150217707 C>A maps to NM_153236.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr7:150217094 C>T maps to NM_153236.3 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:150171544 G>A maps to NM_175571.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:150171328 G>A maps to NM_175571.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:150164370 G>A maps to NM_175571.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:150174549 G>A maps to NM_175571.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:150171155 G>T maps to NM_175571.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:150163851 A>C maps to NM_175571.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr7:150171403 G>T maps to NM_175571.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:150164097 C>T maps to NM_175571.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:102433020 G>A maps to NM_017676.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr5:102423838 A>G maps to NM_017676.2 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:102423838 A>G maps to NM_017676.2 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:102423838 A>G maps to NM_017676.2 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr20:25405914 T>C maps to NM_021067.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:25388531 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr20:25398740 G>A maps to NM_021067.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:41397470 C>T maps to NM_032336.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:14593638 A>G maps to NM_202470.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr1:78585158 A>G maps to NM_017655.4 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:78591630 C>T maps to NM_017655.4 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:78546423 A>G maps to NM_017655.4 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:78585170 C>A maps to NM_017655.4 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr19:3586990 C>T maps to NM_133261.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:3586843 C>T maps to NM_133261.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:27903119 C>T maps to NM_001085454.1 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:110389118 G>A maps to NM_057169.3 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:110397661 C>T maps to NM_057169.3 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr6:121768565 C>A maps to NM_000165.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:121769081 T>G maps to NM_000165.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr6:121768449 C>T maps to NM_000165.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr6:121768961 G>A maps to NM_000165.3 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr6:90604876 A>C maps to NM_032602.1 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:90604333 G>A maps to NM_032602.1 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:20716956 C>T maps to NM_021954.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr13:20716410 C>T maps to NM_021954.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr1:35260314 A>C maps to NM_002060.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:35260152 G>A maps to NM_002060.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:147230605 C>T maps to NM_005266.5 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:147230673 C>A maps to NM_005266.5 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:147230491 A>G maps to NM_005266.5 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:147380681 G>A maps to NM_005267.4 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:147380453 G>A maps to NM_005267.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:147380453 G>A maps to NM_005267.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:147380333 C>T maps to NM_005267.4 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:147380237 C>T maps to NM_005267.4 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr1:147380981 C>T maps to NM_005267.4 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:147380465 C>T maps to NM_005267.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:39340936 G>A maps to NM_030772.4 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:70444046 C>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:70444104 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:70444254 C>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:70443885 G>C did not map to a codon.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr13:20763363 C>T maps to NM_004004.5 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:20763456 C>T maps to NM_004004.5 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:35250422 C>T maps to NM_001005752.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:35250818 C>A maps to NM_001005752.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr1:35223653 C>T maps to NM_005268.2 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:35223626 C>T maps to NM_005268.2 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:35223671 C>T maps to NM_005268.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:35223671 C>T maps to NM_005268.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr13:20797040 A>G maps to NM_001110221.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:20797466 G>A maps to NM_001110221.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:20797214 C>T maps to NM_001110221.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr6:87994537 G>A maps to NM_198568.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr6:87994525 G>T maps to NM_198568.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:42882800 C>A maps to NM_001080383.1 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr17:42882873 G>A maps to NM_001080383.1 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr17:42882603 C>A maps to NM_001080383.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:99526679 C>T maps to NM_181538.2 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:35044681 C>T maps to NM_020660.1 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:35046665 C>T maps to NM_020660.1 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:35896563 G>A maps to NM_153368.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:35896950 G>A maps to NM_153368.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:30745653 G>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:30739084 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:30712587 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:30671718 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:30738758 G>T did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:30742242 G>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:80329179 C>A maps to NM_033214.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:80328850 A>G maps to NM_033214.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:80328946 G>A maps to NM_033214.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr4:80329159 G>A maps to NM_033214.2 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:80328289 A>C maps to NM_033214.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:80329046 A>C maps to NM_033214.2 L103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:141917726 G>A maps to NM_001039547.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:86395296 C>T maps to NM_025211.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr9:86368226 A>G maps to NM_025211.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:69207124 C>T maps to NM_019617.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:69207130 C>T maps to NM_019617.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:69207130 C>T maps to NM_019617.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:69172574 G>A maps to NM_182536.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr23:100655687 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:100653458 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:100658853 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:100653894 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:100658928 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:100652851 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:100658858 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:33058236 T>C maps to NM_000404.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:220107931 C>T maps to NM_024506.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:220104380 G>T maps to NM_024506.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:220104930 G>A maps to NM_024506.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:220108030 G>A maps to NM_024506.3 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:134241039 C>T maps to NM_138342.3 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr11:134212707 C>T maps to NM_138342.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:134238675 G>A did not map to a codon.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr11:134217284 C>T maps to NM_138342.3 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:134177052 C>T maps to NM_001080407.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:134183886 C>A maps to NM_001080407.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:134177061 C>T maps to NM_001080407.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr7:8124621 C>T maps to NM_138426.2 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:8125849 C>A maps to NM_138426.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr15:69561147 A>T maps to NM_015554.1 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:69561213 C>T maps to NM_015554.1 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr15:69561147 A>G maps to NM_015554.1 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:6604636 G>A maps to NM_000170.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:6604709 G>A maps to NM_000170.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:6587267 C>A maps to NM_000170.2 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:6587247 G>T maps to NM_000170.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:6540146 C>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:6645286 C>A maps to NM_000170.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:51696737 C>A maps to NM_181789.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr15:51696534 C>T maps to NM_181789.2 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr16:74499606 G>C maps to NM_012201.5 Y878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:74491799 G>A maps to NM_012201.5 C1079C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:74514292 C>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:74516930 G>T maps to NM_012201.5 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr12:57859466 C>A maps to NM_005269.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:57864568 C>A maps to NM_005269.2 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr12:57863473 C>A maps to NM_005269.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:57857570 G>T maps to NM_005269.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr12:57864796 C>T maps to NM_005269.2 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:57861207 C>T maps to NM_005269.2 H335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:57865675 T>C maps to NM_005269.2 A1051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr12:57865804 C>T maps to NM_005269.2 S1094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:121746828 G>A maps to NM_005270.4 A1113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:121748025 C>T maps to NM_005270.4 F1512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:121684940 G>A maps to NM_005270.4 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:121740293 C>T maps to NM_005270.4 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:121740293 C>T maps to NM_005270.4 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr2:121746681 C>T maps to NM_005270.4 D1064D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:121747165 C>T maps to NM_005270.4 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr2:121684976 G>A maps to NM_005270.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr2:121746765 C>A maps to NM_005270.4 G1092G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:121744155 G>A maps to NM_005270.4 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:121729593 C>T maps to NM_005270.4 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:121684976 G>A maps to NM_005270.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr7:42079689 A>G maps to NM_000168.5 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr7:42004041 C>T maps to NM_000168.5 A1543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr7:42005913 G>C maps to NM_000168.5 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:42012028 C>T maps to NM_000168.5 Q670Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:42004278 G>A maps to NM_000168.5 D1464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr7:42065943 G>A maps to NM_000168.5 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:42004062 G>A maps to NM_000168.5 S1536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:42063090 G>A maps to NM_000168.5 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:42079722 G>T maps to NM_000168.5 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr7:42187876 G>A maps to NM_000168.5 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:42005463 G>T maps to NM_000168.5 I1069I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:42188010 G>A maps to NM_000168.5 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr7:42012039 G>A maps to NM_000168.5 R667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:42064964 C>A maps to NM_000168.5 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:42018277 C>A maps to NM_000168.5 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:42018305 G>A maps to NM_000168.5 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr7:42079836 G>A maps to NM_000168.5 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:42088261 C>T maps to NM_000168.5 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr7:42064964 C>A maps to NM_000168.5 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr7:42065980 C>T maps to NM_000168.5 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr7:42005805 C>T maps to NM_000168.5 T955T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr7:42005277 C>T maps to NM_000168.5 A1131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:42004776 C>T maps to NM_000168.5 P1298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:42004848 G>A maps to NM_000168.5 A1274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:42006213 G>A maps to NM_000168.5 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr7:42004905 C>T maps to NM_000168.5 G1255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:42005949 G>A maps to NM_000168.5 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:144358850 G>A maps to NM_138465.3 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr8:144358562 G>A maps to NM_138465.3 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:75875774 C>T maps to NM_006851.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:75884192 G>A maps to NM_006851.2 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:75741463 A>G maps to ENST00000378695 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr12:75728657 T>C maps to ENST00000378695 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:75763886 G>A maps to ENST00000378695 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr12:75756908 C>T maps to ENST00000378695 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr12:75756908 C>T maps to ENST00000378695 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:75816731 A>G maps to ENST00000378692 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr12:75785030 G>A maps to ENST00000378692 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:36162509 G>A maps to NM_022343.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr1:53990554 C>T maps to NM_147193.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:4385386 G>A maps to NM_032575.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:4387299 G>A maps to NM_032575.2 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:4387494 G>A maps to NM_032575.2 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr9:4118442 C>T maps to NM_001042413.1 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:3937057 G>A maps to NM_001042413.1 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr9:4118115 C>A maps to NM_001042413.1 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr9:4286206 G>A maps to NM_001042413.1 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:4117863 C>T maps to NM_001042413.1 W538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:92713459 A>G maps to NM_053274.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:38650584 G>A maps to NM_006708.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:38650584 G>A maps to NM_006708.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:48631800 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:39024211 C>T maps to NM_002062.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:39034010 C>A maps to NM_002062.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:39047385 G>T maps to NM_002062.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:39025308 G>A maps to NM_002062.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:9739713 C>T maps to NM_004246.1 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr17:9764489 C>T maps to NM_004246.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:9791263 T>C maps to NM_004246.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:9765380 C>T maps to NM_004246.1 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr17:9791263 T>C maps to NM_004246.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:9791263 T>C maps to NM_004246.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:151304088 G>A maps to NM_001146040.1 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:14592499 G>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:14748594 C>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:14548212 T>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:14627284 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:14592669 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:14748344 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:14748515 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:14748562 A>T did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:14550415 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:14625305 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:14627250 C>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:175710030 A>G maps to NM_006529.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr4:175636666 T>C maps to NM_006529.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:175598419 G>A maps to NM_006529.2 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:175598342 G>T maps to NM_006529.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:175565065 G>A maps to NM_006529.2 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:175604003 G>A maps to NM_006529.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr4:175580336 G>C maps to NM_006529.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:102968540 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:102979100 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:102974001 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:102979866 C>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:102962334 A>T did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:102979141 C>G did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:102979018 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:158091609 T>G maps to NM_001166060.1 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr4:158041773 A>G maps to NM_001166060.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:158091875 T>G maps to NM_001166060.1 L497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:158060078 T>C maps to NM_001166060.1 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr4:158065088 G>A maps to NM_001166060.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:193065765 C>A maps to NM_016066.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:131943556 G>T maps to NM_006541.4 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr14:96010335 C>T maps to NM_016417.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr2:191819354 T>C maps to NM_014905.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr12:56868450 G>A maps to NM_013267.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:17683349 C>T maps to NM_024656.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:17679359 C>T maps to NM_024656.2 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:17691596 G>A maps to NM_024656.2 W495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:17683376 C>T maps to NM_024656.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:17679445 C>A maps to NM_024656.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:184006368 C>T maps to NM_015101.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:183914601 G>A maps to NM_015101.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:183942799 G>A maps to NM_015101.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr1:183938580 G>A maps to NM_015101.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr1:183909893 T>C maps to NM_015101.2 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr1:183909863 C>A maps to NM_015101.2 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:138517928 G>T maps to NM_182974.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:138516134 G>T maps to NM_182974.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr9:138516209 G>A maps to NM_182974.2 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr9:138517934 C>A maps to NM_182974.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:138516110 T>C maps to NM_182974.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr9:138516425 G>A maps to NM_182974.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr9:138516110 T>A maps to NM_182974.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:104383248 G>A maps to NM_031302.3 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:104390575 C>T maps to NM_031302.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr12:104397084 C>A did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:104397082 A>G maps to NM_031302.3 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:1263112 C>T maps to NM_001029885.1 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:1262301 G>A maps to NM_001029885.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:4692343 G>A maps to NM_001014985.2 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr19:48176863 C>T maps to NM_015711.3 D11D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:48183158 G>A maps to NM_015711.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:48182984 C>T maps to NM_015711.3 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr19:48201963 G>T maps to NM_015711.3 E1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:48182684 G>A maps to NM_015711.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:48253471 A>G maps to NM_015710.4 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr19:48250286 A>G maps to NM_015710.4 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:48254335 G>A maps to NM_015710.4 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr19:48259943 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:88817494 C>A maps to NM_005271.3 G483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:88818958 G>A maps to NM_005271.3 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr10:88854334 G>A maps to NM_005271.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:120182633 C>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:120182865 T>C did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr23:120183119 T>C did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:120181737 T>C did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:120182803 T>C did not map to a codon.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr23:120181964 C>T did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr23:120181768 C>T did not map to a codon.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr23:120181908 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:120181913 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:120181942 C>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:120181924 G>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:120182436 G>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:120181724 G>A did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:120182024 G>C did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:120181689 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:120182429 G>A did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:120181961 C>A did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:120182599 A>T did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:120182229 G>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:120181732 C>G did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:120181766 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:120182660 G>T did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:182353701 G>A maps to NM_002065.5 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:182355389 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:182357773 G>A maps to NM_002065.5 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:182356407 G>A maps to NM_002065.5 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:182353731 G>A maps to NM_002065.5 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:58477412 G>T maps to NM_201648.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:58722337 C>A maps to NM_080661.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:4861283 C>A maps to NM_032569.3 G492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr16:4864564 G>A maps to NM_032569.3 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:4862180 G>A maps to NM_032569.3 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:150646945 C>T maps to NM_000405.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr2:70081985 A>G maps to NM_178439.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr2:70081985 A>G maps to NM_178439.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:70070297 G>A maps to NM_178439.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:70081982 T>C maps to NM_178439.3 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:70081985 A>G maps to NM_178439.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr2:70064744 C>T maps to NM_178439.3 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr2:70081985 A>G maps to NM_178439.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:70081985 A>G maps to NM_178439.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr2:70076785 G>A maps to NM_178439.3 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr2:70081985 A>G maps to NM_178439.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr2:70076785 G>A maps to NM_178439.3 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr6:1961148 G>A maps to NM_001500.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:1930446 G>A maps to NM_001500.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr1:29019491 T>C maps to NM_006582.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr1:29030746 G>A maps to NM_006582.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:29037129 G>T maps to NM_006582.2 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:62221453 G>A maps to NM_012384.3 H527H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr20:62221609 T>C maps to NM_012384.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:62221642 G>A maps to NM_012384.3 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:39826150 G>A maps to NM_004877.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:19740999 G>A maps to NM_016573.2 C895C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:19746531 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:19744620 T>C maps to NM_016573.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr8:143928004 G>T maps to NM_002066.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:143928000 C>A maps to NM_002066.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr8:143928000 C>T maps to NM_002066.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr8:143928000 C>T maps to NM_002066.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:24777491 G>A maps to NM_015895.3 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:24785864 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:24786005 G>A maps to NM_015895.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:24785963 A>C maps to NM_015895.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:24784335 G>A maps to NM_015895.3 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr6:24784335 G>A maps to NM_015895.3 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:220367115 C>T maps to ENST00000373917 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr3:49759690 G>A maps to NM_013334.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr6:16290696 T>C maps to NM_006877.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:16274666 G>T maps to NM_006877.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:16295323 G>A maps to NM_006877.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:16247137 C>T maps to NM_006877.3 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:16254923 C>T maps to NM_006877.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:16295383 G>A maps to NM_006877.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:24707965 C>A maps to ENST00000348719 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:24702527 C>A maps to ENST00000348719 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr14:24707821 T>C maps to ENST00000348719 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:155655456 C>T maps to NM_003875.2 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:155628620 G>T maps to NM_003875.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:155628647 G>T maps to NM_003875.2 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr3:155633845 A>G maps to NM_003875.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:3118940 C>T maps to NM_002067.2 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:3110297 G>A maps to NM_002067.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr19:3121038 G>C maps to NM_002067.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:3119325 G>A maps to NM_002067.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:3118940 C>T maps to NM_002067.2 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr19:3118940 C>T maps to NM_002067.2 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr7:2834684 G>A maps to NM_007353.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:2771144 C>T maps to NM_007353.2 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:2834752 G>A maps to NM_007353.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:2771129 G>A maps to NM_007353.2 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr7:2770904 G>A maps to NM_007353.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr17:63049766 C>T maps to NM_006572.4 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:63010730 G>A maps to NM_006572.4 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr9:80039056 T>C maps to NM_004297.3 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:80039058 T>A maps to NM_004297.3 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr9:80038942 G>C maps to NM_004297.3 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:80046340 G>A maps to NM_004297.3 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:3155874 C>T maps to NM_002068.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:3150196 G>A maps to NM_002068.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr7:79840296 G>T maps to NM_002069.5 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr7:79833136 T>C maps to NM_002069.5 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:50293659 C>T maps to NM_002070.2 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:50293701 G>A maps to NM_002070.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr3:50290493 C>A maps to NM_002070.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:50290493 C>T maps to NM_002070.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:50289870 G>A maps to NM_002070.2 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:50294445 C>T maps to NM_002070.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:110125088 G>A maps to NM_006496.2 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:110121984 T>C did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr18:11753890 C>T maps to NM_182978.2 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:11753890 C>T maps to NM_182978.2 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr18:11881046 C>T maps to NM_182978.2 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:11868563 C>T maps to NM_182978.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr18:11752476 C>T maps to NM_001142339.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:56370654 C>T maps to NM_020988.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:56362649 C>T maps to NM_020988.2 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:56362682 G>A maps to NM_020988.2 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:56309875 C>T maps to NM_020988.2 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:80412464 G>A maps to NM_002072.3 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:80412493 G>A maps to NM_002072.3 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr9:80412493 G>T maps to NM_002072.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr20:57484421 T>C maps to NM_080425.2 R844R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:57428367 C>T maps to NM_080425.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:57480493 C>T maps to NM_080425.2 Y806Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:57484763 G>A maps to NM_080425.2 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr20:57480493 C>T maps to NM_080425.2 Y806Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:50232222 C>T maps to NM_000172.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:50231060 C>T maps to NM_000172.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr1:110153097 G>T maps to NM_005272.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:1721935 G>A maps to NM_002074.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:1721938 C>T maps to NM_002074.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:1747286 G>A maps to NM_002074.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:1722013 G>A maps to NM_002074.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr22:19776327 G>T maps to NM_053004.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:19808860 C>T maps to NM_053004.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr22:19808857 C>T maps to NM_053004.2 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:180666516 G>A maps to NM_006098.4 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:180668572 G>A maps to NM_006098.4 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:6954916 C>T maps to NM_002075.2 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr12:6952160 C>T maps to NM_002075.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:6952177 G>A maps to NM_002075.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:6950465 G>A maps to NM_002075.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:179132693 G>A maps to NM_021629.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:179131229 C>T maps to NM_021629.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr3:179134311 A>C maps to NM_021629.3 L79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:52425627 G>A maps to NM_016194.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:52446142 C>T maps to NM_016194.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:36236886 C>T maps to NM_001128227.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:36217508 G>A maps to NM_001128227.2 H705H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:235715488 G>T maps to NM_004485.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr19:2515043 G>A maps to NM_052847.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:30514010 C>T maps to NM_005275.3 E554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr6:30521235 A>G maps to NM_005275.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr1:38052988 G>A maps to NM_013285.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:38032455 T>G maps to NM_013285.2 *732Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:38033906 T>C maps to NM_013285.2 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:38058328 T>C maps to NM_013285.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:38032542 G>A maps to NM_013285.2 N703N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:38059444 G>A maps to NM_013285.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:52726984 C>T maps to NM_014366.4 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:54570740 G>A did not map to a codon.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr23:54565496 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:54578344 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:54586996 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:54578769 G>A did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:54584948 T>C did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:54578326 C>T did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:54584947 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:54584907 C>T did not map to a codon.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr4:44719160 T>C maps to NM_138335.1 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:102159941 C>T maps to NM_024312.4 W513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:102158338 G>A maps to NM_024312.4 Q786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:102158708 C>T maps to NM_024312.4 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:102155481 C>T maps to NM_024312.4 R925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:102158935 G>A maps to NM_024312.4 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:1412881 C>T maps to NM_032520.4 H266H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:25279108 G>A maps to NM_001083111.1 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr4:68619927 A>G maps to NM_000406.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr12:65130818 G>A maps to ENST00000418919 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:127644214 C>A maps to NM_002077.3 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:127661694 G>A maps to NM_002077.3 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr9:131019483 G>A maps to NM_004486.4 N957N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:131024928 C>A maps to NM_004486.4 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:131028580 C>T maps to NM_004486.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr9:131022785 G>A maps to NM_004486.4 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:131036173 A>G maps to NM_004486.4 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:131023789 C>T maps to NM_004486.4 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:131030746 G>A maps to NM_004486.4 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:100550994 C>T maps to ENST00000266746 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:133384808 G>A maps to NM_005895.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:133384640 C>T maps to NM_005895.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr12:133384880 A>G maps to NM_005895.3 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:133373205 C>T maps to NM_005895.3 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:37343740 T>C maps to NM_001172713.1 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr3:37368084 C>T maps to NM_001172713.1 Q1592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:37388774 T>C maps to NM_001172713.1 G2203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:37292887 G>A maps to NM_001172713.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:37379194 G>A maps to NM_001172713.1 S2137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:37368057 G>T maps to NM_001172713.1 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr3:37365329 A>G maps to NM_001172713.1 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:37368057 G>T maps to NM_001172713.1 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:37365605 C>T maps to NM_001172713.1 H765H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:37368195 G>T maps to NM_001172713.1 E1629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr3:37365329 A>G maps to NM_001172713.1 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:93286100 T>C maps to NM_005113.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr14:93299648 T>C maps to NM_005113.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr14:93273143 C>G maps to NM_005113.2 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr15:74365092 G>T maps to NM_001038640.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:41363525 C>T maps to NM_001002296.1 R121*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AZ-6598-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:121386351 A>C maps to ENST00000393667 A3180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:121416179 C>A maps to ENST00000393667 E1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:121415559 T>C maps to ENST00000393667 E1270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:121383777 G>A maps to ENST00000393667 R3224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:121413218 C>A maps to ENST00000393667 E2051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:121415009 C>A maps to ENST00000393667 E1454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:121415189 C>A maps to ENST00000393667 E1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:121415675 C>A maps to ENST00000393667 E1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:121411069 C>A maps to ENST00000393667 E2381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:121409665 C>A maps to ENST00000393667 E2849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:121386912 C>T maps to ENST00000393667 Q3143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:121416230 C>A maps to ENST00000393667 E1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:121415637 T>C maps to ENST00000393667 Q1244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:121414026 G>A maps to ENST00000393667 T1781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:121416179 C>A maps to ENST00000393667 E1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:121416221 C>A maps to ENST00000393667 E1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:121416290 C>A maps to ENST00000393667 E1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:121417682 C>A maps to ENST00000393667 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:121441206 C>A maps to ENST00000393667 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:121410359 G>T maps to ENST00000393667 S2617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr3:121412739 T>A maps to ENST00000393667 I2210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:121415637 T>C maps to ENST00000393667 Q1244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr3:121413686 C>A maps to ENST00000393667 E1895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:121410359 G>A maps to ENST00000393667 S2617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:121415637 T>C maps to ENST00000393667 Q1244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:167728166 G>A maps to NM_014498.3 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:167728166 G>A maps to NM_014498.3 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:88694193 C>T maps to ENST00000376023 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr9:88650319 G>A maps to ENST00000376023 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr1:150621062 G>A maps to ENST00000369003 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:204172095 G>A maps to NM_198447.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:155736403 G>A maps to ENST00000368331 R954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:155721660 C>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:155742999 C>A maps to ENST00000368331 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:155732085 G>A maps to ENST00000368331 S1602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:117890830 G>A maps to NM_020399.3 C327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:170521239 T>C maps to NM_152281.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:170521359 C>T maps to NM_152281.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:170521401 A>T maps to NM_152281.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:170521479 T>C maps to NM_152281.2 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:39144333 G>T maps to NM_031899.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr3:39142326 C>T maps to NM_031899.2 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr2:171819382 C>T maps to NM_015530.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:171807860 C>A maps to NM_015530.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr17:28849378 C>T maps to NM_004871.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:28817221 C>T maps to NM_004871.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:28804465 C>A maps to NM_004871.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr17:45012462 C>T maps to NM_054022.2 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:45012462 C>T maps to NM_054022.2 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:101163490 G>A maps to NM_002079.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:101163355 C>A maps to NM_002079.2 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:101163326 G>T maps to NM_002079.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr10:101162406 G>A maps to NM_002079.2 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:101162430 A>G maps to NM_002079.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:37794904 C>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:58750699 C>T maps to NM_002080.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:20329742 G>A maps to NM_001007240.1 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:20335441 C>T maps to NM_001007240.1 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr16:20334242 A>T maps to NM_001007240.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:20329676 C>A maps to NM_001007240.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr16:20335420 C>T maps to NM_001007240.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:20329742 G>A maps to NM_001007240.1 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr16:20335528 G>A maps to NM_001007240.1 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr16:20335528 G>A maps to NM_001007240.1 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr16:20335519 A>G maps to NM_001007240.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr16:20335519 A>G maps to NM_001007240.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:194118297 G>A maps to NM_004488.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr3:194118918 G>A maps to NM_004488.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:194118663 C>T maps to NM_004488.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr3:194118537 G>A maps to NM_004488.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:194118482 A>G maps to NM_004488.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:194118180 C>A maps to NM_004488.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:55526358 A>T maps to NM_001083899.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:55538979 T>C maps to NM_001083899.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:55526127 G>A maps to NM_001083899.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:55525815 A>C maps to NM_001083899.1 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:55525785 C>T maps to NM_001083899.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr19:55527044 A>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:167023579 G>A maps to NM_005814.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:145140274 C>T maps to NM_003801.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:145140892 C>T maps to NM_003801.3 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:145139717 C>T maps to NM_003801.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr10:113933554 A>G maps to NM_020918.4 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:33586713 G>A maps to NM_018025.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:33617618 G>A maps to NM_018025.2 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:33584416 G>A maps to NM_018025.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:217793312 A>G maps to NM_018040.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:217793290 C>A maps to NM_018040.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:217793326 G>A maps to NM_018040.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:217793420 G>A maps to NM_018040.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:27218951 A>G maps to NM_022078.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:27220850 G>A maps to NM_022078.2 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:156565886 C>T maps to NM_015590.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:156565511 G>T maps to NM_015590.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:156565427 T>G maps to NM_015590.3 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:156565192 C>A maps to NM_015590.3 G314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:42541863 G>A maps to NM_001002909.2 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:42477298 G>A maps to NM_001002909.2 R716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:46124753 C>T maps to NM_021639.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:132887942 C>A did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:132795829 G>T did not map to a codon.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr23:132826434 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:132888099 T>A did not map to a codon.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr23:132670252 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:132887894 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:133087214 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:132833958 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr23:132888050 C>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:132670212 G>A did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:132833945 T>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:132437022 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:132440089 T>C did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:132458270 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:132438853 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:132473362 T>C did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:132439866 G>A did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:132438772 C>T did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:132548980 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:92345774 G>A maps to NM_004466.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:92380823 A>G maps to NM_004466.4 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr13:93879816 G>A maps to NM_005708.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:94938666 G>A maps to NM_005708.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr13:95034786 C>T maps to NM_005708.3 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr13:95055410 C>T maps to NM_005708.3 H536H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:5556594 A>G maps to NM_019593.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr20:5528367 A>T maps to NM_019593.3 L653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr20:5559220 G>A maps to NM_019593.3 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:50503259 T>C maps to NM_005276.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr3:32200399 C>T maps to NM_015141.3 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:32181796 G>A maps to NM_015141.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr2:157439369 A>G maps to NM_000408.4 A708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:157425388 A>T maps to NM_000408.4 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:157332646 G>A maps to NM_000408.4 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:157439369 A>G maps to NM_000408.4 A708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:1131642 C>A maps to NM_001505.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr7:1132185 G>A maps to NM_001505.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:67578598 C>T maps to NM_020806.4 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:67390960 G>A maps to NM_020806.4 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr14:67578598 C>T maps to NM_020806.4 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:67589011 C>T maps to NM_020806.4 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr14:67525489 C>T maps to NM_020806.4 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:67389507 C>T maps to NM_020806.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:67525489 C>A maps to NM_020806.4 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:34857273 G>A maps to NM_000175.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:34887519 G>A maps to NM_000175.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:34890197 G>A maps to NM_000175.3 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:34884958 G>A maps to NM_000175.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:34856215 A>G maps to NM_000175.3 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:144296906 C>A maps to NM_178172.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr8:144296927 C>T maps to NM_178172.3 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr23:48970806 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:48976075 A>G did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr6:24480148 G>A maps to NM_001503.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:24448364 G>T maps to NM_001503.2 C506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr6:24429261 A>C maps to NM_001503.2 *841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:24450073 G>A maps to NM_001503.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr6:24437398 G>A maps to NM_001503.2 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:24445774 G>A maps to NM_001503.2 Y673Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:24454353 G>A maps to NM_001503.2 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr6:24462986 T>C maps to NM_001503.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr6:24472838 T>C maps to NM_001503.2 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr6:24447196 G>A maps to NM_001503.2 N563N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:24437458 G>A maps to NM_001503.2 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr4:176622759 T>G maps to NM_005277.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:176556144 T>A maps to NM_005277.3 K250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:13797936 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:13801536 C>A did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:13801596 A>G did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:27206179 G>T maps to NM_018066.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr12:110895383 G>A maps to NM_001164373.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:110897536 G>A maps to NM_001164373.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:23309738 G>A maps to ENST00000435486 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr7:23296643 A>G maps to ENST00000435486 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:23296641 G>T maps to ENST00000435486 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:23299746 C>T maps to ENST00000435486 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:23306205 C>T maps to ENST00000435486 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:23313833 A>G maps to ENST00000435486 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:23286496 C>T maps to ENST00000435486 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr7:23313716 T>C maps to ENST00000435486 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr7:23296641 G>T maps to ENST00000435486 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr7:23307589 C>T maps to ENST00000435486 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:207041029 G>T maps to NM_005279.3 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:136113396 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:136112504 G>T did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:136113692 G>A did not map to a codon.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr23:136113328 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:136113349 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:136112820 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:136112474 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:136112551 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:136113519 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:136113120 A>G did not map to a codon.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr23:136112326 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr23:136113067 A>G did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:136112600 G>A did not map to a codon.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr19:6733589 G>A maps to NM_001080452.1 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:6736656 C>A maps to NM_001080452.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:6731098 C>A maps to NM_001080452.1 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr12:123187812 C>T maps to NM_177551.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:123187041 C>T maps to NM_177551.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr6:46977919 C>A maps to ENST00000283297 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:46977646 C>T maps to ENST00000283297 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:46977919 C>T maps to ENST00000283297 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:47649164 T>A maps to NM_153839.6 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:47646752 G>A maps to NM_153839.6 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:47649053 G>A maps to NM_153839.6 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:47649164 T>C maps to NM_153839.6 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:135494468 G>A did not map to a codon.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr23:135429632 C>T did not map to a codon.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr23:135429259 C>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:135426683 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:135432174 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:135494467 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:135428053 A>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:135494435 T>G did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:135445696 T>A did not map to a codon.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr23:135431089 C>G did not map to a codon.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr23:135432289 T>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:135430060 A>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:135431479 C>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:135482095 G>C did not map to a codon.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr23:135431924 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:135429121 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:135429781 A>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:135470008 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:135496370 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:135428071 T>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:135431053 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:135441479 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:135487943 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:135405204 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:135485466 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:135427097 T>C did not map to a codon.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr23:135430092 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:135480101 C>T did not map to a codon.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr23:135431479 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:135430257 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr23:135431084 T>G did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:135427510 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:135405025 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:135427509 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:135427825 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:135429712 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:135431838 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:135432563 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:135441503 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:135427196 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:135443656 A>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:135443656 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:135443656 A>G did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:135432175 A>G did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:135405025 C>T did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:135443655 A>G did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:135485438 T>C did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:135427510 C>T did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:135443656 A>G did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:135429926 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:135427478 C>T did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:135432175 A>C did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:135429926 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:135427510 C>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:135432095 G>T did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:135429122 T>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:135427477 C>T did not map to a codon.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr2:26537401 G>A maps to NM_001145168.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr2:26535969 G>A maps to NM_001145168.1 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:26535918 C>T maps to NM_001145168.1 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:26539906 G>A maps to NM_001145168.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:26533781 G>A maps to NM_001145168.1 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:26534327 G>A maps to NM_001145168.1 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr2:26537360 A>G maps to NM_001145168.1 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:26534300 C>T maps to NM_001145168.1 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr16:57601917 G>A maps to ENST00000349457 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:57601929 C>T maps to ENST00000349457 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr16:57608786 G>A maps to ENST00000349457 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:57608774 C>T maps to ENST00000349457 Y419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:57608820 C>T maps to ENST00000349457 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr16:57601392 A>G maps to ENST00000349457 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr6:47682171 C>T maps to NM_153838.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:47680211 C>A maps to NM_153838.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:47682675 G>A maps to NM_153838.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr6:47682261 G>A maps to NM_153838.3 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:46825940 A>C maps to NM_015234.4 G1233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:46834662 A>C maps to NM_015234.4 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:46846032 G>A maps to NM_015234.4 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:129518823 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:129518918 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:129518925 C>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:129518507 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:129518962 C>T did not map to a codon.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr13:27333898 C>T maps to NM_005288.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr13:27333265 C>T maps to NM_005288.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:27333241 C>T maps to NM_005288.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr13:27333013 G>A maps to NM_005288.3 C317C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:95347179 G>A maps to NM_181745.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr10:134942297 G>A maps to ENST00000368577 P862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr10:134942525 C>T maps to ENST00000368577 H938H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:37692732 G>A maps to NM_032777.9 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:37672479 G>A maps to NM_032777.9 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr8:37698873 G>A maps to NM_032777.9 P1006P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:22425861 C>T maps to NM_145290.2 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:22425906 C>T maps to NM_145290.2 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr4:22446695 T>C maps to NM_145290.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:142737070 G>A maps to NM_198569.2 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr6:142759475 C>T maps to NM_198569.2 T1183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:142741164 G>A maps to NM_198569.2 W1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr6:142703103 G>A maps to NM_198569.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:100354558 T>C maps to NM_032787.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:100365540 C>T maps to NM_032787.2 N413N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr3:100373846 A>G maps to NM_032787.2 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:100365424 G>T maps to NM_032787.2 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:100362472 G>A maps to NM_032787.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:100413667 G>A maps to NM_032787.2 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:100373864 G>A maps to NM_032787.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr3:100413790 G>A maps to NM_032787.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr3:100364933 C>T maps to NM_032787.2 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:100328753 A>G maps to NM_032787.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:100362472 G>A maps to NM_032787.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr3:100373846 A>G maps to NM_032787.2 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:105517633 G>A maps to NM_013345.2 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr12:131439191 G>A maps to NM_198827.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:131488836 G>A maps to NM_198827.3 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:131561401 C>T maps to NM_198827.3 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:131439190 C>A maps to NM_198827.3 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr12:131561401 C>T maps to NM_198827.3 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:131622749 C>T maps to NM_198827.3 N835N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:131456057 C>A maps to NM_198827.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:131602933 T>C maps to NM_198827.3 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:131488761 C>T maps to NM_198827.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:131620587 A>G maps to NM_198827.3 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr14:59930765 G>A maps to NM_022571.5 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:64054058 T>C maps to NM_001170726.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:236371372 G>A maps to NM_003272.3 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:20043587 G>A maps to NM_001002911.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:20043911 G>A maps to NM_001002911.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:20043314 G>A maps to NM_001002911.2 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:37780516 T>G maps to NM_181791.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:37780372 C>T maps to NM_181791.1 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr7:37780906 C>T maps to NM_181791.1 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr7:37780789 T>A maps to NM_181791.1 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr17:72367916 G>A maps to ENST00000440684 R1152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr17:72366756 G>T maps to ENST00000440684 P1115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:72368474 C>T maps to ENST00000440684 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:72365693 C>T maps to NM_181790.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:9707676 G>T did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:9707584 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:9728807 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:9727427 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:9711618 C>A did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:9711649 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:131487041 C>A maps to NM_207364.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:131487395 T>C maps to NM_207364.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:154147143 G>A maps to NM_001038705.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr3:154056057 A>G maps to NM_001038705.1 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:154146879 G>A maps to NM_001038705.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:154146825 G>A maps to NM_001038705.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr3:154055523 A>G maps to NM_001038705.1 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:154055979 T>G maps to NM_001038705.1 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:154056057 A>G maps to NM_001038705.1 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:98251791 C>T maps to NM_005290.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:98251614 C>T maps to NM_005290.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:145894746 C>T maps to NM_194251.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:145894797 G>T maps to NM_194251.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr11:67218797 G>A maps to NM_206997.1 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:67220113 G>A maps to NM_206997.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:67219844 G>T maps to NM_206997.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr11:67219163 C>T maps to NM_206997.1 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:6313864 C>T maps to NM_207370.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:175304747 C>T maps to NM_152529.5 W730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr2:175311410 A>C maps to NM_152529.5 Y647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:175318518 C>A maps to NM_152529.5 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:119900007 A>G maps to NM_153002.2 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:119886360 G>A maps to NM_153002.2 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:119886033 C>A maps to NM_153002.2 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:119962554 A>C maps to NM_153002.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr3:119892317 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr3:119886769 G>A maps to NM_153002.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:9164618 C>T maps to NM_024980.4 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr10:25887605 T>C maps to NM_020752.2 G1017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:25464648 C>T maps to NM_020752.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr10:25510085 G>A maps to NM_020752.2 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:25701228 G>T maps to NM_020752.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:25701362 C>T maps to NM_020752.2 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:25886861 C>T maps to NM_020752.2 C769C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:25887776 G>A maps to NM_020752.2 W1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr10:25887176 G>A maps to NM_020752.2 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr10:25886864 T>C maps to NM_020752.2 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr3:169802125 G>C maps to NM_014373.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:169802119 T>G maps to NM_014373.2 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:169801858 T>C maps to NM_014373.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr1:168066328 G>A maps to NM_153832.1 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:168059865 A>G maps to NM_153832.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:168059835 C>T maps to NM_153832.1 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:168066364 C>T maps to NM_153832.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr12:6936233 G>A maps to NM_019858.1 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr12:6936245 T>C maps to NM_019858.1 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:6933732 G>C maps to NM_019858.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:128408536 C>T maps to NM_005291.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:128408410 C>T maps to NM_005291.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:128409076 C>T maps to NM_005291.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:128408407 G>A maps to NM_005291.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr2:128408920 G>A maps to NM_005291.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:145584312 G>A maps to NM_024531.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:53106222 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:53106648 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:53106077 G>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:53106712 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:53106636 C>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:53106814 A>G did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:53106507 C>T did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:78427246 T>C did not map to a codon.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr23:78426549 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:78426850 G>A did not map to a codon.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr23:78427246 T>A did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:78427246 T>C did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:78427246 T>C did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:78426850 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:40094103 C>T maps to NM_007223.1 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr15:40093635 C>T maps to NM_007223.1 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr15:40093371 T>C maps to NM_007223.1 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr17:36493076 G>A maps to ENST00000398597 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:36482377 A>G maps to ENST00000398597 P2359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:36485802 C>A maps to ENST00000398597 E1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:36484690 A>G maps to ENST00000398597 P1588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:36482488 C>T maps to ENST00000398597 R2322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:36499332 G>A maps to ENST00000398597 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:36484858 C>T maps to ENST00000398597 Q1532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:36485811 G>A maps to ENST00000398597 Q1215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr17:36484609 T>G maps to ENST00000398597 G1615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:36485791 G>A maps to ENST00000398597 V1221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr17:36499057 G>A maps to ENST00000398597 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:95271477 C>T maps to NM_180989.4 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:57389721 C>T maps to NM_007264.3 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:57389040 C>T maps to NM_007264.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr12:12814167 G>T maps to NM_006143.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:12814167 G>T maps to NM_006143.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:142367939 G>A maps to NM_005293.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:125797610 C>T maps to NM_005294.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:107114795 T>A maps to NM_005295.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:107114561 G>T maps to NM_005295.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:107114612 T>A maps to NM_005295.2 Y36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:107114762 A>G maps to NM_005295.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:200842914 G>A maps to NM_005298.2 E250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:200843190 C>T maps to NM_005298.2 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:200843142 C>T maps to NM_005298.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:200843238 G>T maps to NM_005298.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:200843142 C>A maps to NM_005298.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:125426411 A>G maps to NM_153442.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:125426429 C>T maps to NM_153442.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:125434426 C>T maps to NM_153442.3 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:71804177 G>A maps to NM_018971.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:27720451 A>T maps to NM_005281.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:27720997 C>T maps to NM_005281.2 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr6:167570418 G>A maps to NM_005299.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:167571175 C>T maps to NM_005299.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:51274894 A>G maps to NM_001506.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:51273895 C>T maps to NM_001506.1 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:51274669 G>A maps to NM_001506.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:51274561 C>T maps to NM_001506.1 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:51274739 C>T maps to NM_001506.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:41555565 T>C did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:41555108 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:41555087 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:41555895 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:41555136 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:41555919 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:41555919 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:41555646 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:41555829 T>G did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr23:41555953 T>C did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:41555953 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:41555832 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:241569965 C>A maps to NM_001195381.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:124387106 G>A maps to NM_005302.2 Y438Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr7:124386701 C>T maps to NM_005302.2 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:202097218 C>A maps to NM_004767.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:202097044 G>A maps to NM_004767.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:202097020 G>A maps to NM_004767.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr1:202097158 C>T maps to NM_004767.3 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:133402950 G>A maps to NM_001508.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:133175103 C>T maps to NM_001508.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:133175406 G>A maps to NM_001508.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:133403130 A>G maps to NM_001508.2 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:133402860 G>A maps to NM_001508.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:133402908 G>A maps to NM_001508.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:133402908 G>A maps to NM_001508.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:133402968 C>T maps to NM_001508.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr19:46094047 C>T maps to NM_005282.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:105858884 C>T maps to NM_007227.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:105859133 C>T maps to NM_007227.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:105858845 G>A maps to NM_007227.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:105858860 C>T maps to NM_007227.3 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:150348620 C>G did not map to a codon.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr23:150345371 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:150349078 G>A did not map to a codon.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr23:150345285 G>A did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:150349052 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:150348631 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:150348663 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:150348646 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr23:150348936 C>T did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr23:150348421 G>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:57687918 G>A maps to NM_005682.5 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:57689372 G>A maps to NM_005682.5 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:57690152 C>T maps to NM_005682.5 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr6:110301238 G>A maps to ENST00000414000 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:110301265 C>T maps to ENST00000414000 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:110086369 C>T maps to NM_031936.4 H242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:51989832 C>T maps to NM_080865.3 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:51990612 C>T maps to NM_080865.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr3:51989712 G>A maps to NM_080865.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:51990612 C>T maps to NM_080865.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:51989763 C>T maps to NM_080865.3 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:97247142 C>T maps to NM_030784.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:97246403 G>A maps to NM_030784.2 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:19013106 T>G did not map to a codon.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr23:19051756 G>A did not map to a codon.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr23:19031855 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:19017217 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:19017286 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:19028749 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:19042031 T>G did not map to a codon.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr23:19024376 A>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:19086879 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:19028879 G>A did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:19013019 C>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:19017364 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:19046319 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:19017136 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:19021080 G>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:19026181 C>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:19017254 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:19017361 G>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:19032190 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr14:88478015 G>T maps to NM_003608.3 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:88477964 C>T maps to NM_003608.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:88478054 T>C maps to NM_003608.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:88477895 T>C maps to NM_003608.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr14:91700652 G>A maps to ENST00000238699 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr2:54081476 G>A maps to NM_006794.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:54081161 G>A maps to NM_006794.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:54080989 G>A maps to NM_006794.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:54081848 C>T maps to NM_006794.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:47844349 C>T maps to NM_018485.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:8588792 C>T maps to NM_080819.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:8588876 G>A maps to NM_080819.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr4:8582777 C>T maps to NM_080819.2 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:41586717 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:41586608 A>G did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:94113413 G>T maps to NM_016540.3 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr11:94126649 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:94113377 G>T maps to NM_016540.3 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:54757251 A>G maps to NM_020370.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr12:54757586 G>A maps to NM_020370.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:112724395 G>A maps to NM_018970.6 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr7:112723720 T>C maps to NM_018970.6 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:151012144 C>A maps to NM_023915.3 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:151012379 C>T maps to NM_023915.3 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:101004896 G>A maps to NM_022049.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr1:101004668 C>T maps to NM_022049.2 N49N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr1:101004827 C>T maps to NM_022049.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:145816722 T>C maps to NM_001097612.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:145771640 T>C maps to NM_001097612.1 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:147415651 C>T maps to NM_016334.3 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr16:57714439 G>A maps to NM_170776.4 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:57713180 T>C maps to NM_170776.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:57719788 G>A maps to NM_170776.4 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:57719692 G>T maps to NM_170776.4 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr16:57719605 C>T maps to NM_170776.4 H436H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr5:89988573 T>C maps to NM_032119.3 S2368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:89988573 T>C maps to NM_032119.3 S2368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:90052962 A>G maps to NM_032119.3 E3975E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:90398054 T>A maps to NM_032119.3 Y6110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:90445962 G>A maps to NM_032119.3 T6183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:89949491 G>A maps to NM_032119.3 T1367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:90024545 C>T maps to NM_032119.3 L3408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:90073805 A>G maps to NM_032119.3 T4204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:90449129 G>A maps to NM_032119.3 P6239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:90059211 C>T maps to NM_032119.3 R4071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:89924636 C>T maps to NM_032119.3 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:90016022 C>A maps to NM_032119.3 I3202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:90459617 T>C maps to NM_032119.3 S6274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr5:89990219 C>T maps to NM_032119.3 N2549N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:89925303 T>A maps to NM_032119.3 L596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:90012537 C>A maps to NM_032119.3 R3147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr5:89925238 C>A maps to NM_032119.3 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:90072378 T>C maps to NM_032119.3 G4171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr5:90049488 C>T maps to NM_032119.3 T3740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:90086697 G>A maps to NM_032119.3 W4684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:89953725 T>C maps to NM_032119.3 P1461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:89971180 C>T maps to NM_032119.3 I1744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:90012537 C>T maps to NM_032119.3 R3147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:90368338 C>T maps to NM_032119.3 F6076F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr5:90059177 G>T maps to NM_032119.3 T4059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr5:89981639 G>A maps to NM_032119.3 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:89981703 C>T maps to NM_032119.3 R2128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr5:89979833 G>A maps to NM_032119.3 A2032A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr5:89988573 T>C maps to NM_032119.3 S2368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr5:90012539 A>G maps to NM_032119.3 R3147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:89925238 C>A maps to NM_032119.3 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:89923033 G>T maps to NM_032119.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr5:89988573 T>C maps to NM_032119.3 S2368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:90024538 A>G maps to NM_032119.3 R3405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:101908901 G>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:101911277 T>C did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:101912271 G>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:101912372 G>A did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:101911170 A>G did not map to a codon.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr23:101908989 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:101909505 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:101911922 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:101911586 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:101912259 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:101912589 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:101910434 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:101912650 T>G did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:101911893 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:101910574 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:101912546 T>C did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:101911739 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:101909645 A>G did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:101910846 A>G did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:101910338 T>C did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:101910736 G>T did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:101911284 T>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:101970645 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:101971594 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:101971998 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:101971054 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:101971810 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:101972171 A>C did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:101970996 G>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:101970779 C>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:101971866 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:101971136 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:13061596 C>T maps to NM_003979.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:13061923 C>T maps to NM_003979.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:19884092 C>T maps to NM_016235.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:19883321 G>T maps to NM_016235.1 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:19883243 G>A maps to NM_016235.1 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr16:19884110 C>A maps to NM_016235.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:72436361 C>T maps to NM_022036.2 H194H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:72436808 C>T maps to NM_022036.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr17:72436455 C>A maps to NM_022036.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:72436010 C>T maps to NM_022036.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:72436466 C>T maps to NM_022036.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:72428227 G>A maps to NM_022036.2 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr17:72436625 C>T maps to NM_022036.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr17:72436958 G>T maps to NM_022036.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr6:117130581 A>G maps to NM_148963.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:176026160 C>T maps to NM_052899.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:46998897 C>T maps to NM_014696.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:46999935 G>A maps to NM_014696.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:90170013 C>A maps to NM_198281.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:90169209 G>A maps to NM_198281.2 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr17:80011223 G>A maps to NM_212492.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:7216367 G>A maps to NM_004489.4 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:139232331 C>T maps to NM_001145638.1 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:139243182 G>A maps to NM_001145638.1 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr1:109466730 A>G maps to NM_013296.4 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:109461272 A>G maps to NM_013296.4 K434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:109465145 C>T maps to NM_013296.4 C516C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:109445746 G>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:109461390 C>T maps to NM_013296.4 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr6:32159955 T>C maps to NM_022107.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:145729719 G>A maps to NM_005309.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:49394964 A>T maps to NM_000581.2 C156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:1105427 T>C maps to NM_002085.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr6:28483502 C>T maps to NM_182701.1 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:28472227 G>T maps to NM_182701.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:28474206 C>A did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr6:28474134 C>A maps to NM_182701.1 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:28472133 G>A maps to NM_182701.1 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:28472131 C>T maps to NM_182701.1 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:54459979 A>G maps to NM_001008397.2 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:35501252 C>T maps to NM_020895.3 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr11:123489475 C>T maps to ENST00000456860 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:123474228 C>T maps to ENST00000456860 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:113649642 A>G maps to NM_017577.4 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:113623064 A>G maps to NM_017577.4 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:113634569 T>C maps to NM_017577.4 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr3:113623062 G>T maps to NM_017577.4 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:113623064 A>G maps to NM_017577.4 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr15:72454681 C>T maps to NM_001012642.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:72454681 C>T maps to NM_001012642.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr5:125820112 C>A maps to NM_023927.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr5:125822657 C>A maps to NM_023927.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:125807988 G>A maps to NM_023927.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:18927545 G>A maps to NM_006613.3 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:40356094 G>A maps to NM_004810.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:52407520 C>T maps to NM_181711.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr12:52404888 G>T maps to NM_181711.2 E140*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D5-6929-01A-31D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:52407510 C>T maps to NM_181711.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:50771518 C>T maps to NM_005311.4 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:50685803 G>A maps to NM_005311.4 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr7:50742218 A>G maps to NM_005311.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr2:165365335 G>A maps to NM_004490.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:165378572 C>A maps to NM_004490.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:165349650 G>A maps to NM_004490.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr17:73389682 G>A maps to NM_002086.4 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:37899683 C>T maps to ENST00000445327 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr17:37900873 C>T maps to ENST00000445327 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:11761096 G>T maps to NM_014668.3 E1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr2:11696754 C>A maps to NM_014668.3 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:11720857 C>T maps to NM_014668.3 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:11732965 G>A maps to NM_014668.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:11716530 G>A maps to NM_014668.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:11761107 C>A maps to NM_014668.3 V1374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:11767166 G>A maps to NM_014668.3 A1462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:11777918 G>A maps to NM_014668.3 A1808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:11765287 G>T maps to NM_014668.3 E1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr2:11733022 G>A maps to NM_014668.3 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:11750870 G>A maps to NM_014668.3 A908A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:11716494 T>C maps to NM_014668.3 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr2:11750831 C>T maps to NM_014668.3 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:11720941 G>A maps to NM_014668.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:10139115 C>A maps to NM_198182.2 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:10095061 T>C maps to NM_198182.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:10132240 C>T maps to NM_198182.2 D476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr8:102631912 C>G maps to NM_024915.3 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr8:102611357 G>A maps to NM_024915.3 W359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:102678858 G>A maps to NM_024915.3 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:102585913 C>A maps to NM_024915.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr8:102631900 C>T maps to NM_024915.3 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:102611348 C>A maps to NM_024915.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:102611375 G>A maps to NM_024915.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:24669382 C>T maps to NM_021180.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:24680862 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:24673041 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:24673117 C>T maps to NM_021180.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:24673117 C>T maps to NM_021180.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:24664501 C>T maps to NM_021180.3 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:37432007 C>T maps to NM_012203.1 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:153144074 C>T maps to NM_001114183.1 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:152870528 C>T maps to NM_001114183.1 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr5:153065876 C>T maps to NM_001114183.1 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr5:153065876 C>T maps to NM_001114183.1 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:153065883 C>T maps to NM_001114183.1 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:153026608 C>T maps to NM_001114183.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr5:153065861 T>C maps to NM_001114183.1 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr5:153181926 C>T maps to NM_001114183.1 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:153026521 C>A maps to NM_001114183.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:153078455 C>T maps to NM_001114183.1 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:153190778 A>T maps to NM_001114183.1 G905G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:153077602 G>A did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:153078455 C>T maps to NM_001114183.1 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:158254438 C>T maps to NM_000826.3 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:158284072 G>A maps to NM_000826.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr4:158257028 G>T maps to NM_000826.3 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:158262472 C>A maps to NM_000826.3 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:158284066 C>T maps to NM_000826.3 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:158281187 G>A maps to NM_000826.3 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:158256899 C>T maps to NM_000826.3 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:158142862 C>T maps to NM_000826.3 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr4:158142942 C>T maps to NM_000826.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:158233937 C>A maps to NM_000826.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr4:158284177 C>A maps to NM_000826.3 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:122536907 A>G did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:122319796 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:122387363 A>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:122387196 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:122561804 C>T did not map to a codon.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr23:122532532 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:122599626 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr23:122551380 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:122537276 T>C did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:122561910 A>G did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:122551435 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:122598805 G>A did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:122532555 C>T did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr11:105842715 C>T maps to NM_000829.3 Y790Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr11:105797501 G>A maps to NM_000829.3 W628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:105732882 G>A maps to NM_000829.3 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:105789629 G>T maps to NM_000829.3 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr11:105795378 G>A maps to NM_000829.3 E577E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr11:105804509 A>G maps to NM_000829.3 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:105769107 G>A maps to NM_000829.3 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr11:105774590 C>T maps to NM_000829.3 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:105789577 A>G maps to NM_000829.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:105797619 T>C maps to NM_000829.3 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr11:105845131 G>A maps to NM_000829.3 E835E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr11:105789577 A>G maps to NM_000829.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr11:105845152 A>T maps to NM_000829.3 A842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:105732756 G>A maps to NM_000829.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:87614321 C>T maps to NM_017551.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr10:87966373 G>A maps to NM_017551.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr10:87628865 G>T maps to NM_017551.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:87484301 G>A maps to NM_017551.2 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:87898578 G>A maps to NM_017551.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:87407087 A>G maps to NM_017551.2 Y688Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:87484178 C>T maps to NM_017551.2 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:87362368 C>T maps to NM_017551.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:87362368 C>T maps to NM_017551.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:87966133 G>A maps to NM_017551.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:87373268 G>A maps to NM_017551.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr10:87362143 G>A maps to NM_017551.2 N972N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr10:87484180 G>A maps to NM_017551.2 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr10:87362311 C>T maps to NM_017551.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:87489323 C>T maps to NM_017551.2 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr4:94006177 C>T maps to NM_001510.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr4:94377046 C>T maps to NM_001510.2 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr4:94032028 G>A maps to NM_001510.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr4:93225839 C>T maps to NM_001510.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:94547532 A>G maps to NM_001510.2 G769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:94436426 G>A maps to NM_001510.2 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr4:94377046 C>T maps to NM_001510.2 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:94032100 T>G maps to NM_001510.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:94376914 C>T maps to NM_001510.2 R550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:94436426 G>A maps to NM_001510.2 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr4:94031995 C>A maps to NM_001510.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr4:94344031 C>T maps to NM_001510.2 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr21:31066350 A>G maps to ENST00000327783 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr21:31062246 G>A maps to ENST00000327783 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr21:30961212 C>T maps to ENST00000327783 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr21:30963506 C>T maps to ENST00000327783 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr21:30927522 G>A maps to ENST00000327783 C819C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:30959870 G>A maps to ENST00000327783 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:31023464 C>T maps to ENST00000327783 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr21:31015247 G>A maps to ENST00000327783 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:30933990 G>A maps to ENST00000327783 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr21:31066218 C>T maps to ENST00000327783 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr21:30959732 C>A maps to ENST00000327783 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:30934053 C>T maps to ENST00000327783 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr6:102483220 A>C maps to NM_021956.4 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:101847221 A>G maps to NM_021956.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:102124604 G>T maps to NM_021956.4 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr6:102337633 A>G maps to NM_021956.4 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:102134203 A>C maps to NM_021956.4 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr6:102337642 C>T maps to NM_021956.4 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:102516286 A>G maps to NM_021956.4 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr6:102372583 C>A maps to NM_021956.4 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr6:102516286 A>G maps to NM_021956.4 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:102483232 G>A maps to NM_021956.4 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:102483298 A>G maps to NM_021956.4 E723E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:102124619 A>T maps to NM_021956.4 K222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:37271723 G>A maps to NM_000831.3 Y765Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:37499646 C>T maps to NM_000831.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:37319311 T>C maps to NM_000831.3 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:37307465 G>A maps to NM_000831.3 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr1:37337853 G>A maps to NM_000831.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:37270836 G>A maps to NM_000831.3 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:37346469 G>A maps to NM_000831.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:37346412 G>T maps to NM_000831.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:37267625 C>A maps to NM_000831.3 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:37307402 G>A maps to NM_000831.3 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr1:37271783 G>A maps to NM_000831.3 Y745Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr1:37346391 G>A maps to NM_000831.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:37499643 G>A maps to NM_000831.3 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:37291208 G>A maps to NM_000831.3 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr11:120776003 C>T maps to NM_014619.2 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:120745870 C>T maps to NM_014619.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:120833229 C>T maps to NM_014619.2 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:120702675 C>T maps to NM_014619.2 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:120833229 C>T maps to NM_014619.2 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:120744869 C>A maps to NM_014619.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:120686132 G>A maps to NM_014619.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr11:120776103 C>T maps to NM_014619.2 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr11:120833253 C>T maps to NM_014619.2 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:120702654 G>A maps to NM_014619.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:42566745 C>T maps to NM_002088.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:42526108 G>A maps to NM_002088.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr19:42546715 C>T maps to NM_002088.3 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:42510876 C>A maps to NM_002088.3 E653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr19:42563596 C>A maps to NM_002088.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:140051321 C>T maps to ENST00000371546 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr9:140036502 C>T maps to ENST00000371546 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:10274121 G>A maps to NM_000833.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr16:9943689 G>A maps to NM_000833.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:9857482 C>T maps to NM_000833.3 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr16:9857782 T>C maps to NM_000833.3 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr16:9857857 G>A maps to NM_000833.3 N1181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:10032354 C>T maps to NM_000833.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr16:9943662 G>A maps to NM_000833.3 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:9857524 G>A maps to NM_000833.3 Y1292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:9857809 A>C maps to NM_000833.3 G1197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:10032141 G>T maps to NM_000833.3 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:9858097 G>A maps to NM_000833.3 V1101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:9862887 G>A maps to NM_000833.3 N805N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr16:9857784 G>T maps to NM_000833.3 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:9858454 T>C maps to NM_000833.3 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr16:9857784 G>T maps to NM_000833.3 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr16:9857784 G>A maps to NM_000833.3 R1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr16:9858160 G>A maps to NM_000833.3 H1080H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr16:10273962 G>A maps to NM_000833.3 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:13717507 G>A maps to NM_000834.3 T888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr12:13716759 G>A maps to NM_000834.3 R1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:13768576 C>T maps to NM_000834.3 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:13906540 G>T maps to NM_000834.3 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:13716679 G>A maps to NM_000834.3 R1164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:13722762 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr12:14018868 G>T maps to NM_000834.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:14018868 G>T maps to NM_000834.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:13768146 G>A maps to NM_000834.3 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:14018755 G>A maps to NM_000834.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:13716358 C>T maps to NM_000834.3 A1271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr12:14018866 C>T maps to NM_000834.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr12:13724808 T>C maps to NM_000834.3 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr12:13724808 T>C maps to NM_000834.3 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr12:13724808 T>C maps to NM_000834.3 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:13724808 T>C maps to NM_000834.3 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:72846500 G>A maps to NM_000835.3 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:72846458 G>A maps to NM_000835.3 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:72846744 G>T maps to NM_000835.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:72846774 G>A maps to NM_000835.3 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:72840561 G>A maps to NM_000835.3 I812I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:48945503 G>A maps to NM_000836.2 A846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:48945115 C>T maps to NM_000836.2 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:48925169 C>T maps to NM_000836.2 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:48925181 G>A maps to NM_000836.2 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:48945413 C>T maps to NM_000836.2 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:48945575 C>T maps to NM_000836.2 Y870Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:104432908 G>A maps to NM_133445.2 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:104375759 G>A maps to NM_133445.2 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:104375804 G>A maps to NM_133445.2 Y873Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:104432908 G>A maps to NM_133445.2 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:104335719 G>T maps to NM_133445.2 I1028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr9:104385693 G>A maps to NM_133445.2 D840D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr9:104499568 C>T maps to NM_133445.2 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:104448993 G>A maps to NM_133445.2 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:104432514 A>G maps to NM_133445.2 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr9:104449293 G>A maps to NM_133445.2 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:1005212 G>A maps to NM_138690.1 W571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:1003172 G>A maps to NM_138690.1 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:1005194 C>T maps to NM_138690.1 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr8:145066739 C>T maps to NM_001009184.1 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr8:145066194 C>A maps to NM_001009184.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:66773079 C>T maps to ENST00000359742 W867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:66839252 G>A maps to ENST00000359742 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:66849330 A>C maps to ENST00000359742 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:66856833 G>A maps to ENST00000359742 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:66856866 G>A maps to ENST00000359742 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr12:66771058 T>C maps to ENST00000359742 A876A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:66856836 G>A maps to ENST00000359742 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr12:67072641 G>A maps to ENST00000359742 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:14563272 G>A maps to ENST00000507975 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:14563215 G>A maps to ENST00000507975 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:14583489 G>A maps to ENST00000507975 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr23:48847415 C>T did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:48847415 C>T did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:48830665 C>T did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:48831647 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:48844216 G>C did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:48838221 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:48855684 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:48839839 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:48855870 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:48847438 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:48847366 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:48831599 C>T did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:48832500 C>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:48847480 C>T did not map to a codon.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr13:114321904 C>T maps to NM_002929.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:114321991 G>A maps to NM_002929.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr4:3037162 G>A maps to NM_182982.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:3039117 T>C maps to NM_182982.2 C475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:3021525 G>A maps to NM_182982.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr4:2993971 C>T maps to NM_182982.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:141499328 C>A maps to NM_139209.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr3:141499298 C>T maps to NM_139209.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:141497491 G>A maps to NM_139209.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:141497623 C>T maps to NM_139209.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:141499361 T>C maps to NM_139209.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:141499361 T>C maps to NM_139209.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:141526489 G>T maps to NM_139209.2 G352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr3:141535597 G>A maps to NM_139209.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:47422342 C>T maps to NM_004491.4 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:47423941 G>A maps to NM_004491.4 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:47425364 C>T maps to NM_004491.4 R1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:47424302 G>T maps to NM_004491.4 G791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:47422936 T>C maps to NM_004491.4 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr19:47503611 T>C maps to NM_004491.4 N1389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr19:47423287 G>A maps to NM_004491.4 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr19:47425249 C>T maps to NM_004491.4 S1106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr19:47423192 G>T maps to NM_004491.4 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:47503860 G>A maps to NM_004491.4 S1472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:146625839 G>A maps to NM_000838.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:146720697 G>A maps to NM_000838.3 K841K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr6:146755256 G>A maps to NM_000838.3 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:146351333 C>A maps to NM_000838.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:146351084 C>T maps to NM_000838.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr6:146755394 T>C maps to NM_000838.3 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:146755568 C>T maps to NM_000838.3 H1074H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:146755530 C>T maps to NM_000838.3 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:146755529 G>C maps to NM_000838.3 G1061G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:146755559 T>G maps to NM_000838.3 P1071P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr6:146720535 C>T maps to NM_000838.3 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr6:146350841 C>T maps to NM_000838.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:146351141 C>A maps to NM_000838.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:51749480 C>T maps to NM_000839.3 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:51749276 C>T maps to NM_000839.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:51746991 G>A maps to NM_000839.3 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:86415677 C>T maps to NM_000840.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr7:86415875 C>T maps to NM_000840.2 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:86468839 C>T maps to NM_000840.2 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr7:86468222 C>T maps to NM_000840.2 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:86416106 C>T maps to NM_000840.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:86469091 C>T maps to NM_000840.2 Y754Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:86416106 C>T maps to NM_000840.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr7:86469103 G>T maps to NM_000840.2 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr7:86394865 A>G maps to NM_000840.2 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr6:34059696 G>A maps to NM_000841.1 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:34059846 C>T maps to NM_000841.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr6:34003588 C>T maps to NM_000841.1 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr11:88583231 A>G maps to NM_001143831.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:88386486 G>T maps to NM_001143831.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:88780641 G>T maps to NM_001143831.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:88338055 G>T maps to NM_001143831.2 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:88300510 C>T maps to NM_001143831.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:88583258 G>A maps to NM_001143831.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr11:88242035 G>A maps to NM_001143831.2 I1121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:88242128 G>A maps to NM_001143831.2 G1090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:88330489 T>C maps to NM_001143831.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:88583096 C>T maps to NM_001143831.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr11:88780887 T>C maps to NM_001143831.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:88780887 T>C maps to NM_001143831.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr11:88781019 C>A maps to NM_001143831.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr11:88386357 G>A maps to NM_001143831.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr5:178415972 C>T maps to NM_000843.3 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:178413730 G>A maps to NM_000843.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:178418506 C>A maps to NM_000843.3 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr5:178410141 G>A maps to NM_000843.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:178418521 C>A maps to NM_000843.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:178418552 G>T maps to NM_000843.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:178413703 C>T maps to NM_000843.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:178413955 G>A maps to NM_000843.3 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr5:178413949 G>A maps to NM_000843.3 N463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:6903296 C>T maps to NM_181874.2 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:7621025 C>T maps to NM_181874.2 T811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr3:7620138 C>T maps to NM_181874.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr3:7456753 A>C maps to NM_181874.2 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:7620554 G>A maps to NM_181874.2 V654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:7620140 A>G maps to NM_181874.2 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:7620567 C>A maps to NM_181874.2 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:126173728 G>T maps to NM_001127323.1 C569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:126746724 A>G maps to NM_001127323.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr7:126249445 G>T maps to NM_001127323.1 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:126883204 G>A maps to NM_001127323.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr7:126173578 G>A maps to NM_001127323.1 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:126173854 T>C maps to NM_001127323.1 K527K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:126746619 C>T maps to NM_001127323.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:126542725 A>G maps to NM_001127323.1 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr7:126882787 G>A maps to NM_001127323.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:126173566 G>A maps to NM_001127323.1 Y623Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:126173338 G>T maps to NM_001127323.1 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:126746619 C>T maps to NM_001127323.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:126173065 G>T maps to NM_001127323.1 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr7:126883066 A>G maps to NM_001127323.1 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:42428818 T>C maps to NM_002087.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr17:42427633 C>T maps to NM_002087.2 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:42429833 C>T maps to NM_002087.2 H513H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr17:42427659 G>A maps to NM_002087.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:42428089 C>T maps to NM_002087.2 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:42428523 G>A maps to NM_002087.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr17:42428523 G>A maps to NM_002087.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:42429801 C>T maps to NM_002087.2 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:56892800 G>T maps to NM_002091.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr18:56892827 A>C maps to NM_002091.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:7062675 G>A maps to NM_025196.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr5:148727934 C>T maps to NM_152407.3 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr5:148727864 C>A maps to NM_152407.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:148730652 C>T maps to NM_152407.3 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr23:16168671 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:16168675 T>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:16168589 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:16142155 A>C did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr23:16142159 C>G did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:16168471 C>T did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:16168588 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:113999222 C>A maps to NM_024719.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:48954334 C>T maps to NM_031485.3 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:48956134 C>T maps to NM_031485.3 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:48953745 C>T maps to NM_031485.3 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:43022433 G>T maps to NM_001080476.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:42965061 G>T maps to NM_001080476.2 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:42895391 C>T maps to NM_001080476.2 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:145246230 G>A maps to NM_001080516.1 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:145239333 C>A maps to NM_001080516.1 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr5:145246117 G>A maps to NM_001080516.1 H170H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:38132231 A>G maps to NM_178171.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:38127808 C>T maps to NM_178171.4 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:38131229 C>T maps to NM_178171.4 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr17:38062501 A>G maps to NM_001165958.1 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:130763786 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:130788397 C>T maps to NM_031415.2 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr8:130774935 C>A maps to NM_031415.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:144644473 G>A maps to NM_024736.6 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:13243455 C>T maps to NM_001080555.1 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr12:13238140 C>T maps to NM_001080555.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:13241762 G>A maps to ENST00000405543 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:27895831 G>A maps to NM_001109763.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr19:42737326 G>A maps to NM_019884.2 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:42736813 C>T maps to NM_019884.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:42736732 G>A maps to NM_019884.2 H400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr3:119582445 G>A maps to NM_002093.3 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:119595321 C>A maps to NM_002093.3 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:119582305 A>G maps to NM_002093.3 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr3:119582317 G>T maps to NM_002093.3 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:119585469 C>T maps to NM_002093.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:124094766 C>A maps to NM_000177.4 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:124088884 C>T maps to NM_000177.4 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr9:124094799 T>C maps to NM_000177.4 F756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr9:124073059 C>T maps to NM_000177.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:11969777 G>T maps to NM_002094.3 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:11969777 G>T maps to NM_002094.3 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:51486870 G>A did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:51487266 A>G did not map to a codon.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr23:51487183 A>G did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:51487337 G>A did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:51487273 G>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:51487514 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:30546692 C>T maps to NM_000637.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr8:30546679 G>A maps to NM_000637.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:33533840 G>A maps to NM_000178.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr6:52659006 G>A maps to NM_145740.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr6:52657767 T>C maps to NM_145740.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr6:52615449 T>C maps to NM_000846.4 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:52764808 G>A maps to NM_000847.4 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:52696669 T>C maps to NM_153699.1 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr6:52696669 T>C maps to NM_153699.1 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:52696669 T>C maps to NM_153699.1 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:52696669 T>C maps to NM_153699.1 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr6:52696669 T>C maps to NM_153699.1 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr6:52705590 G>A maps to NM_153699.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:106650579 G>T maps to NM_001031720.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:106766721 A>C maps to NM_001031720.2 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:106766661 C>T maps to NM_001031720.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:110231874 T>G maps to ENST00000369823 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:110282100 G>A maps to NM_000849.4 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr1:110282491 A>G maps to NM_000849.4 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:110199332 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:106039208 G>T maps to NM_183239.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr22:24384225 G>A maps to NM_000853.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr22:24376500 C>T maps to NM_000853.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr14:77791257 C>T maps to NM_145870.2 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:77791257 C>T maps to NM_145870.2 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:28367982 C>T maps to NM_145657.1 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr13:28367931 C>T maps to NM_145657.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:54966585 G>A maps to NM_133267.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:54966804 C>T maps to NM_133267.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:54967858 C>A maps to NM_133267.2 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:144903215 G>A maps to NM_001164629.2 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:144714906 C>A did not map to a codon.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr2:144764887 A>G maps to NM_001164629.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:81662538 G>T maps to NM_015859.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:48847997 C>A maps to NM_172311.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:48896937 C>T maps to NM_172311.2 S1056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:48874069 G>A maps to NM_172311.2 Q993Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr2:48898812 T>A maps to NM_172311.2 Y1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:59931351 A>G maps to NM_004492.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:89325833 G>T maps to NM_001514.5 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:89325690 G>A maps to NM_001514.5 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:89325690 G>A maps to NM_001514.5 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:89325962 C>A maps to NM_001514.5 G89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:89325690 G>A maps to NM_001514.5 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:120500196 C>A maps to NM_005513.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:120489584 C>T maps to NM_005513.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr3:120469686 T>C maps to NM_005513.2 Y96Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr19:6389579 C>T maps to NM_002096.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:6381751 C>T maps to NM_002096.2 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr13:45694852 C>T maps to NM_004128.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr11:18369441 C>T maps to NM_005316.3 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:68868293 G>A maps to NM_001042490.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:124144079 A>G maps to NM_001516.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:124144070 C>T maps to NM_001516.3 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:30879921 G>A maps to NM_001517.4 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr6:30880174 G>A maps to NM_001517.4 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr7:74125429 T>C maps to NM_032999.2 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:74114688 C>T maps to NM_032999.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:73960116 G>A maps to NM_016328.2 E570E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr7:74212035 C>T maps to NM_173537.2 K605K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:74211462 A>G maps to NM_173537.2 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr7:74564622 A>G maps to NM_001003795.2 K790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:27523103 G>A maps to NM_001520.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:27503680 G>A maps to NM_001520.3 C1043C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr16:27475830 G>T maps to NM_001520.3 A1894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:27472724 C>T maps to NM_001520.3 R2092R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:27556753 T>C maps to NM_001520.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr16:27499587 C>T maps to NM_001520.3 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:27506766 G>A maps to NM_001520.3 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:27556782 C>A maps to NM_001520.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:27475893 G>A maps to NM_001520.3 T1873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:27551029 C>T maps to NM_001521.2 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:27560423 G>A maps to NM_001521.2 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:27552106 G>A maps to NM_001521.2 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:27551764 A>C maps to NM_001521.2 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr2:27565766 A>T maps to NM_001521.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:27552096 G>A maps to NM_001521.2 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr2:27566202 C>T maps to NM_001521.2 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:197641321 T>C maps to NM_012086.2 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:197657763 C>T maps to NM_012086.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:197639852 A>G maps to NM_012086.2 N606N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr2:197664263 C>A maps to NM_012086.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:197649604 C>A maps to NM_012086.2 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:197639867 G>A maps to NM_012086.2 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:197641321 T>C maps to NM_012086.2 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr2:197641323 G>T maps to NM_012086.2 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:197639858 T>C maps to NM_012086.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr2:197639858 T>C maps to NM_012086.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:197641321 T>C maps to NM_012086.2 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:197639858 T>C maps to NM_012086.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr9:135554985 A>G maps to NM_012204.2 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr9:135554565 G>A maps to NM_012204.2 E520E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:135553404 C>T maps to NM_012204.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr9:135554145 T>C maps to NM_012204.2 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr9:135554145 T>C maps to NM_012204.2 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:135931466 C>T maps to NM_001122823.1 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr9:135933280 G>T maps to NM_001122823.1 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr9:135929861 C>T maps to NM_001122823.1 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr9:135906412 G>A maps to NM_001122823.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:111283698 G>T maps to NM_138408.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:111288815 A>G maps to NM_138408.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:39112905 G>A maps to NM_004286.4 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:43592281 G>A maps to NM_019096.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:17449471 G>A maps to NM_133644.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:17449381 C>T maps to NM_133644.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:17449773 C>T maps to NM_133644.3 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:1058521 C>T maps to NM_012341.2 R488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:1053032 C>T maps to NM_012341.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:60768526 C>T maps to NM_015666.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:60775931 C>T maps to NM_015666.3 H340H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:46704227 T>C maps to NM_016426.6 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr22:46724614 G>A maps to NM_016426.6 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr22:46704080 C>T maps to NM_016426.6 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr22:46722389 G>T maps to NM_016426.6 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:46704080 C>T maps to NM_016426.6 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:46709818 C>T maps to NM_016426.6 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr22:46704299 G>A maps to NM_016426.6 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:46704797 G>A maps to NM_016426.6 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:54865020 A>C maps to NM_144594.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:42147048 C>T maps to NM_000409.3 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr6:42152594 G>A maps to NM_002098.5 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:42629215 C>T maps to NM_033553.2 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:42620460 C>A maps to NM_007102.2 C67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr11:106647170 C>T maps to ENST00000282249 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:106680721 A>G maps to ENST00000282249 Y563Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:106680925 A>C maps to ENST00000282249 Y495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:106558334 C>T maps to ENST00000282249 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr11:106810250 G>A maps to ENST00000282249 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:106558432 C>A maps to ENST00000282249 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr4:156618123 A>G maps to NM_001130684.1 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:156631716 G>T maps to NM_001130684.1 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:156631865 C>A maps to NM_001130684.1 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr4:156632156 G>A maps to NM_001130684.1 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:156634587 G>A maps to NM_001130684.1 K475K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:156632156 G>A maps to NM_001130684.1 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr4:156638324 C>T maps to NM_001130684.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:156631769 C>T maps to NM_001130684.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:156632280 G>T maps to NM_001130684.1 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:156634362 C>A maps to NM_001130684.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:156643240 A>T maps to NM_001130684.1 K590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr4:156634413 A>G maps to NM_001130684.1 E417E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:156625137 G>T maps to NM_001130684.1 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:156631691 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:156634659 G>A maps to NM_001130684.1 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:156696149 G>A maps to ENST00000502959 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:156725858 G>T maps to ENST00000502959 G579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:156725809 C>A maps to ENST00000502959 Y562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr4:156721097 G>A maps to ENST00000502959 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:14829841 C>T maps to NM_004963.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:14794037 A>G maps to NM_004963.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:14839120 T>C maps to NM_004963.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:14804379 G>T maps to NM_004963.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr12:14849199 C>T maps to NM_004963.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:7909800 C>A maps to NM_000180.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr17:7909844 C>T maps to NM_000180.3 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:7911346 T>A maps to NM_000180.3 Y555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:7915484 C>T maps to NM_000180.3 N591N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:108631829 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:108636279 T>G did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:108652262 A>G did not map to a codon.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr23:108638709 T>G did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:108718574 A>C did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:108718867 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:108619383 C>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:108697079 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:108708573 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:108652306 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:108631835 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:108636217 A>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:108641859 T>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:108697037 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:108652238 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:108708429 G>A did not map to a codon.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr23:108638585 T>C did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:108719135 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:108718727 A>C did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:108719135 G>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:108619391 T>C did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr23:108719135 G>T did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr23:108619205 G>T did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:108619390 T>C did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr23:108619382 T>C did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:108673624 C>A did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:108619382 T>C did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:108641792 C>T did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:108647624 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:108619391 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr23:108635279 C>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:108673622 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:108619392 T>C did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:108719135 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:44696437 C>T maps to NM_021927.2 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:44693685 C>T maps to NM_021927.2 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:44700613 G>A maps to NM_021927.2 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:228334600 C>T maps to ENST00000366720 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:189449041 T>C maps to NM_016315.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:189434817 C>T maps to NM_016315.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr7:65445384 G>A maps to NM_000181.3 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:65444883 G>A maps to NM_000181.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:65432843 G>A maps to NM_000181.3 H509H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:42491369 A>G maps to NM_173601.1 H345H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:42512840 A>G maps to NM_173601.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:73016752 C>T maps to NM_001080393.1 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:73016821 T>C maps to NM_001080393.1 H367H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:72971485 G>A maps to NM_001080393.1 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:72971401 C>T maps to NM_001080393.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:73006458 G>A maps to NM_001080393.1 W311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:148714548 T>C maps to NM_004130.3 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:2795257 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:2795285 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:2778029 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:2777917 G>A did not map to a codon.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr23:2773086 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:2772117 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:2761347 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:2772078 G>A did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:2779654 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:2778087 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:45949081 G>A maps to NM_152312.3 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr11:45948275 G>T maps to NM_152312.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:127413871 G>A maps to NM_002101.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:127447840 G>A maps to NM_002101.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:127451521 A>T maps to NM_002101.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:144826642 G>T maps to NM_198682.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:144801562 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:144801573 T>C maps to NM_198682.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:49490525 G>A maps to NM_002103.4 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:49489139 G>T maps to NM_002103.4 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr19:49486094 C>G did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:49472589 G>A maps to NM_002103.4 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr12:21728844 A>G maps to NM_021957.3 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr12:21721885 G>A maps to NM_021957.3 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:21728931 G>C maps to NM_021957.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:23345739 T>C maps to NM_022482.3 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:54405922 C>T maps to NM_006144.3 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr5:54405922 C>T maps to NM_006144.3 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:54405874 C>T maps to NM_006144.3 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr5:54405874 C>T maps to NM_006144.3 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr14:25100342 A>G maps to ENST00000382542 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr14:25076886 A>G maps to NM_033423.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:54327309 C>A maps to NM_002104.2 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:54327359 C>T maps to NM_002104.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr12:48723598 C>T maps to NM_181788.1 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:48723820 C>A maps to NM_181788.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:48723331 C>T maps to NM_181788.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr3:129268025 T>C maps to NM_153833.1 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:129262075 C>T maps to NM_153833.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:129268073 G>A maps to NM_153833.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:129034715 T>G maps to NM_006026.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr23:154113462 C>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:44882914 C>T maps to ENST00000421098 K67K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:134696261 G>A maps to NM_138610.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr5:134705151 G>A maps to NM_138610.2 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr10:71868831 C>A maps to NM_018649.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:71853556 G>T maps to NM_018649.2 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr4:100869630 C>T maps to NM_002106.3 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:103268204 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:103267816 C>T did not map to a codon.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr23:103268106 C>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:103268036 G>A did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr17:73774968 G>A maps to NM_005324.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:31944833 G>A maps to NM_001013699.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:31944833 G>A maps to NM_001013699.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr1:9305211 T>A maps to NM_004285.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:9324774 G>A maps to NM_004285.3 K741K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:9324273 C>T maps to NM_004285.3 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:9324102 C>T maps to NM_004285.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:9324882 C>T maps to NM_004285.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:42995059 G>T maps to NM_012205.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:42997655 C>T maps to NM_012205.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:115334046 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:115343958 C>T maps to NM_004132.3 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr10:115338461 C>A maps to NM_004132.3 C215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr10:115336948 A>G maps to NM_004132.3 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:115336981 C>T maps to NM_004132.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:115343046 C>T maps to NM_004132.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:99227745 C>T maps to NM_014282.2 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:99250432 A>C maps to NM_014282.2 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:105219220 T>C maps to NM_020771.3 E686E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:105225189 A>C maps to NM_020771.3 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:105244586 C>T maps to NM_020771.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr6:105280964 G>T maps to NM_020771.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:15610009 G>A maps to NM_012260.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:15610009 G>A maps to NM_012260.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:15631060 G>A maps to NM_012260.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:15624435 C>T maps to NM_012260.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr4:108954416 C>T maps to ENST00000351726 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:26437419 C>T maps to NM_000182.4 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:26420586 G>A maps to NM_000182.4 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:26437358 G>A maps to NM_000182.4 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:26424107 A>G maps to NM_000182.4 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr2:26501645 C>T maps to NM_000183.2 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:1872940 G>T maps to NM_005326.4 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr16:1872922 C>T maps to NM_005326.4 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr12:96389490 G>A maps to NM_002108.2 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:96386560 A>G maps to NM_002108.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:96380931 G>A maps to NM_002108.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:174448517 G>T maps to NM_021973.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:174450266 G>A maps to NM_021973.2 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr20:7921006 C>T maps to NM_017545.2 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr20:7894998 C>T maps to NM_017545.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr20:7915283 T>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:119934801 C>T maps to ENST00000361035 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:119936412 C>A maps to ENST00000361035 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:39888991 C>A maps to ENST00000310778 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr17:39889009 G>T maps to ENST00000310778 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr5:82969270 C>T maps to NM_001884.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:82937440 G>A maps to NM_001884.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr5:82937431 G>A maps to NM_001884.3 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:82937377 G>A maps to NM_001884.3 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:82940191 G>T maps to NM_001884.3 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:156594146 G>A maps to NM_021817.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:89424630 G>A maps to NM_178232.2 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr15:89424837 C>T maps to NM_178232.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:19371709 G>A maps to NM_023002.2 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:19371808 G>A maps to NM_023002.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr19:19372261 G>A maps to NM_023002.2 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:46637685 G>T maps to NM_173811.3 Y34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:140056456 G>A maps to NM_002109.3 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:140075139 A>G maps to NM_012208.2 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr5:140077222 C>T maps to NM_012208.2 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr5:140075330 C>T maps to NM_012208.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr19:52217158 G>A maps to NM_001523.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:52222464 G>A maps to NM_001523.2 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr19:52216826 G>A maps to NM_001523.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:122626929 G>A maps to NM_005328.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr8:122641064 C>T maps to NM_005328.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:122641163 G>A maps to NM_005328.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr8:122641019 C>T maps to NM_005328.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr8:122626534 A>G maps to NM_005328.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr8:122626534 A>G maps to NM_005328.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr8:122626972 G>A maps to NM_005328.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:122626534 A>G maps to NM_005328.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:69147348 C>T maps to NM_005329.2 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:69148721 C>T maps to NM_005329.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:172844218 C>A maps to NM_003642.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:172809458 G>A maps to NM_003642.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr2:172844218 C>A maps to NM_003642.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:172841222 A>G maps to NM_003642.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:172844218 C>T maps to NM_003642.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:172841222 A>G maps to NM_003642.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr15:42853576 A>G maps to NM_018097.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:42856036 T>C maps to NM_018097.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:2240604 G>A maps to NM_024511.5 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:2242085 C>T maps to NM_024511.5 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:2233754 C>A maps to NM_024511.5 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:2242085 C>T maps to NM_024511.5 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr4:2233806 C>A maps to NM_024511.5 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr14:23417205 G>A maps to NM_017815.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:36110636 G>A maps to NM_015302.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:19058130 C>T maps to NM_017645.3 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:19058867 C>A maps to NM_017645.3 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:19089513 C>T maps to NM_017645.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr9:19058778 G>A maps to NM_017645.3 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:152721026 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:152721026 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:152734718 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:152735958 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:152734719 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:152735919 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:17166713 G>A maps to NM_033417.1 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:17169424 G>A maps to NM_033417.1 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr5:156456745 A>G maps to NM_001173393.1 *365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:156535949 C>T maps to NM_032782.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:156535936 T>G maps to NM_032782.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:154248122 T>C maps to NM_006118.3 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:154245940 T>C maps to NM_006118.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr11:5255280 A>C maps to NM_000519.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr11:5255331 C>A maps to NM_000519.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:5254223 C>A maps to NM_000519.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:5290788 A>G maps to NM_005330.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr11:5291030 G>T maps to NM_005330.3 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:5270636 C>T maps to ENST00000440157 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:5275631 G>A maps to ENST00000399563 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:5275560 C>T maps to ENST00000399563 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr11:5275626 A>C maps to ENST00000399563 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:231103 C>T maps to NM_005331.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:230981 C>T maps to NM_005331.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:135290430 G>A maps to NM_006620.3 R615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:135358358 G>T maps to NM_001145207.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:135308863 T>C maps to NM_006620.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr6:135290430 G>A maps to NM_006620.3 R615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:135358313 T>C maps to NM_001145207.1 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:11132997 G>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:11139755 C>T did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr23:11130256 C>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:11133058 A>C did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:153219568 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:153228772 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:153221675 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:153229684 C>G did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr23:153229675 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:153218275 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:153220615 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:153216407 C>T did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr23:153223680 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:153219631 C>T did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:153219633 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:153215722 C>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:153229667 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:153215747 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:153224796 C>T did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr12:104487252 G>A maps to NM_013320.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:104459948 G>A maps to NM_013320.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:104476539 A>G maps to NM_013320.2 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:104461819 T>C maps to NM_013320.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:104476680 T>C did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr20:30681688 C>T maps to NM_002110.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:30686921 C>T maps to NM_002110.3 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr20:30686840 A>G maps to NM_002110.3 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:30681739 C>A maps to NM_002110.3 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:30681739 C>T maps to NM_002110.3 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr20:30672338 C>T maps to NM_002110.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr20:30662500 C>T maps to NM_002110.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr20:30671712 C>T maps to NM_002110.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:30686918 C>G maps to NM_002110.3 Y453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr20:30671800 C>T maps to NM_002110.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:121353074 C>A maps to NM_005335.4 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:121351314 G>A maps to NM_005335.4 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr3:121376174 G>A maps to NM_005335.4 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:121356005 G>A maps to NM_005335.4 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:121376174 G>A maps to NM_005335.4 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:121376174 G>A maps to NM_005335.4 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:121355336 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:121353134 C>T maps to NM_005335.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:45353272 C>A maps to NM_021072.2 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:45353285 T>G maps to NM_021072.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:45262514 C>A maps to NM_021072.2 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:45462052 G>A maps to NM_021072.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr5:45262487 C>T maps to NM_021072.2 Q736Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:45262139 C>T maps to NM_021072.2 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:45262220 C>T maps to NM_021072.2 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr5:45262787 G>A maps to NM_021072.2 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:155254391 C>T maps to NM_020897.1 C311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:155257021 C>T maps to NM_020897.1 C512C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:155255669 G>A maps to NM_020897.1 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr15:73622099 C>T maps to NM_005477.2 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr15:73622132 C>T did not map to a codon.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr15:73635794 C>T maps to NM_005477.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:73616240 G>A maps to NM_005477.2 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr15:73617365 C>T maps to NM_005477.2 Q636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr15:73635944 C>T maps to NM_005477.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr15:73615655 G>T maps to NM_005477.2 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:32090675 C>T maps to NM_001525.2 Y348Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AY-4070-01A-01W-1073-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:55147182 G>A maps to NM_001526.3 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:55145213 G>A maps to NM_001526.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:55147218 A>G maps to NM_001526.3 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:55113455 G>A maps to NM_001526.3 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:32793211 G>A maps to NM_004964.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr22:50685353 T>C maps to NM_032019.5 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr3:13538270 C>T maps to NM_024827.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:13538273 C>A maps to NM_024827.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:114277858 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:114264667 G>A maps to ENST00000398283 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr6:114274582 C>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr6:114264667 G>A maps to ENST00000398283 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr6:114264665 T>C maps to ENST00000398283 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:240061382 C>A maps to NM_006037.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:240024583 G>A maps to NM_006037.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr2:240078375 G>A maps to NM_006037.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:240024583 G>A maps to NM_006037.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:240111560 G>A maps to NM_006037.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:240111555 G>A maps to NM_006037.3 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:240024555 G>A maps to NM_006037.3 Q712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr2:240024583 G>A maps to NM_006037.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:42162494 C>T maps to NM_001015053.1 K694K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:42169647 C>T maps to NM_001015053.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:42170837 G>A maps to NM_001015053.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:42157830 G>A maps to NM_001015053.1 N922N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:42156193 C>T maps to NM_001015053.1 V1045V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:48678598 T>C did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:48661608 C>T did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:48678568 G>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:48678597 G>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:48675011 G>A did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:48673138 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:48673090 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:48682587 C>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:48674339 C>T did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:48681848 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:48179651 C>T maps to NM_015401.3 T863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:48192378 C>T maps to NM_015401.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:48180479 G>A maps to NM_015401.3 V820V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr12:48179573 G>A maps to NM_015401.3 D889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:48185743 G>A maps to NM_015401.3 C574C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:71792544 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:71715049 A>C did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:71787871 A>G did not map to a codon.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr7:18767219 G>A maps to NM_178425.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr7:18674250 A>G maps to NM_178425.2 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:18687412 G>A maps to NM_178425.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:18684364 T>G maps to NM_178425.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr7:18869116 C>T maps to NM_178425.2 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:18993806 G>A maps to NM_178425.2 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:18624913 G>A maps to NM_178425.2 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:18687596 C>T maps to NM_178425.2 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:18767261 G>A maps to NM_178425.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:18868782 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:19015576 G>A did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr7:19015543 T>C maps to NM_178425.2 D1046D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr7:18688182 C>A maps to NM_178425.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr7:18767231 G>A maps to NM_178425.2 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:18625093 G>A maps to NM_178425.2 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:18875116 C>T maps to NM_178425.2 Q832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:50555577 G>A maps to NM_002112.3 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:50546374 A>T maps to NM_002112.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr15:50555434 A>G maps to NM_002112.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:50535179 A>G maps to NM_002112.3 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:125597369 C>T maps to NM_016063.2 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:22570268 C>T maps to NM_138574.2 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:22570211 G>A maps to NM_138574.2 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:22570175 C>T maps to NM_138574.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:22570497 G>T maps to NM_138574.2 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr6:22569848 G>A maps to NM_138574.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:22570001 C>T maps to NM_138574.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:22570076 C>T maps to NM_138574.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:22569881 G>A maps to NM_138574.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:22570145 C>T maps to NM_138574.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr6:22570124 G>A maps to NM_138574.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:4488866 G>A maps to ENST00000301284 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:4498824 C>T maps to ENST00000301284 C496C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:7023870 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:6995424 C>T did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:6995413 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:44639368 G>A maps to NM_032124.4 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr18:44660876 A>T maps to NM_032124.4 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:242169307 C>T maps to NM_005336.3 K1220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:242187503 G>A maps to NM_005336.3 Q549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:242173273 G>A maps to NM_005336.3 D1083D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:242194476 G>A maps to NM_005336.3 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:242194884 G>A maps to NM_005336.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:242202286 C>A maps to NM_005336.3 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr2:242170236 G>A maps to NM_005336.3 R1137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr2:242176116 A>G maps to NM_005336.3 D939D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:83724309 T>G did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:83724309 T>G did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:83599448 C>T did not map to a codon.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr23:83723537 G>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:83730394 C>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:83599342 T>C did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:83723612 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:83724416 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:83588782 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:83723565 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:83724170 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:83588785 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:83599384 G>T did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:83576993 A>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:83599349 A>G did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:83730309 C>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:83730287 C>T did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:83724309 T>G did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:83576941 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:83724152 G>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:83723818 C>T did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr1:236748327 T>C maps to NM_018072.5 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr1:236748327 T>C maps to NM_018072.5 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:236757340 C>T maps to NM_018072.5 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:236735751 A>G maps to NM_018072.5 S1222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:236729303 G>T maps to NM_018072.5 V1450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:236758855 G>A maps to NM_018072.5 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:236723046 C>T maps to NM_018072.5 A1579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:236740214 G>A maps to NM_018072.5 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:236750757 C>A maps to NM_018072.5 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:236758906 G>A maps to NM_018072.5 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:810216 C>T maps to NM_017802.3 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:810219 G>A maps to NM_017802.3 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr7:819746 C>T maps to NM_017802.3 D799D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr7:813801 G>A maps to NM_017802.3 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:780542 C>T maps to NM_017802.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:769435 C>T maps to NM_017802.3 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:796447 G>A maps to NM_017802.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:813702 C>T maps to NM_017802.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr16:50134199 C>T maps to NM_182922.2 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:50136234 T>G maps to NM_182922.2 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr14:73965030 G>A maps to ENST00000334988 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr14:31828206 G>A maps to ENST00000389961 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr14:31855709 G>A maps to ENST00000389961 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:37230784 C>T maps to NM_019024.1 L1650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:37234316 T>C maps to NM_019024.1 E1551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:37295977 A>T maps to NM_019024.1 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:37215940 G>T maps to NM_019024.1 S1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:37234316 T>C maps to NM_019024.1 E1551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:37234316 T>C maps to NM_019024.1 E1551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr2:37234316 T>C maps to NM_019024.1 E1551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:37255907 A>G maps to NM_019024.1 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:37234316 T>C maps to NM_019024.1 E1551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:37287828 G>A maps to NM_019024.1 R582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:37215933 A>G maps to NM_019024.1 P1922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:37215846 C>A maps to NM_019024.1 A1951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr2:37234316 T>C maps to NM_019024.1 E1551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:37289139 C>T maps to NM_019024.1 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:58149578 G>T maps to NM_022070.4 C232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr17:58145018 A>G maps to NM_022070.4 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:58125679 G>A maps to NM_022070.4 R873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:58150571 A>T maps to NM_022070.4 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:58123500 A>G maps to NM_022070.4 I953I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:58147082 G>A maps to NM_022070.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:145268002 C>T maps to NM_001099281.1 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr5:41065469 G>A maps to ENST00000296803 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:41033205 G>A maps to ENST00000296803 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:41004968 G>T maps to ENST00000296803 I1307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr5:41004558 G>A maps to ENST00000296803 V1362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:41033159 G>A maps to ENST00000296803 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:40998712 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:13128298 A>G maps to NM_015987.4 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:139498199 C>T maps to NM_016217.2 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:139488183 G>T maps to NM_016217.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr14:31604202 T>C maps to NM_015382.2 T1151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:31576033 G>A maps to NM_015382.2 D2348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:31590657 C>T maps to NM_015382.2 T1723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:93260359 G>A maps to ENST00000446394 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:93252212 A>G maps to ENST00000446394 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:93221092 G>T maps to ENST00000446394 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:45469564 G>A maps to NM_024602.5 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:43351429 A>G maps to NM_015052.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr7:43581519 T>C maps to NM_015052.3 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr7:43495971 T>C maps to NM_015052.3 R859R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:43594233 G>A maps to NM_015052.3 A1518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:43601458 G>A maps to NM_015052.3 S1585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr7:43485074 G>A maps to NM_015052.3 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:43590186 C>T maps to NM_015052.3 Y1464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:43483895 C>T maps to NM_015052.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:43484744 C>T maps to NM_015052.3 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr7:43548588 G>A maps to NM_015052.3 S1296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr7:43495894 G>C did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr7:43591928 C>A maps to NM_015052.3 R1502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:43477672 C>T maps to NM_015052.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr7:43503370 G>T maps to NM_015052.3 E922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr7:43581519 T>C maps to NM_015052.3 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr7:43484555 G>A maps to NM_015052.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr7:43484519 C>T maps to NM_015052.3 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:43503348 C>T maps to NM_015052.3 G914G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:43495908 A>G maps to NM_015052.3 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr7:43360341 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr7:43591928 C>A maps to NM_015052.3 R1502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:43477603 A>G maps to NM_015052.3 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr7:43484504 G>A maps to NM_015052.3 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:43495908 A>G maps to NM_015052.3 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:43484585 G>A maps to NM_015052.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr7:43581519 T>C maps to NM_015052.3 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr2:197183735 G>A maps to NM_020760.1 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:197183957 G>A maps to NM_020760.1 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr2:197085593 G>A maps to NM_020760.1 I1406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:197183633 G>A maps to NM_020760.1 C660C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:197157408 G>A maps to NM_020760.1 D960D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:197066026 C>A maps to NM_020760.1 E1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:197106878 G>A maps to NM_020760.1 F1193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:197187214 G>A maps to NM_020760.1 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:197184563 G>A maps to NM_020760.1 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:197157471 A>G maps to NM_020760.1 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:197143320 G>A maps to NM_020760.1 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr3:124716614 G>T maps to NM_020733.1 I1190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:124728603 G>T maps to NM_020733.1 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:124716599 G>A maps to NM_020733.1 D1195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:124748129 G>A maps to NM_020733.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:124720702 G>T maps to NM_020733.1 I1170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:124732356 G>T maps to NM_020733.1 S689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:124748225 G>A maps to NM_020733.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:66725317 T>C maps to NM_033647.2 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:66703928 T>C maps to NM_033647.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:66698760 A>G maps to NM_033647.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:66704381 G>A maps to NM_033647.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:66703512 C>T maps to NM_033647.2 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr12:66700195 C>T maps to NM_033647.2 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:96341264 T>C maps to NM_018063.3 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr10:96341235 T>C maps to NM_018063.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:96361340 G>T maps to NM_018063.3 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr10:96350505 T>C maps to NM_018063.3 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:96317910 G>T maps to NM_018063.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:96354462 G>A maps to NM_018063.3 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr10:96341235 T>C maps to NM_018063.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr10:96341237 G>A maps to NM_018063.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr4:84376654 C>T maps to NM_133636.2 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr4:84376621 G>C maps to NM_133636.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr4:84342877 C>T maps to NM_133636.2 K929K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr4:84374579 G>A maps to NM_133636.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:84374993 A>G maps to NM_133636.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr4:84368031 C>A maps to NM_133636.2 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr4:84361128 A>G maps to NM_133636.2 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr4:84337943 G>T maps to NM_133636.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:84361128 A>G maps to NM_133636.2 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:185941718 G>A maps to NM_001029887.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:185940189 G>A maps to NM_001029887.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr17:65214734 G>T maps to NM_014877.3 Y62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:65162673 A>G maps to NM_014877.3 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:65141911 G>A maps to NM_014877.3 R906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:65175037 G>A maps to NM_014877.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:65184561 G>A maps to NM_014877.3 Y345Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr9:100693214 T>C maps to NM_018437.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:100692416 T>C maps to NM_018437.3 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:50614571 C>T maps to NM_016173.3 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:50615292 C>T maps to NM_016173.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr3:50609623 T>G maps to NM_016173.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr11:124794735 G>A maps to NM_152722.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr11:124793312 G>A maps to NM_152722.4 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr11:124794705 G>A maps to NM_152722.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:124794735 G>T maps to NM_152722.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:92844816 A>G maps to ENST00000453812 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr7:92848456 A>G maps to ENST00000453812 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:92844957 A>G maps to ENST00000453812 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:92848480 G>A maps to ENST00000453812 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:92844714 A>G maps to ENST00000453812 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr7:92848750 C>A maps to ENST00000453812 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:65476001 A>G did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:65418744 T>C did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:65409718 G>A did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:65418744 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:65408344 A>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:65428019 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:65417597 C>T did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr23:65417720 T>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:65417689 C>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:65390483 C>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:65476001 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:65478741 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:65476002 G>A did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:65476173 T>C did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr23:65420414 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr23:65486453 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:65418744 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:65486451 C>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:65480010 G>A did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:65418744 T>C did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:65418745 T>C did not map to a codon.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr11:93803624 T>C maps to NM_001098672.1 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:93778976 C>T maps to NM_001098672.1 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:93796821 G>A maps to NM_001098672.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:93815600 G>A maps to NM_001098672.1 E578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:93778874 G>A maps to NM_001098672.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:93822101 C>T maps to NM_001098672.1 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:93800852 G>T maps to NM_001098672.1 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr15:63961898 T>C did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr15:64067506 G>A maps to ENST00000261887 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr15:63966955 G>T maps to ENST00000261887 S2477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr15:63946341 G>T maps to ENST00000261887 I3422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr15:63961898 T>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:64041672 A>G maps to ENST00000261887 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:64048887 G>A maps to ENST00000261887 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:63961825 G>T maps to ENST00000261887 S2706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:64067335 G>A maps to ENST00000261887 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:63946355 T>A maps to ENST00000261887 K3418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:63904452 A>G maps to ENST00000261887 D4800D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:63953992 G>T maps to ENST00000261887 Y3043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:64041911 C>A maps to ENST00000261887 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr15:63950777 G>T maps to ENST00000261887 T3188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:63967183 G>A maps to ENST00000261887 G2401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:63966865 C>T maps to ENST00000261887 Q2507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:64067335 G>A maps to ENST00000261887 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:63940270 A>G maps to ENST00000261887 H3625H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:63958317 G>A maps to ENST00000261887 I2785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr15:63961897 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr15:63961898 T>C did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr15:63984736 T>C maps to ENST00000261887 E1901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:28437181 C>T maps to NM_004667.4 S2792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr15:28389861 G>A maps to NM_004667.4 G3699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:28419739 G>A maps to NM_004667.4 H3286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:28377371 G>A maps to NM_004667.4 I4148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr15:28377368 G>T maps to NM_004667.4 A4149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:28419680 A>C maps to NM_004667.4 L3306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:28475599 G>A maps to NM_004667.4 N1574N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:28465670 G>A maps to NM_004667.4 Y1924Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr15:28483841 A>G maps to NM_004667.4 H1218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr15:28419673 G>T maps to NM_004667.4 G3308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:28441424 A>G maps to NM_004667.4 C2732C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:28446657 G>A maps to NM_004667.4 R2554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:28519444 G>A maps to NM_004667.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:28419658 G>A maps to NM_004667.4 R3313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:28456262 G>A maps to NM_004667.4 C2318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:28389920 G>A maps to NM_004667.4 L3680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:28443783 G>A maps to NM_004667.4 G2616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:28386619 G>T maps to NM_004667.4 I3991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr15:28511068 C>T maps to NM_004667.4 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:28517369 G>A maps to NM_004667.4 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:28359949 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:28413594 G>A maps to NM_004667.4 I3457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr15:28431775 A>G maps to NM_004667.4 P2924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr15:28431775 A>G maps to NM_004667.4 P2924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr15:28437271 A>G maps to NM_004667.4 R2762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:28422176 G>A maps to NM_004667.4 S3117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr15:28431775 A>G maps to NM_004667.4 P2924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr15:28499580 C>T maps to NM_004667.4 R985R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:28358282 G>A maps to NM_004667.4 F4722F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr15:28391392 G>A maps to NM_004667.4 S3666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr15:28431775 A>G maps to NM_004667.4 P2924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:89575226 C>T maps to NM_014606.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr4:89625705 A>G maps to NM_014606.1 K963K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:89591404 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:89601315 G>T maps to NM_014606.1 E757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:69773911 C>A maps to NM_022079.2 G314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:69692353 C>T maps to NM_022079.2 K954K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:89407375 T>A maps to NM_016323.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr4:89425436 G>A maps to NM_016323.2 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:89408245 C>T maps to NM_016323.2 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:89415459 G>T maps to NM_016323.2 E808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr4:89380621 G>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr4:89397041 T>C maps to NM_016323.2 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:89397041 T>C maps to NM_016323.2 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:89356890 G>A maps to NM_017912.3 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:89361067 C>T maps to NM_017912.3 V866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:89314664 C>T maps to NM_017912.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:89311818 C>A maps to NM_017912.3 S151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:89356966 C>T maps to NM_017912.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:89311882 G>A maps to NM_017912.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:56973163 G>A maps to NM_014685.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr7:35674830 T>C maps to NM_022373.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:35709863 A>G maps to NM_022373.4 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:35709887 G>A maps to NM_022373.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr7:35673972 G>A maps to NM_022373.4 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:35712872 T>G maps to NM_022373.4 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:35709887 G>A maps to NM_022373.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr7:35674830 T>C maps to NM_022373.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:2461351 C>T maps to NM_001010926.3 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:57232942 A>G maps to NM_003865.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr15:72643471 A>G did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:72668271 T>C maps to ENST00000457859 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:74009341 T>G maps to NM_000521.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:80395185 G>A maps to NM_173620.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:80391634 C>T maps to NM_173620.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:43246671 G>A maps to NM_144608.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:80677779 A>G maps to NM_001040708.1 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:80677926 A>G maps to NM_001040708.1 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr8:80677971 A>T maps to NM_001040708.1 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:126080311 C>T maps to NM_012259.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:126080821 A>G maps to NM_012259.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:126080809 C>T maps to NM_012259.2 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr1:40092691 G>A maps to NM_014571.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:145414831 C>A maps to NM_213653.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:91846474 A>G maps to NM_001017975.3 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr1:91790279 T>G maps to NM_001017975.3 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:91784692 A>T maps to NM_001017975.3 C918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:91844690 C>A maps to NM_001017975.3 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:91742572 A>C maps to NM_001017975.3 L1146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr1:91788554 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:91841284 C>A did not map to a codon.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:91843622 G>T maps to NM_001017975.3 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:91781508 C>T maps to NM_001017975.3 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:120363182 G>A maps to NM_000187.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr7:81386599 G>T maps to NM_000601.4 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:81358973 C>T maps to NM_000601.4 W329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:81359009 G>A maps to NM_000601.4 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:81386589 C>A maps to NM_000601.4 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:81331998 A>G maps to NM_000601.4 R695R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:81386512 G>A maps to NM_000601.4 H158H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr7:81334972 G>C maps to NM_000601.4 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:3449739 G>A maps to ENST00000511533 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:3451016 C>T maps to ENST00000511533 Y620Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:3451115 G>A maps to ENST00000511533 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:3449278 C>T maps to ENST00000511533 D479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:79653371 G>A maps to NM_004712.4 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:79654088 C>T maps to NM_004712.4 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:79653395 C>T maps to NM_004712.4 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:43002175 C>A maps to ENST00000458501 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:43002152 G>T maps to ENST00000458501 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:43037390 A>G maps to ENST00000458501 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:43046738 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:210577962 C>A maps to NM_001170580.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:210761367 G>A maps to NM_001170580.1 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:210577854 G>A maps to NM_001170580.1 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:210847630 C>T maps to NM_001170580.1 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:210797003 C>A maps to NM_001170580.1 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:145640105 A>G maps to NM_022475.1 K586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:145629388 A>G maps to NM_022475.1 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr4:145640087 C>A maps to NM_022475.1 Y580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:100141782 C>T maps to NM_001127258.1 R723R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:100118622 G>A maps to NM_001127258.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:222717192 G>A maps to NM_024746.3 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:222713502 C>T maps to NM_024746.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:222717267 G>A maps to NM_024746.3 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:222713382 A>G maps to NM_024746.3 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr1:222696969 C>T maps to NM_024746.3 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr1:222717195 G>A maps to NM_024746.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr1:222697002 T>C maps to NM_024746.3 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:108072379 C>T maps to NM_007072.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:108076718 C>T maps to NM_007072.2 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:108076979 T>G maps to NM_007072.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr1:70832136 C>T maps to ENST00000432224 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:100534128 T>A maps to NM_033055.2 L269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:100547638 G>A maps to NM_033055.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr9:97207274 C>T maps to NM_032558.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:97177454 C>T maps to NM_032558.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:97218572 G>A maps to NM_032558.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:27669095 G>A maps to NM_152740.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:27582618 G>A maps to NM_152740.3 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:1960067 C>T maps to NM_001098202.1 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:21800479 C>T maps to NM_015094.2 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:21800077 G>A maps to NM_015094.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:21800491 C>A maps to NM_015094.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:62207750 C>T maps to ENST00000394997 H647H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr14:62187186 T>G maps to ENST00000394997 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr14:62207903 A>G maps to ENST00000394997 Q698Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:62211508 C>A maps to ENST00000394997 S728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr14:62207233 C>A maps to ENST00000394997 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:62204875 G>T maps to ENST00000394997 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:62199166 G>T maps to ENST00000394997 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:46834442 C>T maps to NM_152795.2 D581D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:175816443 G>C maps to NM_138820.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:119003386 C>T maps to NM_198971.1 C257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr11:119001462 A>G maps to NM_198971.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:35813655 G>T maps to NM_032593.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr7:75172215 G>A maps to NM_005338.4 G948G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr7:75187557 C>T maps to NM_005338.4 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:75228562 A>G maps to NM_005338.4 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:75185446 G>A maps to NM_005338.4 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:75192286 C>T maps to NM_005338.4 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr7:75187557 C>T maps to NM_005338.4 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr7:75187559 C>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:123333142 C>T maps to NM_003959.1 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr12:123346025 C>T maps to NM_003959.1 Q1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:123345958 A>C maps to NM_003959.1 G1019G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:114483121 C>T maps to ENST00000426820 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:114497325 C>A maps to ENST00000426820 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:114506016 T>C maps to ENST00000426820 C775C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:114511267 T>C maps to ENST00000426820 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:114515839 G>A maps to ENST00000426820 T1184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr1:114508810 T>C maps to ENST00000426820 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:114483985 T>C maps to ENST00000426820 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr1:114500848 C>T maps to ENST00000426820 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:139285296 C>T maps to NM_022740.4 Q767Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:139257864 G>T maps to NM_022740.4 A1135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:139281563 C>T maps to NM_022740.4 R872R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr7:139285281 G>A maps to NM_022740.4 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:139285281 G>T maps to NM_022740.4 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:139315919 C>T maps to NM_022740.4 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr7:139268704 A>G maps to NM_022740.4 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:139257873 C>T maps to NM_022740.4 Q1132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr7:139299209 G>T maps to NM_022740.4 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr7:139268704 A>G maps to NM_022740.4 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:33358676 T>C maps to NM_005734.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:33369439 G>A maps to NM_005734.3 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:33368860 A>G maps to NM_005734.3 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:33368879 A>C maps to NM_005734.3 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:33374672 T>C maps to NM_005734.3 N1069N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr11:33373741 T>A maps to NM_005734.3 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr11:33374798 C>T maps to NM_005734.3 H1111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:40889902 G>A maps to NM_144685.3 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:40889725 C>T maps to NM_144685.3 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:40895491 C>T maps to NM_144685.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:19398254 G>A maps to NM_003325.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:19376059 C>T maps to NM_003325.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:19373156 G>A maps to NM_003325.3 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:30006421 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:26017824 G>A maps to NM_005325.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:26017597 G>A maps to NM_005325.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:27834671 T>C maps to NM_005322.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr6:26056329 C>T maps to NM_005319.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr6:26056473 A>G maps to NM_005319.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:26056015 T>C maps to NM_005319.3 *214W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr6:26056015 T>C maps to NM_005319.3 *214W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr6:26056015 T>C maps to NM_005319.3 *214W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:26234957 C>T maps to NM_005320.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:26107823 G>A maps to NM_005323.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:25726745 G>A maps to NM_170745.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:25726437 G>A maps to NM_170745.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:26124780 C>G maps to NM_003512.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:26217495 A>G maps to NM_021052.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:27101077 G>A maps to NM_021064.4 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:27101044 A>G maps to NM_021064.4 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr6:27114915 A>G maps to NM_080596.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:27782503 A>G maps to NM_021066.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr6:27782170 C>T maps to NM_021066.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:27805771 G>A maps to NM_003510.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr6:27805841 C>T maps to NM_003510.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr6:27833230 A>T maps to NM_003511.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:27860908 G>A maps to NM_003514.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:25727336 C>T maps to NM_170610.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:26124021 A>G maps to NM_003526.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:26124105 G>T maps to NM_003526.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr6:26124114 C>T maps to NM_003526.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr6:26184079 G>A maps to NM_003523.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:26200052 C>A maps to NM_003522.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr6:26199887 C>T maps to NM_003522.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr6:26216634 G>A maps to NM_003518.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr6:26251910 G>A maps to NM_003524.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:26273415 C>T maps to NM_003525.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr6:26273379 T>A maps to NM_003525.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:27100355 C>T maps to NM_021058.3 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:27114412 G>T maps to NM_080593.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr6:27114436 C>T maps to NM_080593.2 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:27775304 T>C maps to NM_003519.3 *127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr6:27783024 C>T maps to NM_003521.2 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:26045821 C>T maps to NM_003531.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr6:26197211 C>A maps to NM_003530.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:26225714 C>T maps to NM_003532.2 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:26271297 A>G maps to NM_003534.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr6:26271213 C>T maps to NM_003534.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:27839709 C>T maps to NM_003533.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr6:26027384 T>C maps to NM_003544.2 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:26027195 T>C maps to NM_003544.2 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:26027288 C>T maps to NM_003544.2 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr6:26027261 G>A maps to NM_003544.2 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr6:26104384 C>T maps to NM_003542.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:26104366 G>A maps to NM_003542.3 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:26189088 G>T maps to NM_003539.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr6:26205096 G>A maps to NM_003545.3 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:26285481 C>T maps to NM_003543.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr6:26285502 C>T maps to NM_003543.3 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr6:27107209 C>T maps to NM_003495.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:27107392 C>T maps to NM_003495.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:27841201 G>A maps to NM_003546.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:149859177 A>G maps to NM_175065.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:149858682 G>A maps to NM_003517.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:149857961 C>A maps to NM_003528.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:14923865 G>T maps to NM_175054.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr12:14923907 A>G maps to NM_175054.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:12162116 A>G maps to NM_002114.2 E2311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:12123783 T>C maps to NM_002114.2 H1252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:12123813 G>A maps to NM_002114.2 W1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr6:12131038 G>A maps to NM_002114.2 R2083R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:12124191 C>T maps to NM_002114.2 F1388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:12123627 C>T maps to NM_002114.2 D1200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:12124191 C>T maps to NM_002114.2 F1388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:12122613 A>G maps to NM_002114.2 R862R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr6:12122613 A>G maps to NM_002114.2 R862R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr6:12122613 A>G maps to NM_002114.2 R862R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:143091852 G>A maps to NM_006734.3 H1341H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr6:143082637 T>C maps to NM_006734.3 S1861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:143091582 G>A maps to NM_006734.3 S1431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:143091162 G>A maps to NM_006734.3 I1571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:143093172 C>T maps to NM_006734.3 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:143074789 G>A maps to NM_006734.3 G2265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:143092431 C>T maps to NM_006734.3 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr6:143081562 G>A maps to NM_006734.3 P1954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr6:143090796 A>G maps to NM_006734.3 L1693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:143081346 G>A maps to NM_006734.3 C2026C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:42045647 G>A maps to NM_024503.3 C1607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:42049343 G>A maps to NM_024503.3 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:42049802 G>A maps to NM_024503.3 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:42048334 G>A maps to NM_024503.3 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:42049976 G>A maps to NM_024503.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:42047531 G>A maps to NM_024503.3 P979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:42045956 T>C maps to NM_024503.3 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:42048470 G>T maps to NM_024503.3 C666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr1:42045956 T>C maps to NM_024503.3 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr1:41976583 G>A maps to NM_024503.3 S2253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:234749796 G>A maps to NM_018410.3 H543H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:234750255 G>A maps to NM_018410.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:234749576 G>A maps to NM_018410.3 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:234750093 T>C maps to NM_018410.3 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:71119779 C>T maps to ENST00000439900 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:71055405 A>G maps to ENST00000439900 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr10:71129341 G>A maps to ENST00000439900 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:71119668 T>C maps to ENST00000439900 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:71139645 G>T maps to ENST00000439900 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:75101435 C>T maps to NM_000189.4 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:75108865 T>G maps to NM_000189.4 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:75108869 G>T maps to NM_000189.4 G535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:75108946 C>T maps to NM_000189.4 Y560Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:75105997 G>A maps to NM_000189.4 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:176316436 G>A maps to NM_002115.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:176309090 C>A maps to NM_002115.2 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr5:176317897 C>T maps to NM_002115.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:70980226 C>T maps to NM_025130.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:71005972 C>T maps to NM_025130.3 H338H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:71025340 C>T maps to NM_025130.3 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:37854536 C>T maps to NM_181786.2 Q614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:37838096 C>T maps to NM_181786.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr19:37853137 T>C maps to NM_181786.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:37853702 C>T maps to NM_181786.2 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:37853618 C>T maps to NM_181786.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:37853461 C>T maps to NM_181786.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:37853014 G>A maps to NM_181786.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:37838730 G>A maps to NM_181786.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:37853629 G>A maps to NM_181786.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:29910691 C>T maps to ENST00000376806 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:29910603 C>A maps to ENST00000376806 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:29910537 C>T maps to ENST00000376806 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:29912171 G>A maps to ENST00000376806 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:29912331 C>A maps to ENST00000376806 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:31323092 C>A did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr6:31324463 C>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:31323307 G>T maps to ENST00000428231 C297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:31238008 T>C maps to ENST00000383329 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:32918305 C>T maps to NM_006120.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:32917126 G>A maps to NM_006120.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr6:32976012 G>T maps to NM_002119.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr6:32975853 G>A maps to NM_002119.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:33041268 G>A maps to NM_033554.2 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:33054012 T>C maps to NM_002121.4 *259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr6:33048602 G>A maps to NM_002121.4 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr6:33043829 G>T maps to NM_002121.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr6:33043848 C>A maps to NM_002121.4 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:32714095 C>T maps to NM_020056.4 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:32713068 T>C maps to NM_020056.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:32411034 A>C maps to NM_019111.4 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:32410355 G>T maps to NM_019111.4 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:32410999 G>T maps to NM_019111.4 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:32557476 G>A maps to NM_002124.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr6:30460336 G>T maps to NM_005516.5 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:29797674 G>T maps to ENST00000376828 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:29796590 C>T maps to ENST00000376828 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:29796494 G>A maps to ENST00000376828 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr6:29797709 G>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr21:38269377 T>C maps to NM_000411.5 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr21:38308961 A>G maps to NM_000411.5 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr21:38302696 G>A maps to NM_000411.5 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr21:38309618 C>T maps to NM_000411.5 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:53345226 C>T maps to NM_002126.4 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr17:53342889 C>A maps to NM_002126.4 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr3:148792014 A>G maps to NM_003071.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:148789068 A>G maps to NM_003071.3 H288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:221053498 G>A maps to NM_021958.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:221053228 C>T maps to NM_021958.3 Y10Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:221055533 C>A maps to NM_021958.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:221053549 C>T maps to NM_021958.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:221053582 G>A maps to NM_021958.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:221053498 G>A maps to NM_021958.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr20:30136865 G>C maps to NM_178581.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr20:30132789 C>T maps to NM_178581.1 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:30126028 C>T maps to NM_178581.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr8:28876382 A>G maps to ENST00000444075 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr8:28876382 A>G maps to ENST00000444075 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr1:186158884 C>T maps to NM_031935.2 R5595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr1:186007066 A>G maps to NM_031935.2 E1917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:186043907 G>T maps to NM_031935.2 A2725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:186151414 C>T maps to NM_031935.2 C5470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:186062738 G>A maps to NM_031935.2 K3378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr1:185976274 C>T maps to NM_031935.2 G1497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:186056761 C>T maps to NM_031935.2 H3116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:185985250 G>T maps to NM_031935.2 E1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:185897791 C>T maps to NM_031935.2 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:186084058 A>G maps to NM_031935.2 R3795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:186147590 G>A maps to NM_031935.2 Q5329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:186084056 C>T maps to NM_031935.2 R3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:186114924 C>T maps to NM_031935.2 C4826C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:186122925 C>T maps to NM_031935.2 Y5021Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:185985315 C>T maps to NM_031935.2 C1712C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:186158893 C>T maps to NM_031935.2 R5598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:186082063 G>T maps to NM_031935.2 E3704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:186114589 C>T maps to NM_031935.2 N4774N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:185834874 C>T maps to NM_031935.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:186008924 G>T maps to NM_031935.2 E2032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr1:186141189 C>T maps to NM_031935.2 N5247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:186120368 T>C maps to NM_031935.2 N4882N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:186007066 A>G maps to NM_031935.2 E1917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:186121954 G>A maps to NM_031935.2 V4990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr1:185987407 A>G maps to NM_031935.2 S1798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr1:186076038 A>G maps to NM_031935.2 T3598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:185932980 T>C maps to NM_031935.2 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:186008858 G>T did not map to a codon.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr1:186043937 T>C maps to NM_031935.2 A2735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:186081958 C>T maps to NM_031935.2 R3669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr1:186113407 G>A maps to NM_031935.2 A4676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr1:185897764 T>C maps to NM_031935.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:186089170 C>T maps to NM_031935.2 G4041G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr1:185970868 G>T maps to NM_031935.2 V1448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:186034454 T>C maps to NM_031935.2 R2533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr1:186039780 A>G maps to NM_031935.2 P2677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr1:186059938 T>C maps to NM_031935.2 L3259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:186113785 C>T maps to NM_031935.2 C4739C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr1:185892579 T>C maps to NM_031935.2 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:186034454 T>C maps to NM_031935.2 R2533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr1:186101470 C>T maps to NM_031935.2 A4414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:186082002 C>T maps to NM_031935.2 D3683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:186084507 G>A maps to NM_031935.2 G3841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:77759490 C>T maps to NM_018200.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:77759490 C>T maps to NM_018200.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:77759490 C>T maps to NM_018200.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr15:77763382 A>G maps to NM_018200.2 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:77763382 A>G maps to NM_018200.2 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr13:31036767 C>T maps to NM_002128.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:174254061 C>T maps to NM_002129.3 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:24134780 G>A maps to NM_000191.2 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:24144013 G>T maps to NM_000191.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:55304333 G>A maps to NM_019036.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:55443835 G>A maps to NM_019036.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:55378898 T>C maps to NM_019036.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:74650509 T>C maps to NM_000859.2 Y517Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr5:43294212 A>C maps to NM_002130.6 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:120295926 G>A maps to NM_005518.3 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:120306817 C>T maps to NM_005518.3 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:26801076 A>G maps to NM_005517.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:26545514 G>T maps to NM_006353.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:80370211 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:80370222 T>C did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:80370222 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:35689037 T>C maps to NM_001003681.2 C564C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:35661586 A>G maps to NM_001003681.2 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:1073568 T>C maps to NM_012292.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:1080705 G>A maps to NM_012292.2 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr19:1068743 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:1080514 G>A maps to NM_012292.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:1080696 C>T maps to NM_012292.2 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:1082960 C>T maps to NM_012292.2 S880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:1074611 G>A did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr19:1080726 G>A maps to NM_012292.2 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:1079992 C>T maps to NM_012292.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr5:143200120 T>A maps to NM_021182.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr22:35782823 C>T maps to NM_002133.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr16:4558051 G>T maps to NM_001127205.1 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:173531331 C>T maps to NM_015980.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr18:61621686 C>T maps to NM_001123366.1 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:124909152 G>A maps to NM_005519.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:124897036 G>A maps to NM_001105574.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr10:124895679 C>T maps to NM_001105574.1 N38N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr12:121426812 C>G maps to NM_000545.5 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr12:121431320 A>G did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:121437179 G>A maps to NM_000545.5 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:121432113 C>T maps to NM_000545.5 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:121431416 C>A maps to NM_000545.5 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:121431480 C>T maps to NM_000545.5 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr12:121431482 A>G maps to NM_000545.5 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:121435307 G>A maps to NM_000545.5 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:121416663 T>C maps to NM_000545.5 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr12:121426773 G>A maps to NM_000545.5 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr12:121426633 A>G did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr12:121431428 G>A maps to NM_000545.5 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr20:43058160 A>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:43048466 C>T maps to ENST00000338692 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr2:138771423 A>G maps to NM_006895.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:137088930 G>A maps to NM_006805.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:54675965 T>G maps to NM_031157.2 Y124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr2:178082496 A>G maps to NM_194247.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:178080512 C>T maps to NM_194247.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:178080621 G>T maps to NM_194247.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:178081264 T>C maps to NM_194247.2 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr2:178083807 T>A maps to NM_194247.2 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:178080569 A>G maps to NM_194247.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr2:178082496 A>G maps to NM_194247.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr2:178082496 A>G maps to NM_194247.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr2:178082496 A>G maps to NM_194247.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:178080390 T>A did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr2:178082475 C>A maps to NM_194247.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr2:178082496 A>G maps to NM_194247.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr5:177637555 C>T maps to NM_031266.2 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:177636357 G>T maps to NM_031266.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:177632872 T>C maps to NM_031266.2 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:177636375 C>T maps to NM_031266.2 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:177633803 G>A maps to NM_031266.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:21699226 A>G maps to NM_031314.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:12908037 C>T maps to NM_001013631.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:12908112 A>G maps to NM_001013631.1 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:12907394 C>A maps to NM_001013631.1 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr4:83277753 G>A maps to NM_031370.2 Y312Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:43883059 G>A maps to NM_001098204.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:179044625 T>G maps to NM_005520.2 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:179043166 G>A maps to NM_005520.2 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr23:100667023 G>A did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr10:70101792 A>G maps to NM_012207.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:70098416 C>T maps to NM_012207.2 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:70101808 T>C maps to NM_012207.2 *347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr10:70101809 G>A maps to NM_012207.2 *347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr10:70101808 T>A maps to NM_012207.2 *347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:70101808 T>A maps to NM_012207.2 *347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr10:70101792 A>G maps to NM_012207.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:70101420 C>T maps to NM_012207.2 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:70101808 T>A maps to NM_012207.2 *347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr10:70101792 A>G maps to NM_012207.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr10:70097031 A>G maps to NM_012207.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr10:70101808 T>A maps to NM_012207.2 *347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr10:70101792 A>G maps to NM_012207.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:86586816 T>A maps to NM_031262.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr9:86588199 C>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:39336534 C>A maps to ENST00000221419 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:39329090 G>A maps to ENST00000221419 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:8553587 C>T maps to NM_005968.3 Y681Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:8528545 C>T maps to NM_005968.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:8551150 C>T maps to NM_005968.3 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:8528539 T>C maps to NM_005968.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:23637492 A>G maps to ENST00000414299 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:23637486 C>T maps to ENST00000414299 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:23650087 G>A maps to ENST00000414299 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:23637408 G>A maps to ENST00000414299 H484H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:245021468 C>T maps to NM_031844.2 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:41811654 A>T maps to NM_007040.3 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr19:41807467 C>T maps to NM_007040.3 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:41774164 C>T maps to NM_007040.3 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:41798172 G>T maps to NM_007040.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr11:62484481 G>A maps to NM_001079559.1 R654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:83347252 G>A maps to NM_031372.2 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:78746815 C>T maps to NM_004272.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:78746935 T>A maps to NM_004272.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:78734966 G>A maps to NM_004272.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr15:83561565 C>T maps to NM_199330.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr15:83527872 G>A maps to NM_199330.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:19040422 C>T maps to NM_004838.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:23745394 C>A maps to NM_020834.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:23746069 G>A maps to NM_020834.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:60324140 A>G maps to NM_015888.4 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:60324140 A>G maps to NM_015888.4 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr1:60324140 A>G maps to NM_015888.4 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr19:12875855 C>T maps to NM_013312.2 K560K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:12875659 G>A maps to NM_013312.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr19:12881825 C>T maps to NM_013312.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr19:12881825 C>A maps to NM_013312.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:42819596 G>A maps to NM_032410.3 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:42863049 C>T maps to NM_032410.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr4:57514897 G>A maps to NM_032495.5 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:57514915 C>A maps to NM_032495.5 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:150679067 C>T maps to NM_032132.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:150680738 A>G maps to NM_032132.4 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:150689638 G>A maps to NM_032132.4 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:150686571 G>A maps to NM_032132.4 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:150689668 G>T maps to NM_032132.4 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:150679067 C>T maps to NM_032132.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr1:150680807 A>G maps to NM_032132.4 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:27135198 G>A maps to NM_005522.4 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:27134328 C>T maps to NM_005522.4 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:27224124 C>T maps to NM_005523.5 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr7:27140434 G>T maps to NM_006735.3 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr7:27140761 G>A maps to NM_006735.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr7:27141043 C>A maps to NM_006735.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr7:27148310 C>T maps to NM_153631.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr7:27150130 G>A maps to NM_153631.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:27147872 C>T maps to NM_153631.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr7:27168962 G>A maps to NM_002141.4 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:27181552 T>C maps to NM_019102.2 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:27185461 C>A maps to NM_024014.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:27204506 G>T maps to NM_152739.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:46607734 G>T maps to NM_002144.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:46608005 G>A maps to NM_002144.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:46607888 G>T maps to NM_002144.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr17:46622180 T>C maps to NM_002145.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:46670936 A>G maps to NM_002147.3 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr17:46670543 G>A maps to NM_002147.3 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr17:46671035 C>T maps to NM_002147.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:46671005 A>G maps to NM_002147.3 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:46685347 G>A maps to NM_004502.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr12:54379510 C>T maps to NM_017409.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:54379402 G>A maps to NM_017409.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:54379165 C>T maps to NM_017409.3 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr12:54379054 T>A maps to NM_017409.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr12:54379510 C>T maps to NM_017409.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:54367138 T>G maps to NM_014212.3 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr12:54350166 G>A maps to NM_173860.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:54339018 G>A maps to NM_017410.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:54448035 G>T maps to NM_153633.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:54447939 G>A maps to NM_153633.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:54447777 G>A maps to NM_153633.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:54403415 C>A maps to NM_022658.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:54396401 C>T maps to NM_006897.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:176982034 C>T maps to NM_002148.3 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:176981992 T>C maps to NM_002148.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:176981725 G>A maps to NM_002148.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:176981812 G>A maps to NM_002148.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:176982034 C>T maps to NM_002148.3 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:176981960 C>T maps to NM_002148.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:176983685 A>G maps to NM_002148.3 E250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr2:176983685 A>G maps to NM_002148.3 E250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr2:176973647 G>A maps to NM_021192.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:176965002 C>T maps to NM_021193.3 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:177036740 C>T maps to NM_006898.4 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:177036842 G>A maps to NM_006898.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr2:177036878 C>T maps to NM_006898.4 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr2:177033964 C>T maps to NM_006898.4 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:177036773 C>T maps to NM_006898.4 Y357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:177017654 C>T maps to NM_014621.2 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:176995441 G>T maps to NM_019558.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:72094680 G>A maps to NM_005143.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:72090143 T>C did not map to a codon.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr16:72094632 G>A maps to NM_005143.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:21072033 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:33354654 C>T maps to NM_002143.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:10560038 C>T maps to NM_002149.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:40149716 C>T maps to NM_016257.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:122294304 G>A maps to NM_002150.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:122287693 A>C maps to NM_002150.2 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:122284776 G>T maps to NM_002150.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr1:45793155 G>A maps to NM_032756.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr1:45793269 C>T maps to NM_032756.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:175439223 A>C maps to NM_000860.4 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:95229808 C>T maps to NM_014485.2 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:35556441 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:35556884 C>T maps to NM_182983.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:35556773 C>T maps to NM_182983.2 G351G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G4-6588-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:72110829 T>C maps to ENST00000228226 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:133632687 T>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:133609218 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:100177446 G>A maps to NM_000195.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:100202988 G>A maps to NM_000195.2 C3C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:100190985 G>A maps to NM_000195.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr10:100195048 G>A maps to NM_000195.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr10:100189547 C>T maps to NM_000195.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr3:148876554 A>G maps to NM_032383.3 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr3:148876527 C>G maps to NM_032383.3 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:148889988 C>T maps to NM_032383.3 R999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr3:148877927 T>C maps to NM_032383.3 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr22:26853922 C>T maps to NM_022081.4 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr22:26860350 C>T maps to NM_022081.4 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:26866722 C>T maps to NM_022081.4 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:26860266 G>A maps to NM_022081.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:26860499 C>A maps to NM_022081.4 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr22:26860749 C>T maps to NM_022081.4 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:18309149 A>G maps to NM_181507.1 C883C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:18313562 G>A maps to NM_181507.1 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr11:18339330 G>C maps to NM_181507.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr10:103826251 C>T maps to NM_024747.4 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:103825902 C>T maps to NM_024747.4 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:84227439 T>G maps to NM_006665.5 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:84227367 G>A maps to NM_006665.5 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:100401681 G>A maps to NM_021828.4 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr10:100219335 G>A maps to NM_021828.4 R592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr10:100380414 C>T maps to NM_021828.4 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:100481430 G>T maps to NM_021828.4 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:100249884 C>A maps to NM_021828.4 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:6462124 G>T maps to NM_000613.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:6452599 T>C maps to NM_000613.2 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:6458682 G>T maps to NM_000613.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:21978604 G>A maps to NM_005144.4 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:533572 G>A maps to NM_005343.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr11:534268 C>A maps to NM_005343.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr11:533307 C>T maps to NM_176795.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr11:63327599 G>A maps to NM_017878.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr11:63233592 G>T maps to NM_054108.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr19:49657291 A>G maps to NM_002152.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:49657558 A>G maps to NM_002152.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:49658155 G>A maps to NM_002152.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:49657708 G>T maps to NM_002152.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:49657602 G>A maps to NM_002152.2 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:49657464 T>G maps to NM_002152.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr19:49657291 A>G maps to NM_002152.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:49657291 A>G maps to NM_002152.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr19:49657291 A>G maps to NM_002152.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:49657210 C>T maps to NM_002152.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:49656856 T>C maps to NM_002152.2 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:49657291 A>G maps to NM_002152.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:186395023 C>A maps to NM_000412.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:186392939 G>A maps to NM_000412.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:186390601 C>T maps to NM_000412.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:186395077 A>G maps to NM_000412.2 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:186394861 G>A maps to NM_000412.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:11301949 C>T maps to NM_001098211.1 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr5:175110301 C>T maps to NM_001131055.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr5:175110301 C>T maps to NM_001131055.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:175111051 C>T maps to NM_001131055.1 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:175112516 C>T maps to NM_001131055.1 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr20:60791115 G>A maps to ENST00000317393 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr18:22056896 G>T maps to NM_021624.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr18:22057129 C>T maps to NM_021624.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr18:22057171 T>C maps to NM_021624.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:152191689 G>T maps to NM_001009931.1 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr1:152192465 G>A maps to NM_001009931.1 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:152191221 G>A maps to NM_001009931.1 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:152192145 G>T maps to NM_001009931.1 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:152185746 G>A maps to NM_001009931.1 G2786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:152192112 T>C maps to NM_001009931.1 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:152192103 G>A maps to NM_001009931.1 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr1:152193212 G>A maps to NM_001009931.1 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:152191581 C>T maps to NM_001009931.1 Q841Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr1:152193447 G>A maps to NM_001009931.1 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr1:152185749 G>A maps to NM_001009931.1 Y2785Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr1:152192826 G>A maps to NM_001009931.1 H426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:20824513 C>T maps to NM_022460.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:87538698 T>C maps to NM_012262.3 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:87538851 T>C maps to NM_012262.3 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:11400897 C>T maps to NM_005114.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:22926817 G>T maps to NM_006043.1 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:22926426 G>A maps to NM_006043.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr16:22826200 C>T maps to NM_006043.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr16:22926516 C>T maps to NM_006043.1 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:13400086 C>T maps to NM_006042.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:13504344 C>T maps to NM_006042.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:13399861 G>A maps to NM_006042.1 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:14248944 C>T maps to NM_006041.1 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:14248461 C>T maps to NM_006041.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:14248392 G>A maps to NM_006041.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:26147121 C>T maps to NM_006040.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:26147115 C>A maps to NM_006040.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr16:26147506 T>C maps to NM_006040.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr16:26147506 T>C maps to NM_006040.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr6:114379254 G>A maps to NM_153612.3 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:114383925 G>A maps to NM_153612.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:114378447 G>T maps to NM_153612.3 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:114378801 G>A maps to NM_153612.3 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:129025996 G>A maps to NM_004807.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:131763095 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:132091051 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:131762414 T>C did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:132091107 G>A did not map to a codon.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr23:132091132 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:131762445 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:131763118 T>A did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr13:97484995 G>A maps to NM_153456.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr13:97484799 G>A maps to NM_153456.2 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:29139966 G>A did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:209879204 C>T maps to NM_005525.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:209880399 G>A maps to NM_005525.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:209880399 G>A maps to NM_005525.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:5687986 G>A maps to NM_198533.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:40706742 G>A maps to NM_000413.2 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:40706440 C>T maps to NM_000413.2 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:53459252 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:53459337 G>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:53458486 C>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr4:88278429 C>A did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr11:43702505 G>A maps to NM_016142.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:88243977 C>A maps to NM_178135.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:88238297 G>T maps to NM_178135.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:88231411 G>T maps to NM_178135.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:49316572 G>A maps to NM_016246.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr19:49318341 C>T maps to NM_016246.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:82131740 C>A maps to NM_002153.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:82069190 T>C maps to NM_002153.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:99006624 C>A maps to NM_000197.1 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:118861657 T>G maps to NM_000414.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:118835235 C>T maps to NM_000414.3 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:162769627 C>T maps to NM_016371.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr1:162766410 G>T maps to NM_016371.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:33173309 A>C maps to NM_014234.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:33173931 G>T maps to NM_014234.3 G225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:120057079 C>T maps to ENST00000235547 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:120056973 C>T maps to ENST00000235547 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr1:120054159 A>G maps to ENST00000235547 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:120057027 T>C maps to ENST00000235547 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr1:120056874 C>T maps to ENST00000235547 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:119964759 A>G maps to NM_000198.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:30999248 C>T maps to NM_025193.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:84163847 G>A maps to NM_031463.4 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:84163351 A>T maps to NM_031463.4 L232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:115216296 T>C maps to NM_032303.4 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:115166385 C>T maps to NM_032303.4 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:115166397 T>C maps to NM_032303.4 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:145537194 A>G did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:122741279 G>A maps to NM_004506.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:122741325 C>T maps to NM_004506.3 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr6:122741288 T>G maps to NM_004506.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:122733803 T>C maps to NM_004506.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:56540489 G>A maps to NM_001080439.1 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:56540184 T>C maps to NM_001080439.1 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr17:56557329 T>C maps to NM_001080439.1 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr17:56540185 G>T maps to NM_001080439.1 S500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr17:56540184 T>C maps to NM_001080439.1 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr19:16263915 C>G maps to NM_032855.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:102568316 G>A maps to NM_001017963.2 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:44216476 G>A maps to NM_007355.2 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:44217154 G>A maps to NM_007355.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:104337538 G>A maps to NM_003299.1 Q638Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:104326698 G>A maps to NM_003299.1 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr12:104340404 G>A maps to NM_003299.1 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:104326615 G>T maps to NM_003299.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:104336432 G>A maps to NM_003299.1 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:104336333 G>A maps to NM_003299.1 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr10:118434522 G>A maps to NM_025015.2 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:118441314 G>A maps to NM_025015.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:118439048 G>A maps to NM_025015.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:118434711 G>T maps to NM_025015.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:118434897 G>T maps to NM_025015.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr20:3722950 C>A maps to NM_052970.4 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:3722989 C>T maps to NM_052970.4 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:3730652 C>T maps to NM_052970.4 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:3731516 C>A maps to NM_052970.4 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr21:15746417 C>T maps to NM_006948.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr10:14896240 A>G maps to NM_016299.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr10:14909739 G>A maps to NM_016299.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:31785269 G>A maps to NM_005345.5 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr6:31778116 C>A maps to NM_005527.3 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:31778362 G>A maps to NM_005527.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:31778528 C>T maps to NM_005527.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:31778435 G>T maps to NM_005527.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:31779077 A>T maps to NM_005527.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:31779380 C>T maps to NM_005527.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:31779008 G>A maps to NM_005527.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:31779077 A>G maps to NM_005527.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr6:31778435 G>T maps to NM_005527.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr6:31778435 G>A maps to NM_005527.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:31779458 A>G maps to NM_005527.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:65009357 C>T maps to NM_021979.3 H597H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:65008469 G>A maps to NM_021979.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:65008439 C>T maps to NM_021979.3 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:65008077 C>T maps to NM_021979.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:65008481 C>T maps to NM_021979.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:65008049 C>T maps to NM_021979.3 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr14:65008523 G>A maps to NM_021979.3 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:65008784 C>T maps to NM_021979.3 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:132425262 A>G maps to NM_002154.3 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:132424190 G>T maps to NM_002154.3 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:132432941 G>A maps to NM_002154.3 K631K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:128744013 C>T maps to ENST00000438626 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:128748545 T>C maps to ENST00000438626 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:128001606 C>T maps to NM_005347.4 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:128001285 C>T maps to NM_005347.4 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr1:161496157 C>A maps to NM_002155.3 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:161494948 G>A maps to NM_002155.3 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:161495317 C>T maps to NM_002155.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:161495452 C>T maps to NM_002155.3 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr11:122928441 T>A maps to NM_006597.3 *647Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:122930712 G>T maps to NM_006597.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:122930691 G>A maps to NM_006597.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:122930448 G>A maps to NM_006597.3 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr11:122930682 A>G maps to NM_006597.3 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr11:122930682 A>G maps to NM_006597.3 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:122930481 G>T maps to NM_006597.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:137894316 C>T maps to NM_004134.6 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:137897306 C>A maps to NM_004134.6 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:137910938 G>A maps to NM_004134.6 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:75933372 C>A maps to NM_001540.3 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr11:111784411 C>A maps to NM_001541.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:111784460 C>A maps to NM_001541.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:53751771 G>A maps to NM_006308.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:53751723 T>C maps to NM_006308.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr5:53751880 C>T maps to NM_006308.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:16343586 G>A maps to ENST00000375714 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:16342209 G>A maps to ENST00000375714 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr12:119617242 C>T maps to NM_014365.2 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:40275056 C>T maps to NM_033194.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:40275014 T>C maps to NM_033194.2 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:122496600 G>A maps to NM_024610.4 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:55790865 G>A maps to NM_012267.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr19:55773996 C>T maps to NM_012267.4 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr2:64685465 A>G maps to NM_014181.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:198361984 G>T maps to NM_199440.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:22201452 G>A maps to NM_005529.5 T1115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:22165465 G>A maps to NM_005529.5 R3334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:22202853 G>A maps to NM_005529.5 N957N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:22214099 C>T maps to NM_005529.5 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:22206926 G>A maps to NM_005529.5 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:22201195 C>T maps to NM_005529.5 T1147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:22169321 G>A maps to NM_005529.5 Q2951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:22174451 G>A maps to NM_005529.5 H2624H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:22213819 C>T maps to NM_005529.5 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:22178679 G>A maps to NM_005529.5 A2257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:22181132 G>A maps to NM_005529.5 R2087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:22188593 G>A maps to NM_005529.5 N1585N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:22179274 G>A maps to NM_005529.5 G2214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:22170703 G>A maps to NM_005529.5 P2851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:22178110 G>A maps to NM_005529.5 C2362C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:31719801 C>T maps to NM_006644.2 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:31725252 C>A maps to NM_006644.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:20398172 G>A maps to NM_001098520.1 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:135593994 C>T did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:135579862 A>G did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:135593313 C>T did not map to a codon.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr23:135593891 C>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:135579948 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:135593918 T>G did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:135592264 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:135586562 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:135593637 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:70921263 C>A maps to NM_002159.2 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:70921235 G>T maps to NM_002159.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:70897792 A>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:63256592 G>A maps to NM_000524.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:63256507 G>A maps to NM_000524.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:63257288 C>T maps to NM_000524.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:63256685 G>A maps to NM_000524.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:63256304 G>T maps to NM_000524.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:63256667 G>A maps to NM_000524.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:63257162 G>A maps to NM_000524.2 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:63256562 G>A maps to NM_000524.2 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:63257036 C>T maps to NM_000524.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:63256508 C>T maps to NM_000524.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:78172882 G>A maps to NM_000863.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:23520214 G>T maps to NM_000864.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:23519785 G>T maps to NM_000864.4 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:87725363 C>A maps to NM_000865.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:88040321 C>T maps to NM_000866.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr3:88040240 C>A maps to NM_000866.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr3:88040588 T>C maps to NM_000866.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:88040240 C>A maps to NM_000866.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr3:88040588 T>C maps to NM_000866.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:47466612 G>A maps to NM_000621.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr13:47409037 C>T maps to NM_000621.3 K450K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr13:47469924 A>G maps to NM_000621.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:47409001 G>A maps to NM_000621.3 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr13:47409195 G>A maps to NM_000621.3 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:114141351 G>A did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:113965789 C>T did not map to a codon.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr23:114082706 G>A did not map to a codon.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr23:114141284 G>A did not map to a codon.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr23:114082669 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:114082715 C>T did not map to a codon.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr23:114141601 C>A did not map to a codon.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr23:114141463 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:114141529 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:114141707 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:113965734 G>C did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:114141779 T>C did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:114141779 T>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:114141873 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr23:114141163 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:114141573 T>C did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:114141606 C>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:114141413 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:114141779 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:113856749 C>T maps to NM_213621.3 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr11:113853874 C>T maps to NM_213621.3 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:113857247 C>T maps to NM_213621.3 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:113815319 C>A maps to NM_006028.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr11:113813724 C>T maps to NM_006028.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:113816682 C>T maps to NM_006028.3 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:183774717 C>T maps to NM_130770.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:183770909 C>T maps to NM_130770.2 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:183778058 G>A maps to NM_130770.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:183756041 A>T maps to NM_001145143.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:183824009 C>A maps to NM_182589.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr3:183823964 G>A maps to NM_182589.2 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:183823205 C>T maps to NM_182589.2 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:183824081 G>A maps to NM_182589.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:183819289 C>T maps to NM_182589.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:183823100 A>G maps to NM_182589.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:147902878 G>T maps to NM_001040173.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr5:147845475 A>G maps to NM_199453.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr7:154863058 G>A maps to NM_024012.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:154876067 C>T maps to NM_024012.2 I315I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-A00A-01A-01W-A005-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr7:154862833 C>T maps to NM_024012.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr7:154863196 C>T maps to NM_024012.2 R196R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G4-6628-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:19992602 C>A maps to NM_000871.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:92508771 G>A maps to NM_019859.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:92617257 C>T maps to NM_019859.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:92617191 G>A maps to NM_019859.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:92503434 T>C maps to NM_019859.3 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:124271581 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:124268173 C>T maps to NM_002775.4 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:124248466 C>T maps to NM_002775.4 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:124249024 C>T maps to NM_002775.4 H220H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:74760019 G>T maps to NM_013247.4 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:8305988 G>A maps to NM_053044.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:8307811 G>A maps to NM_053044.3 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:3227418 A>G maps to NM_002111.6 L2599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr4:3132074 G>A maps to NM_002111.6 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:3214291 G>T maps to NM_002111.6 G2210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:3231708 C>T maps to NM_002111.6 D2735D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:3240323 C>T maps to NM_002111.6 T3014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:3222000 C>A maps to NM_002111.6 V2445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:3208604 G>A maps to NM_002111.6 T1990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:3132047 T>C maps to NM_002111.6 H628H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:3133098 G>A maps to NM_002111.6 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:3240236 C>T maps to NM_002111.6 D2985D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr4:3133386 G>A maps to NM_002111.6 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:3241641 C>T maps to NM_002111.6 A3095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:3129285 C>T maps to NM_002111.6 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:3134295 G>A maps to NM_002111.6 Q748Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr4:3129019 C>T maps to NM_002111.6 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr4:3117137 A>G maps to NM_002111.6 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr4:3156067 C>T maps to NM_002111.6 R1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr21:33296845 C>T maps to NM_014586.1 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr21:33331187 G>A maps to NM_014586.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr21:33371337 G>A maps to NM_014586.1 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr21:33331181 C>T maps to NM_014586.1 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr21:33371488 C>T maps to NM_014586.1 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr21:33371274 G>A maps to NM_014586.1 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:48007442 A>G maps to NM_004507.2 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:48016329 A>G maps to NM_004507.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:48007433 T>A maps to NM_004507.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr6:656637 G>A maps to NM_148959.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:656293 C>T maps to NM_148959.3 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr6:656422 G>A maps to NM_148959.3 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:53631606 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:53565306 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:53573496 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:53616677 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:53674478 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:53565947 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:53672373 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:53581680 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:53571651 A>G did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:53563521 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:53620418 G>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:53574942 T>C did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:53576433 C>T did not map to a codon.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr23:53610836 T>C did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:53566739 T>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:53564589 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:53571566 G>A did not map to a codon.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr23:53596605 G>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:53573423 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:53581672 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:53644316 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:53615445 T>G did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:53562374 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:53591616 C>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:53616744 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:53610811 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:53587255 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:53595718 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:53563201 A>G did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:53563518 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:53654788 A>C did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:53589855 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr23:53571599 C>G did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:53571520 C>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:53603878 T>C did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:53613483 G>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:53563521 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:53622233 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:53658402 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:53565983 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:53577971 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:53655544 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:53602131 C>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:53654406 T>C did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:53577911 A>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:53616553 T>C did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:53563519 A>G did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:53655544 G>A did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr23:53576153 A>G did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:53563521 G>T did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:53654810 T>C did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:53587173 G>A did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:53570858 G>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:53577911 A>T did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:53654408 T>C did not map to a codon.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr23:53654406 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:53564589 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:53579613 T>C did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:53562354 C>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:53576155 G>A did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:53654408 T>C did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:111089028 G>T maps to NM_001040107.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:111089112 G>A maps to NM_001040107.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:111099082 G>A maps to NM_001040107.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:111089136 G>A maps to NM_001040107.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:50338045 C>T maps to NM_153281.1 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:50357377 G>A maps to NM_033158.4 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr3:50357665 C>T maps to NM_033158.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr3:50357182 C>T maps to NM_033158.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:50332325 G>A maps to NM_003549.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:50330947 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:50332885 G>A maps to NM_003549.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:123508774 C>T maps to NM_012269.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr7:123508774 C>T maps to NM_012269.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr7:123509007 C>T maps to NM_012269.2 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:70986496 G>A maps to NM_032821.2 R2119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr16:70952224 G>A maps to NM_032821.2 D2630D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr16:70995967 G>T maps to NM_032821.2 I1953I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:70852283 G>A maps to NM_032821.2 I4872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:70954901 G>T maps to NM_032821.2 T2458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:71025258 C>A maps to NM_032821.2 E1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:70908346 G>A maps to NM_032821.2 H3602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:71065649 G>A maps to NM_032821.2 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:70871622 G>A maps to NM_032821.2 V4403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:70916691 G>A maps to NM_032821.2 V3361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:71015345 G>A maps to NM_032821.2 S1485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:71186685 C>T maps to NM_032821.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:70917970 G>A maps to NM_032821.2 S3276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:71012867 G>A maps to NM_032821.2 L1528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:70913578 C>A maps to NM_032821.2 T3431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:70998800 T>C did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:71021961 T>C maps to NM_032821.2 G1352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:70917898 G>A maps to NM_032821.2 I3300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:70986439 C>A maps to NM_032821.2 E2138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr16:70989428 G>A maps to NM_032821.2 S2054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:70884487 C>A maps to NM_032821.2 E4171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:70894599 C>T maps to NM_032821.2 K3993K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:70897081 G>A maps to NM_032821.2 F3824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:70908753 G>A maps to NM_032821.2 I3541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:70900142 G>A maps to NM_032821.2 F3799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:70908433 G>A maps to NM_032821.2 V3573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:71025258 C>A maps to NM_032821.2 E1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:70989434 G>A maps to NM_032821.2 A2052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:71021859 G>T maps to NM_032821.2 S1386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr16:71196549 G>A maps to NM_032821.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr16:71021901 G>A maps to NM_032821.2 Y1372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:70866822 G>A maps to NM_032821.2 C4608C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:70894773 A>G maps to NM_032821.2 G3935G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:70928359 G>A maps to NM_032821.2 I3079I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:70937700 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:70942695 G>T maps to NM_032821.2 V2690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr16:71127814 G>T maps to NM_032821.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:71098622 A>G maps to NM_032821.2 Y732Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:71008565 G>A maps to NM_032821.2 L1593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr16:71149608 G>A maps to NM_032821.2 C439C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:70916793 G>A maps to NM_032821.2 F3327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:70871622 G>A maps to NM_032821.2 V4403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:70867803 G>A maps to NM_032821.2 G4554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:70937580 C>T maps to NM_032821.2 P2931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:70889065 T>C maps to NM_032821.2 V4135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr16:70955003 G>A maps to NM_032821.2 G2424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr16:70841533 C>A maps to NM_032821.2 G5104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:70928445 C>A maps to NM_032821.2 E3051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr11:118923366 G>A maps to NM_001130991.1 N323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:118921764 G>A maps to NM_001130991.1 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr11:118916313 G>A maps to NM_001130991.1 D997D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:9628326 G>T maps to NM_001039613.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:95050108 G>T maps to ENST00000375660 C122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:220311336 T>C maps to NM_018060.3 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:220300156 C>T maps to NM_018060.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr4:88732602 C>T maps to NM_004967.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr4:88732908 C>A maps to NM_004967.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr4:88732530 T>C maps to NM_004967.3 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr4:88732593 C>T maps to NM_004967.3 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:88732566 A>G maps to NM_004967.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr6:82883136 G>C maps to NM_015525.2 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:82921116 A>C maps to NM_015525.2 Y793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:82925889 G>A maps to NM_015525.2 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:82881216 A>G maps to NM_015525.2 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:82941533 G>A maps to NM_015525.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:82911186 A>C maps to NM_015525.2 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:82927752 A>G maps to NM_015525.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:8153570 G>A maps to ENST00000422063 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:8260939 C>T maps to ENST00000422063 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr7:8198207 A>G maps to ENST00000422063 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr7:8198207 A>G maps to ENST00000422063 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:8167605 A>G maps to ENST00000422063 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:8167617 C>T maps to ENST00000422063 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:203653712 A>G maps to NM_138468.4 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:10395088 G>A maps to NM_000201.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr17:62082580 G>A maps to NM_001099789.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr19:10444908 A>G maps to NM_002162.3 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:10402931 C>T maps to NM_003259.3 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr19:10402231 G>A maps to NM_003259.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:10405275 G>A maps to NM_003259.3 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:10404737 G>A maps to NM_003259.3 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:52905989 G>A maps to NM_016513.4 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:52883235 C>A maps to NM_016513.4 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:6285178 C>T maps to NM_012405.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:204824307 G>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr21:45655308 G>A maps to ENST00000400379 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:73016669 C>T maps to NM_001545.1 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr2:8822450 C>T maps to NM_002166.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr10:94274734 C>T maps to NM_004969.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr10:94250352 C>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:94214245 A>G maps to NM_004969.3 F1005F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:94268596 T>C maps to NM_004969.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:94291643 G>A maps to NM_004969.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:209113110 A>G maps to NM_005896.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:209103913 C>T maps to NM_005896.2 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr2:209113110 A>G maps to NM_005896.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr2:209113208 G>A maps to NM_005896.2 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr15:90631878 T>C maps to NM_002168.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr15:90630360 G>C maps to NM_002168.2 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:90628139 C>T maps to NM_002168.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:90631836 C>T maps to NM_002168.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr15:90631839 G>T maps to NM_002168.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:153052969 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:153053397 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:153053530 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:153055687 G>A did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:153055737 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:153053318 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:1089329 A>C maps to NM_004508.2 L106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:1088637 G>A maps to NM_004508.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:1068667 G>A maps to NM_033261.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:39785484 T>G maps to NM_002164.4 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr8:39785592 C>A maps to NM_002164.4 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:39771449 C>T maps to NM_002164.4 H3H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:39782874 C>T maps to NM_002164.4 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:148579800 A>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:148579831 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:148578047 C>A did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:148564644 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:148568499 G>C did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:998095 G>A maps to NM_000203.3 W626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr18:44682583 G>A maps to NM_016097.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:44682601 C>T maps to NM_016097.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:181058923 G>T maps to NM_016545.4 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:6665015 C>T maps to NM_001193457.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr12:6664616 G>A maps to NM_001193457.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:6664447 G>T maps to NM_001193457.1 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:158990259 C>T maps to ENST00000295809 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:159021626 T>C maps to ENST00000295809 N608N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CK-4952-01A-01D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:41165102 G>T maps to NM_005533.4 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr17:41165641 G>T maps to NM_005533.4 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:79116332 C>T maps to NM_006417.4 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:79121165 C>A maps to NM_006417.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:79121135 C>T maps to NM_006417.4 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:79116327 C>T maps to NM_006417.4 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:79102745 G>A maps to NM_006820.2 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:79101056 A>G maps to NM_006820.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:163144686 T>C maps to NM_022168.2 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:163136601 T>C maps to NM_022168.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:163144662 A>C maps to NM_022168.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:163134116 G>A maps to NM_022168.2 R618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr2:163130454 C>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:163134132 T>C maps to NM_022168.2 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:91162103 G>A maps to NM_001548.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:91143079 G>T maps to NM_001010987.2 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:91066523 A>T maps to NM_001547.4 K271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr10:91066976 C>T maps to NM_001547.4 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:91099705 C>T maps to NM_001549.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:91098876 G>A maps to NM_001549.4 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr10:91177895 C>T maps to NM_012420.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:91177162 C>T maps to NM_012420.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:314977 C>T maps to ENST00000328221 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:320792 G>T maps to NM_021034.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr11:299469 G>A maps to NM_001025295.1 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:25671783 T>C maps to NM_001145728.1 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr12:25699465 C>T maps to NM_001145728.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr9:21440580 T>C maps to NM_024013.1 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr9:21440580 T>C maps to NM_024013.1 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr9:21440947 C>A maps to NM_024013.1 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr9:21440947 C>T maps to NM_024013.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr9:21440947 C>T maps to NM_024013.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr9:21440947 C>T maps to NM_024013.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr9:21367970 C>T maps to NM_006900.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr9:21367970 C>T maps to NM_006900.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr9:21367970 C>T maps to NM_006900.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr9:21239384 T>A maps to NM_002172.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:21239496 G>T maps to NM_002172.2 Y146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr9:21384798 G>T maps to NM_000605.3 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr9:21384798 G>T maps to NM_000605.3 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:21166245 G>A maps to NM_002175.2 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr9:21166464 A>G maps to NM_002175.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr9:21304925 A>C maps to NM_002169.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:21350378 C>A maps to NM_021002.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:21409666 G>A maps to NM_002170.3 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr21:34715864 A>C maps to NM_000629.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr21:34632971 C>G maps to NM_207585.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:21077643 G>A maps to NM_002176.2 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:21077457 G>A maps to NM_002176.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:68551713 G>A maps to NM_000619.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:68551836 G>T maps to NM_000619.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:137519536 C>T maps to NM_000416.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr21:34787246 C>T maps to ENST00000381995 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:21140996 G>A maps to NM_002177.1 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:112096103 A>T maps to NM_001007245.2 K83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:129218764 C>T maps to NM_052985.2 D794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:129185900 C>T maps to NM_052985.2 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:129238529 A>G maps to NM_052985.2 S1248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:129185837 C>T maps to NM_052985.2 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:129237950 C>T maps to NM_052985.2 S1182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:129195609 C>T maps to NM_052985.2 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:129218839 G>T maps to NM_052985.2 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr16:1634322 G>A maps to NM_014714.3 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr16:1642486 G>T maps to NM_014714.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:1634250 G>A maps to NM_014714.3 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:1642285 G>A maps to NM_014714.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:1608111 G>A maps to NM_014714.3 D741D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr16:1614063 C>T maps to NM_014714.3 Q667Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr16:1652490 T>C maps to NM_014714.3 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr16:1570143 G>A maps to NM_014714.3 D1287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:1576065 G>A maps to NM_014714.3 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr16:1642486 G>T maps to NM_014714.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr2:27700127 G>T maps to NM_015662.1 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:27708370 C>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:27684141 G>A maps to NM_015662.1 Y812Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:27703941 G>A maps to NM_015662.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:27693878 G>A maps to NM_015662.1 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:27699567 G>A maps to NM_015662.1 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:27670441 C>T maps to NM_015662.1 T1533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:27702994 G>A maps to NM_015662.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:27668186 G>A maps to NM_015662.1 R1682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:27700127 G>T maps to NM_015662.1 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:27685570 T>C maps to NM_015662.1 E704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:27708304 T>C maps to NM_015662.1 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr22:37159018 G>A maps to ENST00000453009 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr20:42232862 T>G maps to NM_016004.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:42271224 C>T maps to NM_016004.2 H409H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:42247662 C>A maps to NM_016004.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr3:107932812 C>A maps to ENST00000457963 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:107925521 C>A maps to ENST00000457963 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:107932848 C>A maps to ENST00000457963 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr3:107932810 T>C maps to ENST00000457963 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:107884330 G>A maps to ENST00000457963 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:27047366 C>T maps to NM_025103.2 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:160102352 C>T maps to ENST00000326448 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:110618232 C>T maps to NM_014055.3 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:110581325 T>C maps to NM_014055.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:21199960 A>G maps to NM_175605.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:21170366 A>T maps to NM_175605.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:21190018 G>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:69354494 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr23:69368666 C>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:69354426 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:65627715 G>A maps to NM_004884.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:65623079 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:65688223 G>A maps to NM_020962.1 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr15:65687479 C>A maps to NM_020962.1 G510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr15:65682647 C>T maps to NM_020962.1 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr15:65681311 G>T maps to NM_020962.1 P847P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AD-6895-01A-11D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:102811769 T>C maps to NM_001111285.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:102869448 G>A maps to NM_001111285.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:102813361 G>A maps to NM_001111285.1 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:99473523 C>T maps to NM_000875.3 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:99250896 C>T maps to NM_000875.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:99451928 C>T maps to NM_000875.3 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:99486165 C>T maps to NM_000875.3 R1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr15:99491854 C>T maps to NM_000875.3 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:99454652 C>T maps to NM_000875.3 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr15:99500607 C>T maps to NM_000875.3 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr15:99440123 C>A maps to NM_000875.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:2154758 C>T maps to NM_001127598.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr11:2154890 C>T maps to NM_001127598.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:47119660 C>T maps to NM_006546.3 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:47115682 G>A maps to NM_006546.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:47075190 C>A maps to NM_006546.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr17:47115629 C>T maps to NM_006546.3 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:47117433 G>T maps to NM_006546.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:47122408 G>A maps to NM_006546.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:185407396 G>A maps to NM_006548.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:185364845 G>A maps to NM_006548.4 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:23508152 C>A maps to NM_006547.2 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:23358783 A>C maps to NM_006547.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr6:160450626 T>C maps to NM_000876.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:160482959 G>A maps to NM_000876.2 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr6:160500661 C>T maps to NM_000876.2 V1843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:160517474 C>T maps to NM_000876.2 G2220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr6:160491077 C>T maps to NM_000876.2 S1477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:160484558 C>A maps to NM_000876.2 V1261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:160477544 G>A maps to NM_000876.2 T928T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:160468858 C>A maps to NM_000876.2 Y755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:160482535 C>T maps to NM_000876.2 D1088D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr6:160504992 C>A maps to NM_000876.2 R1949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:160471611 C>A maps to NM_000876.2 A874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:160485883 C>T maps to NM_000876.2 R1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:160517552 C>T maps to NM_000876.2 F2246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:160481582 C>T maps to NM_000876.2 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr6:160504992 C>A maps to NM_000876.2 R1949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:1841617 C>T maps to NM_001146006.1 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:1840699 C>T maps to NM_001146006.1 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:38610311 C>T maps to NM_001552.2 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:217559462 G>A maps to NM_000599.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:53494607 G>A maps to NM_002178.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr12:53494598 G>A maps to NM_002178.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr12:53494598 G>A maps to NM_002178.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:57898688 T>C maps to NM_001553.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr4:57898690 C>A maps to NM_001553.1 G244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:46627891 G>A maps to NM_207393.1 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:201174462 C>T maps to NM_001164586.1 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:201187670 G>A maps to NM_001164586.1 T3261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr1:201195000 G>A maps to NM_001164586.1 G3512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:201196223 C>T maps to NM_001164586.1 G3667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:201196295 G>A maps to NM_001164586.1 T3691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr1:201182027 G>A maps to NM_001164586.1 G2669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:68700793 C>T maps to NM_002180.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:68679034 T>C maps to NM_002180.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:68704386 G>A maps to NM_002180.2 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr22:23917202 A>G maps to NM_020070.2 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr22:23915473 C>T maps to NM_020070.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:23235969 C>T maps to ENST00000410090 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:51830994 C>T maps to NM_001101372.1 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:51830349 G>A maps to NM_001101372.1 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr19:51826999 C>T maps to NM_001101372.1 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:130408678 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:130410932 G>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:130417079 T>G did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr23:130408762 C>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:130417004 C>T did not map to a codon.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr23:130409532 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:130409516 T>C did not map to a codon.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr23:130410202 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:130409699 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:130415221 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:130417005 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:130419989 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:130410964 A>G did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:130412065 C>G did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:130420578 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:130409051 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:130409618 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:130409087 G>T did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:130409529 A>T did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:130417179 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:130415207 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:130409959 A>G did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:130410018 C>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:130417004 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:130411893 A>G did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:130409618 C>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:130411871 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:130408154 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:130407780 C>T did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr3:151165413 T>C maps to NM_178822.4 Q785Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:151166328 A>G maps to NM_178822.4 N480N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:151155904 T>C maps to NM_178822.4 K2148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:151166574 C>T maps to NM_178822.4 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:151166574 C>T maps to NM_178822.4 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr3:151155583 G>A maps to NM_178822.4 S2255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:151163625 T>C maps to NM_178822.4 T1381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:151161580 G>A maps to NM_178822.4 R1718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr3:151163625 T>C maps to NM_178822.4 T1381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:151166061 T>C maps to NM_178822.4 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:151161196 C>T maps to NM_178822.4 E1846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr3:151165764 C>T maps to NM_178822.4 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:118623492 A>G did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:118623520 T>C maps to NM_152538.2 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr1:18691748 C>T maps to NM_032880.4 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:18704816 G>A maps to NM_032880.4 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:18661481 C>T maps to NM_032880.4 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:18703403 C>T maps to NM_032880.4 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:18618449 C>T maps to NM_032880.4 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr11:18737204 G>A maps to NM_173588.3 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:18743087 C>T maps to NM_173588.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:18728542 G>T maps to NM_173588.3 Y1166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr11:18743087 C>T maps to NM_173588.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:117146465 G>A maps to NM_001542.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:117120152 G>A maps to NM_001542.2 N1142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:117122056 C>T maps to NM_001542.2 T1117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr1:117142929 C>T maps to NM_001542.2 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr21:41151134 G>A maps to NM_001080444.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr21:41137615 G>A maps to NM_001080444.1 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:21658637 G>A maps to NM_005849.2 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr16:21655619 G>A maps to NM_005849.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:21658805 C>T maps to NM_005849.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:160064893 G>A maps to NM_052868.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:160063611 G>A maps to NM_052868.2 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:159912938 G>A maps to NM_001135050.1 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:159897146 G>T maps to NM_001135050.1 A1176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:159898777 G>A maps to NM_001135050.1 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:159912789 G>A maps to NM_001135050.1 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:159900500 G>A maps to NM_001135050.1 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:159901321 C>T maps to NM_001135050.1 K478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:159901304 C>T maps to NM_001135050.1 W484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:159898276 A>T maps to NM_001135050.1 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:159900059 C>A maps to NM_001135050.1 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:133790547 C>T maps to NM_014987.1 T1024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:133805548 C>T maps to NM_014987.1 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:133816127 G>A maps to NM_014987.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:133789707 C>T maps to NM_014987.1 T1304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:133807827 G>T maps to NM_014987.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:133815977 C>T maps to NM_014987.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr11:133790112 C>T maps to NM_014987.1 R1169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:219920120 G>A maps to NM_002181.3 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:219922284 G>A maps to NM_002181.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:219922287 G>A maps to NM_002181.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr12:99007530 T>C maps to NM_201612.1 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:99007485 G>A maps to NM_201612.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:111668595 G>A maps to NM_003640.3 Q544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:111642367 G>A maps to NM_003640.3 R1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:111659284 C>T maps to NM_003640.3 K845K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:111659549 C>T maps to NM_003640.3 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:111665840 A>G did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:111653501 G>A maps to NM_003640.3 G1047G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr9:111665936 C>T maps to NM_003640.3 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr8:42129644 G>A maps to NM_001556.2 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr1:206649680 G>A maps to NM_014002.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:206649566 C>T maps to NM_014002.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:206653222 C>T maps to NM_014002.3 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:206653375 C>T maps to NM_014002.3 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:50467778 C>T maps to NM_006060.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:50444273 G>A maps to NM_006060.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr7:50444491 G>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:50455121 C>T maps to NM_006060.3 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:213878632 T>C maps to ENST00000342002 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr2:213921695 C>T maps to ENST00000342002 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:213878571 C>A maps to ENST00000342002 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:213872793 G>A maps to ENST00000342002 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:213872490 G>A maps to ENST00000342002 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:213872284 G>T maps to ENST00000342002 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:213872106 G>A maps to ENST00000342002 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:213921659 G>A maps to ENST00000342002 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:37985667 G>A maps to NM_012481.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:37922297 G>A maps to NM_012481.3 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:56426357 A>G maps to NM_022465.3 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:206944269 C>T maps to NM_000572.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:206944308 C>T maps to NM_000572.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:206945753 G>A maps to NM_000572.2 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr1:206944308 C>T maps to NM_000572.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:117870325 C>T maps to NM_001558.3 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr21:34655473 C>T maps to ENST00000433395 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr21:34640816 C>T maps to ENST00000433395 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:34655473 C>T maps to ENST00000433395 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:34656804 T>C maps to NM_001142784.1 H77H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:158750221 G>A maps to NM_002187.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr5:158743719 G>A maps to NM_002187.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr5:158747503 C>T maps to NM_002187.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:158745800 A>G maps to NM_002187.2 H266H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:158747518 G>A maps to NM_002187.2 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr5:158747500 G>A maps to NM_002187.2 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:18174731 T>C maps to NM_005535.1 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:18180497 G>A maps to NM_005535.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr19:18174686 G>A maps to NM_005535.1 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:67838311 A>C maps to NM_001559.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr1:67794050 C>T maps to NM_001559.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:67833572 C>T maps to NM_001559.2 Q442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:131994030 C>A maps to NM_002188.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr23:117875002 T>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:117880926 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:117875023 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:117880918 A>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:117880934 C>T did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:114239843 G>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:114238644 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:114245295 T>C did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:114245294 G>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:114250385 T>A did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:114244111 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:114238657 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:114239864 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:114239864 C>T did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr23:114245295 T>C did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:114251823 G>A did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:114245295 T>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:114250313 G>T did not map to a codon.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr23:114245295 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:114245331 T>C did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:114245331 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:114245295 T>C did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:114245295 T>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:114249066 T>C did not map to a codon.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr10:6002328 C>T did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:81591802 C>T maps to NM_172217.3 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:81558057 G>A maps to NM_172217.3 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr15:81593822 G>A maps to NM_172217.3 E1096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:81601069 A>T maps to NM_172217.3 G1310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:81584975 T>C maps to NM_172217.3 H500H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr15:81592528 C>G maps to NM_172217.3 G954G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:81584924 C>T maps to NM_172217.3 H483H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:148753976 G>A maps to NM_014443.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr22:17579694 T>A maps to NM_014339.5 L114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr22:17579731 C>T maps to NM_014339.5 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:17590421 C>T maps to NM_014339.5 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr22:17590358 C>A maps to NM_014339.5 G750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:53892822 C>T maps to NM_018725.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:53883748 A>G maps to NM_018725.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr3:53883724 A>G maps to NM_018725.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:53891662 G>A maps to NM_018725.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:9959304 G>A maps to NM_153461.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:9962624 A>G maps to NM_153461.2 E269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:57132323 G>A maps to NM_017563.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr3:57131678 C>T maps to NM_017563.3 T684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr3:9944640 C>T maps to NM_153483.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:112025710 C>T maps to NM_001562.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr11:112014428 C>A maps to NM_001562.2 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr11:71711487 C>T maps to NM_001145057.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:103013013 C>T maps to NM_003855.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:102984291 T>C maps to NM_003855.2 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:103006576 C>A maps to NM_003855.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:103013184 C>T maps to NM_003855.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:103053805 T>C maps to NM_003853.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:103040380 C>T maps to NM_003853.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:103053685 C>A maps to NM_003853.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:207013238 C>T maps to NM_153758.2 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:113765446 T>C maps to NM_014440.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:113765446 T>C maps to NM_014440.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr2:113765446 T>C maps to NM_014440.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:113783719 G>A maps to NM_014438.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr2:113742454 C>T maps to NM_019618.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr2:102781636 T>G maps to NM_000877.2 L120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr2:102641016 T>A maps to NM_004633.3 C258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:190366274 C>A maps to NM_002182.3 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr3:190366442 G>T maps to NM_002182.3 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr3:190321957 C>T maps to NM_002182.3 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:29972755 A>G did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:29972685 G>A did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:29301324 G>A did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:29973259 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:29972782 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:29973686 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:29417350 A>G did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:29301319 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:29959774 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:29972783 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:29938089 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr23:29972755 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:29972755 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:29973676 T>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:29973707 A>G did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:29938089 A>G did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:29972754 A>G did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:29414504 C>A did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:29972782 C>A did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:29301233 C>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:29938089 A>G did not map to a codon.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr23:29935626 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:29972755 A>G did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:29973505 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:29972754 A>T did not map to a codon.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr23:29972782 C>T did not map to a codon.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr23:29938104 C>G did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:29414504 C>T did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:29972754 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:29935624 G>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:105011410 C>A did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:104961475 G>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:104961401 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:104478598 T>G did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:104440254 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:105011181 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:104999306 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr23:104984674 C>T did not map to a codon.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr23:105011183 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr23:105011532 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:104999169 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:104961454 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:104999217 G>T did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr23:104984651 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:102968290 C>T maps to NM_016232.4 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr2:102958716 A>G maps to NM_016232.4 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr2:102959786 A>G maps to NM_016232.4 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr2:102836358 G>A maps to NM_003854.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:102851400 C>T maps to NM_003854.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:102808543 G>A maps to NM_003854.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:102818086 A>G maps to NM_003854.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:113888655 T>C maps to NM_173841.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:207039323 C>T maps to NM_018724.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:136714298 C>T maps to NM_144717.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:123534040 C>A maps to NM_021803.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr16:27460465 C>A maps to NM_181079.4 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:24447501 G>A maps to NM_021258.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:24447507 G>A maps to NM_021258.2 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:24449812 C>T maps to NM_021258.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr6:137476132 C>T maps to NM_052962.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:67724297 G>A maps to NM_144701.2 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr14:23844899 C>T maps to NM_022789.3 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:23844899 C>T maps to NM_022789.3 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:28518100 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:28513449 C>T maps to NM_145659.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:28511127 C>T maps to NM_145659.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr19:14159986 G>A maps to NM_004843.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:14159993 C>T maps to NM_004843.2 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:14142704 C>T maps to NM_004843.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:14150595 C>T maps to NM_004843.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:14157075 G>A maps to NM_004843.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:14163074 G>C maps to NM_004843.2 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:14159993 C>T maps to NM_004843.2 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:14162425 C>A maps to NM_004843.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr19:39734289 G>A maps to ENST00000392072 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:39734328 G>T maps to ENST00000392072 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr19:39734312 G>A maps to ENST00000392072 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:24488115 A>G maps to NM_170743.2 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:24483691 G>A maps to NM_170743.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:39788647 G>A maps to NM_172140.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:37535160 C>T maps to ENST00000406505 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:37539610 A>G maps to ENST00000406505 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:37535235 G>A maps to ENST00000406505 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr22:37524753 G>A maps to ENST00000406505 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:70329210 G>A did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:70329169 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:70330359 T>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:70329237 T>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:70328452 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:131398477 C>A maps to NM_000588.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:131396446 C>T maps to NM_000588.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:131396446 C>T maps to NM_000588.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr5:131398417 G>A maps to NM_000588.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr5:131398378 C>T maps to NM_000588.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:122657126 C>T maps to NM_001014336.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:122657018 T>C maps to NM_001014336.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:55202042 G>A maps to NM_139017.4 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:55155338 C>A maps to NM_139017.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:55212641 T>C maps to NM_139017.4 N663N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:6250493 G>T maps to NM_033439.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:70694011 G>A maps to NM_152456.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:70693949 C>T maps to NM_152456.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:1464307 A>G did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:50393250 C>T maps to NM_172374.1 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr16:27367195 C>T maps to NM_000418.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:27353478 C>T maps to NM_000418.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:27373962 A>G maps to NM_000418.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:3139614 G>A maps to NM_000564.3 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:3137078 A>G maps to NM_000564.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:3144391 A>C maps to NM_000564.3 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr3:3137078 A>G maps to NM_000564.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr3:3137078 A>G maps to NM_000564.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:3137078 A>G maps to NM_000564.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:22767171 C>T maps to NM_000600.3 H43H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:22767225 C>T maps to NM_000600.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:55237254 G>A maps to NM_002184.3 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:55251874 A>G maps to NM_002184.3 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr8:79710420 T>A maps to NM_000880.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:35874602 C>T maps to NM_002185.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:35873634 G>A maps to NM_002185.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:135231246 A>G maps to NM_000590.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:155232667 C>G did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:121712752 G>A maps to ENST00000344209 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:121724114 G>A maps to ENST00000344209 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:121725967 G>T maps to ENST00000344209 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:166905933 G>A maps to NM_199351.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr1:166926054 T>C maps to NM_199351.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:10799328 C>T maps to NM_017620.2 G846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:10799954 C>T maps to NM_017620.2 N888N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr19:10787981 T>G maps to NM_017620.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:10789304 C>T maps to NM_017620.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:6629278 C>T maps to NM_001014795.1 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:6630961 C>T maps to NM_001014795.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr11:6630579 G>A maps to NM_001014795.1 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:6629383 G>T maps to NM_001014795.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr11:6629985 C>T maps to NM_001014795.1 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:239090820 A>G maps to NM_030768.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:239079586 G>A maps to NM_030768.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:239082293 C>T maps to NM_030768.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr2:239090818 C>T maps to NM_030768.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr2:239090820 A>G maps to NM_030768.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr2:239102970 T>A maps to NM_030768.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:15234186 G>A maps to NM_006844.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:15227062 C>T maps to NM_006844.3 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:15230828 C>T maps to NM_006844.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:15228698 A>G maps to NM_006844.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr2:86378446 A>G maps to NM_006839.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:86371719 C>A maps to NM_006839.2 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:86398418 C>T maps to NM_006839.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:86378497 T>C maps to NM_006839.2 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr15:75932128 G>T maps to NM_018285.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:131103673 C>T maps to NM_033416.1 Y226Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:131103673 C>T maps to NM_033416.1 Y226Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:131104007 C>T maps to NM_033416.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:43923444 C>T maps to NM_175882.2 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:43923123 C>A maps to NM_175882.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:43922343 C>T maps to NM_175882.2 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:43923396 C>T maps to NM_175882.2 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr8:82572754 A>G maps to NM_001144878.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:82592943 C>T maps to NM_001144878.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:82586097 T>C maps to NM_001144878.1 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr18:12014361 C>T maps to NM_014214.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr18:12030351 C>T maps to NM_014214.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:57878774 A>G maps to NM_017813.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:57890678 A>G maps to NM_017813.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:57876411 T>C maps to NM_017813.3 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:128037056 G>T maps to NM_000883.3 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr3:49065253 G>A maps to NM_000884.2 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:49065919 G>A maps to NM_000884.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr3:49061986 A>G maps to NM_000884.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:49062092 G>A maps to NM_000884.2 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:49062387 G>A maps to NM_000884.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:76640701 G>A maps to NM_001563.2 C737C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr6:76751676 A>G maps to NM_001563.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:76715088 G>T maps to NM_001563.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:76660584 G>A maps to NM_001563.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:76715133 G>T maps to NM_001563.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:76751762 T>A maps to NM_001563.2 K50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:100963521 A>C maps to NM_016247.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr3:100972551 C>T maps to NM_016247.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:100963500 T>C maps to NM_016247.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr3:100962465 G>A maps to NM_016247.2 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:101038553 C>A maps to NM_016247.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:100948264 C>A maps to NM_016247.2 E1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:100962705 G>T maps to NM_016247.2 I823I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:100992555 C>A maps to NM_016247.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:100962377 C>A maps to NM_016247.2 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:100963380 G>A maps to NM_016247.2 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:105037711 C>T maps to NM_032727.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr10:105048339 G>T maps to NM_032727.3 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:62232066 G>A maps to NM_176877.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:62330052 G>A maps to NM_176877.2 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr1:62228766 A>G maps to NM_176877.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:62228852 T>C did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:62582281 T>C maps to NM_176877.2 D1578D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:62365311 G>A maps to NM_176877.2 W1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:62228764 T>C maps to NM_176877.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr11:61906403 G>A maps to NM_001040694.1 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr11:61897349 C>T maps to NM_001040694.1 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr14:105169687 C>T maps to ENST00000252520 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:105173878 A>G maps to ENST00000252520 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:105168004 C>T maps to ENST00000252520 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr14:105169490 G>A maps to ENST00000252520 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:105167737 A>G maps to ENST00000252520 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr14:105180624 C>T maps to ENST00000252520 S1042S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:111372095 C>A maps to NM_005537.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:111372201 A>T maps to NM_005537.3 K398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr4:184432019 G>A maps to NM_001564.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:184432019 G>A maps to NM_001564.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:6761477 G>A maps to NM_001127582.1 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:242651430 C>T maps to NM_032329.4 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:220439782 G>A maps to NM_002191.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:220437215 C>A maps to NM_002191.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr7:41739609 C>T maps to NM_002192.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr7:41729775 G>A maps to NM_002192.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr7:41729775 G>A maps to NM_002192.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr7:41739597 C>T maps to NM_002192.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:41729738 C>A maps to NM_002192.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:121107353 G>A maps to NM_002193.2 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:57843558 C>T maps to NM_005538.2 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr12:57828737 C>T maps to NM_005538.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr12:57843558 C>T maps to NM_005538.2 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:57843333 C>A maps to NM_005538.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:57850222 G>A maps to NM_031479.3 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:57849914 C>T maps to NM_031479.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:30791912 C>T maps to NM_006774.4 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:30793365 G>A maps to NM_006774.4 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:41361828 G>T maps to NM_017553.1 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:41289789 G>T maps to NM_017553.1 I1169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:41352120 G>A maps to NM_017553.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:41384308 A>G maps to NM_017553.1 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr15:41361848 C>T maps to NM_017553.1 W567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr15:41384308 A>G maps to NM_017553.1 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr15:41384308 A>G maps to NM_017553.1 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:74682575 A>T maps to ENST00000452361 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:33059366 G>A maps to NM_001098817.1 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:206874332 G>A maps to NM_017759.4 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:206869247 G>A maps to NM_017759.4 S976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:206921555 G>A maps to NM_017759.4 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr2:191235767 T>C maps to NM_002194.3 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:99170756 C>T maps to NM_001134224.1 C462C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:99169314 C>T maps to NM_001134224.1 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:143191848 G>A maps to NM_003866.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:143324096 A>G maps to NM_003866.2 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr4:143044559 T>C maps to NM_003866.2 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:143094847 A>G maps to NM_003866.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:134463922 G>T maps to NM_005539.3 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:134463922 G>T maps to NM_005539.3 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr1:38332155 C>T maps to ENST00000373026 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:234073070 G>A did not map to a codon.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:234104120 G>A maps to ENST00000359570 K891K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:139326315 C>T maps to NM_019892.3 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:121558055 T>C maps to NM_014937.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:121571327 G>T maps to NM_014937.2 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr10:121586928 G>A maps to NM_014937.2 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr10:121586928 G>A maps to NM_014937.2 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:121586590 C>T maps to NM_014937.2 R900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:121586376 T>C maps to NM_014937.2 D828D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:121586985 G>A maps to NM_014937.2 A1031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr22:31529190 C>A maps to ENST00000331075 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:31529208 C>T maps to ENST00000331075 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr22:31529678 C>T maps to ENST00000331075 I831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:1417236 C>T maps to NM_016532.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr17:1401247 G>A maps to NM_016532.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:1401247 G>T maps to NM_016532.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr17:1401247 G>A maps to NM_016532.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:71941448 T>C maps to NM_001567.3 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:71942172 C>T maps to NM_001567.3 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:71939801 G>A maps to NM_001567.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr11:71942166 C>T maps to NM_001567.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:71948431 G>A maps to NM_001567.3 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:71943723 G>A maps to NM_001567.3 Q589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:71939513 G>A maps to NM_001567.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr11:71941448 T>C maps to NM_001567.3 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr11:71939505 C>T maps to NM_001567.3 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:15197352 C>T maps to NM_001031853.3 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr11:15197550 C>T maps to NM_001031853.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr11:15243144 C>T maps to NM_001031853.3 H361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr11:15134029 T>C maps to NM_001031853.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:155094088 G>A maps to ENST00000344756 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:118864323 C>T maps to NM_016133.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:17927841 G>A maps to NM_005543.2 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr9:5231622 C>T maps to NM_002195.1 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr9:5163995 C>A maps to NM_007179.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:5164169 T>G maps to NM_007179.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:5163998 C>A maps to NM_007179.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr9:5185578 G>C maps to NM_007179.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr9:5164083 G>T maps to NM_007179.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr14:36004285 C>T maps to NM_032594.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr14:36004462 G>A maps to NM_032594.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr19:7142878 A>G maps to NM_000208.2 P830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:7267854 C>T maps to NM_000208.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:7184418 C>T maps to NM_000208.2 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:7267446 C>T maps to NM_000208.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr19:7126640 T>C maps to NM_000208.2 G989G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:7142884 G>A maps to NM_000208.2 D828D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:7166390 G>A maps to NM_000208.2 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:7267487 A>G maps to NM_000208.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:7152849 G>A maps to NM_000208.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:7142950 C>T maps to NM_000208.2 S806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:7267470 G>A maps to NM_000208.2 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:156823895 G>A maps to NM_014215.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:1538449 G>A maps to ENST00000389470 C520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:1532686 C>A maps to ENST00000389470 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:1513224 C>T maps to ENST00000389470 L2192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:1526994 G>A maps to ENST00000389470 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:1538434 C>T maps to ENST00000389470 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:19694644 C>A maps to NM_018142.2 S538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:106613177 G>A maps to NM_020395.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:59945032 G>T maps to NM_020748.2 S1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:59988925 C>T maps to NM_020748.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:59974889 G>T maps to NM_020748.2 Y486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr17:59947157 A>G maps to NM_020748.2 C998C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr17:59947157 A>G maps to NM_020748.2 C998C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:77702195 G>A maps to NM_033547.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr11:77632420 G>A maps to NM_033547.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr11:77639495 G>A maps to NM_033547.3 N421N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:77618836 C>A maps to NM_033547.3 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:62416993 C>T maps to NM_030628.1 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr11:62417128 T>C maps to NM_030628.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:62417263 A>G maps to NM_030628.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:51948377 C>T maps to NM_012141.2 Q690Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:212156109 A>T maps to NM_015434.3 L347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:212193474 G>A maps to NM_015434.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:212148576 A>G maps to NM_015434.3 N582N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:95854637 G>A maps to NM_017864.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr8:95892365 A>G maps to NM_017864.2 T964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:95848844 G>T maps to NM_017864.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:95853793 G>T maps to NM_017864.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:28651403 G>A maps to NM_018250.3 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:28669963 C>T maps to NM_018250.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:28625703 G>A maps to NM_018250.3 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:128564984 C>A maps to NM_015693.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:128627682 C>T maps to NM_015693.3 C610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr4:128564711 A>G maps to NM_015693.3 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr9:103054845 G>A maps to NM_014425.2 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:103004912 C>T maps to NM_014425.2 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:103059316 C>T maps to NM_014425.2 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:103002491 C>T maps to NM_014425.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr9:103055223 C>T maps to NM_014425.2 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:103035211 C>T maps to NM_014425.2 H546H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:49765622 G>A maps to NM_153273.3 D235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:49765637 C>T maps to NM_153273.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr3:49764839 C>T maps to NM_153273.3 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:48730457 A>G maps to ENST00000395509 H142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:33690519 G>A maps to NM_054111.4 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr6:33693313 G>A maps to NM_054111.4 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr6:33690550 A>T maps to NM_054111.4 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:33693298 C>T maps to NM_054111.4 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:33703073 C>T maps to NM_054111.4 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr6:154520844 A>G maps to NM_001130700.1 L289L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3492-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:59955943 G>A maps to NM_152230.4 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:59986857 G>A maps to NM_152230.4 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr10:59976064 T>C maps to NM_152230.4 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:61811234 T>C maps to NM_001134779.1 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:61846249 G>A maps to NM_001134779.1 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr5:61826559 A>G maps to NM_001134779.1 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:61826559 A>G maps to NM_001134779.1 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:44432625 G>T maps to NM_014652.3 E850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr1:44422102 C>T maps to NM_014652.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:44422507 G>A maps to NM_014652.3 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:44423679 C>T maps to NM_014652.3 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:24653065 G>A maps to ENST00000458132 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:24656689 A>G maps to ENST00000458132 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr13:98670827 C>T maps to NM_002271.4 Y920Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr13:98655237 T>C maps to NM_002271.4 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:98637733 C>A maps to NM_002271.4 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr13:98652844 G>T maps to NM_002271.4 G370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:98666300 C>T maps to NM_002271.4 R738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr13:98655134 G>A maps to NM_002271.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:98637841 G>A maps to NM_002271.4 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr13:98673371 C>A maps to NM_002271.4 V1082V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr13:98652846 A>G maps to NM_002271.4 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr13:98673371 C>T maps to NM_002271.4 V1082V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr11:9457897 G>A maps to NM_006391.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:9450679 G>T maps to NM_006391.2 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr11:9462074 T>A maps to NM_006391.2 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:9462074 T>C maps to NM_006391.2 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr11:9462074 T>C maps to NM_006391.2 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:9462006 C>T maps to NM_006391.2 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:9459725 G>A maps to NM_006391.2 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:30805151 C>A maps to NM_006390.3 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:30814200 C>A did not map to a codon.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr12:30792666 G>A maps to NM_006390.3 C757C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:30818180 C>T maps to NM_006390.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:30805936 C>A maps to NM_006390.3 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr12:30829460 G>A maps to NM_006390.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:30787092 C>T maps to NM_006390.3 A941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr12:30789967 C>T maps to NM_006390.3 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:30815298 C>A maps to NM_006390.3 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr12:30792516 A>G maps to NM_006390.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr12:30792516 A>T maps to NM_006390.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr12:30792516 A>G maps to NM_006390.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:30792516 A>G maps to NM_006390.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:30792516 A>G maps to NM_006390.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr12:30792516 A>G maps to NM_006390.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:201823755 C>T maps to NM_018085.4 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:201840383 T>C maps to NM_018085.4 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:201840383 T>C maps to NM_018085.4 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:201837782 C>T maps to NM_018085.4 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:201824264 G>T maps to NM_018085.4 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr9:95397501 G>T maps to NM_022755.5 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:95400509 C>T maps to NM_022755.5 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:95400514 A>C maps to NM_022755.5 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr2:237402431 G>A maps to ENST00000457693 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr2:237272563 C>T maps to ENST00000457693 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr2:237272582 G>T maps to ENST00000457693 S578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:237405952 G>A maps to ENST00000457693 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:237272569 G>A maps to ENST00000457693 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:113633673 G>A maps to ENST00000416617 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:113633673 G>A maps to ENST00000416617 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:2638104 G>T maps to NM_152558.3 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:2629713 G>A maps to NM_152558.3 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:51929109 C>T maps to NM_152397.2 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:197670810 T>C maps to NM_001134435.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr15:67677301 T>C maps to NM_001031715.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:67664696 G>A maps to NM_001031715.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr16:19745075 G>A maps to NM_153208.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:19800168 G>A maps to NM_153208.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:90999444 G>A maps to NM_003870.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:90983842 C>T maps to NM_003870.3 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:91029326 C>T maps to NM_003870.3 D1329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:90997711 G>T maps to NM_003870.3 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:90996085 C>T maps to NM_003870.3 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr15:91016945 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr15:91016136 G>T maps to NM_003870.3 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr15:91020902 G>A maps to NM_003870.3 K1037K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:75967665 C>A maps to NM_006633.2 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:75993921 C>T maps to NM_006633.2 I1439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:75893321 G>A maps to NM_006633.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr5:75996928 G>T maps to NM_006633.2 G1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:75866443 C>T maps to NM_006633.2 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:75993825 A>G maps to NM_006633.2 Q1407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr5:75886317 G>A maps to NM_006633.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr5:75989197 T>C maps to NM_006633.2 I1308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:75973147 A>G maps to NM_006633.2 S1211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr1:156520101 G>T maps to NM_178229.4 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr1:156500096 T>A maps to NM_178229.4 K1402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:156497824 C>T maps to NM_178229.4 T1567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:156507088 C>T maps to NM_178229.4 P1102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:156533378 G>T maps to NM_178229.4 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:156533387 G>A maps to NM_178229.4 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:156504978 G>A maps to NM_178229.4 D1161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:12957129 C>T maps to ENST00000429247 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:12950002 G>A maps to ENST00000429247 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr3:12983256 G>A maps to ENST00000429247 Y44Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:12955014 G>A maps to ENST00000429247 C743C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr3:12978125 C>T maps to ENST00000429247 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:12983247 C>T maps to ENST00000429247 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr23:53283947 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:53280309 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:53272649 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:53271077 G>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:53270966 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:53263409 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:53277314 G>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:53267374 G>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:53265598 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:53277364 C>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:280320 G>A maps to NM_001170738.1 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:266753 C>A maps to NM_001170738.1 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:274925 G>A maps to NM_001170738.1 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:266259 C>T maps to NM_001170738.1 H741H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:123143296 A>C maps to NM_178827.4 L218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:123152250 T>G maps to NM_178827.4 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:123101570 G>T maps to NM_178827.4 S616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:123152342 C>A maps to NM_178827.4 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:123152118 C>T maps to NM_178827.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr7:123152364 A>G maps to NM_178827.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr7:123097467 T>C maps to NM_178827.4 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:153284103 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:153281888 A>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:153278123 C>T did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:153279623 C>T did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:153281982 T>A did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:153284452 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:153284903 A>G did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:10261362 G>T did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr3:10283812 G>A maps to NM_001570.3 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr3:10219696 C>T maps to NM_001570.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:66610952 G>A maps to NM_007199.2 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:66641950 A>C maps to NM_007199.2 *597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr12:66638990 G>A maps to NM_007199.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr12:44171522 A>G maps to NM_016123.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr15:78732215 C>T maps to NM_004136.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:78780589 T>G maps to NM_004136.2 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:131820189 C>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:131820190 T>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:185350152 C>T maps to NM_002199.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:185310141 G>A maps to NM_002199.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:46388204 G>A maps to NM_015649.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr1:234743347 G>A maps to NM_182972.2 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:234743392 G>A maps to NM_182972.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr19:50165871 T>C maps to NM_001571.5 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:50166660 T>C maps to NM_001571.5 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:401481 G>A maps to NM_002460.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:407567 A>G maps to NM_002460.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr7:128587093 A>T maps to NM_001098629.1 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:128587984 G>A maps to NM_001098629.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:128588334 G>T maps to NM_001098629.1 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:209969797 C>A maps to NM_006147.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:209964104 G>T maps to NM_006147.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr1:209964203 G>A maps to NM_006147.2 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:209968701 T>C maps to NM_006147.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr1:209968701 T>C maps to NM_006147.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr11:613428 C>T maps to NM_004031.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:612797 C>T maps to NM_004031.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:85953767 C>T maps to NM_002163.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:85942615 G>A maps to NM_002163.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:85952317 C>T maps to NM_002163.2 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:44222973 C>T maps to NM_019612.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:44222997 G>A maps to NM_019612.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:44223762 C>T maps to NM_019612.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:44097281 C>T maps to NM_001007561.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:44097050 G>A maps to NM_001007561.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:44097416 C>T maps to NM_001007561.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:227660103 C>T maps to NM_005544.2 V1117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:227662785 G>A maps to NM_005544.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:227660991 G>A maps to NM_005544.2 C821C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:227663199 A>C maps to NM_005544.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr13:110435151 C>A maps to NM_003749.2 P1083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:107979348 C>T did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:107979352 G>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:107976288 C>T did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:107975970 G>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:107977820 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:107977128 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:107979514 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:107979515 G>A did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:107978400 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:107977574 C>T did not map to a codon.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr23:107977216 G>A did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:107977906 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:107978206 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:107976398 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:107976788 C>A did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr23:107977757 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:107976195 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:107975821 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:107979261 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:107977960 C>A did not map to a codon.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr23:107978193 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:107976902 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:107978618 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:107979514 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:107976312 G>A did not map to a codon.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr23:107977383 G>A did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:107975896 C>T did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:107979364 C>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:107976576 G>T did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:107976661 T>C did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:107976662 G>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:3599721 C>T maps to NM_024337.3 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:3600750 G>A maps to NM_024337.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr5:3599826 C>T maps to NM_024337.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:3599343 G>A maps to NM_024337.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:3599421 C>T maps to NM_024337.3 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:3599400 G>A maps to NM_024337.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:3599769 C>T maps to NM_024337.3 H236H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:3600252 C>A maps to NM_024337.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:3599808 C>T maps to NM_024337.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:3599796 C>T maps to NM_024337.3 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr5:3599373 G>T maps to NM_024337.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr5:3599604 G>A maps to NM_024337.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:2749565 G>A maps to NM_033267.4 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr5:2749883 C>T maps to NM_033267.4 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:2749529 C>T maps to NM_033267.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr16:54319348 C>T maps to NM_024336.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr16:54318186 G>C maps to NM_024336.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:1881936 G>A maps to NM_016358.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:1879723 C>T maps to NM_016358.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:1879684 C>T maps to NM_016358.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr16:54966516 C>T maps to NM_005853.5 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr16:54966429 A>G maps to NM_005853.5 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:54967688 T>G maps to NM_005853.5 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr16:54967637 G>T maps to NM_005853.5 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:54966714 C>T maps to NM_005853.5 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:55363089 C>T maps to NM_024335.2 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr16:55363200 C>A maps to NM_024335.2 C437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr16:55362882 G>A maps to NM_024335.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr14:74961658 C>T maps to NM_194279.2 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:108961000 C>T maps to NM_213595.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:108957928 C>T maps to NM_014301.3 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:156696859 A>T maps to NM_030980.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:156697177 T>C maps to NM_030980.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:156697177 T>C maps to NM_030980.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr1:156697177 T>C maps to NM_030980.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:50680504 C>T maps to NM_002202.2 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr5:50685715 C>T maps to NM_002202.2 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:50685507 C>T maps to NM_002202.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:76630125 C>T maps to NM_145805.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr15:74467618 C>T maps to NM_201526.1 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:74468110 C>T maps to NM_201526.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:74467615 C>T maps to NM_201526.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr15:74467618 C>T maps to NM_201526.1 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr15:74425415 C>T maps to NM_001130137.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3517-01A-01W-0831-10 chr15:74425250 C>T maps to NM_001130137.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:74426375 T>C maps to NM_001130137.1 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:74426522 C>T maps to NM_001130137.1 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:13269292 A>G maps to NM_080826.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr20:13251242 A>G maps to NM_080826.1 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr20:13279712 G>A maps to NM_080826.1 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:13260402 C>A maps to NM_080826.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:13279766 C>T maps to NM_080826.1 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr20:13279910 G>A maps to NM_080826.1 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:13279616 C>T maps to NM_080826.1 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr20:13260456 C>T maps to NM_080826.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr14:77950698 G>A maps to NM_199296.2 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr14:77944990 C>T maps to NM_199296.2 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr14:77950767 G>C maps to NM_199296.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr14:77942005 G>A maps to NM_199296.2 R550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr7:16348215 A>G maps to NM_001101426.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:16341055 C>T maps to NM_001101426.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:16317776 C>A maps to NM_001101426.3 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:16255734 C>A maps to NM_001101426.3 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr22:35481586 T>C maps to NM_001008494.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr22:35481565 G>A maps to NM_001008494.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr22:35481586 T>C maps to NM_001008494.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr22:35481508 G>A maps to NM_001008494.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:18547601 C>T maps to NM_016368.4 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr19:18546840 C>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:18547214 C>T maps to NM_016368.4 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:310109 C>T maps to NM_032039.2 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:310109 C>T maps to NM_032039.2 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr5:52204741 T>C maps to NM_181501.1 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:52227942 T>C maps to NM_181501.1 Y946Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:52235427 C>T maps to NM_181501.1 N1029N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:52243278 A>G maps to NM_181501.1 L1161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:145532135 C>A maps to NM_003637.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr1:145533508 G>A maps to NM_003637.3 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:145532479 G>A maps to NM_003637.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:145538745 G>T maps to NM_003637.3 E953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:145532772 C>T maps to NM_003637.3 N364N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:145525079 C>T maps to NM_003637.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:145537441 C>T maps to NM_003637.3 R818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:145539727 C>T maps to NM_003637.3 Q1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:145538787 G>T maps to NM_003637.3 E967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:145537497 T>C maps to NM_003637.3 N836N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:145533916 T>C maps to NM_003637.3 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:68643715 T>G maps to ENST00000423218 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:68657110 G>A maps to ENST00000423218 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr15:68617564 G>A maps to ENST00000423218 Y742Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:68612684 G>A maps to ENST00000423218 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:68649616 G>A maps to ENST00000423218 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:68603391 G>A maps to ENST00000423218 G1039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:68607999 G>A maps to ENST00000423218 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:52385774 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:52361726 C>T maps to NM_002203.3 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr5:52285351 G>T maps to NM_002203.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:52356864 C>T maps to NM_002203.3 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:52377520 G>T maps to NM_002203.3 E1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:52377520 G>T maps to NM_002203.3 E1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:52379276 C>T maps to NM_002203.3 F1084F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:52368977 C>T maps to NM_002203.3 N820N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:52338019 C>A maps to NM_002203.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr17:42455813 G>A maps to NM_000419.3 N670N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:42461275 G>A maps to NM_000419.3 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:42453680 C>T maps to NM_000419.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:42458005 G>A maps to NM_000419.3 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:42462331 G>T maps to NM_000419.3 Y261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:42460888 C>T maps to NM_000419.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr17:42461275 G>A maps to NM_000419.3 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr17:42452467 C>T maps to NM_000419.3 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr17:42463480 G>A maps to NM_000419.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr17:48158702 A>T maps to NM_002204.2 V950V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:48156199 G>A maps to NM_002204.2 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:48148247 T>A maps to NM_002204.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:48158723 C>T maps to NM_002204.2 F957F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:48148825 G>A maps to NM_002204.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr17:48148247 T>C maps to NM_002204.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:182347254 T>C maps to NM_000885.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:182388978 T>A did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr2:182344980 G>T maps to NM_000885.4 G248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:182374459 C>T maps to NM_000885.4 R591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr2:182344883 C>T maps to NM_000885.4 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:182394350 G>A maps to NM_000885.4 K838K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr2:182339908 T>C maps to NM_000885.4 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:182360593 A>G maps to NM_000885.4 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr2:182350654 A>G maps to NM_000885.4 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr12:54795450 T>C did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:54812859 G>A maps to NM_002205.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:54803130 G>A maps to NM_002205.2 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:54798245 C>T maps to NM_002205.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:54812949 G>A maps to NM_002205.2 H11H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:54797443 G>A maps to NM_002205.2 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr12:54795877 C>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:54801941 G>A maps to NM_002205.2 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:54795450 T>C did not map to a codon.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr2:173334097 T>C maps to ENST00000264106 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr2:173352084 C>T maps to ENST00000264106 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:173338957 C>A maps to ENST00000264106 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:173356214 T>C maps to ENST00000264106 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:173349577 C>T maps to ENST00000264106 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:56094067 C>T maps to ENST00000347027 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:56092684 C>T maps to ENST00000347027 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:56086714 A>G maps to ENST00000347027 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:56090709 G>T maps to ENST00000347027 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr10:15628599 C>T maps to NM_003638.1 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:15649677 G>A maps to NM_003638.1 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr10:15600155 G>A maps to NM_003638.1 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr10:15600138 A>G maps to NM_003638.1 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:15686118 G>A maps to NM_003638.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr10:15720741 T>C maps to NM_003638.1 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr10:15726084 T>C maps to NM_003638.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr10:15600138 A>G maps to NM_003638.1 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:15646218 T>C maps to NM_003638.1 E702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:15649741 G>A maps to NM_003638.1 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr10:15600138 A>G maps to NM_003638.1 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr10:15600138 A>G maps to NM_003638.1 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr10:15600162 G>A maps to NM_003638.1 A892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:15655756 C>T maps to NM_003638.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:37783230 G>T maps to NM_002207.2 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:37560793 G>T maps to NM_002207.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:37792012 C>T maps to NM_002207.2 R832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr3:37567541 C>T maps to NM_002207.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:37845354 C>T maps to NM_002207.2 Y977Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr3:37860446 A>G maps to NM_002207.2 E1025E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr3:37860446 A>G maps to NM_002207.2 E1025E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr3:37860446 A>G maps to NM_002207.2 E1025E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:31429511 C>T maps to ENST00000444228 N888N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr16:31435466 G>A maps to ENST00000444228 T1084T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr16:31414963 G>T maps to ENST00000444228 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:31435263 C>T maps to ENST00000444228 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr17:3654967 G>A maps to NM_002208.4 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:3651267 C>T maps to NM_002208.4 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:3632788 G>A maps to NM_002208.4 F965F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:3660365 C>T maps to NM_002208.4 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:3663534 G>A maps to NM_002208.4 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:30485550 C>G maps to NM_002209.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:30500670 G>T maps to NM_002209.2 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:30510439 A>G maps to NM_002209.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr16:30507429 G>T maps to NM_002209.2 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:30492795 G>T maps to NM_002209.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:30507431 A>G maps to NM_002209.2 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr16:30486635 G>T maps to NM_002209.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:30516581 G>A maps to NM_002209.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr16:30490515 C>T maps to NM_002209.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:30516596 C>A maps to NM_002209.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr16:30486635 G>A maps to NM_002209.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr16:31336718 G>A maps to NM_001145808.1 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr16:31336304 T>C maps to NM_001145808.1 N773N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:31309241 C>A maps to NM_001145808.1 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:187514612 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:187540444 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:187516813 C>T maps to NM_002210.3 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:187529331 G>A maps to NM_002210.3 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:187533541 G>A maps to NM_002210.3 W829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:31371329 T>A maps to NM_000887.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr16:31383943 C>T maps to NM_000887.3 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:31373160 G>A maps to NM_000887.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:31372439 G>A maps to NM_000887.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:31391911 G>A maps to NM_000887.3 Q1081Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:31374293 C>T maps to NM_000887.3 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr16:31374634 G>T maps to NM_000887.3 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr10:33200928 G>A maps to ENST00000374956 C531C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:33221460 A>G maps to ENST00000374956 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:33200530 A>G maps to ENST00000374956 C592C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:33209232 G>A maps to ENST00000374956 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr10:33211226 T>G maps to ENST00000374956 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr10:33209232 G>A maps to ENST00000374956 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:9554307 T>C maps to NM_004763.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:9558775 G>A maps to NM_004763.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:9548297 C>A maps to NM_004763.3 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:70522348 A>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:70522389 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:70522266 A>G did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:70522291 A>G did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:70523316 A>G did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:70522290 A>G did not map to a codon.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr19:3941068 T>C maps to NM_170678.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr21:46310003 G>A maps to NM_000211.3 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr21:46306324 G>A maps to NM_000211.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr21:46320315 G>A maps to NM_000211.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr21:46313369 C>T maps to NM_000211.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:46309258 G>T maps to NM_000211.3 C603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr21:46320303 G>A maps to NM_000211.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr21:46323313 C>G maps to NM_000211.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr21:46313399 G>T maps to NM_000211.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:45369776 A>G maps to NM_000212.2 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:45369788 G>A maps to NM_000212.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:45368348 G>A maps to NM_000212.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr17:45368327 T>C maps to NM_000212.2 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr17:45362001 G>A maps to NM_000212.2 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:45380165 T>C maps to NM_000212.2 D698D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:63920135 C>T maps to ENST00000371092 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:73723516 G>A maps to NM_001005619.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:73738744 C>T maps to NM_001005619.1 D955D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:73738663 C>T maps to NM_001005619.1 D928D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr17:73739929 G>A maps to NM_001005619.1 A1033A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:73753368 C>T maps to NM_001005619.1 S1752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:73724482 C>T maps to NM_001005619.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:73747157 C>T maps to NM_001005619.1 Y1253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:73746234 G>A maps to NM_001005619.1 Q1120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:73750891 C>A maps to NM_001005619.1 S1448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:124492724 G>A maps to NM_002213.3 C576C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:124483264 G>A maps to NM_002213.3 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:124592291 C>T did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr3:124515541 C>T maps to NM_002213.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:161051920 A>G maps to NM_000888.3 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr2:161055749 A>G maps to NM_000888.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:160994161 G>A maps to NM_000888.3 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:160980352 C>A maps to NM_000888.3 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:160994125 G>A maps to NM_000888.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:160994229 C>A maps to NM_000888.3 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr12:53590401 T>C maps to NM_000889.1 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr12:53590464 G>A maps to NM_000889.1 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:53588113 G>A maps to NM_000889.1 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr12:53586153 G>A maps to NM_000889.1 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:53590470 C>T maps to NM_000889.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:53590407 C>T maps to NM_000889.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:53590401 T>C maps to NM_000889.1 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr12:53590403 C>A maps to NM_000889.1 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:20421483 C>T maps to NM_002214.2 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:20418788 C>T maps to NM_002214.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:20438547 C>T maps to NM_002214.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:20449574 T>C maps to NM_002214.2 D755D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:20445780 C>T maps to NM_002214.2 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr13:102220062 T>C maps to NM_004791.1 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:102231671 C>T maps to NM_004791.1 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:52816026 C>T maps to NM_002215.2 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr3:52820402 C>T maps to NM_002215.2 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr3:52818390 C>T maps to NM_002215.2 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:52820319 G>T maps to NM_002215.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:52822060 C>T maps to NM_002215.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:52813450 C>A maps to NM_002215.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:7772018 T>C maps to NM_002216.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:7759657 C>T maps to NM_002216.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr10:7773925 G>A maps to NM_002216.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:7769666 C>T maps to NM_002216.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:7774341 C>T maps to NM_002216.2 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:7762889 C>T maps to NM_002216.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:7765502 C>T maps to NM_002216.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:7762889 C>T maps to NM_002216.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr10:7791260 C>T maps to NM_002216.2 F935F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:7751088 G>A maps to NM_002216.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:7791194 C>T maps to NM_002216.2 D913D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:52836798 C>A maps to NM_002217.3 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr3:52830615 C>T maps to NM_002217.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:52839830 G>T maps to NM_002217.3 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:52837987 C>T maps to NM_002217.3 N609N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr3:52840986 C>G maps to NM_002217.3 Y709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:52834576 C>T maps to NM_002217.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:52850919 C>T maps to ENST00000485816 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:52848037 G>A maps to ENST00000485816 D897D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr10:7621893 C>T maps to ENST00000256861 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:7618968 G>A maps to ENST00000256861 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:7608173 C>T maps to ENST00000256861 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr10:7621799 G>A maps to ENST00000256861 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:7608140 G>A maps to ENST00000256861 N793N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr10:7618917 G>T maps to ENST00000256861 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:7684020 C>T maps to ENST00000256861 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr10:7621865 G>A maps to ENST00000256861 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr10:7679317 G>A maps to ENST00000256861 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr10:7618500 A>G maps to ENST00000256861 D631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr10:7618797 G>A maps to ENST00000256861 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:7621974 G>A maps to ENST00000256861 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr10:7679197 G>A maps to ENST00000256861 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:54785086 G>A did not map to a codon.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr23:54784282 C>T did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:54776519 G>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:54785156 C>T did not map to a codon.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr23:54784025 C>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:54777528 G>A did not map to a codon.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr23:54784197 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:54783778 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:54776407 G>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:54800556 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:54783891 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:54784765 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:54817415 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:54777533 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:54823488 G>T did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:54784006 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:54814961 A>T did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:54784300 G>C did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:54785180 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:54817286 C>T did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:54785125 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:156667158 C>T maps to NM_005546.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr5:156608042 A>T maps to NM_005546.3 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:156608059 G>A maps to NM_005546.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:156644898 T>A maps to NM_005546.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:160850420 G>A maps to NM_017625.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr1:160914938 G>A maps to NM_080878.2 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:78618569 C>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:78622628 C>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:78619011 C>A did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr23:78618541 T>C did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:78619010 C>T did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:78622661 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:231742780 C>T maps to NM_030926.4 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:231740471 G>T maps to NM_030926.4 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr20:3204032 G>A maps to NM_033453.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:93460300 C>T maps to NM_014216.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:41794644 C>T maps to NM_002220.1 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:226924778 G>A maps to NM_002221.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:226925105 G>A maps to NM_002221.3 N18N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr1:226924247 C>T maps to NM_002221.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:41223585 G>A maps to NM_025194.2 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:4842227 C>T maps to ENST00000356617 R2349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:4712500 C>T maps to ENST00000356617 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr3:4726800 A>C maps to ENST00000356617 R1201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:4706901 G>A maps to ENST00000356617 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:4733006 C>T maps to ENST00000356617 C1332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:4687078 C>T maps to ENST00000356617 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:4687280 C>T maps to ENST00000356617 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:4723090 C>T maps to ENST00000356617 I1046I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:4878492 C>A maps to ENST00000356617 A2686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:4687078 C>T maps to ENST00000356617 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:4829795 G>T maps to ENST00000356617 E2259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr3:4704847 A>G maps to ENST00000356617 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:4821244 G>A maps to ENST00000356617 S2099S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:4704847 A>G maps to ENST00000356617 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr3:4703821 T>C maps to ENST00000356617 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:4824391 C>T maps to ENST00000356617 N2157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:4669537 C>T maps to ENST00000356617 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr12:26592231 G>A maps to NM_002223.2 T2157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:26553156 C>T maps to NM_002223.2 T2478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:26809372 A>G maps to NM_002223.2 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:26648162 G>A maps to NM_002223.2 R1702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:26592231 G>A maps to NM_002223.2 T2157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:26731667 A>G maps to NM_002223.2 C1536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr12:26634156 A>G maps to NM_002223.2 H2010H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:26703214 C>A maps to NM_002223.2 E1680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:26775333 C>A maps to NM_002223.2 E1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:26629849 C>A maps to NM_002223.2 E2072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:26733073 A>G maps to NM_002223.2 T1465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:26834897 G>A maps to NM_002223.2 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:26839562 T>C maps to NM_002223.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:26753042 C>A did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:26835539 T>A maps to NM_002223.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr12:26755413 T>C maps to NM_002223.2 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr12:26553123 C>A maps to NM_002223.2 V2489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr12:26839562 T>C maps to NM_002223.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr12:26809375 C>T maps to NM_002223.2 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr12:26839562 T>C maps to NM_002223.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr12:26580974 C>T maps to NM_002223.2 A2272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr6:33650386 C>T maps to ENST00000374316 S1521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr6:33635678 G>A maps to ENST00000374316 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr6:33626589 G>T maps to ENST00000374316 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:33645292 C>T maps to ENST00000374316 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr6:33648146 G>C maps to ENST00000374316 V1422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:33636849 G>A maps to ENST00000374316 E702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:33648441 C>T maps to ENST00000374316 N1487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:33630360 G>A maps to ENST00000374316 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:33648390 C>T maps to ENST00000374316 S1470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:33657929 C>A maps to ENST00000374316 T2329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr6:33647865 G>T maps to ENST00000374316 E1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:33631648 C>T maps to ENST00000374316 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:33653921 C>T maps to ENST00000374316 G1920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr6:33623570 C>T maps to ENST00000374316 N63N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:33639959 C>T maps to ENST00000374316 D961D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:106075176 G>A maps to NM_033397.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:106074471 G>A maps to NM_033397.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:106075668 C>T maps to NM_033397.2 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:106075458 G>A maps to NM_033397.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:106074921 G>A maps to NM_033397.2 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:96993313 G>A maps to ENST00000420728 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:96993310 C>T maps to ENST00000420728 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:19127144 C>T maps to NM_001034841.3 C454C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr21:35190665 C>T maps to NM_003024.2 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr21:35237556 C>A maps to NM_003024.2 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:35138280 T>G maps to NM_003024.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr21:35169725 C>T maps to NM_003024.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:35140023 C>T maps to NM_003024.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr21:35257410 C>T maps to NM_003024.2 R1581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:24428167 T>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:24536386 G>A maps to NM_006277.2 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:24524838 A>G maps to NM_006277.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:24438974 T>C maps to NM_006277.2 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:24524838 A>G maps to NM_006277.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr2:24438974 T>C maps to NM_006277.2 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:24522815 G>A maps to NM_006277.2 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr1:152883706 C>A maps to NM_005547.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:152883697 G>A maps to NM_005547.2 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:185270653 G>A maps to NM_006469.4 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:185276172 T>G maps to NM_006469.4 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:185270599 A>G maps to NM_006469.4 H287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:128253618 G>A maps to NM_017969.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:128250972 C>A maps to NM_017969.2 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:128247438 C>A maps to NM_017969.2 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:49247794 G>A maps to NM_182575.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:10629301 G>A maps to NM_000214.2 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:10625851 A>G maps to NM_000214.2 D722D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr20:10625565 G>A maps to NM_000214.2 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr20:10622536 G>T maps to NM_000214.2 S859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:10625550 G>A maps to NM_000214.2 C768C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:10626697 G>A maps to NM_000214.2 N640N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:10633194 C>T maps to NM_000214.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:105617981 G>A maps to NM_002226.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:105609121 C>T maps to NM_002226.3 P1209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:105618356 G>A maps to NM_002226.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:105615133 G>A maps to NM_002226.3 D656D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:105612786 C>A maps to NM_002226.3 G882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr14:105614205 C>A maps to NM_002226.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:105622207 G>A maps to NM_002226.3 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:65316528 G>A maps to NM_002227.2 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:65311216 C>T maps to NM_002227.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:65309803 C>T maps to NM_002227.2 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:65344790 G>A maps to NM_002227.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:65323362 G>T maps to NM_002227.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr9:5050789 A>G maps to NM_004972.3 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:5070009 C>T maps to NM_004972.3 N533N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:5089699 C>T maps to NM_004972.3 C866C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:5072562 T>C maps to NM_004972.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr9:5070021 T>C maps to NM_004972.3 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:5064981 G>T maps to NM_004972.3 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:5089769 G>T maps to NM_004972.3 E890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:5072559 C>T maps to NM_004972.3 Y570Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:5072562 T>C maps to NM_004972.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr9:5126757 A>G maps to NM_004972.3 R1122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:5072562 T>C maps to NM_004972.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:5054767 G>T maps to NM_004972.3 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:5126701 G>T maps to NM_004972.3 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr9:5050789 A>G maps to NM_004972.3 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr9:5050789 A>G maps to NM_004972.3 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr9:5072550 A>G maps to NM_004972.3 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:5070027 A>G maps to NM_004972.3 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr9:5078358 C>A maps to NM_004972.3 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr9:5072541 A>G maps to NM_004972.3 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr9:5072535 C>T maps to NM_004972.3 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr9:5078358 C>A maps to NM_004972.3 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr9:5078361 A>G maps to NM_004972.3 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr9:5081728 T>C maps to NM_004972.3 Y813Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr9:5072541 A>G maps to NM_004972.3 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr9:5072535 C>T maps to NM_004972.3 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr19:17949182 G>A maps to NM_000215.3 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:17945418 G>A maps to NM_000215.3 R771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:17947971 G>A maps to NM_000215.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:17943427 G>A maps to NM_000215.3 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:17945717 C>T maps to NM_000215.3 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:17940955 C>T maps to NM_000215.3 E1056E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:17945696 G>A maps to NM_000215.3 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr19:17947959 G>A maps to NM_000215.3 H588H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr19:17953855 T>C maps to NM_000215.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:17943472 G>A maps to NM_000215.3 G845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr19:17948860 C>A maps to NM_000215.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr19:17954227 A>T maps to NM_000215.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:6107361 C>T maps to NM_001099433.1 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:6064098 G>A maps to NM_001099433.1 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:6064098 G>A maps to NM_001099433.1 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:6031496 T>C maps to NM_001099433.1 E797E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr4:6064092 G>A maps to NM_001099433.1 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr4:6114472 G>A maps to NM_001099433.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr4:6082015 C>T maps to NM_001099433.1 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr4:6086640 C>A maps to NM_001099433.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr4:6086640 C>A maps to NM_001099433.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:6107256 C>T maps to NM_001099433.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr4:6064056 G>A maps to NM_001099433.1 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:6055784 C>A maps to NM_001099433.1 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:6086638 T>C maps to NM_001099433.1 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:6086640 C>A maps to NM_001099433.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr4:6086638 T>C maps to NM_001099433.1 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:6082021 C>T maps to NM_001099433.1 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:147040951 C>T maps to NM_014790.3 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr5:147027949 G>A maps to NM_014790.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:147023704 G>A maps to NM_014790.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:147019218 G>T maps to NM_014790.3 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:147040852 C>T maps to NM_014790.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:147024556 T>C maps to NM_014790.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:147051260 G>A maps to NM_014790.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:147040666 C>T maps to NM_014790.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr5:147040768 G>A maps to NM_014790.3 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr10:133931041 C>A maps to NM_001105521.2 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:133930993 C>T maps to NM_001105521.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:133930822 C>T maps to NM_001105521.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr10:133967291 G>A maps to NM_001105521.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:27071112 C>T maps to NM_021219.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr11:134014175 C>T maps to NM_032801.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:134010570 C>T maps to NM_032801.3 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:15497072 G>T maps to NM_004973.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr6:15496484 G>A maps to NM_004973.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:15410530 C>A maps to NM_004973.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr6:15487703 G>A maps to NM_004973.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr6:15496952 G>A maps to NM_004973.2 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:15496484 G>A maps to NM_004973.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:15501480 C>T maps to NM_004973.2 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr6:15487599 G>T maps to NM_004973.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr6:15496643 G>A maps to NM_004973.2 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr7:139790914 G>A maps to NM_030647.1 G935G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:139829299 A>G maps to NM_030647.1 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr7:139824535 T>A maps to NM_030647.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr10:64950668 A>G maps to NM_032776.1 Y2092Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:64974009 G>A maps to NM_032776.1 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:27230280 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:27221851 C>T maps to NM_001145348.1 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:42127825 G>A maps to NM_005090.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:42138967 C>T maps to NM_005090.3 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr15:42133103 G>A did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr15:42136769 C>T maps to NM_005090.3 C558C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:42137878 C>T maps to NM_005090.3 Y698Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:75149493 G>A maps to NM_020647.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr8:75156994 G>A maps to NM_020647.2 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:75227148 G>A maps to NM_020647.2 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:75227255 C>A maps to NM_020647.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr20:42788652 G>A maps to NM_020433.4 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr20:42788955 C>T maps to NM_020433.4 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr20:42747217 G>T maps to NM_020433.4 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr20:42815177 G>A maps to NM_020433.4 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:87678035 G>T maps to NM_020655.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:87678419 C>T maps to NM_020655.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:87678281 C>T maps to NM_020655.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr16:87678137 G>C maps to NM_020655.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr16:87677885 C>T maps to NM_020655.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr16:87723888 C>T maps to NM_020655.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:87637036 C>T maps to NM_020655.2 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr14:24041119 G>A maps to NM_032452.2 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr8:143747255 C>T maps to NM_003724.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:143745920 G>A maps to NM_003724.2 C519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:96124635 C>T maps to NM_003772.3 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:96125217 G>T maps to NM_003772.3 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:12903367 C>A maps to NM_002229.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:39913987 G>A maps to NM_021991.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:39919375 C>T maps to NM_021991.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr17:39923762 G>A maps to NM_021991.2 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr17:39927935 T>C maps to NM_021991.2 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:39914754 C>A maps to NM_021991.2 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:8504843 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:8503640 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:8565121 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:8538563 C>A did not map to a codon.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr23:8538694 C>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:8555879 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:8565161 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr23:8538694 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:8522062 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:8536406 G>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:8504872 A>G did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:8553364 T>C did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:8503820 A>G did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:8503698 A>C did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:8591672 T>C did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:8591672 T>C did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:124157797 C>T maps to NM_001024660.3 R1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:124132315 G>T did not map to a codon.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr3:124415079 G>A maps to NM_001024660.3 T2559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:124352709 T>G maps to NM_001024660.3 G1825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr3:124174097 G>A maps to NM_001024660.3 T1207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:123988075 C>A maps to NM_001024660.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:124415064 C>T maps to NM_001024660.3 H2554H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:124376625 A>G maps to NM_001024660.3 R2003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:124390732 C>T maps to NM_001024660.3 F2309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:124103813 C>T maps to NM_001024660.3 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:124438049 C>T maps to NM_001024660.3 S2898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr3:124053278 G>A maps to NM_001024660.3 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:124114127 C>T maps to NM_001024660.3 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr3:124114157 G>A maps to NM_001024660.3 A711A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:124237248 T>C maps to NM_003947.4 D1644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:124415064 C>T maps to NM_001024660.3 H2554H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:124418863 G>A maps to NM_001024660.3 V2660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr3:123953790 G>T did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr3:124413266 A>G maps to NM_001024660.3 P2498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:124175533 C>T maps to NM_001024660.3 H1269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr3:124438028 C>T maps to NM_001024660.3 N2891N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:124436190 C>T maps to NM_001024660.3 Q2792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:124157817 A>G maps to NM_001024660.3 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr3:124398309 G>A maps to NM_001024660.3 T2441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr9:710975 C>T maps to NM_015158.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:711527 C>T maps to NM_015158.2 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:712565 C>T maps to NM_015158.2 C600C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:712652 T>C maps to NM_015158.2 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:712346 C>T maps to NM_015158.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:713321 C>T maps to NM_015158.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:712442 C>T maps to NM_015158.2 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:732410 A>T maps to NM_015158.2 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr9:712598 C>T maps to NM_015158.2 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:712712 C>T maps to NM_015158.2 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:11280609 G>A maps to NM_015493.6 D823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr1:62728926 C>T maps to NM_181712.4 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr1:62739026 C>T maps to NM_181712.4 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr1:62740016 T>C maps to NM_181712.4 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr1:62740087 C>A maps to NM_181712.4 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr1:62740564 G>A maps to NM_181712.4 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:62740331 G>T maps to NM_181712.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr17:40265765 G>A maps to NM_021078.2 R805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:40266544 G>A maps to NM_021078.2 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:20113889 C>T maps to NM_003884.4 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:20167465 G>T maps to NM_003884.4 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:20167576 G>T maps to NM_003884.4 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:20181724 G>T maps to NM_003884.4 E625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:20156372 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:20167542 C>T maps to NM_003884.4 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:20189911 G>A maps to NM_003884.4 W746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:20167407 G>A maps to NM_003884.4 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:65486178 G>A maps to NM_182710.1 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:65486549 C>T maps to NM_182710.1 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:149922786 A>G maps to NM_007044.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr18:44626630 G>T maps to ENST00000356157 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:44584698 G>A maps to ENST00000356157 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr18:44589401 A>G maps to ENST00000356157 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:57789766 C>T maps to NM_005886.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr16:57778418 C>A maps to NM_005886.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:15370550 C>T maps to NM_201628.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:15421414 C>T maps to NM_201628.2 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:15382592 C>T maps to NM_201628.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:15441124 C>T maps to NM_201628.2 N774N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:15390115 C>T maps to NM_201628.2 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:15441058 C>T maps to NM_201628.2 D752D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:15420751 G>A maps to NM_201628.2 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:15392283 G>A maps to NM_015209.2 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:170371184 A>G maps to ENST00000419050 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:170366659 T>G maps to NM_006063.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr2:170366587 C>T maps to NM_006063.2 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:127642851 C>T maps to NM_207335.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:127642968 T>A maps to NM_207335.2 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr3:127646782 G>A maps to NM_207335.2 W416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr15:65369923 C>T maps to NM_001101362.2 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:32910159 A>G maps to NM_015483.2 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:32909136 C>T maps to NM_015483.2 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:32910228 C>T maps to NM_015483.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr11:105924395 G>A maps to NM_198439.2 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:105924395 G>A maps to NM_198439.2 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:105924209 G>A maps to NM_198439.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr11:105924395 G>A maps to NM_198439.2 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:47594907 G>A maps to NM_018095.4 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:47597233 G>A maps to NM_018095.4 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr3:42727419 T>C maps to NM_152393.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:42727160 G>A maps to NM_152393.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:42727229 C>T maps to NM_152393.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:42730191 C>T maps to NM_152393.2 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr13:41705066 A>G maps to NM_152903.4 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:41705573 G>A maps to NM_152903.4 C358C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:41706151 G>A maps to NM_152903.4 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:41767337 A>G maps to NM_032138.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:41768027 G>A maps to NM_032138.4 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:41767283 T>C maps to NM_032138.4 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:67054329 G>A maps to NM_032505.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:67058347 G>T maps to NM_032505.2 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:67053714 C>A maps to NM_032505.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:67054512 A>C maps to NM_032505.2 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr3:67053984 T>C maps to NM_032505.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:85262220 G>A maps to NM_020122.4 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:85273315 C>T maps to NM_020122.4 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr12:5020810 C>T maps to NM_000217.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:5020762 C>T maps to NM_000217.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:5021005 G>A maps to NM_000217.2 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr12:5021227 T>C maps to NM_000217.2 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:5020687 C>T maps to NM_000217.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr12:5021641 G>A maps to NM_000217.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:5020693 G>A maps to NM_000217.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:5021170 G>A maps to NM_000217.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:5020693 G>A maps to NM_000217.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:5020975 G>A maps to NM_000217.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:111061265 G>A maps to NM_005549.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:111060911 G>T maps to NM_005549.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr1:111060809 A>G maps to NM_005549.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:111061292 G>A maps to NM_005549.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:111060743 C>T maps to NM_005549.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr1:111060809 A>G maps to NM_005549.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:111060743 C>T maps to NM_005549.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr1:111145943 T>C maps to NM_004974.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:111146660 G>A maps to NM_004974.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:111216552 A>G maps to NM_002232.3 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:111215835 G>A maps to NM_002232.3 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:111216507 G>A maps to NM_002232.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:111216990 G>T maps to NM_002232.3 Y147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr1:111217038 G>A maps to NM_002232.3 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr11:30033739 G>A maps to NM_002233.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:30034063 G>A maps to NM_002233.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr11:30034117 G>C maps to NM_002233.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:30032626 G>T maps to NM_002233.2 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:30034090 T>A maps to NM_002233.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:30034021 G>A maps to NM_002233.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr11:30032881 C>A maps to NM_002233.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:30032949 G>A maps to NM_002233.2 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:30032388 C>A maps to NM_002233.2 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:30033966 G>A maps to NM_002233.2 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr11:30032815 G>A maps to NM_002233.2 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:5153831 C>T maps to NM_002234.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:5154302 G>A maps to NM_002234.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:5154332 C>T maps to NM_002234.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr12:5153894 C>T maps to NM_002234.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr12:5153831 C>T maps to NM_002234.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:4919788 G>A maps to NM_002235.3 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:4920760 G>T maps to NM_002235.3 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:4920385 C>T maps to NM_002235.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:4920577 C>A maps to NM_002235.3 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr19:49574066 C>T maps to NM_031886.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:155838591 C>T maps to NM_172160.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:156009753 C>T maps to NM_172159.3 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:156232160 C>T maps to NM_172159.3 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:156254532 A>G maps to NM_172159.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:156234149 G>A maps to NM_172159.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:7828430 G>T maps to NM_004732.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr20:47989825 G>A maps to NM_004975.2 D757D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:47991073 G>A maps to NM_004975.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr20:48098513 G>A maps to NM_004975.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:47990839 G>A maps to NM_004975.2 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr20:47991223 A>G maps to NM_004975.2 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:48098545 G>T maps to NM_004975.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:73480178 C>T maps to NM_004770.2 H70H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:73850022 C>T maps to NM_004770.2 D811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:73480332 G>T maps to NM_004770.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:73480446 C>T maps to NM_004770.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:73480428 C>T maps to NM_004770.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr8:73848483 C>T maps to NM_004770.2 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:73850088 C>T maps to NM_004770.2 C833C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:73849336 C>T maps to NM_004770.2 Q583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:73848939 T>C maps to NM_004770.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr8:73848939 T>C maps to NM_004770.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr8:73849038 C>T maps to NM_004770.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:17793357 C>T maps to NM_001112741.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:17793864 G>A maps to NM_001112741.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:17793339 G>A maps to NM_001112741.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:17757686 C>T maps to NM_001112741.1 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr11:17794077 A>C maps to NM_001112741.1 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:17793312 C>T maps to NM_001112741.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:17757917 C>T maps to NM_001112741.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr11:17803256 G>T maps to NM_001112741.1 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:17803274 G>A maps to NM_001112741.1 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr12:75444802 A>G maps to NM_139137.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:75601403 G>A maps to NM_139137.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:75601436 G>A maps to NM_139137.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr12:75601157 G>A maps to NM_139137.2 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:75444935 C>T maps to NM_139137.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:50831808 G>A maps to NM_004977.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:110765854 C>A maps to NM_004978.4 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:48820018 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:48826068 C>T did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:48826536 C>T did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:48819869 G>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:48819931 G>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:48823472 A>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:48826247 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:48825776 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:48825716 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:48825997 G>T did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:48819925 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:48819933 C>T did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:48819915 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:48826167 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:119915498 G>T maps to NM_012281.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:119915210 C>T maps to NM_012281.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:119915528 C>T maps to NM_012281.2 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr7:120385962 C>T maps to NM_012281.2 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr7:119915012 C>T maps to NM_012281.2 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:119915153 C>T maps to NM_012281.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:120385962 C>T maps to NM_012281.2 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:120385946 C>T maps to NM_012281.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr7:120373092 C>T maps to NM_012281.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr7:120382616 C>T maps to NM_012281.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr7:120387857 G>A maps to NM_012281.2 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr7:119915721 G>T maps to NM_012281.2 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr1:112525120 G>A maps to ENST00000315987 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:112524862 C>T maps to ENST00000315987 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:112524694 G>A maps to ENST00000315987 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:112524272 C>T maps to ENST00000315987 W359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:112318746 C>T maps to ENST00000315987 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:112524505 G>A maps to ENST00000315987 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr21:35821695 G>A maps to NM_000219.3 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr21:35821815 G>A maps to NM_000219.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:108868048 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:108868111 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:108868202 A>T did not map to a codon.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr21:35743073 A>G maps to NM_172201.1 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr11:74168467 C>T maps to NM_005472.4 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:223917679 C>A maps to NM_080671.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:223917685 C>T maps to NM_080671.2 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:11052956 C>T maps to NM_002236.4 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:11053424 G>A maps to NM_002236.4 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:11052651 C>T maps to NM_002236.4 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:11053475 G>A maps to NM_002236.4 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:49620782 G>T maps to NM_002237.3 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr20:49626414 C>T maps to NM_002237.3 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:49620611 G>A maps to NM_002237.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr20:49621343 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:77659146 C>T maps to NM_012283.1 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr18:77659089 C>T maps to NM_012283.1 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:42720047 G>A maps to NM_133329.5 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:84270674 G>A maps to NM_172347.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr16:84270731 G>A maps to NM_172347.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:84270938 G>A maps to NM_172347.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:211256163 C>T maps to NM_172362.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr1:210971069 G>A maps to NM_172362.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:211192196 G>T maps to NM_172362.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:211276868 A>G maps to NM_172362.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:211192409 G>T maps to NM_172362.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:210857393 C>A maps to NM_172362.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:210857324 T>C maps to NM_172362.2 R756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:150649926 G>A maps to NM_000238.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:150644715 G>A maps to NM_000238.2 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:150649785 C>T maps to NM_000238.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:150656804 C>T maps to NM_000238.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:49951333 G>A maps to NM_012284.1 Q950Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:49934796 C>A maps to NM_012284.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:49948273 C>T maps to NM_012284.1 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:49943395 G>A maps to NM_012284.1 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:40312201 C>T maps to NM_012285.2 A970A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr17:40328183 G>A maps to NM_012285.2 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr17:40314328 G>T maps to NM_012285.2 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:40312438 A>G maps to NM_012285.2 N891N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:40321503 G>A maps to NM_012285.2 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr17:40321521 G>A maps to NM_012285.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr17:40318432 G>C maps to NM_012285.2 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr17:40312255 C>T maps to NM_012285.2 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr14:63174948 G>A maps to NM_139318.3 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr14:63269179 C>T maps to NM_139318.3 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr14:63174903 C>T maps to NM_139318.3 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:63246580 C>T maps to NM_139318.3 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:63483595 G>T maps to NM_139318.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:63316465 G>A maps to NM_139318.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:63416956 G>T maps to NM_139318.3 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr14:63175089 G>A maps to NM_139318.3 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:63174351 T>C maps to NM_139318.3 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr14:63416872 C>T maps to NM_139318.3 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr14:63447925 C>T maps to NM_139318.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr17:61613229 C>T maps to NM_030779.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:61613391 C>T maps to NM_030779.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:61607791 C>T maps to NM_030779.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:163253255 G>A maps to NM_033272.2 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:163291906 G>A maps to NM_033272.2 I585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:163291708 G>A maps to NM_033272.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:163693277 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr2:163693155 G>A maps to NM_033272.2 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:163292017 G>A maps to NM_033272.2 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:163302671 G>A maps to NM_033272.2 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:19432084 C>T maps to NM_144633.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr3:19575026 G>A maps to NM_144633.2 E920E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:19389272 G>A maps to NM_144633.2 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr3:19295237 C>T maps to NM_144633.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:19498290 A>G maps to NM_144633.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:19479729 C>T maps to NM_144633.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:19322774 T>C maps to NM_144633.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:19384205 C>T maps to NM_144633.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:19436649 C>T maps to NM_144633.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:19575410 C>T maps to NM_144633.2 S1048S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:170145871 C>T maps to NM_001034837.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr5:169780957 C>T maps to NM_001034838.1 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:103588870 C>T maps to NM_014591.4 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:103587994 G>A maps to NM_014591.4 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:96040895 C>A maps to NM_013434.4 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:96047432 T>C maps to NM_013434.4 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:96012788 C>T maps to NM_001034914.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr4:20852165 A>G maps to ENST00000382152 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr4:20736355 A>G maps to ENST00000382152 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:20751287 G>A maps to ENST00000382152 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr11:128709970 G>C maps to NM_000220.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:128709886 C>T maps to NM_000220.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:128709055 C>T maps to NM_000220.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:128709616 C>T maps to NM_000220.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr11:128709850 A>T maps to NM_000220.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr11:128709601 T>C maps to NM_000220.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:128709601 T>C maps to NM_000220.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:160011737 G>A maps to NM_002241.4 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:160012073 G>A maps to NM_002241.4 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:17409451 G>A maps to NM_000525.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr17:21319682 G>A maps to NM_021012.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr17:21319682 G>A maps to NM_021012.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr17:21319406 C>T maps to NM_021012.4 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:21318734 C>T maps to NM_021012.4 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr17:21319217 G>A maps to NM_021012.4 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:233633035 C>T maps to NM_002242.4 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:48965193 G>A maps to NM_170720.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:48965634 C>T maps to NM_170720.1 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr21:39671395 T>C maps to NM_170736.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:68128269 C>T maps to NM_018658.1 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:68129305 C>T maps to NM_018658.1 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:68172223 C>T maps to NM_000891.2 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:68171230 C>T maps to NM_000891.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:155711563 A>G maps to NM_002239.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:155711554 T>C maps to NM_002239.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:155711677 T>A maps to NM_002239.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr22:38823966 G>A maps to NM_152868.1 Y57Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr22:38824020 C>T maps to NM_152868.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:128781341 C>T maps to NM_000890.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:21919127 G>A maps to NM_004982.2 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:160057393 C>T maps to NM_004983.2 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr14:88652211 C>T maps to NM_138318.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr14:88658592 C>T maps to NM_138318.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:88654453 C>A did not map to a codon.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr14:88654445 G>A maps to NM_138318.2 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:47748882 G>A maps to NM_022055.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr14:90650863 C>T maps to NM_022054.2 N248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr14:90528866 C>T maps to NM_022054.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:90650503 C>T maps to NM_022054.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr14:90650621 C>T maps to NM_022054.2 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr14:90650863 C>T maps to NM_022054.2 N248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:90650452 A>G did not map to a codon.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr20:43378884 C>T maps to ENST00000372861 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr20:43379115 C>T maps to ENST00000372861 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr20:43379202 C>A maps to ENST00000372861 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr6:39284129 G>A maps to NM_032115.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:39286807 G>A maps to NM_032115.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:118957016 C>T maps to NM_181840.1 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:118957202 C>A maps to NM_181840.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:215408304 G>A maps to NM_001017425.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr1:215259846 G>A maps to NM_001017425.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:215342563 C>T maps to NM_001017425.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr1:215259780 G>A maps to NM_001017425.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr1:215368302 C>T maps to NM_001017425.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:26950856 C>T maps to NM_002246.2 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:26951123 G>A maps to NM_002246.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:64065618 G>A maps to ENST00000422670 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr11:64060651 C>T maps to ENST00000422670 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:39162423 G>A maps to NM_003740.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:39158872 G>A maps to NM_003740.3 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:39162095 C>T maps to NM_003740.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr6:39196841 G>A maps to NM_003740.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr6:39196737 C>T maps to NM_003740.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:38817248 G>A maps to NM_004823.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:38817446 C>T maps to NM_004823.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr19:38817898 G>A maps to NM_004823.1 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:65360923 C>T maps to NM_005714.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:65363021 C>T maps to NM_033347.1 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr8:140715143 G>T maps to NM_016601.2 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:140715157 G>A maps to NM_016601.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr8:140715169 G>A maps to NM_016601.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:140631061 G>A maps to NM_016601.2 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:140630761 C>T maps to NM_016601.2 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:78647230 C>T maps to NM_001161352.1 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr10:78729808 C>T maps to NM_001161352.1 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr10:78832989 C>T maps to NM_001161352.1 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr10:78844405 C>T maps to NM_001161352.1 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:78844405 C>T maps to NM_001161352.1 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:78651306 G>A maps to NM_001161352.1 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr10:78649240 A>T maps to NM_001161352.1 A1143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:78647241 C>A maps to NM_001161352.1 E1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:169805926 G>A maps to NM_004137.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:178560712 G>A maps to NM_005832.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:178543547 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:178543411 G>T maps to NM_005832.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:178968763 A>C maps to NM_171830.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr12:70824351 C>T maps to NM_014505.4 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:18092780 C>T maps to ENST00000222249 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:18092834 C>T maps to ENST00000222249 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:113698822 C>T maps to NM_021614.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr5:113831878 G>T maps to NM_021614.2 *580Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:113699682 C>T maps to NM_021614.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:113831788 C>T maps to NM_021614.2 H550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:113698897 C>T maps to NM_021614.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:154842344 C>T maps to NM_002249.4 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:154698472 G>A maps to NM_002249.4 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr1:154842122 G>A maps to NM_002249.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:154744706 G>T maps to NM_002249.4 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr19:44276190 G>T maps to NM_002250.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:44284896 G>T maps to NM_002250.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:44284854 C>T maps to NM_002250.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:44284855 G>T maps to NM_002250.2 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr19:44273604 G>A maps to NM_002250.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:2592621 G>A maps to NM_000218.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr11:2869031 C>T maps to NM_000218.2 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr11:2604687 T>C maps to NM_000218.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr20:62059788 C>A did not map to a codon.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr20:62076170 G>A maps to NM_172107.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:62070033 G>A maps to NM_172107.2 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:62046274 C>T maps to NM_172107.2 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr20:62038263 G>A maps to NM_172107.2 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr20:62076131 G>A maps to NM_172107.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:62076705 A>G maps to NM_172107.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr20:62046373 G>A maps to NM_172107.2 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr20:62039876 G>A maps to NM_172107.2 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:133150175 G>A maps to NM_004519.2 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr8:133492422 C>A maps to NM_004519.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:133141865 G>C maps to NM_004519.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:133142132 C>T maps to NM_004519.2 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:133187753 T>C maps to NM_004519.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:133182600 G>A maps to NM_004519.2 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:133192427 G>A maps to NM_004519.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:133141589 C>T maps to NM_004519.2 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:133152339 G>A maps to NM_004519.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr8:133142228 C>A maps to NM_004519.2 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr8:133150175 G>A maps to NM_004519.2 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr8:133196544 G>A maps to NM_004519.2 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr8:133196523 G>A maps to NM_004519.2 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr1:41304080 G>A maps to NM_004700.3 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:41304173 G>A maps to NM_004700.3 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:41289855 C>T maps to NM_004700.3 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:73815036 T>C maps to NM_001160133.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr6:73843165 C>T maps to NM_001160133.1 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:73751663 C>T maps to NM_001160133.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:73751727 C>T maps to NM_001160133.1 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:73904500 C>T maps to NM_001160133.1 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:73904617 G>T maps to NM_001160133.1 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:73830222 C>T maps to NM_001160133.1 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:73904329 A>G maps to NM_001160133.1 K683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:73843257 C>A maps to NM_001160133.1 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:73787159 C>T maps to NM_001160133.1 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:73787519 T>C maps to NM_001160133.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:50594588 G>T maps to NM_173605.1 *273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr20:43726866 G>A maps to NM_002251.3 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:99440977 G>A maps to NM_020697.2 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:99441586 G>A maps to NM_020697.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:99440383 C>T maps to NM_020697.2 C59C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:99440302 G>A maps to NM_020697.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:99440836 C>T maps to NM_020697.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:99440362 C>T maps to NM_020697.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:99440734 G>A maps to NM_020697.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:99440278 C>T maps to NM_020697.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:99440359 G>A maps to NM_020697.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr2:18113141 C>G maps to NM_002252.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr2:18113663 C>T maps to NM_002252.3 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr2:18112709 G>A maps to NM_002252.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:18112958 G>A maps to NM_002252.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr2:18112823 C>T maps to NM_002252.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:18113026 G>A maps to NM_002252.3 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:18112770 C>T maps to NM_002252.3 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr2:18113666 T>C maps to NM_002252.3 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:138656878 C>T maps to ENST00000298480 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:138667154 G>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:138660694 C>T maps to ENST00000298480 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr9:138667249 C>A maps to ENST00000298480 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:138646969 T>G maps to ENST00000298480 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr9:138662915 C>T maps to ENST00000298480 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:138676731 G>A maps to ENST00000298480 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:138606560 C>T maps to ENST00000298480 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:196309549 C>T maps to NM_198503.2 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:196227416 G>A maps to NM_198503.2 R1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:196577421 G>A maps to NM_198503.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr1:196285077 G>A maps to NM_198503.2 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:196285056 A>G maps to NM_198503.2 D816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:196303053 C>T maps to NM_198503.2 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:196461467 T>A maps to NM_198503.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr1:196367691 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr1:196394992 T>A maps to NM_198503.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:196311351 G>A maps to NM_198503.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:196398704 A>G did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr1:196250055 A>G maps to NM_198503.2 C948C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:196461467 T>A maps to NM_198503.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:36788656 C>T maps to NM_001031836.2 D975D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr8:36691177 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:36793212 T>C maps to NM_001031836.2 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr8:36644849 T>C maps to NM_001031836.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:36780116 C>T maps to NM_001031836.2 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr8:36788638 C>T maps to NM_001031836.2 H969H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:36722015 G>A maps to NM_001031836.2 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:36675179 C>A maps to NM_001031836.2 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:110986290 C>T maps to NM_014379.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr8:110986362 G>A maps to NM_014379.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:110984486 C>A maps to NM_014379.2 G331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:2718981 C>T maps to NM_133497.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr9:2717856 C>T maps to NM_133497.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:2718551 C>T maps to NM_133497.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr18:24035850 C>T maps to NM_001142730.1 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr18:24035849 G>A maps to NM_001142730.1 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr18:24126928 G>T maps to NM_001142730.1 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr12:109898512 G>A maps to NM_031954.3 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:109895803 G>T maps to NM_031954.3 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:109895808 C>T maps to NM_031954.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:109898553 G>A maps to NM_031954.3 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr17:7256821 G>T maps to NM_001002914.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:7256473 C>T maps to NM_001002914.2 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:29937180 G>T maps to NM_178863.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr16:29934512 G>A maps to NM_178863.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:34302405 G>A maps to ENST00000422820 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr5:143586927 A>G maps to NM_020768.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:67354508 G>A maps to NM_001100915.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr16:67325600 C>T maps to NM_001100915.1 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr16:67330088 G>A maps to NM_001100915.1 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:67328038 G>A maps to NM_001100915.1 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:67354713 A>G maps to NM_001100915.1 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:67327879 A>G maps to NM_001100915.1 C595C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:67337073 G>A maps to NM_001100915.1 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:73045323 G>T maps to NM_015353.1 G117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:36449465 G>A maps to NM_173562.3 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:36449445 C>T maps to NM_173562.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:77885012 T>C maps to NM_001029859.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:77885522 G>A maps to NM_001029859.1 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:77884837 G>A maps to NM_001029859.1 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr1:215759897 C>T maps to NM_016121.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:215759844 G>T maps to NM_016121.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:215777558 G>A maps to NM_016121.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:215747443 C>T maps to NM_016121.3 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:45768663 C>T maps to NM_198404.2 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:44450234 G>A maps to NM_198353.2 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr4:44176886 T>A maps to NM_198353.2 K448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:44177064 T>C maps to NM_198353.2 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:44177007 G>A maps to NM_198353.2 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:44450066 G>A maps to NM_198353.2 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:44449814 C>T maps to NM_198353.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr4:44450183 C>T maps to NM_198353.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:25301822 C>A maps to NM_017634.3 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr13:103440255 T>C maps to NM_024089.2 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr13:103440258 T>A maps to NM_024089.2 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr13:103443451 C>T maps to NM_024089.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr13:103441516 A>G maps to NM_024089.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr13:103441516 A>G maps to NM_024089.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:108350129 C>T maps to NM_153705.4 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr11:108350192 G>A maps to NM_153705.4 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr11:108350192 G>A maps to NM_153705.4 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr19:48892815 A>G maps to NM_006801.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr19:48892938 C>T maps to NM_006801.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:6509364 G>T maps to NM_006854.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:6502801 G>A maps to NM_006854.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr7:6502801 G>A maps to NM_006854.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr22:38870606 C>T maps to NM_016657.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:23395102 T>C maps to NM_001009999.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:23408840 G>A maps to NM_001009999.2 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr1:23403831 C>T maps to NM_001009999.2 Q616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:18222189 C>T maps to ENST00000388870 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr6:18186010 C>T maps to ENST00000388870 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:18160179 G>A maps to ENST00000388870 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:66995524 C>T maps to NM_012308.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:67012859 C>T maps to NM_012308.2 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr11:67020275 T>C maps to NM_012308.2 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:67013526 T>C maps to NM_012308.2 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr11:67022387 C>T maps to NM_012308.2 R1117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:122016704 A>G did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:121947648 G>T maps to ENST00000377071 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:121970783 G>T maps to ENST00000377071 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr12:122017933 T>C maps to ENST00000377069 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr2:86678323 G>A maps to NM_001146688.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:86676997 G>A maps to NM_001146688.1 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr2:86693887 T>C maps to NM_001146688.1 C467C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:86683679 C>T maps to NM_001146688.1 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:86709167 C>T maps to NM_001146688.1 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:86718176 T>C maps to NM_001146688.1 H1249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:86693887 T>C maps to NM_001146688.1 C467C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:137721890 C>T maps to NM_016604.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr5:137708406 G>A maps to NM_016604.3 W79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:137713510 C>T maps to NM_016604.3 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:137763000 C>T maps to NM_016604.3 N1542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:137727724 C>T maps to NM_016604.3 R802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:137753248 C>T maps to NM_016604.3 R1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:137761257 C>T maps to NM_016604.3 F1466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:137727724 C>T maps to NM_016604.3 R802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:137727576 G>T maps to NM_016604.3 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:137727864 T>C maps to NM_016604.3 N848N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr5:137708418 T>C maps to NM_016604.3 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:137760002 C>A maps to NM_016604.3 I1404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr5:137722108 T>C maps to NM_016604.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr5:137721784 G>C maps to NM_016604.3 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr5:137722108 T>C maps to NM_016604.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:137727671 C>A maps to NM_016604.3 S784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr5:137734081 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:44126082 G>A maps to NM_014663.2 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:44163575 C>T maps to NM_014663.2 N911N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr1:44169932 T>A maps to NM_014663.2 I1029I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:44163620 C>A maps to NM_014663.2 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:44159774 T>C did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr19:5110772 C>A maps to NM_015015.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:5135471 C>T maps to NM_015015.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:5077405 C>T maps to NM_015015.2 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:5131360 C>T maps to NM_015015.2 Y530Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:5144087 C>T maps to NM_015015.2 G887G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:5144081 C>T maps to NM_015015.2 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:5131962 G>C maps to NM_015015.2 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr9:6986380 A>T maps to NM_015061.3 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr9:7049127 A>G maps to NM_015061.3 E784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:7128094 C>T maps to NM_015061.3 S880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:6880039 C>T maps to NM_015061.3 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:7049127 A>G maps to NM_015061.3 E784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr9:7049127 A>G maps to NM_015061.3 E784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr11:94730721 C>T maps to NM_018039.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:416930 C>A maps to NM_001042603.1 E1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:402278 C>T maps to NM_001042603.1 K1504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:493229 C>T maps to NM_001042603.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr12:394750 A>T maps to NM_001042603.1 A1648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:202719810 A>G maps to ENST00000367264 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:202715397 A>G maps to ENST00000367264 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:202715085 G>A maps to ENST00000367264 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:202718089 C>A maps to ENST00000367264 E703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:53239680 G>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:53226050 T>G did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:53223692 A>G did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:53223795 C>G did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:53222252 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:53223861 C>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:53230865 A>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:53223601 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:53230751 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:53245276 C>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:53239600 C>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:53246445 C>T did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:53245373 T>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:53223694 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:53222675 C>T did not map to a codon.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr23:53225899 C>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:53226071 T>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:53239622 G>T did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:53239741 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:53230865 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr23:53246446 G>A did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:53245373 T>C did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:53223694 A>G did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:53223692 A>G did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:53240684 T>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:53246446 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:53224535 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr24:21869539 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr24:21878583 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr24:21903630 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr24:21877536 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr24:21868175 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr24:21868340 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr24:21883188 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr24:21869128 C>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr24:21870832 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:44945147 A>C did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:44929487 A>G did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:44929212 T>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:44966704 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:44922737 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:44922957 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:44950066 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:44918491 T>C did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:44918514 A>G did not map to a codon.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr23:44929141 C>T did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:44929210 G>C did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:44941969 A>G did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:44928929 A>G did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:44942736 T>C did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr23:44937741 T>C did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr23:44879926 A>G did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr23:44942736 T>C did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:44922759 C>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:44921909 G>A did not map to a codon.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr23:44966704 T>C did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:44966704 T>C did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:44966704 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:44966704 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr23:44929210 G>T did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:44950067 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:44950066 G>A did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:44937741 T>C did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:44918490 G>T did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:44929212 T>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:44879925 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:7751759 C>T maps to NM_001080424.1 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr17:7756647 G>T maps to NM_001080424.1 E1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:55979623 G>A maps to NM_002253.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr4:55968145 C>T maps to NM_002253.2 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr4:55972080 C>T maps to NM_002253.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:55968583 A>G maps to NM_002253.2 N693N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:55955592 G>A maps to NM_002253.2 R1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:55964941 G>T maps to NM_002253.2 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr4:55946254 T>C maps to NM_002253.2 G1308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr4:55962504 T>C maps to NM_002253.2 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:55948735 C>T maps to NM_002253.2 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:55955583 C>A maps to NM_002253.2 E1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:55976855 C>T maps to NM_002253.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr4:55953805 G>T maps to NM_002253.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr4:55972961 C>A maps to NM_002253.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr4:55962504 T>C maps to NM_002253.2 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr4:55955083 G>T maps to NM_002253.2 S1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:55984888 G>A maps to NM_002253.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr4:55979623 G>A maps to NM_002253.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:10610685 G>A maps to NM_203500.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:10599901 C>T maps to NM_203500.1 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr19:10610685 G>A maps to NM_203500.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:142640915 G>A maps to NM_000420.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:142658093 G>T maps to NM_000420.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr7:142643344 C>T maps to NM_000420.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:142641420 C>A maps to NM_000420.2 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr7:142658513 G>A maps to NM_000420.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:142640108 G>T maps to NM_000420.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:142641481 A>G maps to NM_000420.2 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:91449560 C>T maps to NM_007035.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:91449731 G>A maps to NM_007035.3 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr6:73951829 C>A maps to ENST00000370385 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:73933895 G>A maps to ENST00000370385 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:73935079 C>T maps to ENST00000370385 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:62407112 G>T maps to NM_152688.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:62757845 T>C maps to NM_152688.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:62688063 C>T maps to NM_152688.2 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:62442600 C>T maps to NM_152688.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr6:62390873 T>C maps to NM_152688.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr6:62688003 A>G maps to NM_152688.2 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:136569777 C>T maps to NM_006558.1 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:136659305 C>T maps to NM_006558.1 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr2:27322320 C>A maps to NM_006488.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:24900829 C>A maps to NM_015299.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:24900094 G>A maps to NM_015299.2 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr14:24902053 C>T maps to NM_015299.2 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:6416503 G>A maps to NM_003685.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:6417825 G>A maps to NM_003685.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:6417825 G>A maps to NM_003685.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:2824722 C>T maps to NM_014878.4 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:2829935 C>T maps to NM_014878.4 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:2824764 G>A maps to NM_014878.4 H362H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:2831281 T>C maps to NM_014878.4 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr9:2831317 A>G maps to NM_014878.4 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:2820068 C>T maps to NM_014878.4 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr1:19563663 A>G maps to NM_015047.1 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:19561644 C>A maps to NM_015047.1 G471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:19566919 C>T maps to NM_015047.1 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:19549292 C>T maps to NM_015047.1 E804E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr17:26970190 G>T maps to NM_014680.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:26946934 C>T maps to NM_014680.2 V1821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:26961745 G>A maps to NM_014680.2 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:26948517 T>C did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:26966622 G>C maps to NM_014680.2 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:26951282 G>A maps to NM_014680.2 R1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:26962000 A>G maps to NM_014680.2 P868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:26942126 G>A maps to NM_014680.2 G2221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:141313815 T>G maps to NM_014773.3 Y303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:141316761 G>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:141318089 G>A maps to NM_014773.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:141305001 C>T maps to NM_014773.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:141312890 C>T maps to NM_014773.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:141312905 G>A maps to NM_014773.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:141309145 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:48641497 C>T maps to NM_001080394.1 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:85699804 C>T maps to NM_014615.2 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:85701893 A>G maps to NM_014615.2 P1093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:85682156 G>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:85682272 C>T maps to NM_014615.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:85682236 C>T maps to NM_014615.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:85689337 C>T maps to NM_014615.2 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:85690023 C>T maps to NM_014615.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr17:73487442 T>C maps to ENST00000375248 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:73486820 G>A maps to ENST00000375248 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:73493258 C>T maps to ENST00000375248 C1135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:73487857 C>T maps to ENST00000375248 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr8:126051125 T>C maps to ENST00000377985 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:126056843 G>A maps to ENST00000377985 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:126044523 C>T maps to ENST00000377985 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr8:126091119 G>A maps to ENST00000377985 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:197444886 G>A maps to NM_014687.1 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr3:197404370 C>T maps to NM_014687.1 K824K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr4:6862867 C>T maps to NM_014743.2 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:6865717 A>G maps to NM_014743.2 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:6860227 G>A maps to NM_014743.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:6843913 C>T maps to NM_014743.2 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr4:6862993 A>G maps to NM_014743.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:6865105 T>C maps to NM_014743.2 N999N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr4:6862993 A>G maps to NM_014743.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr4:6862993 A>G maps to NM_014743.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:42796379 C>T maps to NM_015349.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr6:42823598 G>A maps to NM_015349.1 E684E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:42824930 C>T maps to NM_015349.1 H737H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:42832928 C>T maps to NM_015349.1 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr6:42819928 C>T maps to NM_015349.1 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr14:70175423 C>T maps to NM_014734.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:105353354 C>T maps to ENST00000453495 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:105351710 T>C maps to ENST00000453495 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr14:105353410 G>A maps to ENST00000453495 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr14:105359414 C>T maps to ENST00000453495 S1363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr14:105352849 C>T maps to ENST00000453495 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:105350273 G>A maps to ENST00000453495 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr14:105353833 G>A maps to ENST00000453495 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr14:105353413 G>A maps to ENST00000453495 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:105359864 G>A maps to ENST00000453495 V1384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr14:75150176 G>A maps to NM_001039479.1 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:24569027 G>A maps to NM_014809.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:24556934 G>T maps to NM_014809.3 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:24569153 G>C maps to NM_014809.3 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:24601307 G>A maps to NM_014809.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:24580178 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:24566863 G>T maps to NM_014809.3 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr6:24572914 C>T maps to NM_014809.3 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:24588923 C>T maps to NM_014809.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr1:35925907 G>A maps to NM_024874.4 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:35944645 G>T maps to NM_024874.4 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:35920053 C>T maps to NM_024874.4 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:35936529 A>G maps to NM_024874.4 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:35932297 T>G did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr19:34832719 G>T maps to NM_014686.3 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:34821221 G>A maps to NM_014686.3 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:34832353 C>T maps to NM_014686.3 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:34818947 G>A maps to NM_014686.3 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr19:34833277 T>A maps to NM_014686.3 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr19:34833067 G>A maps to NM_014686.3 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr9:114159343 C>T maps to NM_001080398.1 W1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:114184239 T>C maps to NM_001080398.1 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:114145500 G>A maps to NM_001080398.1 R1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:114148717 C>A maps to NM_001080398.1 E1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:114188021 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:114184212 C>T maps to NM_001080398.1 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:114204674 G>A maps to NM_001080398.1 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr20:36611956 A>G maps to NM_014657.1 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr20:36641627 A>G maps to NM_014657.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr20:36641830 A>G maps to NM_014657.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr20:36641605 A>G maps to NM_014657.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr20:36641605 A>G maps to NM_014657.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr20:36634761 G>A maps to NM_014657.1 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:127768626 G>A maps to NM_014702.4 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:127768484 C>A maps to NM_014702.4 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:4821213 C>T maps to ENST00000450194 C776C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:4823395 C>T maps to ENST00000450194 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:4830401 C>T maps to ENST00000450194 F1390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:4829561 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:4827793 G>A maps to ENST00000450194 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:4823932 C>T maps to ENST00000450194 Q952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:46385779 C>T maps to NM_001142397.1 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:15730007 C>T maps to NM_014647.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:15694351 G>A maps to NM_014647.3 G1582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:15719471 G>A maps to NM_014647.3 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:15711259 G>A maps to NM_014647.3 S951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:15716816 G>A maps to NM_014647.3 Q812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:43913761 C>T maps to NM_015284.2 F2293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:43916045 G>A maps to NM_015284.2 Q2499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:43896001 A>G maps to NM_015284.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:43900105 C>T maps to NM_015284.2 Q1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:43891291 G>A maps to NM_015284.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:43903089 G>A maps to NM_015284.2 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:43907462 C>A maps to NM_015284.2 T1673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:43902866 G>A maps to NM_015284.2 A1121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr1:43909338 G>A maps to NM_015284.2 S2000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:43896332 C>T maps to NM_015284.2 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr1:43891606 G>A maps to NM_015284.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:43913357 G>A maps to NM_015284.2 S2244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:43914115 A>T maps to NM_015284.2 A2411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:47154078 G>A maps to NM_014774.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:85111190 C>T maps to NM_014732.2 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr16:85112552 C>T maps to NM_014732.2 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:85111073 G>A maps to NM_014732.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:22677556 C>T maps to ENST00000446597 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:22606958 A>G maps to ENST00000446597 G965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr12:22677465 G>T maps to ENST00000446597 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:22643109 T>C maps to ENST00000446597 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr12:22622718 A>G maps to ENST00000446597 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:27761539 C>T maps to NM_015202.2 R1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr16:27760971 C>T maps to NM_015202.2 H897H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr16:27782956 G>A maps to NM_015202.2 P1394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:27786317 C>T maps to NM_015202.2 D1454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:27772845 C>A maps to NM_015202.2 I1248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:27732944 C>T maps to NM_015202.2 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:27788247 G>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:27692718 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:27784441 C>T maps to NM_015202.2 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:27784499 C>T maps to NM_015202.2 R1427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:27760998 C>T maps to NM_015202.2 F906F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr16:27752011 T>C maps to NM_015202.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr16:27720201 G>A maps to NM_015202.2 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:3754079 G>A maps to NM_014704.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:3761502 G>A maps to NM_014704.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:3753079 G>T maps to NM_014704.3 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:3751575 A>T maps to NM_014704.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:3765181 G>A maps to NM_014704.3 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:3765295 G>A maps to NM_014704.3 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr13:42385433 G>A maps to NM_015058.1 R664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:42144706 G>A maps to NM_015058.1 R1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:42407523 C>T maps to NM_015058.1 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:42293844 G>A maps to NM_015058.1 R1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:42385400 C>A maps to NM_015058.1 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:42189136 G>A maps to NM_015058.1 G1565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:42275626 T>G maps to NM_015058.1 R1089R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:42293844 G>A maps to NM_015058.1 R1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr13:42407523 C>A maps to NM_015058.1 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:42357990 C>T maps to NM_015058.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr13:42481810 C>A maps to NM_015058.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:59006846 A>G maps to ENST00000354386 V1549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:58910814 C>T maps to ENST00000354386 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:138378009 C>T maps to NM_014811.3 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:138379338 G>T maps to NM_014811.3 G995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:138376739 C>T maps to NM_014811.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:138378380 C>T maps to NM_014811.3 D675D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:138376709 G>A maps to NM_014811.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:138379010 G>A maps to NM_014811.3 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:138376901 G>A maps to NM_014811.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr9:138377852 A>G maps to NM_014811.3 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:138378080 C>T maps to NM_014811.3 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:138379922 C>T maps to NM_014811.3 D1189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:46690059 G>A maps to NM_001142673.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr17:2599529 G>A maps to NM_015229.3 Q733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:2604776 C>T maps to NM_015229.3 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr17:2595378 G>A maps to NM_015229.3 V1152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:2597229 G>A maps to NM_015229.3 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:2605319 G>A maps to NM_015229.3 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr17:2595945 G>A maps to NM_015229.3 T1080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:55359871 G>A maps to NM_001098815.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:55356355 G>T maps to NM_001098815.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:55367298 A>G maps to NM_001098815.1 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:6515397 C>T maps to NM_014804.2 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr17:6493870 A>G maps to NM_014804.2 D840D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:6526884 C>A maps to NM_014804.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:6498334 G>A maps to NM_014804.2 I799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:6503774 A>G maps to NM_014804.2 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:39879308 G>A maps to NM_015038.1 V1124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:39877451 C>T maps to NM_015038.1 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:39879404 C>T maps to NM_015038.1 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:96976412 A>G maps to NM_015323.4 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:96971051 T>C maps to NM_015323.4 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:96985289 A>G maps to NM_015323.4 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr6:97001345 C>G maps to NM_015323.4 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:96988490 T>C maps to NM_015323.4 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:8784115 G>T maps to ENST00000456698 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:8793057 C>T maps to ENST00000306329 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr18:8826043 G>A maps to ENST00000456698 T1831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:8826091 G>A maps to ENST00000456698 E1847E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:8798207 G>A maps to ENST00000456698 E1104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr18:8825246 C>A maps to ENST00000456698 R1566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr14:55864123 G>A maps to NM_014924.3 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:19465237 G>A maps to NM_015329.3 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:19453375 G>A maps to NM_015329.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:19465226 C>T maps to NM_015329.3 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:19449694 C>T maps to NM_015329.3 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:19459984 C>T maps to NM_015329.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:19465237 G>A maps to NM_015329.3 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:19454736 G>T maps to NM_015329.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:67213390 C>T maps to NM_001040715.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:67214416 G>A maps to NM_001040715.1 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:75554005 T>C maps to NM_015037.2 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:75557174 G>A maps to NM_015037.2 S1158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:75561108 G>A maps to NM_015037.2 A1787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr10:75561117 C>T maps to NM_015037.2 D1790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:75553645 G>A maps to NM_015037.2 T823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:154523385 G>A maps to NM_001131007.1 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:5461141 G>A maps to NM_015325.1 K565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr5:5461208 C>T maps to NM_015325.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:5437216 G>A maps to NM_015325.1 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:5460574 T>C maps to NM_015325.1 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:5441305 A>C maps to NM_015325.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:5463071 G>T maps to NM_015325.1 E1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr5:5460574 T>C maps to NM_015325.1 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:5476148 G>A maps to NM_015325.1 A2159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:84922729 G>A maps to NM_014895.2 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:84883775 T>G maps to NM_014895.2 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:84870528 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:84895037 A>G maps to NM_014895.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:84894935 C>T maps to NM_014895.2 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr18:29488731 C>T maps to NM_014939.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:29429526 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:29450465 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:29497583 C>T maps to NM_014939.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr18:29493391 T>C maps to NM_014939.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr18:29470816 G>A maps to NM_014939.3 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr15:79760680 C>A maps to NM_015206.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr15:79748575 C>T maps to NM_015206.2 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr15:79748965 G>T maps to NM_015206.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr15:79749916 C>A maps to NM_015206.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:79748611 G>A maps to NM_015206.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:79749655 C>T maps to NM_015206.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr15:79760680 C>T maps to NM_015206.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr15:79750483 C>T maps to NM_015206.2 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr15:79760680 C>A maps to NM_015206.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:105536270 C>T maps to NM_015275.1 R610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr12:105509007 G>A did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr12:105509007 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:34971555 C>T maps to NM_015297.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr9:34972434 C>T maps to NM_015297.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:34972416 C>T maps to NM_015297.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:34971552 C>T maps to NM_015297.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:123161330 C>T maps to NM_015312.3 P1498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr4:123097022 C>A maps to NM_015312.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr4:123167884 G>A maps to NM_015312.3 T1744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:123268839 C>T maps to NM_015312.3 N4345N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:123267853 A>G maps to NM_015312.3 A4270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:123140631 T>G maps to NM_015312.3 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:123257357 G>T maps to NM_015312.3 G3954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:123280859 T>C maps to NM_015312.3 H4928H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:123107365 G>A maps to NM_015312.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr4:123161216 T>C maps to NM_015312.3 P1460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr4:123197174 T>C maps to NM_015312.3 F2863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:123107296 G>A maps to NM_015312.3 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:123113406 G>T maps to NM_015312.3 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:123269833 C>T maps to NM_015312.3 N4414N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr4:123192487 C>T maps to NM_015312.3 S2603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:123168411 A>T maps to NM_015312.3 G1804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:123131032 G>A maps to NM_015312.3 W664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:141365038 G>A maps to NM_001080392.1 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:141364764 G>A maps to NM_001080392.1 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:34371528 C>T maps to NM_020702.3 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr9:34371825 G>A maps to NM_020702.3 N372N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:34371129 C>T maps to NM_020702.3 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:34372404 G>A maps to NM_020702.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr9:34371186 C>T maps to NM_020702.3 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:175782624 G>A maps to NM_020444.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:118220566 T>C did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:118242430 A>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:118250600 G>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:118221580 G>T did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:118223473 T>G did not map to a codon.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr23:118222471 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:118223410 C>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:118223688 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:118221268 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:118219433 T>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:118222003 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:118215412 T>G did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:118220566 T>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:118220566 T>C did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:118223499 C>T did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:118221321 G>A did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:118223314 G>A did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:118239037 A>G did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:118221611 T>C did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:118221604 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr23:118220566 T>C did not map to a codon.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr23:118223671 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:118221044 G>T did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr4:57181653 G>A maps to NM_020722.1 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr4:57181614 C>T maps to NM_020722.1 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:57181467 C>T maps to NM_020722.1 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:57181854 C>T maps to NM_020722.1 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:57181041 C>T maps to NM_020722.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr4:57181854 C>T maps to NM_020722.1 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr4:57182505 G>A maps to NM_020722.1 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:57182718 G>A maps to NM_020722.1 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:57181005 G>A maps to NM_020722.1 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr4:57181320 C>A maps to NM_020722.1 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr10:24832275 C>T maps to NM_019590.3 N1359N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:24833361 T>C maps to NM_019590.3 G1721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:24809123 C>T maps to NM_019590.3 D750D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:24822123 G>A maps to NM_019590.3 E1124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:24835060 G>A maps to NM_019590.3 P1880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:24832767 A>G maps to NM_019590.3 P1523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:24832002 C>T maps to NM_019590.3 F1268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:24669979 G>A maps to NM_019590.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:24762497 T>G maps to NM_019590.3 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:24835241 G>T maps to NM_019590.3 E1941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr10:24790374 T>C maps to NM_019590.3 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr10:24835063 G>A maps to NM_019590.3 Q1881Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr10:24762209 C>A maps to NM_019590.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr10:24831849 G>A maps to NM_019590.3 K1217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr10:24790422 G>A maps to NM_019590.3 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr10:24762209 C>G maps to NM_019590.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr10:24832404 T>C maps to NM_019590.3 D1402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:138655232 G>A maps to NM_020340.4 V1750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:138635000 C>A maps to NM_020340.4 R1424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:138559695 T>C maps to NM_020340.4 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:138615204 G>A maps to NM_020340.4 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:138584110 C>T maps to NM_020340.4 N497N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:138640843 A>G maps to NM_020340.4 P1493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:128690181 G>A maps to NM_020741.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:44127953 C>T maps to NM_015443.3 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr17:44144024 G>A maps to NM_015443.3 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:44249214 G>A maps to NM_015443.3 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:44249367 C>A maps to NM_015443.3 G48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:44143917 A>G maps to NM_015443.3 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:72307153 G>A maps to NM_014431.2 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr10:72300889 C>T maps to NM_014431.2 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr10:72297622 C>A maps to NM_014431.2 Y428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:72300994 C>T maps to NM_014431.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:70776072 C>T maps to NM_015634.3 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:97271204 A>G maps to ENST00000421845 D621D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:109743461 C>T maps to NM_020775.3 D971D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:109734382 G>A maps to NM_020775.3 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:109743446 C>T maps to NM_020775.3 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:109742790 C>A maps to NM_020775.3 I913I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr1:109707160 C>T maps to NM_020775.3 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:109731686 G>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:109734345 A>C did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:86547860 C>T did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr7:86568139 G>A maps to NM_001142749.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:86539265 C>A maps to NM_001142749.2 E741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:86509807 G>A maps to NM_001142749.2 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr18:34801988 A>G maps to NM_020776.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:34424254 G>T maps to NM_020776.1 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:52901774 G>A maps to NM_019600.2 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:52901855 C>A maps to NM_019600.2 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:52901774 G>A maps to NM_019600.2 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:52892395 A>G maps to NM_019600.2 D859D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:101833634 T>C maps to NM_020802.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:101793450 C>T maps to NM_020802.2 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:101834363 T>A maps to NM_020802.2 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:101815011 C>T maps to NM_020802.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:232941227 G>A maps to NM_019090.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:232941347 C>T maps to NM_019090.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr3:113753851 T>C maps to NM_020817.1 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr3:113723482 C>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:113720467 G>A maps to NM_020817.1 R713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:113729789 G>C maps to NM_020817.1 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:113697175 G>A maps to NM_020817.1 Y821Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr3:113753851 T>C maps to NM_020817.1 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr3:113753851 T>C maps to NM_020817.1 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr14:94060162 G>A maps to ENST00000393153 W1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr14:94060162 G>A maps to ENST00000393153 W1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr14:94008967 C>T maps to ENST00000393153 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:94155036 T>G maps to ENST00000393153 P2373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:94089143 C>A maps to ENST00000393153 I1877I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr14:94063746 C>A maps to ENST00000393153 S1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:94088465 C>T maps to ENST00000393153 S1651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr14:94088627 G>A maps to ENST00000393153 P1705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:94083571 G>A maps to ENST00000393153 P1404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:94109927 G>T maps to ENST00000393153 E2038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:94120313 G>A maps to ENST00000393153 S2136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:94155060 A>G maps to ENST00000393153 G2381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr14:94088192 C>T maps to ENST00000393153 I1560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr14:94066970 A>C maps to ENST00000393153 T1143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr14:94079269 C>T maps to ENST00000393153 S1316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr14:94100937 G>T maps to ENST00000393153 E1952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr14:94173121 C>T maps to ENST00000393153 L2616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:94088747 C>T maps to ENST00000393153 A1745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr14:94103631 A>G maps to ENST00000393153 P1990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:94088508 G>T maps to ENST00000393153 E1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr14:94063747 A>G maps to ENST00000393153 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr14:94083478 T>C maps to ENST00000393153 Y1373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr14:94089038 A>G maps to ENST00000393153 E1842E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:94158129 G>A maps to ENST00000393153 A2497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:94110010 G>A maps to ENST00000393153 P2065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:95531418 T>C maps to NM_015496.3 Q769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:95539106 C>T maps to NM_015496.3 Q455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:95543298 C>A maps to NM_015496.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr8:95531232 G>A maps to NM_015496.3 Y831Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:95539334 G>A maps to NM_015496.3 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:186112011 G>A maps to NM_020827.1 H113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:5756351 T>C maps to ENST00000414202 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr9:5732428 G>A maps to ENST00000414202 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr9:5765497 C>T maps to ENST00000414202 R976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:5720641 A>G maps to ENST00000414202 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:5763199 C>T maps to ENST00000414202 R725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:5765690 C>T maps to ENST00000414202 F1010F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:30318281 G>A maps to NM_020848.2 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:30316766 G>A maps to NM_020848.2 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:30315481 T>A maps to NM_020848.2 K1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:30315457 C>A maps to NM_020848.2 E1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:30316631 G>T maps to NM_020848.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:30317420 G>A maps to NM_020848.2 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr10:30316484 C>T maps to NM_020848.2 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr10:30318026 C>T maps to NM_020848.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr10:30317774 A>G maps to NM_020848.2 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:30316106 C>T maps to NM_020848.2 A990A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:30317186 G>A maps to NM_020848.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:13219626 A>G maps to NM_020853.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr12:13219626 A>G maps to NM_020853.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:13232898 C>T maps to NM_020853.1 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr12:13214521 A>G maps to NM_020853.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr12:13219626 A>G maps to NM_020853.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr12:13208680 C>A maps to NM_020853.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:13211469 C>T maps to NM_020853.1 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr18:59894634 G>A maps to NM_020854.3 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr18:59888720 C>T maps to NM_020854.3 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:59954689 T>C maps to NM_020854.3 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr18:59925178 A>G did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr2:226447359 G>A maps to NM_020864.1 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:226446721 C>T maps to NM_020864.1 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:226447107 C>A maps to NM_020864.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr2:226516163 C>A maps to NM_020864.1 C615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:226446729 G>A maps to NM_020864.1 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr2:226447137 G>A maps to NM_020864.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:226447383 G>A maps to NM_020864.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:226447602 C>T maps to NM_020864.1 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr2:226273791 C>T maps to NM_020864.1 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr2:226273703 T>C maps to NM_020864.1 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr2:226273691 T>C maps to NM_020864.1 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:226273818 T>C did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:33235373 G>A maps to NM_020888.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:33237296 G>A maps to NM_020888.2 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:33236768 C>T maps to NM_020888.2 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:33236801 C>T maps to NM_020888.2 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:108276233 C>A maps to NM_020890.2 E681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr3:108282016 T>C maps to NM_020890.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:108300978 A>C maps to NM_020890.2 L143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr3:108271107 T>C maps to NM_020890.2 E840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr3:108282016 T>C maps to NM_020890.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr3:108282016 T>C maps to NM_020890.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:108271107 T>C maps to NM_020890.2 E840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:108282016 T>C maps to NM_020890.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr3:108271107 T>C maps to NM_020890.2 E840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr3:108282016 T>C maps to NM_020890.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:108271107 T>C maps to NM_020890.2 E840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr9:100085203 G>A did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr9:100105779 T>C maps to ENST00000375206 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:100071718 G>A maps to ENST00000375206 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:100116894 C>A maps to ENST00000375206 S1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:100136873 C>T maps to ENST00000375206 L1539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr9:100082483 C>T maps to ENST00000375206 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:100128908 C>T maps to ENST00000375206 C1361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:100132330 C>T maps to ENST00000375206 F1428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:100079421 C>T maps to ENST00000375206 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr4:1349005 C>T maps to NM_020894.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:1348625 G>A maps to NM_020894.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:35105806 G>T maps to NM_025182.2 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr9:35108000 G>A maps to NM_025182.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:7675416 C>T maps to NM_001080429.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:7676701 G>A maps to NM_001080429.2 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:7673040 G>A maps to NM_001080429.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr19:7681484 C>T maps to NM_001080429.2 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:7670157 C>T maps to NM_001080429.2 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr19:7676704 G>A maps to NM_001080429.2 P469P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3710-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr7:138583737 G>T maps to NM_001164665.1 I1270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:138579114 A>G maps to NM_001164665.1 T1335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:138602325 C>T maps to NM_001164665.1 Q682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:138552735 G>T maps to NM_001164665.1 A1638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:138602337 C>T maps to NM_001164665.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:138554377 G>A maps to NM_001164665.1 R1561*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:138522707 G>A maps to ENST00000413208 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:138603324 G>A maps to NM_001164665.1 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:138602775 C>T maps to NM_001164665.1 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:138604074 G>A maps to NM_001164665.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:138566204 C>T maps to NM_001164665.1 T1386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:56917664 C>A maps to NM_020931.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:56918107 G>T maps to NM_020931.2 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:56918832 T>G maps to NM_020931.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:56918728 C>T maps to NM_020931.2 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr10:118687303 G>A maps to NM_001127211.1 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:118711511 G>A maps to NM_001127211.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:118687337 T>A maps to NM_001127211.1 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:118681001 G>A maps to NM_001127211.1 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr16:84529351 A>G maps to NM_020947.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:180886030 C>A maps to NM_020950.1 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:180914591 C>T maps to NM_020950.1 C1147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr18:43450590 G>T maps to NM_020964.2 R2056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr18:43502541 G>A maps to NM_020964.2 R955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr18:43535196 T>A maps to NM_020964.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr18:43481064 C>T maps to NM_020964.2 P1514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:43532513 G>A maps to NM_020964.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:43531189 C>A maps to NM_020964.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:43529530 A>G maps to NM_020964.2 C472C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:43502446 C>T maps to NM_020964.2 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr18:43524010 A>G maps to NM_020964.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr18:43450590 G>T maps to NM_020964.2 R2056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr18:43462236 A>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:44692577 C>T maps to NM_001099294.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr22:44681336 C>T maps to NM_001099294.1 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr22:44681450 G>A maps to NM_001099294.1 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:18377716 C>T maps to NM_001145304.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:18377287 A>G maps to NM_001145304.1 Y354Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:18378025 C>T maps to NM_001145304.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr19:18375559 C>T maps to NM_001145304.1 Q930Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:18368694 G>T maps to NM_001145304.1 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr19:18377746 G>A maps to NM_001145304.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr2:176804340 G>A maps to NM_030650.1 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:176794922 A>G maps to NM_030650.1 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr2:176804338 T>C maps to NM_030650.1 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:176802225 G>T maps to NM_030650.1 Y300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:176804340 G>T maps to NM_030650.1 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:176803095 A>G maps to NM_030650.1 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:176804340 G>A maps to NM_030650.1 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr1:1897851 G>A maps to ENST00000434971 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr1:1888151 C>T maps to ENST00000434971 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:1922359 C>T maps to ENST00000434971 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr1:1896470 G>A maps to ENST00000434971 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr20:36869245 A>G maps to NM_001029864.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr20:36867996 T>C maps to NM_001029864.1 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:36868044 A>C maps to NM_001029864.1 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr20:36841700 C>A maps to NM_001029864.1 E1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:36869734 C>A maps to NM_001029864.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr9:20874702 T>C maps to NM_017794.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr9:20874702 T>C maps to NM_017794.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:20995591 G>A maps to NM_017794.3 K1790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:20740294 A>G maps to NM_017794.3 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:20823038 T>C maps to NM_017794.3 N615N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr9:20874702 T>C maps to NM_017794.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr9:20923667 G>T maps to NM_017794.3 P954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr9:20874702 T>C maps to NM_017794.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr9:20885120 T>C maps to NM_017794.3 F839F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:233518253 C>T maps to NM_032435.2 Q970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr1:233511708 C>T maps to NM_032435.2 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:233490666 T>C maps to NM_032435.2 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:233515415 A>G maps to NM_032435.2 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:233507805 G>A maps to NM_032435.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:105881194 C>T maps to NM_032424.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:61331037 C>T maps to NM_001129993.1 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:111587860 G>T maps to NM_153369.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr6:111587448 C>T maps to NM_153369.2 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:111587428 C>T maps to NM_153369.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:111588136 G>T maps to NM_153369.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr6:111587085 C>T maps to NM_153369.2 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:111587451 C>T maps to NM_153369.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr6:111587907 T>C maps to NM_153369.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:30653495 C>T maps to NM_133471.3 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:30652244 G>A maps to NM_133471.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:30647004 C>T maps to NM_133471.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:115337397 G>A maps to NM_133465.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:115337310 T>C maps to NM_133465.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:115336995 C>A maps to NM_133465.2 Y212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:115336896 A>G maps to NM_133465.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr8:22472457 C>T maps to NM_021174.5 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:22475863 C>T maps to NM_021174.5 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:11983400 C>T maps to ENST00000376576 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:113374321 A>G maps to NM_001009899.2 P2069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr3:113379973 T>C maps to NM_001009899.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:113377261 T>C maps to NM_001009899.2 S1089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:113378524 T>C maps to NM_001009899.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:113374120 T>C maps to NM_001009899.2 S2136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:113378721 G>A maps to NM_001009899.2 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:113373811 A>G maps to NM_001009899.2 H2239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:113375694 G>A maps to NM_001009899.2 Q1612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr3:113376106 C>T maps to NM_001009899.2 Q1474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:73963796 G>A did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:73963105 A>G did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:73963269 C>A did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:73965421 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:73961696 C>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:73963170 A>G did not map to a codon.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr23:73961166 G>T did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr23:73961714 C>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:73960440 G>A did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:73960333 A>G did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:73964130 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:73961285 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:73961055 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:73963605 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:73962430 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:73960874 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:73964048 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:73960246 T>G did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:73963699 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr23:73962294 T>C did not map to a codon.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr23:73961846 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:73964003 C>A did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:73961554 T>C did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:73964067 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:73960045 C>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:73963170 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr23:73962574 A>C did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr23:73963794 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:73963292 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:73964262 A>G did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:73961170 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:73960066 G>A did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:73960504 A>G did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr23:73961569 C>A did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:73963794 C>T did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:73963105 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:73959989 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:73964161 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:73962187 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:73965420 C>T did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:73962382 C>T did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:73963292 G>T did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:73963290 A>G did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:73963291 G>T did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:73963795 A>G did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:73963106 G>T did not map to a codon.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr9:5929075 T>C maps to NM_001017969.2 E822E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr9:5919743 C>T maps to NM_001017969.2 A2084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:5969126 G>T maps to NM_001017969.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:5988523 C>T maps to NM_001017969.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:5969205 G>T maps to NM_001017969.2 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:5968823 A>C maps to NM_001017969.2 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr2:8926462 T>C maps to NM_020738.2 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:8926158 A>G maps to NM_020738.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr2:8926462 T>C maps to NM_020738.2 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr2:8926462 T>C maps to NM_020738.2 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr2:8957798 G>A maps to NM_020738.2 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:8917023 T>G did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr2:8926116 G>A maps to NM_020738.2 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr10:94381171 C>T maps to NM_004523.3 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr10:94368931 A>G maps to NM_004523.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:94390004 G>T maps to NM_004523.3 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr9:116854682 C>T maps to ENST00000259410 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:116854667 T>C maps to ENST00000259410 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:116854275 C>A maps to ENST00000259410 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:116858732 G>T maps to ENST00000259410 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:17785747 G>A maps to NM_022113.4 D1162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr6:17794481 G>A maps to NM_022113.4 Q1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr6:17855843 C>T maps to NM_022113.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:17781485 G>T maps to NM_022113.4 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:17852250 G>A maps to NM_022113.4 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:17826139 G>A maps to NM_022113.4 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:17834190 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:17788052 T>C maps to NM_022113.4 R1105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr8:28950279 C>T maps to NM_015254.3 P1480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr8:29006249 G>A maps to NM_015254.3 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:28976450 C>T maps to NM_015254.3 A1198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:28988067 T>C maps to NM_015254.3 G1019G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:29013283 C>T maps to NM_015254.3 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:200534366 G>A maps to NM_014875.2 R1301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:200584664 C>T maps to NM_014875.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:200529893 G>A maps to NM_014875.2 L1396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:200523718 G>A maps to NM_014875.2 Q1482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:200569230 C>A maps to NM_014875.2 E771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:200571039 G>A maps to NM_014875.2 N712N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr1:200534780 T>C maps to NM_014875.2 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr1:200522806 A>G maps to NM_014875.2 P1552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:200587485 T>C maps to NM_014875.2 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr1:200524531 T>C maps to NM_014875.2 E1468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:200534780 T>C maps to NM_014875.2 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr3:44867869 T>C maps to NM_020242.2 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr3:44816853 G>A maps to NM_020242.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr20:16359604 C>T maps to NM_024704.4 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr20:16496282 G>A maps to NM_024704.4 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:16293063 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:16360035 C>A maps to NM_024704.4 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:16362363 C>A maps to NM_024704.4 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:16506734 A>G did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:16337013 G>A maps to NM_024704.4 C1194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:16488668 G>A maps to NM_024704.4 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:16359475 C>T maps to NM_024704.4 Q1057Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:21036309 G>A maps to NM_020816.2 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:21031327 C>T maps to NM_020816.2 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:21044100 C>T maps to NM_020816.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:21031009 G>A maps to NM_020816.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:21011456 G>A maps to NM_020816.2 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:21031192 C>T maps to NM_020816.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:21031102 A>G maps to NM_020816.2 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:20991148 C>T maps to NM_020816.2 E1006E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:21009283 G>A maps to NM_020816.2 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:21031303 C>T maps to NM_020816.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr1:21041997 G>A maps to NM_020816.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:28110258 G>A maps to NM_031217.3 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:28057917 A>G maps to NM_031217.3 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:28057999 T>C maps to NM_031217.3 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:28080608 G>A maps to NM_031217.3 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:28106235 G>A maps to NM_031217.3 Y339Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:28090850 G>A maps to NM_031217.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:43005517 G>A maps to ENST00000438933 R730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:72350655 A>G maps to NM_153209.3 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:72324589 C>T maps to NM_153209.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:72343980 C>T maps to NM_153209.3 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:72348406 C>T maps to NM_153209.3 Y636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:72349058 C>T maps to NM_153209.3 Q694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:241664737 C>T maps to ENST00000373308 S1410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:241689888 G>A maps to ENST00000373308 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr2:241702208 C>T maps to ENST00000373308 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr2:241657525 G>A maps to ENST00000373308 S1766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:241697883 G>A maps to ENST00000373308 Y825Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:241706365 G>A maps to ENST00000373308 C550C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr2:241724507 C>T maps to ENST00000373308 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr2:241660416 C>T maps to ENST00000373308 S1602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:241706335 G>A maps to ENST00000373308 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:241727560 G>A maps to ENST00000373308 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr1:10408753 C>T maps to ENST00000377086 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:10342533 T>C maps to ENST00000377086 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr1:10428580 C>T maps to ENST00000377086 S1603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:10435088 G>A maps to ENST00000377086 Q1758Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:10423349 C>A maps to ENST00000377086 V1438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:10397495 C>T maps to ENST00000377086 N1109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:10436626 G>A maps to ENST00000377086 P1811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:10318672 A>G maps to ENST00000377086 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:10363931 G>T maps to NM_183416.3 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:10327511 G>A maps to ENST00000377086 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:10338109 G>T maps to ENST00000377086 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:10357060 T>C maps to ENST00000377086 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:10434406 C>A maps to ENST00000377086 P1660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:4906118 G>A maps to NM_006612.5 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:4925673 C>T maps to NM_006612.5 H766H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:4923938 C>T maps to NM_006612.5 Q635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:4925925 G>A maps to NM_006612.5 Q850Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:4910315 G>A maps to NM_006612.5 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:137519020 C>T maps to NM_005733.2 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:137522047 T>G maps to NM_005733.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr10:91498347 A>G maps to ENST00000416354 E1280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:91476229 C>A maps to ENST00000416354 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:91479363 C>T maps to ENST00000416354 N541N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:91498345 G>T maps to ENST00000416354 E1280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr10:91497687 T>C maps to ENST00000416354 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:91498837 G>A maps to ENST00000416354 K1330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:91497600 T>C maps to ENST00000416354 I1031I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:91488914 G>T maps to ENST00000416354 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr10:91479225 T>C maps to ENST00000416354 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:39725575 C>T maps to ENST00000395670 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:39724053 G>A maps to ENST00000395670 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:39701481 G>A maps to ENST00000395670 R1444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:39763921 C>T maps to ENST00000395670 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:200959388 G>A maps to NM_017596.2 P969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:200972806 C>T maps to NM_017596.2 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:200956018 C>T maps to NM_017596.2 T1214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:200969855 G>A maps to NM_017596.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:200956152 G>A maps to NM_017596.2 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:200943294 G>A maps to NM_017596.2 Y1601Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:200967533 G>A maps to NM_017596.2 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr1:200956254 G>A maps to NM_017596.2 T1161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:200944770 C>T maps to NM_017596.2 T1477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr16:29810337 C>T maps to NM_007317.1 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr15:69728553 G>A maps to NM_138555.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:69732651 T>C maps to NM_138555.1 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:69729011 G>A maps to NM_138555.1 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:69737381 T>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:34257971 C>A maps to NM_194313.2 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr6:168440793 C>T maps to NM_030615.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:168443256 C>T maps to NM_030615.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:104638913 C>T maps to NM_015656.1 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:104642340 A>G maps to NM_015656.1 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:104642295 C>T maps to NM_015656.1 F1057F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:104643039 G>A maps to NM_015656.1 P1305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr14:104618707 G>A maps to NM_015656.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:245850754 C>T maps to NM_018012.3 L1490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr1:245704128 C>T maps to NM_018012.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:245862259 G>A maps to NM_018012.3 A2033A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:245849263 C>T maps to NM_018012.3 G993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:245861564 C>T maps to NM_018012.3 I1994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:245849092 C>T maps to NM_018012.3 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr1:245847621 C>T maps to NM_018012.3 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr1:245849896 C>T maps to NM_018012.3 S1204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:245766054 C>T maps to NM_018012.3 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:245849608 C>T maps to NM_018012.3 S1108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:245850997 G>A maps to NM_018012.3 P1571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:86468744 T>C maps to NM_017576.1 E1052E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:86465163 C>A maps to NM_017576.1 E1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr5:61668327 T>C maps to NM_001098511.1 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:51901827 C>T maps to NM_032559.4 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr17:51901674 A>T maps to NM_032559.4 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:51902010 A>G maps to NM_032559.4 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:51901920 C>T maps to NM_032559.4 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr17:51901554 C>T maps to NM_032559.4 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:51900888 G>A maps to NM_032559.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr17:51900744 G>A maps to NM_032559.4 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr17:51900948 C>T maps to NM_032559.4 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:45226122 C>T maps to NM_006845.3 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:132070010 C>A maps to ENST00000403231 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr20:30897912 T>C maps to NM_004798.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:30898104 T>C maps to NM_004798.3 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr20:30897717 C>T maps to NM_004798.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr20:30914651 A>G maps to NM_004798.3 E609E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr20:30904343 A>G maps to NM_004798.3 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr20:30914651 A>G maps to NM_004798.3 E609E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr20:30914651 A>G maps to NM_004798.3 E609E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr20:30914651 A>G maps to NM_004798.3 E609E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr20:30904349 C>T maps to NM_004798.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:26203928 C>T maps to NM_002254.6 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:26203964 G>A maps to NM_002254.6 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:26203451 G>A maps to NM_002254.6 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:26203514 G>T maps to NM_002254.6 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:26204015 G>A maps to NM_002254.6 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:69626849 T>C did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:69510345 C>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:69549267 C>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:69594038 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:69639928 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:69622447 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:69623880 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:69563578 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:69563562 C>T did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:69516974 G>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:69510632 A>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:69626848 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:69573595 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:69510632 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:69615879 G>T did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr23:69563730 A>G did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:69510632 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr23:69573528 G>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:69549350 A>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:69595980 G>A did not map to a codon.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr5:154396043 C>A maps to NM_001099293.1 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:154394111 C>T maps to NM_001099293.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:154394054 T>C maps to NM_001099293.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr5:154395555 C>T maps to NM_001099293.1 R713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:154396161 G>T maps to NM_001099293.1 E915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:154393791 G>T maps to NM_001099293.1 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:154396907 C>A maps to NM_001099293.1 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:57966448 C>T maps to NM_004984.2 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr10:32320138 A>G maps to NM_004521.2 N481N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:32322807 C>A maps to NM_004521.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:32307308 C>A maps to NM_004521.2 E792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:32329376 C>A maps to NM_004521.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr10:32329376 C>A maps to NM_004521.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:149799245 C>T maps to NM_004522.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:149829955 C>T maps to NM_004522.1 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:149818508 C>A maps to NM_004522.1 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:149856969 G>A maps to NM_004522.1 K748K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:149793853 C>A maps to NM_004522.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:149818508 C>A maps to NM_004522.1 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:149847636 C>T maps to NM_004522.1 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:149803530 C>T maps to NM_004522.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr6:39328175 G>A maps to NM_145027.4 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:39311554 G>A maps to NM_145027.4 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:39552760 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:39507856 G>A maps to NM_145027.4 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:39607481 G>A maps to NM_145027.4 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:39507856 G>A maps to NM_145027.4 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:39554174 G>T maps to NM_145027.4 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:39507856 G>A maps to NM_145027.4 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr15:90177027 G>A maps to NM_198525.2 N827N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:47277618 C>A maps to NM_182902.3 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:47278067 C>A maps to NM_182902.3 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:47282432 T>C maps to NM_182902.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:169953797 G>A maps to NM_014970.2 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:145694022 G>A maps to NM_145754.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr8:145697821 T>C maps to NM_145754.2 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:145698667 G>A maps to NM_145754.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr16:57803504 A>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:57805496 G>A maps to NM_005550.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:7798065 C>A maps to NM_012311.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:7811292 A>G maps to NM_012311.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:7811249 C>A maps to NM_012311.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:55286659 G>A maps to ENST00000291633 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:55295207 C>T maps to ENST00000291633 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr19:55286842 C>T maps to ENST00000291633 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:55284860 T>A maps to ENST00000291633 C49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr19:55295258 C>A maps to ENST00000291633 C373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr19:55285016 C>T maps to ENST00000291633 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:55294413 G>T maps to ENST00000291633 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:55263913 C>T maps to NM_015868.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr19:55258835 C>T maps to NM_015868.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:55263913 C>T maps to NM_015868.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:55316284 C>T maps to ENST00000396289 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:55317454 C>T maps to ENST00000396289 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr19:55316443 C>T maps to ENST00000396289 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:55358642 C>T maps to NM_012314.3 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr19:55331399 C>T maps to ENST00000355608 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:55331399 C>T maps to ENST00000355608 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:55333224 C>T maps to ENST00000355608 H287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr19:55331208 C>T maps to ENST00000355608 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:55329016 A>G maps to ENST00000355608 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr19:55331210 G>T maps to ENST00000355608 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr19:55331399 C>T maps to ENST00000355608 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr19:55363597 C>T maps to NM_006737.2 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr19:55239242 G>T maps to NM_153443.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr19:55247472 C>T maps to NM_153443.3 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr19:55241223 G>A maps to NM_153443.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr19:55239325 T>A maps to NM_153443.3 L202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:55241085 C>T maps to NM_153443.3 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:55301510 G>A maps to NM_001015070.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:158063473 A>G maps to ENST00000368173 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:36351525 C>T maps to NM_199180.2 N295N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3510-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:126343241 G>A maps to NM_032531.3 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr11:126396493 G>A maps to NM_032531.3 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:126301338 C>T maps to NM_032531.3 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:126391321 T>C maps to NM_032531.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr4:55592133 T>C maps to NM_000222.2 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr4:55595594 A>G maps to NM_000222.2 E695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:55593598 A>G maps to NM_000222.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:55592059 C>T maps to NM_000222.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:55595594 A>G maps to NM_000222.2 E695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr4:55593583 A>G maps to NM_000222.2 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr4:55561897 G>A maps to NM_000222.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr4:55561912 C>T maps to NM_000222.2 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr4:55593652 A>G maps to NM_000222.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:55597499 T>C maps to NM_000222.2 D716D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr4:55561885 C>T maps to NM_000222.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr4:55604627 C>T maps to NM_000222.2 R946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:55593486 A>G maps to NM_000222.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr4:55595594 A>G maps to NM_000222.2 E695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:55602764 G>A maps to NM_000222.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr4:55592043 A>T maps to NM_000222.2 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr4:55594222 A>G maps to NM_000222.2 K642K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr4:55593583 A>G maps to NM_000222.2 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr4:55599324 C>A maps to NM_000222.2 I817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:55594222 A>G maps to NM_000222.2 K642K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr4:55597499 T>C maps to NM_000222.2 D716D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:55594213 T>C maps to NM_000222.2 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr4:55593664 T>C maps to NM_000222.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr4:55594213 T>C maps to NM_000222.2 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr4:55595585 A>G maps to NM_000222.2 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:55593664 T>C maps to NM_000222.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr4:55594213 T>A maps to NM_000222.2 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr4:55593583 A>G maps to NM_000222.2 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr4:55561828 A>G maps to NM_000222.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:55603373 T>C maps to NM_000222.2 D910D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr4:55561702 A>G maps to NM_000222.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr4:55599288 C>A maps to NM_000222.2 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:55594177 G>A maps to NM_000222.2 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr4:55593634 T>C maps to NM_000222.2 N567N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr4:55599259 A>T maps to NM_000222.2 R796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr4:55602951 C>A maps to NM_000222.2 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr4:55592166 G>A maps to NM_000222.2 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr4:55573315 C>T maps to NM_000222.2 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr4:55589771 C>T maps to NM_000222.2 Y418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr4:55589768 T>C maps to NM_000222.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr4:55593616 G>A maps to NM_000222.2 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr4:55593643 C>T maps to NM_000222.2 Y570Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:55593626 G>T maps to NM_000222.2 G565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr4:55595600 T>C maps to NM_000222.2 H697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr4:55592202 A>G maps to NM_000222.2 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr4:55593634 T>C maps to NM_000222.2 N567N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr4:55593664 T>C maps to NM_000222.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr4:55593586 C>A maps to NM_000222.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr4:55593616 G>A maps to NM_000222.2 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr4:55599312 A>G maps to NM_000222.2 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr4:55593676 A>G maps to NM_000222.2 K581K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr4:55561828 A>G maps to NM_000222.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr4:55593487 C>T maps to NM_000222.2 Q549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr4:55599285 G>T maps to NM_000222.2 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:88910243 G>A maps to NM_000899.4 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:88939540 G>A maps to NM_000899.4 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr13:33638145 G>A maps to NM_004795.3 P954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:33635273 G>A maps to NM_004795.3 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr13:33635102 C>T maps to NM_004795.3 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr13:33591261 C>T maps to NM_004795.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:33629244 C>T maps to NM_004795.3 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:33638205 T>C maps to NM_004795.3 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr13:33635087 C>T maps to NM_004795.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:39450176 T>C maps to NM_175737.3 C1002C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:39448220 C>T maps to NM_175737.3 C625C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:39448175 C>T maps to NM_175737.3 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:39448253 C>T maps to NM_175737.3 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:39448919 C>A maps to NM_175737.3 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr14:104136616 A>G maps to ENST00000445352 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:104123944 G>A maps to ENST00000445352 A280A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-A01R-01A-21W-A096-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:45852817 C>T maps to NM_177417.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:45849908 A>G maps to NM_177417.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr19:45851969 G>A maps to NM_177417.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:43038168 G>A maps to NM_201523.1 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr6:43039322 G>A maps to NM_201523.1 W443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:103663383 C>T maps to NM_005655.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:10186296 T>C maps to NM_003597.4 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:10192393 A>G maps to NM_003597.4 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr2:10188450 C>T maps to NM_003597.4 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:31664330 C>T maps to NM_015995.2 C232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:130418116 C>T maps to NM_138693.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:126070727 C>T maps to NM_014079.3 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:126071519 G>T maps to NM_014079.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:44596341 C>T maps to NM_173484.3 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:44584620 G>A maps to NM_173484.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr1:44595812 C>T maps to NM_173484.3 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr9:110250386 G>A maps to NM_004235.4 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:73636105 C>T maps to NM_001730.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr13:73636639 C>T maps to NM_001730.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr23:56310885 G>C did not map to a codon.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr23:56310910 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:56296627 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:56310900 C>T did not map to a codon.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr23:56296650 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:56310880 G>A did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:56310907 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:56291902 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:56310796 G>A did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:73028201 C>T maps to NM_001206.2 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr9:73002808 C>T maps to NM_001206.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:50244913 G>A maps to NM_014315.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr14:50241351 C>T maps to NM_014315.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:42986628 G>A maps to NM_057161.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:87795631 C>T maps to NM_017566.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:87743030 C>T maps to NM_017566.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:27944793 T>C maps to NM_020782.1 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:27933781 C>A maps to NM_020782.1 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:18809736 G>A maps to NM_152375.2 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:18808308 G>A maps to NM_152375.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:18809655 C>T maps to NM_152375.2 C727C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:18809358 G>A maps to NM_152375.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:18809628 C>T maps to NM_152375.2 C718C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:50987857 C>T maps to NM_138433.3 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:50987348 C>T maps to NM_138433.3 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr22:50987713 C>T maps to NM_138433.3 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:50987863 G>A maps to NM_138433.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:205312363 C>T maps to NM_018203.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:205312624 G>A maps to NM_018203.1 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:205312639 G>C maps to NM_018203.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:205312381 G>A maps to NM_018203.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:205312381 G>A maps to NM_018203.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:205308364 C>T maps to NM_018203.1 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr1:205306703 G>A maps to NM_018203.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr3:49213086 G>A maps to NM_173546.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:49210330 A>T maps to NM_173546.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr3:49212313 G>A maps to NM_173546.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr13:70314647 G>A maps to NM_020866.2 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:70681773 T>A maps to NM_020866.2 K20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr13:70514321 T>C maps to NM_020866.2 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:70371055 G>A maps to NM_020866.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:70456524 C>A maps to NM_020866.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr13:70535455 G>C maps to NM_020866.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:70413147 G>A maps to NM_020866.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:70456473 T>G maps to NM_020866.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:70371074 T>C maps to NM_020866.2 K478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr13:70681804 G>A maps to NM_020866.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:40001823 C>T maps to NM_152467.3 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:39994204 G>T maps to NM_152467.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:40001805 G>A maps to NM_152467.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:40001601 C>T maps to NM_152467.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:39994379 T>C did not map to a codon.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr17:39998467 T>C maps to NM_152467.3 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr17:40001913 G>A maps to NM_152467.3 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr17:40004471 A>G maps to NM_152467.3 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:40010657 T>G maps to NM_018143.1 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:202880232 C>T maps to NM_021633.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:202861787 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:202866002 A>C maps to NM_021633.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:202887481 A>G maps to NM_021633.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr23:117043324 G>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:117033339 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:117043787 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:117079436 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr23:117043308 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:117043551 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:117035804 A>G did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:117053528 C>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:30260414 C>T maps to NM_020805.1 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:30257203 G>A maps to NM_020805.1 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr18:30321954 G>A maps to NM_020805.1 D335D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AD-6895-01A-11D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr18:30260480 G>A maps to NM_020805.1 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:30260461 C>A maps to NM_020805.1 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr18:30349972 C>T maps to NM_020805.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr18:30350035 G>A maps to NM_020805.1 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr23:24024790 C>G did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:24006566 A>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:24006373 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:24006145 C>T did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr23:24006568 C>T did not map to a codon.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:898540 C>T maps to NM_198317.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:47385308 C>T maps to NM_025010.4 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:47364151 C>T maps to NM_025010.4 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:47361204 T>C maps to NM_025010.4 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:47374762 C>T maps to NM_025010.4 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:166231810 C>T maps to NM_001161521.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:166231873 C>T maps to NM_001161521.1 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:173685205 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:173726262 C>T maps to NM_014458.3 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:173744968 A>G maps to NM_014458.3 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:20812121 C>T maps to NM_032775.3 W426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:20800819 G>A maps to NM_032775.3 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:20812115 G>A maps to NM_032775.3 Y428Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:170605953 G>A maps to NM_144711.5 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:170592043 G>T maps to NM_144711.5 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr2:170606125 G>T maps to NM_144711.5 G521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:170591634 T>C maps to NM_144711.5 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr3:183388919 G>A maps to NM_017644.3 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:183390265 C>T maps to NM_017644.3 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr15:86312669 G>A maps to NM_022480.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:86311412 G>A maps to NM_022480.3 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:86312900 G>A maps to NM_022480.3 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr15:86312254 T>A maps to NM_022480.3 K263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:18778747 C>T maps to NM_018316.1 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:45403534 G>A maps to ENST00000355081 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:136997638 G>A maps to NM_017415.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:137013263 G>A maps to NM_017415.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr6:53519320 G>A maps to NM_001003760.4 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:53519148 G>A maps to NM_001003760.4 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr6:53519023 C>T maps to NM_001003760.4 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr6:97587058 T>C maps to NM_052904.3 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:97578796 G>A maps to NM_052904.3 W526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr6:97562260 C>G maps to NM_052904.3 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr6:97533141 G>A maps to NM_052904.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr6:97587058 T>C maps to NM_052904.3 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:21675867 G>A did not map to a codon.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr23:21674283 G>A did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:21674364 G>A did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:21675345 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:21675703 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:21674282 C>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:21674155 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:21675633 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:21675337 C>T did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:21674811 G>T did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:21674233 G>T did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:21674706 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:21675079 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:84690958 C>T maps to NM_024731.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:84690778 G>A maps to NM_024731.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:84693511 C>T maps to NM_024731.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:84695204 C>T maps to NM_024731.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:84691174 C>T maps to NM_024731.2 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:124658143 G>A maps to NM_001081675.2 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:124658143 G>A maps to NM_001081675.2 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:124665025 G>A maps to NM_001081675.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:124664058 G>A maps to NM_001081675.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr8:124664167 G>A maps to NM_001081675.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:86880693 C>A did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:86919933 A>C did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:86890728 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:86773014 G>A did not map to a codon.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr23:86887357 T>A did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:86873007 C>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:86873110 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:86772938 C>A did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:86877328 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:86890687 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:86773065 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr23:86887325 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:86919876 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:86887339 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:86888767 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:86890681 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:86887278 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:86880631 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:86773203 A>G did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr23:86873049 T>C did not map to a codon.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr23:86773150 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:86880672 A>G did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:86773220 T>C did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr23:86773089 G>T did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:86873049 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:86888869 A>C did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:86919824 G>C did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:86873049 T>C did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr23:86880674 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:86888776 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:86887340 G>A did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr4:39114765 G>A maps to NM_015990.4 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:39064632 G>T maps to NM_015990.4 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:39077635 T>C maps to NM_015990.4 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:183217381 G>T maps to NM_130446.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:183209810 G>A maps to NM_130446.2 C590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:23163400 G>A maps to NM_001031710.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr7:23145762 C>T maps to NM_001031710.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:23164665 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr4:88091664 A>C maps to NM_020803.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr4:88099710 G>T maps to NM_020803.3 C338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:21333609 C>A maps to NM_018847.2 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:21333217 G>A maps to NM_018847.2 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:21333882 C>A maps to NM_018847.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:21334807 C>T maps to NM_018847.2 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr9:21333994 T>C maps to NM_018847.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:51322485 C>A maps to NM_002257.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:51325113 C>T maps to NM_002257.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:51527970 G>A maps to NM_144947.1 F72F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G4-6588-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:51535129 A>G did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr19:51535183 G>A maps to NM_019598.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:51563757 C>T maps to NM_015596.1 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:51330320 G>A maps to NM_017509.2 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:51329966 C>T maps to NM_017509.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:51380301 G>C did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:51381739 T>C maps to NM_005551.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:51359598 C>T maps to NM_001648.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr19:51359502 A>G maps to NM_001648.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:51412666 G>T maps to NM_004917.3 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:51411647 G>A maps to NM_004917.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:51412665 C>A maps to NM_004917.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:51413937 G>A maps to NM_004917.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:51451970 G>A maps to NM_012427.4 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:51483523 G>A maps to NM_005046.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr19:51485144 G>A maps to NM_005046.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:51499470 C>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:51509927 C>A maps to NM_012315.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:51512494 A>G maps to NM_012315.1 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:187177155 A>G maps to ENST00000511608 K547K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:187171544 C>T maps to ENST00000511608 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:187178495 G>T maps to ENST00000511608 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr4:187177215 C>A maps to ENST00000511608 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr2:48713779 A>G maps to NM_001135629.2 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:48692654 G>A maps to NM_001135629.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:48713881 A>G maps to NM_001135629.2 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr12:9750664 G>A maps to NM_002258.2 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr12:9751097 T>C maps to NM_002258.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:9751132 C>A maps to NM_002258.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr12:10601883 A>G maps to NM_213658.2 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:10601877 C>T maps to NM_213658.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:10601973 G>A maps to NM_213658.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr12:10588527 G>A maps to NM_002260.3 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:10583715 C>T maps to NM_002260.3 *232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr12:10462062 A>G maps to ENST00000381908 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:139164426 G>A maps to NM_198508.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:10539532 A>G maps to NM_007360.3 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr12:10532338 G>A maps to NM_007360.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:241731805 C>T maps to NM_003679.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:241725625 C>T maps to NM_003679.3 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:241752098 G>A maps to NM_003679.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:241752098 G>A maps to NM_003679.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr1:241725481 C>T maps to NM_003679.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:135020786 C>T maps to ENST00000368572 G1244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:135015104 C>T maps to ENST00000368572 F1032F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:135032399 C>T maps to ENST00000368572 F1583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:135015188 C>T maps to ENST00000368572 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr10:135027568 C>T maps to ENST00000368572 N1542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:135024986 C>T maps to ENST00000368572 Q1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr10:135020390 G>A maps to ENST00000368572 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:135024946 G>A maps to ENST00000368572 S1312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr10:134981057 C>T maps to ENST00000368572 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:186459484 G>T maps to NM_001102416.2 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:186435378 T>C maps to NM_001102416.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:186460081 G>T maps to NM_001102416.2 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:186459579 C>T maps to NM_001102416.2 H465H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr12:123067397 G>A maps to NM_014708.4 V1043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:123028752 T>C maps to NM_014708.4 H202H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:123042010 G>A maps to NM_014708.4 W451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:123075942 T>G maps to NM_014708.4 L1396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr12:123057756 C>A maps to NM_014708.4 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:123087764 C>T maps to NM_014708.4 I1692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:123055445 A>G maps to NM_014708.4 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:123041999 C>T maps to NM_014708.4 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:122186227 C>A maps to NM_002264.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr3:122145980 G>A maps to NM_002264.3 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr17:66039223 C>A maps to NM_002266.2 Y225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:66039283 G>A maps to NM_002266.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr17:66033286 T>C maps to NM_002266.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr17:66033286 T>C maps to NM_002266.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr17:66033286 T>C maps to NM_002266.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:66033286 T>C maps to NM_002266.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:50279757 T>G maps to NM_002267.3 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:50280283 C>A maps to NM_002267.3 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:50279802 G>A maps to NM_002267.3 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:160253672 C>A maps to NM_002268.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:160254612 G>A maps to NM_002268.3 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:160253640 A>G maps to NM_002268.3 H53H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr6:117045495 G>A maps to NM_002269.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:117045495 G>A maps to NM_002269.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:32635542 G>A maps to NM_012316.4 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:45748171 T>C maps to NM_002265.4 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr17:45734426 G>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:152733140 G>A maps to NM_001025231.1 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr1:152733155 C>T maps to NM_001025231.1 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:152732459 C>T maps to NM_001025231.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:152733155 C>T maps to NM_001025231.1 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:152732420 C>T maps to NM_001025231.1 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:152732429 C>T maps to NM_001025231.1 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:152732463 G>T maps to NM_001025231.1 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:152732459 C>T maps to NM_001025231.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:152733791 T>C maps to NM_001025231.1 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:152732438 A>G maps to NM_001025231.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr19:47979857 G>A maps to NM_007059.2 H371H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:25380235 A>G maps to NM_033360.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr12:25362803 T>C maps to NM_004985.3 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:25398258 C>T maps to NM_033360.2 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr12:25398252 C>T maps to NM_033360.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr12:25380322 T>A maps to NM_033360.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr12:25398288 T>C maps to NM_033360.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:25398237 A>G maps to NM_033360.2 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr12:25398213 T>G maps to NM_033360.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:25380283 T>C maps to NM_033360.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:25398249 T>C maps to NM_033360.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr12:25378559 T>C maps to NM_033360.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr12:25398288 T>C maps to NM_033360.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr12:25398273 G>T maps to NM_033360.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr12:25398294 T>C maps to NM_033360.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr12:25398258 C>A maps to NM_033360.2 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:149430364 G>T maps to NM_032534.2 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:149430820 C>T maps to NM_032534.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:149417174 C>T maps to NM_032534.2 H37H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:149419994 C>T maps to NM_032534.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr7:149430328 G>A maps to NM_032534.2 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr7:149417989 G>A maps to NM_032534.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:8273549 G>A maps to NM_213597.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:88327746 T>C maps to NM_016618.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:88327917 C>A maps to NM_016618.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:29536342 C>T maps to NM_032045.4 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:29533510 G>A maps to NM_032045.4 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr22:29494867 G>T maps to NM_032045.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:3016743 C>T maps to NM_172229.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:10670497 C>T maps to NM_023008.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:10670299 G>A maps to NM_023008.3 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:10668647 G>A maps to NM_023008.3 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:91863866 G>A maps to NM_194456.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:91865793 G>A maps to NM_194456.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:91870400 C>T maps to NM_194456.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:91871371 C>T maps to NM_194456.1 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:91864910 G>A maps to NM_194456.1 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:91871373 G>T maps to NM_194456.1 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:75902206 C>T maps to NM_007043.6 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr12:75902131 G>A maps to NM_007043.6 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:53074033 G>A maps to NM_006121.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr12:53069198 G>A maps to NM_006121.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr12:53072387 A>G maps to NM_006121.3 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr12:53072387 A>G maps to NM_006121.3 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr12:53068991 G>A maps to NM_006121.3 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:53069342 A>G maps to NM_006121.3 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:53072387 A>G maps to NM_006121.3 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:38975820 G>A maps to NM_000421.3 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr17:38978507 G>T maps to NM_000421.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:38976348 T>C maps to NM_000421.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:38976407 C>A maps to NM_000421.3 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:39022966 G>A maps to NM_000223.3 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr17:39023369 C>T maps to NM_000223.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:39659269 G>A maps to NM_153490.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr17:39659586 G>A maps to NM_153490.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:39742774 A>G maps to NM_000526.4 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr17:39671924 G>T maps to NM_002275.3 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:39673065 G>A maps to NM_002275.3 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:39670277 G>T maps to NM_002275.3 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:39766746 C>T maps to NM_005557.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:39768796 G>A maps to NM_005557.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:39777274 C>T maps to NM_000422.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:39776786 C>T did not map to a codon.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr17:39041266 G>A maps to NM_019010.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:39036874 C>T maps to NM_019010.2 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr17:39034545 C>T maps to NM_019010.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:38812820 G>A maps to NM_152349.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:39092582 G>A maps to NM_015515.3 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:39081673 C>A maps to NM_015515.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr17:39081619 C>T maps to NM_015515.3 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr17:38854569 A>G maps to NM_019016.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:38854865 T>C maps to NM_019016.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr17:38906789 C>T maps to NM_181534.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr17:38906693 G>A maps to NM_181534.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:38907524 G>A maps to NM_181534.3 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:38907479 T>A maps to NM_181534.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:38925239 G>A maps to NM_181539.4 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:38926570 G>A maps to NM_181539.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:38928281 G>A maps to NM_181539.4 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:38926218 G>A maps to NM_181539.4 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:38935870 C>T maps to NM_181537.3 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr17:38936089 C>T maps to NM_181537.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:38935972 C>T maps to NM_181537.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:38936668 C>T maps to NM_181537.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr17:38953512 G>A maps to NM_181535.3 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:38954594 G>A maps to NM_181535.3 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:38954594 G>A maps to NM_181535.3 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:38953254 G>A maps to NM_181535.3 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr17:38953470 C>T maps to NM_181535.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr17:38950145 G>T maps to NM_181535.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:38953263 G>A maps to NM_181535.3 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr12:53185036 G>A maps to ENST00000309505 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:53185501 C>T maps to ENST00000309505 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:53189439 A>G maps to ENST00000309505 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:39553728 G>A maps to ENST00000393998 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:39553196 G>A maps to ENST00000393998 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:39552806 C>T maps to ENST00000393998 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr17:39553647 G>A maps to ENST00000393998 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:39553695 G>T maps to ENST00000393998 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:39623481 C>T maps to NM_002278.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:39620557 G>A maps to NM_002278.3 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr17:39619218 G>A maps to NM_002278.3 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:39503152 G>A maps to NM_004138.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:39505668 G>A maps to NM_004138.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:39521516 C>T maps to ENST00000394004 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr17:39521218 G>A maps to ENST00000394004 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr17:39538252 C>T maps to NM_021013.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr17:39535941 G>A maps to NM_021013.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr17:39538252 C>T maps to NM_021013.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr17:39637022 G>A maps to NM_002280.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:39637034 G>A maps to NM_002280.4 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:39643227 G>A maps to NM_003771.4 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:39645729 G>A maps to NM_003771.4 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr17:39580622 G>A maps to NM_003770.4 H51H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr17:39580421 G>A maps to NM_003770.4 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr17:39577725 G>A maps to NM_003770.4 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr17:39578362 C>T maps to NM_003770.4 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr17:39595460 G>A maps to NM_006771.3 H242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr17:39597059 G>T maps to NM_006771.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:39596891 G>T maps to NM_006771.3 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr17:39596777 C>A maps to NM_006771.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:39118724 C>A maps to NM_213656.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr17:39115040 C>A maps to NM_213656.3 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:53201438 G>A maps to NM_002272.2 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr12:53202523 G>A maps to NM_002272.2 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:53203199 G>A maps to NM_002272.2 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr12:53207848 A>G maps to NM_002272.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr12:53200957 A>G maps to NM_002272.2 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:53207428 G>A maps to NM_002272.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:52908905 G>A maps to NM_000424.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:52913759 G>A maps to NM_000424.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:52910511 G>A maps to NM_000424.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:52911000 G>A maps to NM_000424.3 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:52882329 G>A maps to NM_005554.3 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:52884931 G>A maps to NM_005554.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:52886666 G>A maps to NM_005554.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr12:52886879 A>G maps to NM_005554.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:52886879 A>G maps to NM_005554.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr12:52885373 G>A maps to NM_005554.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr12:52886879 A>G maps to NM_005554.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:52842637 G>A maps to NM_005555.3 H397H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:52841347 G>A maps to NM_005555.3 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:52844260 G>A maps to NM_005555.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:52843390 G>T maps to NM_005555.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:52842643 G>A maps to NM_005555.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:52863031 G>A maps to NM_173086.4 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:52865893 C>T maps to NM_173086.4 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:52863046 G>A maps to NM_173086.4 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr12:52635260 G>A maps to NM_005556.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:52941727 G>A maps to NM_033448.2 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:52941700 G>T maps to NM_033448.2 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:52946513 G>A maps to NM_033448.2 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:52946435 G>T maps to NM_033448.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:52994909 C>T maps to NM_080747.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:52981482 C>A maps to NM_080747.2 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr12:52981482 C>T maps to NM_080747.2 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:52985382 G>A maps to NM_080747.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:53012017 C>T maps to NM_175068.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:53010107 C>T maps to NM_175068.2 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:53012086 G>A maps to NM_175068.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:53012245 G>A maps to NM_175068.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr12:53009975 G>A maps to NM_175068.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:53002018 G>A maps to NM_175068.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr12:53008437 C>T maps to NM_175068.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:53012062 A>G maps to NM_175068.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr12:52967276 G>T maps to NM_175053.3 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr12:52967150 G>A maps to NM_175053.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:52966394 C>T maps to NM_175053.3 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:52967108 G>A maps to NM_175053.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr12:52960827 C>T maps to NM_175053.3 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:52827847 G>A maps to ENST00000252245 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr12:52818429 C>A maps to ENST00000252245 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:52818501 G>A maps to ENST00000252245 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:52827677 T>C maps to ENST00000252245 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:52822433 G>A maps to ENST00000252245 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:52827608 G>A maps to ENST00000252245 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:53165747 A>G maps to NM_015848.4 H390H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:53164856 C>T maps to NM_015848.4 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr12:53166626 C>A maps to NM_015848.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:53164964 C>T maps to NM_015848.4 Q434Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:53096885 A>G maps to NM_175078.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:53091463 A>G did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:53096687 G>T maps to NM_175078.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:53091587 C>T maps to NM_175078.2 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:53089555 C>T maps to NM_175078.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:53091587 C>T maps to NM_175078.2 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:53241776 C>T maps to NM_173352.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:53238405 G>A maps to NM_173352.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr12:53240568 G>A maps to NM_173352.2 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr12:53216978 A>G maps to NM_175834.2 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:53217736 G>A maps to NM_175834.2 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr12:53293651 G>A maps to NM_002273.3 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:53293651 G>A maps to NM_002273.3 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr12:53293651 G>A maps to NM_002273.3 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr12:53298480 G>T maps to NM_002273.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr12:52567467 G>A maps to NM_182507.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr12:52585638 A>G maps to NM_182507.2 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:52680170 C>T maps to NM_002281.3 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:52680107 G>A maps to NM_002281.3 C483C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr12:52685195 G>A maps to NM_002281.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr12:52680062 G>A maps to NM_002281.3 C498C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:52714939 G>A maps to NM_002282.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:52711470 G>A maps to NM_002282.3 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr12:52714810 G>A maps to NM_002282.3 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:52710344 G>A maps to NM_002282.3 H316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr12:52708507 G>A maps to NM_002282.3 N463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:52778970 T>C maps to NM_033045.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:52774232 G>A maps to NM_033045.3 C446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:52761081 G>A maps to NM_002283.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr12:52758834 C>A maps to NM_002283.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:52756664 C>T maps to NM_002283.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:52695750 C>T maps to NM_002284.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:52699160 T>C maps to NM_002284.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:52699061 C>T maps to NM_002284.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:39723596 G>A maps to NM_000226.3 Y600Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:39723992 G>A maps to NM_000226.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:39723829 C>A maps to NM_000226.3 G523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr17:39197430 T>A maps to NM_030967.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr17:39197553 G>T maps to NM_030967.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:39197466 T>C maps to NM_030967.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr17:39190656 G>A maps to NM_030966.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:39182990 C>T maps to NM_031957.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr21:45959373 G>A maps to NM_198691.2 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr21:46066470 C>T maps to NM_198692.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr21:46066872 T>C maps to NM_198692.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr21:46066872 T>C maps to NM_198692.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr21:46117133 C>T maps to NM_198699.1 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr21:46117241 C>T maps to NM_198699.1 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr21:46117187 C>T maps to NM_198699.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr21:45971161 C>T maps to NM_198693.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr21:45978001 G>A maps to NM_198696.2 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:46011651 G>T maps to NM_198688.2 C238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:46020892 C>T maps to ENST00000380102 C124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr21:46021402 G>A maps to ENST00000380102 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr21:46032493 C>A maps to NM_198695.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr21:46032493 C>T maps to NM_198695.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:32253396 C>T maps to NM_175858.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr21:31768661 C>A maps to NM_181599.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr21:31768679 C>T maps to NM_181599.2 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr21:31768691 C>T maps to NM_181599.2 Y96Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:31744303 G>A maps to NM_181621.3 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr21:31797816 A>G maps to NM_181622.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr21:31798086 C>A maps to NM_181622.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr21:31802949 C>T maps to NM_181600.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr21:31802880 C>A maps to NM_181600.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr21:31812683 C>T maps to NM_181623.1 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr21:31852582 G>A maps to NM_181607.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:31852582 G>A maps to NM_181607.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr21:31852600 G>T maps to NM_181607.1 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:31859640 A>G maps to NM_181608.1 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr21:31864089 G>A maps to ENST00000433652 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr21:31869395 C>T maps to ENST00000433652 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:31869356 G>T maps to ENST00000433652 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr21:31869395 C>T maps to ENST00000433652 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr21:31874363 G>A maps to NM_181611.1 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:31874354 G>A maps to NM_181611.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr21:31933554 G>A maps to ENST00000437381 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr21:31933569 G>A maps to ENST00000437381 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr21:31988928 A>G maps to ENST00000399871 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr21:32127645 G>A maps to NM_181619.1 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:32119403 A>G maps to NM_181617.1 Y39Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr21:31973484 G>T maps to NM_181620.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr21:31973480 C>A maps to NM_181620.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr21:31720804 T>C maps to NM_181624.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr21:31654986 C>T maps to NM_001085455.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr21:31654986 C>T maps to NM_001085455.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr21:31692299 G>A maps to NM_203405.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr21:31691795 C>A maps to NM_203405.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr21:31691837 A>T maps to NM_203405.1 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr21:31709437 T>C maps to NM_001077711.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr21:31709707 C>T maps to NM_001077711.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr21:31709681 G>T maps to NM_001077711.1 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:39156096 G>A maps to NM_031959.2 C3C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:39274084 C>T maps to NM_033059.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr17:39280056 A>G maps to NM_031854.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr17:39324103 A>G maps to NM_033187.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:39324040 G>T maps to NM_033187.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr17:39305836 G>T maps to NM_033188.3 C61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:39240691 G>A maps to ENST00000377731 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr17:39254123 C>G maps to NM_031960.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:71277217 C>T maps to NM_001012710.1 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr11:71293685 G>C maps to ENST00000376535 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:71293679 G>A maps to ENST00000376535 G68G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A6-6653-01A-11D-1771-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-3518-01A-02W-0833-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:1628994 T>C maps to ENST00000359229 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:1628931 G>A maps to ENST00000359229 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:1629078 G>A maps to ENST00000359229 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:1643257 C>T maps to ENST00000359229 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:1651189 C>T maps to NM_001001480.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr11:1651120 T>A maps to NM_001001480.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr11:1718645 G>A maps to NM_001012416.1 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:1718717 C>T maps to NM_001012416.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:71238579 C>T maps to NM_001012503.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr11:71249124 A>G maps to NM_021046.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr21:31964901 C>T maps to NM_181605.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr21:31964934 C>G maps to ENST00000399871 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:32185412 G>A maps to NM_175857.3 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:39406160 G>A maps to NM_033191.2 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:39406205 A>C maps to NM_033191.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:39406256 C>A maps to NM_033191.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr17:39394488 G>C maps to NM_031963.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:155142285 G>A maps to NM_173852.3 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:25931720 G>A maps to ENST00000268763 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr17:25932506 C>T maps to ENST00000268763 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:25915544 C>T maps to ENST00000268763 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:118199117 G>T maps to ENST00000339824 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr12:118199153 G>A maps to ENST00000339824 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:117962829 G>A maps to ENST00000339824 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:117964917 T>C maps to ENST00000339824 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr12:117969477 G>T maps to ENST00000339824 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:118405897 C>A maps to ENST00000339824 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:117996344 G>A maps to ENST00000339824 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:118105387 C>T maps to ENST00000339824 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:117977584 C>T maps to ENST00000339824 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:118198880 C>T maps to ENST00000339824 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr12:117914381 G>A maps to ENST00000339824 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:118293320 G>A maps to ENST00000339824 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr12:117977575 G>T maps to ENST00000339824 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:119210363 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:119209401 C>T maps to NM_152305.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr14:56130758 G>A maps to NM_001079521.1 K1059K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr14:56119763 A>G maps to NM_001079521.1 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr14:56079104 A>G maps to NM_001079521.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:134322795 G>T maps to NM_178554.4 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:134322978 G>A maps to NM_178554.4 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:134323299 C>T maps to NM_178554.4 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr2:143799647 G>T maps to NM_003937.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:143743578 G>A maps to NM_003937.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:143799662 C>A maps to NM_003937.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:143718296 G>A maps to NM_003937.2 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:143713791 G>A maps to NM_003937.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:153136337 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:153134973 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:153134318 T>C did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:153130950 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:153136599 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:153129361 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr23:153136381 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:153128275 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:153135085 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:153130410 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:153128249 G>A did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:153133314 T>C did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:153130781 G>A did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:153133528 G>A did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:153136542 T>C did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:153136542 T>C did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr23:153136543 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:153133314 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:153133787 G>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:153137804 G>A did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:153136542 T>C did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:153130574 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:62675768 A>G maps to NM_019079.4 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:62675768 A>G maps to NM_019079.4 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:62672749 C>T maps to NM_019079.4 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:62672750 G>T maps to NM_019079.4 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:50736035 G>A maps to NM_024884.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:42143190 C>T maps to NM_015478.6 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:42168893 G>A maps to NM_032107.4 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:42143189 G>A maps to NM_015478.6 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr20:42162720 G>A maps to NM_032107.4 W507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:42169451 C>T maps to NM_032107.4 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:42143778 C>T maps to NM_032107.4 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr20:42161501 C>T maps to NM_032107.4 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr20:42143742 C>A maps to NM_032107.4 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr20:42162982 A>T maps to NM_032107.4 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr22:41620993 C>T maps to NM_031488.4 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:41620169 C>T maps to NM_031488.4 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr22:41620121 A>G maps to NM_031488.4 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:130372526 G>A maps to NM_032438.2 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr6:130389526 T>C maps to NM_032438.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr6:130387571 T>C maps to NM_032438.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr6:130376383 G>A maps to NM_032438.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr6:130389526 T>C maps to NM_032438.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr18:6244485 C>T maps to NM_173464.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:5960140 T>C maps to NM_173464.3 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr18:5969541 C>T maps to NM_173464.3 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:71553241 T>C maps to NM_016027.2 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:71553173 G>T maps to NM_016027.2 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:201352291 G>A maps to NM_005558.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:201353947 C>A maps to NM_005558.3 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:153706666 C>A did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr19:54868558 C>T maps to NM_002287.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr19:54866900 C>T maps to NM_002287.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:54871662 C>T maps to NM_002287.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:54868157 G>T maps to NM_002287.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr19:54866936 G>A maps to NM_002287.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr19:55019331 T>C maps to NM_002288.3 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr19:55019331 T>C maps to NM_002288.3 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr18:6982565 G>A maps to NM_005559.2 N1940N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr18:6986258 G>A maps to NM_005559.2 H1752H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr18:6942194 G>A maps to NM_005559.2 R3037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr18:7032091 A>C maps to NM_005559.2 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:6948486 G>A maps to NM_005559.2 S2875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr18:7026006 G>A maps to NM_005559.2 C791C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr18:6986297 C>T maps to NM_005559.2 P1739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr18:7012041 G>A maps to NM_005559.2 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr18:7049145 C>T maps to NM_005559.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:7014008 G>A maps to NM_005559.2 C1056C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr18:7008591 T>A maps to NM_005559.2 S1339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:6964725 A>G maps to NM_005559.2 S2424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr18:7010270 C>T maps to NM_005559.2 K1267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:6978336 C>T maps to NM_005559.2 T2016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr18:7044736 G>A maps to NM_005559.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:6950819 G>T maps to NM_005559.2 V2786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:6978321 G>A maps to NM_005559.2 S2021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:6982582 C>A maps to NM_005559.2 E1935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:6966163 G>A maps to NM_005559.2 Y2344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:6986174 G>A maps to NM_005559.2 H1780H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:6986306 G>A maps to NM_005559.2 Y1736Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:6978321 G>A maps to NM_005559.2 S2021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:6958661 C>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr18:7037642 G>A maps to NM_005559.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:6978288 C>T maps to NM_005559.2 L2032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:7049076 G>A maps to NM_005559.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr18:6986225 C>T maps to NM_005559.2 A1763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr18:7033057 A>G maps to NM_005559.2 N696N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr6:129813141 T>C maps to NM_000426.3 A2665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:129637185 G>T maps to NM_000426.3 E1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:129475791 C>T maps to NM_000426.3 C390C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:129636999 C>T maps to NM_000426.3 R1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:129725025 C>T maps to NM_000426.3 S1929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr6:129785588 C>T maps to NM_000426.3 R2383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:129759857 C>A maps to NM_000426.3 L2012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:129649443 C>T maps to NM_000426.3 R1400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:129691104 C>T maps to NM_000426.3 L1643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:129470224 T>C maps to NM_000426.3 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:129722391 C>T maps to NM_000426.3 S1823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:129823818 G>T maps to NM_000426.3 E2754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:129813060 A>G maps to NM_000426.3 Q2638Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr6:129635867 A>G maps to NM_000426.3 P1160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:129371127 G>T maps to NM_000426.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:129381034 A>G maps to NM_000426.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:129824274 C>T maps to NM_000426.3 S2799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:129833511 T>C maps to NM_000426.3 G2954G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr6:129641721 T>C maps to NM_000426.3 R1366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:129723617 T>C maps to NM_000426.3 S1904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:129762060 C>T maps to NM_000426.3 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:129828677 A>G maps to NM_000426.3 A2916A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:129419442 G>A maps to NM_000426.3 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr6:129802421 T>C maps to NM_000426.3 V2529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:129636914 C>A maps to NM_000426.3 A1248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:129785497 C>T maps to NM_000426.3 S2352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr18:21413904 C>T maps to ENST00000416669 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:21478925 A>C maps to ENST00000416669 V1913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr18:21496634 C>A maps to ENST00000416669 G2635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr18:21333776 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:21422468 C>T maps to ENST00000416669 G1151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr18:21330991 C>T maps to ENST00000416669 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr18:21526172 A>G maps to ENST00000416669 G3094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr18:21396412 C>T maps to ENST00000416669 C705C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr18:21474874 C>T maps to ENST00000416669 C1824C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:21451417 C>T maps to ENST00000416669 S1599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:21355756 C>A maps to ENST00000416669 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:21447863 C>T maps to ENST00000416669 R1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr18:21419835 C>A maps to ENST00000416669 P1095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:112480076 C>T maps to NM_001105206.1 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:112466058 G>A maps to NM_001105206.1 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:112508650 C>T did not map to a codon.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr6:112508672 G>A maps to NM_001105206.1 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr6:112430729 G>A maps to NM_001105206.1 R1794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:112512940 G>T maps to NM_001105206.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:112460991 G>T maps to NM_001105206.1 I1024I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:112537589 C>T maps to NM_001105206.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:112462024 A>G maps to NM_001105206.1 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:112494004 T>C maps to NM_001105206.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:112463410 C>T maps to NM_001105206.1 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:112466085 C>A maps to NM_001105206.1 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:112508789 G>A maps to NM_001105206.1 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:112462662 G>A maps to NM_001105206.1 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:112496623 G>T maps to NM_001105206.1 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr6:112506503 G>A maps to NM_001105206.1 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr6:112462024 A>G maps to NM_001105206.1 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr6:112462024 A>G maps to NM_001105206.1 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr6:112443317 G>A maps to NM_001105206.1 H1458H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr6:112450237 A>G maps to NM_001105206.1 Y1391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:60893638 G>C maps to NM_005560.3 T2370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:60907445 T>C maps to NM_005560.3 E1178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:60908963 G>A maps to NM_005560.3 C957C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:60912682 T>C maps to NM_005560.3 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:60927348 C>T maps to NM_005560.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:60927411 G>A maps to NM_005560.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr20:60894812 G>A maps to NM_005560.3 A2266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:60887285 G>A maps to NM_005560.3 S3149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:60897448 C>T maps to NM_005560.3 P2074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:60908504 G>A maps to NM_005560.3 Y1018Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:60894848 G>T maps to NM_005560.3 A2254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:60906107 G>A maps to NM_005560.3 H1210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:60908522 C>T maps to NM_005560.3 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr20:60887234 C>T maps to NM_005560.3 A3166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr20:60903418 C>T maps to NM_005560.3 L1510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr7:107575916 G>C maps to NM_002291.2 L1377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr7:107602081 G>A maps to NM_002291.2 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:107603376 G>A maps to NM_002291.2 Y610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr7:107580510 G>A maps to NM_002291.2 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr7:107599740 C>A maps to NM_002291.2 G881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:107572774 G>A maps to NM_002291.2 G1412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:49168287 G>A maps to NM_002292.3 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:49169730 C>T maps to NM_002292.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr3:49162720 G>C maps to NM_002292.3 G895G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr3:49162242 A>G maps to NM_002292.3 C1000C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:49169706 C>T maps to NM_002292.3 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr3:49169730 C>T maps to NM_002292.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr3:49162571 C>T maps to NM_002292.3 R917R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr3:49169732 G>T maps to NM_002292.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:209803238 A>G maps to NM_000228.2 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:209790825 G>A maps to NM_000228.2 Q1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:209801425 C>T maps to NM_000228.2 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:209788720 C>T maps to NM_000228.2 Q1138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:209789960 C>T maps to NM_000228.2 E1079E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:107738989 G>A maps to NM_007356.2 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:107717448 G>T maps to NM_007356.2 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:107703377 G>A maps to NM_007356.2 C1041C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:107743597 G>A maps to NM_007356.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:107704410 G>A maps to NM_007356.2 C952C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:107743537 G>T maps to NM_007356.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr7:107748207 C>T maps to NM_007356.2 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr7:107752376 G>A maps to NM_007356.2 C69C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:183093868 T>C maps to NM_002293.3 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:183083762 C>T maps to NM_002293.3 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:183084688 A>G maps to NM_002293.3 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:183085789 C>T maps to NM_002293.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:183091038 C>T maps to NM_002293.3 C724C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:183105701 C>T maps to NM_002293.3 I1432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr1:183093868 T>C maps to NM_002293.3 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:183093868 T>C maps to NM_002293.3 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr1:183196725 C>T maps to NM_005562.2 H454H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:183196761 C>T maps to NM_005562.2 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:183212498 A>G maps to NM_005562.2 P1182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr9:133911588 C>T maps to ENST00000355048 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr9:133961019 G>A maps to ENST00000355048 A1392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr9:133952672 C>T maps to ENST00000355048 G1243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr9:133920994 C>T maps to ENST00000355048 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:133901729 C>T maps to ENST00000355048 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:133932373 A>C maps to ENST00000355048 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:133954657 G>A maps to ENST00000355048 T1300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:133954657 G>A maps to ENST00000355048 T1300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:133945209 G>A maps to ENST00000355048 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr13:113975947 G>A maps to NM_005561.3 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:113975923 C>T maps to NM_005561.3 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr13:113975908 G>A maps to NM_005561.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:113963965 C>A maps to NM_005561.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:119590508 A>C did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:119602984 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:119602989 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:119565256 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:119575596 T>G did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:119573097 C>A did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr3:182871490 C>T maps to NM_014398.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:182871751 G>A maps to NM_014398.3 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr3:182853604 G>A maps to NM_014398.3 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:182872114 T>C maps to NM_014398.3 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr3:182871685 G>A maps to NM_014398.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:211341093 A>C maps to NM_001136575.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:55492954 G>A maps to NM_018697.3 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:55479742 C>T maps to NM_018697.3 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:37515022 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:37534927 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:17609064 C>T maps to NM_015907.2 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:17585154 T>C maps to NM_015907.2 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr2:20240748 A>G maps to NM_014713.4 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr8:98837350 C>G maps to ENST00000378722 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:98827574 G>A maps to ENST00000378722 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:31206722 C>T maps to NM_006762.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr22:33700432 G>A maps to NM_133642.3 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr22:34157382 A>G maps to NM_133642.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr22:34046574 G>A maps to NM_133642.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:33679273 G>A maps to NM_133642.3 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr22:33712111 G>A maps to NM_133642.3 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr22:33712111 G>A maps to NM_133642.3 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:154185461 G>A maps to ENST00000377643 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr5:154179580 G>A maps to ENST00000377643 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:154185461 G>A maps to ENST00000377643 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:154173699 T>C maps to ENST00000377643 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr5:154185464 T>C maps to ENST00000377643 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:154181565 G>T did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:154173477 G>C maps to ENST00000377643 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:129035843 G>T maps to NM_018078.2 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:129120605 T>G maps to NM_018078.2 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:50822862 T>C maps to ENST00000429001 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:50860752 T>C maps to ENST00000429001 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr12:50869314 C>T maps to ENST00000429001 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:50867886 G>A maps to ENST00000429001 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:859146 G>A maps to NM_015155.1 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:909764 C>T maps to NM_015155.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:871158 G>T maps to NM_015155.1 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:890956 G>A maps to NM_015155.1 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr10:859015 G>A maps to NM_015155.1 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:858907 A>G maps to NM_015155.1 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:910081 G>A maps to NM_015155.1 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:71124594 G>A maps to NM_018357.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr15:71125191 T>A maps to NM_018357.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:71125092 G>A maps to NM_018357.2 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:71125257 G>A maps to NM_018357.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr4:113570807 A>G maps to ENST00000509061 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr4:113570786 A>G maps to ENST00000509061 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr4:113571626 G>A maps to ENST00000509061 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr4:113570807 A>G maps to ENST00000509061 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr4:113570807 A>G maps to ENST00000509061 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr4:113570807 A>G maps to ENST00000509061 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:145537355 A>G maps to NM_020117.9 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:145519820 G>A maps to NM_020117.9 D698D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr5:145508575 G>A maps to NM_020117.9 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:145493695 G>A maps to NM_020117.9 G1168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:145529244 T>A maps to NM_020117.9 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:145552288 G>A maps to NM_020117.9 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr5:145508639 A>G maps to NM_020117.9 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:145536998 G>A maps to NM_020117.9 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:64732727 C>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:64744105 G>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:64751241 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:64751241 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:64751241 C>T did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:64744052 T>C did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:64751241 C>T did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:64749521 C>T did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:64744052 T>C did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:37070657 A>G maps to NM_006148.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:37074955 C>T maps to NM_006148.2 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:37054771 C>T maps to NM_006148.2 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr15:100943016 C>T maps to ENST00000394113 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr15:100942968 G>A maps to ENST00000394113 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:8321861 C>T maps to NM_024552.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr19:8322866 C>T maps to NM_024552.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:50532370 G>A maps to NM_147190.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr16:28997966 G>A maps to NM_014387.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:28997738 G>A maps to NM_014387.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr16:28997873 G>A maps to NM_014387.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:73639038 C>T maps to NM_032464.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr6:150004718 A>G maps to NM_004690.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:150004718 A>G maps to NM_004690.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:150001473 T>C maps to NM_004690.2 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:150001187 G>A maps to NM_004690.2 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:150005459 A>G maps to NM_004690.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:149982975 C>T maps to NM_004690.2 P1094P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:150005468 T>C maps to NM_004690.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:150004718 A>G maps to NM_004690.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr6:150005468 T>C maps to NM_004690.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:150005468 T>C maps to NM_004690.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr13:21549227 T>C maps to NM_014572.2 E1016E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr13:21549308 G>A maps to NM_014572.2 Y989Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:21557816 G>A maps to NM_014572.2 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:21549230 G>A maps to NM_014572.2 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr13:21620045 T>C maps to NM_014572.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:21553889 G>A maps to NM_014572.2 F904F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr13:21562244 G>A maps to NM_014572.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr13:21620045 T>C maps to NM_014572.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:203743595 C>T maps to NM_017773.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:111414780 C>T maps to ENST00000375615 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:111420381 C>A maps to ENST00000375615 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:30480469 G>T maps to NM_030915.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr20:36982722 C>T maps to NM_004139.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:225594519 C>T maps to NM_194442.1 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:225607069 C>A maps to NM_194442.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:225607069 C>A maps to NM_194442.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr1:225599131 G>C maps to NM_194442.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:225598019 G>T maps to NM_194442.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:102987298 C>A maps to NM_006562.4 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:102987496 G>A maps to NM_006562.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:102988410 G>A maps to NM_006562.4 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:74725140 G>A maps to NM_001009812.1 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:68118555 C>T maps to ENST00000380035 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:68126113 G>A maps to ENST00000380035 K946K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:68118546 C>T maps to ENST00000380035 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:80197161 G>A maps to NM_181714.3 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr6:80198891 C>A maps to NM_181714.3 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr6:80198860 T>A maps to NM_181714.3 K391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:80197421 C>A maps to NM_181714.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:80197583 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:80223131 C>A maps to NM_181714.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr21:40794963 C>A maps to NM_152505.3 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:67974067 G>A maps to NM_000229.1 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:67976842 G>A maps to NM_000229.1 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr16:67973854 A>G maps to NM_000229.1 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:152785041 C>A maps to NM_178349.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:152785074 C>A maps to NM_178349.1 C51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:152749023 C>T maps to NM_178354.2 C59C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr1:152749164 C>T maps to NM_178354.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:152671529 C>T maps to NM_178428.3 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:152659414 C>T maps to NM_014357.4 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:152659417 G>A maps to NM_014357.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:152659327 C>T maps to NM_014357.4 C3C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:152648577 C>T maps to NM_178429.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr1:152648628 T>C maps to NM_178429.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:152595318 G>A maps to NM_178431.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:152573449 C>T maps to NM_178434.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr1:152538447 G>A maps to NM_178435.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:152681679 C>T maps to NM_178356.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:152484108 C>T maps to NM_178438.4 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:32742271 C>T maps to ENST00000373562 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:32745785 C>A maps to ENST00000373562 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:30682501 T>C maps to NM_182551.3 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr2:30863098 C>A maps to NM_182551.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr9:138415759 G>A maps to NM_002297.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:139637333 G>A maps to NM_001001712.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:139849826 G>A maps to NM_178536.3 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:139658165 C>T maps to NM_203347.1 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:130915391 C>T maps to ENST00000373013 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr9:138556090 C>T maps to ENST00000277526 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:17886169 G>T maps to NM_001166139.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:17847355 G>A maps to NM_153686.7 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:17963556 T>C maps to NM_001166139.1 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:46716515 C>T maps to NM_002298.4 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr13:46701725 T>G maps to NM_002298.4 *628C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:169688115 C>A maps to NM_005565.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:169680131 C>T maps to NM_005565.3 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr5:169697804 C>T maps to NM_005565.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr5:169677769 T>C maps to NM_005565.3 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr5:169714972 C>T did not map to a codon.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:136567501 G>A maps to NM_002299.2 F805F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr2:136547321 C>T maps to NM_002299.2 A1794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr2:136575429 G>A maps to NM_002299.2 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:136575459 G>A maps to NM_002299.2 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:136561515 G>A maps to NM_002299.2 Y1549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:136567495 G>A maps to NM_002299.2 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:136594286 G>A maps to NM_002299.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:136566313 G>T maps to NM_002299.2 A1201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:136564709 A>G maps to NM_002299.2 S1387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:136567186 G>A maps to NM_002299.2 G910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:136566313 G>T maps to NM_002299.2 A1201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:136566313 G>T maps to NM_002299.2 A1201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr2:136564709 A>G maps to NM_002299.2 S1387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:136548387 C>T maps to NM_002299.2 T1725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr2:136566474 G>A maps to NM_002299.2 Q1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:136587195 C>T maps to NM_002299.2 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:136562576 C>T maps to NM_002299.2 T1408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr15:66857031 G>A maps to NM_207338.2 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr15:66853526 G>T maps to NM_207338.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:66853376 G>A maps to NM_207338.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:66840911 C>T maps to NM_207338.2 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr15:66856251 G>A maps to NM_207338.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr15:66853376 G>A maps to NM_207338.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr4:16504334 C>T maps to NM_001290.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr4:16597346 G>A maps to NM_001290.3 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr10:88441413 C>T maps to NM_001171610.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr10:88485963 C>T maps to NM_001171610.1 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:88441539 G>A maps to NM_001171610.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:88478581 C>T maps to NM_001171610.1 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr11:18421012 C>T maps to NM_001165414.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr11:18421028 G>T maps to NM_001165414.1 G89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr11:18421030 A>G maps to NM_001165414.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:18499236 G>T maps to NM_144972.4 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:18485521 A>G maps to NM_144972.4 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr15:59500146 A>G maps to NM_033195.1 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:21788475 T>G maps to NM_002300.6 *335C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr11:18467843 T>C maps to NM_017448.3 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:18460141 G>A maps to NM_017448.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:75148863 G>A maps to NM_153486.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr16:75146525 G>C maps to NM_153486.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr16:75148773 G>C maps to NM_153486.3 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:11240345 G>A maps to NM_000527.4 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:11222253 C>T maps to NM_000527.4 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:11223987 C>T maps to NM_000527.4 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:11240342 C>A maps to NM_000527.4 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:11224234 C>T maps to NM_000527.4 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:54477846 G>T maps to NM_001010978.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:25889634 T>C maps to NM_015627.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:140270953 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:140270953 C>T did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:140271018 C>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:140270810 A>G did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr22:44893391 T>C maps to NM_032287.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr22:44893391 T>A maps to NM_032287.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr13:53277819 T>C maps to NM_007015.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr13:53313174 G>A maps to NM_007015.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:135286972 G>T maps to NM_002302.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:226074669 C>T maps to NM_020997.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:226076646 C>T maps to NM_020997.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:226127301 T>C did not map to a codon.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr1:226127173 C>T maps to NM_003240.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:226128746 G>A maps to NM_003240.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr1:153177314 C>T maps to NM_001010857.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:205388379 C>T maps to ENST00000367153 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr12:65612389 G>A maps to NM_014319.4 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr12:65564764 C>A maps to NM_014319.4 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr12:65564842 A>G maps to NM_014319.4 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:65564842 A>G maps to NM_014319.4 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:54659536 C>T maps to NM_024316.1 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr19:54963366 C>T maps to ENST00000431846 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr19:54966190 C>A maps to ENST00000431846 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:54964804 C>T maps to ENST00000431846 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:54967271 G>A maps to ENST00000431846 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:54969676 C>T maps to ENST00000431846 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:54963437 T>C maps to ENST00000431846 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:54974754 G>A maps to NM_198988.1 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:54974070 C>A maps to NM_198988.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:54973998 C>T maps to NM_198988.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:52245363 T>C maps to NM_138792.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:127894590 C>T maps to NM_000230.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:66074505 G>A maps to NM_002303.5 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:66036154 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:66102052 T>C maps to NM_002303.5 G951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:66087081 G>A maps to NM_002303.5 V846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:66075694 C>T maps to NM_002303.5 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:66067524 G>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:66075661 T>G maps to NM_002303.5 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:43213938 G>A maps to NM_022356.3 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:43221251 A>C maps to NM_022356.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:43212436 C>T maps to NM_022356.3 Q714Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr1:43224899 G>T maps to NM_022356.3 Y260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:43223486 T>C maps to NM_022356.3 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:189688658 A>G maps to NM_018192.3 D613D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:189700880 T>C maps to NM_018192.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr3:189689719 T>C maps to NM_018192.3 E592E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:189675700 T>G maps to NM_018192.3 *709Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr3:189700881 G>T maps to NM_018192.3 S426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:189711982 G>A maps to NM_018192.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr3:189688658 A>G maps to NM_018192.3 D613D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr3:189688658 A>G maps to NM_018192.3 D613D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr3:189675794 T>G did not map to a codon.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr12:6940434 G>A maps to NM_014262.3 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:6946897 G>T maps to NM_014262.3 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr12:6946220 G>T maps to NM_014262.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:6939162 G>A maps to NM_014262.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:1838220 G>A maps to NM_012318.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:38262005 G>A maps to ENST00000379957 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:38257890 C>T maps to ENST00000379957 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:2552827 A>C maps to NM_001166355.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:38074570 C>T maps to NM_002305.3 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr22:38074612 C>T maps to NM_002305.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:63276300 C>T maps to NM_001142535.1 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:63277353 A>G maps to NM_001142535.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr19:40197277 C>T maps to NM_203471.1 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:40197994 G>A maps to NM_203471.1 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:55611841 A>G maps to NM_002306.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:76968407 A>G maps to NM_005567.3 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:39292966 G>A maps to NM_006149.3 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:236711335 G>T maps to NM_201545.1 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr17:20359951 G>A maps to ENST00000324290 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr10:95557041 G>T maps to NM_005097.2 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:95557001 C>A maps to NM_005097.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:25005708 G>A maps to NM_018176.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:25014121 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr8:22005675 G>T maps to NM_139278.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:22006170 G>A maps to NM_139278.2 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:22006443 C>T maps to NM_139278.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr8:22006350 C>T maps to NM_139278.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr19:35622733 G>T maps to NM_139284.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr19:35616165 G>A maps to NM_139284.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:35616129 G>T maps to NM_139284.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr19:35617793 G>A maps to NM_139284.2 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr14:93180172 G>A maps to NM_005606.6 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:93176021 G>A maps to NM_005606.6 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:93180173 G>A maps to NM_005606.6 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:93178265 C>T maps to NM_005606.6 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:93172962 G>A maps to NM_005606.6 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr14:93172944 C>T maps to NM_005606.6 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:27389487 G>A maps to NM_018490.2 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:27389932 G>A maps to NM_018490.2 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr11:27389487 G>A maps to NM_018490.2 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:27389695 G>A maps to NM_018490.2 C858C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:27412665 G>A maps to NM_018490.2 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:27389487 G>A maps to NM_018490.2 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:27389899 A>G maps to NM_018490.2 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr12:71977931 T>C maps to NM_003667.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:71978360 C>T maps to NM_003667.2 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:71977625 G>A maps to NM_003667.2 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:202276526 G>A maps to NM_001017403.1 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr1:202245514 C>T maps to NM_001017403.1 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:202245514 C>T maps to NM_001017403.1 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:202205113 C>T maps to NM_001017403.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:202287248 C>T maps to NM_001017403.1 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr1:202287605 T>C maps to NM_001017403.1 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:202288214 C>A maps to NM_001017403.1 P928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:202245649 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:63990450 C>T maps to NM_016571.2 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:63990375 C>T maps to NM_016571.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:63990584 C>A maps to NM_016571.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:63990441 C>T maps to NM_016571.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:206775703 G>A maps to NM_006893.2 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:206782795 G>T maps to NM_006893.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:206769078 C>T maps to NM_006893.2 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:49519471 C>T maps to NM_000894.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:49519507 A>G maps to NM_000894.2 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:49519540 C>T maps to NM_000894.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:48950765 G>A maps to NM_000233.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:48914955 G>A maps to NM_000233.3 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:48950761 G>A maps to NM_000233.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:48915351 T>A maps to NM_000233.3 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr2:48925806 G>A maps to NM_000233.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr2:48915351 T>G maps to NM_000233.3 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr13:40175188 A>G maps to NM_005780.2 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:111914527 A>G did not map to a codon.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr23:111914501 C>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr7:103969379 C>T maps to NM_199000.2 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:9594219 G>A maps to NM_198560.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:9594237 G>A maps to NM_198560.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:9547735 G>A maps to NM_198560.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:35773617 G>A maps to NM_182548.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:35773632 C>T maps to NM_182548.3 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr6:35782473 C>T maps to NM_182548.3 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:35300116 C>T maps to NM_005568.3 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:126794964 G>A maps to NM_004789.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:126794889 G>A maps to NM_004789.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:139092438 G>A maps to NM_014564.3 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:180235526 G>A maps to NM_033343.3 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:180243560 C>A maps to NM_033343.3 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:113907077 G>A maps to NM_022363.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr12:113905103 G>A maps to NM_022363.2 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:124976612 T>C maps to NM_014368.3 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:124979347 G>A maps to NM_014368.3 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:124989231 C>T maps to NM_014368.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:124979386 G>A maps to NM_014368.3 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:124979539 G>A maps to NM_014368.3 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:124979524 G>A maps to NM_014368.3 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:124976627 C>T maps to NM_014368.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr1:75609593 A>G maps to NM_001001933.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:197881672 T>C maps to NM_001014434.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:197890485 G>T maps to NM_020204.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:197890478 C>T maps to NM_020204.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:197898313 G>A maps to NM_020204.2 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr5:38481810 T>C maps to NM_002310.5 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:38496681 C>A maps to NM_002310.5 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:38496538 T>C maps to NM_002310.5 K610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:38484962 T>C maps to NM_002310.5 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr5:38493713 C>A maps to NM_002310.5 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:38490300 C>A maps to NM_002310.5 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:38527353 A>G maps to NM_002310.5 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:38496691 T>C maps to NM_002310.5 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr5:38484941 G>T maps to NM_002310.5 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:38496579 G>A maps to NM_002310.5 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:38493780 C>T maps to NM_002310.5 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr19:48626506 G>A maps to NM_000234.1 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:48634422 G>A maps to NM_000234.1 H577H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:48619176 G>A maps to NM_000234.1 R877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:48643324 G>T maps to NM_000234.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:48634410 G>A maps to NM_000234.1 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr19:48626223 G>A maps to NM_000234.1 Y733Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr19:48653078 G>C maps to NM_000234.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:48640864 G>A maps to NM_000234.1 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr19:48631262 C>T maps to NM_000234.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:33329031 A>G maps to NM_013975.3 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:33319683 G>A maps to NM_013975.3 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:33319587 G>A maps to NM_013975.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:108861362 C>A maps to NM_001098268.1 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:108861786 G>A maps to NM_001098268.1 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:108861204 G>T maps to NM_001098268.1 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:108861525 C>T maps to NM_001098268.1 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr13:108861825 G>A maps to NM_001098268.1 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr19:55106754 T>C maps to NM_006863.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:55106796 C>A maps to NM_006863.1 C197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:55107951 C>T maps to NM_006863.1 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:55106397 C>A maps to NM_006863.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr19:55106787 G>A maps to NM_006863.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:54800066 G>A maps to ENST00000251375 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:54803091 G>A maps to ENST00000251375 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr19:54803580 G>A maps to ENST00000251375 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr19:54803121 G>T maps to ENST00000251375 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:54848836 G>A maps to NM_012276.3 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr19:54849483 G>A maps to NM_012276.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:54848196 C>T maps to NM_012276.3 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr19:54849480 T>G maps to NM_012276.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:54818814 G>A maps to NM_021250.2 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:54822753 G>T maps to NM_021250.2 C214*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D5-6540-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr19:54746124 G>A maps to ENST00000407860 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:54742837 G>A maps to NM_024318.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr19:54745722 C>A maps to ENST00000270464 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:55145458 G>A maps to ENST00000427581 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr19:55144530 C>T maps to ENST00000427581 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:55144608 G>A maps to ENST00000427581 W403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:55143035 C>T maps to ENST00000427581 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr19:54783323 G>A maps to ENST00000391747 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:54722657 C>T maps to NM_001081450.1 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr19:54721072 G>A maps to NM_001081450.1 Y596Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:54724665 C>T maps to NM_001081450.1 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr19:55175847 C>T maps to ENST00000391733 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr19:54761029 A>G maps to NM_001081442.1 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr19:54756851 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:51883762 G>A maps to NM_030657.3 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:50642470 C>A maps to NM_001113546.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:50570974 C>A maps to NM_001113546.1 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr12:50571179 T>C maps to NM_001113546.1 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:41608015 C>T maps to NM_014988.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:41694391 C>T maps to NM_014988.2 R1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr4:41608015 C>T maps to NM_014988.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:41362913 C>A maps to NM_014988.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr3:45636916 C>T maps to NM_014240.2 N182N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr3:45636880 T>C maps to NM_014240.2 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:45636880 T>C maps to NM_014240.2 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr7:73522253 C>T maps to NM_002314.2 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr22:31672975 T>C maps to NM_001031801.1 D637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr22:31655979 G>A maps to NM_001031801.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:26737970 C>T maps to NM_024674.4 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:26738003 C>T maps to NM_024674.4 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:26738030 C>T maps to NM_024674.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:105406004 C>G maps to NM_001004317.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr19:36244069 C>T maps to NM_019104.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:83900138 C>T maps to NM_194282.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr4:83857171 G>A maps to NM_194282.2 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:81283027 A>G did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:226454021 A>T maps to ENST00000366807 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:77907530 G>A maps to NM_032808.5 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr15:77906538 G>A maps to NM_032808.5 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:77907600 G>A maps to NM_032808.5 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:77907693 G>A maps to NM_032808.5 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr15:77907843 C>T maps to NM_032808.5 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr9:27950126 C>T maps to NM_152570.1 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:27949622 G>A maps to NM_152570.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:27950327 G>A maps to NM_152570.1 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:27950486 G>T maps to NM_152570.1 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr9:27948944 G>A maps to NM_152570.1 N575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr15:101114012 A>T maps to NM_001040616.2 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr15:101114264 A>C maps to NM_001040616.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:101109660 C>A maps to NM_001040616.2 E686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:101115219 G>T maps to NM_001040616.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:90983568 C>A maps to NM_000235.2 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:90974674 C>T maps to NM_000235.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:90984920 A>G maps to NM_000235.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr10:90974776 C>T maps to NM_000235.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:58840565 G>A maps to NM_000236.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:58830635 C>T maps to NM_000236.2 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:58830574 G>A maps to NM_000236.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:58834827 G>A maps to NM_000236.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:58830604 C>A maps to NM_000236.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:42931184 C>T maps to NM_005357.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:42930734 C>T maps to NM_005357.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:42914539 G>A maps to NM_005357.2 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:42911847 C>T maps to NM_005357.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr19:42930863 T>C maps to NM_005357.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr19:42930863 T>C maps to NM_005357.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr19:42931263 C>T maps to NM_005357.2 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:47095889 C>T maps to NM_006033.2 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:47107830 C>A maps to NM_006033.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr3:185251380 A>G maps to NM_139248.2 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:185252726 T>C maps to NM_139248.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:185251460 C>A maps to NM_139248.2 G142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr21:15554163 C>T maps to NM_198996.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr10:90366438 T>C maps to NM_001010939.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:90484306 C>T maps to NM_001080518.1 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:90499787 G>A maps to NM_001080518.1 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr10:90503074 T>C maps to NM_001080518.1 H319H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:90534232 C>T maps to NM_001102469.1 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:99779232 G>A maps to NM_015929.3 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:11647525 G>A maps to NM_001136472.1 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:11650406 C>T maps to NM_001136472.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:96430579 C>A maps to NM_153234.4 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr5:96432518 G>T maps to NM_153234.4 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:145492368 T>C maps to NM_153713.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:18145295 C>T maps to NM_004140.3 R955R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:73559410 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:73569138 G>T maps to NM_001031803.1 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:73555350 A>G maps to NM_001031803.1 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:66517748 T>C maps to NM_032338.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr15:75116801 C>T maps to NM_021819.2 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:75108621 G>A maps to NM_021819.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:75105269 G>A maps to NM_021819.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:97377600 C>T maps to NM_001142292.1 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:156629549 G>A maps to ENST00000354505 Y32Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:156476846 T>C maps to ENST00000354505 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:49496937 A>G maps to NM_018113.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr12:49497479 C>T maps to NM_018113.2 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:49491460 G>A maps to NM_018113.2 H488H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr12:49495284 G>A maps to NM_018113.2 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr12:49498248 G>A maps to NM_018113.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:36122382 A>G maps to NM_001007527.1 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:36122431 G>T maps to NM_001007527.1 S357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:36143289 C>G maps to NM_001007527.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:36116584 A>C maps to NM_001007527.1 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:8574499 A>G maps to NM_014583.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:8590577 G>T maps to NM_014583.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr3:8607281 C>T maps to NM_014583.2 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:8607209 C>A maps to NM_014583.2 C272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:8578903 G>A maps to NM_014583.2 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:8607326 C>T maps to NM_014583.2 C311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr16:1004604 A>G maps to ENST00000262301 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr16:921263 G>A maps to ENST00000262301 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:920742 G>A maps to ENST00000262301 Y406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:50943764 T>C did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr22:50943655 A>G did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr22:50944505 G>A maps to NM_033200.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:197707246 G>A maps to NM_001136049.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:197687178 G>A maps to NM_001136049.2 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:197751529 A>G maps to NM_001136049.2 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:156104723 G>A maps to NM_170707.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:126154738 A>G maps to NM_005573.3 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr5:126154714 G>A maps to NM_005573.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:2432481 A>G maps to NM_032737.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:2433928 G>A maps to NM_032737.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:87805290 G>A maps to NM_006769.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:76382227 T>C maps to ENST00000357063 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr13:76427278 G>A maps to ENST00000357063 Q1402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:76423369 C>T maps to ENST00000357063 R1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:76395393 A>G maps to ENST00000357063 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:76407281 C>T maps to ENST00000357063 F945F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:76378668 A>G maps to ENST00000357063 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr13:76393660 C>T maps to ENST00000357063 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr1:201869576 T>C maps to NM_012134.2 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr1:201868808 A>G maps to NM_012134.2 N444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:123296067 C>T maps to NM_207163.1 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:123302395 C>T maps to NM_207163.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:123301951 C>A maps to NM_207163.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:123302398 C>T maps to NM_207163.1 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:123302974 C>T maps to NM_207163.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:123302968 T>C maps to NM_207163.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:69169037 G>A maps to NM_198271.3 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:69171272 G>A maps to NM_198271.3 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr7:97822458 G>A maps to NM_014916.3 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:97820087 G>A maps to NM_014916.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:97821198 C>T maps to NM_014916.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:97816230 C>T maps to NM_014916.3 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:97821737 T>G maps to NM_014916.3 L654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:97823187 C>T maps to NM_014916.3 P1137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr7:97800899 G>A maps to NM_014916.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr7:97822794 C>T maps to NM_014916.3 H1006H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:49001280 C>T maps to NM_001080434.1 T1044T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr19:49002993 C>T maps to NM_001080434.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr19:49004661 C>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:49001625 G>A maps to NM_001080434.1 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:49002945 G>A maps to NM_001080434.1 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:165179968 G>A maps to NM_177398.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:165182976 C>T maps to NM_177398.3 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:165324787 G>A maps to NM_177398.3 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:165173272 G>A maps to NM_177398.3 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr1:165182991 A>G maps to NM_177398.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr1:165175151 G>A maps to NM_177398.3 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:129455810 G>A maps to NM_001174147.1 E250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:129458247 G>A maps to NM_001174147.1 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr9:129453246 C>T maps to NM_001174147.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr9:129458244 G>A maps to NM_001174147.1 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:129458672 C>T maps to NM_001174147.1 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr3:100170633 T>C maps to ENST00000489752 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:100170780 T>C maps to ENST00000489752 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr5:96315040 A>G maps to NM_005575.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:96349421 A>G maps to NM_005575.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr5:96349497 C>T maps to NM_005575.2 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:54344825 T>C maps to NM_001126328.1 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:54439944 A>G maps to NM_001126328.1 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr4:54364912 C>T maps to NM_001126328.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr4:54344825 T>A maps to NM_001126328.1 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr13:28155765 T>C maps to NM_153371.3 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr13:28155767 C>A maps to NM_153371.3 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr13:28143397 A>G maps to NM_153371.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr5:135188256 C>T maps to ENST00000420621 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:135188325 C>A maps to ENST00000420621 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:96906264 C>T maps to NM_001037228.1 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:96906136 C>T maps to NM_001037228.1 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr16:20826320 A>G maps to NM_030941.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:5694843 G>A maps to NM_004793.2 D694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:5696268 G>A maps to NM_004793.2 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:5714216 G>A maps to NM_004793.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:5694897 G>A maps to NM_004793.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr16:48382146 A>G maps to NM_031490.2 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:48381504 C>T maps to NM_031490.2 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:12583291 G>A maps to NM_152271.3 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr8:12583305 A>T maps to NM_152271.3 L698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:12586831 C>T maps to NM_152271.3 K566K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:12580615 G>A maps to NM_152271.3 Q771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:12580760 T>C maps to NM_152271.3 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:12580613 T>C maps to NM_152271.3 Q771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr2:100906746 C>T maps to NM_198461.3 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr2:100911976 G>A maps to NM_198461.3 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:118145808 A>G did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:118109560 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:118151530 A>T did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:118112392 A>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:118109297 G>A did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr23:118109342 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:118109107 C>G did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr23:118124452 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:153233505 C>T maps to NM_000427.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:153234354 G>A maps to NM_000427.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:121405746 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr8:23217749 A>T maps to NM_002318.2 C128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:23160837 G>A maps to NM_002318.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:23198682 G>A maps to NM_002318.2 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:23217701 G>A maps to NM_002318.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:23167239 G>A maps to NM_002318.2 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:74761051 G>A maps to NM_032603.2 C715C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr2:74762840 G>A maps to NM_032603.2 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:74763994 C>T maps to NM_032603.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:74763191 A>G maps to NM_032603.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:100022770 C>T maps to NM_032211.6 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr10:100022615 C>T maps to NM_032211.6 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr10:100012212 G>A maps to NM_032211.6 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr10:100015391 C>T maps to NM_032211.6 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr6:161006127 C>G maps to NM_005577.2 S1413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:160977156 G>A maps to NM_005577.2 R1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:161007483 C>A maps to NM_005577.2 E1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:161012013 G>T maps to NM_005577.2 S1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:161010684 G>A maps to NM_005577.2 R1283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:160966490 G>T maps to NM_005577.2 Y1793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:160966562 G>A maps to NM_005577.2 Y1769Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr6:160977187 C>T maps to NM_005577.2 R1614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:161010684 G>A maps to NM_005577.2 R1283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:161015089 G>A maps to NM_005577.2 R1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:161027578 G>A maps to NM_005577.2 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr6:160998232 G>T maps to NM_005577.2 T1522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:113637853 G>A maps to NM_057159.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr9:113703929 A>T maps to NM_057159.2 C188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:19735208 G>A maps to NM_004720.5 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:19737772 C>T maps to NM_004720.5 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:19737441 G>A maps to NM_004720.5 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:19737847 G>A maps to NM_004720.5 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr1:85331320 C>T maps to NM_012152.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:78010402 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:78010732 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:78011051 G>A did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:78010950 T>C did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr23:78011284 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:78011370 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:78011464 G>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:78010950 T>C did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:78010950 T>C did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:78011285 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr13:48986283 A>G maps to NM_005767.5 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr13:48985899 G>A maps to NM_005767.5 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:1463912 G>A maps to NM_024830.3 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:1474766 G>A maps to NM_024830.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:1466993 C>T maps to NM_024830.3 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr5:1474673 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:55565845 T>C maps to NM_017839.4 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:55613059 G>T maps to NM_017839.4 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:55584950 C>T maps to NM_017839.4 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr12:7125610 G>A maps to NM_005768.5 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:7087510 C>T maps to NM_005768.5 W344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr12:7087510 C>T maps to NM_005768.5 W344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr15:34656397 C>T maps to NM_153613.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:34654499 C>A maps to NM_153613.2 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:211956633 A>G maps to NM_014873.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:211956631 C>T maps to NM_014873.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:14274138 C>T maps to NM_001008701.2 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:14272286 C>T maps to NM_001008701.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:14261915 C>T maps to NM_001008701.2 P1398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:14263353 G>T maps to NM_001008701.2 I1170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:14273598 G>A maps to NM_001008701.2 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr19:14263247 A>G maps to NM_001008701.2 G1179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:14272229 G>A maps to NM_001008701.2 H473H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:82402429 G>A maps to ENST00000370717 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr1:82409062 G>T maps to ENST00000370717 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:82302677 T>A maps to ENST00000370717 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:82416776 C>A maps to ENST00000370717 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:82436146 T>G maps to ENST00000370717 G957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:82456537 A>G maps to ENST00000370717 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:82302707 T>C maps to ENST00000370717 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr4:62910253 G>A maps to ENST00000506720 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:62758609 G>T maps to ENST00000506720 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:62758569 C>T maps to ENST00000506720 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:62542541 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:62596343 G>T maps to ENST00000506720 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:62936364 G>A maps to ENST00000506720 P1494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:62758609 G>T maps to ENST00000506720 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:62903567 C>A maps to ENST00000506720 G1237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:62935884 T>C maps to ENST00000506720 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:62778476 T>C did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr4:62936391 G>A maps to ENST00000506720 E1503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:62849102 T>C maps to ENST00000506720 I1006I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:11911637 C>T maps to ENST00000396099 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr2:11905834 G>A maps to ENST00000396099 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:11922442 G>A maps to ENST00000396099 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr18:2925362 C>T maps to NM_014646.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr18:2960784 G>C maps to NM_014646.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr20:39978801 C>T maps to NM_022896.1 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:19809336 G>T maps to NM_000237.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr8:19809368 G>A maps to NM_000237.2 W113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:19813367 G>T maps to NM_000237.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr8:19811856 A>G maps to NM_000237.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr8:19811856 A>G maps to NM_000237.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:19797007 C>T maps to NM_000237.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr8:19811856 A>G maps to NM_000237.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr8:19811856 A>G maps to NM_000237.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:56326938 G>A maps to NM_006151.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr17:56329647 C>T maps to NM_006151.2 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:56345255 A>G maps to NM_006151.2 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:188327172 G>A maps to NM_005578.3 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:188592143 C>T maps to NM_005578.3 C572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:188242499 C>T maps to NM_005578.3 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:188202392 A>G maps to NM_005578.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:104071607 A>C maps to NM_017753.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:814917 G>A maps to NM_024888.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:814911 G>A maps to NM_024888.1 H191H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:99764654 A>G maps to NM_014839.4 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:99771645 C>T maps to NM_014839.4 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:99772385 C>T maps to NM_014839.4 R704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:99772046 C>T maps to NM_014839.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:99772217 G>A maps to NM_014839.4 K648K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:99762350 G>T maps to NM_014839.4 G156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:99730157 G>A maps to NM_014839.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr1:99771794 C>T maps to NM_014839.4 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:99772184 G>A maps to NM_014839.4 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:99470050 G>A maps to NM_001037317.1 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:99358628 C>A maps to NM_001037317.1 *322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:99380373 C>A maps to NM_001037317.1 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:99470137 G>A maps to NM_001037317.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:99470074 G>A maps to NM_001037317.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr4:151358007 T>C maps to NM_006726.3 G2274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:151356802 G>A maps to NM_006726.3 R2338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:151791716 C>T maps to NM_006726.3 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:151835448 A>G maps to NM_006726.3 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr4:151392831 C>T maps to NM_006726.3 W2215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr4:151511865 G>A maps to NM_006726.3 A2075A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:151186900 C>T maps to NM_006726.3 W2855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:151752981 A>G maps to NM_006726.3 N1572N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:151774073 C>A maps to NM_006726.3 E930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr4:151773762 A>C maps to NM_006726.3 T1033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:151773585 C>T maps to NM_006726.3 E1092E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:151392788 G>A maps to NM_006726.3 L2229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:151392835 G>A maps to NM_006726.3 R2214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:151773135 C>T maps to NM_006726.3 A1242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:151358009 C>A maps to NM_006726.3 G2274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:151388881 A>G maps to NM_006726.3 N2252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:151773135 C>T maps to NM_006726.3 A1242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:151231426 G>T maps to NM_006726.3 V2612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr4:151749555 A>G maps to NM_006726.3 N1649N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr4:151408966 G>A maps to NM_006726.3 F2167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:151207133 T>C maps to NM_006726.3 T2701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:47315952 C>T maps to NM_001164211.1 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr13:47243224 C>T maps to NM_001164211.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:114357700 A>G did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:114468418 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:114404901 A>G did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:114398325 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:114400447 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:114414218 A>C did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:114468452 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:114414072 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:114422923 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:114419005 C>A did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:114422933 C>A did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:114414296 C>G did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:114400493 T>A did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:114358546 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:197559083 C>A maps to ENST00000425562 S333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr3:197559135 A>G maps to ENST00000425562 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:100179502 G>A maps to NM_002319.3 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:100180079 G>A maps to NM_002319.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:100176035 C>T maps to NM_002319.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr7:100175008 C>T maps to NM_002319.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr7:100175316 G>A maps to NM_002319.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:801248 G>A maps to NM_145886.3 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:800166 G>A maps to NM_145886.3 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr11:800205 G>A maps to NM_145886.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:39805745 G>A maps to NM_020862.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:39798947 C>T maps to NM_020862.1 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:39805145 C>T maps to NM_020862.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:39805373 G>A maps to NM_020862.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:39805646 G>A maps to NM_020862.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:39804758 G>A maps to NM_020862.1 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:39804659 G>A maps to NM_020862.1 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:40399634 G>A maps to NM_020737.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:40400276 G>C maps to NM_020737.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr6:40360116 G>A maps to NM_020737.1 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr6:40360416 C>T maps to NM_020737.1 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr6:40359912 C>T maps to NM_020737.1 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr6:40400555 G>A maps to NM_020737.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:40400057 A>G maps to NM_020737.1 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:40399550 G>T maps to NM_020737.1 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr6:40359912 C>T maps to NM_020737.1 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:40400585 G>A maps to NM_020737.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:36431076 C>A maps to NM_024509.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr19:36431493 T>C maps to NM_024509.1 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:36431682 G>A maps to NM_024509.1 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:66625712 C>T maps to NM_024036.4 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr14:42361133 G>A maps to NM_152447.3 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr14:42356403 C>T maps to NM_152447.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr14:42361073 C>T maps to NM_152447.3 N669N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr14:42355881 G>A maps to NM_152447.3 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:42357162 T>A maps to NM_152447.3 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr14:42357162 T>C maps to NM_152447.3 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr14:42356016 T>C maps to NM_152447.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr14:42356010 T>C maps to NM_152447.3 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr14:42355884 C>A maps to NM_152447.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:4538845 A>G maps to NM_052972.2 H50H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:4538113 G>A maps to NM_052972.2 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:4538287 C>T maps to NM_052972.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:133863331 C>T maps to NM_144648.1 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr7:133859312 T>C maps to NM_144648.1 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr7:133832998 T>C maps to NM_144648.1 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:133842866 G>A maps to NM_144648.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:133842813 C>T maps to NM_144648.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:66460605 G>A maps to NM_015541.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr3:66431103 G>A maps to NM_015541.2 A984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:66449391 A>G did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:66444464 G>A maps to NM_015541.2 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:113641349 C>A maps to NM_014813.1 S372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:113653131 T>C maps to NM_014813.1 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:113666710 T>C maps to NM_014813.1 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr12:59276711 G>T maps to NM_153377.3 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:59274636 C>T maps to NM_153377.3 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr12:59266419 A>G maps to NM_153377.3 C1098C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:59271266 G>T maps to NM_153377.3 C817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr10:85991808 G>A maps to NM_015613.2 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:85984097 C>A maps to NM_001017924.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:110788953 G>A maps to NM_198506.2 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:25257301 T>C maps to ENST00000354454 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr12:57574513 C>T maps to NM_002332.2 G1817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:57574201 C>T maps to NM_002332.2 L1776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:57603908 C>T maps to NM_002332.2 N4179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:57550569 T>C maps to NM_002332.2 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:57603499 C>T maps to NM_002332.2 D4096D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:57595352 C>T maps to NM_002332.2 C3473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:57574573 C>T maps to NM_002332.2 D1837D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:57538863 C>A maps to NM_002332.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr12:57590874 C>A maps to NM_002332.2 G3001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:57552323 C>T maps to NM_002332.2 H567H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:57590781 C>T maps to NM_002332.2 G2970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:57581233 C>T maps to NM_002332.2 C2342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:57571281 C>A maps to NM_002332.2 R1423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:57579419 C>T maps to NM_002332.2 D2190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:57588432 G>A maps to NM_002332.2 T2714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:57549890 C>T maps to NM_002332.2 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr12:57548291 C>T maps to NM_002332.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr12:57574967 C>T maps to NM_002332.2 V1852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:57603917 C>T maps to NM_002332.2 C4182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr14:23344654 C>T maps to NM_014045.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:23344654 C>T maps to NM_014045.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:23345173 C>T maps to NM_014045.3 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:23346453 T>A maps to NM_014045.3 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr14:23346253 C>T maps to NM_014045.3 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:150158534 C>T maps to NM_032832.5 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:105509339 G>A maps to NM_013437.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:105503358 C>A maps to NM_013437.4 G708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:105511688 C>A maps to NM_013437.4 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:105503742 G>A maps to NM_013437.4 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:105509255 G>A maps to NM_013437.4 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:105601062 G>A maps to NM_013437.4 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:141299384 T>G maps to NM_018557.2 P2450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:141816551 G>A maps to NM_018557.2 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr2:141356295 A>G maps to NM_018557.2 N2366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:141458143 A>G maps to NM_018557.2 C2158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:141457894 G>A maps to NM_018557.2 I2241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:141816551 G>A maps to NM_018557.2 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr2:141819774 G>A maps to NM_018557.2 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:141143558 A>G maps to NM_018557.2 P3478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr2:141130649 A>G maps to NM_018557.2 C3565C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr2:141093239 T>C maps to NM_018557.2 R4020R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:141093242 G>A maps to NM_018557.2 T4019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr2:141643836 T>C maps to NM_018557.2 R1278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr2:140990837 G>A maps to NM_018557.2 R4573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr2:141115595 G>A maps to NM_018557.2 R3783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr2:141641426 G>T maps to NM_018557.2 A1376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:141458143 A>G maps to NM_018557.2 C2158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:141458143 A>G maps to NM_018557.2 C2158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:142888292 G>C maps to NM_018557.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:141299471 C>T maps to NM_018557.2 S2421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:141298622 A>G maps to NM_018557.2 L2478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:141055454 C>A maps to NM_018557.2 G4297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:140990783 C>A maps to NM_018557.2 E4591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:141819755 G>T maps to NM_018557.2 S367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:141298559 C>A maps to NM_018557.2 E2499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:141294249 C>A maps to NM_018557.2 S2514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:141806669 A>G maps to NM_018557.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:141214164 T>C maps to NM_018557.2 K3274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:141751585 G>A maps to NM_018557.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr2:141259267 C>T maps to NM_018557.2 P2946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:140990768 C>A maps to NM_018557.2 E4596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:141215138 G>T maps to NM_018557.2 S3236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:141660546 C>T maps to NM_018557.2 K1236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr2:141751585 G>A maps to NM_018557.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:141986890 A>T maps to NM_018557.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr2:141571321 C>A maps to NM_018557.2 G1755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:141665551 T>C maps to NM_018557.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr2:141253146 G>T maps to NM_018557.2 C3007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:141473603 A>G maps to NM_018557.2 R1987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:141294273 T>C maps to NM_018557.2 K2506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr2:141473603 A>G maps to NM_018557.2 R1987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:141214101 G>T maps to NM_018557.2 T3295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr2:141459304 G>A maps to NM_018557.2 R2138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:140990825 C>A maps to NM_018557.2 G4577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:141201989 G>A maps to NM_018557.2 F3401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr2:141946090 A>G maps to NM_018557.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:141214113 G>T maps to NM_018557.2 A3291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:141641543 T>C maps to NM_018557.2 P1337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr2:141214101 G>A maps to NM_018557.2 T3295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:141294267 G>T maps to NM_018557.2 S2508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr2:140990760 C>A maps to NM_018557.2 V4598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr2:141245248 G>A maps to NM_018557.2 I3060I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr2:141113956 G>T maps to NM_018557.2 R3828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr2:141641543 T>A maps to NM_018557.2 P1337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr2:141665551 T>C maps to NM_018557.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:141108398 G>A maps to NM_018557.2 G3953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:141113986 A>T maps to NM_018557.2 C3818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:141459404 T>C maps to NM_018557.2 A2104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr2:141232881 G>A maps to NM_018557.2 C3150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:142238097 G>A maps to NM_018557.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr2:141680654 G>A maps to NM_018557.2 C1066C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:141072519 G>A maps to NM_018557.2 C4263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:170009382 A>G maps to NM_004525.2 N4129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:170034510 G>A maps to NM_004525.2 R3399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:170063044 A>G maps to NM_004525.2 S2395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:170030537 G>A maps to NM_004525.2 C3635C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:170038097 G>A maps to NM_004525.2 R3343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr2:170053529 C>T maps to NM_004525.2 T2863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:170145602 C>T maps to NM_004525.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:170137024 G>A maps to NM_004525.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:170048490 C>T maps to NM_004525.2 P2961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr2:170103910 G>T maps to NM_004525.2 S962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:170063556 G>A maps to NM_004525.2 R2225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:170025079 G>A maps to NM_004525.2 G3868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:170048427 G>A maps to NM_004525.2 Y2982Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr2:170068565 G>A maps to NM_004525.2 F2064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:170003384 G>A maps to NM_004525.2 F4225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:170048451 G>A maps to NM_004525.2 G2974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:170094627 C>T maps to NM_004525.2 A1493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:170129545 G>A maps to NM_004525.2 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:170101287 G>A maps to NM_004525.2 T1115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:170147493 A>G maps to NM_004525.2 H261H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:170025079 G>A maps to NM_004525.2 G3868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:170097702 G>A maps to NM_004525.2 N1280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:169996996 G>T maps to NM_004525.2 C4389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:170002289 G>A maps to NM_004525.2 R4319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:170025142 G>A maps to NM_004525.2 F3847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:170177302 C>T maps to NM_004525.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:170034510 G>A maps to NM_004525.2 R3399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:170147487 A>T maps to NM_004525.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:170034510 G>A maps to NM_004525.2 R3399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr2:169989188 C>T maps to NM_004525.2 V4541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:170013935 G>T maps to NM_004525.2 I3988I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:170030573 T>G maps to NM_004525.2 S3623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:170044660 G>A maps to NM_004525.2 F3049F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:170072804 G>A maps to NM_004525.2 I1928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:170092578 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:169985520 A>G did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr2:170147487 A>G maps to NM_004525.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:170070305 T>C maps to NM_004525.2 A1967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:170063044 A>G maps to NM_004525.2 S2395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:169985567 T>C maps to NM_004525.2 R4585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:170034508 T>C maps to NM_004525.2 R3399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr2:170127567 G>T maps to NM_004525.2 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr2:170034508 T>C maps to NM_004525.2 R3399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr2:170048526 C>T maps to NM_004525.2 S2949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr2:170066148 G>A maps to NM_004525.2 R2095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:170092466 G>A maps to NM_004525.2 C1601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr2:170066029 C>A maps to NM_004525.2 L2134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:170034510 G>A maps to NM_004525.2 R3399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr2:170147487 A>G maps to NM_004525.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr2:170063044 A>G maps to NM_004525.2 S2395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:170034508 T>C maps to NM_004525.2 R3399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr2:170063044 A>G maps to NM_004525.2 S2395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr2:170070305 T>C maps to NM_004525.2 A1967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:170070305 T>C maps to NM_004525.2 A1967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:170094612 C>T maps to NM_004525.2 T1498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:186298109 C>A maps to ENST00000362004 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:186296769 G>A maps to ENST00000362004 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:186295363 A>G maps to ENST00000362004 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:33695660 T>C maps to NM_002333.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:33697931 A>G maps to NM_002333.3 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:33687651 C>T maps to NM_002333.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:33696191 C>A maps to NM_002333.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:46886688 G>A maps to ENST00000256991 D1757D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:46897067 G>A maps to ENST00000256991 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:68181190 G>A maps to NM_002335.2 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:68183853 C>T maps to NM_002335.2 D962D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:68177404 C>T maps to NM_002335.2 N705N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr11:68157387 C>T maps to NM_002335.2 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:68201130 C>T maps to NM_002335.2 P1275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:68177494 C>T maps to NM_002335.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:68181334 G>A maps to NM_002335.2 V894V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr11:68204450 C>T maps to NM_002335.2 S1365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:68204432 C>T maps to NM_002335.2 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr22:25755849 G>A maps to NM_001135772.1 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr22:25755984 C>T maps to NM_001135772.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr12:12397326 T>C maps to NM_002336.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr12:12284833 A>G maps to NM_002336.2 S1297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:12397353 G>A maps to NM_002336.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:12397409 C>A maps to NM_002336.2 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:12315227 C>T maps to NM_002336.2 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:12283786 C>T maps to NM_002336.2 Q1337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr12:12274062 G>T maps to NM_002336.2 S1613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:53715075 G>A maps to NM_004631.3 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:53736980 T>C maps to NM_004631.3 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr1:53729947 C>T maps to NM_004631.3 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:53755305 G>A maps to NM_004631.3 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr1:53746280 C>T maps to NM_004631.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:53715063 G>A maps to NM_004631.3 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:3517866 C>T maps to NM_002337.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:3516637 G>A maps to NM_002337.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:3534049 G>A maps to NM_002337.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:44161385 A>G maps to NM_133259.3 D893D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:44201297 A>G maps to NM_133259.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:44161914 G>A maps to NM_133259.3 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:44132915 C>T maps to NM_133259.3 A1093A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:44209476 C>T maps to NM_133259.3 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr2:44173337 G>A maps to NM_133259.3 D708D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:44171016 C>A maps to NM_133259.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:53761654 G>T maps to NM_018214.4 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:53660104 C>T maps to NM_018214.4 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:145745669 T>C maps to NM_014665.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr5:195137 C>T maps to NM_001080478.1 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr3:194080473 C>T maps to NM_001135057.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:194080098 G>A maps to NM_001135057.2 C564C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr3:194081480 G>T maps to NM_001135057.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr3:194080857 G>A maps to NM_001135057.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:194080242 G>A maps to NM_001135057.2 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:25435757 A>G maps to NM_017640.5 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:25466139 G>A maps to NM_017640.5 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:25538130 C>T maps to NM_017640.5 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:25495348 G>T maps to NM_017640.5 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:25594677 A>G maps to NM_017640.5 E1014E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:24529214 C>T maps to NM_138360.3 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr14:24528349 G>A maps to NM_138360.3 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:24523640 C>T maps to NM_138360.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr14:24530140 T>C maps to NM_138360.3 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr14:24530767 C>T maps to NM_138360.3 A789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:50121795 G>A maps to NM_001006939.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:26998047 G>A maps to NM_022901.2 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr3:46586739 T>A maps to NM_024512.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr10:72100453 C>T maps to NM_207119.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:72061169 C>T maps to NM_207119.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:7021986 C>T maps to NM_201650.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:7023195 G>A maps to NM_006992.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr12:7021986 C>T maps to NM_201650.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:7023195 G>A maps to NM_006992.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:18502853 C>T maps to NM_145256.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:134162529 C>T maps to NM_001143759.1 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr10:134178934 C>T maps to NM_030626.2 Q433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:134174959 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:67244004 G>A maps to NM_001004055.1 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr21:45877261 C>T maps to NM_030891.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr18:7231579 G>A maps to NM_001105581.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:7232011 C>T maps to NM_001105581.1 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:7231663 G>A maps to NM_001105581.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr18:7231559 C>T maps to NM_001105581.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:169574262 G>A maps to NM_024727.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:169578355 T>C maps to NM_024727.2 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:76372417 T>C maps to NM_001128922.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:76371706 G>A maps to NM_001128922.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr11:76372063 G>T maps to NM_001128922.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:196387059 T>C maps to NM_198565.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:196387044 C>T maps to NM_198565.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:196387638 C>T maps to NM_198565.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr3:196387317 G>A maps to NM_198565.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:67401277 C>A maps to NM_018296.5 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:67384146 C>T maps to NM_018296.5 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:67404901 G>A maps to NM_018296.5 E417E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:67405063 G>A maps to NM_018296.5 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:62855862 C>T maps to NM_199340.2 S1467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr17:62892265 A>G maps to NM_199340.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:30349706 C>T maps to ENST00000327564 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:30376269 C>T maps to ENST00000327564 R872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr17:30376235 A>G maps to ENST00000327564 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr17:30376235 A>G maps to ENST00000327564 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:100620622 C>A maps to NM_144620.2 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:100626047 A>G maps to NM_144620.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:100624847 G>A maps to NM_144620.2 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:100626080 C>A maps to NM_144620.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr3:26751684 G>A maps to NM_052953.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr3:26751471 C>T maps to NM_052953.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr3:26751177 C>T maps to NM_052953.2 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:26751757 A>T maps to NM_052953.2 K199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr7:127670303 C>A maps to NM_022143.4 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:70650575 G>A maps to NM_017768.4 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:70625064 C>A maps to NM_017768.4 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:70625080 G>A maps to NM_017768.4 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:70654894 C>T maps to NM_017768.4 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:46751171 G>A maps to ENST00000254454 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:46745900 G>A maps to ENST00000254454 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:46746203 T>C maps to ENST00000254454 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr1:54423899 G>A maps to NM_052940.3 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:54417827 T>G maps to NM_052940.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:122677315 G>T maps to NM_001098519.1 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:122676005 G>A maps to NM_001098519.1 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:122672261 C>T maps to NM_001098519.1 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:122685441 G>A maps to NM_001098519.1 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:79986487 G>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:79985612 C>T maps to NM_144999.2 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:17907768 G>A maps to NM_031294.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:71272442 G>T maps to NM_017691.3 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:71300726 C>T maps to NM_017691.3 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:51022287 G>A maps to NM_001080457.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr19:51021871 G>A maps to NM_001080457.1 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:51021622 G>A maps to NM_001080457.1 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:51022360 G>A maps to NM_001080457.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr19:51021274 G>A maps to NM_001080457.1 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:51022198 C>T maps to NM_001080457.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:51021043 A>C maps to NM_001080457.1 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:51021280 G>A maps to NM_001080457.1 N563N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr19:51021937 G>A maps to NM_001080457.1 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:40136945 A>G maps to NM_020929.1 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:40136309 A>G maps to NM_020929.1 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:40137659 A>T maps to NM_020929.1 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr11:40137376 G>A maps to NM_020929.1 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:40137191 C>T maps to NM_020929.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:40137422 C>T maps to NM_020929.1 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr11:40137535 C>A maps to NM_020929.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:40136969 A>G maps to NM_020929.1 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:40137689 G>T maps to NM_020929.1 C51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr11:40137797 A>G maps to NM_020929.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr11:40136780 C>T maps to NM_020929.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:40137605 C>T maps to NM_020929.1 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:84182610 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:84188195 G>T maps to NM_178452.4 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:84199397 G>A maps to NM_178452.4 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:84205902 C>T maps to NM_178452.4 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:84188206 A>G maps to NM_178452.4 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr16:84188206 A>G maps to NM_178452.4 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:165533004 C>A maps to NM_001005214.3 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr1:165532889 C>T maps to NM_001005214.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr1:165532856 C>A maps to NM_001005214.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:165513682 C>T maps to NM_001005214.3 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:56954755 C>T maps to NM_001005210.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:551726 G>A maps to NM_198075.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:552568 C>T maps to NM_198075.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:120053900 C>A maps to NM_001099678.1 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:120053798 G>A maps to NM_001099678.1 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:120053823 T>C maps to NM_001099678.1 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:48460411 C>T maps to NM_018509.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr8:133623563 G>A maps to ENST00000250173 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:52860895 C>T maps to NM_001024611.1 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr4:52860943 C>T maps to NM_001024611.1 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:52861933 G>A maps to NM_001024611.1 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:52861339 C>T maps to NM_001024611.1 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:52869386 A>G did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:67926707 A>G maps to ENST00000421742 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:70502289 T>C maps to NM_020794.2 N719N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:70486782 G>T maps to NM_020794.2 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:70505049 C>T maps to NM_020794.2 Y1143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:70257785 C>T maps to NM_020794.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr1:70303930 G>A maps to NM_020794.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:70505049 C>T maps to NM_020794.2 Y1143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:70541890 C>A maps to NM_020794.2 I1416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:70225997 G>A maps to NM_020794.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:70504818 C>T maps to NM_020794.2 I1066I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:70226018 C>T maps to NM_020794.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:70451956 G>A maps to NM_020794.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:70504929 C>T maps to NM_020794.2 F1103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:70518809 G>A maps to NM_020794.2 P1366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:70257749 C>T maps to NM_020794.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:70504344 C>A maps to NM_020794.2 V908V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr1:70502307 G>T did not map to a codon.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr9:131670711 C>T maps to NM_001127244.1 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:131670900 C>T maps to NM_001127244.1 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:131670816 C>T maps to NM_001127244.1 D458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:131671053 C>T maps to NM_001127244.1 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:90049516 C>A maps to NM_015350.2 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:90048829 C>A maps to NM_015350.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:90179037 T>C maps to NM_032270.4 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr1:90179904 A>G maps to NM_032270.4 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:90180366 G>A maps to NM_032270.4 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:90178953 C>A maps to NM_032270.4 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:90399379 A>G maps to NM_001134479.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:90400651 A>G maps to NM_001134479.1 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:90399442 C>T maps to NM_001134479.1 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr1:90398819 A>T maps to NM_001134479.1 K65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr1:90400033 G>A maps to NM_001134479.1 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:90400780 C>T maps to NM_001134479.1 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:90400780 C>T maps to NM_001134479.1 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:7960607 C>A maps to NM_025061.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:7964495 C>T maps to NM_025061.3 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:86049828 C>T maps to NM_033402.4 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:238672329 A>G maps to NM_001137552.1 Q658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:238671318 T>C maps to NM_001137552.1 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:238629419 T>C maps to NM_001137552.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr2:238647927 C>T maps to ENST00000391999 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:238672668 C>T maps to NM_001137552.1 N771N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr2:238672327 C>T maps to NM_001137552.1 Q658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr2:238672329 A>G maps to NM_001137552.1 Q658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr3:37170567 G>A maps to NM_006309.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr3:37125234 G>A maps to NM_006309.2 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:37116573 G>A maps to NM_006309.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:37107770 G>A maps to NM_006309.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:37125234 G>A maps to NM_006309.2 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:37170567 G>A maps to NM_006309.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:37125282 T>C maps to NM_006309.2 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:85449779 C>T maps to NM_001079910.1 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:85438563 G>T maps to NM_001079910.1 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:85450751 C>T maps to NM_001079910.1 C727C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:85450932 C>T maps to NM_001079910.1 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:85517982 G>A maps to NM_001079910.1 Q1231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:85546924 T>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:85450940 C>T maps to NM_001079910.1 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:85449609 G>T maps to NM_001079910.1 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr12:85449557 A>G maps to NM_001079910.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:85449551 A>G maps to NM_001079910.1 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:85449555 C>T maps to NM_001079910.1 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr12:85449557 A>G maps to NM_001079910.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr12:85449557 A>G maps to NM_001079910.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr12:85450050 G>T maps to NM_001079910.1 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:85441130 A>G maps to NM_001079910.1 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr12:85449557 A>G maps to NM_001079910.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr12:85449557 A>G maps to NM_001079910.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr12:85517938 C>T maps to NM_001079910.1 R1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:74507398 C>A maps to NM_001105659.1 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:74507441 C>T maps to NM_001105659.1 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:169555316 C>T maps to NM_001080460.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:169540725 A>G maps to NM_001080460.1 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:101528845 C>T maps to NM_024652.3 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:101608974 C>T maps to NM_024652.3 G1990G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:101605891 C>T maps to NM_024652.3 V1750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:101608986 C>T maps to NM_024652.3 F1994F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:101550768 C>T maps to NM_024652.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr12:40761488 T>C maps to NM_198578.3 H2502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr12:40714896 C>T maps to NM_198578.3 R1693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:40715969 T>G maps to NM_198578.3 P1768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:40626105 G>T maps to NM_198578.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:40699633 C>A maps to NM_198578.3 V1275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr12:40757341 C>T maps to NM_198578.3 C2389C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:40692093 C>A maps to NM_198578.3 S1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:40696663 A>G maps to NM_198578.3 E1190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:40757341 C>T maps to NM_198578.3 C2389C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr12:40728800 C>A maps to NM_198578.3 P1930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr12:40761488 T>C maps to NM_198578.3 H2502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:40713868 C>A maps to NM_198578.3 S1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:40714884 G>T maps to NM_198578.3 E1689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr12:40704252 T>C maps to NM_198578.3 P1446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr12:40745480 C>T maps to NM_198578.3 T2174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr12:40734167 C>A maps to NM_198578.3 P2007P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:40715838 C>T maps to NM_198578.3 R1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:40696663 A>G maps to NM_198578.3 E1190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr12:40696663 A>G maps to NM_198578.3 E1190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr12:40734147 C>T maps to NM_198578.3 L2001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr12:40714899 C>T maps to NM_198578.3 L1694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:40657657 T>C maps to NM_198578.3 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:204587944 C>T maps to NM_201630.1 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:204588985 C>T maps to NM_201630.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:204588855 G>A maps to NM_201630.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:204588085 G>A maps to NM_201630.1 N345N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:110763238 C>A maps to NM_018334.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:110764892 G>T maps to NM_018334.4 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:110764589 G>T maps to NM_018334.4 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:110763517 C>T maps to NM_018334.4 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr7:110763028 G>A maps to NM_018334.4 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr7:110763238 C>A maps to NM_018334.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:6022852 G>A maps to NM_152611.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr20:6022798 G>A maps to NM_152611.3 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr20:6022423 C>T maps to NM_152611.3 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:6022627 C>T maps to NM_152611.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:6021781 T>C maps to NM_152611.3 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:80530416 C>T maps to NM_178839.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:80529444 G>A maps to NM_178839.4 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:80530443 A>G maps to NM_178839.4 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:138209669 G>A maps to NM_015564.2 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr10:68687196 C>T maps to NM_178011.3 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:68687951 G>A maps to NM_178011.3 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:76975859 C>T maps to NM_001134745.1 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:77746571 G>T maps to NM_001134745.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:77746784 G>A maps to NM_001134745.1 F70F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D5-6930-01A-11D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:77746238 C>T maps to NM_001134745.1 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:76975864 T>G maps to NM_001134745.1 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:130263313 C>T maps to NM_001005374.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:1943778 C>T maps to NM_001163926.1 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:71819877 C>T maps to NM_001145309.1 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:102112682 C>T maps to NM_152892.1 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:102108194 C>T maps to NM_152892.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:102106650 C>A maps to NM_152892.1 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:102110269 C>T maps to NM_152892.1 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr3:115738437 G>T maps to NM_002338.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr3:115560698 G>T maps to NM_002338.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr3:194387245 G>A maps to NM_018385.2 F94F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3877-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:38027408 C>A maps to NM_014462.1 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:157181010 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:157182238 C>T maps to NM_173491.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:34712511 G>T maps to NM_001114093.1 G413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:34712519 T>C maps to NM_001114093.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:34710472 T>A maps to NM_001114093.1 L320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:34699873 C>T maps to NM_001114093.1 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr19:34706499 G>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:60701442 G>A maps to NM_144703.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr20:60699715 G>A maps to NM_144703.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:60701400 C>T maps to NM_144703.2 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:14223155 C>T maps to NM_014463.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:14223146 C>T maps to NM_014463.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr19:18423464 G>A maps to NM_012321.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:7760396 G>A maps to NM_032356.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:1908735 G>T maps to ENST00000381758 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:35753458 C>T maps to NM_205834.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr21:47625799 C>T maps to NM_002340.5 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:21229416 T>C maps to ENST00000381541 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:21172233 A>G maps to ENST00000381541 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:21196340 A>C maps to ENST00000381541 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:21220307 C>T maps to ENST00000381541 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:21176139 G>T maps to ENST00000381541 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:21174469 T>C maps to ENST00000381541 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr6:31555084 G>A maps to NM_007161.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr6:31556309 G>T maps to NM_007161.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:96410826 G>A maps to NM_000895.1 H314H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:33468796 C>T maps to ENST00000354476 R649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:33412139 A>C maps to ENST00000354476 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:33585829 C>T maps to ENST00000354476 C1390C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:33500089 C>T maps to ENST00000354476 T935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:33585832 G>T maps to ENST00000354476 P1391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:33622347 C>T maps to ENST00000354476 V1662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:33622299 C>T maps to ENST00000354476 C1646C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:33412085 G>A maps to ENST00000354476 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:33590515 C>T maps to ENST00000354476 L1554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:33585704 G>T maps to ENST00000354476 E1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:33413791 G>A maps to ENST00000354476 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr2:33468798 A>G maps to ENST00000354476 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:33359827 G>A maps to ENST00000390003 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:74971550 C>T maps to NM_000428.2 E1461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr14:74999213 G>A maps to NM_000428.2 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr14:75019733 G>T maps to NM_000428.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:75017916 C>T maps to NM_000428.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:74968276 G>A maps to NM_000428.2 F1729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:74999210 C>T maps to NM_000428.2 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:65318624 G>A maps to NM_001130144.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:65308345 G>A maps to NM_001130144.2 H991H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:41125282 A>G maps to ENST00000308370 V1100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:41114435 C>T maps to ENST00000308370 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:41118977 C>T maps to ENST00000308370 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr19:41135352 G>A maps to ENST00000308370 A1590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr19:41122906 G>A maps to ENST00000308370 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:6494268 G>A maps to NM_002342.1 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:6495551 T>C maps to NM_002342.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:46486805 G>A maps to NM_002343.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:46479467 G>A maps to NM_002343.3 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr3:46490413 G>A maps to NM_002343.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr15:41797488 A>G maps to NM_002344.5 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr15:41801322 G>A maps to NM_002344.5 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:41804356 G>A maps to NM_002344.5 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:144178912 C>T maps to NM_032860.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:144171287 T>C maps to NM_032860.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr6:144171287 T>C maps to NM_032860.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:144171287 T>C maps to NM_032860.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr6:144171287 T>C maps to NM_032860.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:258091 C>T maps to NM_201412.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr16:258075 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:139094362 G>T maps to NM_016019.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:48823106 A>G maps to ENST00000393227 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:91502239 C>A maps to NM_002345.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr12:91502248 G>T maps to NM_002345.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:23417972 G>A maps to NM_001142546.1 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:23420565 C>T maps to NM_001142546.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:23420001 C>T maps to NM_001142546.1 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr1:23418665 G>A maps to NM_001142546.1 R697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:23420264 C>A maps to NM_001142546.1 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:23418834 C>T maps to NM_001142546.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:23419152 G>T maps to NM_001142546.1 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr1:23417828 G>A maps to NM_001142546.1 R976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr11:24759821 G>T maps to NM_001009909.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:24750822 C>T maps to NM_001009909.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:24753701 T>G maps to NM_001009909.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:24750753 C>A maps to NM_001009909.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:24927589 C>T maps to NM_001009909.2 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:24750748 G>T maps to NM_001009909.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:114536676 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:114536640 C>T did not map to a codon.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr23:114540854 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:114536595 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:114541191 T>C did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:114524367 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:158390213 C>T maps to NM_020169.3 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:144102803 C>T maps to NM_002346.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr8:144240223 G>A maps to NM_001130478.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:144239714 C>A maps to NM_001130478.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:160663514 A>C maps to NM_001198759.1 G1653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:160661554 T>G maps to NM_002349.3 *1723Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:160738668 A>G maps to NM_001198759.1 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:160708783 C>T maps to NM_001198759.1 S937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:160714926 A>G maps to NM_001198759.1 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:160738725 T>C maps to NM_001198759.1 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:160706637 G>T maps to NM_001198759.1 S1001S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:160661610 G>A maps to NM_002349.3 R1705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:160735778 A>C maps to NM_001198759.1 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:160697257 G>A maps to NM_001198759.1 I1163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:6589068 C>T maps to NM_004271.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:160783636 C>T maps to ENST00000263285 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:160784471 C>T maps to ENST00000263285 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:160788096 C>T maps to ENST00000263285 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr1:160771691 C>T maps to NM_001033667.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:74939063 A>C maps to NM_015364.4 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:4283620 G>A maps to NM_017816.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:4283620 G>A maps to NM_017816.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:99901198 C>A maps to NM_174898.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:99901283 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:99901198 C>A maps to NM_174898.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:99858877 G>A maps to NM_175735.3 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:99861829 G>A maps to NM_175735.3 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:99861811 G>A maps to NM_175735.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:13210474 G>A maps to NM_005583.4 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:13211694 C>T maps to NM_005583.4 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr8:56911008 T>C maps to NM_002350.2 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr8:56911008 T>C maps to NM_002350.2 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:133426000 A>G maps to ENST00000409034 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:43969662 G>A maps to NM_014400.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:42342335 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:42342039 C>T maps to NM_173506.4 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:42342105 G>A maps to NM_173506.4 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:150064895 C>T maps to NM_177964.3 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:54963679 A>G maps to ENST00000419058 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:20926936 G>A maps to NM_020424.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr12:25357173 A>G maps to NM_001001660.2 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr15:52017158 G>A maps to NM_153374.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:89821056 G>T maps to NM_198273.1 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:100269824 C>A maps to NM_152449.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr1:235969924 T>C maps to NM_000081.2 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:235922804 C>T maps to NM_000081.2 T2116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr1:235884036 G>A maps to NM_000081.2 Q3162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:235973132 G>A maps to NM_000081.2 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr1:235884127 C>G maps to NM_000081.2 L3131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr1:235922693 G>A maps to NM_000081.2 S2153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:235972014 A>G maps to NM_000081.2 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr1:235956856 A>G maps to NM_000081.2 C1354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr1:235884119 A>C maps to NM_000081.2 L3134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr1:235860530 G>A maps to NM_000081.2 Y3472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:235972458 A>G maps to NM_000081.2 C553C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:235850344 C>G maps to NM_000081.2 V3568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:235884034 C>T maps to NM_000081.2 Q3162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:235955344 T>C maps to NM_000081.2 L1399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:235972335 A>G maps to NM_000081.2 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:235938332 T>G maps to NM_000081.2 I1838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:235969924 T>C maps to NM_000081.2 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:29581595 C>T maps to NM_032517.4 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:29599978 G>A maps to NM_032517.4 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:45877274 G>A maps to NM_020347.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr3:45877151 G>A maps to NM_020347.2 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:45868914 G>A maps to NM_020347.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr22:21350077 G>A maps to NM_006767.3 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:21350368 C>T maps to NM_006767.3 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:21344775 A>C maps to NM_006767.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr8:20112431 G>A maps to NM_021020.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr8:20112392 C>T maps to NM_021020.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:20110556 G>A maps to NM_021020.2 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:20107373 G>A maps to NM_021020.2 Y550Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr10:102763706 C>A maps to NM_032429.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:102763427 C>A maps to NM_032429.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr13:36049846 A>G maps to NM_005584.4 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:36049984 G>A maps to NM_005584.4 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr4:151505047 G>A maps to NM_006439.4 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr7:20199539 G>A maps to NM_182762.3 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr7:20198744 A>G maps to NM_182762.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:20199638 G>T maps to NM_182762.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr7:20199638 G>T maps to NM_182762.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr7:20198105 T>A maps to NM_182762.3 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr7:20193971 G>A maps to NM_182762.3 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr1:39903561 C>T maps to ENST00000361689 D3975D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:39749084 G>A maps to ENST00000361689 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:39913440 T>C maps to ENST00000361689 L4554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:39749132 G>A maps to ENST00000361689 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:39927612 G>A maps to ENST00000361689 G5135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:39788323 G>A maps to ENST00000361689 S1363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:39823378 G>A maps to ENST00000361689 R1857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:39818812 C>T maps to ENST00000361689 S1716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:39800846 G>T maps to ENST00000289893 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:39888437 T>C maps to ENST00000361689 L3277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:39798901 G>A maps to ENST00000289893 K654K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:39801101 G>T maps to ENST00000289893 E1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:39823309 C>T maps to ENST00000361689 S1834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:39888475 G>A maps to ENST00000361689 L3289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:39824376 A>G maps to ENST00000361689 R1922R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:39776596 A>G maps to ENST00000361689 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:39800846 G>T maps to ENST00000289893 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:39776557 G>A maps to ENST00000361689 R1057R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:39800846 G>T maps to ENST00000289893 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:39900159 G>A maps to ENST00000361689 E3818E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr1:39905072 T>C maps to ENST00000361689 A4057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:39913184 G>T maps to ENST00000361689 E4504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:39945599 T>G maps to ENST00000361689 R5275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:39847751 A>G maps to ENST00000361689 E2530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:39905072 T>C maps to ENST00000361689 A4057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:63782753 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr11:63767720 G>A maps to NM_014067.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr20:15866409 C>T maps to ENST00000310348 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr20:15210667 A>G maps to ENST00000310348 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr20:15412072 C>A maps to ENST00000310348 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:15866409 C>T maps to ENST00000310348 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr20:15967378 G>A maps to ENST00000310348 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:2252881 C>T maps to NM_003550.2 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:1997329 G>A maps to NM_003550.2 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:120981441 G>T maps to NM_002358.3 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:120981336 G>T maps to NM_002358.3 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:43604139 C>T maps to NM_001003690.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:11735153 C>T maps to ENST00000376669 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:504745 G>A maps to NM_130760.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr11:47345226 C>T maps to NM_003682.3 C1461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:47346037 C>T maps to NM_003682.3 G1544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:47333362 C>A maps to NM_003682.3 I1413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:47348330 C>T maps to NM_003682.3 R1589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:47296578 C>T maps to NM_003682.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:47308065 G>A maps to NM_003682.3 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:47297479 G>A maps to NM_003682.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:47297654 C>T maps to NM_003682.3 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:47311027 C>T maps to NM_003682.3 R934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:47336865 C>A maps to NM_003682.3 I1455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:47308065 G>A maps to NM_003682.3 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:47296476 G>A maps to NM_003682.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr4:1332341 C>T maps to ENST00000505177 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr4:1305834 C>T maps to ENST00000505177 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:1305894 C>T maps to ENST00000505177 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr4:1332380 C>A maps to ENST00000505177 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:166991079 T>C maps to NM_032858.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:166990395 T>C maps to NM_032858.1 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:166991079 T>C maps to NM_032858.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:166958618 T>G maps to NM_032858.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:166974587 C>T maps to NM_032858.1 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr1:166991079 T>C maps to NM_032858.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr1:166991079 T>C maps to NM_032858.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr1:166991079 T>C maps to NM_032858.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr1:166991079 T>C maps to NM_032858.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr1:166991079 T>C maps to NM_032858.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:145161277 A>G maps to NM_032272.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr20:39317230 C>T maps to NM_005461.3 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr19:35786681 G>A maps to NM_002361.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr19:35793483 G>A maps to NM_002361.3 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:35801522 C>T maps to NM_002361.3 C531C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:35800807 C>T maps to NM_002361.3 C421C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:35804249 G>T maps to NM_002361.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:35790469 C>T maps to NM_002361.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr19:35800912 C>T maps to NM_002361.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr19:35801483 C>T maps to NM_002361.3 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:152482662 T>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:152482629 T>G did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:152482482 A>G did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr23:152482176 T>C did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:152482497 A>G did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:152482177 T>C did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:152482678 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:152482541 T>C did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:152482724 A>G did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:152482724 A>G did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:152482178 T>C did not map to a codon.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr23:152482498 A>G did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:152482482 A>G did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:152482178 T>C did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:152482570 G>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:152482823 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:152482541 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:152482178 T>C did not map to a codon.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr23:151304072 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:151303449 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:151304045 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:151303737 T>C did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr23:151303886 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:151900288 C>T did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr23:151900695 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:151900442 G>T did not map to a codon.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr23:151900717 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:151900710 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:151900291 A>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:151900301 C>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:151900304 C>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:151900735 G>A did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:151900056 T>G did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:151900607 G>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:151900024 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:151900188 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:151935643 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:151935509 C>A did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:151935884 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:151935745 C>T did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:151092592 G>T did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:151092826 G>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:151092593 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:151092652 G>A did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:151092798 A>G did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:151092592 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:151092581 C>T did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:151283739 T>G did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:151283786 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:151869730 G>A did not map to a codon.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr23:151870122 C>G did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:151869998 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:151870202 G>A did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:151869844 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:151869900 C>G did not map to a codon.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:149013285 G>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:149013204 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:149013270 C>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:30268901 A>G did not map to a codon.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr23:30269334 G>A did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:30269389 G>A did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:30269391 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:30269210 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:30269408 C>T did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:30268663 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:30269391 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:30269582 C>T did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:30269386 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:30268779 T>G did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:30268698 C>A did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:27839884 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:27840331 C>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:27839979 T>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:35820799 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:35820381 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:35821138 C>A did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:35820615 T>C did not map to a codon.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr23:26157599 A>C did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:26157772 A>T did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:26157645 C>T did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:26157611 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:26157473 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:26157694 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr23:26157112 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:26158115 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:30236760 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:30237447 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr23:30237090 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:30237102 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:30236764 G>A did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:30236764 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:30237218 C>T did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:30236764 G>A did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:30236764 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:30236764 G>T did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:30236711 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:30236764 G>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:30254360 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:30254424 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:30254478 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:30254728 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:30254360 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:30254375 T>C did not map to a codon.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr23:30254731 A>G did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:30254157 C>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:30254670 G>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:30261040 T>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:30260603 C>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:30260898 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:30260500 C>T did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:30260981 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr23:30260953 G>T did not map to a codon.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr23:30260295 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:30260301 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:30261001 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:30260638 C>A did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:30260759 A>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:26212304 T>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:26212647 T>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:26212719 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:26212722 G>T did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:26212559 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:26212921 T>C did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:140995105 G>A did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:140995936 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:140993456 C>T did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:140995758 T>C did not map to a codon.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr23:140993194 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:140993631 C>A did not map to a codon.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr23:140995679 T>A did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr23:140996490 T>A did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:140995760 C>A did not map to a codon.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr23:140995937 G>A did not map to a codon.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr23:140994880 T>G did not map to a codon.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr23:140996327 A>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:140994644 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:140995236 C>T did not map to a codon.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr23:140994516 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:140994777 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:140995444 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:140994259 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:140995219 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:140993848 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:140993953 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:140994420 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:140994590 C>G did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:140995605 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr23:140995442 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:140995708 C>T did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:140993225 G>A did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:140996191 T>C did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:140994976 C>T did not map to a codon.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr23:140996523 G>T did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:140995758 T>C did not map to a codon.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr23:140996327 A>C did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:140996074 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:140995606 C>T did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:140996191 T>C did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:140993276 G>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:140995030 G>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:140995605 G>A did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:141291256 T>G did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:141291127 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:141290743 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:141291559 G>A did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:141291352 G>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:141290686 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:141291247 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:141290945 T>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:141291291 G>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:140984799 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:140983102 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:140985440 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:140984571 C>T did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:140984456 C>G did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:140969256 T>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:140967175 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:140985598 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr23:140985313 A>T did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr23:140985210 T>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:140985059 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:140969574 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:140953274 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:140969400 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:140983126 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:140984995 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:140969328 C>T did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:140926109 G>T did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr23:140969479 C>A did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:140969192 C>T did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:140969327 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:140953280 G>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:51643298 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:51640085 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:51638271 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:51640146 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:51637797 C>T did not map to a codon.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr23:51639688 C>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:51637808 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:51637827 C>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:51640041 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:51638174 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:51639965 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:51640361 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:51638326 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:51638316 G>A did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:51639603 C>T did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:51644741 G>A did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:51639634 T>C did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:51639974 C>T did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:54837740 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:54836360 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:54838050 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:54835801 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:54836305 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:54841864 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:54836399 T>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:54836152 A>G did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:54837359 G>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:54838087 T>C did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:54835769 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:54835768 C>G did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:54839944 C>T did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:54841194 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:54837499 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:75648745 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:75648675 C>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:75649384 T>G did not map to a codon.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr23:75650967 G>A did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:75649321 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:75650736 T>G did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:75649843 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:75651109 G>A did not map to a codon.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr23:75649460 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:75649926 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:75649460 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:75649328 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:75650124 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:75649985 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:75649353 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:75648501 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:75650481 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:75649096 C>A did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:75650068 C>G did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:75650241 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:75651143 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:75003407 C>A did not map to a codon.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr23:75004319 C>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:75004572 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:75004796 G>A did not map to a codon.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr23:75004644 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:75003527 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:75004085 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:75004559 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr3:184429510 C>T maps to NM_022149.4 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr23:55479047 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:55479289 C>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:55479104 T>C did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:55478843 G>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:55478851 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:23889901 G>A maps to NM_019066.4 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr15:23890183 C>T maps to NM_019066.4 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr15:23890459 G>T maps to NM_019066.4 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr3:65365101 C>T maps to NM_001033057.1 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr3:65342499 G>A maps to NM_001033057.1 A1314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:65349232 G>A maps to NM_001033057.1 G1134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:65342577 T>C maps to NM_001033057.1 K1288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:65365101 C>T maps to NM_001033057.1 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:65361531 G>A maps to NM_001033057.1 D1028D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:65425575 C>T maps to NM_001033057.1 Q416Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:65415200 G>A maps to NM_001033057.1 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:78131027 G>A maps to NM_012301.3 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:77885458 G>T maps to NM_012301.3 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:78636480 G>A maps to NM_012301.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr7:77885569 G>A maps to NM_012301.3 D579D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr7:79082450 C>T maps to NM_012301.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:77824233 T>C maps to NM_012301.3 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:77885458 G>T maps to NM_012301.3 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:77885692 G>T maps to NM_012301.3 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr7:77762213 G>A maps to NM_012301.3 H1065H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr7:79082402 G>A maps to NM_012301.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:77824190 G>A maps to NM_012301.3 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr7:78636412 C>T maps to NM_012301.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr7:77885614 C>T maps to NM_012301.3 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr7:78636412 C>T maps to NM_012301.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:77764395 G>A maps to NM_012301.3 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:114184953 C>T maps to NM_001142782.1 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:114201750 C>A maps to NM_001142782.1 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:114184533 C>T maps to NM_001142782.1 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:114196467 C>T maps to NM_001142782.1 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr1:114196482 C>T maps to NM_001142782.1 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr1:114215317 G>A maps to NM_001142782.1 Q1000Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:114224861 C>T maps to ENST00000369617 Y1144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:49019267 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:49021089 G>A did not map to a codon.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr23:49021371 C>G did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr12:10760469 A>G maps to NM_018048.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:10758963 T>C maps to NM_018048.3 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:10758963 T>C maps to NM_018048.3 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr12:10758963 T>C maps to NM_018048.3 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:77086341 G>A did not map to a codon.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr23:77086303 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:77130932 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:77131028 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:77150987 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:77112284 C>T did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr23:77086309 G>T did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:10830845 G>A maps to NM_005906.3 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr6:10818201 A>G maps to NM_005906.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:10802141 G>A maps to NM_005906.3 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:10796326 C>T maps to NM_005906.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:10803997 G>A maps to NM_005906.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr6:10802141 G>A maps to NM_005906.3 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr6:10802139 T>C maps to NM_005906.3 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:33346510 G>T maps to NM_032509.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:33347838 T>C maps to NM_032509.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:33346652 C>A maps to NM_032509.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:95715345 C>T maps to NM_002371.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:95715372 A>G maps to NM_002371.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:110849335 G>A maps to NM_005434.4 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr2:110845226 G>A maps to NM_005434.4 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:110845253 G>A maps to NM_005434.4 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:56367781 G>A maps to NM_006785.2 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:56414741 T>C maps to NM_006785.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:56348531 G>T maps to NM_006785.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:56376622 C>T maps to NM_006785.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:72840703 T>C maps to NM_153267.4 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:139749737 C>T maps to ENST00000392881 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:139748723 C>A maps to ENST00000392881 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:139748723 C>T maps to ENST00000392881 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr9:139747569 G>A maps to ENST00000392881 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:179198182 A>G maps to NM_014757.4 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:179192400 C>T maps to NM_014757.4 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:179192374 C>T maps to NM_014757.4 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr5:179195975 T>C maps to NM_014757.4 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:95825238 T>C maps to NM_032427.1 Q652Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:95825256 T>C maps to NM_032427.1 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:95712225 G>A maps to NM_032427.1 G1119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:95825259 T>C maps to NM_032427.1 Q645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:95712129 G>T maps to NM_032427.1 I1151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr11:95712435 G>A maps to NM_032427.1 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:95825403 C>T maps to NM_032427.1 Q597Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:95825400 C>T maps to NM_032427.1 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:95825367 C>T maps to NM_032427.1 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:140811119 C>T maps to ENST00000509479 Q490Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:140641423 G>A maps to ENST00000509479 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:140640908 C>T maps to ENST00000509479 P995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:140640662 T>C maps to ENST00000509479 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:140811077 C>T maps to ENST00000509479 Q504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:140812012 G>A maps to ENST00000509479 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:141074237 C>A maps to ENST00000509479 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:140810699 C>T maps to ENST00000509479 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr4:140640557 T>C maps to ENST00000509479 A1112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr4:140811134 T>C maps to ENST00000509479 K485K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr4:140811122 T>C maps to ENST00000509479 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr4:140641397 G>A maps to ENST00000509479 N832N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:149671591 G>A did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:149613799 T>A did not map to a codon.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr23:149639552 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:149613800 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:149638449 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:149638971 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:149638865 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:149638671 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:149638161 C>T did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:149671654 A>G did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:149639571 C>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:149639500 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:149638694 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr23:149638239 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:149638665 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:149671753 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:149671780 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:49218634 G>A maps to NM_001130915.1 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:119510997 G>A maps to NM_005907.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:118042172 A>G maps to NM_006699.3 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:117910987 A>G maps to NM_006699.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:139990825 G>A maps to NM_016219.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr9:140001200 C>T maps to NM_016219.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:140001847 C>T maps to NM_016219.3 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:139995455 G>T did not map to a codon.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr9:139982603 C>G maps to NM_016219.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:26109125 C>T maps to NM_020379.2 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:26073198 C>A maps to NM_020379.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:109106065 T>G maps to NM_002372.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:109120628 T>C did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:109120588 A>G maps to NM_002372.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr5:109120588 A>G maps to NM_002372.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr5:109120586 G>T maps to NM_002372.2 G574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr5:109120588 A>G maps to NM_002372.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:91454701 G>A maps to NM_006122.2 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:91453435 G>A maps to NM_006122.2 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:91462968 C>A maps to NM_006122.2 V1135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr15:91461421 A>G did not map to a codon.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr15:91450063 G>A maps to NM_006122.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:12776598 C>T maps to NM_000528.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr19:12760988 G>T maps to NM_000528.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:12757523 C>T maps to NM_000528.3 P982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:12774184 G>A maps to NM_000528.3 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:12767855 G>A maps to NM_000528.3 N478N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:6588822 G>A maps to NM_015274.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:6612991 C>T maps to NM_015274.1 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr4:6612877 C>T maps to NM_015274.1 N812N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:6594920 C>T maps to NM_015274.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:6610887 C>T maps to NM_015274.1 N623N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr4:6611770 C>T maps to NM_015274.1 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:6612964 G>A maps to NM_015274.1 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:103611845 G>A maps to NM_005908.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr4:103560993 G>C maps to NM_005908.3 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:103610841 C>A did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr4:103645117 C>T maps to NM_005908.3 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:103644075 G>A maps to NM_005908.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr4:103645118 C>T maps to NM_005908.3 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:38265460 C>T maps to NM_001113482.1 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:38265331 T>C maps to NM_001113482.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:51423766 G>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:12482966 G>A maps to NM_018050.2 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:43590969 G>A did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr23:43592001 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:43572003 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:43572005 A>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:43572022 T>C did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr23:43572005 A>G did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:43515632 A>G did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:43634461 T>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:43656479 G>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:43655117 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:43655119 C>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:43652773 A>G did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:43652773 A>G did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:43652773 A>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:43818920 C>A maps to ENST00000382031 P1988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr15:43818800 C>T maps to ENST00000382031 H1948H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr15:43814033 C>T maps to ENST00000382031 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:43817291 G>A maps to ENST00000382031 E1445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr15:43815239 G>A maps to ENST00000382031 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:43820387 T>C maps to ENST00000382031 P2477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:71491264 G>T maps to NM_005909.3 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:71479568 G>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:71495358 C>T maps to NM_005909.3 Y2059Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr5:71495025 G>A maps to NM_005909.3 R1948R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr5:71493159 C>T maps to NM_005909.3 S1326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:71492790 A>C maps to NM_005909.3 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:71493384 G>T maps to NM_005909.3 P1401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:71490039 C>T maps to NM_005909.3 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:71492658 C>T maps to NM_005909.3 F1159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:71494953 G>A maps to NM_005909.3 E1924E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:71482515 G>T maps to NM_005909.3 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:71491720 G>T maps to NM_005909.3 E847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:71493858 G>A maps to NM_005909.3 T1559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr5:71491215 A>G maps to NM_005909.3 E678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:71494557 C>A maps to NM_005909.3 S1792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr5:71494449 C>A maps to NM_005909.3 P1756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr5:71492181 C>T maps to NM_005909.3 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr5:71495793 C>T maps to NM_005909.3 P2204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr5:71491215 A>G maps to NM_005909.3 E678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:71491215 A>G maps to NM_005909.3 E678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr5:71491974 C>T maps to NM_005909.3 A931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr5:71491156 G>T maps to NM_005909.3 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:172943958 A>G maps to NM_199227.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:172935726 G>A maps to NM_199227.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:172945100 G>A maps to NM_199227.1 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:172945097 C>T maps to NM_199227.1 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr20:33147623 G>A maps to NM_181509.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:117013965 C>T maps to NM_001085481.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:17835935 C>T maps to NM_018174.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:17831772 C>T maps to NM_018174.4 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:17837537 C>T maps to NM_018174.4 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:210560394 C>A maps to NM_002374.3 V1167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:210560883 G>A maps to NM_002374.3 E1330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:210569289 G>A maps to NM_001039538.1 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:210557472 A>G maps to NM_002374.3 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr2:210559908 A>G maps to NM_002374.3 S1005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr2:210594577 C>T maps to NM_002374.3 G1720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr2:210518020 C>T maps to NM_002374.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr2:210560568 C>A maps to NM_002374.3 I1225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr2:210559978 G>T maps to NM_002374.3 E1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr2:210574734 T>A maps to NM_002374.3 S1610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:210574836 C>T maps to NM_002374.3 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr2:210559701 C>T maps to NM_002374.3 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr2:210543311 G>A maps to NM_002374.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:210558766 G>T maps to NM_002374.3 E625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:210559008 G>T maps to NM_002374.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:210517995 A>G maps to NM_002374.3 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:210561045 C>T maps to NM_002374.3 D1384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:210574836 C>T maps to NM_002374.3 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr2:210559008 G>A maps to NM_002374.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:210559247 C>A maps to NM_002374.3 S785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:210574836 C>T maps to NM_002374.3 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:210570347 A>G maps to NM_002374.3 R1543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr2:210560955 T>C maps to NM_002374.3 P1354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:210560574 T>C maps to NM_002374.3 S1227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr2:210559008 G>A maps to NM_002374.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr2:210517974 T>C maps to NM_002374.3 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:210559008 G>A maps to NM_002374.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:210560754 C>T maps to NM_002374.3 I1287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:210588404 C>T maps to NM_001039538.1 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr15:66782946 C>T maps to NM_002755.3 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:4099262 G>A maps to NM_030662.3 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:4110605 G>A maps to NM_030662.3 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:4110554 G>A maps to NM_030662.3 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:4101260 C>T maps to NM_030662.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr17:21208415 C>T maps to NM_145109.2 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:12028636 A>G maps to ENST00000415385 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr17:12032541 G>C maps to ENST00000415385 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:12013720 A>G maps to ENST00000415385 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr17:12028613 G>T maps to ENST00000415385 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr17:12028635 C>A maps to ENST00000415385 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr17:11984783 A>G maps to ENST00000415385 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:12032541 G>A maps to ENST00000415385 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:11998918 G>T maps to ENST00000415385 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:12011199 G>T maps to ENST00000415385 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:12013690 G>A did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr17:11984783 A>G maps to ENST00000415385 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr17:11984783 A>G maps to ENST00000415385 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr17:12032541 G>A maps to ENST00000415385 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr17:12043153 A>G did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr15:67893021 G>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:67515569 G>T maps to NM_002758.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:67522793 G>A maps to NM_002758.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr17:67513688 C>T maps to NM_002758.3 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:7977228 G>A maps to ENST00000425613 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:7977204 C>T maps to ENST00000425613 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr19:7975164 C>T maps to ENST00000425613 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr19:7968850 C>T maps to ENST00000425613 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:56180601 G>T maps to NM_005921.1 G1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:56171124 C>T maps to NM_005921.1 Y651Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:56178350 T>C maps to NM_005921.1 S1108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:56161770 C>A maps to NM_005921.1 S423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:56152565 C>T maps to NM_005921.1 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:40704384 C>T maps to NM_002446.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:40720988 G>A maps to NM_002446.3 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:65375276 C>T maps to NM_002419.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:65366952 C>T maps to NM_002419.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:65366865 G>A maps to NM_002419.3 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:53875004 G>A maps to NM_001193511.1 S880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:53880277 C>A maps to NM_001193511.1 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:53881046 C>T maps to NM_001193511.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:53880737 C>T maps to NM_001193511.1 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:53876135 C>T maps to NM_001193511.1 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:185183577 C>A maps to NM_004721.3 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:185169093 C>T maps to NM_004721.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:185146659 G>A maps to NM_004721.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:185200168 C>T maps to NM_004721.3 D942D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:185181424 C>T maps to NM_004721.3 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:185190892 C>T maps to NM_004721.3 R592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr3:185198025 T>C maps to NM_004721.3 H836H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr3:185184656 C>T maps to NM_004721.3 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:43344491 G>A maps to ENST00000344686 I799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:43347912 C>T maps to ENST00000344686 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr17:43364145 T>C maps to ENST00000344686 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr23:19387305 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:19416380 G>T did not map to a codon.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr23:19392614 C>T did not map to a codon.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr23:19389552 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:19379674 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:19410478 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:19431490 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr23:19413201 C>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:19392619 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:19431518 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:19380950 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:19380859 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:19390894 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:19410501 T>C did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:19379456 C>T did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr23:19389112 G>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:19378901 C>T did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:19431488 A>G did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:19416379 C>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:19391705 C>T did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:19431487 G>T did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:19378899 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:19390820 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:128075797 C>A maps to NM_006609.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:61762930 T>C maps to NM_203351.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:61768520 C>T maps to NM_203351.1 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:161470761 G>A maps to NM_005922.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:161527660 G>A maps to NM_005922.2 T1324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr6:161470824 A>G maps to NM_005922.2 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:161530873 C>T maps to NM_005922.2 L1442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr6:161455386 C>T maps to NM_005922.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr6:161491637 A>G did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr6:161530786 G>T maps to NM_005922.2 E1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr6:161491656 T>C maps to NM_005922.2 D575D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr6:161530788 A>G maps to NM_005922.2 E1413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:161455303 T>C maps to NM_005922.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:161536208 G>T maps to NM_005922.2 G1561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr6:137019676 A>T maps to NM_005923.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:136923078 G>A maps to NM_005923.3 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr6:136913364 G>A maps to NM_005923.3 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr6:136932438 G>T maps to NM_005923.3 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:27685944 C>T maps to NM_004672.3 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:27688703 G>A maps to NM_004672.3 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr6:91281511 T>C maps to NM_145331.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:30739281 T>C maps to NM_005204.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:30747104 G>A maps to NM_005204.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:30747086 G>A maps to NM_005204.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:71209215 G>A maps to NM_033141.2 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:71199901 C>T maps to NM_033141.2 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr14:71209233 A>G maps to NM_033141.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr14:71199901 C>T maps to NM_033141.2 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr3:47910709 C>T maps to ENST00000426837 A2134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:48040302 G>A maps to ENST00000426837 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:39106865 A>G maps to NM_001042600.1 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr11:64557097 T>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:64569921 G>A maps to NM_004579.2 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr11:64557097 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:64559486 C>T maps to NM_004579.2 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr2:39553360 A>G maps to NM_003618.2 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:39570589 T>A maps to NM_003618.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:39553345 T>G maps to NM_003618.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:39499510 A>C maps to NM_003618.2 L629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr2:39605228 A>G maps to NM_003618.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr2:39485579 A>G maps to NM_003618.2 C793C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:102476160 G>A maps to NM_145686.2 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:102505285 C>A maps to NM_145686.2 G1256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:102501694 T>G maps to NM_145686.2 S1125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:102472486 C>T maps to NM_145686.2 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:102448225 G>A maps to NM_145686.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:102504298 G>A maps to NM_145686.2 E1213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:102504325 G>A maps to NM_145686.2 G1222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr2:102476235 G>A maps to NM_145686.2 Q538Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr2:102483018 C>T maps to NM_145686.2 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:50952320 G>A maps to NM_198794.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:75319276 A>G maps to NM_033063.1 H332H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:75298895 A>G maps to NM_033063.1 D550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:75319308 G>A maps to NM_033063.1 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr6:136693764 T>C maps to NM_001198609.1 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:136709571 C>T maps to NM_001198609.1 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:136683597 C>A maps to NM_001198609.1 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:136681168 G>A maps to NM_001198609.1 R632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:36636899 C>T maps to NM_018067.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr1:36636770 G>A maps to NM_018067.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr1:36641854 G>C maps to NM_018067.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:20074856 T>C did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:20031736 C>A did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:20071060 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:20074901 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:20034396 G>A did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:20028953 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:20062619 T>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:20034354 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:20071023 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:20081635 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:20029076 A>G did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:20043109 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:135302950 T>C did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:135313852 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:135326875 C>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:135323359 G>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:135302950 T>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:135323322 T>G did not map to a codon.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr23:135318470 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:135328415 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:135328252 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:135302996 A>C did not map to a codon.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr23:135328414 C>G did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:135314111 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:135312620 A>G did not map to a codon.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr23:135326814 T>C did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:135313784 G>A did not map to a codon.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr23:135328444 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:135302951 C>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:135313852 G>A did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:135326814 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:135326816 T>C did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:135328253 G>A did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr4:156281553 T>C maps to NM_001039580.1 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:156276981 C>T maps to NM_001039580.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:156281508 C>T maps to NM_001039580.1 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:156281394 A>G maps to NM_001039580.1 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr4:156281553 T>C maps to NM_001039580.1 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr4:156269026 G>A maps to NM_001039580.1 R618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:86952562 T>A maps to NM_138982.2 K378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr4:87022343 G>T maps to NM_138982.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:86952529 C>A maps to NM_138982.2 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr4:86952560 C>T maps to NM_138982.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr4:87022226 C>T maps to NM_138982.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr4:87022331 G>T maps to NM_138982.2 C201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr22:50703849 G>A maps to NM_002751.5 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr22:50694121 G>A maps to NM_002969.3 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr6:36104512 G>A maps to NM_002754.3 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr6:36044344 C>T maps to NM_139012.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:144800416 T>C maps to NM_139021.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:144804019 C>T maps to NM_139021.2 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:55529640 G>A maps to NM_144578.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:55529754 A>G maps to NM_144578.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr16:30128009 G>A maps to NM_002746.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr18:48190345 C>T maps to NM_002747.3 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:48252488 C>A maps to NM_002747.3 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr18:48255905 C>T maps to NM_002747.3 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr18:48241534 C>T maps to NM_002747.3 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr18:48190732 C>T maps to NM_002747.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:52338848 T>C maps to NM_002748.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr15:52342334 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr17:19285385 C>T maps to NM_139034.2 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:19282362 C>T maps to NM_139034.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:19284469 C>T maps to NM_139034.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:49628328 C>A maps to NM_139049.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:49635146 C>T maps to NM_139049.1 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr10:49628259 T>C maps to NM_139049.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:49612909 C>T maps to NM_139049.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:49628259 T>C maps to NM_139049.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:49628277 A>G maps to NM_139049.1 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:49628340 T>C maps to NM_139049.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr10:49628295 G>A maps to NM_139049.1 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr10:49628328 C>A maps to NM_139049.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:49618120 G>A maps to NM_139049.1 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:45926728 C>T maps to NM_005456.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:45926728 C>T maps to NM_005456.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:45924464 C>T maps to NM_005456.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:45924649 C>T maps to NM_005456.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr11:45925671 T>C maps to NM_005456.2 Y542Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:45924190 C>T maps to NM_005456.2 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr22:51044277 G>T maps to ENST00000329492 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:1816798 C>T maps to NM_015133.3 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:1816389 C>A maps to NM_015133.3 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr5:179691818 C>A maps to NM_002752.4 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:179691839 C>T did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr5:179696363 T>C maps to NM_002752.4 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:128347856 G>A maps to NM_001006617.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:206904102 C>A maps to NM_032960.2 Y254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:206902134 C>T maps to NM_032960.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:50679203 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:50677937 T>C did not map to a codon.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr15:42103095 G>A maps to NM_001128608.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr15:42107483 C>T maps to NM_001128608.1 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:42116161 C>A maps to NM_001128608.1 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr15:42113250 T>G maps to NM_001128608.1 T907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:42115702 C>T maps to NM_001128608.1 I1225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr15:42107533 C>T maps to NM_001128608.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr15:42104312 G>A maps to NM_001128608.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr4:100806728 T>C maps to NM_021970.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:100806799 G>A maps to NM_021970.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:32682068 G>T maps to NM_014268.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:32677529 C>A maps to NM_014268.2 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr18:32650251 T>C maps to NM_014268.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:27245205 A>G maps to NM_012326.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr2:27249185 G>A maps to NM_012326.2 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:44060772 G>A maps to NM_001123066.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr17:44039726 C>T maps to NM_001123066.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:164506986 G>A maps to ENST00000514618 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:164507056 T>C maps to ENST00000514618 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:164466826 G>A maps to ENST00000514618 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr17:60814040 C>T maps to NM_152598.2 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:60813804 G>T maps to NM_152598.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr17:60879072 C>T maps to NM_152598.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr5:126250630 C>T maps to NM_178450.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:126213942 C>T maps to NM_178450.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:217142428 G>A maps to NM_020814.2 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr2:217142407 G>A maps to NM_020814.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:217142455 G>A maps to NM_020814.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr10:94110874 G>T maps to NM_017824.4 G250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:94100497 G>T maps to NM_017824.4 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:94100535 T>G maps to NM_017824.4 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:94070897 C>T maps to NM_017824.4 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:10400941 A>G maps to NM_005885.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:10378901 G>T maps to NM_005885.2 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:10411624 C>T maps to NM_005885.2 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:10402701 C>T maps to NM_005885.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:160619446 C>T maps to NM_022826.2 C650C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:160604451 C>T maps to NM_022826.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:45953758 G>T maps to NM_145021.4 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:119750833 C>T maps to NM_006770.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:119750787 C>T maps to NM_006770.3 C447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:119731936 C>T maps to NM_006770.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:220824027 C>T maps to NM_018650.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:220835399 C>T maps to NM_018650.3 C760C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:220773170 G>A maps to NM_018650.3 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:220808728 T>C maps to NM_018650.3 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:220805568 C>T maps to NM_018650.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:220835213 T>A maps to NM_018650.3 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr1:220805597 T>C maps to NM_018650.3 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:220777409 T>C maps to NM_018650.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr11:63668513 T>C maps to NM_001039469.2 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:63662725 T>A maps to NM_001039469.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:63672422 T>C maps to NM_001039469.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:63662749 C>A maps to NM_001039469.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:103871546 C>T maps to ENST00000335102 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:103933479 C>T maps to ENST00000335102 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr19:45783969 C>T maps to NM_031417.3 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:45766420 G>A maps to NM_031417.3 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:45781284 A>G maps to NM_031417.3 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:57906609 G>A maps to NM_004990.2 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr12:57883317 C>T maps to NM_004990.2 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:57894202 T>C maps to NM_004990.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr12:57909764 A>G maps to NM_004990.2 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:198571019 C>T maps to NM_138395.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:71674476 G>A maps to NM_001017967.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:71668219 C>T maps to NM_052858.3 F240F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3854-01A-01W-0900-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:160328502 C>T maps to NM_002377.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:160327992 T>C maps to NM_002377.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr6:160328640 G>A maps to NM_002377.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr3:186961368 C>A maps to NM_139125.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:186953693 G>A maps to NM_139125.3 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:186954082 G>A maps to NM_139125.3 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:186978604 G>A maps to NM_139125.3 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:187003786 G>A maps to NM_139125.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr3:186978652 G>A maps to NM_139125.3 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:186953582 G>A maps to NM_139125.3 C692C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:186971085 T>C maps to NM_139125.3 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:186968078 C>A maps to NM_139125.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:186968081 A>G maps to NM_139125.3 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:186968084 C>T maps to NM_139125.3 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:186978565 G>A maps to NM_139125.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:11087510 G>A maps to NM_006610.2 R498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:11105507 G>A maps to NM_006610.2 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:11106989 G>A maps to NM_006610.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:11087277 T>C maps to NM_006610.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:12979493 G>A maps to NM_014975.2 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr19:12981911 C>T maps to NM_014975.2 P1063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:12969201 G>A maps to NM_014975.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:46500712 C>T maps to NM_015112.2 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:46500504 C>T maps to NM_015112.2 L1388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:46499743 G>A did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr1:46493447 A>G maps to NM_015112.2 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:46489566 T>G maps to NM_015112.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:46498269 C>T maps to NM_015112.2 H1139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:18239255 T>C maps to NM_015016.1 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:18260478 C>T maps to NM_015016.1 I1291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:18235112 C>T maps to NM_015016.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:18235489 G>A maps to NM_015016.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:18232705 T>G maps to NM_015016.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:18255819 C>T maps to NM_015016.1 G911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:18245670 C>T maps to NM_015016.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:18254617 G>A maps to NM_015016.1 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr19:18232539 C>T maps to NM_015016.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:66445254 C>T maps to NM_001164664.1 R1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:66459344 C>T maps to NM_001164664.1 S1446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:66426062 G>T maps to NM_001164664.1 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:66396318 C>T maps to NM_001164664.1 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:66460997 C>T maps to NM_001164664.1 S1997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr5:66459074 C>T maps to NM_001164664.1 P1356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:27444510 G>A maps to NM_001172303.1 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:27444534 A>T maps to NM_001172303.1 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:82036320 G>A maps to NM_000429.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:82034844 T>C maps to NM_000429.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:85769870 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:162945285 C>T maps to NM_013283.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:3785088 G>A maps to NM_139355.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:3781622 C>A maps to NM_002378.3 G243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:3784188 G>A maps to NM_002378.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:3784855 C>T maps to NM_002378.3 W34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr19:3778228 T>C maps to NM_002378.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:99019455 G>A did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr8:99019455 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr8:99015934 C>T maps to ENST00000254898 C417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:43934162 C>T maps to ENST00000372754 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:138661139 C>T maps to ENST00000394800 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr5:138658193 C>T maps to ENST00000394800 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:29819983 C>T maps to NM_001042539.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:29821440 G>A maps to NM_002383.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr22:36007074 C>T maps to NM_203377.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:47800681 G>T maps to ENST00000424334 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:47800163 G>A maps to ENST00000424334 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr18:47800167 A>G maps to ENST00000424334 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr18:51731393 G>A maps to NM_003927.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:1592594 C>T maps to NM_003926.5 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:1578476 G>A maps to NM_003926.5 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:1585062 G>A maps to NM_003926.5 N87N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:129156093 A>G maps to NM_003925.1 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:149227413 A>G maps to ENST00000404807 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:149226510 C>T maps to ENST00000404807 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:149247619 G>A maps to ENST00000404807 L1473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr2:149243446 G>A maps to ENST00000404807 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:149227206 C>A maps to ENST00000404807 I565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:149248082 G>T maps to ENST00000404807 G1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:149227012 A>C maps to ENST00000404807 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:149240763 C>T maps to ENST00000404807 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:149216413 G>T maps to ENST00000404807 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:57920715 G>A maps to NM_052897.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:57920574 G>A maps to NM_052897.3 Q549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:57922489 G>A maps to NM_052897.3 R954R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:57922312 C>T maps to NM_052897.3 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:54528265 G>C maps to NM_000242.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr5:89757099 G>A maps to NM_203406.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:152163153 T>C maps to NM_021038.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:152132785 G>T maps to NM_021038.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:152018065 A>G maps to NM_021038.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:97986570 G>A maps to ENST00000376673 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr13:98043600 C>T maps to ENST00000376673 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr13:97999188 G>A maps to ENST00000376673 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:131540363 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:131525081 A>G did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:20118733 G>A maps to NM_001080480.1 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:20128942 G>A maps to NM_001080480.1 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:20113187 C>T maps to NM_001080480.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:20152982 G>T maps to NM_001080480.1 C39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:20152901 C>T maps to NM_001080480.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:9017321 C>T maps to NM_138799.2 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:74701983 G>A maps to NM_001025101.1 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr18:74728808 C>T maps to NM_001025101.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:74700830 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:49284279 G>A maps to ENST00000389496 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:49270164 T>C maps to ENST00000389496 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:49272707 T>C maps to ENST00000389496 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:49280158 G>A maps to ENST00000389496 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:49297753 G>A maps to ENST00000389496 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:84094362 C>T maps to NM_003791.2 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:84088185 T>A maps to NM_003791.2 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr16:84132697 C>T maps to NM_003791.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00W-01A-01W-A005-10 chr16:84132810 G>A maps to NM_003791.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:84127330 G>A maps to NM_003791.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:21863434 C>G did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:21857877 T>G did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:21861307 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:21900626 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:21896684 A>C did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:13885484 G>A maps to NM_000529.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:13885283 G>T maps to NM_000529.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr18:13885321 A>G maps to NM_000529.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:13885199 G>A maps to NM_000529.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:13885337 G>T maps to NM_000529.2 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr18:13884764 G>A maps to NM_000529.2 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr18:13885321 A>G maps to NM_000529.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:54824096 C>T maps to ENST00000371389 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:54824846 C>T maps to ENST00000371389 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:54824342 C>T maps to ENST00000371389 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr20:54824096 C>T maps to ENST00000371389 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr20:54824096 C>T maps to ENST00000371389 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr20:54824045 C>T maps to ENST00000371389 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr20:54824096 C>T maps to ENST00000371389 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr18:58038874 G>A maps to NM_005912.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr18:58038832 C>A maps to NM_005912.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:119182875 C>T maps to NM_006500.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:119182824 G>A maps to NM_006500.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:119181067 C>T maps to NM_006500.2 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:119182284 C>T maps to NM_006500.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:119181806 G>T maps to NM_006500.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:119182269 C>T maps to NM_006500.2 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr9:37888382 G>A maps to NM_033412.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr9:37888376 T>C maps to NM_033412.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr9:37888378 G>A maps to NM_033412.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:37887932 C>T maps to NM_033412.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:37888378 G>A maps to NM_033412.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr9:37888378 G>A maps to NM_033412.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr9:37887938 G>A maps to NM_033412.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:29340258 G>A maps to NM_001034172.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:103349452 G>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:103349503 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:103349541 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:103349266 G>A did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:103349601 G>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:103349892 C>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:103349038 C>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:43533164 A>G maps to NM_173467.4 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:43533164 A>G maps to NM_173467.4 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:112403843 C>T maps to NM_001085377.1 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr5:112439975 C>T maps to NM_001085377.1 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:112437518 G>A maps to NM_001085377.1 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:112389628 G>A maps to NM_001085377.1 C747C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:112420977 G>A maps to NM_001085377.1 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:112389604 G>A maps to NM_001085377.1 D755D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:112676263 C>T maps to NM_001085377.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:182790188 A>G maps to NM_020166.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr3:182740299 C>A maps to NM_020166.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr3:182812386 C>T maps to NM_020166.3 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:182756918 G>A maps to NM_020166.3 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:182759396 G>A maps to NM_020166.3 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:70939653 C>T maps to NM_022132.4 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:138678857 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:138670551 T>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:138697170 C>T did not map to a codon.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr23:138713584 T>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:138687891 C>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:138687894 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:138698523 G>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:138708866 G>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:138679645 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:138667315 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:138713627 C>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:138701839 A>T did not map to a codon.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr23:138698561 T>G did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:138728982 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:138698446 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:138678715 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:138708884 T>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:138708446 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:138697074 A>G did not map to a codon.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr23:138697074 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:138708834 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:138679711 T>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:138697074 A>G did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:138678728 G>C did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:138679646 A>G did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:138697170 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:138697074 A>G did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:138713582 A>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:138724630 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:138699727 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:113735526 G>A maps to NM_001112732.1 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr13:113718649 C>T maps to NM_001112732.1 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr13:113669098 C>T maps to NM_001112732.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:113731374 C>T maps to NM_001112732.1 R561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:113740564 T>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:182947475 C>A maps to NM_015078.2 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:182910844 A>G maps to NM_015078.2 N986N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:182947475 C>A maps to NM_015078.2 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:182948758 C>A maps to NM_015078.2 E637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:183056613 G>A maps to NM_015078.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:183056613 G>A maps to NM_015078.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:183059354 G>A maps to NM_015078.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:182925517 G>A maps to NM_015078.2 R864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:183028714 G>A maps to NM_015078.2 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:183097179 G>A maps to NM_015078.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:41075556 C>T maps to NM_005297.3 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:41075523 G>A maps to NM_005297.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:100395798 C>A maps to NM_032503.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr6:100390993 G>T maps to NM_032503.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:150550851 A>G maps to NM_021960.4 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:13217612 G>T maps to NM_182751.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:13214442 A>G maps to NM_182751.2 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:13237166 G>A maps to NM_182751.2 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:127336908 C>T maps to NM_004526.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:127323811 G>A maps to NM_004526.2 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:127325560 C>T maps to NM_004526.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:127338033 C>T maps to NM_004526.2 Y726Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:127336234 C>T maps to NM_004526.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:127334775 C>T maps to NM_004526.2 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:127339939 C>A maps to NM_004526.2 R825R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:127339644 C>T maps to NM_004526.2 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr3:127325075 C>T maps to NM_004526.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:127339941 G>A maps to NM_004526.2 R825R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:52138561 T>C maps to ENST00000419835 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:52147553 G>A maps to ENST00000419835 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr21:47678995 T>C maps to NM_003906.3 V1197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr21:47685377 G>A maps to NM_003906.3 Q1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr21:47687020 C>T maps to NM_003906.3 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr21:47685881 C>T maps to NM_003906.3 A996A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr21:47655321 G>A maps to NM_003906.3 Q1935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr21:47705017 A>G maps to NM_003906.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr21:47678851 C>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr21:47676821 G>A maps to NM_003906.3 D1271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr21:47697543 G>A maps to NM_003906.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:48882365 C>T maps to NM_182746.1 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:48882380 C>T maps to NM_182746.1 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr8:48889247 A>G maps to NM_182746.1 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:48875322 G>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:48878897 C>T maps to NM_182746.1 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr22:35812390 C>T maps to NM_006739.3 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:35812692 C>T maps to NM_006739.3 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:35811868 G>A maps to NM_006739.3 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:136609033 G>A maps to NM_005915.4 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:136630400 G>A maps to NM_005915.4 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:136616993 G>A maps to NM_005915.4 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr2:136614432 C>G maps to NM_005915.4 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr7:99695276 G>A maps to NM_005916.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:99691888 G>A maps to NM_005916.3 Y585Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr7:99693566 G>A maps to NM_005916.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:99693773 G>T maps to NM_005916.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr20:5935881 T>G maps to NM_032485.4 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:5948090 A>G maps to NM_032485.4 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:5963806 T>C maps to NM_032485.4 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:5939373 T>C did not map to a codon.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr20:5953799 T>C maps to NM_032485.4 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:119232908 C>A maps to ENST00000316316 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:7591777 C>T maps to NM_020533.2 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:7595257 G>A maps to NM_020533.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:7592773 C>T maps to NM_020533.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:85422114 G>T maps to NM_153259.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:85418169 C>T maps to NM_153259.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr1:85397197 A>G maps to NM_153259.2 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:85422114 G>T maps to NM_153259.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:85510877 G>A maps to NM_018298.9 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:85499837 G>A maps to NM_018298.9 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:85498410 C>A maps to NM_018298.9 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:85510877 G>A maps to NM_018298.9 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:6500518 C>A maps to NM_024596.3 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:6289058 C>T maps to NM_024596.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:94253666 C>T maps to NM_024717.4 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr5:94248558 G>A maps to NM_024717.4 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr5:94044282 A>G maps to NM_024717.4 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:94289033 G>A maps to NM_024717.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:94206574 A>G did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr15:94983490 T>C maps to NM_018349.3 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:94928754 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:94882594 G>A maps to NM_018349.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:94841689 C>A maps to NM_018349.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:95019950 C>T maps to NM_018349.3 R833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:119746060 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:119739273 A>C did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr6:30671315 T>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:30681043 A>G maps to NM_014641.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:30671906 T>G maps to NM_014641.2 R1685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:30675777 C>A maps to NM_014641.2 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:30673671 T>C maps to NM_014641.2 S1096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr6:30671315 T>C did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr6:30671308 G>A maps to NM_014641.2 V1856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:114655784 C>T maps to NM_199072.4 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:114619804 C>A maps to NM_199072.4 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:114582351 T>C maps to NM_199072.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:37623565 C>T maps to ENST00000297153 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr6:37622185 C>A maps to ENST00000297153 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:37622672 C>T maps to ENST00000297153 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:37623624 G>A maps to ENST00000297153 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr6:37623624 G>A maps to ENST00000297153 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:37613718 C>T maps to ENST00000297153 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr6:37619823 G>A maps to ENST00000297153 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:37631750 G>T maps to ENST00000297153 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr6:37620105 G>A maps to ENST00000297153 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr6:37615056 G>T maps to ENST00000297153 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:47530614 C>A maps to NM_001113498.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:47601050 T>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:47530476 G>A maps to NM_001113498.2 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr14:47504436 C>T maps to NM_001113498.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr14:47342699 A>G maps to NM_001113498.2 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:63826411 C>T maps to NM_005917.3 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:207613840 T>C maps to NM_001039845.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:207613840 T>C maps to NM_001039845.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:207613840 T>C maps to NM_001039845.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:207619969 G>A maps to NM_001039845.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:207622056 A>G maps to NM_001039845.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:207611124 G>A maps to NM_001039845.1 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr2:207622056 A>G maps to NM_001039845.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr2:207613840 T>C maps to NM_001039845.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:68696400 A>G maps to NM_017440.4 N657N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:68715402 A>G maps to NM_017440.4 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr12:68707264 G>C maps to NM_017440.4 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:204515954 G>T maps to NM_002393.3 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr1:204507404 C>A maps to NM_002393.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:90406179 A>T maps to NM_014611.1 S3094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:90422424 T>C maps to NM_014611.1 G2433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr6:90422424 T>C maps to NM_014611.1 G2433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:90353806 G>A maps to NM_014611.1 R5570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:90410545 T>C maps to NM_014611.1 Q2819Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:90421899 T>A maps to NM_014611.1 A2502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr6:90415870 G>A maps to NM_014611.1 V2685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr6:90422465 G>A maps to NM_014611.1 R2420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:90504336 C>T maps to NM_014611.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:90394602 C>A maps to NM_014611.1 E3941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:90354763 G>T maps to NM_014611.1 I5524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:90503485 C>A maps to NM_014611.1 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:90371808 A>G maps to NM_014611.1 D4854D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:90396699 G>A maps to NM_014611.1 T3831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:90424430 G>A maps to NM_014611.1 S2300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:90503841 A>G maps to NM_014611.1 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:90499590 C>A maps to NM_014611.1 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:90425448 G>A maps to NM_014611.1 P2261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr6:90410536 G>T maps to NM_014611.1 V2822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr6:90411651 G>A maps to NM_014611.1 I2759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:90405335 G>A maps to NM_014611.1 Y3253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr6:90385898 C>T maps to NM_014611.1 W4189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr6:90383869 G>A maps to NM_014611.1 D4400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:24684959 A>G maps to NM_138476.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:24684995 A>C maps to NM_138476.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:83947498 A>C maps to NM_002395.4 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:83921693 A>G maps to NM_002395.4 C556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:83938568 C>A maps to NM_002395.4 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:83938568 C>A maps to NM_002395.4 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:48473461 G>T maps to NM_002396.4 E555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr18:48439179 C>T maps to NM_002396.4 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr18:48458684 C>T maps to NM_002396.4 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr18:48447079 T>C maps to NM_002396.4 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:86267656 G>A maps to NM_001014811.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:86209055 C>T maps to NM_001014811.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:86157427 G>A maps to NM_001014811.1 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:86152470 G>A maps to NM_001014811.1 Y555Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:86382833 G>A maps to NM_001014811.1 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr11:86152476 G>A maps to NM_001014811.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:42981068 G>T maps to NM_014623.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:42980324 T>C maps to NM_014623.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:168810803 G>A maps to NM_004991.3 R1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:168807792 T>C maps to NM_004991.3 P1132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:168834288 A>T maps to NM_004991.3 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:168833700 C>A maps to NM_004991.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr3:168802732 C>T maps to NM_004991.3 A1228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:168813033 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:168833982 G>A maps to NM_004991.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:168807840 A>G maps to NM_004991.3 D1116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:153296218 G>A did not map to a codon.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr23:153296367 T>C did not map to a codon.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr23:153296276 T>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:153296859 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:153296444 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:153295962 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:29533343 G>A maps to NM_016011.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:29529713 G>A maps to NM_016011.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr17:37565608 A>G maps to NM_004774.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:37566097 T>C maps to NM_004774.3 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr17:37571512 A>G maps to NM_004774.3 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:37565965 A>G maps to NM_004774.3 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr17:37565608 A>G maps to NM_004774.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr5:6372669 C>T maps to NM_032286.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:70338702 G>T did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:70352330 A>C did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:70349908 A>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:70357674 A>G did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:70351421 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:70354957 G>A did not map to a codon.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr23:70355012 C>A did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:70354692 T>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:70360551 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:70340985 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:70342197 T>C did not map to a codon.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr23:70338702 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:70339252 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:70341593 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:70345912 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:70357412 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr23:70348243 C>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:70348498 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:70360634 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:70346923 C>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:70360622 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:70360634 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:70360707 G>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:70352365 C>T did not map to a codon.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr23:70357675 C>T did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:70345336 C>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:70345908 C>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:70351419 G>A did not map to a codon.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr23:70346885 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:70345298 C>A did not map to a codon.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr3:151083643 C>T maps to NM_053002.4 N1029N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:151093948 G>T maps to NM_053002.4 E1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:151093867 G>T maps to NM_053002.4 E1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:150804739 T>C maps to NM_053002.4 Y9Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:151127074 G>A maps to NM_053002.4 R1920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:150911302 C>A maps to NM_053002.4 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:151131059 C>T maps to NM_053002.4 R2057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:150877656 T>A maps to NM_053002.4 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:151102859 C>T maps to NM_053002.4 R1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:151067869 T>C maps to NM_053002.4 C723C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:150845632 G>T maps to NM_053002.4 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:150874029 C>T maps to NM_053002.4 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr3:151094628 C>T maps to NM_053002.4 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:150883244 A>G maps to NM_053002.4 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:150877857 C>T maps to NM_053002.4 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:60040328 C>T maps to NM_005121.2 T1616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:60032839 A>G maps to NM_005121.2 C1957C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:60072619 C>A maps to NM_005121.2 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:60039086 G>T maps to NM_005121.2 I1706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:116444150 C>T maps to NM_015335.4 G768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:116424914 G>A maps to NM_015335.4 Y1371Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:116443772 G>A maps to NM_015335.4 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:116424166 G>A maps to NM_015335.4 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:116457643 C>T maps to NM_015335.4 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:116457745 C>T maps to NM_015335.4 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr12:116444159 C>T maps to NM_015335.4 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:116446576 T>C maps to NM_015335.4 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr12:116457631 G>A maps to NM_015335.4 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr12:116424202 C>T maps to NM_015335.4 P1402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:116460324 C>T maps to NM_015335.4 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:40514223 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:40514248 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:40556294 C>T did not map to a codon.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr23:40522177 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:40585997 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:40518831 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:40523638 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:40560443 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:40514247 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:40568631 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:40514311 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:40539308 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:40571468 C>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:40514247 G>A did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:40514311 A>G did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:40514310 A>G did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:40569381 C>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:40523720 G>T did not map to a codon.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr23:40573907 G>A did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:40573073 A>G did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:40569252 T>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr22:20920815 G>A maps to NM_001003891.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr22:20920812 A>G maps to NM_001003891.1 Q250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:93545133 G>A maps to NM_004268.4 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr11:93545019 T>A maps to NM_004268.4 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:28657193 C>T maps to NM_017638.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:57472444 C>T maps to ENST00000431606 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:57472197 G>A maps to ENST00000431606 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr6:41884655 G>A maps to NM_004275.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:27175555 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:27181261 T>C maps to NM_004264.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:136208360 G>A maps to NM_133640.3 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:131914182 C>A maps to ENST00000403834 E1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:131943026 T>C maps to ENST00000403834 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:131915247 G>A maps to ENST00000403834 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr6:131908845 C>A maps to ENST00000403834 V1366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr17:38176534 G>T maps to NM_014815.3 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr17:38182512 G>A maps to NM_014815.3 H627H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr17:38185173 G>A maps to NM_014815.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr19:50333134 G>A maps to NM_030973.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:50334642 A>T maps to NM_030973.3 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:50339042 G>A maps to NM_030973.3 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:16687290 G>A maps to NM_004831.3 H450H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:134769349 G>A maps to NM_004269.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:17625363 C>A maps to NM_025205.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr17:6553390 G>A maps to NM_016060.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr13:48654028 G>A maps to NM_014166.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr13:48664501 C>A maps to NM_014166.2 G60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr14:71064414 T>A maps to ENST00000430055 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:43852633 A>G maps to NM_052877.3 H102H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:17380492 G>A maps to NM_018019.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:17394790 C>T maps to NM_018019.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr15:100185845 C>G maps to ENST00000338042 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr15:100215616 C>T maps to ENST00000338042 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:100211574 C>T maps to ENST00000338042 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr5:88057094 C>T maps to NM_002397.4 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:88057040 G>A maps to NM_002397.4 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr5:88047697 G>A maps to NM_002397.4 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr1:156452363 G>A maps to NM_005920.2 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:156438636 A>G maps to NM_005920.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:156446854 G>A maps to NM_005920.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:156452246 G>T maps to NM_005920.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:156450649 G>A maps to NM_005920.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr16:3304260 C>T maps to NM_000243.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:3293533 G>A maps to NM_000243.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:3293269 G>A maps to NM_000243.2 H739H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:3299658 G>T maps to NM_000243.2 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:3297215 G>A maps to NM_000243.2 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:3293491 C>T maps to NM_000243.2 W665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr16:3293506 T>C maps to NM_000243.2 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:126776450 G>T maps to NM_032446.2 G752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:126771137 T>G maps to NM_032446.2 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:126770442 C>T maps to NM_032446.2 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr5:126770430 C>T maps to NM_032446.2 C631C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr5:126755841 C>T maps to NM_032446.2 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:126732227 C>T maps to NM_032446.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:126734481 C>T maps to NM_032446.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:3413231 C>T maps to ENST00000452816 T1318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:3431147 G>T maps to ENST00000452816 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:3427407 G>A maps to ENST00000452816 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:3415795 G>A maps to ENST00000452816 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:3417647 T>C maps to ENST00000452816 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:3427350 A>G maps to ENST00000452816 C485C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:3496398 G>A maps to ENST00000452816 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:3428618 G>A maps to ENST00000452816 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr1:3410410 G>A maps to ENST00000452816 D1512D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr1:3440763 G>A maps to ENST00000452816 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:42855622 C>T maps to ENST00000251268 C966C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:42860344 C>T maps to ENST00000251268 A1501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr19:42873064 C>T maps to ENST00000251268 N2184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr19:42848894 G>A maps to ENST00000251268 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:42873727 C>T maps to ENST00000251268 N2229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:42874381 A>G maps to ENST00000251268 S2292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr19:42848972 C>T maps to ENST00000251268 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:42838253 C>T maps to ENST00000251268 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr19:42857653 C>T maps to ENST00000251268 P1196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:42847686 C>T maps to ENST00000251268 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:123370070 C>T maps to ENST00000426959 E472E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr22:42150015 A>C maps to NM_152513.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:42191506 G>A maps to NM_152513.3 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:42095604 G>A maps to NM_152513.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:42119977 C>A maps to NM_152513.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:15014592 G>T maps to NM_001080836.2 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:66667040 C>T maps to ENST00000407092 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:47910727 G>A maps to NM_020160.1 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:36671108 G>A maps to NM_014791.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr9:36671003 A>C maps to NM_014791.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr9:36643023 G>T maps to NM_014791.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:36669326 G>T maps to NM_014791.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:36665549 G>A maps to NM_014791.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr9:36665549 G>A maps to NM_014791.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr9:36671030 T>C maps to NM_014791.2 H514H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr9:36657326 A>G maps to NM_014791.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:32157143 C>T maps to NM_015955.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:64575146 C>T maps to NM_130804.2 W225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:64573792 G>T maps to NM_130804.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:64577289 G>A maps to NM_130804.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:64575133 C>A maps to NM_130804.2 G230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr11:64571898 C>T maps to NM_130804.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:64575482 A>T maps to NM_130804.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr11:64574542 T>C maps to NM_130804.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:64573792 G>T maps to NM_130804.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr11:64571898 C>T maps to NM_130804.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:15652182 T>C maps to NM_005924.4 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:15652020 C>T maps to NM_005924.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:15725739 C>T maps to NM_005924.4 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:15725802 G>A maps to NM_005924.4 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr7:15725619 G>A maps to NM_005924.4 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:15725619 G>A maps to NM_005924.4 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:15725808 G>A maps to NM_005924.4 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:46793177 C>T maps to NM_005588.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:46803220 A>G maps to NM_005588.2 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr6:46797207 T>C maps to NM_005588.2 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:29790485 C>T maps to NM_005925.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:88767381 T>C maps to ENST00000395102 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr4:88766499 G>A maps to ENST00000395102 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:88766985 A>G maps to ENST00000395102 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:88767087 C>T maps to ENST00000395102 N387N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr4:88766448 C>T maps to ENST00000395102 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:112754942 C>T maps to NM_006343.2 N498N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:112779061 C>T maps to NM_006343.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:112686790 C>A maps to NM_006343.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:112686982 A>G maps to NM_006343.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr2:112777033 C>T maps to NM_006343.2 A708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:90321303 T>A maps to NM_001039958.1 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:130140341 C>T maps to NM_002402.2 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr7:130138110 C>T maps to NM_002402.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:116417464 T>C maps to NM_001127500.1 H1112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:116411649 A>C maps to NM_001127500.1 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr7:116417503 T>C maps to NM_001127500.1 C1125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr7:116419007 T>C maps to NM_001127500.1 T1191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:116339710 G>A maps to NM_001127500.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:116419007 T>C maps to NM_001127500.1 T1191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr7:116423408 C>T maps to NM_001127500.1 D1246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:116339933 A>C maps to NM_001127500.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:116418996 C>T maps to NM_001127500.1 R1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr7:116423414 T>C maps to NM_001127500.1 Y1248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:116417482 T>C maps to NM_001127500.1 N1118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:116339800 A>G maps to NM_001127500.1 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr7:116417464 T>C maps to NM_001127500.1 H1112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr7:116418845 A>G maps to NM_001127500.1 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr7:116339935 G>A maps to NM_001127500.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr7:116417464 T>C maps to NM_001127500.1 H1112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr7:116339605 G>T maps to NM_001127500.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:116423408 C>T maps to NM_001127500.1 D1246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:116339851 A>G maps to NM_001127500.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:99964419 C>T maps to NM_015143.2 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:95907610 G>A maps to NM_006838.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:95907610 G>A maps to NM_006838.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:95905700 C>A maps to NM_006838.3 S332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:95879728 G>T maps to NM_006838.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:81043110 G>A maps to NM_001004431.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:81050972 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:2341477 C>T maps to NM_024086.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:2324078 C>T maps to NM_024086.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:2323296 A>G maps to NM_024086.3 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:2323691 C>A maps to NM_024086.3 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:2324093 C>T maps to NM_024086.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:2376926 A>G maps to NM_024086.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr14:21460325 C>T maps to NM_001029991.1 H136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:21464381 C>T maps to NM_001029991.1 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:28232737 T>C maps to NM_001113528.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:132396373 T>C maps to NM_014064.2 C68C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:132397679 C>T maps to NM_014064.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:62434412 C>T maps to NM_001043229.1 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:171753043 G>A maps to NM_015935.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:128141864 T>C maps to NM_018396.2 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr18:2544200 C>T maps to NM_022840.3 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:2539099 A>G maps to NM_022840.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:170677752 G>A maps to NM_014168.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:170677752 G>A maps to NM_014168.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:15452873 C>A maps to NM_152396.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:15466509 G>T maps to NM_152396.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:15452852 C>T maps to NM_152396.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:51323740 G>A maps to NM_014033.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:172248668 A>T maps to NM_024770.3 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:21624075 G>A maps to NM_016025.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr16:21629218 A>G maps to NM_016025.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:156047144 G>A maps to NM_001093725.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:156047456 G>T maps to NM_001093725.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:156047087 C>T maps to NM_001093725.1 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr1:156046949 G>A maps to NM_001093725.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:82336622 C>T maps to NM_032246.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:82336307 G>A maps to NM_032246.3 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:82335545 C>T maps to NM_032246.3 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr15:82335626 G>A maps to NM_032246.3 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:82335584 G>A maps to NM_032246.3 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:1556851 C>T maps to NM_001174118.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:1556530 G>A maps to NM_001174118.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:44105191 G>A maps to NM_005926.2 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr15:44116731 G>C maps to NM_005926.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:170912956 G>A maps to NM_021647.6 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr4:170912543 G>A maps to NM_021647.6 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr4:170913260 G>A maps to NM_021647.6 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr4:170912846 G>A maps to NM_021647.6 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:170912633 A>G maps to NM_021647.6 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr4:170926875 G>A maps to NM_021647.6 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:228195396 C>T maps to NM_020194.4 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr2:228195479 C>T maps to NM_020194.4 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:228211953 G>A maps to NM_020194.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:228195389 A>G maps to NM_020194.4 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr2:228195387 G>T maps to NM_020194.4 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr2:228211953 G>A maps to NM_020194.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr15:89449967 C>T maps to NM_005928.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:89444811 C>T maps to NM_005928.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:8747631 G>T maps to NM_004225.2 T979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr8:8747607 G>A maps to NM_004225.2 C987C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr8:8748393 G>A maps to NM_004225.2 H725H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:196744060 G>A maps to NM_005929.5 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:196754752 G>A maps to NM_005929.5 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:196742358 C>T maps to NM_005929.5 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:179082174 A>G maps to NM_033540.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:179076696 C>T maps to NM_033540.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:179093042 C>T maps to NM_033540.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr3:179095151 T>C maps to NM_033540.2 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr3:179082162 C>T maps to NM_033540.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:179082174 A>G maps to NM_033540.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr22:37876329 G>A maps to NM_002405.3 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:37876260 G>A maps to NM_002405.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr22:37876305 C>T maps to NM_002405.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:119215345 G>A maps to NM_031433.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:119216196 C>A maps to NM_031433.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:158538002 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:74763522 T>C maps to NM_024311.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:74774409 C>T maps to NM_024311.2 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:74740545 C>T maps to NM_024311.2 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:40432534 G>A maps to NM_001136493.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:40422814 A>G maps to NM_001136493.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:40422814 A>G maps to NM_001136493.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:24244588 A>G maps to ENST00000338315 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr2:24240388 C>T maps to ENST00000338315 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:205554082 G>A maps to NM_181644.4 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr1:205549032 C>T maps to NM_181644.4 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:205561350 C>T maps to NM_181644.4 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr12:53647044 C>T maps to NM_001170790.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr2:191353392 C>T maps to NM_017694.3 H547H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:8701483 G>A maps to NM_152599.3 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:679899 C>T maps to ENST00000404286 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr4:128863226 G>A maps to NM_152778.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:103335130 G>A maps to NM_032718.3 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:103335394 G>A maps to NM_032718.3 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:103334922 G>A maps to NM_032718.3 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:103348856 A>G maps to NM_032718.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:103335079 G>A maps to NM_032718.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr2:103348781 T>C maps to NM_032718.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr2:103343361 A>G maps to NM_032718.3 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:103343421 G>A maps to NM_032718.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:103343415 T>C maps to NM_032718.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr2:103348781 T>C maps to NM_032718.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:103335466 G>A maps to NM_032718.3 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:42050031 C>T maps to ENST00000219905 R2445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:42049991 T>C maps to ENST00000219905 C2431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:42042254 G>A maps to ENST00000219905 Q2199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:41989088 A>G maps to ENST00000219905 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr15:42041073 C>T maps to ENST00000219905 R1867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:42041073 C>T maps to ENST00000219905 R1867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:42041936 T>C maps to ENST00000219905 T2093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:42052727 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:42041564 C>A maps to ENST00000219905 T1969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr15:41961970 T>C maps to ENST00000219905 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:41989133 A>G maps to ENST00000219905 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr15:42057084 A>G maps to ENST00000219905 E2631E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:141727536 T>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:141805648 C>T maps to ENST00000475668 S2741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:141740553 C>T maps to ENST00000475668 V802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:141763375 C>A maps to ENST00000475668 P1445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:141803232 G>A maps to ENST00000475668 T2727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:141795483 C>T maps to ENST00000475668 G2527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr7:141754648 G>C maps to ENST00000475668 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:141747642 G>T maps to ENST00000475668 E853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr7:141764253 C>T maps to ENST00000475668 D1472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr7:141758100 T>C maps to ENST00000475668 D1264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr7:141765233 G>A maps to ENST00000475668 T1528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:141740553 C>A maps to ENST00000475668 V802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:141758085 C>T maps to ENST00000475668 I1259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr7:141763386 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr7:141754630 G>A maps to ENST00000475668 E1079E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:141765185 A>G maps to ENST00000475668 T1512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr5:180219290 C>T maps to NM_001114617.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:180218780 G>A maps to NM_001114617.1 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:180219356 G>A maps to NM_001114617.1 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:180219188 G>A maps to NM_001114617.1 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:50088492 C>T maps to NM_002408.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:39883450 C>A maps to NM_001098270.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:39884005 C>T maps to NM_001098270.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr22:39884665 C>T maps to NM_001098270.1 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr22:39884017 C>T maps to NM_001098270.1 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:39883544 G>T maps to NM_001098270.1 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:99294773 C>T maps to NM_012214.2 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:99242037 G>T maps to NM_012214.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr2:99260499 C>T maps to NM_012214.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:86373821 G>A maps to ENST00000393205 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:86374175 G>A maps to ENST00000393205 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:86373588 T>C maps to ENST00000393205 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr2:135206336 C>T maps to NM_002410.3 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:74921059 A>G maps to NM_198955.1 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:74928733 C>A maps to NM_198955.1 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr17:74878254 C>A maps to NM_198955.1 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr7:88423874 G>A maps to NM_152706.2 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:43280158 C>T maps to NM_153361.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:43280467 C>T maps to NM_153361.2 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:43246105 C>T maps to NM_153361.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:43280710 G>A maps to NM_153361.2 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:43280576 G>T maps to NM_153361.2 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:43246020 C>T maps to NM_153361.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:43280117 G>T maps to NM_153361.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr5:43280633 C>A maps to NM_153361.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:43246059 G>T maps to NM_153361.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:43280518 T>C maps to NM_153361.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:43280398 C>T maps to NM_153361.2 H293H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr7:22532993 G>A maps to ENST00000441815 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr10:103563618 G>A maps to NM_012215.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:103558937 C>T maps to NM_012215.3 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr10:103546266 C>A maps to NM_012215.3 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:103558651 G>A maps to NM_012215.3 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr3:127429436 G>C maps to NM_007283.5 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:127441392 G>A maps to NM_007283.5 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:15035138 G>A maps to NM_001190839.1 Y107Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:4733848 C>T maps to NM_015246.2 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr16:4718285 T>C maps to NM_015246.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:4702777 C>A maps to NM_015246.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:165624621 C>T maps to ENST00000367886 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:41282871 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:39717053 G>T maps to NM_054024.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:39717209 G>T maps to NM_054024.3 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:39717064 G>A maps to NM_054024.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:222801761 G>A maps to NM_198551.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:222805553 G>T maps to NM_198551.2 E1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:222838682 G>T maps to NM_198551.2 E1816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:222828061 G>T maps to NM_198551.2 E1512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:222838682 G>T maps to NM_198551.2 E1816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:222802488 G>T maps to NM_198551.2 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr1:222803381 G>A maps to NM_198551.2 Q940Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr18:19378062 C>T maps to NM_020774.2 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr18:19383881 T>C maps to NM_020774.2 C462C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr18:19429213 A>G maps to NM_020774.2 E817E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:19444494 C>T maps to NM_020774.2 C963C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr18:19429213 A>G maps to NM_020774.2 E817E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr18:19378064 A>G maps to NM_020774.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr18:19427017 G>A maps to NM_020774.2 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr18:19378062 C>T maps to NM_020774.2 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr18:19378062 C>T maps to NM_020774.2 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:1564899 G>A maps to NM_080875.2 A954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:1565022 C>T maps to NM_080875.2 C971C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:1559289 C>T maps to NM_080875.2 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:1558767 G>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:1563984 C>T maps to NM_080875.2 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:1563966 C>T maps to NM_080875.2 D804D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:109771201 G>A maps to NM_022765.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:109770005 G>A maps to NM_022765.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:109775021 G>A maps to NM_022765.3 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr6:109771705 G>A maps to NM_022765.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr6:109775291 G>T maps to NM_022765.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr6:109772808 C>T maps to NM_022765.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:12264315 G>A maps to NM_014632.2 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:12263786 C>T maps to NM_014632.2 H788H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr11:12247784 C>T maps to NM_014632.2 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:18347515 G>A maps to NM_001136004.1 C1042C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr22:18368739 G>A maps to NM_015241.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr22:18304841 C>T maps to NM_015241.2 S1134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:18314815 C>T maps to NM_015241.2 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:18314680 C>T maps to NM_015241.2 E998E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr22:18301133 G>A maps to NM_015241.2 H1431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:18383722 G>T maps to NM_015241.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr11:12379869 C>T maps to NM_032867.2 N644N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:12315194 G>T maps to NM_032867.2 G73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr22:38308428 C>T maps to NM_033386.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr22:38318138 C>T maps to NM_033386.2 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr22:38333779 A>G maps to NM_033386.2 E817E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:38315059 A>G maps to NM_033386.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:1481876 C>T maps to NM_182924.3 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:1484388 C>T maps to NM_182924.3 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr7:1477569 G>A maps to NM_182924.3 H786H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr23:10535191 C>G did not map to a codon.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr23:10534980 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:10422948 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:10437806 G>A did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:10417722 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:10491219 A>G did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:10463675 T>C did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:38664219 C>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:38664252 G>A did not map to a codon.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr23:107148849 C>A did not map to a codon.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr23:107160961 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:107170079 A>G did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:107084274 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:107097884 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:107170237 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:107084413 G>T did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:107084209 C>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:67391873 G>A maps to NM_001077700.2 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:67391831 G>T maps to NM_001077700.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:67450306 T>G maps to NM_001077700.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:67425378 G>T maps to NM_001077700.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:67391891 G>A maps to NM_001077700.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:325647 C>T maps to NM_017550.1 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr19:312206 G>A maps to NM_017550.1 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr5:56233407 G>A maps to ENST00000381226 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:56234735 C>A maps to ENST00000381226 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:12089126 T>C maps to NM_021933.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:12089315 C>T maps to NM_021933.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:97680435 G>A maps to NM_153182.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr3:97668724 A>G maps to NM_153182.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:4797527 T>C maps to NM_153827.4 P910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:89312067 C>T maps to NM_004897.4 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr22:50925837 C>T maps to NM_017584.5 R14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:24448989 C>A maps to NM_005932.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:24415491 G>A maps to NM_005932.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr14:37969284 G>T maps to NM_001195296.1 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr14:37838759 G>A maps to NM_001195296.1 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:5392743 C>T maps to NM_024039.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr3:70008522 A>G maps to ENST00000448226 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:69915452 T>C maps to NM_198177.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr3:70008540 C>T maps to ENST00000448226 H383H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr3:70014170 G>A maps to ENST00000448226 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr3:70008501 C>T maps to ENST00000448226 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:69988314 C>T maps to ENST00000448226 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr3:69986986 C>T maps to ENST00000448226 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr3:70008520 C>A maps to ENST00000448226 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:70014383 G>A maps to ENST00000448226 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr10:129899557 C>A maps to NM_002417.4 T3223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:129903620 C>T maps to NM_002417.4 R2161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr10:129906251 C>T maps to NM_002417.4 A1284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr10:129901496 C>T maps to NM_002417.4 T2869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:129906149 C>T maps to NM_002417.4 Q1318Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:129905804 C>T maps to NM_002417.4 A1433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr10:129905212 G>A maps to NM_002417.4 R1631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:129904778 C>T maps to NM_002417.4 T1775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:129910277 A>G maps to NM_002417.4 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:129914797 C>T maps to NM_002417.4 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:129903299 T>C maps to NM_002417.4 T2268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:129913348 A>G maps to NM_002417.4 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:129913657 A>G maps to NM_002417.4 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr10:129906941 C>T maps to NM_002417.4 T1054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr10:129913657 A>G maps to NM_002417.4 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr10:129913861 G>A maps to NM_002417.4 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr10:129913657 A>G maps to NM_002417.4 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr10:129913657 A>G maps to NM_002417.4 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr10:129903299 T>C maps to NM_002417.4 T2268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:10386113 G>A maps to NM_170784.1 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr20:10386092 C>T maps to NM_170784.1 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:40814581 G>A maps to NM_020831.3 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:40807639 G>A maps to NM_020831.3 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:40827436 C>T maps to NM_020831.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr16:14354944 C>T maps to NM_014048.3 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:14306212 T>C maps to NM_014048.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:14340859 C>T maps to NM_014048.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr16:14339511 T>C maps to NM_014048.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr16:14339512 T>A maps to NM_014048.3 L403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:14306226 G>A maps to NM_014048.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:131072013 T>C maps to NM_013255.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:131072000 T>C maps to NM_013255.4 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:131128439 A>G maps to NM_013255.4 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:47027227 G>T maps to NM_003684.4 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:47030718 G>T maps to NM_003684.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr19:2043517 G>A maps to NM_199054.2 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:2046282 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:140159572 C>A maps to NM_013446.3 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:140158887 A>T maps to NM_013446.3 Y230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:140154927 C>T maps to NM_013446.3 Q401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr7:140154430 G>A maps to NM_013446.3 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr3:12610427 C>T maps to NM_014160.3 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:23811282 G>A maps to NM_005664.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:23811186 G>A maps to NM_005664.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:23811186 G>A maps to NM_005664.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr15:23811141 C>A maps to NM_005664.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr15:23811090 C>A maps to NM_005664.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:23811309 C>T maps to NM_005664.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr17:56291735 G>A maps to NM_017777.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:28030432 G>A maps to NM_173576.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr10:27964187 A>T maps to NM_173576.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:50515323 G>A maps to NM_015166.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:50502483 C>T maps to NM_015166.3 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:121134167 A>G maps to NM_014730.2 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:121134167 A>G maps to NM_014730.2 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr12:121134117 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr12:121134137 T>C maps to NM_014730.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr3:158320711 C>T maps to NM_001195432.1 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:158320711 C>T maps to NM_001195432.1 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:158322929 C>G maps to NM_001195432.1 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:185623533 C>A maps to NM_024629.3 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr12:6858125 G>A maps to NM_005439.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:6859908 A>G maps to NM_005439.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr3:37055999 C>A maps to NM_000249.3 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:37053325 T>C maps to NM_000249.3 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr3:37042540 T>C maps to NM_000249.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr3:37092042 T>C maps to NM_000249.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr3:37067240 T>C maps to NM_000249.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:37042537 A>G maps to NM_000249.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:37089174 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-AY-6197-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:37061890 G>A maps to NM_000249.3 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:37038199 G>A maps to NM_000249.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr3:37092044 G>A maps to NM_000249.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr3:37056035 G>A did not map to a codon.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:37038154 A>G maps to NM_000249.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:37083821 G>A maps to NM_000249.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:37038199 G>A maps to NM_000249.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:37053590 G>A did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr3:37038154 A>G maps to NM_000249.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr3:37042540 T>C maps to NM_000249.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr3:37083823 T>C did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr3:37090069 G>A maps to NM_000249.3 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr3:37038154 A>G maps to NM_000249.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:37055999 C>A maps to NM_000249.3 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr3:37050324 C>T maps to NM_000249.3 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr3:37038107 A>G did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:37083821 G>A maps to NM_000249.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr3:37083821 G>A maps to NM_000249.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr3:37083821 G>A maps to NM_000249.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr14:75485654 G>A maps to NM_001040108.1 S1373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr14:75483835 A>G maps to NM_001040108.1 C1437C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:75514365 C>A maps to NM_001040108.1 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:74716631 C>A maps to NM_152649.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:74708894 G>A maps to NM_152649.2 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr16:74716631 C>A maps to NM_152649.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:74712829 T>C maps to NM_152649.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr16:74716631 C>A maps to NM_152649.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:118376881 G>A maps to NM_001197104.1 A3425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:118376815 G>A maps to NM_001197104.1 P3403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:118373177 C>T maps to NM_001197104.1 R2191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:118372553 C>T maps to NM_001197104.1 R2163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:118343016 G>A maps to NM_001197104.1 K381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:118352613 A>G maps to NM_001197104.1 E1273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:118369216 C>T maps to NM_001197104.1 R1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:118392074 C>T maps to NM_001197104.1 A3862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:118373665 C>A maps to NM_001197104.1 S2353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:118373659 C>T maps to NM_001197104.1 I2351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:118374604 A>G maps to NM_001197104.1 G2666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:118343235 G>A maps to NM_001197104.1 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:118368730 A>G maps to NM_001197104.1 E1915E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr11:118368706 T>C maps to NM_001197104.1 A1907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr11:118374634 T>C maps to NM_001197104.1 T2676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr11:118342932 A>G maps to NM_001197104.1 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:118342930 C>T maps to NM_001197104.1 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr11:118374634 T>C maps to NM_001197104.1 T2676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:118344457 C>T maps to NM_001197104.1 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr12:49425257 T>C maps to NM_003482.3 A4410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr12:49436527 A>G maps to NM_003482.3 L1926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr12:49434220 G>A maps to NM_003482.3 F2444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:49433710 C>T maps to NM_003482.3 S2614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:49435970 G>A maps to NM_003482.3 Q2004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:49445836 C>T maps to NM_003482.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:49448765 T>C maps to NM_003482.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr12:49416545 G>T maps to NM_003482.3 R5389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:49427266 G>A maps to NM_003482.3 Q3741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:49432270 G>T maps to NM_003482.3 T2956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:49433599 T>C maps to NM_003482.3 G2651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:49445872 T>C maps to NM_003482.3 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:49432624 T>A maps to NM_003482.3 P2838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:49433710 C>A maps to NM_003482.3 S2614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr12:49434973 C>T maps to NM_003482.3 P2193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:49431286 G>T maps to NM_003482.3 S3284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:49431436 G>A maps to NM_003482.3 D3234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:49438282 G>A maps to NM_003482.3 C1662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr12:49418643 G>A maps to NM_003482.3 G5290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr12:49443596 C>G maps to NM_003482.3 R1258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr12:49440151 G>A maps to NM_003482.3 Q1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:49426352 C>T maps to NM_003482.3 Q4045Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:49420325 G>A maps to NM_003482.3 P5141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:49438548 G>A maps to NM_003482.3 T1647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:49432772 C>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:151873534 G>A maps to ENST00000355193 N3001N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr7:151836803 G>A maps to ENST00000355193 R4863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:151879228 G>T maps to ENST00000355193 R1906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:151896507 T>A maps to ENST00000355193 R1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:151949111 C>T maps to ENST00000355193 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr7:151859336 T>C maps to ENST00000355193 E3775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr7:151904486 T>A maps to ENST00000355193 K1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr7:151884822 T>C maps to ENST00000355193 A1590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:151917680 G>A maps to ENST00000355193 S1213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:151879604 C>T maps to ENST00000355193 Q1780Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:151879427 C>T maps to ENST00000355193 T1839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:151962265 G>A maps to ENST00000355193 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:151891205 G>A maps to ENST00000355193 G1516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:152055684 C>T maps to ENST00000355193 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:151846090 G>A maps to ENST00000355193 I4364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:151846090 G>A maps to ENST00000355193 I4364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr7:152027815 C>A maps to ENST00000355193 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:151874770 T>C maps to ENST00000355193 R2589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:151878104 T>C maps to ENST00000355193 G2280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:151962265 G>A maps to ENST00000355193 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr7:151962208 A>G maps to ENST00000355193 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:151945336 C>A maps to ENST00000355193 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:152009029 C>A maps to ENST00000355193 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr7:151878641 T>C maps to ENST00000355193 P2101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr7:151962208 A>G maps to ENST00000355193 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr7:151891204 C>A maps to ENST00000355193 G1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:151859996 A>G maps to ENST00000355193 P3555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:152012244 G>A maps to ENST00000355193 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr7:151851175 C>T maps to ENST00000355193 A4122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr7:151859567 C>T maps to ENST00000355193 T3698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:151860620 A>G maps to ENST00000355193 N3347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr7:152027786 T>C maps to ENST00000355193 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr7:151962265 G>A maps to ENST00000355193 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr7:151891204 C>A maps to ENST00000355193 G1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr7:151859336 T>C maps to ENST00000355193 E3775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:36220996 C>T maps to NM_014727.1 Q1683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:36229430 C>G maps to NM_014727.1 A2707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:36218612 G>A maps to NM_014727.1 G1439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr19:36220120 G>A maps to NM_014727.1 W1614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:36210432 A>G maps to NM_014727.1 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:36210687 C>T maps to NM_014727.1 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:36213367 G>A maps to NM_014727.1 R855R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:36218438 C>T maps to NM_014727.1 S1406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:36217195 C>T maps to NM_014727.1 D1315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr19:36222960 C>T maps to NM_014727.1 R1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:36218127 C>T maps to NM_014727.1 Q1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:104752462 C>T maps to NM_182931.2 H1420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr7:104752614 C>A maps to NM_182931.2 S1471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:104749676 T>C did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:104702671 T>C maps to NM_182931.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr7:104748222 C>T maps to NM_182931.2 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:104747107 G>A maps to NM_182931.2 T912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:104753707 A>C maps to NM_182931.2 G1835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr7:104752615 A>G maps to NM_182931.2 S1471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:6262286 C>T maps to NM_005934.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr19:6230613 C>T maps to NM_005934.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:21959472 C>A maps to NM_004641.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:21962634 G>T maps to NM_004641.3 G470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:20448234 A>G maps to NM_004529.2 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr9:20363526 G>A maps to NM_004529.2 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:20413790 C>T maps to NM_004529.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:20413784 C>T maps to NM_004529.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr9:20414309 A>G maps to NM_004529.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:20414327 G>A maps to NM_004529.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:20414303 G>A maps to NM_004529.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:168298979 C>T maps to ENST00000400822 Y470Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:168352446 C>T maps to ENST00000400822 P1463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:168352152 G>A maps to ENST00000400822 P1365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:168294540 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:168273001 G>T maps to ENST00000400822 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:168352855 C>T maps to ENST00000400822 R1600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr17:36874204 A>G maps to NM_005937.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:36872707 C>T maps to NM_005937.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:36874165 C>T maps to NM_005937.3 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr17:36865797 C>T maps to NM_005937.3 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:36874204 A>G maps to NM_005937.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:36874204 A>G maps to NM_005937.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:36872019 C>A maps to NM_005937.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr17:36874204 A>G maps to NM_005937.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:36874204 A>G maps to NM_005937.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr17:36874204 A>G maps to NM_005937.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:33768829 C>T maps to NM_002418.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr13:49796455 T>C maps to NM_001507.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:238436065 C>T maps to NM_024101.5 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:238455286 A>G maps to NM_024101.5 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:238428569 C>T maps to NM_024101.5 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:238461076 C>T maps to NM_024101.5 F591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:2257074 C>T maps to NM_022372.4 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:2256582 G>A maps to NM_022372.4 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:40721585 G>A maps to NM_170607.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr12:122611847 G>A maps to NM_014938.3 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr12:122620112 C>T maps to NM_014938.3 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:122619867 C>A maps to NM_014938.3 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr12:122614612 A>C maps to NM_014938.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:122618268 T>G maps to NM_014938.3 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:73038600 G>T maps to NM_032951.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:146560392 C>T maps to NM_172250.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr4:146560419 G>A maps to NM_172250.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:146575223 C>T maps to NM_172250.2 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr4:146575150 C>A maps to NM_172250.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:146563620 T>G maps to NM_172250.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:146575165 C>T maps to NM_172250.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:45973110 G>A maps to NM_015506.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr2:150436109 A>G maps to NM_015702.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr2:150426562 G>C maps to NM_015702.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:150436156 G>A maps to NM_015702.2 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr7:4949577 G>T maps to NM_001100600.1 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:4955700 T>C maps to NM_001100600.1 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr7:4947152 G>A maps to NM_001100600.1 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:154802116 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:154834775 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:154864955 C>T maps to NM_007289.2 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr3:154832894 T>C maps to NM_007289.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr3:154832897 C>T maps to NM_007289.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:2522494 G>A maps to NM_033467.3 F758F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:2540787 G>A maps to NM_033467.3 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:135047189 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:135055809 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:102663438 C>T maps to NM_002421.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:102668817 G>A maps to NM_002421.3 H2H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:102650064 T>C maps to NM_002425.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr11:102650064 T>C maps to NM_002425.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr22:24125718 C>T maps to NM_005940.3 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr22:24121513 C>T maps to NM_005940.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:102742636 G>A maps to ENST00000326227 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:102737048 T>A maps to ENST00000326227 K348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:102825295 G>A maps to NM_002427.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:102822867 G>A maps to NM_002427.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:102825295 G>A maps to NM_002427.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:102818622 C>T maps to NM_002427.3 W403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:23311891 C>T maps to NM_004995.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr14:23312610 C>T maps to NM_004995.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:58078950 C>T maps to NM_002428.2 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:58076250 C>T maps to NM_002428.2 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:89086955 G>A maps to NM_005941.4 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:89131039 A>G maps to NM_005941.4 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:89068423 G>T maps to NM_005941.4 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:89053709 G>T maps to NM_005941.4 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:89053945 T>G maps to NM_005941.4 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:89198759 G>A maps to NM_005941.4 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr8:89128915 T>C maps to NM_005941.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr8:89198827 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr8:89053811 A>G maps to NM_005941.4 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:132326241 C>T maps to NM_016155.4 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:132325231 G>A maps to NM_016155.4 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:132325198 C>T maps to NM_016155.4 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr12:132335650 A>G maps to NM_016155.4 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:56233349 T>C maps to NM_002429.4 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:56231633 G>A maps to NM_002429.4 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:56230984 C>T maps to NM_002429.4 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:55519286 G>A maps to NM_004530.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr16:55517981 T>C maps to NM_004530.4 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:55518014 A>G maps to NM_004530.4 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr16:55539302 T>C maps to NM_004530.4 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:55513486 G>A maps to NM_004530.4 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:55519307 C>T maps to NM_004530.4 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr16:55530858 G>T maps to NM_004530.4 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:55530930 G>T maps to NM_004530.4 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr16:55539302 T>C maps to NM_004530.4 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:102479782 C>A maps to NM_004771.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:102480738 G>A maps to NM_004771.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr11:102465370 G>A maps to NM_004771.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:127455251 A>G maps to NM_147191.1 H563H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr10:127460874 C>A maps to NM_147191.1 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:33834788 C>T maps to NM_006690.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:33851678 G>A maps to NM_006690.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr16:3100088 G>T maps to NM_022468.4 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr16:3100374 C>A maps to NM_022468.4 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:5011092 T>G maps to NM_021801.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:102567145 G>A maps to NM_022122.2 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:102573487 T>C maps to NM_022122.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr11:102573487 T>C maps to NM_022122.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:102573776 C>T maps to NM_022122.2 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:102564710 C>A maps to NM_022122.2 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:34093568 G>A maps to NM_024302.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:34106075 C>T maps to NM_024302.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:34093821 G>A maps to NM_024302.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr17:34105994 C>T maps to NM_024302.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:102714244 G>A maps to NM_002422.3 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:102709279 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:102711280 G>A maps to NM_002422.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr11:102709883 G>T maps to NM_002422.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:102398387 A>G maps to NM_002423.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:102398359 G>A maps to NM_002423.3 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:102587058 A>G maps to NM_002424.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:102593329 G>A maps to NM_002424.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:102593304 G>A maps to NM_002424.2 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr11:102587058 A>G maps to NM_002424.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:102587061 G>A maps to NM_002424.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr20:44639627 C>T maps to NM_004994.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:44641993 C>A maps to NM_004994.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr4:90856192 T>C maps to NM_007351.2 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:90856340 G>T maps to NM_007351.2 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:90856465 C>T maps to NM_007351.2 Y545Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:90856381 T>C maps to NM_007351.2 H517H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:90856186 T>G maps to NM_007351.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr4:90857545 G>A maps to NM_007351.2 A905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:90857446 G>A maps to NM_007351.2 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr4:90856090 C>T maps to NM_007351.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr4:90830531 A>G maps to NM_007351.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr4:90874313 A>G maps to NM_007351.2 V1144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr10:88705346 T>A maps to NM_024756.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:88703124 G>A maps to NM_024756.2 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:88705160 G>A maps to NM_024756.2 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:88704133 C>T maps to NM_024756.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:99236706 T>C maps to ENST00000422291 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr22:28192811 G>A maps to NM_002430.2 D1240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:28146920 G>A maps to NM_002430.2 F1315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr22:28193096 C>T maps to NM_002430.2 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:61275147 T>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:154279642 G>T maps to NM_032117.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:154318376 C>T maps to NM_032117.2 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:158815444 A>G maps to NM_002432.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:158815561 C>T maps to NM_002432.1 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:158812141 G>T maps to NM_002432.1 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr15:56736871 C>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr15:56748623 G>A maps to NM_018365.2 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:56735674 C>A maps to NM_018365.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr15:56726334 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:2298368 C>T maps to NM_020310.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:2290938 A>G maps to NM_020310.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:2290368 C>T maps to NM_020310.2 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:2290369 G>T maps to NM_020310.2 S525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:2298446 G>A maps to NM_020310.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:156798450 G>A maps to NM_005515.3 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr14:93649801 C>T maps to NM_022151.4 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:1501639 C>T maps to NM_001172223.1 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:71824641 T>C maps to ENST00000396051 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:74386316 A>C maps to NM_018221.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:27359142 G>A maps to NM_024761.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr9:27455338 C>A maps to NM_024761.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr9:27455338 C>A maps to NM_024761.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:198400288 T>C maps to NM_015387.3 N53N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:39543706 C>T maps to ENST00000311042 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr3:39543700 T>A maps to ENST00000311042 C47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr18:33780038 G>A maps to NM_017947.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:33775271 C>T maps to NM_017947.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:39880019 A>G maps to ENST00000425303 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:39881118 C>T maps to ENST00000425303 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:52397999 G>A maps to NM_004531.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:52397990 A>G maps to NM_004531.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:49575972 G>C maps to NM_014484.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:29638161 C>A maps to NM_002433.4 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:29638496 A>G maps to NM_002433.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr6:29638161 C>A maps to NM_002433.4 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr6:29638161 C>A maps to NM_002433.4 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr6:29638161 C>A maps to NM_002433.4 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr2:223554147 G>A maps to NM_058165.2 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr11:75439154 C>T maps to NM_025098.2 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr11:75442240 C>T maps to NM_025098.2 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:75440014 C>T maps to NM_025098.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr2:74688662 C>T maps to NM_006302.2 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:74692098 C>A maps to NM_006302.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:74688677 A>G maps to NM_006302.2 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:49948231 C>T maps to NM_032355.3 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:49948980 G>A maps to NM_032355.3 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:49946703 G>A maps to NM_032355.3 N600N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:49947568 G>A maps to NM_032355.3 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:77232018 C>T maps to NM_014940.2 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:62949800 C>T maps to ENST00000393630 R1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:62972281 C>T maps to ENST00000393630 V1525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:62954439 A>G maps to ENST00000393630 V1194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:62918893 G>A maps to ENST00000393630 Q380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:62949800 C>T maps to ENST00000393630 R1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:62892770 C>T maps to ENST00000393630 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:62931428 G>A maps to ENST00000393630 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:62940739 C>T maps to ENST00000393630 R882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:62902205 C>T maps to ENST00000393630 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:108776287 G>A maps to NM_014429.3 N359N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:108723720 A>G maps to NM_014429.3 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr3:108698423 C>T maps to NM_014429.3 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:108788594 C>T maps to NM_014429.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr3:108698498 C>T maps to NM_014429.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:108819277 G>A maps to NM_014429.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:31335683 G>A maps to ENST00000397641 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:31335683 G>A maps to ENST00000397641 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:31337447 T>G maps to ENST00000397641 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:106185854 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:106201598 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:106184785 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:106186339 G>A did not map to a codon.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr23:106205287 T>C did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:106186274 T>C did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:106224217 C>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:106242956 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:106224213 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:174537512 G>A maps to NM_006792.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:174537329 G>A maps to NM_006792.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr15:79165391 C>T maps to NM_206839.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:102931128 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr23:102931341 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:102931451 C>T did not map to a codon.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr23:102931700 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:2316482 G>A maps to NM_024848.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr1:2268236 G>A maps to NM_024848.1 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:2268230 G>A maps to NM_024848.1 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:122107284 G>A maps to NM_173855.4 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:122090687 C>A maps to NM_173855.4 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:124929178 C>T maps to NM_198469.2 N60N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:124936829 C>T maps to NM_198469.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr9:124929124 C>T maps to NM_198469.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:57025551 G>A maps to NM_005372.1 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:57026172 G>A maps to NM_005372.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:57025881 G>A maps to NM_005372.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr8:57026160 C>T maps to NM_005372.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:57025881 G>A maps to NM_005372.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:57025881 G>A maps to NM_005372.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:220971259 G>A maps to NM_022746.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:134023213 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:134031040 C>T did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:134033373 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:134033160 A>G did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:14891815 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:14918717 A>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:14929501 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:14937799 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:14936876 T>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:100212640 C>T maps to NM_023948.4 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:100210605 G>A maps to NM_023948.4 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:100212598 G>A maps to NM_023948.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:113235388 G>A maps to NM_020963.3 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:113242339 C>T maps to NM_020963.3 R873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:113235434 C>T maps to NM_020963.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:113236717 C>T maps to NM_020963.3 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr1:113236719 G>A maps to NM_020963.3 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:113239121 C>T maps to NM_020963.3 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:113238837 C>A maps to NM_020963.3 Y616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:50589174 A>G maps to NM_018995.2 A913A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:50537978 C>T maps to NM_018995.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr22:50591565 G>A maps to NM_018995.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr22:50547177 A>C maps to NM_018995.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:50599251 C>T maps to NM_018995.2 R1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr22:50553669 C>T maps to NM_018995.2 D418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr22:50552082 C>T maps to NM_018995.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:50580544 A>G maps to NM_018995.2 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr22:50537978 C>T maps to NM_018995.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr22:50555693 G>A maps to NM_018995.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:50581574 C>T maps to NM_018995.2 C761C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:132695874 A>G maps to NM_015529.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:132694079 A>G maps to NM_015529.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr6:132722370 C>T maps to NM_015529.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:13162712 A>G maps to ENST00000319217 D1112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr9:13219686 T>C maps to ENST00000319217 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:13113021 G>A maps to ENST00000319217 V1863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:13158036 G>A maps to ENST00000319217 S1144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:13113029 T>G maps to ENST00000319217 R1861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:13138000 A>C maps to ENST00000319217 A1385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr9:13224465 C>A maps to ENST00000319217 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:13188863 G>A maps to ENST00000319217 N761N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:13183487 A>G maps to ENST00000319217 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr9:13193255 C>T maps to ENST00000319217 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:13107074 G>A maps to ENST00000319217 G2034G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr9:13186266 A>G did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:58980299 C>T maps to NM_001039396.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:71376507 A>C maps to NM_005791.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:71360657 T>C maps to NM_005791.2 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:71360378 A>G maps to NM_005791.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:71377103 A>T maps to NM_005791.2 K669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:71376477 A>G maps to NM_005791.2 K597K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:82185046 T>C maps to NM_005792.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:82182421 T>G maps to NM_005792.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr13:20244397 C>T maps to ENST00000414242 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:123694600 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:123679028 A>G maps to NM_022782.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:43805050 C>T maps to NM_005373.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:43814979 C>T maps to NM_005373.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:43805161 T>C maps to NM_005373.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:4359932 G>A maps to ENST00000262967 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:4354114 C>T maps to ENST00000262967 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:56349188 C>T maps to ENST00000340482 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:56357220 G>A maps to ENST00000340482 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:56356741 C>T maps to ENST00000340482 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:154014610 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:154007498 G>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:154010016 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:154014598 A>C did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:154009555 C>T did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:154020121 C>T did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:154020121 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:41959855 G>A maps to NM_005374.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:41958515 G>A maps to NM_005374.3 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:41955243 G>A maps to NM_005374.3 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:41886433 G>A maps to ENST00000398393 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:202512532 G>A maps to NM_033066.2 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:67779398 T>C maps to NM_022474.2 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:24681354 T>C maps to ENST00000409253 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:24690172 C>T maps to ENST00000409253 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:24690297 A>G maps to ENST00000409253 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:28408645 T>C did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr10:28408645 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr10:28408643 C>T maps to NM_173496.3 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr18:11886524 G>A maps to ENST00000344987 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:43831103 G>A maps to NM_001044370.1 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:43870766 G>A maps to NM_001044370.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:43821074 C>T maps to NM_001044370.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr22:43831124 C>T maps to NM_001044370.1 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:43901441 C>A maps to NM_001044370.1 Y309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:30601839 C>T maps to NM_001584.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:30557685 C>T maps to NM_001584.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr11:30435826 C>T maps to NM_001584.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr11:30433113 G>A maps to NM_001584.2 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:17030119 T>C maps to NM_015134.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr17:17083922 C>T maps to NM_201274.2 S1016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:17046907 C>T maps to NM_015134.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:17057705 G>A maps to NM_015134.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:17080619 G>A maps to NM_015134.2 A951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:17078650 G>A maps to NM_015134.2 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:15489930 C>T maps to NM_001128423.1 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:161276675 G>A maps to ENST00000360451 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:161276705 G>A maps to ENST00000360451 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr11:118133201 A>G maps to NM_144765.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:118111081 G>A maps to NM_198275.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:181021614 C>T maps to NM_001531.2 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:181022718 T>G maps to NM_001531.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr10:17865236 G>T maps to NM_002438.2 G76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:60743590 C>T maps to NM_006039.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:60744868 C>T maps to NM_006039.3 N364N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:60766268 C>T maps to NM_006039.3 D1094D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:60753788 C>T maps to NM_006039.3 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:60755962 C>T maps to NM_006039.3 Y717Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr17:60742278 C>T maps to NM_006039.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:94189483 G>T maps to NM_005591.3 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:94204876 G>A maps to NM_005591.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:94200976 A>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:94204873 G>A maps to NM_005591.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:6711317 C>T maps to NM_203462.2 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr11:3249981 G>A maps to ENST00000328215 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:68773516 G>A maps to NM_145015.4 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr11:68772955 G>A maps to NM_145015.4 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:18956300 C>A maps to NM_147199.3 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr11:18955440 G>A maps to NM_147199.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:18159393 C>T maps to NM_054031.3 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:18159570 C>T maps to NM_054031.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:18159291 C>T maps to NM_054031.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr11:18158958 G>A maps to NM_054031.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:13879215 C>T maps to NM_032285.2 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:13879818 C>T maps to NM_001031727.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:48331523 G>A maps to NM_001127176.1 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:48333091 G>T maps to NM_001127176.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr18:48333091 G>T maps to NM_001127176.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:78804605 G>A maps to NM_020236.3 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:45904066 A>G maps to NM_145255.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:66204699 A>G maps to NM_016050.3 H116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr8:121432150 G>A maps to NM_014078.5 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:44081705 G>A maps to NM_032111.2 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr6:44081840 A>G maps to NM_032111.2 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr6:44081902 G>A maps to NM_032111.2 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr6:44081840 A>G maps to NM_032111.2 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:59573999 G>A maps to NM_017840.3 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr11:59573999 G>A maps to NM_017840.3 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:59574125 G>A maps to NM_017840.3 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:59573980 G>A maps to NM_017840.3 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr11:59573999 G>A maps to NM_017840.3 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:59573969 T>C maps to NM_017840.3 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:6703634 T>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:160218322 C>T maps to NM_014161.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:75879784 T>C did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr6:43022179 A>T maps to NM_015950.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:43024169 C>T maps to NM_015950.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:154346363 C>A maps to NM_014180.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:48445497 A>G maps to NM_016504.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:419103 G>T maps to NM_006428.4 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr16:419153 G>A maps to NM_006428.4 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:131219300 A>G maps to ENST00000425847 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:131186979 G>T maps to ENST00000425847 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:131208879 C>T maps to ENST00000425847 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:131217091 C>A maps to ENST00000425847 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:42971990 G>A maps to NM_031903.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:42977102 G>A maps to NM_031903.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr19:17417127 G>A maps to NM_023937.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:86434314 C>T maps to NM_016622.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:54681869 A>G maps to NM_016491.3 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:54666224 C>T maps to NM_016491.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:54670965 A>G did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:73897918 G>A maps to NM_032478.3 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr21:26978812 A>G maps to NM_080794.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr19:10369174 G>C maps to NM_146387.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:140446781 G>A maps to NM_032477.2 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:93881316 T>C maps to NM_172177.2 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr12:93873235 T>C maps to NM_172177.2 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr12:93881355 A>G maps to NM_172177.2 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:36478049 A>G maps to NM_032351.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr15:89010599 C>T maps to NM_022163.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:89008971 G>A maps to NM_022163.3 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr3:179316464 T>A maps to NM_020409.2 K134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:73536801 C>T maps to NM_016055.5 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:6601441 G>A maps to NM_016497.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr1:228295955 C>T maps to NM_181462.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:228294607 A>G maps to NM_181462.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:42181907 G>A maps to NM_018141.3 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:174983882 G>T maps to NM_022100.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:36921819 G>A maps to NM_031280.3 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:36921511 A>G maps to NM_031280.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:75010657 A>T maps to NM_016065.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr10:75011557 G>A maps to NM_016065.3 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr7:56020920 A>G maps to ENST00000426595 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr6:30590649 T>C maps to NM_014046.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr6:30590649 T>C maps to NM_014046.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:139062963 G>A maps to NM_020191.2 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr3:139069895 T>C maps to NM_020191.2 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr3:139065783 C>A maps to NM_020191.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:55918608 T>C maps to NM_016070.3 S76S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A6-5661-01A-01D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:15100903 C>T maps to NM_022497.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:71522027 T>C maps to ENST00000431255 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:44809447 G>A maps to NM_016640.3 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:44809333 G>A maps to NM_016640.3 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:140710259 G>A maps to NM_053035.2 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:27877079 A>G maps to NM_021821.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:95753104 C>T maps to NM_031902.3 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:95774085 A>G maps to NM_031902.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:95766249 C>T maps to NM_031902.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:73258674 G>T maps to NM_015971.3 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:105705440 G>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr9:125033217 C>A maps to NM_138777.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:19584371 C>T maps to NM_016183.3 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr11:10615704 G>T maps to NM_001098579.1 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:10597935 G>T maps to NM_001098579.1 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:10647679 C>A maps to NM_001098579.1 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr11:10647905 G>C maps to NM_001098579.1 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr11:10622525 C>T maps to NM_001098579.1 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:60233496 T>A maps to NM_152866.2 L147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr11:60235859 A>G maps to NM_152866.2 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:60235877 G>A maps to NM_152866.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr11:60229852 A>G maps to NM_152866.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:60229852 A>G maps to NM_152866.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:60557837 C>T maps to NM_206893.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:60559754 C>A maps to NM_206893.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:60565967 C>T maps to NM_206893.3 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:60274226 G>A maps to NM_017716.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:60264814 C>T maps to NM_017716.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:60170494 C>A maps to NM_032597.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:60183787 C>T maps to NM_032597.3 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:60184291 G>A maps to NM_032597.3 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:60531413 G>T maps to NM_001098835.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:60531415 G>A maps to NM_001098835.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:60198331 T>C maps to NM_023945.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr11:60201281 A>C maps to NM_023945.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:60201266 T>A maps to NM_023945.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:59947309 G>A maps to NM_152852.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:59949074 G>A maps to NM_152852.1 H42H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:60160213 C>T maps to NM_206939.1 Y201Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:60156996 A>G maps to NM_206939.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:60482507 G>A maps to NM_031457.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr11:60468359 G>T maps to NM_031457.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:60482507 G>A maps to NM_031457.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:72755975 C>T maps to NM_005098.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:72756050 G>A maps to NM_005098.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr8:72756314 G>A maps to NM_005098.3 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:72755906 C>T maps to NM_005098.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:72754916 T>C maps to NM_005098.3 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:72756398 C>T maps to NM_005098.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:17998105 C>T maps to NM_001105569.1 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:17998105 C>T maps to NM_001105569.1 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:17998174 C>T maps to NM_001105569.1 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:17997994 G>A maps to NM_001105569.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr2:17998345 G>A maps to NM_001105569.1 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:17998237 G>A maps to NM_001105569.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:47698202 T>C did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:47643475 C>A maps to NM_000251.1 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:47637471 C>A maps to NM_000251.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:47702308 A>G maps to NM_000251.1 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:47643532 G>A maps to NM_000251.1 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:47698179 G>T maps to NM_000251.1 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:47707841 T>C maps to NM_000251.1 C822C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:47656895 A>G maps to NM_000251.1 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:47637471 C>A maps to NM_000251.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:47637471 C>A maps to NM_000251.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:47703560 C>T maps to NM_000251.1 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:47698179 G>T maps to NM_000251.1 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr2:47639566 A>G maps to NM_000251.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:47690270 A>G maps to NM_000251.1 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:47703632 A>G maps to NM_000251.1 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:47707955 G>A maps to NM_000251.1 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:47639683 A>G maps to NM_000251.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:47703560 C>T maps to NM_000251.1 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:47703630 C>A maps to NM_000251.1 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr2:47639566 A>G maps to NM_000251.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:47709946 G>A maps to NM_000251.1 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:47703630 C>T maps to NM_000251.1 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:47657019 C>A maps to NM_000251.1 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr2:47630536 G>A maps to NM_000251.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr2:47637471 C>A maps to NM_000251.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr2:47707841 T>C maps to NM_000251.1 C822C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:47703630 C>T maps to NM_000251.1 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:47657019 C>A maps to NM_000251.1 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr2:47639683 A>G maps to NM_000251.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:47657019 C>A maps to NM_000251.1 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:47690183 A>G maps to NM_000251.1 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:47657019 C>A maps to NM_000251.1 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:79968145 T>C maps to NM_002439.3 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:80057475 C>T maps to NM_002439.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr1:76378571 A>T maps to NM_002440.2 *937Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:76349321 T>G maps to NM_002440.2 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:76262813 C>T maps to NM_002440.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:76342619 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:31729319 C>A maps to ENST00000375742 I720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:31728553 C>T maps to ENST00000375742 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:48026312 T>C maps to NM_000179.2 Y397Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:48026573 A>G maps to NM_000179.2 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:48033779 C>T maps to NM_000179.2 R1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:48027965 A>G maps to NM_000179.2 E948E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:48026579 T>G maps to NM_000179.2 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:48027957 G>T maps to NM_000179.2 E946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:48030772 T>C maps to NM_000179.2 C1129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr2:48018227 C>T maps to NM_000179.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:48027957 G>T maps to NM_000179.2 E946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:48033752 G>T maps to NM_000179.2 E1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:48025814 A>G maps to NM_000179.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:48030685 G>A maps to NM_000179.2 T1100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr2:48027431 T>C maps to NM_000179.2 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr2:48026543 G>A maps to NM_000179.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:48026648 G>A maps to NM_000179.2 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr2:48030631 G>A maps to NM_000179.2 P1082P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr2:48032119 T>C maps to NM_000179.2 I1170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:48026576 G>A maps to NM_000179.2 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr2:48032086 C>T maps to NM_000179.2 Y1159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr2:48026990 C>A maps to NM_000179.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr2:48026990 C>T maps to NM_000179.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr2:48028193 G>A maps to NM_000179.2 R1024R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:120795684 C>T maps to NM_002442.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:55693380 A>G maps to NM_138962.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr3:135870638 G>A maps to NM_018133.3 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:135870849 C>T maps to NM_018133.3 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:135870890 C>A maps to NM_018133.3 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:11782015 A>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:11780324 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:11790782 G>T did not map to a codon.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr23:11793181 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:11783732 G>A did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr23:11778981 G>A did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:11781905 C>A did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:11781906 T>G did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:11783734 G>A did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:11783731 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:11776437 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:824437 A>G maps to NM_001025190.1 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:824957 G>A maps to NM_001025190.1 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr16:830430 A>G maps to NM_001025190.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:830331 G>A maps to NM_001025190.1 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:823209 G>A maps to NM_001025190.1 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr16:830430 A>G maps to NM_001025190.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:830460 A>C maps to NM_001025190.1 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr16:830625 C>T maps to NM_001025190.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr16:830601 C>T maps to NM_001025190.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr23:64958438 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:64955210 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:64956697 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:64949370 T>C did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:64955133 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr23:64949376 C>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:64951036 A>G did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:64949461 C>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:64958388 C>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:16026013 C>A maps to ENST00000445506 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr8:16026092 T>A maps to ENST00000445506 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:16026257 G>T maps to ENST00000445506 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr8:16001118 T>G maps to ENST00000445506 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:16026262 C>A maps to ENST00000445506 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:65672637 G>A maps to NM_198080.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:65672613 C>T maps to NM_198080.3 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:49722250 C>T maps to NM_020998.3 E563E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:49725253 G>T maps to NM_020998.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:49936644 G>A maps to NM_002447.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:49932678 A>G maps to NM_002447.2 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:49933626 C>T did not map to a codon.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr23:131205096 C>A did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:131188723 G>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:131207039 A>G did not map to a codon.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr23:131207039 A>C did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:131207039 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:131202296 T>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:131202274 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr23:131205096 C>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr2:190922145 A>G maps to NM_005259.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr2:190922145 A>G maps to NM_005259.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr2:190922145 A>G maps to NM_005259.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:155582979 C>T maps to NM_018116.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:155582058 G>A maps to NM_018116.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:4864488 G>A maps to NM_002448.3 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:174156372 G>A maps to NM_002449.4 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:56673218 C>T maps to NM_005946.2 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:56693003 C>T maps to ENST00000394501 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:56667675 C>T maps to NM_176870.2 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:105927235 C>T maps to NM_004689.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:105926763 C>T maps to NM_004689.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:62362965 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr11:62363335 C>T maps to NM_004739.2 W381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr11:62365833 C>A maps to NM_004739.2 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr11:62363579 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:42883418 T>C maps to ENST00000405094 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:42931390 T>C maps to ENST00000405094 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:21854769 C>A maps to NM_002451.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:21837922 C>T maps to NM_002451.3 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr8:121467705 T>G maps to NM_022045.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:121530952 G>T maps to NM_022045.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr8:121466096 G>T maps to NM_022045.3 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr8:121466098 A>G maps to NM_022045.3 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr8:121528344 A>G maps to NM_022045.3 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr8:121531005 T>C maps to NM_022045.3 C853C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:36936737 G>A maps to ENST00000373627 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:36946352 C>T maps to ENST00000373627 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:47652108 G>A maps to NM_014342.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:47652600 C>A maps to NM_014342.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:154293800 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:154293798 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:154292253 C>A did not map to a codon.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr23:154290228 G>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:98703261 T>C maps to NM_178812.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:98673341 C>T maps to NM_178812.3 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr8:98731335 C>T maps to NM_178812.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr8:98725893 C>G maps to NM_178812.3 S426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:91503609 G>T maps to NM_006980.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr8:97251898 C>T maps to NM_015942.3 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:97256268 G>A maps to NM_015942.3 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:97269237 G>A maps to NM_015942.3 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:97269237 G>A maps to NM_015942.3 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:97258105 G>A maps to NM_015942.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr8:97251799 T>C maps to NM_015942.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:97256269 A>G maps to NM_015942.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:242035469 C>T maps to NM_182501.3 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:242036798 G>A maps to NM_182501.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr2:242035427 G>A maps to NM_182501.3 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:242035628 A>G maps to NM_182501.3 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:38281059 G>A maps to NM_005955.2 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:93602421 T>C maps to NM_007358.3 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr1:93586104 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:65312547 C>T maps to NM_139242.3 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr15:65313911 C>A maps to NM_139242.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:65295575 G>A maps to NM_139242.3 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:66620201 G>T maps to NM_014637.3 G297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:66620171 C>T maps to NM_014637.3 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr8:66617138 G>A maps to NM_014637.3 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr10:135233088 G>A maps to NM_138384.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr10:135216217 C>T maps to NM_138384.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:64916195 C>T maps to NM_005956.3 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:64906863 G>T maps to NM_005956.3 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:151270258 G>A maps to NM_015440.3 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:151258062 G>A maps to NM_015440.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:151258062 G>A maps to NM_015440.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:151281424 C>T maps to NM_015440.3 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:151239761 G>A maps to NM_015440.3 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:151265683 C>T maps to NM_015440.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:74437139 T>C maps to NM_006636.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr4:75041091 C>T maps to NM_001144978.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr1:11854076 G>T maps to ENST00000376585 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:86580240 G>A maps to NM_001159377.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:55490955 T>G maps to NM_002453.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr2:55473507 T>C maps to NM_002453.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:55479742 T>C maps to NM_002453.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:55473528 A>G maps to NM_002453.2 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:55476539 G>A maps to NM_002453.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:28014363 A>C maps to NM_152912.4 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:28014414 G>A maps to NM_152912.4 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr11:68478346 G>A maps to NM_004923.3 H443H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:149807466 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr23:149826405 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:149787598 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:149814260 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:149828206 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:149787547 G>A did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr23:149809888 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:149818310 T>C did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:149924191 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:149899044 A>G did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:149931105 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:149905863 G>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:149901047 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:149898588 G>A did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:149901187 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:149924280 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:149899075 G>T did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:149901048 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:149931090 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:149899020 G>T did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:149905123 T>C did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr23:149924176 C>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:149901047 C>T did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:149901047 C>T did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:149912837 G>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:149912832 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:31251114 G>A maps to NM_017762.2 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:149906940 G>A maps to NM_001145862.1 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:149907506 G>T maps to NM_001145862.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:149903216 G>A maps to NM_001145862.1 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:149905326 G>A maps to NM_001145862.1 H319H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:149901544 G>C maps to NM_001145862.1 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr5:32242201 C>A maps to NM_001040446.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:32233962 G>T maps to NM_001040446.1 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:32239118 G>A maps to NM_001040446.1 N444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:32230401 T>A maps to NM_001040446.1 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:32248912 G>A maps to NM_001040446.1 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:32229918 G>A maps to NM_001040446.1 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:31217358 G>A maps to NM_014967.4 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:31222789 C>T maps to NM_014967.4 C944C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr11:95568510 G>T maps to NM_016156.5 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:95582864 C>T maps to NM_016156.5 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:95569470 A>G maps to NM_016156.5 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:95568590 C>A maps to NM_016156.5 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:95590774 C>A maps to NM_016156.5 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:30412560 C>T maps to NM_021090.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr22:30418070 C>T maps to NM_021090.3 C1093C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:30415930 C>T maps to NM_021090.3 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr22:30415771 C>T maps to NM_021090.3 H708H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr22:30416521 C>A maps to NM_021090.3 C958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:56572381 G>A maps to NM_004687.4 R1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:56570268 G>A maps to NM_004687.4 G1085G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:56569119 G>A maps to NM_004687.4 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr17:56573507 C>T maps to NM_004687.4 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:25835928 A>G maps to NM_004685.3 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr13:25825816 T>C maps to NM_004685.3 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr13:25826043 G>A maps to NM_004685.3 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:25825855 T>A maps to NM_004685.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:17157568 T>G maps to NM_004686.4 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:63615228 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:63574684 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:63488790 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:63569907 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:63555987 C>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:63574744 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:63574745 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:63574685 T>C did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:63574744 C>T did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:63576201 A>G did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:63574685 T>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:63574732 T>C did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:11172455 C>T maps to NM_015458.3 H332H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr8:11180158 C>A maps to NM_015458.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:11162469 C>T maps to NM_015458.3 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr8:11167105 C>T maps to NM_015458.3 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr8:11174255 A>G maps to NM_015458.3 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr4:187455385 G>A maps to NM_005958.3 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr4:187455586 A>G maps to NM_005958.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr11:92714700 C>T maps to NM_005959.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr11:92714937 C>A maps to NM_005959.3 Y183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:92715226 G>T maps to NM_005959.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:92715267 C>T maps to NM_005959.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:74207529 C>T maps to NM_001123226.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:74183286 A>G maps to NM_001123226.1 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:11319442 G>A maps to NM_004958.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:11194520 G>A maps to NM_004958.3 I1711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:11174455 G>A maps to NM_004958.3 L2407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:11293465 C>A maps to NM_004958.3 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:11300543 G>A maps to NM_004958.3 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:11184571 A>G maps to NM_004958.3 S2215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:11288778 C>T maps to NM_004958.3 Q992Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:11259382 T>C maps to NM_004958.3 K1395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:11319343 G>A maps to NM_004958.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr1:11259382 T>C maps to NM_004958.3 K1395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:11190717 G>A maps to NM_004958.3 N1827N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:30823312 G>A maps to ENST00000439838 W289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:30625758 A>G maps to ENST00000358107 D381D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:30602717 C>T maps to ENST00000358107 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:135614712 T>C maps to NM_145808.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:237044081 G>A maps to NM_000254.2 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:237052622 C>T maps to NM_000254.2 N998N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:153311146 C>T maps to NM_019041.5 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:7870967 G>T maps to NM_024010.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr8:125575040 C>T maps to NM_014751.4 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:125575100 G>T maps to NM_014751.4 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr8:125565658 G>A maps to NM_014751.4 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:125568559 C>A maps to NM_014751.4 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:100534203 C>T maps to ENST00000511045 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:100543834 C>T maps to ENST00000511045 Q866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:100528110 T>C maps to ENST00000511045 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:100529981 G>A maps to ENST00000511045 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr4:100543933 C>T maps to ENST00000511045 Q899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:100530060 G>T maps to ENST00000511045 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:100534164 C>A maps to ENST00000511045 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:100534267 G>T maps to ENST00000511045 G757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:100510831 A>G maps to ENST00000511045 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr4:100543935 A>G maps to ENST00000511045 Q899Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:100534287 T>C maps to ENST00000511045 D763D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr4:100543935 A>G maps to ENST00000511045 Q899Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:17573336 G>T maps to NM_001001924.2 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:17611975 C>T maps to NM_001001924.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:17612668 C>T maps to NM_001001924.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:17612658 C>A maps to NM_001001924.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:17612658 C>A maps to NM_001001924.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:17612272 A>G maps to NM_001001924.2 D348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr8:17611705 G>A maps to NM_001001924.2 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr13:29898825 A>G maps to NM_001033602.2 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:29600335 G>T maps to NM_001033602.2 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr13:29601036 G>A maps to NM_001033602.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr13:29600346 A>T maps to NM_001033602.2 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:30072637 C>T maps to NM_001033602.2 H1264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr13:29599905 C>T maps to NM_001033602.2 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:30062050 C>T maps to NM_001033602.2 T1148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:29599704 G>A maps to NM_001033602.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr13:30062122 C>T maps to NM_001033602.2 D1172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr13:29855976 G>A maps to NM_001033602.2 A937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:29933441 G>A maps to NM_001033602.2 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr13:29599896 G>A maps to NM_001033602.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:30014149 C>T maps to NM_001033602.2 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr13:29599395 C>T maps to NM_001033602.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:29599704 G>A maps to NM_001033602.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr13:29599861 T>C maps to NM_001033602.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr13:29600811 C>T maps to NM_001033602.2 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:29599602 C>A maps to NM_001033602.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr13:29599665 C>T maps to NM_001033602.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:30062050 C>T maps to NM_001033602.2 T1148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:177195385 G>A maps to NM_006554.4 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr2:177191625 C>T maps to NM_006554.4 A94A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-A010-01A-01W-A00E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:124646424 A>C maps to NM_033049.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:124646628 G>A maps to NM_033049.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:124627179 C>T maps to NM_033049.3 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:124635227 C>T maps to NM_033049.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:124627080 A>G maps to NM_033049.3 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr3:124631968 C>T maps to NM_033049.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:26584786 G>A maps to NM_001135091.1 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:26587348 C>T maps to NM_001135091.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr19:9073804 T>C maps to NM_024690.2 S4547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:9071467 A>G maps to NM_024690.2 T5326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr19:9049992 T>C maps to NM_024690.2 G10546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr19:9089507 A>G maps to NM_024690.2 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr19:9068746 A>C maps to NM_024690.2 P6233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:9089939 G>A maps to NM_024690.2 H625H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr19:9088844 A>C maps to NM_024690.2 T990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:9088588 C>A maps to NM_024690.2 E1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr19:9069778 A>C maps to NM_024690.2 T5889T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:9061420 T>C maps to NM_024690.2 P8675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:9063556 G>T maps to NM_024690.2 P7963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:9084476 A>G maps to NM_024690.2 T2446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr19:9047676 C>T maps to NM_024690.2 V11318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:9005697 G>A maps to NM_024690.2 D13236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr19:9058006 C>A maps to NM_024690.2 A9813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr19:9068377 A>T maps to NM_024690.2 I6356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr19:9077503 G>T maps to NM_024690.2 V3314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:9089903 G>A maps to NM_024690.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:9066841 C>T maps to NM_024690.2 L6868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:9067609 G>T maps to NM_024690.2 A6612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:9002612 G>A maps to NM_024690.2 P13401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:9088346 T>C maps to NM_024690.2 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr19:9049662 G>A maps to NM_024690.2 V10656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr19:9057574 G>A maps to NM_024690.2 T9957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:9061150 G>T maps to NM_024690.2 I8765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:9062106 C>A maps to NM_024690.2 E8447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:9062986 G>T maps to NM_024690.2 V8153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:9066496 G>T maps to NM_024690.2 V6983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr19:9089221 C>A maps to NM_024690.2 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr19:9091400 T>C maps to NM_024690.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr19:9046601 G>T maps to NM_024690.2 R11677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:9067147 C>T maps to NM_024690.2 S6766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:9086114 C>T maps to NM_024690.2 E1900E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:9038095 G>T maps to NM_024690.2 S12060S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:9047190 C>T maps to NM_024690.2 E11480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:9057841 C>T maps to NM_024690.2 P9868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:9059880 A>G maps to NM_024690.2 L9189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:9083659 C>A maps to NM_024690.2 E2719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:9087545 G>T maps to NM_024690.2 T1423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr19:9072478 A>G maps to NM_024690.2 F4989F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr19:9062791 G>A maps to NM_024690.2 D8218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr19:9059932 C>T maps to NM_024690.2 S9171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr19:8982157 G>A maps to NM_024690.2 N14039N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:9085799 G>T maps to NM_024690.2 V2005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:9091106 G>T maps to NM_024690.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr19:9087602 T>C maps to NM_024690.2 K1404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:9048528 A>G maps to NM_024690.2 V11034V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:9026264 G>A maps to NM_024690.2 L12241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:9075919 T>C maps to NM_024690.2 T3842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:8969275 C>T maps to NM_024690.2 A14356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:9064561 C>T maps to NM_024690.2 S7628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:9072886 C>T maps to NM_024690.2 E4853E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:9087896 C>T maps to NM_024690.2 E1306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:9090805 C>A maps to NM_024690.2 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr19:9087725 A>G maps to NM_024690.2 A1363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr19:9061042 G>A maps to NM_024690.2 T8801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:9054348 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:9067260 C>A maps to NM_024690.2 E6729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:9068980 G>A maps to NM_024690.2 I6155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:9077748 C>A maps to NM_024690.2 E3233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:9088129 A>G maps to NM_024690.2 L1229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:9090538 C>A maps to NM_024690.2 G426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:9090652 C>A maps to NM_024690.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr19:9083886 A>T maps to NM_024690.2 L2643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:9089507 A>G maps to NM_024690.2 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:9009334 C>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:9085733 G>T maps to NM_024690.2 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr19:8961960 G>A maps to NM_024690.2 C14472C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr19:9049152 C>T maps to NM_024690.2 T10826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:9073804 T>C maps to NM_024690.2 S4547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr19:9085169 T>C maps to NM_024690.2 T2215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr19:9070810 T>C maps to NM_024690.2 T5545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr19:9089507 A>G maps to NM_024690.2 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:9049647 T>G maps to NM_024690.2 T10661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr19:9066445 A>G maps to NM_024690.2 S7000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr19:9058870 G>T maps to NM_024690.2 T9525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr19:9018505 C>T maps to NM_024690.2 K12556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:9027222 G>A maps to NM_024690.2 S12221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr19:9047603 C>A maps to NM_024690.2 E11343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr19:9070909 G>T maps to NM_024690.2 P5512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:9076211 G>T maps to NM_024690.2 S3745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr19:8996453 G>T maps to NM_024690.2 I13706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr19:9074935 C>T maps to NM_024690.2 S4170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr19:9089507 A>G maps to NM_024690.2 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr19:9085169 T>C maps to NM_024690.2 T2215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:9089882 C>T maps to NM_024690.2 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:9073981 A>G maps to NM_024690.2 S4488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:9065668 T>C maps to NM_024690.2 S7259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:9066445 A>G maps to NM_024690.2 S7000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:9068725 C>T maps to NM_024690.2 L6240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:100685894 C>A maps to NM_001040105.1 S3733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr7:100684113 T>C maps to NM_001040105.1 S3139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:100681866 A>G maps to NM_001040105.1 S2390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr7:100677279 T>C maps to NM_001040105.1 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr7:100679649 T>C maps to NM_001040105.1 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:100679064 A>G maps to NM_001040105.1 P1456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:100685235 T>C maps to NM_001040105.1 G3513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:100683156 G>A maps to NM_001040105.1 T2820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:100681443 A>C maps to NM_001040105.1 T2249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:100676661 C>T maps to NM_001040105.1 D655D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr7:100696329 T>C maps to NM_001040105.1 S4389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:100701312 G>A maps to NM_001040105.1 T4490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:100693863 G>A maps to NM_001040105.1 E4274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:100675545 C>T maps to NM_001040105.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr7:100683308 T>G maps to NM_001040105.1 L2871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:100686648 T>C maps to NM_001040105.1 S3984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr7:100685238 A>G maps to NM_001040105.1 E3514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr7:100675089 T>C maps to NM_001040105.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:100675089 T>C maps to NM_001040105.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr7:100685235 T>C maps to NM_001040105.1 G3513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:100677555 A>G maps to NM_001040105.1 T953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr7:100686996 A>G maps to NM_001040105.1 T4100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:100679799 G>A maps to NM_001040105.1 P1701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr7:100680243 T>C maps to NM_001040105.1 P1849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr7:100678404 T>C maps to NM_001040105.1 A1236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr7:100679778 T>C maps to NM_001040105.1 S1694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr7:100686648 T>C maps to NM_001040105.1 S3984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr7:100686648 T>C maps to NM_001040105.1 S3984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr7:100675341 C>T maps to NM_001040105.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr7:100675089 T>C maps to NM_001040105.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:1090914 C>A maps to ENST00000441003 T1270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:1094686 G>A maps to ENST00000441003 T1925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:1098724 G>A maps to ENST00000441003 S2365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:1095704 G>A maps to ENST00000441003 T2072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr11:1094842 C>T maps to ENST00000441003 N1977N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:1094827 C>A maps to ENST00000441003 I1972I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr11:1093013 C>G maps to ENST00000441003 T1611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:1093526 C>T maps to ENST00000441003 P1782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:1093502 T>C maps to ENST00000441003 T1774T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:195453309 G>A maps to ENST00000447234 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr3:195453369 G>A maps to ENST00000447234 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:195453132 C>T maps to ENST00000447234 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr6:30954260 C>T maps to NM_001010909.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:30954242 A>C maps to NM_001010909.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr3:195489066 C>G maps to NM_018406.5 S4801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:195487764 G>A maps to NM_018406.5 N4946N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:195490916 G>A maps to NM_018406.5 P4681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr3:195478121 G>T maps to NM_018406.5 T5201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr3:195479922 T>A maps to NM_018406.5 L5169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:1269215 G>A maps to ENST00000447027 T3705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:1250445 C>T maps to ENST00000447027 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr11:1258282 G>A maps to ENST00000447027 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr11:1258294 A>G maps to ENST00000447027 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:1272602 C>A maps to ENST00000447027 A4834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:1269623 C>T maps to ENST00000447027 T3841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr11:1268585 C>A maps to ENST00000447027 S3495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:1256558 C>T maps to ENST00000447027 H935H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:1267259 C>A maps to ENST00000447027 T3053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:1264895 C>T maps to ENST00000447027 T2265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr11:1256377 C>T maps to ENST00000447027 Y901Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:1272692 C>T maps to ENST00000447027 T4864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:1281904 C>T maps to ENST00000447027 C5675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:1252674 C>A maps to ENST00000447027 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr11:1271267 G>A maps to ENST00000447027 P4389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:1267118 C>T maps to ENST00000447027 T3006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:1267454 G>A maps to ENST00000447027 T3118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:1244392 C>T maps to ENST00000447027 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:1267133 C>T maps to ENST00000447027 S3011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:1269890 C>A maps to ENST00000447027 A3930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:1270808 C>A maps to ENST00000447027 A4236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:1277969 C>T maps to ENST00000447027 N5405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr11:1276472 G>A maps to ENST00000447027 P5292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:1271198 C>A maps to ENST00000447027 S4366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:1282616 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:1264784 C>A maps to ENST00000447027 T2228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:1025310 G>A maps to NM_005961.2 H952H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:1017538 G>T maps to NM_005961.2 S1754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:1036631 C>T maps to NM_005961.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:1016917 C>T maps to NM_005961.2 R1961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr11:1016170 G>A maps to NM_005961.2 A2210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr11:1017022 G>A maps to NM_005961.2 H1926H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:1025855 G>A maps to NM_005961.2 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:1026421 G>A maps to NM_005961.2 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr11:1027446 C>T maps to NM_005961.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:1019353 C>T maps to NM_005961.2 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:1023620 C>T maps to NM_005961.2 T1138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:1020711 T>C maps to NM_005961.2 P1204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:1026418 G>A maps to NM_005961.2 D818D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:1026939 C>T did not map to a codon.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr4:71346820 C>T maps to NM_152291.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:71347157 G>T maps to NM_152291.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr4:71346826 A>G maps to NM_152291.2 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr4:71346646 C>T maps to NM_152291.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr14:57741240 T>C maps to ENST00000431972 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:57741090 C>T maps to ENST00000431972 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:20829736 G>A maps to NM_024544.2 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:20827341 G>A maps to NM_024544.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:1366354 G>T maps to NM_032853.3 G447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:105451437 C>A did not map to a codon.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr23:105450574 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:105449906 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:105451038 A>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:105450023 C>T did not map to a codon.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr23:105449567 T>A did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr23:105451297 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:105450142 T>C did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:105450660 T>C did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:105450658 A>G did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:105450660 T>C did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:105451018 A>G did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:105450701 A>G did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr23:105451018 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:105450121 G>C did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:105450701 A>G did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:105450549 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:103340829 C>T maps to NM_001018116.1 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:65632543 C>T maps to NM_025128.4 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:65632008 G>T maps to NM_025128.4 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:65632702 C>T maps to NM_025128.4 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr11:65631347 C>T maps to NM_025128.4 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:65630910 A>G maps to NM_025128.4 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr9:113509956 C>T maps to ENST00000189978 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:113530240 G>A maps to ENST00000189978 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr9:113563183 G>C maps to ENST00000189978 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:113538933 A>G maps to ENST00000189978 K467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:113530126 C>A maps to ENST00000189978 Y322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:52867384 G>T maps to ENST00000504329 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:49427118 C>A maps to NM_000255.3 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr6:49421312 C>T maps to NM_000255.3 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:8015902 T>C maps to NM_201280.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:45795091 C>T maps to NM_001128425.1 Q512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:45798118 G>A maps to NM_001128425.1 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr16:88721711 G>A maps to NM_002461.1 H264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:88719737 G>A maps to NM_002461.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr12:110032873 C>T maps to NM_001114185.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:110012683 A>G maps to NM_001114185.1 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr16:29857517 C>T maps to NM_017458.3 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:29845082 C>A maps to NM_017458.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:29848185 C>A maps to NM_017458.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr16:29848185 C>T maps to NM_017458.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr16:29848185 C>T maps to NM_017458.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr16:29848185 C>T maps to NM_017458.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:42807912 C>T maps to NM_001144925.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr21:42807879 C>T maps to NM_001144925.1 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr21:42780010 C>T maps to NM_002463.1 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr21:42749083 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:42749783 C>A maps to NM_002463.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr21:42748940 C>T maps to NM_002463.1 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr21:42752028 C>T maps to NM_002463.1 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr2:70148880 G>T maps to NM_002357.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:70143278 T>C maps to NM_002357.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:70142521 G>A maps to NM_002357.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:112039788 C>T maps to NM_130439.3 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:3228182 G>A did not map to a codon.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr23:3241452 A>G did not map to a codon.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr23:3228256 C>T did not map to a codon.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr23:3241275 A>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:3248398 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:3248801 T>C did not map to a codon.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr23:3248772 C>G did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:3235603 G>A did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:3228552 C>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:3240231 C>T did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:3242300 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:3238721 T>C did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:3238274 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:3229334 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:3235844 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:3228940 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:3242449 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:3242527 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:3227962 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:3229423 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:3240191 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:3240873 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:3240771 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:3248199 A>C did not map to a codon.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr23:3240325 G>T did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:3228954 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:3241255 T>C did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:3241316 T>C did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:3241353 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:3261695 A>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:3228196 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:3242789 T>G did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:3229633 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:3239908 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:3240763 G>A did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:3235261 G>A did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:3241452 A>G did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:3261723 C>T did not map to a codon.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr23:3242751 T>C did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:3229632 C>A did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:3238127 G>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:3229370 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:3241558 A>G did not map to a codon.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr23:3242853 C>T did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr23:3241451 A>G did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:3242676 G>A did not map to a codon.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr23:3235152 G>A did not map to a codon.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr23:3235331 G>A did not map to a codon.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr23:3240723 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:3242751 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:3229307 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:3235194 G>A did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:3248416 C>A did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:3228227 C>T did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:3248741 G>A did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:3248743 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:3239926 T>C did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:3261757 G>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:3240591 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:74673705 G>A maps to NM_001008528.1 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:54377385 G>A maps to NM_001020818.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:135518400 C>T maps to NM_001130173.1 D502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:135511347 T>C maps to NM_001130173.1 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:4444823 C>T maps to NM_001105538.1 A1077A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:67478939 A>G maps to NM_001080416.2 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:67511349 G>A maps to NM_001080416.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr20:42331533 G>A maps to NM_002466.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:42331371 C>T maps to NM_002466.2 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:42338650 G>A maps to NM_002466.2 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr20:42338692 G>A maps to NM_002466.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:102040627 C>T maps to NM_002465.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:102023263 C>A maps to NM_002465.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:102030491 T>C maps to NM_002465.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:102025457 G>A maps to NM_002465.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:102010986 T>C maps to NM_002465.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:102023210 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:102025860 C>T maps to NM_002465.2 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:102054960 G>A maps to NM_002465.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:102043106 A>G maps to NM_002465.2 K422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:102061582 T>C maps to NM_002465.2 D810D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:50967706 G>A maps to NM_004533.3 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr19:50958866 C>T maps to NM_004533.3 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:50940924 G>A maps to NM_004533.3 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:50944250 C>T maps to NM_004533.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:50954151 C>T maps to NM_004533.3 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr19:50958539 T>C maps to NM_004533.3 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr19:50958539 T>C maps to NM_004533.3 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:50958803 T>C maps to NM_004533.3 D747D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr19:50957407 C>T maps to NM_004533.3 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:47364189 G>A maps to ENST00000399249 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:47372916 G>A maps to ENST00000399249 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:47354768 C>T maps to ENST00000399249 V1102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr11:47360143 A>G maps to ENST00000399249 D745D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:47372949 G>A maps to ENST00000399249 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:47358999 C>T maps to ENST00000399249 A848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:47354170 C>T maps to ENST00000399249 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:203143675 C>T maps to NM_004997.2 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:109839516 G>T maps to NM_001010985.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:109839552 C>T maps to NM_001010985.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:128752783 C>T maps to NM_002467.4 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:39333279 A>G maps to NM_012333.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr13:77748600 G>A maps to NM_015057.4 R1832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:77657195 G>A maps to NM_015057.4 S3669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:77862313 G>A maps to NM_015057.4 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr13:77740557 T>C maps to NM_015057.4 K2082K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr13:77842066 A>G maps to NM_015057.4 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr13:77792003 C>A maps to NM_015057.4 G1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:77755923 G>T maps to NM_015057.4 S1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:77853003 C>A maps to NM_015057.4 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:77780955 G>A maps to NM_015057.4 R1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:77817967 C>A maps to NM_015057.4 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr13:77669575 T>C maps to NM_015057.4 Q3372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:77632487 C>A maps to NM_015057.4 G4398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr13:77700629 G>A maps to NM_015057.4 C2569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:77695604 A>G maps to NM_015057.4 S2681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr13:77792022 C>T maps to NM_015057.4 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr13:77841994 A>G maps to NM_015057.4 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:77631118 A>G did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr13:77700454 C>A maps to NM_015057.4 E2628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:77671937 T>C maps to NM_015057.4 K3117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr13:77760024 A>G maps to NM_015057.4 C1475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr13:77754357 T>C maps to NM_015057.4 R1679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:77672276 C>T maps to NM_015057.4 S3004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr13:77760024 A>G maps to NM_015057.4 C1475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:48601069 T>C maps to NM_032133.4 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:48604742 G>A maps to NM_032133.4 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:48594670 T>C maps to NM_032133.4 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:48606425 C>A maps to NM_032133.4 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr17:48598489 C>T maps to NM_032133.4 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:48602275 C>T maps to NM_032133.4 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:48598789 C>T maps to NM_032133.4 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:40363564 G>A maps to NM_001033082.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:40363241 C>T maps to NM_001033082.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr2:16085897 G>T maps to NM_005378.4 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:16085669 G>A maps to NM_005378.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:153042886 C>A maps to NM_025107.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:38182002 C>T maps to NM_001172567.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:38182050 C>T maps to NM_001172567.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:48451807 A>G did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr15:48460906 T>C maps to NM_016132.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:48458200 C>A maps to NM_016132.3 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:48435190 C>A maps to NM_016132.3 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr15:48443732 G>A maps to NM_016132.3 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:69063303 C>T maps to NM_138768.2 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:241066276 C>T maps to NM_138336.1 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:81110943 G>A maps to NM_005593.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:81110898 C>T maps to NM_005593.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:81111150 C>T maps to NM_005593.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr12:81111114 C>T maps to NM_005593.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:81101719 C>A maps to NM_002469.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:81101629 C>A maps to NM_002469.2 C44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr12:81101647 G>A maps to NM_002469.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:81101644 C>T maps to NM_002469.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr12:81101617 C>A maps to NM_002469.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:81101767 C>T maps to NM_002469.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:10404438 G>A maps to NM_005963.3 V1242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:10406460 A>G maps to NM_005963.3 D932D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr17:10419515 G>A maps to NM_005963.3 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:10400684 C>A maps to NM_005963.3 E1484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:10404996 C>A maps to NM_005963.3 E1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr17:10402357 G>T maps to NM_005963.3 S1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:10395822 G>A maps to NM_005963.3 A1910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:10408740 G>A maps to NM_005963.3 D754D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr17:10395822 G>A maps to NM_005963.3 A1910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:10416087 G>A maps to NM_005963.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr17:10408740 G>A maps to NM_005963.3 D754D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:10419536 G>T maps to NM_005963.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:10400652 T>C maps to NM_005963.3 E1494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:8384695 G>A maps to ENST00000360416 H1736H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr17:8421971 A>G maps to ENST00000360416 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr17:8417148 C>T maps to ENST00000360416 A856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr17:8424544 G>A maps to ENST00000360416 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:8396258 G>A maps to ENST00000360416 D1431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:8379184 G>A maps to ENST00000360416 S1987S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr17:8395620 T>C maps to ENST00000360416 G1555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:8383480 T>C maps to ENST00000360416 S1848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr17:8421971 A>G maps to ENST00000360416 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:8381673 C>T maps to ENST00000360416 A1896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr16:15814061 G>A maps to NM_001040114.1 A1640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr16:15808818 C>T maps to NM_001040114.1 T1918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:15839008 G>A maps to NM_001040114.1 Q840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr16:15853492 G>T maps to NM_001040114.1 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:15813510 G>T maps to NM_001040114.1 I1678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:15850311 C>T maps to NM_001040114.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr16:15876246 G>A maps to NM_001040114.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:15850221 G>A maps to NM_001040114.1 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:15835631 T>C maps to NM_001040114.1 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:15857722 G>T maps to NM_001040114.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:15932001 G>T maps to NM_001040114.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:15835328 C>T maps to NM_001040114.1 Q957Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:15815482 G>A maps to NM_001040114.1 A1465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr16:15854402 T>C maps to NM_001040114.1 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr16:15854402 T>C maps to NM_001040114.1 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:10204897 G>A maps to NM_003802.2 D1930D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:10204902 G>A maps to NM_003802.2 R1929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:10222145 G>A maps to NM_003802.2 D1233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:10225010 G>A maps to NM_003802.2 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:10263383 C>A maps to NM_003802.2 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:10212577 G>A maps to NM_003802.2 S1714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:10222352 C>T maps to NM_003802.2 Q1164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:10216010 G>A maps to NM_003802.2 C1415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:10222460 C>T maps to NM_003802.2 A1128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:10233777 C>T maps to NM_003802.2 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:10219234 T>C maps to NM_003802.2 A1282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr17:10222451 C>T maps to NM_003802.2 T1131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:10215230 G>A maps to NM_003802.2 Q1510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:10222451 C>T maps to NM_003802.2 T1131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:50755951 C>T maps to NM_001145809.1 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:50760715 C>G maps to NM_001145809.1 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:50755918 G>A maps to NM_001145809.1 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:50775221 C>T maps to NM_001145809.1 D1096D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr19:50812950 G>A maps to NM_001145809.1 E2005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr3:108195348 A>G maps to NM_014981.1 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:108172898 G>A maps to NM_014981.1 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:108175728 A>G maps to NM_014981.1 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:108211961 G>T maps to NM_014981.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:108205370 G>A maps to NM_014981.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:108156423 T>C maps to NM_014981.1 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr3:108129643 G>T maps to NM_014981.1 V1447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr3:108156425 G>T maps to NM_014981.1 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:108129460 C>T maps to NM_014981.1 E1508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:108129643 G>A maps to NM_014981.1 V1447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:108156456 C>A maps to NM_014981.1 R1075R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:10451104 C>A maps to NM_017534.5 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:10447328 C>A maps to NM_017534.5 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:10447415 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:10430094 C>T maps to NM_017534.5 A1336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:10438391 C>T maps to NM_017534.5 Q726Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-A01T-01A-21W-A096-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:10440718 G>T maps to NM_017534.5 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr17:10428767 G>A maps to NM_017534.5 Q1513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:10428144 G>A maps to NM_017534.5 Q1634*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D5-6538-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr17:10431063 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-F4-6570-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:10534927 G>A maps to NM_002470.2 D1762D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:10541230 G>A maps to NM_002470.2 R1251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr17:10539140 C>A maps to NM_002470.2 E1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:10558264 G>A maps to NM_002470.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:10555850 G>A maps to NM_002470.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr17:10541368 C>T maps to NM_002470.2 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr17:10533509 G>A maps to NM_002470.2 R1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr17:10535885 C>T maps to NM_002470.2 G1621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr17:10545860 C>T maps to NM_002470.2 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr17:10543074 C>A maps to NM_002470.2 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr17:10535885 C>T maps to NM_002470.2 G1621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr17:10537388 G>A maps to NM_002470.2 Y1489Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr17:10358093 A>G maps to NM_017533.2 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:10356158 C>A maps to NM_017533.2 E1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:10346760 A>C maps to NM_017533.2 A1917A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr17:10354158 G>A maps to NM_017533.2 R1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:10351710 A>G did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr17:10350416 T>C maps to NM_017533.2 A1694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:10351974 A>G maps to NM_017533.2 D1497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:10356624 C>T maps to NM_017533.2 E985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:10367996 C>T did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr17:10350374 T>C maps to NM_017533.2 Q1708Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:10348418 G>A maps to NM_017533.2 S1780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:10351203 C>T maps to NM_017533.2 Q1632Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr14:23866460 A>G maps to NM_002471.3 N656N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr14:23871679 G>A maps to NM_002471.3 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:23858216 G>A maps to NM_002471.3 C1342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:23871811 C>A did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr14:23865557 C>T maps to NM_002471.3 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr14:23893325 G>A maps to NM_000257.2 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:23886518 G>A maps to NM_000257.2 A1454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:23892881 C>T maps to NM_000257.2 K991K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr14:23900137 G>A maps to NM_000257.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:23886789 G>A maps to NM_000257.2 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:23902830 G>T maps to NM_000257.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr14:23896794 C>T maps to NM_000257.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr14:23892857 C>A maps to NM_000257.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:23895252 G>A maps to NM_000257.2 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:23902830 G>T maps to NM_000257.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:23902758 G>A maps to NM_000257.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:23887429 G>A maps to NM_000257.2 L1386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr14:23901920 C>A maps to NM_000257.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:23897771 G>A maps to NM_000257.2 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:23899002 C>T maps to NM_000257.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr14:23897840 G>A maps to NM_000257.2 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:23886747 A>T maps to NM_000257.2 A1439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr14:23884311 C>T maps to NM_000257.2 A1817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr14:23887510 G>A maps to NM_000257.2 R1359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr14:23901905 G>A maps to NM_000257.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr14:23884981 G>A maps to NM_000257.2 I1671I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:33577718 C>T maps to NM_020884.3 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:33584894 C>T maps to NM_020884.3 S1134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr20:33567543 G>A maps to NM_020884.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:33567226 C>T maps to NM_020884.3 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:10315797 G>A maps to NM_002472.2 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:10322010 C>T maps to NM_002472.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:10322058 C>T maps to NM_002472.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr17:10304036 C>T maps to NM_002472.2 A1135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:10304271 C>A maps to NM_002472.2 E1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:10300221 C>T maps to NM_002472.2 T1420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr17:10299903 G>A maps to NM_002472.2 L1498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr17:10304430 G>C maps to NM_002472.2 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr22:36684871 C>T maps to NM_002473.4 R1557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr22:36690988 G>A maps to NM_002473.4 Q1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:36680257 G>A maps to NM_002473.4 A1882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:36716408 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:36722639 C>T maps to NM_002473.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:36718563 G>A maps to NM_002473.4 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:36737436 G>A maps to NM_002473.4 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr22:36680481 G>A maps to NM_002473.4 D1853D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:36715603 C>T maps to NM_002473.4 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr22:36701973 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:36715603 C>T maps to NM_002473.4 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr22:36689852 C>T maps to NM_002473.4 K1298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr22:36702076 A>G maps to NM_002473.4 H686H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:36680308 G>A maps to NM_002473.4 A1865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:36684898 C>T maps to NM_002473.4 L1548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:36718472 C>T did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:211179706 C>A maps to NM_079420.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr2:211179700 C>T maps to NM_079420.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:211163183 A>G maps to NM_079420.2 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:211158972 G>T maps to NM_079420.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:211179700 C>T maps to NM_079420.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr7:101259513 G>A maps to NM_138403.4 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:101256989 G>A maps to NM_138403.4 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:101265427 G>A maps to NM_138403.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:46904871 G>T maps to NM_000258.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:45299064 C>T maps to NM_002476.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:45299147 C>T maps to NM_002476.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:673733 C>T maps to NM_002477.1 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:56553876 G>A maps to NM_079423.3 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:44180601 G>T maps to ENST00000457314 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:35173355 C>T maps to NM_006097.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:16144085 A>G maps to NM_013262.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:16145532 C>T maps to NM_013262.3 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:16145301 C>T maps to NM_013262.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:123357033 C>T maps to NM_053025.3 A1615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:123375976 A>C maps to NM_053025.3 P1428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:123367897 G>A maps to NM_053025.3 P1445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:123426707 G>A maps to NM_053025.3 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:123426686 G>A maps to NM_053025.3 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:123457863 C>T maps to NM_053025.3 W156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr3:123359227 G>A maps to NM_053025.3 I1581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:123452621 G>A maps to NM_053025.3 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:30407388 G>A maps to NM_033118.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr20:30414647 T>C maps to NM_033118.3 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:30409337 A>C maps to NM_033118.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr20:30414647 T>C maps to NM_033118.3 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:30408103 C>T maps to NM_033118.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr20:30414505 G>T maps to NM_033118.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr16:46764539 C>T maps to NM_182493.2 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:46746654 G>A maps to NM_182493.2 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr6:2689128 C>A maps to NM_001012418.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:2693069 G>A maps to NM_001012418.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:2693018 T>C maps to NM_001012418.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr6:2679590 G>A maps to NM_001012418.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:2689134 T>C maps to NM_001012418.3 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:2685591 C>T maps to NM_001012418.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr6:2689128 C>A maps to NM_001012418.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr6:2749438 C>T maps to NM_001012418.3 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr6:2689128 C>A maps to NM_001012418.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr16:30387813 C>T maps to NM_013292.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:169500312 C>A maps to NM_018657.4 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr5:16685900 C>T maps to NM_012334.2 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:16681493 C>T maps to NM_012334.2 A1436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:16699595 G>A maps to NM_012334.2 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:16794863 G>A maps to NM_012334.2 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:16681986 G>A maps to NM_012334.2 I1394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:16668424 G>A maps to NM_012334.2 I2012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:16680190 G>A maps to NM_012334.2 Y1469Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:16701527 C>T maps to NM_012334.2 E992E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:16701746 C>T maps to NM_012334.2 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:16701125 C>T maps to NM_012334.2 G1126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:18030173 C>A maps to ENST00000205890 I1312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:18075480 C>T maps to ENST00000205890 S3409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr17:18023040 C>T maps to ENST00000205890 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:18022119 G>A maps to ENST00000205890 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:18022464 C>T maps to ENST00000205890 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:18052640 C>T maps to ENST00000205890 D2356D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:18065944 C>T maps to ENST00000205890 F3188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:18054760 C>T maps to ENST00000205890 F2569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:18025335 A>C maps to ENST00000205890 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:18077226 C>T maps to ENST00000205890 L3495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr17:18074950 G>A did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr13:109379897 C>T maps to NM_015011.1 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr13:109318423 G>T maps to NM_015011.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:109379897 C>T maps to NM_015011.1 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr13:109459145 T>C maps to NM_015011.1 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:109672057 G>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr13:109753196 C>T maps to NM_015011.1 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr13:109779803 G>A maps to NM_015011.1 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr13:109617155 C>T maps to NM_015011.1 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr13:109475608 C>A maps to NM_015011.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr13:109318423 G>A maps to NM_015011.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:109318489 C>T maps to NM_015011.1 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:109753196 C>T maps to NM_015011.1 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr13:109777544 G>T maps to NM_015011.1 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:109753196 C>T maps to NM_015011.1 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr13:109318303 T>C maps to NM_015011.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:109472755 G>A maps to NM_015011.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr13:109475608 C>T maps to NM_015011.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr13:109379843 C>T maps to NM_015011.1 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr13:109793563 C>T maps to NM_015011.1 D1646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:109779749 G>A maps to NM_015011.1 S1279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr13:109475608 C>T maps to NM_015011.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr13:109475563 C>G maps to NM_015011.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr13:109475608 C>T maps to NM_015011.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr13:109793143 C>T maps to NM_015011.1 S1506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr13:109438059 C>T maps to NM_015011.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr17:27401880 G>A maps to NM_078471.3 H2024H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:27438767 A>C maps to NM_078471.3 Y904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:27447684 G>T maps to NM_078471.3 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr17:27423863 G>A maps to NM_078471.3 R1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:27449223 C>T maps to NM_078471.3 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr22:26348302 C>T maps to ENST00000407587 R1964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr22:26168327 G>T maps to ENST00000407587 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:26264330 G>A maps to ENST00000407587 A1312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:26348310 C>T maps to ENST00000407587 I1966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr22:26168326 C>T maps to ENST00000407587 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr22:26173602 G>A maps to ENST00000407587 Q643Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr22:26422788 G>A maps to ENST00000407587 T2285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr22:26164209 C>T maps to ENST00000407587 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr22:26422651 C>T maps to ENST00000407587 L2240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr22:26422608 T>C maps to ENST00000407587 P2225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr22:26348302 C>T maps to ENST00000407587 R1964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr22:26294299 C>T maps to ENST00000407587 D1567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:34870294 G>A maps to NM_001163735.1 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:34859017 C>A maps to NM_001163735.1 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:34871818 G>A maps to NM_001163735.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr17:34866661 C>T maps to NM_001163735.1 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:34863246 G>A maps to NM_001163735.1 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:192228933 C>T maps to NM_001130158.1 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:192246225 C>T maps to NM_001130158.1 N408N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:192261218 G>A maps to NM_001130158.1 W764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr2:192228893 A>G maps to NM_001130158.1 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:192256912 C>T maps to NM_001130158.1 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:192234333 C>T maps to NM_001130158.1 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:192141728 G>A maps to NM_001130158.1 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr2:192246225 C>T maps to NM_001130158.1 N408N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr2:192246225 C>T maps to NM_001130158.1 N408N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:1385798 C>T maps to NM_001080779.1 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:1381996 C>T maps to NM_001080779.1 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:1378232 G>A maps to NM_001080779.1 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr17:1381978 G>A maps to NM_001080779.1 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr17:30980959 T>C maps to NM_015194.1 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:31048195 G>A maps to NM_015194.1 Y586Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:31039082 G>A maps to NM_015194.1 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:31048132 C>T maps to NM_015194.1 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr17:31107777 C>T maps to NM_015194.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr17:31102938 G>A maps to NM_015194.1 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:31048189 A>G maps to NM_015194.1 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:59519756 A>G maps to NM_004998.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:59510158 C>T maps to NM_004998.2 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr15:59455417 G>A maps to NM_004998.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr15:59445907 G>A maps to NM_004998.2 S987S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:59523957 C>T maps to NM_004998.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr15:59470678 G>A maps to NM_004998.2 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:8612994 G>A maps to NM_012335.3 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:8617024 G>A maps to NM_012335.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:8587342 G>A maps to NM_012335.3 C1046C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:8609318 G>A maps to NM_012335.3 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:8619537 C>T maps to NM_012335.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:8612994 G>A maps to NM_012335.3 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:8616650 G>A maps to NM_012335.3 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:8601851 G>A maps to NM_012335.3 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:8595421 G>A maps to NM_012335.3 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr19:8616668 G>A maps to NM_012335.3 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:8595115 G>A maps to NM_012335.3 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:8619555 G>A maps to NM_012335.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:8615467 G>A maps to NM_012335.3 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr19:8613156 G>A maps to NM_012335.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:8620541 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:8601411 G>A maps to NM_012335.3 Y623Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:45010210 G>A maps to NM_033054.2 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr7:45010505 C>T maps to NM_033054.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:45009365 G>A maps to NM_033054.2 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:109843731 C>A maps to NM_001101421.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:109834287 C>A maps to NM_001101421.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:109847384 T>C maps to NM_001101421.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr12:109870752 A>G maps to NM_001101421.3 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:109835589 A>G maps to NM_001101421.3 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr10:26446312 T>C maps to NM_017433.4 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:26355940 C>T maps to NM_017433.4 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:26432507 G>A maps to NM_017433.4 K798K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr10:26446312 T>C maps to NM_017433.4 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr10:26457645 C>T maps to NM_017433.4 F1039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr10:26463392 T>C maps to NM_017433.4 H1400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr10:26286167 A>T maps to NM_017433.4 G163G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3947-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:26446394 C>T maps to NM_017433.4 R984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:26465718 T>C maps to NM_017433.4 G1461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:26446394 C>T maps to NM_017433.4 R984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr10:26446429 T>C maps to NM_017433.4 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:26446394 C>T maps to NM_017433.4 R984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:26443676 C>T maps to NM_017433.4 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr10:26463053 T>C maps to NM_017433.4 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr10:26463392 T>C maps to NM_017433.4 H1400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr10:26315320 T>C maps to NM_017433.4 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr10:26463392 T>C maps to NM_017433.4 H1400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:26436438 C>T maps to NM_017433.4 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr10:26462789 G>A maps to NM_017433.4 E1199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:26377145 C>A maps to NM_017433.4 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:171258114 C>T maps to NM_138995.3 D681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr2:171256714 C>T maps to NM_138995.3 Y603Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:171070974 C>A maps to NM_138995.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:171259489 T>G maps to NM_138995.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:171056671 G>T maps to NM_138995.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:171191937 G>T maps to NM_138995.3 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:171242700 C>T maps to NM_138995.3 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:171264304 A>G maps to NM_138995.3 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:171056682 A>T maps to NM_138995.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:171399428 C>T maps to NM_138995.3 Q1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:171264304 A>C maps to NM_138995.3 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr2:171248950 A>G maps to NM_138995.3 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr2:171238586 G>T maps to NM_138995.3 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:171258105 C>T maps to NM_138995.3 D678D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:171248911 A>G maps to NM_138995.3 G566G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-F4-6703-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr2:171259366 A>G maps to NM_138995.3 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:171056661 T>C maps to NM_138995.3 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr2:171242700 C>T maps to NM_138995.3 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:171323203 T>C maps to NM_138995.3 F999F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr15:52720717 G>A maps to ENST00000358212 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:52688563 T>C maps to ENST00000358212 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:52659252 G>A maps to ENST00000358212 I1045I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:52702588 G>A maps to ENST00000358212 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:52697557 G>A maps to ENST00000358212 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:52702532 G>A maps to ENST00000358212 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:52668719 G>T maps to ENST00000358212 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:52675316 G>A maps to ENST00000358212 I661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr15:52611291 C>T maps to ENST00000358212 K1733K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:47463626 G>A maps to NM_001080467.2 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr18:47367797 C>T maps to NM_001080467.2 T1546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr18:47431167 C>A maps to NM_001080467.2 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:47363954 G>A maps to NM_001080467.2 N1690N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:47463696 G>T maps to NM_001080467.2 S608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:47500922 C>T maps to NM_001080467.2 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr18:47516891 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:47421352 G>T maps to NM_001080467.2 I1001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:47563302 G>T maps to NM_001080467.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr18:47421508 G>A maps to NM_001080467.2 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr18:47364071 T>C maps to NM_001080467.2 S1651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr18:47421414 G>A maps to NM_001080467.2 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr18:47369685 C>T maps to NM_001080467.2 A1512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:52536688 G>A maps to NM_018728.3 R752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:52561976 C>A maps to NM_018728.3 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr15:52571805 G>A maps to NM_018728.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr15:52571796 G>A maps to NM_018728.3 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:52534343 G>A maps to NM_018728.3 R819R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr15:52517285 T>C maps to NM_018728.3 E1117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:52536601 G>A maps to NM_018728.3 R781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr15:52517285 T>C maps to NM_018728.3 E1117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:52564911 T>C maps to NM_018728.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:76538311 T>C maps to ENST00000428345 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr6:76576653 G>A maps to ENST00000428345 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr6:76602248 T>C maps to ENST00000428345 A983A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:76596597 C>T maps to ENST00000428345 R849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:76621387 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:76572316 A>G maps to ENST00000428345 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:76608089 G>A maps to ENST00000428345 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:76901881 C>T maps to NM_000260.3 F1297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:76858896 G>A maps to NM_000260.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr11:76900478 C>T maps to NM_000260.3 C1198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr11:76915211 C>T maps to NM_000260.3 A1806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr11:76917222 C>T maps to NM_000260.3 V1906V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:76893641 C>T maps to NM_000260.3 G1094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:76912559 C>A maps to NM_000260.3 G1640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:128366374 G>A maps to ENST00000389524 T912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:128367091 G>A maps to ENST00000389524 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:128335808 C>T maps to ENST00000389524 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:128367425 C>T maps to ENST00000389524 A1009A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:128384647 C>T maps to ENST00000389524 F1412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:128322878 C>T maps to ENST00000389524 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:128341822 C>T maps to ENST00000389524 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:128388810 C>T maps to ENST00000389524 A1630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr15:72302776 C>T maps to ENST00000424560 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr15:72119271 C>T maps to ENST00000424560 S2503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr15:72152108 G>A maps to ENST00000424560 C2111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr15:72193639 C>T maps to ENST00000424560 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:72190037 G>A maps to ENST00000424560 T1602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr15:72118929 A>G maps to ENST00000424560 F2617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:72190967 A>G maps to ENST00000424560 V1292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:72119283 G>A maps to ENST00000424560 V2499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr19:17317575 C>T maps to NM_004145.3 L1825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:17264831 G>T maps to NM_004145.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:17318011 G>A maps to NM_004145.3 S1861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr19:17305559 G>A maps to NM_004145.3 R1108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr19:17321537 G>A maps to NM_004145.3 K1937K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:17318053 G>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:171605265 G>A maps to NM_000261.1 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:171621715 C>T maps to NM_000261.1 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:12569537 G>T maps to NM_001146312.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:12666669 C>T maps to NM_001146312.1 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr17:12666520 C>T maps to NM_001146312.1 Q841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:12639563 C>T maps to NM_001146312.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:12649280 G>A maps to NM_001146312.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:12666633 C>T maps to NM_001146312.1 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr17:12666825 C>T maps to NM_001146312.1 D942D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:12647715 C>T maps to NM_001146312.1 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr17:12639487 G>A maps to NM_001146312.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:12656545 G>A maps to NM_001146312.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:17741472 G>A maps to NM_002478.4 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr11:17743018 G>C maps to NM_002478.4 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:17741433 C>T maps to NM_002478.4 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:17741736 G>A maps to NM_002478.4 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:17741757 G>A maps to NM_002478.4 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:17741784 C>T maps to NM_002478.4 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:17741457 C>T maps to NM_002478.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr10:95141117 G>T maps to NM_013451.3 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:95083094 C>A maps to NM_013451.3 V1764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:95129488 C>T maps to NM_013451.3 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr10:95241873 G>T maps to NM_013451.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr10:95093571 C>T maps to NM_013451.3 T1554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:95089559 C>A maps to NM_013451.3 E1615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:95163931 A>G maps to NM_013451.3 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr10:95107443 G>A maps to NM_013451.3 T1393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:95152698 C>T maps to NM_013451.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:95134653 G>A maps to NM_013451.3 R723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:3100420 C>T maps to NM_003803.3 T1193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:3067277 A>G maps to NM_003803.3 G1680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:3067412 G>A maps to NM_003803.3 G1635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:3102488 G>A maps to NM_003803.3 V1186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:3164278 G>A maps to NM_003803.3 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:3164278 G>A maps to NM_003803.3 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:3164278 G>A maps to NM_003803.3 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:3083881 A>C maps to NM_003803.3 A1463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:2088723 G>A maps to NM_003970.2 P1293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:2063768 T>C maps to NM_003970.2 C1066C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr8:2041892 C>T maps to NM_003970.2 D700D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr8:2054289 G>C maps to NM_003970.2 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr8:2026859 G>A maps to NM_003970.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr8:2054107 C>T maps to NM_003970.2 D937D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:2017608 G>A maps to NM_003970.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr8:2046691 C>T maps to NM_003970.2 D773D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:2071142 G>T maps to NM_003970.2 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr8:2000350 G>A maps to NM_003970.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr8:2020569 C>T maps to NM_003970.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:2000383 G>A maps to NM_003970.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr8:2048807 T>G maps to NM_003970.2 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr8:2063846 T>C maps to NM_003970.2 I1092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:2005486 C>A maps to NM_003970.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:2046691 C>T maps to NM_003970.2 D773D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr8:2017616 G>A did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr8:2057291 T>A maps to NM_003970.2 I1050I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:24418755 T>C maps to ENST00000330966 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr1:24419509 G>A maps to ENST00000330966 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:24416132 C>T maps to ENST00000330966 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:24418800 G>A maps to ENST00000330966 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:24409191 G>A maps to ENST00000330966 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:24435060 G>A maps to ENST00000330966 H22H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr1:24433673 T>C maps to ENST00000330966 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:24400656 G>T maps to ENST00000330966 T988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr1:24433673 T>C maps to ENST00000330966 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr1:24418785 G>A maps to ENST00000330966 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:75394371 G>A maps to NM_021245.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr10:75393677 G>T maps to NM_021245.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:120079272 C>T maps to NM_016599.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:150056295 C>T maps to NM_133371.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr10:69902840 A>T maps to NM_032578.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:69882047 C>T maps to NM_032578.2 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:69970160 G>A maps to NM_032578.2 T1304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:69881294 C>T maps to NM_032578.2 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:69933999 G>A maps to NM_032578.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:46404833 G>A maps to NM_001012643.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:46394573 T>C maps to NM_001012643.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:46394204 G>A maps to NM_001012643.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:40251394 C>T maps to NM_015460.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:40285998 C>T maps to NM_015460.2 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr3:40231827 G>A maps to NM_015460.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:40085591 G>A maps to NM_015460.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:40192647 G>T maps to NM_015460.2 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:40293390 T>G maps to NM_015460.2 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:40251394 C>T maps to NM_015460.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:40085744 C>T maps to NM_015460.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr3:40085598 C>T maps to NM_015460.2 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:40231768 C>T maps to NM_015460.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:59147758 C>T maps to NM_001085487.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:59139307 A>G maps to NM_001085487.1 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:31129151 G>A maps to NM_182958.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr17:47895363 C>T maps to NM_007067.4 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:47893247 A>G maps to NM_007067.4 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:41801476 C>A maps to NM_006766.3 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:41790673 C>T maps to NM_006766.3 Q1688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:41794924 G>A maps to NM_006766.3 I1067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:41812836 G>A maps to NM_006766.3 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr8:41801474 T>C maps to NM_006766.3 E673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:41836161 C>T maps to NM_006766.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:41798494 C>T maps to NM_006766.3 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr8:41832335 A>G maps to NM_006766.3 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr8:41812839 G>A maps to NM_006766.3 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:76781901 A>G maps to NM_012330.2 E1095E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:76781904 G>A maps to NM_012330.2 E1096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr10:76789081 C>T maps to NM_012330.2 P1500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:76788805 C>T maps to NM_012330.2 H1408H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:76789768 C>T maps to NM_012330.2 S1729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr10:76780499 G>A maps to NM_012330.2 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:76781874 A>G maps to NM_012330.2 E1086E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:76744839 T>C maps to NM_012330.2 V792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:76788787 T>G maps to NM_012330.2 S1402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr10:76788700 A>G maps to NM_012330.2 E1373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr10:76789171 A>G maps to NM_012330.2 G1530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:76781868 G>A maps to NM_012330.2 E1084E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:76781895 G>A maps to NM_012330.2 E1093E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:76789970 C>T maps to NM_012330.2 R1797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr10:76789435 T>C maps to NM_012330.2 S1618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr20:62871773 G>A maps to NM_004535.2 K1113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:1926103 C>T maps to ENST00000399161 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:1843078 G>A maps to ENST00000399161 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:1946985 G>A maps to ENST00000399161 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:1946752 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr2:1893036 G>A maps to ENST00000399161 D832D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:1947057 C>T maps to ENST00000399161 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:1796155 G>A maps to ENST00000399161 H1119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:1946754 G>A maps to ENST00000399161 N168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:1895919 G>A maps to ENST00000399161 H724H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:1843057 C>T maps to ENST00000399161 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:1921019 G>A maps to ENST00000399161 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:1914052 G>T maps to ENST00000399161 C592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr19:59082474 G>A maps to NM_198055.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:48582025 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr16:48577114 G>A maps to NM_153029.3 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr4:40103896 C>A maps to NM_018177.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:40103770 C>T maps to NM_018177.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr4:40138608 A>G maps to NM_018177.3 E1564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:32977299 G>A maps to NM_052818.2 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr13:32978396 G>T maps to NM_001079691.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr13:32978396 G>T maps to NM_001079691.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:33016915 G>T maps to NM_033111.3 C586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr13:33095541 A>C maps to NM_033111.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:21331635 G>A maps to NM_174928.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr13:21306049 C>T maps to NM_174928.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:153197861 C>T did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:153195524 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:80246827 C>T maps to NM_032693.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:140306064 G>A maps to NM_057175.3 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:140297536 G>T maps to NM_057175.3 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:140280894 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:140282982 C>T maps to NM_057175.3 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:140258062 A>G maps to NM_057175.3 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:41932461 G>A maps to NM_024561.4 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:112479878 C>A maps to NM_024953.3 E802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:112506796 C>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:112528532 G>A maps to NM_024953.3 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:88632425 C>T maps to NM_024635.3 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:117828388 C>T maps to NM_016200.4 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:113440684 G>A maps to NM_025146.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:113442821 G>A maps to NM_025146.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:89907026 A>G maps to NM_005467.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr11:89916140 C>T maps to NM_005467.3 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:89867943 C>T maps to NM_005467.3 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:64815819 G>A maps to ENST00000340252 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:64824938 G>A maps to ENST00000340252 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:64824857 T>C maps to ENST00000340252 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:64825616 G>T maps to ENST00000340252 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:57486937 C>T maps to NM_005967.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:57485186 C>T maps to NM_005967.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:57485738 C>T maps to NM_005967.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr12:57111932 T>C maps to NM_001113203.1 T1127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:57113624 G>A maps to NM_001113203.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:57114641 T>C maps to NM_001113203.1 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:57106971 G>A maps to NM_001113203.1 I1991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr12:57106971 G>A maps to NM_001113203.1 I1991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:57114305 C>A maps to NM_001113203.1 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:57110131 C>A maps to NM_001113203.1 G1728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr17:59668490 C>T maps to NM_199290.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:138903745 C>T maps to NM_144653.3 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:1686081 G>A maps to ENST00000344463 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:1685600 C>T maps to ENST00000344463 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr11:71192997 G>T maps to NM_018161.4 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:71189490 G>A maps to NM_018161.4 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr16:66842913 A>G maps to ENST00000359087 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr16:66860651 C>A maps to ENST00000359087 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:66860486 C>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:66844644 G>A maps to ENST00000359087 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr4:164067002 A>G maps to NM_138386.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr22:42462728 G>A maps to NM_000262.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:71300651 C>T maps to NM_017567.4 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:71303789 C>T maps to NM_017567.4 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:71304725 C>T maps to NM_017567.4 C314C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr17:40696066 G>A maps to NM_000263.3 A681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr17:40695184 C>T maps to NM_000263.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:5075658 C>T maps to NM_016256.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr16:5083892 C>T maps to NM_016256.3 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:42085054 C>A maps to NM_153006.2 G455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:42085968 A>G maps to NM_153006.2 *535W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:130829374 G>A maps to NM_197956.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr5:70308328 G>A maps to NM_004536.2 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr13:101736062 C>T maps to NM_052867.2 P1194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr13:101797213 C>A maps to NM_052867.2 E625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr13:101717781 G>A maps to NM_052867.2 G1526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr13:101726980 G>A maps to NM_052867.2 V1329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr13:101890180 G>A maps to NM_052867.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:101735171 G>T maps to NM_052867.2 I1251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:101795439 G>A maps to NM_052867.2 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:101714451 G>A maps to NM_052867.2 S1541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:101997704 G>A maps to NM_052867.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:101735216 C>T maps to NM_052867.2 P1236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr13:101759853 G>A maps to NM_052867.2 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr13:101710291 T>C maps to NM_052867.2 S1674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr13:101756744 G>A maps to NM_052867.2 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr13:102030995 A>G maps to NM_052867.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:101707841 T>G did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr13:102030995 A>G maps to NM_052867.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr13:101717781 G>A maps to NM_052867.2 G1526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr13:101936301 G>A maps to NM_052867.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:105909679 A>G maps to NM_005746.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr7:105915442 T>C maps to NM_005746.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr7:105904029 T>C maps to NM_005746.2 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr7:105909679 A>G maps to NM_005746.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:7945720 A>G maps to NM_024865.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:7942306 G>T maps to NM_024865.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:46417942 C>T maps to NM_001029861.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:76447057 T>C maps to NM_139207.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr23:72434106 T>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:72434219 C>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:72433102 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:72433266 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:72433915 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:72434108 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:72433111 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:72434152 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:72434204 C>T did not map to a codon.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr23:72433258 G>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:72433380 A>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:72434276 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:92927846 C>T did not map to a codon.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr23:92927637 T>A did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:92928043 G>A did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:92926911 C>T did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:92927339 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:92927281 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:92928018 A>C did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:92927788 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:92927640 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:92926797 C>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:92928229 G>A did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:92928156 G>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:92927362 T>C did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:92928039 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:92928042 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:89618590 C>T maps to NM_153757.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:48006731 G>A maps to NM_003827.2 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr20:23361923 A>G maps to ENST00000431864 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr20:23358021 G>A maps to ENST00000431864 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:23360087 A>G maps to ENST00000431864 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:102760571 T>C maps to ENST00000455523 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:102760526 C>T maps to ENST00000455523 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:102768974 C>T maps to ENST00000455523 W156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:10548363 G>A maps to NM_003826.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:144657866 A>G maps to ENST00000276844 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:50863112 A>G maps to NM_004851.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:50861881 G>A maps to NM_004851.1 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:80426677 T>G maps to ENST00000374611 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:80422206 C>T maps to ENST00000374611 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:80430461 G>A maps to ENST00000374611 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:783295 A>G did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:55270049 A>C maps to NM_004539.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:78270614 A>G maps to NM_024678.4 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:78270601 C>A maps to NM_024678.4 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:78279746 A>G maps to NM_024678.4 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:46080715 G>A maps to NM_002482.3 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:46080015 C>T maps to NM_002482.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:46079808 G>A maps to NM_002482.3 E516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:46073488 G>A maps to NM_002482.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:18074437 C>T maps to NM_001160176.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr11:34162751 G>A maps to NM_024662.2 V903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:34153749 C>T maps to NM_024662.2 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:3534842 C>T maps to NM_024845.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:3532545 C>T maps to NM_024845.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr8:18258185 T>C maps to NM_000015.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr8:18257782 A>T maps to NM_000015.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:18258304 A>G maps to NM_000015.2 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr8:18258185 T>C maps to NM_000015.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:73868506 C>T maps to NM_003960.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:73868248 G>A maps to NM_003960.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:72767940 G>A maps to NM_015654.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr1:201752710 G>A maps to ENST00000367296 P845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:201777569 C>T maps to ENST00000367296 H1290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:201781601 C>A maps to ENST00000367296 T1678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:201687829 C>T maps to ENST00000367296 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:201782298 C>T maps to ENST00000367296 G1751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:201687679 G>A maps to ENST00000367296 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:201749584 C>T maps to ENST00000367296 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr1:201777274 C>T maps to ENST00000367296 T1281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:201789018 C>T maps to ENST00000367296 R1865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr11:20065669 C>T maps to ENST00000396087 D1040D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:20005784 C>T maps to ENST00000396087 D943D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:19914120 G>A maps to ENST00000396087 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:20005745 G>A maps to ENST00000396087 R930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:20136217 G>A maps to ENST00000396087 Q2406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:19955766 G>A maps to ENST00000396087 Q682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:20136259 C>T maps to ENST00000396087 V2420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:20112465 T>C maps to ENST00000396087 L1911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr11:19954818 T>C maps to ENST00000396087 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:20075652 G>A maps to ENST00000396087 T1526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:19955643 C>A maps to ENST00000396087 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:20127271 C>T maps to ENST00000396087 I2339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:19954914 G>A maps to ENST00000396087 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:19955157 C>A maps to ENST00000396087 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:20066700 C>T maps to ENST00000396087 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr11:20070510 C>T maps to ENST00000396087 N1403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr12:78512066 C>T maps to NM_014903.4 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr12:78401198 C>T maps to NM_014903.4 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr12:78531116 G>A maps to NM_014903.4 S1534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:78593172 C>T maps to NM_014903.4 R2171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:78444657 G>A maps to NM_014903.4 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:78515773 T>C maps to NM_014903.4 G1268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:78570997 G>A maps to NM_014903.4 E1734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:78582044 A>G maps to NM_014903.4 A1914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr12:78444546 C>A maps to NM_014903.4 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr12:78444542 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:78582420 C>T maps to NM_014903.4 S1951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:78400556 T>C maps to NM_014903.4 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:78400772 A>G maps to NM_014903.4 K485K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr12:78591080 G>T maps to NM_014903.4 G2094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:78582080 C>A maps to NM_014903.4 T1926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr12:78579378 A>G did not map to a codon.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr12:78362414 C>T maps to NM_014903.4 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr12:78513593 C>T maps to NM_014903.4 V1206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:15564501 C>A maps to NM_015909.2 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:15698716 C>T maps to NM_015909.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:15698734 A>C maps to NM_015909.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr2:15564501 C>T maps to NM_015909.2 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:15694240 A>G maps to NM_015909.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:15470730 T>C maps to NM_015909.2 R1446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:15542316 C>A maps to NM_015909.2 E1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:15493714 C>A maps to NM_015909.2 E1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:15506733 G>A maps to NM_015909.2 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:15615948 C>A maps to NM_015909.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:15417143 G>A maps to NM_015909.2 H1740H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr2:15330509 A>G maps to NM_015909.2 I2150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:35770248 T>C maps to ENST00000400445 L1726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr13:35745582 A>C maps to ENST00000400445 R1473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr13:36241641 C>T maps to ENST00000400445 R2845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:36129210 A>G maps to ENST00000400445 E2298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:36241563 G>T maps to ENST00000400445 G2819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:35615081 G>T maps to ENST00000400445 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:35756665 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr13:35806652 G>A maps to ENST00000400445 A1891A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:35731364 C>A maps to ENST00000400445 G934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:35685095 C>T maps to ENST00000400445 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr13:36223811 G>A maps to ENST00000400445 P2576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:35615081 G>T maps to ENST00000400445 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:36026302 G>T maps to ENST00000400445 E2127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:36225940 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:36242644 C>A maps to ENST00000400445 S2913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:36245076 T>G maps to ENST00000400445 A2930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr13:35745554 T>A maps to ENST00000400445 S1463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr13:35806756 G>T did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr13:35806743 C>T maps to ENST00000400445 L1922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr13:35624520 C>T maps to ENST00000400445 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr13:35685047 C>T maps to ENST00000400445 H645H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:36026232 G>A maps to ENST00000400445 T2103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr13:35683424 A>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:36026370 A>T maps to ENST00000400445 A2149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:204031987 C>T maps to NM_001114132.1 R1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:204064098 A>G maps to NM_001114132.1 G2360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:204000785 G>A maps to NM_001114132.1 L1371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr2:204055106 T>C maps to NM_001114132.1 L2277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr2:204034490 C>A maps to NM_001114132.1 R1978R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:47041758 G>A maps to NM_015175.1 S1390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:47043177 G>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:47046043 G>A maps to NM_015175.1 A2086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:47040311 C>T maps to NM_015175.1 D1109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:47037426 C>T maps to NM_015175.1 C679C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:47048572 A>G maps to NM_015175.1 V2384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:19969885 A>G maps to NM_182744.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:19983462 C>T maps to NM_182744.2 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:90967611 T>C maps to NM_002485.4 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr8:90990527 T>C maps to NM_002485.4 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:90967611 T>C maps to NM_002485.4 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr8:90990527 T>C maps to NM_002485.4 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr8:90990527 T>C maps to NM_002485.4 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr8:90993048 A>G maps to NM_002485.4 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr8:90967611 T>C maps to NM_002485.4 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:16895568 G>A maps to NM_017940.3 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:145301792 A>G maps to NM_001039703.4 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:148594437 T>A maps to NM_001170755.1 L604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:148594471 G>A maps to NM_001170755.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:21809743 G>A maps to NM_032264.2 Q589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:21798067 T>C maps to NM_032264.2 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:21797206 C>T maps to NM_032264.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:120381831 C>T maps to NM_001047980.1 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:120378665 G>A maps to NM_001047980.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr1:144619345 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:41343476 G>T maps to NM_005899.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:102705046 G>T maps to NM_032041.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:102701563 G>A maps to NM_032041.2 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:113085202 T>G maps to ENST00000316851 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:113105854 C>T maps to ENST00000316851 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr11:113078647 C>T maps to ENST00000316851 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr11:113105794 C>T maps to ENST00000316851 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:113105854 C>T maps to ENST00000316851 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:113126683 C>T maps to ENST00000316851 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr11:113105875 G>A maps to ENST00000316851 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr11:113131040 C>T maps to ENST00000316851 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr21:22696778 C>T maps to NM_004540.2 C232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr21:22906884 G>T maps to NM_004540.2 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr21:22696811 C>T maps to NM_004540.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr21:22804560 G>A maps to NM_004540.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:22804552 G>T maps to NM_004540.2 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:22849745 G>A maps to NM_004540.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:22707893 G>A maps to NM_004540.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr21:22656720 G>A did not map to a codon.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr21:22906868 C>A maps to NM_004540.2 S765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr21:22710715 T>C maps to NM_004540.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr21:22790889 G>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:22910244 C>A maps to NM_004540.2 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr21:22656720 G>T did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr21:22664430 C>T maps to NM_004540.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr21:22804491 C>T maps to NM_004540.2 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr21:22707872 C>T maps to NM_004540.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr21:22710715 T>C maps to NM_004540.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr19:19360683 G>T maps to NM_004386.2 T1310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr19:19338513 C>T maps to NM_004386.2 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr12:6639918 C>T maps to NM_014865.3 I1300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr12:6637401 C>T maps to NM_014865.3 P1069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:6619271 G>T maps to NM_014865.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr12:6623982 C>G maps to NM_014865.3 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr12:6618881 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:134073970 G>T maps to NM_015261.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:134038945 G>A maps to NM_015261.2 F1035F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:134054647 C>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:17826619 G>A maps to NM_022346.3 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:17826671 G>T maps to NM_022346.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:17842266 T>G maps to NM_022346.3 G935G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:17819712 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr4:17818884 T>C maps to NM_022346.3 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:17841762 G>T maps to NM_022346.3 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:158468255 C>T maps to NM_017760.5 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:158455004 C>A maps to NM_017760.5 E624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:158439242 C>A maps to NM_017760.5 E1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:97009879 T>C maps to NM_015341.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr2:97009957 G>A maps to NM_015341.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:97034756 T>C maps to NM_015341.3 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:97031621 C>T maps to NM_015341.3 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:100403139 T>C maps to NM_002486.4 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:100417227 T>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:196664497 C>T maps to NM_007362.3 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:196664404 G>A maps to NM_007362.3 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:39691371 C>T maps to NM_001001414.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:39691347 G>A maps to NM_001001414.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:36026369 C>T maps to NM_001014839.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:36026544 C>T maps to NM_001014839.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:36029470 C>T maps to NM_001014839.1 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:172363468 A>G maps to NM_001146276.1 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:172351567 G>C maps to NM_001146276.1 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:172353834 A>G maps to NM_001146276.1 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:183556090 G>T maps to NM_001127651.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:183543622 C>T maps to NM_001127651.2 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:183556057 G>A maps to NM_001127651.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:183534890 G>A maps to NM_001127651.2 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr22:37260140 C>T maps to NM_013416.3 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:37260971 C>T maps to NM_013416.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:37267714 C>T maps to NM_013416.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr22:37263467 C>T maps to NM_013416.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:136646929 A>G maps to NM_006153.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:136664707 C>T maps to NM_006153.4 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:106471729 C>T maps to NM_001004720.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:106497916 C>T maps to NM_001004720.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:106498381 G>A maps to NM_001004720.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:106497916 C>T maps to NM_001004720.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:183860523 G>A maps to NM_205842.1 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:183868017 C>T maps to NM_205842.1 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:54920344 G>A maps to NM_005337.4 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr12:54925590 C>T maps to NM_005337.4 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr12:54893248 G>A maps to NM_005337.4 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:54932672 C>A maps to NM_005337.4 A1063A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr12:54920383 A>G maps to NM_005337.4 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr12:54930003 T>C maps to NM_005337.4 S1016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr12:54922030 G>A maps to NM_005337.4 W792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr12:54893248 G>T maps to NM_005337.4 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr12:54893224 C>G maps to NM_005337.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:133541623 C>T maps to NM_207363.2 P920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:133483209 G>A maps to NM_207363.2 S1901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:133483296 G>A maps to NM_207363.2 S1872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:133542553 G>A maps to NM_207363.2 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:133547619 G>A maps to NM_207363.2 H356H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:133539950 A>T maps to NM_207363.2 L1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr2:133538711 A>T maps to NM_207363.2 C1654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:133542436 A>G maps to NM_207363.2 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:133542055 T>C maps to NM_207363.2 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:133541260 C>T maps to NM_207363.2 P1041P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr2:133542615 C>A maps to NM_207363.2 E590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:133547634 G>T maps to NM_207363.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr2:133547619 G>A maps to NM_207363.2 H356H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:50189854 C>T maps to NM_001037806.3 E596E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:50189329 G>A maps to NM_001037806.3 C771C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:50185660 T>C maps to NM_001037806.3 S1322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr12:50185726 G>A maps to NM_001037806.3 A1300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:50185812 G>A maps to NM_001037806.3 R1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:48717269 G>A maps to NM_016453.2 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:48716029 C>T maps to NM_016453.2 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:232320208 G>A maps to NM_005381.2 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:232320767 G>A maps to NM_005381.2 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:232323763 G>A maps to NM_005381.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:232326287 G>A maps to NM_005381.2 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr2:232320316 G>A maps to NM_005381.2 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:232320316 G>A maps to NM_005381.2 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr2:232325560 A>G maps to NM_005381.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:3204719 C>T maps to NM_020170.3 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr19:3207445 C>T maps to NM_020170.3 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:24991196 G>A maps to NM_003743.4 T1421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:24991145 C>T maps to NM_003743.4 G1404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:24951212 T>C maps to NM_003743.4 C918C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:24952626 G>A maps to NM_003743.4 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:24964906 G>A maps to NM_003743.4 P1186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr2:24933966 T>C maps to NM_003743.4 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:24928072 T>C maps to NM_003743.4 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr8:71069189 G>A maps to NM_006540.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:71060637 C>T maps to NM_006540.2 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr8:71071753 T>C maps to NM_006540.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:71078927 C>A maps to NM_006540.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr8:71039197 G>A maps to NM_006540.2 Q1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr8:71075721 A>G maps to NM_006540.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr8:71069189 G>T maps to NM_006540.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr8:71078927 C>T maps to NM_006540.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr20:46279856 G>A maps to NM_181659.2 Q1261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr20:46279862 G>A maps to NM_181659.2 Q1263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:46252780 G>A maps to NM_181659.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr20:46264827 T>C maps to NM_181659.2 D566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:46277795 T>A maps to NM_181659.2 P1198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:46281692 G>A maps to NM_181659.2 Q1380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:46262345 G>A maps to NM_181659.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr10:51581336 C>T maps to NM_001145260.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:44698915 G>A maps to NM_020967.2 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:44699119 G>A maps to NM_020967.2 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr20:44691132 G>A maps to NM_020967.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr20:44699149 G>A maps to NM_020967.2 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr20:33303155 C>A maps to NM_014071.2 A2054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr20:33337888 C>T maps to NM_014071.2 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:33330798 G>A maps to NM_014071.2 S1087S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:33303142 G>A maps to NM_014071.2 R2059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr20:33345740 C>T maps to NM_014071.2 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:33330546 C>T maps to NM_014071.2 S1171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr20:33330879 G>A maps to NM_014071.2 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr20:33345746 T>C maps to NM_014071.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr20:33338032 A>T maps to NM_014071.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr20:33329664 C>T maps to NM_014071.2 S1465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:33337267 G>A maps to NM_014071.2 N910N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr6:126210969 G>A maps to NM_181782.4 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:126211857 A>C maps to NM_181782.4 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr6:126243867 G>A maps to NM_181782.4 W804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:15961009 C>T maps to ENST00000395857 S2085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:16024539 C>A maps to ENST00000395857 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:16029502 C>T maps to ENST00000395857 S509S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-A010-01A-01W-A00E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:15969003 C>T maps to ENST00000395857 A1597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:15968277 T>C maps to ENST00000395857 G1684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr17:15973734 C>T maps to ENST00000395857 P1435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:16012202 C>T maps to ENST00000395857 E693E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:16001703 G>A maps to ENST00000395857 R949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:16024378 C>T maps to ENST00000395857 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:16004982 C>T maps to ENST00000395857 T773T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr17:15971319 G>A maps to ENST00000395857 S1559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:124856704 C>T maps to NM_006312.4 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:124950760 C>T maps to NM_006312.4 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:124832780 C>T maps to NM_006312.4 K1315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:124835268 G>A maps to NM_006312.4 D1243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr12:124829398 G>A maps to NM_006312.4 P1493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:124831352 A>C maps to NM_006312.4 R1379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:124856680 G>A maps to NM_006312.4 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr12:124904571 G>A maps to NM_006312.4 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr12:124856836 G>A maps to NM_006312.4 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:124809980 G>A maps to NM_006312.4 C2511C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:124886969 G>A maps to NM_006312.4 N540N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:124887098 T>C maps to NM_006312.4 Q497Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:124824664 C>T maps to NM_006312.4 S1865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr19:55421378 C>T maps to NM_004829.5 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr19:55420746 G>T maps to NM_004829.5 G167*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A6-6653-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:41318517 T>G maps to NM_004828.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:41318496 G>A maps to NM_004828.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr6:31557742 A>G maps to NM_147130.2 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr9:132988708 T>G maps to NM_014286.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:160321857 C>A maps to NM_015331.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:160323963 C>A maps to NM_015331.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:160327988 C>T maps to NM_015331.2 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:160319949 G>A maps to NM_015331.2 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:160324012 C>T maps to NM_015331.2 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:2578015 C>T maps to NM_006101.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr18:2595454 A>G maps to NM_006101.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:15761297 T>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:15788109 C>T maps to NM_001143979.1 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:15771692 G>A maps to NM_001143979.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:8358112 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:141511419 T>C maps to NM_030571.3 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:141511396 G>T maps to NM_030571.3 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr13:80095012 G>A maps to NM_019080.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:80095081 T>C maps to NM_019080.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:23931487 G>A maps to NM_002487.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:23931647 G>A maps to NM_002487.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr15:23931755 G>A maps to NM_002487.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:29561224 G>A maps to NM_138704.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:140110117 C>T maps to NM_001144026.1 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:140107030 C>T maps to NM_001144026.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:43817825 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr8:134274321 G>T maps to NM_006096.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:134251195 G>A maps to NM_006096.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr8:134260980 C>T maps to NM_006096.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:21490566 G>A maps to NM_201537.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:21491462 C>T maps to NM_201537.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr14:21490581 C>T maps to NM_201537.1 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr14:21490016 G>A maps to NM_201537.1 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:21491452 G>A maps to NM_201537.1 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr20:35282006 G>T maps to ENST00000373803 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:35288784 G>A maps to ENST00000373803 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr20:35315899 T>A maps to ENST00000373803 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr20:35288778 G>A maps to ENST00000373803 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:149918809 C>T maps to NM_001543.4 C486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr5:149914444 C>T maps to NM_001543.4 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:149901094 C>T maps to NM_001543.4 Y93Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:149932867 C>T maps to NM_001543.4 R875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr10:75566082 G>A maps to NM_003635.3 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr4:118975346 C>T maps to NM_004784.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:119064809 G>T maps to NM_004784.2 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr4:118975856 T>C maps to NM_004784.2 H264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr4:115997241 T>C maps to NM_022569.1 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr4:115997241 T>C maps to NM_022569.1 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:115997436 G>T maps to NM_022569.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:115998158 G>A maps to NM_022569.1 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr4:115773914 T>C maps to NM_022569.1 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr4:115997241 T>C maps to NM_022569.1 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:119007320 C>T did not map to a codon.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr23:119005967 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:240960716 A>G maps to ENST00000404554 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:240954169 G>A maps to ENST00000404554 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:240951032 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:140026865 C>T maps to NM_002488.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:140027138 G>A maps to NM_002488.4 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:10977770 C>T maps to NM_002489.2 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:123185667 A>G maps to NM_005000.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr9:124910447 G>A maps to NM_014222.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:124906618 A>G maps to NM_014222.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:124914612 C>T maps to NM_014222.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:124906618 A>G maps to NM_014222.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:23598553 G>A maps to NM_005003.2 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr15:41687143 C>T maps to NM_016013.2 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:97339060 C>A maps to NM_014165.3 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:47003917 G>A did not map to a codon.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr23:47001817 G>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:47002068 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr7:140402693 C>A maps to NM_004546.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr3:120320070 C>T maps to NM_004547.5 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:120320109 T>C maps to NM_001168331.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:179332766 C>T maps to NM_002492.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:179334769 G>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:179341726 C>T maps to NM_002492.2 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:14677653 C>T maps to NM_004146.4 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:14677706 G>A maps to NM_004146.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:77790753 G>A maps to NM_004549.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:206991489 G>A maps to ENST00000455934 R669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr2:206997667 C>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:206988980 T>C maps to ENST00000455934 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:206994850 G>A maps to ENST00000455934 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:161173224 A>G did not map to a codon.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr1:161176279 C>T maps to NM_004550.4 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:52942235 G>A did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr5:1814532 C>T maps to ENST00000469176 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:67800438 C>T maps to NM_002496.3 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:67803781 C>T maps to NM_002496.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr11:67377973 G>A maps to NM_007103.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr18:9122636 C>T maps to NM_021074.4 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr21:44323481 T>C maps to NM_021075.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr21:44329046 G>A maps to NM_021075.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr21:44323481 T>C maps to NM_021075.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr21:44323481 T>C maps to NM_021075.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:44323382 G>A maps to NM_021075.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:152482050 A>G maps to NM_001164507.1 S3483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr2:152550884 G>A maps to NM_001164507.1 D616D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:152528900 G>T maps to NM_001164507.1 V1427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr2:152354773 C>A maps to NM_001164507.1 S8069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:152362071 C>A maps to NM_001164507.1 E7888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:152362069 T>C maps to NM_001164507.1 E7888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:152584336 C>T maps to NM_001164507.1 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr2:152484189 G>A maps to NM_001164507.1 S3330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr2:152527650 G>A maps to NM_001164507.1 G1464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:152417135 G>A maps to NM_001164507.1 H6428H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:152507180 G>A maps to NM_001164507.1 D2378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:152383461 G>A maps to NM_001164507.1 L7305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:152500574 G>A maps to NM_001164507.1 D2571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:152394411 G>A maps to NM_001164507.1 R7026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:152541390 G>A maps to NM_001164507.1 A912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:152511794 G>A maps to NM_001164507.1 L2266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:152376261 G>A maps to NM_001164507.1 F7500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:152417609 C>A maps to NM_001164507.1 E6372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:152471029 C>T maps to NM_001164507.1 P3787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:152544142 G>A maps to NM_001164507.1 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:152350674 C>A maps to NM_001164507.1 S8193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:152506853 C>A maps to NM_001164507.1 G2423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:152371376 C>T maps to NM_001164507.1 T7657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:152342309 G>A maps to NM_001164507.1 T8514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:152425129 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:152467089 A>G maps to NM_001164507.1 D3986D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:152512664 A>G did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr2:152381064 G>T maps to NM_001164507.1 I7446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr2:152409184 C>T did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:152362069 T>C maps to NM_001164507.1 E7888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:152409233 A>G maps to NM_001164507.1 D6596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:152482050 A>G maps to NM_001164507.1 S3483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr2:152528930 G>A maps to NM_001164507.1 D1417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr2:152477449 G>T maps to NM_001164507.1 R3515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:152589658 G>A maps to NM_001164507.1 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:152521900 G>A maps to NM_001164507.1 A1728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:152363467 C>T maps to NM_001164507.1 T7837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:21124456 T>A maps to ENST00000430741 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:21098789 G>A maps to ENST00000430741 F854F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:21074831 G>A maps to ENST00000430741 Y965Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:21074777 G>A maps to ENST00000430741 I983I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr10:21097466 A>G maps to ENST00000430741 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr10:21101809 G>A maps to ENST00000430741 D804D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr10:21101809 G>A maps to ENST00000430741 D804D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr10:21129729 C>A maps to ENST00000430741 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:91929793 G>A maps to NM_022351.4 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr16:84024175 G>A maps to NM_019065.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr16:84024157 G>A maps to NM_019065.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:84024133 G>A maps to NM_019065.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr20:32248099 C>T maps to NM_031232.3 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr12:8245637 A>G maps to NM_015509.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr12:8245637 A>G maps to NM_015509.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr12:97313767 T>C maps to NM_001135175.1 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr12:97330427 G>A maps to NM_001135175.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:56208894 G>A maps to ENST00000508342 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:56155253 T>C maps to ENST00000508342 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:56155178 A>G maps to ENST00000508342 D621D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:56155238 G>A maps to ENST00000508342 C601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr15:56155112 A>G maps to ENST00000508342 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:56208642 A>G maps to ENST00000508342 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:56208834 G>A maps to ENST00000508342 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr15:56208960 G>A maps to ENST00000508342 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr18:56033343 G>A maps to NM_001144967.1 W649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:55990491 C>T maps to NM_001144967.1 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr18:56035034 G>A maps to NM_001144967.1 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr18:56018257 A>G maps to NM_001144967.1 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:55992307 G>A maps to NM_001144967.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:11185670 C>T maps to NM_006403.3 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:11185844 C>T maps to NM_006403.3 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr6:11185547 G>A maps to NM_006403.3 C784C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:11185844 C>T maps to NM_006403.3 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:11213516 T>C maps to NM_006403.3 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:11191045 C>T maps to NM_006403.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:29886484 G>A maps to NM_021076.3 P952P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr22:29886007 C>A maps to NM_021076.3 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:24813234 G>A maps to ENST00000221169 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:24811752 C>A maps to ENST00000221169 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:24813468 G>A maps to ENST00000221169 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:24811735 G>C maps to ENST00000221169 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:24772061 G>A maps to NM_005382.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:24774807 G>A maps to NM_005382.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:24771383 C>T maps to NM_005382.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:24773236 G>A maps to NM_005382.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr1:72058512 G>A maps to NM_173808.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:71873176 C>T maps to NM_173808.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr1:72076743 C>T maps to NM_173808.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:72163742 C>A maps to NM_173808.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:75641602 G>A maps to NM_024608.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr8:11643754 G>A maps to NM_145043.2 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:178256850 C>T maps to NM_018248.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:178274762 A>C maps to NM_018248.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:178283507 G>A maps to NM_018248.2 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:178283451 T>C maps to NM_018248.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr4:178283451 T>C maps to NM_018248.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr4:178283451 T>C maps to NM_018248.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr4:178283451 T>C maps to NM_018248.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr4:170523745 T>C maps to ENST00000507142 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr4:170523706 T>C maps to ENST00000507142 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:170384420 G>A maps to ENST00000507142 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr4:170321505 A>T maps to ENST00000507142 A1239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:170345784 C>T maps to ENST00000507142 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr4:170498216 A>G maps to ENST00000507142 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr4:170321764 G>A maps to ENST00000507142 C1207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr4:170508742 A>G maps to ENST00000507142 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr4:170498216 A>G maps to ENST00000507142 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:170498216 A>G maps to ENST00000507142 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr4:170508742 A>G maps to ENST00000507142 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr4:170508742 A>G maps to ENST00000507142 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:170354745 G>A maps to ENST00000507142 C945C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:27332146 T>C maps to ENST00000396636 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:27346425 C>T maps to ENST00000396636 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr3:27332146 T>C maps to ENST00000396636 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:130887691 G>T maps to NM_024800.4 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:130871279 C>T maps to NM_024800.4 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:130852755 T>C maps to NM_024800.4 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:130962338 A>G maps to NM_024800.4 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:130884282 G>T maps to NM_024800.4 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:130889729 T>C maps to NM_024800.4 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:52725345 G>T maps to NM_002498.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:52728226 C>A maps to NM_002498.2 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:52771703 T>C maps to NM_003157.4 R777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr3:52777433 T>C maps to NM_003157.4 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr13:52661488 G>A maps to NM_199289.1 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr13:52639602 G>A maps to NM_199289.1 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:52639734 C>T maps to NM_199289.1 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:52667335 G>A maps to NM_199289.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr13:52676385 G>A maps to NM_199289.1 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:127089683 C>T maps to NM_001166171.1 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr9:127089650 G>A maps to NM_001166171.1 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr9:127083820 C>T maps to NM_001166171.1 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:198288567 C>T maps to NM_133494.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:198201739 G>A maps to NM_133494.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:27065716 C>T maps to NM_178170.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr17:27068231 C>T maps to NM_178170.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:27061207 T>C did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr17:27068192 T>A maps to NM_178170.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr14:75553927 A>G maps to NM_033116.4 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:75567725 G>A maps to NM_033116.4 C657C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:75557977 G>A maps to NM_033116.4 R813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:75576447 G>T maps to NM_033116.4 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr14:75580923 A>G maps to NM_033116.4 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:140344072 T>C maps to NM_001130969.1 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:20805296 G>T maps to NM_006157.3 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr11:20968916 T>C maps to NM_006157.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:20968916 T>C maps to NM_006157.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr11:21250968 G>A maps to NM_006157.3 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr12:44902736 G>A maps to NM_001145107.1 Q861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:45097532 G>A maps to NM_001145107.1 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:45059270 A>G maps to NM_001145107.1 C530C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr12:44915940 G>A maps to NM_001145107.1 R723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr12:45170848 A>G maps to NM_001145107.1 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:44902731 G>A maps to NM_001145107.1 C862C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr12:44926361 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:45097553 G>A maps to NM_001145107.1 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:45168538 C>A maps to NM_001145107.1 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:45169848 C>A maps to NM_001145107.1 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr12:44926361 A>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr15:73409115 T>C maps to NM_002499.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:73418869 C>A maps to NM_002499.3 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:73528769 G>A maps to NM_002499.3 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:73590696 C>T maps to NM_002499.3 R1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:73562483 C>T maps to NM_002499.3 D876D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:156643276 G>A maps to NM_006617.1 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:156641951 C>T maps to NM_006617.1 E676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr1:156640547 T>C maps to NM_006617.1 L1144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:5498099 C>T maps to NM_001047160.1 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:5494321 C>A maps to NM_001047160.1 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:5494837 C>T maps to NM_001047160.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:5496269 C>T maps to NM_001047160.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr18:70417778 C>G maps to NM_153181.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr18:70461477 C>T maps to NM_153181.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr18:70526130 T>C maps to NM_153181.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:47162458 C>T maps to NM_018092.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:47120188 G>A maps to NM_018092.3 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:47163237 G>T maps to NM_018092.3 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:47162394 G>A maps to NM_018092.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:47117581 C>T maps to NM_018092.3 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr6:31829869 C>T maps to NM_000434.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:31829854 G>A maps to NM_000434.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr6:31827957 G>A maps to NM_000434.3 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:233899361 C>A maps to NM_005383.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:233897446 C>T maps to NM_005383.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:242757596 G>A maps to NM_001167599.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:242758232 G>A maps to NM_001167599.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:7221384 G>A maps to NM_032442.2 P1353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:7230149 G>A maps to NM_032442.2 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:7229597 G>A maps to NM_032442.2 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:7230149 G>A maps to NM_032442.2 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:7231161 C>T maps to NM_032442.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:7220893 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:182542518 A>G maps to NM_002500.2 *357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr2:182542762 C>T maps to NM_002500.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:182543230 C>T maps to NM_002500.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:182542900 C>T maps to NM_002500.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:37762591 C>T maps to NM_006160.3 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:37762570 G>A maps to NM_006160.3 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr12:55420537 C>T maps to NM_021191.2 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr12:55420484 C>T maps to NM_021191.2 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr7:31378582 G>A maps to NM_022728.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr7:31378399 G>A maps to NM_022728.2 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:31378053 C>A maps to NM_022728.2 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr7:31378707 C>A maps to NM_022728.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:31378198 G>T maps to NM_022728.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr7:31378426 G>A maps to NM_022728.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:134870878 G>A maps to NM_006161.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr5:134870972 G>A maps to NM_006161.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:113435914 C>T maps to NM_024019.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:113436103 G>A maps to NM_024019.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:71332228 G>A maps to NM_020999.3 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:78408291 G>A maps to NM_144573.3 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:78407847 A>G maps to NM_144573.3 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr1:78399083 C>T maps to NM_144573.3 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:78383808 G>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:78408366 C>T maps to NM_144573.3 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr17:29556080 A>G maps to NM_001042492.2 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr17:29575999 A>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:29559778 C>T maps to NM_001042492.2 Q1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr17:29586048 G>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr17:29546064 G>T maps to NM_001042492.2 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr17:29677226 C>T maps to NM_001042492.2 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr17:29528488 C>A maps to NM_001042492.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:29687578 A>G maps to NM_001042492.2 G2745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr17:29677294 T>A maps to NM_001042492.2 P2472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:29556080 A>G maps to NM_001042492.2 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:29562640 C>A maps to NM_001042492.2 R1241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:29677330 C>A maps to NM_001042492.2 S2484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:29683508 A>G maps to NM_001042492.2 S2549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:29556483 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:29677309 C>A maps to NM_001042492.2 P2477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:29701166 C>T maps to NM_001042492.2 I2838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr17:29588726 A>G did not map to a codon.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr17:29654737 C>A maps to NM_001042492.2 R1830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:29662015 T>C maps to NM_001042492.2 S1991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:29677294 T>A maps to NM_001042492.2 P2472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr17:29588726 A>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr17:29546051 A>G maps to NM_001042492.2 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr17:29486095 A>G maps to NM_001042492.2 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:29677226 C>T maps to NM_001042492.2 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:29684325 C>T maps to NM_001042492.2 R2637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:29687608 C>A maps to NM_001042492.2 L2755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr17:29562980 C>T maps to NM_001042492.2 R1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:29553696 C>A maps to NM_001042492.2 S749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr17:29684029 A>G maps to NM_001042492.2 S2597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:29546051 A>G maps to NM_001042492.2 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr17:29586048 G>T did not map to a codon.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr17:29667608 A>G maps to NM_001042492.2 A2336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr17:29496909 T>C maps to NM_001042492.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:29683508 A>G maps to NM_001042492.2 S2549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr17:29592289 T>C maps to NM_001042492.2 L1590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr17:29562692 G>A maps to NM_001042492.2 W1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr17:29654770 A>G maps to NM_001042492.2 Q1841Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr17:29556177 G>T maps to NM_001042492.2 G849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr17:29687578 A>T maps to NM_001042492.2 G2745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:29486044 T>C maps to NM_001042492.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr17:29496968 A>G maps to NM_001042492.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr17:29562642 A>G maps to NM_001042492.2 R1241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:29679349 C>T maps to NM_001042492.2 V2511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr17:29486025 A>G did not map to a codon.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr17:29546136 G>A did not map to a codon.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr17:29679273 G>A did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:29592289 T>C maps to NM_001042492.2 L1590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr17:29592289 T>C maps to NM_001042492.2 L1590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr17:29548884 T>C maps to NM_001042492.2 H553H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr17:29508726 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr17:29576110 C>T maps to NM_001042492.2 R1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr17:29677309 C>A maps to NM_001042492.2 P2477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr17:29588752 A>G maps to NM_001042492.2 R1534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr17:29664431 A>G maps to NM_001042492.2 L2158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:29562980 C>T maps to NM_001042492.2 R1306*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-F4-6807-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:29559777 G>A maps to NM_001042492.2 A1125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr17:29560068 T>C maps to NM_001042492.2 V1182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr17:29664407 A>G maps to NM_001042492.2 R2150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr17:29548865 A>G did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr17:29562626 A>G did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr17:29664407 A>G maps to NM_001042492.2 R2150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr17:29654552 C>T maps to NM_001042492.2 R1769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr17:29684284 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:29497002 C>T maps to NM_001042492.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:29679273 G>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:29683508 A>G maps to NM_001042492.2 S2549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:29508753 T>C maps to NM_001042492.2 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr17:29533377 C>A maps to NM_001042492.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:29546105 C>T maps to NM_001042492.2 H537H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:29679432 G>A did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr22:30038188 A>G did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr22:30069332 C>T maps to NM_181832.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr22:30054176 G>T did not map to a codon.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr22:30054253 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:30077550 C>T maps to NM_181832.2 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr22:30035155 A>G maps to NM_181832.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr22:30057325 G>T maps to NM_181832.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr22:30035155 A>G maps to NM_181832.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:30069332 C>T maps to NM_181832.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr22:30051665 G>C did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr22:30067835 C>T maps to NM_181832.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr22:30050698 A>G maps to NM_181832.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr22:30035155 A>G maps to NM_181832.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr22:30051659 A>G maps to NM_181832.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:30032762 C>A maps to NM_181832.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr22:30032762 C>A maps to NM_181832.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr22:30050698 A>G maps to NM_181832.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr22:30035098 A>G maps to NM_181832.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:30035140 T>C maps to NM_181832.2 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr22:30038188 A>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr22:30061034 G>A maps to NM_181832.2 K289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr22:30054175 A>G did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr22:30070830 A>G maps to NM_181832.2 K449K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr22:30050643 A>G did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr22:30032813 A>G maps to NM_181832.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr22:30051596 T>C maps to NM_181832.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr22:30054211 C>T maps to NM_181832.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr22:30035140 T>C maps to NM_181832.2 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr22:30035097 C>A maps to NM_181832.2 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr22:30051596 T>C maps to NM_181832.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr22:30054175 A>G did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr22:30051659 A>G maps to NM_181832.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr22:30054211 C>T maps to NM_181832.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr22:30051656 C>T maps to NM_181832.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr22:30070822 A>G did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr22:30032746 G>A maps to NM_181832.2 W41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr22:30050665 T>C maps to NM_181832.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr22:30069353 C>T maps to NM_181832.2 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr22:30070858 C>T maps to NM_181832.2 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr22:30070891 C>T maps to NM_181832.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr22:30050643 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr22:30070881 A>G maps to NM_181832.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr22:30054240 C>T maps to NM_181832.2 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr22:30069416 C>T maps to NM_181832.2 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr22:30051596 T>C maps to NM_181832.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr22:30032793 C>T maps to NM_181832.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:30054198 T>C maps to NM_181832.2 Y207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr22:30069362 C>T maps to NM_181832.2 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:42805530 C>T maps to NM_145912.5 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:204978742 C>T maps to ENST00000367172 C1223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:204937482 C>T maps to ENST00000367172 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:204923323 G>A maps to ENST00000367172 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:204913508 C>T maps to ENST00000367172 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr1:204942403 C>A maps to ENST00000367172 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:204937476 C>T maps to ENST00000367172 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:204953167 G>A maps to ENST00000367172 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr1:204950994 C>T maps to ENST00000367172 R773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:204943898 C>T maps to ENST00000367172 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr1:204978799 C>T maps to ENST00000367172 R1242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr1:204953227 C>T maps to ENST00000367172 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:204956568 C>T maps to ENST00000367172 R939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr1:204943328 G>A maps to ENST00000367172 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr16:69681174 T>C maps to NM_138713.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr16:69726307 C>T maps to NM_138713.2 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:69689702 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr18:77171120 G>A maps to NM_172387.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:77170865 C>T maps to NM_172387.1 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:77170862 G>A maps to NM_172387.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr18:77170997 G>A maps to NM_172387.1 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:50092116 G>A maps to NM_012340.3 H471H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:50139714 G>A maps to NM_012340.3 C355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr20:50139645 C>T maps to NM_012340.3 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr20:50049243 G>A maps to NM_012340.3 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr20:50140068 G>T maps to NM_012340.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:68224770 A>G maps to NM_173165.2 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:68200794 C>T maps to NM_173165.2 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:24841677 C>T maps to NM_001136022.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr14:24839674 A>G maps to NM_001136022.1 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr14:24839258 C>A maps to NM_001136022.1 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:24844890 G>A maps to NM_001136022.1 E696E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:24838822 G>A maps to NM_001136022.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:54686928 A>G maps to NM_001136023.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:54686852 C>A maps to NM_001136023.1 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr17:46136900 G>C maps to ENST00000362042 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:46136912 C>T maps to ENST00000362042 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:26225318 C>T maps to NM_004289.6 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr1:61553862 C>T maps to NM_001145512.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr1:61872391 G>A maps to NM_001145512.1 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr9:14307411 C>T maps to ENST00000397581 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:14150222 C>A maps to ENST00000397581 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:14307185 G>A maps to ENST00000397581 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:14307165 C>T maps to ENST00000397581 W128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:3452507 C>T maps to ENST00000269778 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:94172200 C>T maps to NM_005384.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:94172545 G>A maps to NM_005384.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:94171972 C>T maps to NM_005384.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:13136326 G>T maps to ENST00000397661 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr19:13189496 G>A maps to ENST00000397661 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr4:103488230 G>T maps to NM_003998.3 G116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:103505915 G>T maps to NM_003998.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:103528828 T>C maps to NM_003998.3 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:104160228 G>A maps to NM_001077494.1 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:104160935 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr14:35871224 C>T maps to NM_020529.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr19:36380911 A>G maps to ENST00000352614 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:36387010 C>T maps to ENST00000352614 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:31526321 C>A maps to NM_005007.3 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:31526297 C>T maps to NM_005007.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:31526336 A>C maps to NM_005007.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:101572404 T>C maps to NM_031419.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:129747234 C>T maps to NM_006165.3 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:129739447 C>A maps to NM_006165.3 G1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:129744712 A>G maps to NM_006165.3 H676H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:33294461 G>T maps to NM_002504.4 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:33352712 C>T maps to NM_002504.4 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:47853935 A>G maps to NM_152995.4 R815R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:41062196 A>T maps to NM_002505.4 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr1:41223897 C>T maps to ENST00000308733 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr14:77732898 G>A maps to NM_021257.3 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:23947228 G>A maps to NM_001042635.1 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:23944941 T>C maps to NM_001042635.1 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:233748704 G>A maps to NM_019850.2 C529C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:233785014 G>A maps to NM_019850.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr2:233750019 G>A maps to NM_019850.2 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:233750055 G>A maps to NM_019850.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:233759569 G>A maps to NM_019850.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:233791862 C>T maps to NM_019850.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:115828849 G>A maps to NM_002506.2 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:115828996 G>A maps to NM_002506.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:115829296 A>G maps to NM_002506.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:47583925 C>A maps to NM_002507.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr17:47587999 C>T maps to NM_002507.3 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:47583910 G>A maps to NM_002507.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:102632481 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:102632644 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:102632629 A>G did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:25770802 C>A maps to NM_018297.3 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:25781137 G>A maps to NM_018297.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr15:90814446 C>G maps to NM_001033088.1 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:90815010 C>T maps to NM_001033088.1 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:103911034 C>A maps to NM_139173.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:103866372 G>T maps to NM_139173.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:103970156 G>A maps to NM_178833.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:103964458 G>A maps to NM_178833.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:116380915 G>A maps to NM_005599.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr6:18122198 G>T maps to NM_198586.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:18122369 T>C maps to NM_198586.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:18122345 A>G maps to NM_198586.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr6:18121982 C>G maps to NM_198586.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:115662228 G>T did not map to a codon.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr10:115661631 C>T maps to NM_198514.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr10:115661490 C>T maps to NM_198514.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:42071038 G>T maps to ENST00000402458 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:17750441 G>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:17750143 A>G did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:17750486 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:17710527 A>G did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:17739579 A>G did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:17746105 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:17750147 C>T did not map to a codon.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr23:17742543 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:17705888 A>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:17750036 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:17750207 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:17743727 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:17745045 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:17745046 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:17746116 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:17750347 T>C did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:17705899 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:17750058 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:17745120 T>G did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr23:17743956 T>C did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:17746786 A>G did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:17745632 C>T did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:17710475 G>A did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr23:17746117 G>A did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:17743981 C>T did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:17750206 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:17750208 C>T did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:17710475 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:17742490 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:17750347 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:17745771 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:71352008 C>A did not map to a codon.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr23:71360135 C>T did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:71359950 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:71358705 G>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:71359503 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:71358768 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:71359299 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr23:71358843 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:71359836 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:71359815 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:71359688 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:71362116 T>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:71357065 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:71359488 G>T did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:71363198 T>C did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:71360407 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:71360492 C>T did not map to a codon.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr3:49462420 G>A maps to NM_032316.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:236189325 G>A maps to NM_002508.2 C618C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr1:236189409 C>T maps to NM_002508.2 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:236156945 C>T maps to NM_002508.2 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:236192895 G>A maps to NM_002508.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:236212061 G>A maps to NM_002508.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr1:236175230 G>A maps to NM_002508.2 C839C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr1:236189439 C>T maps to NM_002508.2 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:236141178 G>A maps to NM_002508.2 I1244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:236189235 G>T maps to NM_002508.2 I648I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr1:236144993 C>T maps to NM_002508.2 A1048A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:236157065 G>A maps to NM_002508.2 C878C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr1:236205354 G>A maps to NM_002508.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr1:236208774 G>C maps to NM_002508.2 S245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr1:236212085 C>A maps to NM_002508.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:236195893 C>T maps to NM_002508.2 Q448Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:236212100 G>A maps to NM_002508.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:52534587 C>T maps to NM_007361.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr14:52534611 G>C maps to NM_007361.3 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:52477690 T>A maps to NM_007361.3 K1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr14:52477601 T>C maps to NM_007361.3 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr14:52477601 T>C maps to NM_007361.3 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:201768296 C>T maps to NM_001136039.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:201756680 C>T maps to NM_001136039.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:201756680 C>T maps to NM_001136039.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:51208425 G>A maps to NM_020921.3 T1774T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:51259465 C>T maps to NM_020921.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr14:51219333 G>A maps to NM_020921.3 L1618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr14:51239693 T>C maps to NM_020921.3 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr14:51259465 C>T maps to NM_020921.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:51223928 G>A maps to NM_020921.3 Y1273Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:51211026 G>A maps to NM_020921.3 S1707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:51226987 C>T maps to NM_020921.3 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr14:51230542 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:51196405 C>T maps to NM_020921.3 P1971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:51223676 G>A maps to NM_020921.3 I1357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr14:51221339 C>A maps to NM_020921.3 E1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr14:51221337 T>C maps to NM_020921.3 E1559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr14:51221337 T>C maps to NM_020921.3 E1559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr14:51239693 T>C maps to NM_020921.3 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:51259462 C>T maps to NM_020921.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr14:51223868 C>T maps to NM_020921.3 E1293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr14:51221337 T>C maps to NM_020921.3 E1559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:51225254 G>A maps to NM_020921.3 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr14:51239693 T>C maps to NM_020921.3 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr12:675224 C>T maps to NM_016533.4 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr12:674562 C>T maps to NM_016533.4 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr20:25434250 G>A maps to NM_025176.4 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr20:25507058 G>A maps to NM_025176.4 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:25469915 G>A maps to NM_025176.4 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:25459617 G>T maps to NM_025176.4 C714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr16:69375524 A>G maps to NM_016101.4 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:23048918 G>A maps to NM_144599.4 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:23014496 C>T maps to NM_030922.6 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr4:48036954 C>G maps to NM_207330.1 G173G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A6-5660-01A-01D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:24795491 C>T maps to NM_020448.4 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:24766675 C>T maps to NM_020448.4 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:24768666 C>A maps to NM_020448.4 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr1:24779983 G>T maps to NM_020448.4 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:24768663 C>T maps to NM_020448.4 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:156899376 C>T maps to NM_001099287.1 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr5:156894063 A>G maps to NM_001099287.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:156887237 C>T maps to NM_001099287.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:37026374 T>C maps to NM_133433.3 T1918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:37061003 C>T maps to NM_133433.3 R2582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr5:37019432 A>G maps to NM_133433.3 E1647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:37052523 A>G maps to NM_133433.3 T2373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:37052508 A>G maps to NM_133433.3 Q2368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:36985781 C>T maps to NM_133433.3 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr5:36985786 G>A maps to NM_133433.3 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:37019430 G>T maps to NM_133433.3 E1647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr5:37019432 A>G maps to NM_133433.3 E1647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:36985863 C>G maps to NM_133433.3 S861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:37020619 A>G maps to NM_133433.3 K1690K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:37019432 A>G maps to NM_133433.3 E1647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr5:37019432 A>G maps to NM_133433.3 E1647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr5:37026374 T>C maps to NM_133433.3 T1918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:37006463 C>T maps to NM_133433.3 N1287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:36976463 T>C maps to NM_133433.3 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:29957619 G>A maps to NM_003634.2 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr22:29956798 G>T maps to NM_003634.2 Y210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr9:107513400 A>C maps to NM_015469.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:107513234 A>C did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:52525419 G>A maps to NM_007184.3 T1265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:52521682 C>T maps to NM_007184.3 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:52521274 C>A maps to NM_007184.3 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:52526017 C>T maps to NM_007184.3 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:52492814 C>T maps to NM_007184.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:52505923 C>T maps to NM_007184.3 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:100058050 T>G did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr1:31654747 C>T maps to NM_024522.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:63659612 C>T maps to NM_173688.2 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:61878932 G>A maps to NM_152864.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:61881301 C>T maps to NM_152864.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:119077503 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:119070327 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:119070615 T>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:119077310 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:119068480 T>C did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:28227472 G>A maps to NM_001007531.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:28227547 G>A maps to NM_001007531.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:28228054 C>T maps to NM_001007531.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr6:28228097 C>T maps to NM_001007531.1 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:28227718 G>A maps to NM_001007531.1 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:50659454 G>A maps to NM_033119.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:50667158 C>T maps to NM_033119.3 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:50667214 C>T maps to NM_033119.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:51875675 A>G maps to NM_005601.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:23942373 A>G maps to NM_020345.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:45661945 A>G maps to NM_198478.3 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:45656446 C>T maps to NM_198478.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:118726447 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:118724903 A>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:118723999 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:118723741 A>G did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:118724026 G>A did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:118724538 G>C did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:42680648 A>G maps to NM_005385.3 A1151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:42680192 G>A maps to NM_005385.3 G999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:36986893 G>A maps to NM_001079668.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:36986602 G>A maps to NM_001079668.2 H362H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr14:36986893 G>A maps to NM_001079668.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:21492731 C>T maps to NM_002509.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:21492749 G>A maps to NM_002509.2 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr5:172659670 G>A maps to NM_004387.3 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:172659670 G>A maps to NM_004387.3 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:37050637 C>T maps to NM_014360.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr8:23538844 C>T maps to NM_006167.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:23539068 G>A maps to NM_006167.3 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:13543766 C>T maps to NM_001189.3 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr8:41504033 G>T maps to ENST00000425142 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:33460468 C>T maps to NM_018096.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr17:33463389 G>A maps to NM_018096.3 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr17:33460441 G>C maps to NM_018096.3 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:33464118 G>A maps to NM_018096.3 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:173997152 G>A maps to NM_014932.2 K454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr3:173998300 G>A maps to NM_014932.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:173997236 T>C maps to NM_014932.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:173525590 C>T maps to NM_014932.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr3:173525521 C>A maps to NM_014932.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr3:173997110 T>A maps to NM_014932.2 Y440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:173997242 C>G maps to NM_014932.2 Y484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:7315506 G>A maps to NM_020795.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:7318452 C>T maps to NM_020795.2 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:7318862 C>T maps to NM_020795.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:7318114 C>T maps to NM_020795.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:70387486 A>G did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:70367791 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:70389349 G>A did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:70387437 C>T did not map to a codon.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr23:70389789 G>A did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:70387357 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:70389283 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:70387253 T>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:70375106 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:70387355 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:70389791 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:70367944 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:70367719 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:70387083 T>C did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:70389799 G>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:70367694 G>A did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:70387495 G>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:5947359 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:5811020 G>A did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:5827265 C>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:5810934 A>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:5811120 T>C did not map to a codon.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr23:5827153 A>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:5821414 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:5821623 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:5811129 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:5811292 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:5811553 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:6069177 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:5811553 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr23:6069465 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:5821527 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr23:5811431 C>T did not map to a codon.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr23:5821545 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:5821797 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:5947386 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:5821254 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:5811553 C>T did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:5811554 G>A did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:5811268 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:5821237 G>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:6069119 C>T did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr23:5821284 G>A did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:5810990 A>C did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:5947402 G>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:5827265 C>T did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:6069403 T>G did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:6069222 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:5827265 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:5811014 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:5811009 A>G did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:5827226 G>A did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:5827265 C>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:5821255 G>A did not map to a codon.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr24:16942082 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr24:16845405 A>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr24:16845415 G>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr24:16734353 T>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr24:16952603 G>A did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr24:16952991 G>A did not map to a codon.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr24:16941908 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr24:16835134 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:16734145 C>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr24:16942232 G>A did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr24:16734218 T>G did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:26369982 C>T maps to NM_016231.4 H28H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:26495676 T>C maps to NM_016231.4 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:26370039 C>T maps to NM_016231.4 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr17:26495664 A>G maps to NM_016231.4 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr17:26495664 A>G maps to NM_016231.4 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr5:65105484 C>T maps to NM_020726.4 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:3598190 G>A maps to ENST00000448023 G951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr16:3613716 C>T maps to ENST00000448023 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:3613578 G>A maps to ENST00000448023 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr16:3614703 C>T maps to ENST00000448023 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:3614340 C>T maps to ENST00000448023 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:3594301 G>A maps to ENST00000448023 D979D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:32476185 G>T maps to NM_021209.4 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:32475575 G>A maps to NM_021209.4 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:32475575 G>A maps to NM_021209.4 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:32476083 G>A maps to NM_021209.4 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:32477623 G>A maps to NM_021209.4 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:32475575 G>A maps to NM_021209.4 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:32475264 C>T maps to NM_021209.4 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr2:32475575 G>A maps to NM_021209.4 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:32475575 G>A maps to NM_021209.4 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr2:32475575 G>A maps to NM_021209.4 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:57059997 C>T maps to NM_032206.3 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:57075483 C>T maps to NM_032206.3 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr16:57088994 C>T maps to NM_032206.3 G1216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr16:57089380 A>G maps to NM_032206.3 V1232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr16:57089398 G>A maps to NM_032206.3 L1238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:57059641 C>T maps to NM_032206.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:57060669 C>T maps to NM_032206.3 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:57101297 G>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:57075411 C>T maps to NM_032206.3 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:57110815 T>C did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:57067560 G>A maps to NM_032206.3 Q841Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:57110757 C>T maps to NM_032206.3 V1593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:57062289 G>T maps to NM_032206.3 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr16:57081522 G>A maps to NM_032206.3 P1135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:57088669 C>T maps to NM_032206.3 Q1172*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AZ-4315-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:57060258 G>A maps to NM_032206.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:57101379 C>A maps to NM_032206.3 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:57108584 C>T maps to NM_032206.3 Q1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:5421176 C>A maps to NM_033004.3 E1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:5418360 G>A maps to NM_033004.3 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:5418352 A>G maps to NM_033004.3 F1381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:5433981 C>T maps to NM_033004.3 T1113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:5485320 G>A maps to NM_033004.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr17:5462644 C>T maps to NM_033004.3 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:5442786 G>A maps to NM_033004.3 R940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:5424245 G>A maps to NM_033004.3 Y1290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:5436615 G>A maps to NM_001033053.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr17:5456843 C>T maps to NM_033004.3 W797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr17:5436263 G>A maps to NM_033004.3 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:5462685 G>A maps to NM_033004.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:5487051 G>A maps to NM_033004.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:5445347 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:7981448 A>C maps to NM_176821.3 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:7981808 G>A maps to NM_176821.3 N450N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:56303830 G>T maps to NM_145007.3 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:56321606 G>A maps to NM_145007.3 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:56303800 G>A maps to NM_145007.3 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:56313092 G>T maps to NM_145007.3 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:56297090 G>T maps to NM_145007.3 S1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:56303725 G>A maps to NM_145007.3 Y818Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:56307596 G>A maps to NM_145007.3 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:54308640 A>G maps to ENST00000391773 N770N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:54308607 G>A maps to ENST00000391773 N781N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:54313883 C>T maps to ENST00000391773 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:54318222 C>T maps to ENST00000391773 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr19:54314258 C>T maps to ENST00000391773 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr19:54314207 C>T maps to ENST00000391773 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:54313766 C>T maps to ENST00000391773 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:54312935 G>A maps to ENST00000391773 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr19:56423970 T>C maps to NM_176810.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:56407360 G>A maps to NM_176810.2 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:56423174 C>A maps to NM_176810.2 E670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr19:56419174 G>T maps to NM_176810.2 C810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:56407478 C>T maps to NM_176810.2 A988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:56423387 C>A maps to NM_176810.2 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:56413555 C>T maps to NM_176810.2 Q878Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:56423589 G>A maps to NM_176810.2 C531C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:7063772 C>T maps to NM_176822.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:7063966 G>A maps to NM_176822.3 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:7081193 C>T maps to NM_176822.3 S901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:7059960 T>C maps to NM_176822.3 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:7068057 G>A maps to NM_176822.3 K706K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr11:7071012 A>G maps to NM_176822.3 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:7064450 T>C maps to NM_176822.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:7064450 T>C maps to NM_176822.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:7060038 G>A maps to NM_176822.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:7078952 T>C maps to NM_176822.3 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr11:7064450 T>C maps to NM_176822.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:55481607 C>A maps to NM_017852.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr19:55494412 G>A maps to NM_017852.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:55494667 C>T maps to NM_017852.3 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:55493030 C>T maps to NM_017852.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:55496561 C>T maps to NM_017852.3 D726D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr19:55512226 C>A maps to NM_017852.3 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:55494745 C>T maps to NM_017852.3 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr19:55494895 C>T maps to NM_017852.3 Y610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:55494661 T>C maps to NM_017852.3 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr19:55494667 C>T maps to NM_017852.3 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:247587257 G>A maps to NM_004895.4 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:247587914 C>A maps to NM_004895.4 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:247592938 C>T maps to NM_004895.4 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:247611745 G>A maps to NM_004895.4 A1017A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr1:247608057 C>T maps to NM_004895.4 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:247588025 G>A maps to NM_004895.4 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:247588581 G>T maps to NM_004895.4 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:247607360 G>A maps to NM_004895.4 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:247588700 G>A maps to NM_004895.4 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:247582320 C>T maps to NM_004895.4 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:247611778 G>A maps to NM_004895.4 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr1:247607360 G>A maps to NM_004895.4 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr1:247587252 C>T maps to NM_004895.4 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr1:247607360 G>A maps to NM_004895.4 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:247607360 G>A maps to NM_004895.4 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr1:247607360 G>A maps to NM_004895.4 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr19:56369457 C>T maps to NM_134444.4 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:56369349 G>A maps to NM_134444.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:56370114 C>T maps to NM_134444.4 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:56388502 G>A maps to NM_134444.4 T889T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr19:56369914 G>T maps to NM_134444.4 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:56369445 C>T maps to NM_134444.4 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr19:56370009 C>T maps to NM_134444.4 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:56369497 C>T maps to NM_134444.4 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:56369355 G>A maps to NM_134444.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:56390276 G>T maps to NM_134444.4 V938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:56379185 C>T maps to NM_134444.4 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:56369313 G>A maps to NM_134444.4 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:56370585 C>A maps to NM_134444.4 V609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:56369394 C>T maps to NM_134444.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr19:56369634 G>A maps to NM_134444.4 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:56379149 G>A maps to NM_134444.4 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:56369988 C>T maps to NM_134444.4 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:56370507 C>T maps to NM_134444.4 N583N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr19:56539386 C>T maps to NM_153447.4 Y596Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:56515424 C>T maps to NM_153447.4 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:56539245 C>T maps to NM_153447.4 D549D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:56539284 T>A maps to NM_153447.4 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:56511132 G>T maps to NM_153447.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr19:56539284 T>C maps to NM_153447.4 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr19:56538759 G>A maps to NM_153447.4 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr19:56515123 A>G maps to NM_153447.4 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:56538441 G>T maps to NM_153447.4 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:280783 C>T maps to NM_138329.1 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr11:280822 G>A maps to NM_138329.1 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr11:281404 C>T maps to NM_138329.1 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:280108 C>T maps to NM_138329.1 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:281680 G>A maps to NM_138329.1 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:55451376 G>A maps to ENST00000446217 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr19:55450488 G>A maps to ENST00000446217 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:55449587 C>T maps to ENST00000446217 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr19:55450902 G>A maps to ENST00000446217 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:55449587 C>T maps to ENST00000446217 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:55451283 C>T maps to ENST00000446217 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:56466459 C>T maps to NM_176811.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:56467244 G>A maps to NM_176811.2 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr19:56466995 A>G maps to NM_176811.2 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr19:56465978 C>T maps to NM_176811.2 H185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:56466122 C>T maps to NM_176811.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:56466194 C>A maps to NM_176811.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:56490888 C>T maps to NM_176811.2 C1002C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:56466233 C>T maps to NM_176811.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr19:56467268 A>G maps to NM_176811.2 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:56481918 C>T maps to NM_176811.2 D797D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:56482026 G>A maps to NM_176811.2 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:56466122 C>T maps to NM_176811.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr19:56467268 A>G maps to NM_176811.2 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr19:56459345 C>A maps to NM_176811.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:56459618 C>T maps to NM_176811.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:56244623 G>A maps to NM_176820.2 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:56243687 G>A maps to NM_176820.2 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr19:56244541 G>A maps to NM_176820.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr19:56243633 C>T maps to NM_176820.2 Q521Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:56244307 C>A maps to NM_176820.2 G297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr19:56244482 T>C maps to NM_176820.2 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:56249635 C>T maps to NM_176820.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:56220322 T>C maps to NM_176820.2 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:56243792 C>T maps to NM_176820.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:56244785 G>A maps to NM_176820.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr19:56249671 A>G maps to NM_176820.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:56244116 G>A maps to NM_176820.2 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:56249534 C>T maps to NM_176820.2 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:56223302 G>A maps to NM_176820.2 C902C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:56244554 T>C maps to NM_176820.2 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:119044620 G>A maps to NM_024618.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr6:142409378 G>A maps to NM_002511.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:142409489 C>T maps to NM_002511.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr6:142409417 G>A maps to NM_002511.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:142396808 G>A maps to NM_002511.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:160945046 A>G maps to ENST00000472947 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr3:160952912 T>C maps to ENST00000472947 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:160958905 C>T maps to ENST00000472947 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:49231763 C>T maps to ENST00000393198 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr3:48336642 G>A maps to NM_005793.3 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:48336667 C>T maps to NM_005793.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr2:152139414 C>T maps to NM_004688.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:183253905 C>T maps to NM_015039.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:139279991 G>A maps to ENST00000296202 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr16:4519367 G>A maps to NM_020677.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:101096959 C>T maps to NM_001011717.1 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:43181078 C>T maps to NM_021079.3 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:43180339 C>T maps to NM_021079.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:43181245 T>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:15151790 T>C maps to ENST00000378143 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr10:15161467 G>A maps to ENST00000378143 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:56465342 C>A maps to NM_006681.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:232393452 C>A maps to NM_006056.4 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr5:151784440 C>T maps to NM_020167.4 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:151775092 T>C maps to NM_020167.4 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:151784440 C>T maps to NM_020167.4 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:151784059 C>A maps to NM_020167.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:151784059 C>T maps to NM_020167.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:151775122 A>G maps to NM_020167.4 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr5:151784059 C>A maps to NM_020167.4 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:114183099 C>T maps to NM_006169.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:114167364 T>C maps to NM_006169.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:43644409 G>T maps to NM_182977.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:43675707 G>A maps to NM_182977.2 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:43656074 G>A maps to NM_182977.2 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:43645490 G>A maps to NM_182977.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr5:43656056 A>G maps to NM_182977.2 E725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr16:69778880 A>G maps to NM_014062.1 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:69776393 G>A maps to NM_014062.1 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr1:891301 C>A did not map to a codon.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:881626 G>A maps to NM_015658.3 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr10:96121491 T>A maps to NM_022451.9 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:96117943 T>C maps to NM_022451.9 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr10:96116943 A>G maps to NM_022451.9 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:96093960 C>T maps to NM_022451.9 T792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:96112150 C>A maps to NM_022451.9 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:96116976 A>G maps to NM_022451.9 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:132632254 C>T maps to NM_024078.1 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:30491973 G>T maps to NM_006092.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:30491958 G>A maps to NM_006092.2 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:50745612 G>A maps to NM_022162.1 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:50746017 C>T maps to NM_022162.1 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr16:50733459 G>A maps to NM_022162.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:50750886 T>C did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr16:50745532 C>T maps to NM_022162.1 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:72192775 C>T maps to NM_018055.4 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:54672055 C>T maps to NM_005450.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:54671700 C>T maps to NM_005450.4 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr17:65730491 A>G maps to NM_015462.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr17:65717543 G>A maps to NM_015462.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr18:31463226 C>A maps to NM_003787.4 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr18:31538358 G>A maps to NM_003787.4 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:31685022 T>C maps to NM_003787.4 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:31432849 G>A maps to NM_003787.4 R625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr18:31538216 G>A maps to NM_003787.4 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr18:31685022 T>C maps to NM_003787.4 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr18:31685022 T>C maps to NM_003787.4 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:33466674 C>T maps to NM_022917.4 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr9:33463427 C>T maps to NM_022917.4 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr9:33470050 G>A maps to NM_022917.4 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr6:13616699 A>G maps to NM_016167.3 R111R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-A010-01A-01W-A00E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr1:6610546 A>G maps to NM_024654.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:103919774 G>T maps to ENST00000405356 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:103921992 C>T maps to ENST00000405356 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:103919007 C>T maps to ENST00000405356 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:103921313 T>C maps to ENST00000405356 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr7:156755709 C>T maps to NM_138400.1 N584N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:156761800 G>A maps to NM_138400.1 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr7:156743148 G>T maps to NM_138400.1 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:156756621 C>T maps to NM_138400.1 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:14969012 C>T maps to ENST00000456867 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:18549976 G>T maps to NM_001004060.1 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:18544424 G>A maps to NM_001004060.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:70514184 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:70514211 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:70514289 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:70514083 G>A did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:70514365 T>C did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:70517237 C>T did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:70516720 G>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:70517749 C>T did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:70514364 T>C did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr4:2943380 G>A maps to NM_003703.1 H709H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:2949305 G>A maps to NM_003703.1 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:2955255 G>A maps to NM_003703.1 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:2959394 C>A maps to NM_003703.1 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:2951823 G>A maps to NM_003703.1 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:6670869 C>A maps to ENST00000382421 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:6673108 G>A maps to ENST00000382421 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:6669389 G>A maps to ENST00000382421 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:6670195 G>A maps to ENST00000382421 D449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:2638681 G>A maps to NM_006392.2 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:2636274 C>T maps to NM_006392.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:2638795 T>C maps to NM_006392.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:2635575 C>A maps to NM_006392.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr20:2637438 C>T maps to NM_006392.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr20:2637854 G>A maps to NM_006392.2 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:203130679 G>T maps to NM_015934.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:203157514 G>T maps to NM_015934.3 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr12:117665293 T>C maps to ENST00000338101 P1220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:117723944 C>T maps to ENST00000338101 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:117657906 G>A maps to ENST00000338101 D1415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:117665299 G>T maps to ENST00000338101 S1218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:117749303 G>A maps to ENST00000338101 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:117664495 G>A maps to ENST00000338101 F1266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:117768724 G>A maps to ENST00000338101 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr12:117710315 G>A maps to ENST00000338101 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:117725889 T>C maps to ENST00000338101 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:117749285 A>C maps to ENST00000338101 Y279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:117726008 C>A maps to ENST00000338101 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:117669913 G>A maps to ENST00000338101 D1120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:117725931 C>T maps to ENST00000338101 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr12:117710225 G>A maps to ENST00000338101 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:117718628 G>A maps to ENST00000338101 H475H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:162335354 C>T maps to NM_014697.2 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr1:162336848 C>A maps to NM_014697.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:162337070 C>T maps to NM_014697.2 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:26106045 G>A maps to NM_000625.4 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:26109126 G>A maps to NM_000625.4 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr7:150709474 G>A maps to NM_000603.4 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:150710861 C>T maps to NM_000603.4 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr7:150710873 C>T maps to NM_000603.4 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:150704192 C>T maps to NM_000603.4 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:50063216 C>T maps to NM_015953.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:50063225 A>G maps to NM_015953.3 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:50059647 G>A maps to NM_015953.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr9:139390631 C>T maps to NM_017617.3 W2520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:139391767 C>T maps to NM_017617.3 S2141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:139410037 G>A maps to NM_017617.3 C600C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr9:139399156 C>T maps to NM_017617.3 R1662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr9:139391197 T>C maps to NM_017617.3 A2331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:139391506 G>T maps to NM_017617.3 S2228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:139395075 G>A maps to NM_017617.3 A1954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr9:139390834 C>A maps to NM_017617.3 A2452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr9:139401425 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:139390831 C>T maps to NM_017617.3 V2453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:139399414 C>T maps to NM_017617.3 V1576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:139411817 G>A maps to NM_017617.3 C487C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr9:139391209 C>T maps to NM_017617.3 R2327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr9:139401047 G>A maps to NM_017617.3 P1315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:139396479 G>A maps to NM_017617.3 D1815D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr9:139402426 G>A maps to NM_017617.3 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr9:139399354 G>A maps to NM_017617.3 L1596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:139410091 G>A maps to NM_017617.3 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr9:139390996 C>T maps to NM_017617.3 Q2398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:139395153 G>A maps to NM_017617.3 G1928G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:139412252 G>A maps to NM_017617.3 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:139413064 G>A maps to NM_017617.3 C359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:120506200 C>T maps to NM_024408.2 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:120512209 G>A maps to NM_024408.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr1:120572584 T>C maps to NM_024408.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:120462192 G>A maps to NM_024408.2 S1841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr1:120480045 G>A maps to NM_024408.2 I1127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr1:120468283 G>A maps to NM_024408.2 H1385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:120462051 T>C maps to NM_024408.2 S1888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:120466474 A>G maps to NM_024408.2 V1548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:120502117 A>G maps to NM_024408.2 N641N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:120458146 G>A maps to NM_024408.2 R2400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr1:120466368 G>A maps to NM_024408.2 Q1584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr1:120458146 G>T maps to NM_024408.2 R2400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:120506308 G>A maps to NM_024408.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:120458146 G>A maps to NM_024408.2 R2400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:145282013 G>T maps to ENST00000454606 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:145273433 C>T maps to ENST00000454606 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:145282013 G>T maps to ENST00000454606 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:15295103 A>C did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr19:15297970 G>A maps to NM_000435.2 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:32188995 G>A maps to NM_004557.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:32181561 G>A maps to NM_004557.3 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:32163261 T>C maps to NM_004557.3 P1988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:32180663 G>A maps to NM_004557.3 C821C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr6:32170046 G>A maps to NM_004557.3 C1187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr6:32180305 G>A maps to NM_004557.3 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:32188308 C>A maps to NM_004557.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:32172106 T>C maps to NM_004557.3 Q975Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:32172124 G>A maps to NM_004557.3 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr6:32190297 A>T maps to NM_004557.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:32190297 A>T maps to NM_004557.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr6:32168770 G>T maps to NM_004557.3 V1384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr6:32172106 T>C maps to NM_004557.3 Q975Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:32188181 C>A maps to NM_004557.3 G387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:32187495 G>A maps to NM_004557.3 C461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:79917422 G>A maps to NM_178493.5 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:79911109 C>T maps to NM_178493.5 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:79913409 G>A maps to NM_178493.5 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr8:120428843 T>C maps to NM_002514.3 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr8:120428843 T>C maps to NM_002514.3 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr8:120430511 A>G maps to NM_002514.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr14:26917692 T>C maps to ENST00000449198 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr14:26949341 A>C maps to ENST00000449198 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:46444149 G>A maps to NM_002516.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:46444041 G>A maps to NM_002516.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr19:46443732 G>A maps to NM_002516.2 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:46444176 C>T maps to NM_002516.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:100105206 G>A did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:100117758 G>T did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr23:100118199 A>G did not map to a codon.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr23:100104797 T>C did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:100117757 C>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:100106249 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:155757593 C>A maps to NM_015718.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr6:155764484 C>T maps to NM_015718.2 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:155764541 G>A maps to NM_015718.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:155750118 C>T maps to NM_015718.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:155743923 G>A maps to NM_015718.2 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:89133505 G>A maps to NM_016931.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:69328218 G>C maps to NM_024505.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:69349005 C>T maps to NM_024505.3 F756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:140320737 G>A maps to NM_006647.1 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:140322512 C>T maps to NM_006647.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:140328421 C>T maps to NM_006647.1 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:47542318 C>T maps to NM_002517.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:101606815 G>A maps to NM_002518.3 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:101606758 C>T maps to NM_002518.3 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr2:101609868 C>T maps to NM_002518.3 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:101592010 C>T maps to NM_002518.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr14:34268982 C>T maps to NM_001164749.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr14:33408527 G>A maps to NM_001164749.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:33684749 A>G maps to NM_173159.2 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:34269153 C>T maps to NM_001164749.1 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr11:66192331 C>A maps to NM_178864.3 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:66192379 C>T maps to NM_178864.3 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr11:108031924 A>G maps to NM_002519.2 S1296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:108032091 A>G maps to NM_002519.2 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:108043043 C>T maps to NM_002519.2 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:108059884 C>T maps to NM_002519.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr11:108044480 T>C maps to NM_002519.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:108043330 C>A maps to NM_002519.2 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:108059853 G>A maps to NM_002519.2 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr11:108044480 T>C maps to NM_002519.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr11:108032260 T>C maps to NM_002519.2 S1184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:62737887 G>A maps to NM_005286.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:62737875 C>T maps to NM_005286.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:21121136 A>G maps to NM_000271.4 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr18:21119409 C>T maps to NM_000271.4 S940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:21136548 G>A maps to NM_000271.4 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr18:21119856 G>A maps to NM_000271.4 Q905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr18:21121350 C>T maps to NM_000271.4 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:21152066 G>A maps to NM_000271.4 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr18:21134753 G>A maps to NM_000271.4 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr18:21119839 G>A maps to NM_000271.4 G910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr18:21136494 G>A maps to NM_000271.4 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr18:21119427 T>C maps to NM_000271.4 R934R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:44579110 G>A maps to NM_013389.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:44578621 C>T maps to NM_013389.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:44574087 G>A maps to NM_013389.2 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:44579683 C>T maps to NM_013389.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr7:44556454 G>A maps to NM_013389.2 P1149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr7:44579746 G>A maps to NM_013389.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr7:44578420 A>G maps to NM_013389.2 C525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:139935637 G>A maps to ENST00000371600 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:57269509 C>T maps to NM_024663.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:45695736 C>T maps to NM_006310.3 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:45691039 T>A maps to NM_006310.3 Y748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:72015309 G>A maps to ENST00000277942 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:72015285 C>T maps to ENST00000277942 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:72897707 G>A maps to NM_004885.2 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:72897734 C>T maps to NM_004885.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:72897734 C>T maps to NM_004885.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr4:73012745 G>A maps to NM_004885.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:110922732 C>T did not map to a codon.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr2:110922273 C>T maps to NM_000272.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:110962481 G>A maps to NM_000272.3 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:132435693 C>A maps to ENST00000393156 G244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:132403520 T>C maps to ENST00000393156 K1149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:132411560 G>A maps to ENST00000393156 H804H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:132415579 G>A maps to ENST00000393156 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:132420335 C>T maps to ENST00000393156 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:5967243 C>T maps to NM_015102.2 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:6008218 C>T maps to NM_015102.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr1:5935109 G>A maps to NM_015102.2 A956A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:5965732 C>T maps to NM_015102.2 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:5935091 C>T maps to NM_015102.2 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:5924499 G>A maps to NM_015102.2 A1298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:36321823 A>G maps to NM_004646.3 P1172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:36341339 C>T maps to NM_004646.3 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:36333317 C>T maps to NM_004646.3 A823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr19:36332761 C>T maps to NM_004646.3 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:36340013 C>T maps to NM_004646.3 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr19:36333350 G>A maps to NM_004646.3 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr19:36321766 G>T maps to NM_004646.3 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:179526214 G>A maps to NM_014625.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:182775293 G>T maps to NM_030769.1 G53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr1:182772898 C>T maps to NM_030769.1 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr1:182787733 G>A maps to NM_030769.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr1:182787733 G>T maps to NM_030769.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:170837562 T>C maps to NM_002520.6 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr5:170818325 T>G maps to NM_002520.6 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr8:21882971 G>T maps to NM_182795.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:106888414 C>T maps to ENST00000503451 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:106861717 C>T maps to ENST00000503451 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:106888342 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:106861794 T>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:11918406 G>A maps to NM_002521.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:11918770 C>T maps to NM_002521.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:153661759 G>A maps to NM_000906.3 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr1:153661482 G>A maps to NM_000906.3 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr1:153657470 G>T maps to NM_000906.3 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:153655937 T>C maps to NM_000906.3 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:153654302 C>A maps to NM_000906.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:35800707 T>C maps to NM_003995.3 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:35801151 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:35805896 C>T maps to NM_003995.3 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr9:35799667 C>T maps to NM_003995.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:35807070 T>C maps to NM_003995.3 F857F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr9:35809391 C>T maps to NM_003995.3 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:35792701 C>T maps to NM_003995.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:32712304 G>A maps to ENST00000265074 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:32724816 T>A maps to ENST00000265074 C261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:32739000 C>T maps to ENST00000265074 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:32780865 C>T maps to ENST00000265074 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr3:50387110 A>G maps to NM_006545.4 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:162720 G>A maps to ENST00000399953 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:162759 C>T maps to ENST00000399953 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:34867049 C>T maps to NM_207172.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:73879928 G>A maps to NM_012428.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:73889441 G>A maps to NM_012428.3 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr17:78444660 G>A maps to NM_002522.3 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:78445639 G>A maps to NM_002522.3 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr7:98254456 C>T maps to NM_002523.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr7:98257874 C>T maps to NM_002523.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:98257718 C>T maps to NM_002523.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:39218697 A>G maps to NM_014293.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:25266338 G>A maps to NM_022150.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:25266585 T>C maps to NM_022150.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr7:25268010 A>G maps to NM_022150.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:24324930 G>A maps to NM_000905.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:24324975 C>T maps to NM_000905.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr7:24325008 G>A maps to NM_000905.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:24325015 C>T maps to NM_000905.3 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:156135717 C>T maps to NM_000910.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:156135750 T>C maps to NM_000910.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:164272078 T>C maps to NM_006174.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:164272750 T>C maps to NM_006174.2 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:69752396 C>T maps to NM_000903.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:3019825 G>A maps to NM_000904.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:30327156 C>T did not map to a codon.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr23:30322933 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:30322826 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:30327205 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:30322738 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:30326799 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:30326562 G>A did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:30326908 C>A did not map to a codon.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr23:30326860 G>A did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:30326827 G>A did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:30326791 C>T did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr23:30327206 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:30327299 C>G did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:27238446 G>T maps to NM_021969.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:38251834 A>G maps to NM_021724.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:38251837 C>T maps to NM_021724.3 W369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:38252038 G>A maps to NM_021724.3 Y302Y. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-A02K-01A-21W-A096-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:38250297 G>A maps to NM_021724.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:23997526 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:24006650 G>T maps to NM_005126.4 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:50881011 C>T maps to NM_007121.4 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:50881460 G>A maps to NM_007121.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr19:50881824 G>A maps to NM_007121.4 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:50881535 C>T maps to NM_007121.4 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:47290159 C>T maps to NM_005693.2 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:47280784 G>A maps to NM_005693.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:47290240 C>T maps to NM_005693.2 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr12:100904823 G>A maps to ENST00000392986 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:100904616 G>A maps to ENST00000392986 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr12:100934588 A>G maps to ENST00000392986 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:100926236 T>C maps to ENST00000392986 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr12:100934586 C>T maps to ENST00000392986 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:100934586 C>A maps to ENST00000392986 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:119528943 C>A maps to NM_022002.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:119528925 C>T maps to NM_022002.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:95452182 A>G maps to NM_003297.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr12:95422202 G>A maps to NM_003297.2 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:15055250 A>G maps to NM_003298.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:15055241 C>T maps to NM_003298.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr6:108492734 C>T maps to ENST00000368983 C70C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:108508663 C>A maps to ENST00000368983 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:108496083 G>A maps to ENST00000368983 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:108497788 C>T maps to ENST00000368983 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr15:72105742 A>G maps to NM_014249.2 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:72105838 C>A maps to NM_014249.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:72104775 G>A maps to NM_014249.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:92929487 C>T maps to NM_005654.4 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:92924091 G>A maps to NM_005654.4 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:92923851 C>T maps to NM_005654.4 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:92923701 C>T maps to NM_005654.4 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:92923818 C>T maps to NM_005654.4 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:96877677 C>A maps to NM_021005.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr19:17343289 C>T maps to NM_005234.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:142661519 G>T maps to NM_001024094.1 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:142693600 T>C maps to NM_001024094.1 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr5:142779552 G>A maps to NM_001024094.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:142779903 C>T maps to NM_001024094.1 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:142780377 A>G maps to NM_001024094.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr5:142680224 C>T maps to NM_001024094.1 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr4:149115999 A>G maps to ENST00000511528 Y641Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:149073663 C>T maps to ENST00000511528 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr4:149181244 A>G maps to ENST00000511528 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:149356389 G>A maps to ENST00000511528 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:149357214 A>G maps to ENST00000511528 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:149357282 G>A maps to ENST00000511528 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:157182438 G>A maps to NM_006186.3 H538H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:127262608 C>T maps to NM_004959.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr9:127265587 C>T maps to NM_004959.4 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:200080382 C>T maps to NM_205860.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:200089982 C>T maps to NM_205860.1 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr1:200012983 G>A maps to NM_205860.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr10:115368214 G>A maps to ENST00000369358 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr10:115391315 G>A maps to ENST00000369358 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:115406695 C>A maps to ENST00000369358 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:115349556 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:115355413 G>A maps to ENST00000369358 R1510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr10:115384632 G>A maps to ENST00000369358 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:115391351 T>C maps to ENST00000369358 E594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr10:115380455 C>T maps to ENST00000369358 R935R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr10:115377231 A>G maps to ENST00000369358 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr1:115256536 T>C maps to NM_002524.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr1:115256563 T>C maps to NM_002524.3 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:115256536 T>C maps to NM_002524.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:115256565 C>A maps to NM_002524.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr1:115258751 T>C maps to NM_002524.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:115256515 A>G maps to NM_002524.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:115256533 A>G maps to NM_002524.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:115258751 T>C maps to NM_002524.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr1:115256533 A>G maps to NM_002524.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr1:115258753 C>A maps to NM_002524.3 G10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr1:115256527 T>C maps to NM_002524.3 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:115256506 T>C maps to NM_002524.3 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr1:115256536 T>C maps to NM_002524.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:64913851 C>T maps to NM_030759.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:27664046 C>T maps to ENST00000379863 H469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:27656160 G>A maps to ENST00000379863 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr2:27660136 G>A maps to ENST00000379863 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:144919270 C>T maps to NM_178564.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr8:144919840 C>T maps to NM_178564.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr7:107824876 A>G maps to ENST00000379032 Y739Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:107807428 G>A maps to ENST00000379032 R1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr7:107799942 A>T maps to ENST00000379032 P1214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr7:107838418 G>A maps to ENST00000379032 N444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:107872815 G>A maps to ENST00000379032 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr7:107790558 T>C maps to ENST00000379032 G1241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr7:107790558 T>C maps to ENST00000379032 G1241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr7:107799942 A>T maps to ENST00000379032 P1214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:52256236 G>A maps to NM_002525.2 Q1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:52272550 C>T maps to NM_002525.2 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:52263976 C>A maps to NM_002525.2 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:52255242 A>G maps to NM_002525.2 V1153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:129367174 G>T maps to ENST00000393231 G440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr7:129297322 G>A maps to ENST00000393231 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr8:32621346 G>A maps to NM_013956.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:32613972 C>T maps to NM_013956.3 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr8:32463199 C>T maps to NM_013956.3 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:139245160 G>A maps to NM_013982.2 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:139422206 G>A maps to NM_013982.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:139251346 G>A maps to NM_013982.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:139244718 G>A maps to NM_013983.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr5:139231307 T>C maps to NM_013982.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:139260459 G>A maps to NM_013982.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:83635728 G>T maps to ENST00000404547 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:84745231 C>T maps to ENST00000404547 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:84118576 C>A maps to ENST00000404547 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:84744537 G>T did not map to a codon.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr21:16339844 T>C maps to NM_003489.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr21:16337366 C>T maps to NM_003489.3 A1049A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:105153674 C>T did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:105153754 T>C did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:105153754 T>C did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:105156666 G>T did not map to a codon.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr23:105152737 G>C did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:105152902 A>G did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:105153513 A>T did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:105161621 C>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:105153756 A>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:105193632 C>T did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:105132333 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:105161579 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:105178363 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:105139511 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:105125724 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:105167143 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:105168790 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:105189925 A>T did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:105153754 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:105168909 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:105190374 G>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:105132355 T>C did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr23:105132355 T>C did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:105156667 A>G did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:105153262 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:30657190 A>G maps to NM_007243.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:5999292 G>A maps to NM_016588.2 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr16:67919691 C>T maps to NM_198443.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:67920035 C>T maps to NM_198443.1 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr10:33510659 A>G maps to NM_003873.5 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:33502630 C>A maps to NM_003873.5 G433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr10:33559762 G>A maps to NM_003873.5 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:33510659 A>G maps to NM_003873.5 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:33552751 G>A maps to NM_003873.5 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr2:206628479 G>A maps to NM_201266.1 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:206608116 A>G maps to NM_201266.1 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:206607960 A>G maps to NM_201266.1 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:206610474 C>T maps to NM_201266.1 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:206630205 C>T maps to NM_201266.1 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:206587238 C>T maps to NM_201266.1 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:206610474 C>T maps to NM_201266.1 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:206614474 G>T maps to NM_201266.1 G605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:24134687 G>T maps to NM_080723.4 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr6:24145873 C>T maps to NM_080723.4 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:334170 G>A maps to NM_024958.2 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:334206 A>G maps to NM_024958.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr20:333870 G>A maps to NM_024958.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:5824274 C>T maps to NM_004558.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr2:50847270 T>C maps to ENST00000404971 E443E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:50149332 G>T maps to ENST00000404971 R1465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr2:51255075 G>A maps to ENST00000404971 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:51254931 C>T maps to ENST00000404971 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr2:50149200 G>A maps to ENST00000404971 R1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:50149312 C>T maps to ENST00000404971 T1471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:50149132 C>T maps to ENST00000404971 A1531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:50318599 A>C maps to ENST00000404971 V1233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr2:51255219 G>A maps to ENST00000404971 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr2:50765424 G>A maps to ENST00000404971 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:51255120 G>A maps to ENST00000404971 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr2:50149303 G>A maps to ENST00000404971 V1474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:50699478 G>T maps to ENST00000404971 S1107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:51254751 G>A maps to ENST00000404971 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:50282141 T>G maps to ENST00000404971 R1293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr2:50149093 C>T maps to ENST00000404971 E1544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:50755763 G>T maps to ENST00000404971 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr2:50850730 C>T maps to ENST00000404971 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:51254787 C>T maps to ENST00000404971 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:50723067 G>A maps to ENST00000404971 A1055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:64434905 A>G maps to NM_015080.3 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr11:64457916 G>A maps to NM_015080.3 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:64390410 G>A maps to NM_015080.3 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:64375324 G>T maps to NM_015080.3 G1494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr11:64434761 G>A maps to NM_015080.3 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:64390431 C>T maps to NM_015080.3 A1322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:64417956 C>T maps to NM_015080.3 T1024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr14:79432446 C>T maps to NM_004796.4 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr14:79269960 A>G did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr14:79175639 C>T maps to NM_004796.4 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr14:79181438 C>T maps to NM_004796.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr14:79434627 C>A maps to NM_004796.4 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr14:80328135 C>T maps to NM_004796.4 Y1005Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:79181454 G>T maps to NM_004796.4 G300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:79181447 C>T maps to NM_004796.4 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:80130200 C>T maps to NM_004796.4 D802D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:79432437 C>A maps to NM_004796.4 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:176675252 C>T maps to NM_022455.4 P1523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:176721367 C>A maps to NM_022455.4 P2333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr5:176719031 A>G maps to NM_022455.4 E2112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:176631232 C>T maps to NM_022455.4 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:176631232 C>T maps to NM_022455.4 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:176687161 C>T maps to NM_022455.4 C1713C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr5:176687050 T>C maps to NM_022455.4 A1676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr5:176721628 T>C maps to NM_022455.4 P2420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr5:176637844 C>T maps to NM_022455.4 C815C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr5:176721628 T>C maps to NM_022455.4 P2420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:152034379 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:152037426 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:152031171 C>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:152037490 T>C did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:44791240 T>C maps to NM_006178.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr20:1424437 C>A maps to ENST00000476071 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr20:1426390 G>A maps to ENST00000476071 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:212911989 G>A maps to NM_015471.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:59498271 A>G maps to NM_001144772.1 G897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:59513892 G>A maps to NM_001144772.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:59547898 C>T maps to NM_001144772.1 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr8:59508177 T>C maps to NM_001144772.1 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr8:59508177 T>C maps to NM_001144772.1 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr8:59508177 T>C maps to NM_001144772.1 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr8:59535941 G>A maps to NM_001144772.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr8:59508168 C>T maps to NM_001144772.1 W645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr8:59512378 C>T maps to NM_001144772.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:126163506 T>C maps to NM_173685.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr8:126379012 C>T maps to NM_173685.2 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:6600149 G>A maps to NM_017755.5 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:6600245 G>A maps to NM_017755.5 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:6625724 C>T maps to NM_017755.5 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:93803154 C>T maps to NM_022072.3 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:72717830 G>A maps to NM_148956.2 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:18903473 C>A maps to NM_182543.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr10:18937508 T>C maps to NM_182543.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr10:18937508 T>C maps to NM_182543.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:40800864 T>C maps to NM_024677.4 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:40129062 C>T maps to NM_032526.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:40126792 G>A maps to NM_032526.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr2:18765443 G>A maps to ENST00000455492 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr2:18765812 G>A maps to ENST00000455492 Y307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:18765992 C>T maps to ENST00000455492 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr10:104934673 A>G maps to NM_001134373.1 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:104860806 A>G maps to NM_001134373.1 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:104849518 T>C maps to NM_001134373.1 K532K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr10:104852955 G>A maps to NM_001134373.1 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:104861042 G>A maps to NM_001134373.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:104866422 A>G maps to NM_001134373.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:104853795 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:104849491 G>T maps to NM_001134373.1 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:33054410 A>C maps to NM_001002010.1 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr7:33057182 G>A maps to NM_001002010.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr7:33057182 G>C maps to NM_001002010.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:39991472 G>A maps to NM_052935.4 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr17:39981861 C>A maps to NM_052935.4 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:39991472 G>A maps to NM_052935.4 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr17:39991351 G>A maps to NM_052935.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:39985115 C>A maps to NM_052935.4 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:39991472 G>A maps to NM_052935.4 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr6:116559378 A>G maps to NM_152729.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:52559101 G>A maps to NM_001134231.1 H408H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:52558719 C>T maps to NM_001134231.1 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:52559311 C>A did not map to a codon.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr12:104171696 C>A maps to NM_001031701.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:104171678 G>A maps to NM_001031701.2 H525H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:104192412 G>A maps to NM_001031701.2 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr12:104171696 C>A maps to NM_001031701.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr12:104171669 G>A maps to NM_001031701.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr6:86181102 C>T maps to NM_002526.2 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr17:17209933 C>T maps to ENST00000379552 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr16:15134970 A>G maps to NM_173474.2 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:5541507 G>A maps to NM_001102654.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:5603409 C>T maps to NM_001102654.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:132016295 G>A maps to NM_001144058.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:132177682 G>A maps to NM_001144058.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:132204991 C>T maps to NM_001144058.1 C340C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:132016193 G>T maps to NM_001144058.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:132082018 T>G maps to NM_001144058.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:132016191 C>A maps to NM_001144058.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:8926151 G>A maps to NM_004822.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:9083184 T>C maps to NM_004822.2 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:96077382 G>A maps to NM_021229.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr12:96131892 G>T maps to NM_021229.3 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:96063914 G>A maps to NM_021229.3 C506C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:96106999 G>A maps to NM_021229.3 N327N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:107867034 T>C maps to NM_001113226.1 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:107867154 C>T maps to NM_001113226.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:107691370 G>A maps to NM_001113226.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:107937895 A>G maps to NM_001113226.1 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:108023242 C>T maps to NM_001113226.1 C467C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr1:107691238 G>A maps to NM_001113226.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:135073411 G>A maps to NM_032536.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:135042235 G>A maps to NM_032536.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr9:135073567 C>T maps to NM_032536.2 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr9:135102319 C>T maps to NM_032536.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr9:135073620 G>A maps to NM_032536.2 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:135073714 C>T maps to NM_032536.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:135117320 C>T maps to NM_032536.2 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:156843449 G>A maps to NM_002529.3 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:156845887 G>A maps to NM_002529.3 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:156849015 G>A maps to NM_002529.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:156851305 G>T maps to NM_002529.3 E755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:156849052 C>A maps to NM_002529.3 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr1:156834170 C>T maps to NM_002529.3 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:156849052 C>A maps to NM_002529.3 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:156843677 C>T maps to NM_002529.3 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:156851380 C>A maps to NM_002529.3 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:156844711 G>T maps to NM_002529.3 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:156844711 G>A maps to NM_002529.3 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr9:87570407 C>T maps to NM_006180.3 D716D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:87359924 G>A maps to NM_006180.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:87285818 C>T maps to NM_006180.3 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:87570245 G>A maps to NM_006180.3 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr9:87285695 C>T maps to NM_006180.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr9:87359903 G>A maps to NM_006180.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr15:88472556 A>G maps to NM_001012338.1 G666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr15:88679133 G>C maps to NM_001012338.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:88679226 C>T maps to NM_001012338.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:88423512 G>T maps to NM_001012338.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr15:88679814 G>A maps to NM_001012338.1 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:88472460 G>A maps to NM_001012338.1 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:88483984 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:88679835 A>G maps to NM_001012338.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:88472522 G>A maps to NM_001012338.1 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:88423601 G>T maps to NM_001012338.1 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr15:88678614 C>A maps to NM_001012338.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:88799240 C>T maps to NM_001012338.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr15:88690582 C>A maps to NM_001012338.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr15:88423601 G>T maps to NM_001012338.1 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr15:88678527 C>A maps to NM_001012338.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr15:88679226 C>T maps to NM_001012338.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr15:88669525 G>A maps to NM_001012338.1 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr15:88679187 C>T maps to NM_001012338.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr20:61340984 C>T maps to NM_002531.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:61341203 C>T maps to NM_002531.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:106480509 A>G did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:106461626 G>A maps to NM_014840.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:106461101 C>T maps to NM_014840.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:106460825 G>A maps to NM_014840.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr12:106461530 G>T maps to NM_014840.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr12:106532326 C>T maps to NM_014840.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:205272952 G>T maps to ENST00000441520 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:205273312 G>T maps to ENST00000441520 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:151052896 G>A maps to ENST00000355851 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:151064063 C>T maps to ENST00000355851 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:151057300 G>A maps to ENST00000355851 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:151073787 G>A maps to ENST00000355851 Q520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:151071274 C>T maps to ENST00000355851 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:151046310 A>G maps to ENST00000355851 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:151052875 C>T maps to ENST00000355851 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr7:151065857 C>A maps to ENST00000355851 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr16:10850620 G>A maps to NM_002484.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr16:1836795 C>A maps to NM_012225.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr14:32031389 A>G maps to NM_025152.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr19:49422361 G>T maps to NM_006184.5 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:49404124 G>A maps to NM_006184.5 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:17336926 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:110308764 G>A maps to NM_032869.3 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:110255471 C>T maps to NM_032869.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr7:2290566 C>T maps to NM_198954.1 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:2284214 C>T maps to NM_198954.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:51076059 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:51075978 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:51238947 G>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:51239140 C>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:102891659 G>A maps to NM_031438.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:145587746 G>T maps to NM_001012758.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:21964960 C>A maps to NM_024815.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr8:21965839 G>T maps to NM_024815.3 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr9:34343314 C>T maps to NM_147173.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:56468723 T>C maps to NM_007006.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:34256676 G>A maps to NM_006703.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:12212731 C>T maps to ENST00000378937 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr10:12219830 G>A maps to ENST00000378937 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:123814372 T>C maps to NM_007083.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr16:77775567 G>T maps to NM_001105663.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr16:77759351 G>A maps to NM_001105663.1 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr16:77775615 C>T maps to NM_001105663.1 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:88356153 G>A maps to NM_024047.3 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr4:88379088 T>C maps to NM_024047.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:88378998 G>A maps to NM_024047.3 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:163318798 G>T maps to NM_145697.2 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:163297331 C>T maps to NM_145697.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:163295870 T>C maps to NM_145697.2 N10N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:163318800 A>G maps to NM_145697.2 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:27613817 T>C maps to NM_020772.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:27614197 G>A maps to NM_020772.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr17:27613076 T>C maps to NM_020772.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr17:27613076 T>C maps to NM_020772.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr17:27614012 C>T maps to NM_020772.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr17:27613076 T>C maps to NM_020772.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:71715792 G>A maps to ENST00000393695 R1973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:71730541 G>A maps to ENST00000393695 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:71726160 C>T maps to ENST00000393695 Q802Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr11:71715793 G>C maps to ENST00000393695 R1972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:71725650 C>T maps to ENST00000393695 A972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr14:73743429 T>C maps to NM_001005743.1 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr14:73750954 G>A maps to NM_001005743.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:73822371 C>A maps to NM_001005743.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr14:73743303 C>T maps to NM_001005743.1 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr19:41188692 G>A maps to NM_004756.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:41186950 G>A maps to NM_004756.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:41173885 C>T maps to NM_004756.3 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:41173897 T>C maps to NM_004756.3 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:69129078 C>T maps to NM_020401.2 N819N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:69094532 C>T maps to NM_020401.2 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:229613422 C>T maps to NM_018230.2 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:229631309 T>C maps to NM_018230.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:229631743 C>T maps to NM_018230.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:229588390 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:229602464 C>T maps to NM_018230.2 E705E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr1:229633911 C>A maps to NM_018230.2 G264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:229623210 A>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:229631309 T>C maps to NM_018230.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr1:229623210 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:229625812 T>C maps to NM_018230.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:17637423 T>C maps to ENST00000430136 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:17637423 T>C maps to ENST00000430136 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:17706513 C>T maps to ENST00000430136 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:17637603 C>T maps to ENST00000430136 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:17629252 T>G maps to ENST00000430136 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:17637423 T>C maps to ENST00000430136 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:17624927 A>C maps to ENST00000430136 S1377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr6:17637423 T>C maps to ENST00000430136 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:37351390 A>G maps to NM_153485.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr5:37309297 T>C maps to NM_153485.1 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:37307532 C>T maps to NM_153485.1 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:37294428 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:37333655 A>C maps to NM_153485.1 L476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:47861509 A>G maps to NM_015231.1 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr11:47829976 G>A maps to NM_015231.1 C782C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:47837186 T>C maps to NM_015231.1 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:47820008 G>A maps to NM_015231.1 R968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr11:47869813 G>A maps to NM_015231.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:131742952 A>G maps to NM_015354.1 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:131755473 A>G did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr9:131767583 C>T maps to NM_015354.1 N1504N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:131763974 G>A maps to NM_015354.1 L1337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr9:131745223 C>T maps to NM_015354.1 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr9:131760507 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:135261102 G>A maps to NM_015135.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:135310091 G>T maps to NM_015135.2 E1554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr7:135292025 C>T maps to NM_015135.2 H1034H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr7:135261806 T>C maps to NM_015135.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:135301841 T>C maps to NM_015135.2 R1179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:135279309 T>C maps to NM_015135.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:135261154 G>T maps to NM_015135.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:135290952 G>T maps to NM_015135.2 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:135303258 G>T maps to NM_015135.2 E1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr7:135304253 C>T maps to NM_015135.2 A1349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:135301838 A>G maps to NM_015135.2 V1178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr7:135269580 T>C maps to NM_015135.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:135279314 A>C maps to NM_015135.2 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:135285706 G>T maps to NM_015135.2 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:13413397 G>A maps to NM_024923.2 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr3:13438875 G>T maps to NM_024923.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:13421213 G>A maps to NM_024923.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:13427774 C>A maps to NM_024923.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:13379369 G>A maps to NM_024923.2 R1173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr3:13417901 A>G maps to NM_024923.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr3:13384686 A>G maps to NM_024923.2 R984R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr3:13378358 G>A maps to NM_024923.2 A1204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:13381377 G>A maps to NM_024923.2 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:13401880 G>A maps to NM_024923.2 N681N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:153991413 G>A maps to NM_207308.2 R1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr1:153995647 G>A maps to NM_207308.2 I1416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:154115958 C>T maps to NM_207308.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:154029379 G>A maps to NM_207308.2 R1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:153995641 C>T maps to NM_207308.2 E1418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:154101768 T>G maps to NM_207308.2 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:154112415 G>A maps to NM_207308.2 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr1:154018593 C>T maps to NM_207308.2 W1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:154125254 C>T maps to NM_207308.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:134021533 C>A maps to ENST00000451030 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:134098222 G>A maps to ENST00000451030 S1937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr9:134073014 G>C maps to ENST00000451030 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr9:134073833 C>T maps to ENST00000451030 A1652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:134049502 C>T maps to ENST00000451030 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:134106046 C>T maps to ENST00000451030 F2036F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:134067622 T>G maps to ENST00000451030 T1202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:183995218 T>C maps to NM_138285.3 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:102471143 G>A maps to NM_024057.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr12:102512170 A>G maps to NM_024057.2 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:150063667 G>T maps to NM_198887.1 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr22:45574338 T>C maps to NM_007172.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:45574146 C>A maps to NM_007172.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:77065314 C>T maps to ENST00000458189 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr4:77039263 C>T maps to ENST00000458189 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr4:77039263 C>A maps to ENST00000458189 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:73227670 C>T maps to NM_024844.3 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr17:73208119 C>T maps to NM_024844.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:5319981 T>C maps to NM_002532.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr17:5322835 C>T maps to NM_002532.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:56871555 C>T maps to NM_014669.3 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:56867318 G>A did not map to a codon.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr11:3707399 C>T maps to NM_016320.4 L1493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:3746391 A>C maps to NM_016320.4 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr7:23221817 G>A maps to ENST00000413919 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:118015230 G>A maps to NM_138459.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:67899132 G>A did not map to a codon.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr1:224495770 T>G maps to NM_002533.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr1:224468865 G>A maps to NM_002533.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:224415333 G>A maps to NM_002533.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:224475557 G>A maps to NM_002533.2 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr19:16918827 C>T maps to ENST00000438489 R1390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:16872933 G>T maps to ENST00000438489 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:16918874 C>T maps to ENST00000438489 S1405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:16890160 C>T maps to ENST00000438489 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr19:16910773 C>T maps to ENST00000438489 R1179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr19:16874746 G>T maps to ENST00000438489 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:16884018 C>T maps to ENST00000438489 C831C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:16908585 C>G maps to ENST00000438489 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:16910773 C>T maps to ENST00000438489 R1179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:16860310 G>A maps to ENST00000438489 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:16883956 G>T maps to ENST00000438489 E811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:16860010 C>T maps to ENST00000438489 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:16918931 C>T maps to ENST00000438489 F1424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:16902372 C>T maps to ENST00000438489 A1051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:16910914 C>T maps to ENST00000438489 Y1226Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:16861114 G>A maps to ENST00000438489 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:62563804 G>T maps to NM_006362.4 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr11:62561812 C>T maps to NM_006362.4 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr11:62561845 G>A maps to NM_006362.4 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:101581400 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr23:101581391 C>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:102337990 T>C did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:102334344 G>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:102337990 T>C did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:102338376 G>C did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:102334192 T>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:102337745 G>A did not map to a codon.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr23:102339358 C>T did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:102334799 T>G did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:102338372 C>T did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:102337990 T>C did not map to a codon.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr23:101092587 G>A did not map to a codon.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr23:101096064 G>C did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:101092604 T>G did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr23:101096737 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr23:101096730 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:101096494 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:726898 G>A maps to NM_022463.3 H195H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:722781 C>T maps to NM_022463.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr17:726976 G>C maps to NM_022463.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:8791131 G>T maps to NM_152745.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:139429226 A>G maps to NM_007226.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:139429094 C>T maps to NM_007226.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:139429160 C>T maps to NM_007226.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr2:139428866 T>C maps to NM_007226.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr2:139428866 T>C maps to NM_007226.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:139428868 C>A maps to NM_007226.2 G140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr2:139428866 T>C maps to NM_007226.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr2:139429226 A>G maps to NM_007226.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:139429082 G>A maps to NM_007226.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:47656211 C>T maps to ENST00000513748 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:57619331 G>A maps to NM_007224.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:57619421 C>A maps to NM_007224.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:23334947 G>A maps to NM_013248.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:108780175 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:108780232 C>T did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:108780176 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:24884653 C>A maps to NM_025081.2 S1233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:24885193 C>T maps to NM_025081.2 Y1413Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:24884848 G>A maps to NM_025081.2 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:24879174 C>A maps to NM_025081.2 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:41333576 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:41334070 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:41333643 G>A did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:41333733 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:41333576 G>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:41333650 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:120099745 G>A maps to NM_178507.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:120099760 C>T maps to NM_178507.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:113346600 C>T maps to NM_001032409.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:113348964 A>G maps to NM_001032409.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:113440862 G>T maps to NM_016817.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:113379409 T>C maps to NM_006187.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:113386913 G>A maps to NM_006187.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:113398966 C>T maps to NM_006187.2 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:121458636 G>T maps to NM_003733.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:126086642 T>C maps to NM_000274.3 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:151740685 C>A maps to ENST00000321531 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr1:151742725 C>T maps to ENST00000321531 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:105670311 C>A maps to NM_024928.4 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr10:105670369 C>T maps to NM_024928.4 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr9:138439762 C>T maps to NM_014582.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr9:136082706 G>A maps to NM_014581.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr1:228466999 G>A maps to NM_001098623.1 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:228437747 C>T maps to NM_001098623.1 C1372C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr1:228432198 G>A maps to NM_001098623.1 A1136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:228511098 G>T maps to NM_001098623.1 V5148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:228402695 C>T maps to NM_001098623.1 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:228548203 G>A maps to NM_052843.2 A6537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:228560417 C>T maps to NM_001098623.1 Y7313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:228480449 C>T maps to NM_001098623.1 C3610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:228494677 G>A maps to NM_001098623.1 E4001E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:228467934 C>T maps to NM_001098623.1 G2573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:228538629 G>A maps to NM_001098623.1 P6135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:228462348 C>T maps to NM_001098623.1 C1920C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:228506747 C>T maps to NM_001098623.1 D4765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:228503689 C>T maps to NM_001098623.1 N4385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:228471426 C>T maps to NM_001098623.1 C2987C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr1:228402046 A>G maps to NM_001098623.1 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:228527714 G>A maps to NM_001098623.1 A5776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr1:228495836 G>A maps to NM_001098623.1 G4164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:228495134 G>A maps to NM_001098623.1 T4123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:228554729 C>T maps to NM_001098623.1 C6494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:228564497 T>A maps to NM_001098623.1 S7654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:228496001 G>C maps to NM_001098623.1 L4219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:228547966 G>A maps to NM_052843.2 T6458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:228554786 A>G maps to NM_001098623.1 R6513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:228566393 G>A maps to NM_001098623.1 A7935A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:228399510 G>A maps to NM_001098623.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr1:228554786 A>G maps to NM_001098623.1 R6513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr1:228520597 G>A maps to NM_001098623.1 T5230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:228554723 C>A maps to NM_001098623.1 I6492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:228527714 G>T maps to NM_001098623.1 A5776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr1:228554784 C>T maps to NM_001098623.1 R6513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:228467044 G>A maps to NM_001098623.1 T2432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:228481087 C>T maps to NM_001098623.1 N3634N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:228506600 C>T maps to NM_001098623.1 A4716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr1:228538596 C>T maps to NM_001098623.1 D6124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:228494621 C>T maps to NM_001098623.1 R3983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr1:228464197 G>T maps to NM_001098623.1 E2090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr1:228509754 G>T maps to NM_001098623.1 A5071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:228504578 C>T maps to NM_001098623.1 D4485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:228511239 C>T maps to NM_001098623.1 G5195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr1:228509502 G>A maps to NM_001098623.1 V4987V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:228444565 C>T maps to NM_001098623.1 V1508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:228470776 C>T maps to NM_001098623.1 D2843D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:228538629 G>T maps to NM_001098623.1 P6135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:228461587 G>A maps to NM_001098623.1 W1752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:228401965 C>T maps to NM_001098623.1 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:228462438 C>T maps to NM_001098623.1 G1950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:228471372 C>T maps to NM_001098623.1 T2969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:228509610 G>A maps to NM_001098623.1 P5023P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:228399549 G>A maps to NM_001098623.1 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:228464307 G>A maps to NM_001098623.1 V2126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:220432022 G>A maps to NM_015311.2 H603H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr2:220419339 G>A maps to NM_015311.2 Q1578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:220432903 C>T maps to NM_015311.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:220431645 T>C maps to NM_015311.2 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:220431578 G>A maps to NM_015311.2 Q703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:220420976 C>T maps to NM_015311.2 V1458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:220428116 G>A maps to NM_015311.2 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:220428290 G>A maps to NM_015311.2 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr2:220432656 G>A maps to NM_015311.2 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:220416383 C>T maps to NM_015311.2 P1850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:220428119 G>A maps to NM_015311.2 C879C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:133053908 G>A maps to ENST00000262283 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:133053366 G>A maps to ENST00000262283 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:133045400 C>T maps to ENST00000262283 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr8:133036961 G>T maps to ENST00000262283 C612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr15:28260068 C>T maps to NM_000275.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr15:28228547 A>G maps to NM_000275.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr15:28273045 C>T maps to NM_000275.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:28202749 G>A maps to NM_000275.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:28196948 A>G maps to NM_000275.2 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:28267659 C>T maps to NM_000275.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:28117029 T>C maps to NM_000275.2 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:28326975 C>T maps to NM_000275.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:28200301 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:28211896 C>T maps to NM_000275.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr15:28273113 G>A maps to NM_000275.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:28267659 C>T maps to NM_000275.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:28228547 A>G maps to NM_000275.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:17337927 C>T maps to NM_024578.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:68805444 A>C maps to NM_002538.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr7:97617860 C>G did not map to a codon.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr23:128696443 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:128692880 C>A did not map to a codon.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr23:128696443 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:128724128 T>C did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:128696443 A>G did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:128691384 C>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:128696420 C>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:128710478 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:128721028 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:128703272 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:128722239 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:128699841 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:128710311 C>A did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:128696443 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:128724128 T>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:128696441 A>G did not map to a codon.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr23:128691316 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:128691315 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:128701259 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:128696464 C>A did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:128724128 T>C did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr23:128724128 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:128709185 G>A did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:128701242 C>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:71068609 T>C maps to NM_017855.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:71063813 A>G maps to NM_017855.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:71062447 G>T maps to NM_017855.3 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:71062431 T>A maps to NM_017855.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:10584767 A>G maps to NM_002539.1 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr2:10583627 A>T maps to NM_002539.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:10584374 G>A maps to NM_002539.1 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:10581945 T>C maps to NM_002539.1 Q341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:10583400 G>A maps to NM_002539.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr2:10584353 C>A maps to NM_002539.1 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:10582161 A>G maps to NM_002539.1 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr8:103563969 T>C maps to NM_024410.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:131262482 T>A maps to NM_153435.1 Y877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:131221878 T>C maps to NM_153435.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:131247108 C>T maps to NM_153435.1 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:86852673 C>A maps to ENST00000370567 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:197382 G>T maps to NM_053280.3 G27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:197576 G>A maps to NM_053280.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:198473 G>A maps to NM_053280.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr11:197576 G>A maps to NM_053280.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:464278 C>T maps to NM_182577.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:8249133 A>G maps to NM_153007.4 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr17:8248733 C>T maps to NM_153007.4 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:123556125 A>C did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:123518180 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:123519820 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:123779166 C>T did not map to a codon.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr23:123517571 C>T did not map to a codon.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr23:123518055 T>C did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:123517614 G>T did not map to a codon.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr23:123787618 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:123518564 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:123554655 G>A did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr23:123515057 A>C did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr23:123697601 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:123514663 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:123657429 G>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:123518689 G>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:123785912 T>C did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:124097561 T>C did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:123517996 G>A did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:124030086 A>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:123514977 G>A did not map to a codon.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr23:123587293 T>C did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:123630895 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:123540293 T>C did not map to a codon.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr23:124097530 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:123518403 A>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:123539053 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:124028163 A>G did not map to a codon.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr23:123657428 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:123587225 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:123615731 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:124028185 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr23:123654487 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr23:123514918 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:123554200 C>T did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:124028200 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:124097459 T>C did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:123518288 C>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:123785912 T>C did not map to a codon.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr23:123785781 C>T did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:123514662 C>A did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:123517986 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:123519747 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:123870943 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr23:123517633 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:123517952 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:123526138 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:123680798 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:123787482 G>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:123785953 C>A did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:124097454 T>C did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:123587268 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:123775704 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:124029954 T>C did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:123526086 G>A did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:123556127 A>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:123517768 C>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:123654499 T>C did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:123775706 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:123630894 C>T did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:123538888 T>C did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:123554388 G>A did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:123556298 G>A did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:123785912 T>C did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:123518055 T>C did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:123518055 T>C did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:123775706 T>C did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:123519761 C>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:123556261 C>A did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:123517987 C>T did not map to a codon.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr23:123775704 A>G did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:123587237 A>T did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:123775706 T>C did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:123785912 T>C did not map to a codon.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr23:123787608 T>A did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:123805676 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:123517891 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:123517987 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:123516662 C>A did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:124030054 A>G did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:123517633 T>C did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:123517572 A>G did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:123654448 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:123699347 C>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:124029954 T>C did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:123514662 C>A did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:124030054 A>G did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:123657429 G>A did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr23:124030027 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:123615778 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:123514498 G>A did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:123775704 A>G did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:167689472 G>A maps to NM_001122679.1 R2652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:167379599 G>A maps to NM_001122679.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:167674777 C>T maps to NM_001122679.1 F2269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr5:167617468 G>T maps to NM_001122679.1 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr5:167626007 C>T maps to NM_001122679.1 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:167642230 C>T maps to NM_001122679.1 C1335C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:166802452 C>T maps to NM_001122679.1 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:167489224 C>A maps to NM_001122679.1 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:167674558 C>T maps to NM_001122679.1 Y2196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:167626885 C>T maps to NM_001122679.1 I1051I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr5:167553786 C>T maps to NM_001122679.1 H746H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:167674072 C>T maps to NM_001122679.1 D2034D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:167671460 C>T maps to NM_001122679.1 R1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:166711916 C>A maps to NM_001122679.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr5:167627063 C>T maps to NM_001122679.1 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr5:167379629 C>T maps to NM_001122679.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:167674825 C>T maps to NM_001122679.1 S2285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:183601837 C>A maps to NM_001080477.1 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:183603087 C>A maps to NM_001080477.1 C652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:183676245 C>T maps to NM_001080477.1 R1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:183713900 C>T maps to NM_001080477.1 R2026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr4:183245349 C>T maps to NM_001080477.1 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:183675914 C>T maps to NM_001080477.1 Y1465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:183714058 G>A maps to NM_001080477.1 T2078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:183601837 C>A maps to NM_001080477.1 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:183601867 C>T maps to NM_001080477.1 Y604Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:183714670 T>C maps to NM_001080477.1 F2282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:183720957 C>T maps to NM_001080477.1 N2518N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr4:183721101 C>T maps to NM_001080477.1 S2566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:183650166 C>T maps to NM_001080477.1 C806C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:183245349 C>T maps to NM_001080477.1 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:78387406 G>A maps to NM_001098816.2 I1762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:78369638 G>A maps to NM_001098816.2 R2592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:78419558 G>T maps to NM_001098816.2 G1352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:78399261 G>A maps to NM_001098816.2 S1699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr11:78369306 C>T maps to NM_001098816.2 A2702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:78387406 G>A maps to NM_001098816.2 I1762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:78381416 G>A maps to NM_001098816.2 D1991D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:78381548 G>A maps to NM_001098816.2 F1947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:78574129 G>A maps to NM_001098816.2 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:78381092 G>A maps to NM_001098816.2 N2099N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:78525372 G>A maps to NM_001098816.2 C583C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:78565254 G>A maps to NM_001098816.2 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:78775930 G>A maps to NM_001098816.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:78523350 G>A maps to NM_001098816.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:78602314 G>A maps to NM_001098816.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr11:78780857 G>T maps to NM_001098816.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr11:78413331 G>A maps to NM_001098816.2 A1442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:13785264 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:13778509 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:13778817 G>A did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:13778790 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:13786312 G>A did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr23:13787190 A>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:13762632 C>T did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:13774705 G>C did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:13753379 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:13778509 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:13778308 A>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:13779230 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:44714839 C>T maps to ENST00000444676 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:44684942 T>C maps to ENST00000444676 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr7:44687326 C>T maps to ENST00000444676 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:44736043 C>T maps to ENST00000444676 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr7:44737335 G>T maps to ENST00000444676 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:44721374 C>T maps to ENST00000444676 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:44737085 C>T maps to ENST00000444676 Y738Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr7:44737813 C>T maps to ENST00000444676 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:44733560 C>T maps to ENST00000444676 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:50944453 C>T maps to NM_018245.2 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:50952142 G>T maps to NM_018245.2 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:50955200 G>A maps to NM_018245.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:50954813 G>A maps to NM_018245.2 H426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:56509958 C>T maps to NM_018233.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:123463778 C>T maps to ENST00000228922 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:61444400 C>T maps to NM_007346.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:95152321 G>A maps to NM_033014.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr23:70787406 G>C did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:70782797 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:70775879 C>G did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:70783200 A>G did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:70777502 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:70793482 C>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:70775133 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:70782731 G>A did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:70757810 T>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:70757810 T>C did not map to a codon.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr10:74658647 C>T maps to NM_152635.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:74684189 G>T maps to NM_152635.1 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr10:74684315 C>T maps to NM_152635.1 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:174943721 C>A maps to ENST00000409546 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr2:175006597 T>C maps to ENST00000409546 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr2:175006588 A>G maps to ENST00000409546 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:175006597 T>C maps to ENST00000409546 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr2:175006588 A>G maps to ENST00000409546 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr2:175006597 T>C maps to ENST00000409546 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:15103763 G>T maps to NM_018324.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr9:138011624 G>A maps to NM_014279.4 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:137982069 G>A maps to NM_014279.4 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:138011655 C>T maps to NM_014279.4 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:9965419 C>T maps to NM_058164.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:9965026 C>T maps to NM_058164.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr19:9965377 G>A maps to NM_058164.2 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:9965017 G>A maps to NM_058164.2 Y403Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:102462312 A>G maps to NM_058170.2 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:102296353 G>T maps to ENST00000338858 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr1:102269826 A>G maps to ENST00000338858 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:102269835 A>G maps to ENST00000338858 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr13:53603148 T>C maps to NM_006418.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:53617311 G>T maps to NM_006418.3 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr13:53616067 T>C maps to NM_006418.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr13:53603176 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:7531358 G>A maps to NM_198474.3 W383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:127549349 C>T maps to NM_182487.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:127549423 C>T maps to NM_182487.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:127549504 C>T maps to NM_182487.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:127563820 C>T maps to NM_182487.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr9:127549501 G>T maps to NM_182487.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:127570177 C>A maps to NM_182487.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:127572537 C>T maps to NM_182487.2 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr9:127572249 A>G maps to NM_182487.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr9:127557401 C>T maps to NM_182487.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:127561610 C>T maps to NM_182487.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:127572543 G>A maps to NM_182487.2 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr1:161967993 G>A maps to ENST00000451379 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:161953998 G>A maps to ENST00000451379 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr1:161953842 G>A maps to ENST00000451379 D626D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr21:34399406 G>A maps to NM_005806.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:137814968 C>T maps to NM_175747.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr6:137815016 G>A maps to NM_175747.2 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:58971763 G>A maps to NM_145243.3 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:58946768 C>T maps to NM_145243.3 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:58999993 C>A maps to NM_145243.3 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:95178990 C>A maps to NM_005014.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:95179819 T>A maps to NM_005014.2 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr9:95179144 A>G maps to NM_005014.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr9:95179144 A>G maps to NM_005014.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr9:95179144 A>G maps to NM_005014.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr9:95179144 A>G maps to NM_005014.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:95179819 T>A maps to NM_005014.2 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:29622458 T>C maps to NM_002544.4 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:29622227 G>A maps to NM_002544.4 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:76814136 G>A maps to NM_006189.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr15:53081838 G>A maps to NM_004498.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:53081136 G>A maps to NM_004498.1 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr18:55143729 C>T maps to NM_004852.2 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr6:74079007 G>A maps to NM_001080507.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:74079352 C>A maps to NM_001080507.2 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr6:74079007 G>A maps to NM_001080507.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr3:193382708 T>G maps to NM_130837.2 L901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:98105697 T>G maps to NM_033207.3 *142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr11:132307167 C>T maps to NM_002545.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:132306127 T>C maps to NM_002545.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:132306563 C>T maps to NM_002545.3 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:132307146 G>A maps to NM_002545.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr23:67293119 C>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:67273522 A>G did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:67283807 G>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:67293105 C>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:67283807 G>T did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:67283809 T>C did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:67283807 G>T did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:67432019 T>G did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:67283809 T>C did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:145113683 G>A maps to ENST00000360660 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:145107139 G>A maps to ENST00000360660 H1131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr8:145111299 G>A maps to ENST00000360660 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr8:145113262 G>A maps to ENST00000360660 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:153416215 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:153418513 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:153418413 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:153418523 C>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:153421858 G>T did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:153459018 T>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:153496124 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:241767690 G>A maps to NM_014322.2 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:241757981 G>A maps to NM_014322.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:241767828 G>A maps to NM_014322.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:241761092 C>T maps to NM_014322.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:241767566 G>A maps to NM_014322.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:88423483 C>T maps to NM_001030015.2 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:88417833 C>T maps to NM_001030015.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:88419192 C>A maps to NM_001030015.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:47759708 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:47776029 G>A maps to ENST00000489301 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:29189569 T>C maps to NM_000911.3 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:54142294 G>A maps to NM_000912.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr8:54142312 G>A maps to NM_000912.3 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:54142288 G>A maps to NM_000912.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:54142009 G>A maps to NM_000912.3 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:62729283 G>A maps to NM_000913.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:62724276 G>T maps to NM_000913.3 G68G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AZ-4315-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:62729154 G>A maps to NM_000913.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:62729409 G>A maps to NM_000913.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:154412195 C>T maps to NM_001145279.1 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr6:154412345 C>T maps to NM_001145279.1 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:154360921 C>T maps to NM_001145279.1 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:154411263 A>G maps to NM_001145279.1 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:154412274 C>T maps to NM_001145279.1 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr6:154412384 G>A maps to NM_001145279.1 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:154414473 C>T maps to NM_001008505.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr6:154360813 C>T maps to NM_001145279.1 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr6:154414562 A>G maps to NM_001008505.1 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr6:154360589 C>T maps to NM_001145279.1 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:203465246 C>T maps to NM_014359.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr1:203465174 G>T maps to NM_014359.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:203467830 C>T maps to NM_014359.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:13174188 C>T maps to NM_021980.4 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:13160938 C>T maps to NM_021980.4 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:13174182 C>T maps to NM_021980.4 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr10:13167990 A>G maps to NM_021980.4 Q398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr10:13167990 A>G maps to NM_021980.4 Q398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr10:13167514 G>T maps to NM_021980.4 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:6897946 G>A maps to NM_207186.2 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:6867797 T>C maps to ENST00000379831 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr11:6867509 C>T maps to ENST00000379831 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr11:7949612 T>G maps to NM_001004461.1 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr12:55615515 G>A maps to NM_001005280.1 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:48596460 G>A maps to NM_001004134.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:55735228 T>A maps to NM_001005491.1 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr11:55735459 G>A maps to NM_001005491.1 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:55735675 A>G maps to NM_001005491.1 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:29408340 C>T maps to NM_013941.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:29408484 G>A maps to NM_013941.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:29408295 C>T maps to NM_013941.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:22102377 G>A maps to NM_001005466.1 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:22102476 A>G maps to NM_001005466.1 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr14:22038125 G>A maps to NM_001005465.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:22038674 G>A maps to NM_001005465.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr14:22038053 G>T maps to NM_001005465.1 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr14:22038671 T>C maps to NM_001005465.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:123886346 C>T maps to ENST00000375021 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:123886568 C>T maps to ENST00000375021 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:123887117 G>A maps to NM_001004462.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:123886823 G>A maps to NM_001004462.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:123887171 T>C maps to NM_001004462.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:123886823 G>A maps to NM_001004462.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:123886898 C>T maps to NM_001004462.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr11:123909291 C>T maps to NM_001004463.1 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:123909126 G>A maps to NM_001004463.1 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr11:123909231 G>T maps to NM_001004463.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr11:123900523 G>A maps to NM_001004464.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr11:123901252 T>G maps to ENST00000375021 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:123900427 C>T maps to NM_001004464.1 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr11:123901210 G>A maps to ENST00000375021 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:123900337 C>T maps to NM_001004464.1 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr11:123901210 G>A maps to ENST00000375021 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:15918448 G>A maps to NM_013940.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:15918640 G>A maps to NM_013940.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr19:15918100 C>T maps to NM_013940.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:15839209 C>T maps to NM_013939.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr19:15838975 C>T maps to NM_013939.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:15839044 C>T maps to NM_013939.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:16060635 C>T maps to NM_001004465.1 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:15905787 C>A maps to NM_001004466.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:15905217 C>T maps to NM_001004466.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:159409667 C>T maps to NM_012351.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr1:159283477 C>T maps to NM_001004467.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:159283756 T>C maps to NM_001004467.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:159283477 C>T maps to NM_001004467.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:159283723 G>A maps to NM_001004467.1 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr1:159284218 G>A maps to NM_001004467.1 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:159284368 G>A maps to NM_001004467.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr1:159504869 A>T maps to NM_001004469.1 *310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:159505499 G>A maps to NM_001004469.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:159505014 C>T maps to NM_001004469.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr1:159505128 G>C maps to NM_001004469.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr1:159505431 G>T maps to NM_001004469.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:158436254 C>T maps to NM_001004473.1 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:56031445 C>T maps to NM_206899.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:57995507 C>T maps to NM_001004471.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:57995612 G>T maps to NM_001004471.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr11:57995626 G>T maps to NM_001004471.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:57995921 G>A maps to NM_001004471.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:57995713 G>A maps to NM_001004471.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:158450236 C>T maps to NM_001004472.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:158450596 T>A maps to NM_001004472.1 Y310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:123847441 G>A maps to NM_001004474.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:123848245 A>G maps to NM_001004474.1 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:123847795 G>A maps to NM_001004474.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:123848008 T>G maps to NM_001004474.1 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:123848122 G>A maps to NM_001004474.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr11:59480924 G>A maps to NM_001005324.1 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:59480736 G>A maps to NM_001005324.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:59480616 C>T maps to NM_001005324.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr11:58034982 G>A maps to NM_207374.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:58034970 C>T maps to NM_207374.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:158549452 A>G maps to NM_001004477.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:158549275 G>A maps to NM_001004477.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr1:158548945 C>T maps to NM_001004477.1 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:158576569 T>C maps to NM_001004478.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:158576254 G>A maps to NM_001004478.1 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr6:29394569 G>T maps to NM_013937.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:20666270 C>T maps to NM_001005503.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:20665971 C>T maps to NM_001005503.1 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr14:20665628 C>T maps to NM_001005503.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr22:16449558 G>T maps to NM_001005239.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr14:20711204 C>T maps to NM_001004479.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:20711159 C>A maps to NM_001004479.1 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:20711036 T>C maps to NM_001004479.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:20692404 T>G maps to NM_001004480.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr14:20691876 T>C maps to NM_001004480.1 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:248004940 C>T maps to NM_001001959.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr1:248005087 C>A maps to NM_001001959.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:248005042 G>A maps to NM_001001959.1 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:248004945 G>A maps to NM_001001959.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:29364553 C>T maps to NM_013936.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:29342464 G>T maps to NM_030959.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:29342155 G>T maps to NM_030959.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:29342842 C>A maps to ENST00000396806 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr6:29342734 G>A maps to ENST00000396806 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:29342125 C>T maps to NM_030959.2 Q313Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:45799429 C>T maps to NM_001004297.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:45799153 G>A maps to NM_001004297.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr9:107367305 C>G maps to NM_001004481.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:107298488 A>G maps to NM_001001961.1 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:107288800 C>T maps to NM_001001919.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:107288806 C>T maps to NM_001001919.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:107289055 A>C maps to NM_001001919.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:107360992 T>C maps to NM_001004482.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr9:107360992 T>C maps to NM_001004482.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:107332342 C>T maps to NM_001004483.1 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr9:107331861 G>A maps to NM_001004483.1 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:107332342 C>T maps to NM_001004483.1 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr9:107332185 A>G maps to NM_001004483.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:107380260 G>T maps to NM_001001956.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:107380412 A>G maps to NM_001001956.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:107380212 G>C maps to NM_001001956.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr9:107457622 G>A maps to NM_001004484.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr9:107457526 G>A maps to NM_001004484.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:107457553 C>T maps to NM_001004484.1 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr9:107267334 T>C maps to NM_001004485.1 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:107266779 T>A maps to NM_001004485.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:107267379 C>T maps to NM_001004485.1 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr9:107266590 A>G maps to NM_001004485.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:247835434 T>C maps to NM_001005487.1 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:130678701 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:130678461 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:130678855 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr23:130678702 G>A did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr23:130678281 C>G did not map to a codon.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr9:35870161 A>G maps to NM_001004487.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr9:35870161 A>G maps to NM_001004487.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:247978491 G>T maps to NM_001001966.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:247978617 G>T maps to NM_001001966.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr1:247978437 G>T maps to NM_001001966.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:248512474 C>T maps to NM_001001918.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:248512741 C>T maps to NM_001001918.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:29275134 G>A maps to NM_030946.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:29275148 C>A maps to NM_030946.1 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:29275012 C>T maps to NM_030946.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:3119639 C>A maps to NM_014565.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr9:125391061 G>C maps to NM_001004450.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr9:125390977 C>A maps to NM_001004450.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:247921327 G>A maps to NM_012353.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:247920898 G>A maps to NM_012353.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:247921360 A>T maps to NM_012353.2 C116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:247921381 A>G maps to NM_012353.2 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr1:247920772 C>T maps to NM_012353.2 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:247920774 G>A maps to NM_012353.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:2995828 G>T maps to NM_002548.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:3301266 C>T maps to NM_003553.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:3337108 G>T maps to NM_003554.1 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:3336709 G>A maps to NM_003554.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:3254831 G>T maps to NM_012360.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:3254671 C>A maps to NM_012360.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:3030179 G>A maps to ENST00000381953 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:3030101 G>T maps to ENST00000381953 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:3030107 G>A maps to ENST00000381953 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:15198439 C>T maps to NM_001004713.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:15198535 C>T maps to NM_001004713.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:15197902 C>A maps to NM_001004713.1 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:15198244 C>T maps to NM_001004713.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:15198308 C>T maps to NM_001004713.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:15198235 C>T maps to NM_001004713.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr19:15198451 G>A maps to NM_001004713.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:15198877 A>G maps to NM_001004713.1 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr9:125239587 G>A maps to NM_001004451.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:125239293 G>T maps to NM_001004451.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:125240138 G>A maps to NM_001004451.1 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:125273547 C>A maps to ENST00000444856 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr9:125273429 C>A maps to ENST00000444856 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:125282009 G>T maps to NM_001004452.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr9:125281979 C>A maps to NM_001004452.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:125562826 C>T maps to NM_080859.1 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:125562517 C>T maps to NM_080859.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:125562439 C>T maps to NM_080859.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:125424584 C>A maps to ENST00000373686 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr9:125424242 G>T maps to ENST00000373686 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:125438016 G>A maps to NM_001005234.1 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr9:125486297 C>A maps to NM_001005235.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:125512494 G>T maps to ENST00000373684 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr9:125330267 C>T maps to NM_001004454.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr19:9204468 C>T maps to ENST00000305465 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:9204354 C>T maps to ENST00000305465 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:125289158 G>T maps to ENST00000359439 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:125289098 C>T maps to ENST00000359439 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:125288893 G>A maps to ENST00000359439 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr9:125289521 C>T maps to ENST00000359439 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:125316436 T>G maps to NM_001004457.1 L330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:125316107 C>A maps to NM_001004457.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:125315557 G>A maps to NM_001004457.1 W37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:125316166 G>A maps to NM_001004457.1 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:125377084 G>A maps to NM_012364.1 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:125377666 C>A maps to NM_012364.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr7:143792499 T>G maps to NM_001004135.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr7:143793069 C>T maps to NM_001004135.1 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr7:143792232 C>T maps to NM_001004135.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr7:143792808 G>A maps to NM_001004135.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr7:143747796 C>A maps to NM_012365.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:143956019 C>T maps to NM_001005328.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:99474173 C>T maps to NM_001005276.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:6807162 C>A maps to NM_001004489.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:6789861 G>A maps to NM_001004490.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:6789408 G>T maps to NM_001004490.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr11:6789378 T>C maps to NM_001004490.1 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:6789444 G>A maps to NM_001004490.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr11:6789378 T>C maps to NM_001004490.1 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:6789369 G>A maps to NM_001004490.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:6789378 T>C maps to NM_001004490.1 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:248129157 A>T maps to NM_001004491.1 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:74800046 C>A maps to NM_001005285.1 G238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:247614507 C>T maps to NM_001004492.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:247615089 G>T maps to NM_001004492.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:247615146 G>A maps to NM_001004492.1 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:247614974 G>A maps to NM_001004492.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:29054809 G>T maps to NM_001005226.2 C72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:27925038 C>T maps to NM_012367.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:27925290 A>C maps to NM_012367.1 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:3406857 G>A maps to NM_012368.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:247695740 C>A maps to NM_198074.4 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:6913725 T>C maps to NM_003700.1 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr11:6912966 T>A maps to NM_003700.1 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:6942838 C>T maps to NM_001004684.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:6942480 C>A maps to NM_001004684.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr7:143657545 T>C maps to NM_012369.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr7:143657083 T>G maps to NM_012369.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr7:143632418 T>C maps to NM_001004685.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr7:143632420 G>A maps to NM_001004685.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:143633236 A>T maps to NM_001004685.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:247752482 C>A maps to NM_001001915.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:247768890 G>T maps to NM_001001914.1 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:247769681 C>T maps to NM_001001914.1 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:247768890 G>T maps to NM_001001914.1 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:247769027 C>A maps to NM_001001914.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr1:248685372 G>A maps to NM_001013355.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:248685228 C>T maps to NM_001013355.1 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr1:248685642 G>A maps to NM_001013355.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr1:248685525 T>C maps to NM_001013355.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:248685294 C>T maps to NM_001013355.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr1:248685288 C>T maps to NM_001013355.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:248685525 T>C maps to NM_001013355.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr1:248685525 T>C maps to NM_001013355.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr1:248685525 T>C maps to NM_001013355.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:29430313 C>A maps to NM_030883.3 V256V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3977-01A-01W-0995-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-A010-01A-01W-A00E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:29556270 C>T maps to NM_007160.3 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:29079939 G>A maps to NM_001005216.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:29080338 C>T maps to NM_001005216.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:114090629 G>A maps to ENST00000374428 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:248262919 G>A maps to NM_175911.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:248262847 G>A maps to NM_175911.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:248263243 A>G maps to NM_175911.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr1:248263243 A>G maps to NM_175911.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:248263243 A>G maps to NM_175911.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:248201883 T>C maps to NM_001004686.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:248201883 T>A maps to NM_001004686.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:248112938 T>A maps to NM_001001963.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr1:248112938 T>C maps to NM_001001963.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr1:248112908 C>T maps to NM_001001963.1 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:248343302 C>T maps to NM_001004688.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:248402565 T>C maps to NM_017504.1 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:248402844 A>G maps to NM_017504.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:248403115 G>T maps to NM_017504.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:248402896 C>T maps to NM_017504.1 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr1:248402565 T>C maps to NM_017504.1 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr1:248308998 C>T maps to NM_001004690.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:248309015 C>T maps to NM_001004690.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:248487420 G>A maps to NM_001004691.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:248487281 C>A maps to NM_001004691.1 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:35957816 G>T maps to NM_019897.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr9:35957426 G>A maps to NM_019897.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:248569327 C>T maps to NM_030904.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr1:248570068 G>T maps to NM_030904.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr1:248570143 C>A maps to NM_030904.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:248570398 C>A maps to NM_030904.1 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:248756790 C>T maps to NM_001004693.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:248789661 G>A maps to NM_001001964.1 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:248789634 G>T maps to NM_001001964.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:248790375 A>G maps to NM_001001964.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr1:248789634 G>A maps to NM_001001964.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:248790144 G>T maps to NM_001001964.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:248458364 G>T maps to NM_001004692.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr1:248616139 C>A maps to NM_001004136.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr1:248813351 G>T maps to NM_001001824.1 Y278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:248813771 G>A maps to NM_001001824.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:248813941 G>A maps to NM_001001824.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr1:248436750 C>T maps to NM_001004695.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr1:248525115 C>A maps to NM_001004696.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:248551172 C>T maps to NM_001005471.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr1:248551277 C>T maps to NM_001005471.1 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:248551598 G>A maps to NM_001005471.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:248084903 C>T maps to NM_001005522.1 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:180581952 G>A maps to NM_206880.1 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:180581977 C>T maps to NM_206880.1 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr5:180582343 C>A maps to NM_206880.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr5:180582343 C>A maps to NM_206880.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:29012622 A>G maps to NM_030903.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:29012163 A>G maps to NM_030903.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr1:248059394 T>C maps to NM_001001957.2 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:248058989 G>A maps to NM_001001957.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:248059403 C>T maps to NM_001001957.2 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:248059355 C>A maps to NM_001001957.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:247654758 C>A maps to NM_001004698.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:247654839 C>T maps to NM_001004698.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:180166677 A>G maps to NM_001001657.1 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr5:180166926 G>A maps to NM_001001657.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:180166896 C>T maps to NM_001001657.1 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:180166995 C>T maps to NM_001001657.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:8842178 C>T maps to NM_001004699.1 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:8842058 G>A maps to NM_001004699.1 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:3195086 G>A maps to ENST00000397187 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr17:3195801 C>A maps to ENST00000397187 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr17:3181737 G>A maps to NM_002551.3 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:3324553 A>G maps to NM_012373.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:3324784 C>T maps to NM_012373.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:3324355 A>G maps to NM_012373.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:55135806 C>T maps to NM_001005275.1 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:55111518 T>C maps to NM_001005274.1 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:55110865 T>C maps to NM_001005274.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr11:55110865 T>C maps to NM_001005274.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr11:48510481 C>T maps to NM_001005512.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr11:51411756 G>A maps to NM_001005272.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:51411756 G>T maps to NM_001005272.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr11:51411696 G>A maps to NM_001005272.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:51411509 C>A maps to NM_001005272.3 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:51411989 G>A maps to NM_001005272.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr11:48239116 T>C maps to NM_001005470.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:48238564 G>A maps to NM_001005470.1 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:48238498 G>A maps to NM_001005470.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:48238918 C>A maps to NM_001005470.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr11:55370957 T>A maps to NM_001004700.1 K298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:55371372 G>A maps to NM_001004700.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:55371420 A>T maps to NM_001004700.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:55370930 C>A maps to NM_001004700.1 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr11:55371456 T>C maps to NM_001004700.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:50003775 T>A maps to NM_001005270.2 K88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr11:49974324 C>T maps to NM_001001955.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr11:49974225 C>G maps to NM_001001955.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:49973979 G>A maps to NM_001001955.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:49974621 C>T maps to NM_001001955.2 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:55322877 G>T maps to NM_001001920.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr11:55321799 A>G maps to NM_001001920.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr11:55322678 T>C maps to NM_001001920.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:55321789 C>A maps to NM_001001920.1 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr11:55322678 T>C maps to NM_001001920.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr11:55322678 T>C maps to NM_001001920.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr11:55322678 T>C maps to NM_001001920.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:55340358 C>T maps to NM_001004701.2 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:48347010 T>G maps to NM_001004702.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:51515835 C>T maps to NM_001004703.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:51515475 C>A maps to NM_001004703.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr11:51515862 A>G maps to NM_001004703.1 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr11:55433100 C>T maps to NM_001004704.1 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:56232780 C>T maps to NM_012374.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:56232615 C>A maps to NM_012374.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr17:56232603 G>A maps to NM_012374.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:56232600 T>C maps to NM_012374.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:59245543 C>A maps to NM_001004705.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:59244928 A>C maps to NM_001004705.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:59271891 C>T maps to NM_001004706.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr11:59271221 C>A maps to NM_001004706.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr11:59271711 C>T maps to NM_001004706.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:56247576 T>C maps to NM_001004707.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:123810832 G>A maps to NM_001001965.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:123810598 T>C maps to NM_001001965.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:123810763 C>A maps to NM_001001965.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr11:123811042 T>C maps to NM_001001965.1 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:59224747 C>T maps to NM_001004708.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr11:59225155 G>A maps to NM_001004708.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr14:22133652 G>A maps to NM_001001912.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr15:102346251 T>C maps to NM_001005326.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr15:102346251 T>C maps to NM_001005326.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:102346377 T>C maps to NM_001005326.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr14:20404577 C>T maps to NM_001004063.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr14:20404532 T>C maps to NM_001004063.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr14:20404256 T>C maps to NM_001004063.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr14:20404720 G>A maps to NM_001004063.2 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:20502353 G>T maps to NM_001004714.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:20502845 C>T maps to NM_001004714.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:20482571 G>T maps to NM_001004712.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr14:20482659 G>T maps to NM_001004712.1 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:20443687 C>A maps to NM_001005486.1 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr14:20444054 C>T maps to NM_001005486.1 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:20586305 C>T maps to NM_001004715.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:20585618 C>A maps to NM_001004715.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr14:20586242 A>G maps to NM_001004715.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr14:20345166 C>A maps to NM_001005501.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:20345145 T>C maps to NM_001005501.1 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr14:20388944 C>A maps to NM_001005483.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:20389031 C>T maps to NM_001005483.1 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:20389115 G>A maps to NM_001005483.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr14:20389103 G>T maps to NM_001005483.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr14:20528493 C>T maps to NM_001004717.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr14:20528253 T>C maps to NM_001004717.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr14:20528232 C>T maps to NM_001004717.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:20248973 C>T maps to NM_001005500.1 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:22368742 C>A maps to NM_001004719.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr14:20295717 C>A maps to NM_001004723.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr15:22382837 C>T maps to NM_001005241.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr15:22382942 T>C maps to NM_001005241.1 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr14:20612085 C>T maps to NM_001004724.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr14:20612745 T>C maps to NM_001004724.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr14:20612745 T>A maps to NM_001004724.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr14:20612745 T>C maps to NM_001004724.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr14:20612454 G>T maps to NM_001004724.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:55406282 A>T maps to NM_001004124.1 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:55405953 T>C maps to NM_001004124.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:55406747 C>T maps to NM_001004124.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr14:20215705 G>A maps to NM_172194.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:20216359 C>A maps to NM_172194.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:48328628 T>C maps to NM_001004725.1 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr11:48328640 C>T maps to NM_001004725.1 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:48328241 G>A maps to NM_001004725.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:48328640 C>T maps to NM_001004725.1 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:48328625 C>T maps to NM_001004725.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:55418648 C>A maps to NM_001004059.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:55418889 G>T maps to NM_001004059.2 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:55418784 C>A maps to NM_001004059.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr11:55418396 C>T maps to NM_001004059.2 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr11:48286059 C>T maps to NM_001004726.1 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:48285591 T>C maps to NM_001004726.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:48266700 C>T maps to NM_001004727.1 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr11:48267293 C>A maps to NM_001004727.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:4967599 G>T maps to NM_001005329.1 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:4928754 G>A maps to NM_001004749.1 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:4929078 C>A maps to NM_001004749.1 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:4929324 C>A maps to NM_001004749.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:4928899 G>T maps to NM_001004749.1 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr11:4929198 C>T maps to NM_001004749.1 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:4929537 A>C maps to NM_001004749.1 *313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr11:5345047 A>G maps to NM_033180.4 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr11:5344729 C>T maps to NM_033180.4 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:5322957 G>A maps to NM_033179.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:5322810 G>T maps to NM_033179.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr11:5364066 C>A maps to NM_001005567.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:5364181 G>A maps to NM_001005567.1 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:5364391 A>G maps to NM_001005567.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:5373426 A>G maps to NM_001004750.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:5373597 A>C maps to NM_001004750.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr11:5373477 G>T maps to NM_001004750.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:4674157 C>T maps to NM_152430.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:4674343 G>A maps to NM_152430.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr11:4703038 C>T maps to NM_030774.3 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr11:4790478 A>T maps to ENST00000380383 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr11:4842656 G>A maps to NM_001004753.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr11:4842792 C>T maps to NM_001004753.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr11:4842728 G>A maps to NM_001004753.1 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr11:4842927 G>T maps to NM_001004753.1 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:4843352 A>G maps to NM_001004753.1 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:4944641 G>A maps to NM_001005237.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:4945422 G>A maps to NM_001005237.1 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:4944972 G>T maps to NM_001005237.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:4945056 G>A maps to NM_001005237.1 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:4936269 G>A maps to NM_001005238.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:4936062 G>T maps to NM_001005238.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:4936380 G>A maps to NM_001005238.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:4936869 G>A maps to NM_001005238.1 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:5462456 A>G maps to NM_001005288.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:5474837 G>T maps to NM_001004754.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:5475048 G>T maps to NM_001004754.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:5020400 C>A maps to NM_001004755.1 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:5410669 A>G maps to NM_001004756.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:5411326 C>A maps to NM_001004756.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr11:5411389 C>T maps to NM_001004756.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:5410664 C>T maps to NM_001004756.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:5410684 G>A maps to NM_001004756.2 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:5443852 A>G maps to NM_001004757.2 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:5443975 C>T maps to NM_001004757.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:4870072 G>T maps to NM_001004758.1 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:4869963 G>A maps to NM_001004758.1 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:4870096 G>T maps to NM_001004758.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:4869963 G>A maps to NM_001004758.1 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr11:4903875 A>G maps to NM_001004759.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:4903825 C>T maps to NM_001004759.1 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr11:4903503 C>T maps to NM_001004759.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:5221605 G>A maps to NM_001004760.2 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:5221312 G>A maps to NM_001004760.2 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:5221177 G>A maps to NM_001004760.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:5173257 T>C maps to NM_012375.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:5173119 T>C maps to NM_012375.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr11:5172993 A>G maps to NM_012375.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:5153488 G>T maps to NM_001005160.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:5153614 G>T maps to NM_001005160.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr11:4388613 C>T maps to NM_001005161.3 Q304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr11:4388694 C>T maps to NM_001005161.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr11:5603050 G>A maps to NM_001005162.2 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr11:5603050 G>A maps to NM_001005162.2 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:5510463 C>A maps to NM_001005163.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:5080740 G>A maps to NM_001005164.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:5080028 G>A maps to NM_001005164.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr11:5080374 A>G maps to NM_001005164.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:5080197 C>T maps to NM_001005164.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:5906175 C>A maps to NM_001005165.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr11:5862647 T>A maps to ENST00000379946 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:5862356 A>G maps to ENST00000379946 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr11:5566240 C>A maps to NM_001005289.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:4615414 C>T maps to ENST00000450052 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:4608338 G>T maps to NM_001005170.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr11:4608707 C>T maps to NM_001005170.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:5068048 T>G maps to NM_001001916.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr11:5067892 C>T maps to NM_001001916.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:4510478 C>T maps to NM_001005171.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr11:4510283 C>T maps to NM_001005171.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:4510882 G>A maps to NM_001005171.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:4471423 C>T maps to NM_001005172.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:4471096 C>T maps to NM_001005172.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:6008058 C>T maps to NM_001005173.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr11:6008034 C>T maps to NM_001005173.2 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:6007521 A>G maps to NM_001005173.2 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr11:6008109 G>A maps to NM_001005173.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:6007674 G>A maps to NM_001005173.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:4567178 C>A maps to NM_001004137.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:4566482 G>A maps to NM_001004137.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:5841693 G>A maps to NM_001005174.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:5842224 C>T maps to NM_001005174.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:5776812 T>C maps to NM_001005175.2 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr11:5776743 C>T maps to NM_001005175.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:5776827 A>G maps to NM_001005175.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:5776410 G>A maps to NM_001005175.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:5799162 C>T maps to NM_001001922.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:5798955 T>A maps to NM_001001922.2 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:4825379 G>T maps to ENST00000380382 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:4825181 G>A maps to ENST00000380382 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:4824866 G>T maps to ENST00000380382 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:4825511 C>T maps to ENST00000380382 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:6220548 G>A maps to NM_001005178.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr11:6048910 G>T maps to NM_001001917.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr11:6048469 A>G maps to NM_001001917.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:6048454 C>T maps to NM_001001917.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr11:6048826 C>A maps to NM_001001917.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:6048727 C>T maps to NM_001001917.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:5969451 C>T maps to NM_001003443.2 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:5969196 C>T maps to NM_001003443.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:5757841 G>A maps to NM_001005180.2 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:6129151 T>C maps to NM_001005181.1 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr11:6129814 A>G maps to NM_001005181.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr11:6129814 A>G maps to NM_001005181.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr11:59211351 A>G maps to NM_001004728.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr11:59211349 C>T maps to NM_001004728.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr11:59211349 C>T maps to NM_001004728.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr3:97806441 C>G maps to NM_054106.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr11:56756786 T>C maps to NM_001005323.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:59132242 C>T maps to NM_001004729.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:56409426 G>A maps to NM_001002925.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:56409549 G>A maps to NM_001002925.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr11:56409030 G>A maps to NM_001002925.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:56409426 G>A maps to NM_001002925.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:55798412 C>T maps to NM_001001921.1 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:55798583 C>A maps to NM_001001921.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr11:55798442 T>C maps to NM_001001921.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:55798730 T>A maps to NM_001001921.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:55798730 T>C maps to NM_001001921.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:21623809 G>T maps to NM_001004731.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:21623755 G>T maps to NM_001004731.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:58206976 G>A maps to NM_001004733.2 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:58206849 G>A maps to NM_001004733.2 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr11:58126176 T>C maps to NM_001005489.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:58126161 G>A maps to NM_001005489.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr11:58190500 C>T maps to NM_001005566.2 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:58170591 A>T maps to NM_001005469.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:58170144 G>A maps to NM_001005469.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:125551927 G>A maps to NM_001001923.1 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:55541761 G>A maps to NM_001001967.1 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:55541011 C>T maps to NM_001001967.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:55563633 T>G maps to NM_001004735.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr11:55563237 T>C maps to NM_001004735.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:55563273 C>A maps to NM_001004735.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr11:55563699 T>A maps to NM_001004735.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:55563432 T>C maps to NM_001004735.1 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:55606628 C>T maps to NM_001005496.1 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr11:55606991 C>T maps to NM_001005496.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr11:55606640 C>A maps to NM_001005496.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr11:55606331 A>G maps to NM_001005496.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr11:55606580 G>T maps to NM_001005496.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:55587695 G>A maps to ENST00000395203 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:55761879 T>C maps to NM_003697.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:55761294 A>G maps to NM_003697.1 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:55761515 C>A maps to NM_003697.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:55761777 C>T maps to NM_003697.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr11:55762041 C>T maps to NM_003697.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:97851906 C>T maps to NM_001005338.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:97852456 A>T maps to NM_001005338.1 K306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:97851849 G>A maps to NM_001005338.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:97887716 A>C maps to NM_001005515.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr3:97888307 T>C maps to NM_001005515.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr3:97888307 T>C maps to NM_001005515.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:97887707 T>G maps to NM_001005515.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr3:98001793 A>G maps to NM_001005482.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:98001793 A>G maps to NM_001005482.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr3:98001889 T>C maps to NM_001005482.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr3:98001793 A>G maps to NM_001005482.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr3:98002357 C>A maps to NM_001005482.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:98001793 A>G maps to NM_001005482.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:98001847 C>A maps to NM_001005482.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr3:97984009 C>A maps to NM_001005479.1 Y294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:97983781 C>T maps to NM_001005479.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr3:97983781 C>T maps to NM_001005479.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:55703830 G>A maps to NM_006637.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:55703726 C>T maps to NM_006637.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:55703860 T>G maps to NM_006637.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:55702964 C>T maps to NM_006637.1 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:55944980 C>T maps to NM_001005492.1 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:55944593 C>A maps to NM_001005492.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr3:98189344 T>C maps to NM_001004736.2 *309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr3:98189346 A>G maps to NM_001004736.2 *309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:98216964 C>G maps to NM_001004737.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:98216982 T>C maps to NM_001004737.1 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr3:98216961 A>G maps to NM_001004737.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:98217147 C>A maps to NM_001004737.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr3:98216961 A>G maps to NM_001004737.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr3:98109983 G>T maps to NM_001005516.1 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:98073299 C>A maps to NM_001005517.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:98073095 C>T maps to NM_001005517.1 H133H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:98073320 C>A maps to NM_001005517.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:98073002 T>G maps to NM_001005517.1 Y102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:55579091 G>A maps to NM_001004738.1 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr11:55579544 G>T maps to NM_001004738.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:55595260 C>A maps to NM_001004739.1 C189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:55595260 C>T maps to NM_001004739.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:56345140 G>A maps to NM_001004741.1 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr11:56310187 C>T maps to NM_001005245.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:56310595 T>G maps to NM_001005245.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:56237700 A>C maps to NM_001004742.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:56237172 C>T maps to NM_001004742.1 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:56237628 C>T maps to NM_001004742.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:56237700 A>G maps to NM_001004742.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:56258204 A>G maps to NM_001005282.1 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:56258444 T>C maps to NM_001005282.1 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr11:56258225 A>C maps to NM_001005282.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:56230604 G>T maps to NM_001004743.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr11:7818264 G>T maps to NM_153444.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:7847318 G>T maps to NM_153445.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:56185348 G>A maps to NM_001004744.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:56185492 A>G maps to NM_001004744.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr11:56185149 G>A maps to NM_001004744.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:56184841 G>T maps to NM_001004744.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:56185014 G>A maps to NM_001004744.1 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:56043491 C>A maps to NM_001004745.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:56043860 C>A maps to NM_001004745.1 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:56043791 C>T maps to NM_001004745.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr11:56000490 T>G maps to NM_001004746.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr11:55999590 A>T maps to NM_001004746.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr11:55999590 A>T maps to NM_001004746.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:56000450 G>A maps to NM_001004746.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr11:56000325 A>C maps to NM_001004746.1 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:55999590 A>T maps to NM_001004746.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr11:55999590 A>T maps to NM_001004746.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:55999764 C>T maps to NM_001004746.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:56020316 C>T maps to NM_001004747.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:56020328 T>G maps to NM_001004747.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr6:29323444 G>T maps to NM_030876.5 Y176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:29323908 C>A maps to NM_030876.5 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr6:29323189 C>T maps to NM_030876.5 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:29323941 C>A maps to NM_030876.5 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr6:29323084 G>A maps to NM_030876.5 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr11:55681275 C>T maps to NM_001001960.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr11:55681964 A>G maps to NM_001001960.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:143701445 C>A maps to NM_001005281.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr2:240969702 G>A maps to NM_001005853.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:240985204 G>A maps to NM_173351.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:240985306 G>A maps to NM_173351.1 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:240985213 G>T maps to NM_173351.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:240984766 G>A maps to NM_173351.1 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:55714889 T>C maps to NM_001005182.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:55715022 C>T maps to NM_001005182.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:55714574 C>T maps to NM_001005182.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:55714457 C>A maps to NM_001005182.1 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:55714733 C>A maps to NM_001005182.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:55715216 A>G maps to NM_001005182.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:55714457 C>A maps to NM_001005182.1 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:55846461 T>C maps to NM_054105.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:55725678 C>T maps to NM_054104.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:55945640 C>T maps to NM_001005494.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:55688899 C>A maps to NM_001005493.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:55688083 T>C maps to NM_001005493.1 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:55794636 G>T maps to NM_001005518.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr12:55886732 C>G maps to NM_001005519.1 S196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr12:55641442 C>A maps to NM_001005490.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr12:55641793 C>T maps to NM_001005490.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:55641264 C>A maps to NM_001005490.1 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:55641650 G>T maps to NM_001005490.1 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:55641679 G>A maps to NM_001005490.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr12:55759367 A>G maps to NM_001005497.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:55759559 A>G maps to NM_001005497.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr1:247875721 G>T maps to NM_001005286.1 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:247875849 C>A maps to NM_001005286.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:247875328 C>T maps to NM_001005286.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr1:158670124 G>A maps to NM_001005279.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:158669553 C>A maps to NM_001005279.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:158687572 C>T maps to ENST00000368146 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:158687572 C>T maps to ENST00000368146 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:158687275 G>A maps to ENST00000368146 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:158687896 G>A maps to ENST00000368146 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr1:158735896 C>T maps to NM_001005185.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:158735965 A>G maps to NM_001005185.1 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:158735653 G>A maps to NM_001005185.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:158746957 G>A maps to NM_001005278.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:158746611 G>A maps to NM_001005278.1 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:57798681 T>G maps to NM_001005186.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:57799098 C>T maps to NM_001005186.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:21108946 C>A maps to NM_001001968.1 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:123813681 G>A maps to NM_001005187.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:123814296 G>A maps to NM_001005187.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:123814125 G>T maps to NM_001005187.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr11:123624863 G>A maps to NM_001005188.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:123624776 G>A maps to NM_001005188.1 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:158517442 T>C maps to NM_001005189.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr1:158517442 T>C maps to NM_001005189.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:158517778 G>T maps to NM_001005189.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:14938282 C>T maps to NM_017506.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:14938735 G>A maps to NM_017506.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:14938348 G>A maps to NM_017506.1 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:14910332 G>A maps to NM_198944.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:14910660 G>A maps to NM_198944.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:15052824 G>A maps to NM_012377.1 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:15052698 G>T maps to NM_012377.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr19:9296784 C>T maps to NM_175883.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr19:9296784 C>T maps to NM_175883.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr19:9296786 G>A maps to NM_175883.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:9296784 C>T maps to NM_175883.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:9325017 A>G maps to NM_001005191.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:9362738 G>T maps to NM_001079935.1 *340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:9225896 G>A maps to ENST00000293614 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:9213940 G>A maps to NM_001005193.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:9213718 G>T maps to NM_001005193.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:9213856 C>T maps to NM_001005193.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr19:9237556 G>A maps to NM_001001958.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr19:9237176 G>A maps to NM_001001958.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:9236903 G>A maps to NM_001001958.1 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr11:124440425 T>A maps to NM_001005194.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr11:124440425 T>C maps to NM_001005194.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:124413511 G>A maps to NM_001005195.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:124252918 G>A maps to NM_001005468.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr11:124293906 C>A maps to NM_001005196.1 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:124294277 G>A maps to NM_001005196.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:124310066 C>T maps to NM_012378.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:124310897 G>A maps to NM_012378.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr11:124180530 G>T maps to NM_001002917.1 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr11:124189868 A>G maps to NM_001002918.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:124189373 A>G maps to NM_001002918.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:124189159 A>G maps to NM_001002918.1 *312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr11:124189868 A>G maps to NM_001002918.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:123777206 T>G maps to NM_001005197.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:124120466 T>C maps to ENST00000341493 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr11:124120431 G>T maps to ENST00000341493 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:124095708 C>A maps to NM_001007249.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:56057802 C>A maps to NM_001005199.1 G246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:56058406 C>T maps to NM_001005199.1 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:56058172 G>A maps to NM_001005199.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr11:55873039 T>C maps to NM_001005200.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr11:55873183 C>G maps to NM_001005200.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:55873207 C>T maps to NM_001005200.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:55872802 G>A maps to NM_001005200.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:55889986 C>T maps to NM_001005201.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr11:55890369 T>C maps to NM_001005201.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:55861445 C>A maps to NM_001003750.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:56128418 G>T maps to NM_001005205.1 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr11:56128009 A>G maps to NM_001005205.1 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:55904864 C>T maps to NM_001004064.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr11:56113951 A>C maps to NM_001002907.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:56113867 C>A maps to NM_001002907.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:56113867 C>A maps to NM_001002907.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:56113822 T>C maps to NM_001002907.1 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:56086255 A>T maps to NM_001005202.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr11:56086253 C>T maps to NM_001005202.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:56086172 C>T maps to NM_001005202.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr11:56086459 C>T maps to NM_001005202.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:56086519 G>A maps to NM_001005202.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr11:55927528 G>A maps to NM_001004058.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:55927361 C>T maps to NM_001004058.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:48919887 C>A maps to NM_001005203.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:142723544 C>T maps to NM_001001658.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:141618746 T>C maps to NM_001001656.1 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:141618902 C>T maps to NM_001001656.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:141619148 G>A maps to NM_001001656.1 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr7:141619328 C>T maps to NM_001001656.1 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:56468210 C>T maps to NM_001013358.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:56510876 G>A maps to NM_001005284.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr11:56511136 A>G maps to NM_001005284.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:56510788 C>A maps to NM_001005284.1 G167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr11:56510545 C>A maps to NM_001005284.1 G248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:57947110 C>T maps to NM_001005212.3 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr11:57947605 T>C maps to NM_001005212.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr11:57947605 T>C maps to NM_001005212.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr7:102079549 G>A maps to NM_032831.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr11:69482287 C>T maps to NM_153451.2 *138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:52867825 G>A maps to NM_004153.3 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:52854182 A>C maps to NM_004153.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:52854886 A>G did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:52863404 C>T maps to NM_004153.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:52850924 A>T maps to NM_004153.3 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:52859245 G>T maps to NM_004153.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:201796102 T>C maps to NM_006190.4 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:201800456 C>A maps to NM_006190.4 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:88326096 C>A maps to NM_181837.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:88326096 C>A maps to NM_181837.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:88311548 C>T maps to NM_181837.2 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:148693242 C>A maps to NM_181742.3 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:103824452 C>T maps to NM_002553.3 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:103838177 C>A maps to NM_002553.3 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:103828731 A>G maps to NM_002553.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:117086076 C>T maps to NM_000607.2 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:117087088 C>T maps to NM_000607.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:117087163 G>A maps to NM_000607.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:117086073 G>A maps to NM_000607.2 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr9:117093886 G>A maps to NM_000608.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:117094196 C>T maps to NM_000608.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:56212842 A>G maps to NM_014182.4 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr12:58088057 G>A maps to NM_006812.3 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:58114604 G>A maps to NM_006812.3 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:58109595 C>T maps to NM_006812.3 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:59369197 C>T maps to NM_002556.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:59376001 G>A maps to NM_002556.2 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr22:31137318 C>T maps to NM_030758.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:31301829 C>T maps to NM_030758.3 N794N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr3:31743922 G>A maps to NM_017784.4 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:31921212 G>A maps to NM_017784.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:31871612 G>A maps to NM_017784.4 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:31703605 G>A maps to NM_017784.4 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:125295146 C>T maps to NM_022776.4 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr3:125298790 T>C maps to NM_022776.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:21891974 A>G maps to NM_080597.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr18:21897127 A>G maps to NM_080597.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr18:21758089 A>G maps to NM_080597.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr18:21759757 C>T maps to NM_080597.2 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:60868921 C>T maps to NM_144498.1 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:60859134 G>A maps to NM_144498.1 W302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr20:60856152 C>T maps to NM_144498.1 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr20:60847221 T>C maps to NM_144498.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr20:60847221 T>C maps to NM_144498.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr20:60847221 T>C maps to NM_144498.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr7:24874212 C>T maps to NM_015550.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:24874170 G>A maps to NM_015550.2 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:24844018 G>A maps to NM_015550.2 Q828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:24874338 A>G maps to NM_015550.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:24846423 A>G maps to NM_015550.2 P805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:24874131 C>T maps to NM_015550.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr11:3122914 C>T maps to NM_020896.3 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:179260183 T>C maps to ENST00000392505 V926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:179253813 T>C maps to ENST00000392505 H770H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179260238 C>T maps to ENST00000392505 R945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:179259090 A>G maps to ENST00000392505 V900V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr2:179197764 A>G maps to ENST00000392505 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:45890712 G>T maps to NM_145798.2 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr17:45886547 G>A maps to NM_145798.2 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:45896351 C>T maps to NM_145798.2 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:45897127 G>A maps to NM_145798.2 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:76752585 G>A maps to NM_020841.4 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:76791623 C>T maps to NM_020841.4 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:76791500 A>G maps to NM_020841.4 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr12:76791500 A>T maps to NM_020841.4 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:52248307 T>C maps to ENST00000428468 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:52227575 T>C maps to ENST00000428468 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:52135134 C>T maps to ENST00000428468 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:54599074 C>T maps to NM_206818.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:36889028 G>A maps to ENST00000356637 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr14:20920174 G>A maps to NM_017807.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:190618906 G>A maps to NM_022353.2 H258H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:90926356 G>A maps to NM_001126111.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:90933396 A>C maps to NM_001126111.1 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr8:90921810 G>T maps to NM_001126111.1 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:30661133 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:38884013 C>T maps to NM_003999.2 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:38933485 G>A maps to NM_003999.2 P960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr5:38919093 C>T maps to NM_003999.2 C505C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:38932600 T>C maps to NM_003999.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr5:38885487 C>T maps to NM_003999.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:38904606 T>A did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr5:38881804 C>T maps to NM_003999.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr5:38884139 G>T maps to NM_003999.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:38933485 G>A maps to NM_003999.2 P960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:19553461 C>T maps to NM_145260.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr8:99961221 G>A maps to ENST00000457907 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr8:99961419 C>T maps to ENST00000457907 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr8:99961776 G>A maps to ENST00000457907 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:99961561 G>T maps to ENST00000457907 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:99961557 G>T maps to ENST00000457907 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr8:99963856 C>A maps to ENST00000457907 C410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr6:108370455 C>T did not map to a codon.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr6:108370485 G>C maps to NM_014028.3 S307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:195954566 G>A maps to NM_152672.5 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:195960018 T>C maps to NM_152672.5 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:195959312 A>T maps to NM_152672.5 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:195954985 G>A maps to NM_152672.5 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr3:195955790 C>T maps to NM_152672.5 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr23:38268010 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:38240638 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:38240671 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:38229106 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:38262956 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:38226585 T>C did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:38262942 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:38226679 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:38268186 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:38260562 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:38229106 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:38229106 G>A did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:38268218 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr23:38268219 A>G did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:38271180 G>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:38268220 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:38268249 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr16:21721275 C>A maps to ENST00000286149 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:21737951 A>G maps to ENST00000286149 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:21690359 G>T maps to ENST00000286149 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:21742247 A>T maps to ENST00000286149 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr16:21716597 G>A maps to ENST00000286149 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:26700550 G>T maps to NM_194248.2 R761R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:26686942 C>T maps to NM_194248.2 A1664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:26702188 C>A maps to NM_194248.2 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:26684705 G>A maps to NM_194248.2 F1797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:26706356 G>A maps to NM_194248.2 Y455Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr2:26683818 C>A maps to NM_194248.2 G1871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:26725283 C>A maps to NM_194248.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:26686954 G>A maps to NM_194248.2 D1660D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr2:26684994 G>A maps to NM_194248.2 D1749D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr2:26717863 G>A maps to NM_194248.2 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:26684669 G>A maps to NM_194248.2 S1809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr2:26683737 G>A maps to NM_194248.2 N1898N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:26689713 G>A maps to NM_194248.2 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:26696096 G>A maps to NM_194248.2 F1212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:26698244 G>T maps to NM_194248.2 I1036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:26687830 G>A maps to NM_194248.2 D1622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:26717863 G>A maps to NM_194248.2 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:26686837 G>A maps to NM_194248.2 I1699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:26700045 C>T maps to NM_194248.2 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr2:26684573 G>A maps to NM_194248.2 D1841D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:26717938 G>A maps to NM_194248.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:26690265 G>A maps to NM_194248.2 P1398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr2:26705322 G>A maps to NM_194248.2 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:26688697 G>A maps to NM_194248.2 I1547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr3:161214626 T>G maps to NM_001080440.1 L11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr3:161214690 G>A maps to NM_001080440.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:161221571 C>T maps to NM_001080440.1 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr4:4199525 C>T maps to NM_177998.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:4199525 C>T maps to NM_177998.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:4199525 C>A maps to NM_177998.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:4214705 A>G maps to NM_177998.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr4:4199525 C>A maps to NM_177998.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr4:4199525 C>A maps to NM_177998.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:72926890 C>T maps to NM_178160.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:72926905 G>A maps to NM_178160.2 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr17:72921011 C>T maps to NM_178160.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:72926905 G>A maps to NM_178160.2 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:72939746 C>T maps to NM_178233.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr17:72939781 C>T maps to NM_178233.1 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:72937722 C>T maps to NM_178233.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:72943029 C>T maps to NM_178233.1 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:72939781 C>T maps to NM_178233.1 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:72942999 A>G maps to NM_178233.1 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:72943539 C>A maps to NM_178233.1 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr2:241078760 C>T maps to NM_148961.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:76933026 G>A maps to NM_032109.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:76932822 C>T maps to NM_032109.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:76932807 G>A maps to NM_032109.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:20230875 T>C maps to NM_015207.1 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr4:146059157 G>A maps to ENST00000447906 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr4:146059565 C>T maps to ENST00000447906 P787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr4:146073788 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr4:146073754 A>G maps to ENST00000447906 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr4:146062618 G>C maps to ENST00000447906 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:146076750 C>A maps to ENST00000447906 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr4:146058809 G>T maps to ENST00000447906 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr4:146058809 G>A maps to ENST00000447906 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:48783166 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:48792073 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:48801472 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:48781141 G>A did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:48814790 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:48781140 C>G did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:48780944 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:48814354 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:48791844 G>A did not map to a codon.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr23:69282839 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:69283014 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:69282932 C>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:69282522 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:69282601 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:69282696 G>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:69282885 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:92097011 A>T maps to NM_016023.3 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:92096313 G>T maps to NM_016023.3 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr15:31776528 C>T maps to ENST00000382902 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:31776858 C>T maps to ENST00000382902 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr15:31819494 G>A maps to ENST00000382902 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr15:31795897 T>C maps to ENST00000382902 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:31776528 C>T maps to ENST00000382902 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr15:31776489 C>T maps to ENST00000382902 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:31776399 G>A maps to ENST00000382902 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:149943066 A>G maps to NM_020205.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr1:149943014 G>A maps to NM_020205.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:149916817 T>C maps to NM_020205.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:63283354 C>T maps to NM_014562.3 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:63282688 C>T maps to NM_014562.3 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:57271010 C>T maps to NM_021728.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:57270952 G>A maps to NM_021728.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:1946082 G>A maps to NM_080822.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:29592359 G>A maps to NM_183378.2 F1055F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:29630139 T>G maps to NM_183378.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:7722945 T>C maps to NM_198185.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:7716873 G>A maps to NM_198185.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:7716873 G>A maps to NM_198185.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:7716873 G>A maps to NM_198185.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:111966275 A>G maps to ENST00000369728 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:111968027 G>A maps to ENST00000369728 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:111969246 G>A maps to ENST00000369728 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:18005450 G>A maps to NM_021220.2 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:23239776 C>A maps to NM_005015.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:23240697 C>T maps to NM_005015.3 N473N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr5:41861483 T>G maps to NM_000436.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr5:41862744 A>G maps to NM_000436.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:42990500 C>G maps to NM_148962.4 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:42990086 G>A maps to NM_148962.4 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:42990263 G>A maps to NM_148962.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr2:42990344 G>A maps to NM_148962.4 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr13:97639560 A>C maps to NM_080818.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:16343188 T>C maps to NM_138381.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:16336470 G>A maps to NM_138381.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:107763042 T>C maps to NM_001198533.1 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr8:107752648 T>C maps to NM_001198533.1 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr8:107695512 C>G maps to NM_001198533.1 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:107722931 G>A maps to NM_001198533.1 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:107718975 T>C maps to NM_001198533.1 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:107719144 G>T maps to NM_001198533.1 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:25833011 T>C maps to NM_017897.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr3:38232256 T>C maps to NM_005109.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:38291456 G>A maps to NM_005109.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr3:38289199 A>G maps to NM_005109.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:8794785 G>A maps to NM_000916.3 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:8809555 G>A maps to NM_000916.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr3:8794698 G>A maps to NM_000916.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:3802293 G>A maps to NM_002558.2 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:3807232 G>A maps to NM_002558.2 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:133196075 G>A maps to NM_170683.2 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr11:57118270 C>T maps to NM_002559.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:57135569 C>T maps to NM_002559.2 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:121660837 C>T maps to NM_002560.2 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:121670261 G>A maps to NM_002560.2 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:3593914 C>T maps to ENST00000435558 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:3582948 C>T maps to ENST00000435558 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:152554204 C>T maps to NM_002563.2 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:152554161 C>T maps to NM_002563.2 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:152554518 C>T maps to NM_002563.2 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr23:78216601 G>T did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr23:78216490 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:78216743 C>T did not map to a codon.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr23:78216598 G>A did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:78216068 A>G did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:78216070 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:78216896 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:78216926 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:78216808 T>G did not map to a codon.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr23:78216744 G>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:78216070 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:78216863 G>A did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr23:78216947 G>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:78216714 A>G did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:78216070 C>T did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:78216070 C>T did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:78216070 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:78216069 C>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:78216919 T>C did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:151056582 G>A maps to NM_022788.3 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:151056621 G>A maps to NM_022788.3 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:151046190 C>T maps to NM_176894.2 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:151045814 A>G maps to NM_176894.2 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:151046063 G>A maps to NM_176894.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr3:150931684 A>G maps to NM_014879.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:150931531 G>A maps to NM_014879.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr3:150931684 A>G maps to NM_014879.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr3:150931192 T>C maps to NM_014879.3 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:150931192 T>C maps to NM_014879.3 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:150931885 A>C maps to NM_014879.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr3:150931192 T>C maps to NM_014879.3 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:72945323 C>T maps to NM_176071.1 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr11:72946049 C>T maps to NM_176071.1 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:72945893 C>T maps to NM_176071.1 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr23:69478522 G>A did not map to a codon.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr23:69478882 C>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:69478394 A>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:69478797 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:69478680 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:69479030 G>A did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:69479278 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:69479139 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:69478740 C>T did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:69479313 G>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:1584668 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:74806706 G>A maps to NM_000917.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr10:74813220 G>A maps to NM_000917.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr10:74810836 G>A maps to NM_000917.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:131546130 C>T maps to NM_001142599.1 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr5:131531143 G>T maps to NM_001142599.1 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:131539540 C>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:131534058 G>A maps to NM_001142598.1 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:79803018 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:79803529 G>A maps to NM_000918.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:73611328 A>G maps to NM_025155.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:73598465 A>C maps to NM_025155.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr11:73610246 C>T maps to NM_025155.1 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:101733745 C>T maps to NM_002568.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:101727767 C>A maps to NM_002568.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr8:101730497 A>C maps to NM_002568.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr20:43550281 C>T maps to NM_001124756.1 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr20:43545458 C>T maps to NM_001124756.1 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr20:43567370 G>A maps to NM_001124756.1 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr13:25670977 C>T maps to NM_030979.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr13:25672111 C>T maps to NM_030979.2 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr13:25671835 G>A maps to NM_030979.2 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr13:25670863 T>C maps to NM_030979.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:25670419 C>T maps to NM_030979.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:25671919 A>G maps to NM_030979.2 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:25670497 C>T maps to NM_030979.2 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:25670500 G>A maps to NM_030979.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr13:25670398 C>T maps to NM_030979.2 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr13:25671805 T>A maps to NM_030979.2 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:25670870 C>T maps to NM_030979.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:40036955 G>A maps to NM_001135653.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:40033519 T>C did not map to a codon.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr23:90690623 C>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:90691571 A>C did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:90690784 C>T did not map to a codon.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr23:90690741 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:90691590 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:90690878 A>G did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:90691132 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:90690693 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:90691013 T>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:90690897 A>G did not map to a codon.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr23:90691443 C>T did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:90691013 T>C did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:90691135 C>A did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:90691011 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:90690840 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:23790966 G>T maps to NM_004643.3 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:88932015 G>A maps to NM_001080487.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr6:163149299 C>T maps to NM_152410.2 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr6:163483285 C>T maps to NM_152410.2 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:163510304 C>T maps to NM_152410.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:20728957 C>A maps to ENST00000503585 C247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:65977858 C>T maps to NM_018026.2 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:66001369 C>T maps to NM_018026.2 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr11:65995009 T>C maps to NM_018026.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:105849151 C>T maps to ENST00000458164 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr14:105858022 G>A maps to ENST00000458164 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:105858022 G>A maps to ENST00000458164 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:34499406 C>T maps to NM_020804.3 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:34498364 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:34499544 C>T maps to NM_020804.3 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:34498247 A>G maps to NM_020804.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr22:43267389 C>T maps to NM_001184970.1 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:43267470 A>G maps to NM_001184970.1 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:43278310 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:43287009 C>T maps to NM_001184970.1 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:43272242 C>T maps to NM_001184970.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:43287078 G>A maps to NM_001184970.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr22:43287078 G>A maps to NM_001184970.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr22:43267431 C>T maps to NM_001184970.1 W464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr22:43287099 G>T maps to NM_001184970.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:47200990 G>A maps to NM_016223.4 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:17570737 A>T maps to NM_013358.2 *664C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr1:17552648 C>T maps to NM_013358.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:17559315 T>C maps to NM_013358.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:17396636 G>T maps to NM_007365.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr1:17594443 C>G maps to NM_016233.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:17593255 C>T maps to NM_016233.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:17682534 G>A maps to NM_012387.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:17668606 G>A maps to NM_012387.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:17666243 C>T maps to NM_012387.2 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:17727795 C>T maps to NM_207421.3 C649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:17722085 A>C maps to NM_207421.3 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:17715014 C>A maps to NM_207421.3 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:17727810 G>A maps to NM_207421.3 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:17727810 G>A maps to NM_207421.3 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:138454171 G>A maps to NM_002571.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr19:39879771 G>A maps to NM_019088.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:39877360 G>A maps to NM_019088.2 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr17:2573467 T>C maps to NM_000430.3 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:117038270 G>A maps to NM_002572.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr11:117038249 C>T maps to NM_002572.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr11:117038249 C>A maps to NM_002572.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:26299184 A>G maps to NM_000437.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:81889138 G>A maps to NM_018440.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr8:81905414 G>A maps to NM_018440.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:49455856 G>A did not map to a codon.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr23:55116493 G>A did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:55116477 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:55117813 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:55117792 A>G did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:55117031 C>A did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr23:55117044 T>C did not map to a codon.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr23:55117792 A>G did not map to a codon.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr23:55117791 A>G did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr23:55117791 A>G did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:55117044 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:55247040 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:55249163 A>G did not map to a codon.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr12:103306634 G>T maps to NM_000277.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:103245492 G>C maps to NM_000277.1 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:103240684 T>C maps to NM_000277.1 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:103246705 T>C maps to NM_000277.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:103246707 G>A maps to NM_000277.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr12:103249073 T>C maps to NM_000277.1 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr12:103238122 A>G maps to NM_000277.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:57318147 A>C maps to NM_001079525.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:71417007 T>C maps to NM_020459.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:77064624 G>A maps to NM_001128620.1 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:77054910 C>T maps to NM_001128620.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:77066712 G>A maps to NM_001128620.1 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:77054910 C>T maps to NM_001128620.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr3:196509540 A>G maps to NM_002577.4 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr3:196509540 A>G maps to NM_002577.4 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:110406926 G>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:110406914 A>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:110439783 G>A did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:110406251 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:110406197 A>G did not map to a codon.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr23:110439070 G>T did not map to a codon.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr23:110437579 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:110406217 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:110366477 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:110463592 T>A did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:110366487 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:110439733 A>G did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr23:110391100 T>C did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:110385411 C>T did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:110366488 C>A did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:110391101 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:110385392 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:110406162 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr23:110406250 C>T did not map to a codon.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr23:110416302 G>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:110366488 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:110459767 T>C did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:110437552 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:39669068 G>A maps to NM_005884.3 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr19:39669110 C>T maps to NM_005884.3 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr19:39669140 G>A maps to NM_005884.3 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:39668358 C>T maps to NM_005884.3 D510D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:39663673 G>A maps to NM_005884.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:40565546 G>A maps to NM_020168.4 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:40565544 A>T did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr15:40564918 C>T maps to NM_020168.4 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr20:9523319 G>A maps to NM_177990.2 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr20:9546754 G>A maps to NM_177990.2 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr20:9561250 G>A maps to NM_177990.2 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr20:9561103 G>A maps to NM_177990.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:9546782 C>T maps to NM_177990.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr20:9561103 G>A maps to NM_177990.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr20:9560790 C>T did not map to a codon.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr20:9546782 C>T maps to NM_177990.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr20:9546761 G>A maps to NM_177990.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr20:9560845 G>T maps to NM_177990.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr20:9560845 G>T maps to NM_177990.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:9546559 G>A maps to NM_177990.2 R488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:23646756 C>T maps to NM_024675.3 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:23646861 A>G maps to NM_024675.3 N335N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr16:23614974 G>A maps to NM_024675.3 D1122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:23625393 T>C maps to NM_024675.3 Q1044Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:23649186 C>T maps to NM_024675.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:23646408 T>C maps to NM_024675.3 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:23641668 T>C maps to NM_024675.3 Q602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:23646408 T>C maps to NM_024675.3 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:23619228 G>A maps to NM_024675.3 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr16:23652433 T>C maps to NM_024675.3 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:169432681 C>A maps to NM_001166108.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:169819807 C>A maps to NM_001166108.1 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr4:169433389 C>T maps to NM_001166108.1 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:169433290 A>G maps to NM_001166108.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:169433515 A>G maps to NM_001166108.1 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:740361 G>A maps to NM_002579.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:112705428 C>T maps to ENST00000413420 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr9:112705362 C>T maps to ENST00000413420 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr1:100154415 T>C maps to NM_017734.4 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:100127900 C>A maps to NM_017734.4 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:100133241 C>T maps to NM_017734.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:100152268 C>T maps to NM_017734.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:100152314 C>A maps to NM_017734.4 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:100154403 T>G maps to NM_017734.4 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:100159608 G>A maps to NM_017734.4 K549K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:100154787 G>A maps to NM_017734.4 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:102295722 C>T maps to NM_000919.3 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:102285660 G>A maps to NM_000919.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr5:102361012 G>T maps to NM_000919.3 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:102295710 C>T maps to NM_000919.3 N346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:102355500 A>G maps to NM_000919.3 E813E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:102285289 C>A maps to NM_000919.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:102364750 C>T maps to NM_000919.3 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:102342599 C>A maps to NM_000919.3 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:35453963 G>A maps to NM_015430.2 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr11:35454224 G>A maps to NM_015430.2 N631N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr12:56719181 A>G maps to NM_001127460.2 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr12:56712896 C>G maps to NM_001127460.2 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:56712168 T>C maps to NM_001127460.2 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:56718840 A>G maps to NM_001127460.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr12:56718840 A>G maps to NM_001127460.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr12:56718840 A>G maps to NM_001127460.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr13:28851444 A>G maps to NM_175854.7 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr13:28851444 A>G maps to NM_175854.7 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr13:28834682 C>T maps to NM_175854.7 R450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:28851444 A>G maps to NM_175854.7 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:28771468 G>T maps to NM_175854.7 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr13:28851444 A>G maps to NM_175854.7 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr13:28851444 A>G maps to NM_175854.7 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:91359115 C>T maps to NM_148977.1 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr20:3893257 G>C maps to NM_153638.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr20:3903937 G>A maps to NM_153638.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:167988396 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:2452248 G>A maps to ENST00000425477 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:2451264 G>A maps to ENST00000425477 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr11:93912905 T>A maps to NM_015368.3 C228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr11:124489803 C>A maps to NM_052959.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:124487187 C>T maps to NM_052959.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:124489452 C>T maps to NM_052959.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:124482945 C>T maps to NM_052959.2 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:124489743 A>G maps to NM_052959.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:135204868 G>A maps to NM_152911.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:78915895 C>T maps to NM_173797.3 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:50261799 G>A maps to NM_001040284.2 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:50257141 G>T maps to NM_001040284.2 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:50257162 C>T maps to NM_001040284.2 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:50245356 C>T maps to NM_001040284.2 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:6749756 G>A maps to NM_006999.4 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:6738839 T>C maps to NM_006999.4 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:6746493 C>T maps to NM_006999.4 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:6748658 T>C maps to NM_006999.4 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:6746400 T>C maps to NM_006999.4 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:6751177 G>A maps to NM_006999.4 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:6750564 G>A maps to NM_006999.4 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr19:39589258 C>T maps to NM_001004318.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr19:39600715 C>A maps to NM_001004318.2 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:73733455 C>T maps to ENST00000427855 P1139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:73720620 C>A maps to ENST00000427855 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:73731401 C>T maps to ENST00000427855 A1031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:73730933 C>T maps to ENST00000427855 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr14:73729421 C>A maps to ENST00000427855 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr14:73732188 A>G maps to ENST00000427855 R1079R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr14:73727446 C>T maps to ENST00000427855 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr14:73726172 C>T maps to ENST00000427855 H635H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:97010500 G>A maps to NM_032632.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:96993810 C>T maps to NM_032632.3 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr14:97022204 T>G maps to NM_032632.3 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:4900288 C>A maps to NM_020144.4 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:61014657 A>G maps to NM_022894.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr2:61014657 A>G maps to NM_022894.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:118997554 T>C maps to NM_002581.3 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr9:119115106 C>T maps to NM_002581.3 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr9:119065126 G>A maps to NM_002581.3 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:119097182 T>A maps to NM_002581.3 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:118950378 C>T maps to NM_002581.3 N454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:118949775 C>T maps to NM_002581.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:118973927 C>A maps to NM_002581.3 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr9:118950120 G>A maps to NM_002581.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr9:119144732 C>T maps to NM_002581.3 D1579D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:118997514 G>A maps to NM_002581.3 E777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:118949880 G>A maps to NM_002581.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr9:118997589 T>C maps to NM_002581.3 F802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr9:119094679 T>C maps to NM_002581.3 Y1110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr9:119130026 G>T maps to NM_002581.3 R1533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr9:118949775 C>T maps to NM_002581.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:118950084 C>T maps to NM_002581.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:176809334 C>T maps to NM_020318.2 D1743D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:176564650 C>T maps to NM_020318.2 N637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:176811589 A>G maps to NM_020318.2 *1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:176526088 G>T maps to NM_020318.2 G211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:176811560 C>A maps to NM_020318.2 R1783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr1:176526090 A>G maps to NM_020318.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:176525599 G>T maps to NM_020318.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:176681110 G>A maps to NM_020318.2 W1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:176564269 C>A maps to NM_020318.2 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr1:176681023 G>A maps to NM_020318.2 W1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr1:176675572 T>C maps to NM_020318.2 G1148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr1:176709305 C>T maps to NM_020318.2 D1375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:176564551 C>T maps to NM_020318.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr1:176526210 A>G maps to NM_020318.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr1:176564659 C>T maps to NM_020318.2 D640D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:176526210 A>G maps to NM_020318.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr1:176564443 C>T maps to NM_020318.2 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr1:176659318 C>T maps to NM_020318.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:89474520 T>G maps to NM_001015880.1 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:89501114 G>T maps to NM_001015880.1 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:89503292 G>A maps to NM_001015880.1 W462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:79841701 T>C maps to NM_001040202.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:69689833 C>A maps to NM_017705.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:69677129 C>A maps to NM_017705.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:156214002 C>T maps to NM_024897.2 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:156213888 C>T maps to NM_024897.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:156215648 G>A maps to NM_198406.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:156216023 G>A maps to NM_198406.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:26189781 C>T maps to NM_178422.5 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:142681572 G>A maps to NM_198504.2 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:142681977 C>T maps to NM_198504.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:34400255 G>A maps to NM_019619.3 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:34400353 C>A maps to NM_019619.3 G1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:34400366 G>A maps to NM_019619.3 N1267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr10:34620075 C>T maps to NM_019619.3 A937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:34630664 A>G maps to NM_019619.3 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:34985344 A>G maps to NM_019619.3 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:205986365 C>T maps to ENST00000406610 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:206166410 C>T maps to ENST00000406610 F872F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:205986515 C>T maps to ENST00000406610 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:205550902 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:205829990 C>T maps to ENST00000406610 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr2:205983734 C>T maps to ENST00000406610 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:206050506 C>T maps to ENST00000406610 D648D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:67696270 C>T maps to NM_016948.2 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:49366259 C>T maps to NM_032521.2 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr18:77918229 G>A maps to NM_032510.3 H185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:77918085 C>T maps to NM_032510.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:162683628 C>A maps to NM_004562.2 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:162864401 C>T maps to NM_004562.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr6:162683710 G>A maps to NM_004562.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr1:8045029 C>T maps to NM_001123377.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:183547472 T>C maps to NM_018622.5 E351E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:183551526 C>T maps to NM_018622.5 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr4:75937686 G>A maps to NM_015393.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:14721034 C>T maps to NM_002582.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:14530618 C>T maps to NM_002582.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:14702916 G>A maps to NM_002582.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:226573297 G>A maps to NM_001618.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:226576428 T>G maps to NM_001618.3 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr1:226564877 G>A maps to NM_001618.3 N624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:226551744 G>A maps to NM_001618.3 I895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:226549776 G>A maps to NM_001618.3 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:226564877 G>A maps to NM_001618.3 N624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:226566919 G>A maps to NM_001618.3 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:226552774 G>A maps to NM_001618.3 H862H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:226564877 G>A maps to NM_001618.3 N624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr1:226549713 G>A maps to NM_001618.3 T973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr8:145058185 G>A maps to NM_032789.3 D589D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr12:3931097 G>A maps to NM_020367.4 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:3921558 T>C maps to NM_020367.4 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr7:139746808 T>A did not map to a codon.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr7:139756917 G>A maps to NM_022750.2 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:139724512 G>A maps to NM_022750.2 C651C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:139746808 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr7:139737584 C>T maps to NM_022750.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:139727143 C>T maps to NM_022750.2 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr7:139746808 T>C did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr7:139746808 T>A did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:122439111 T>C maps to NM_017554.2 P1606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:122439186 G>A maps to NM_017554.2 T1631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr3:122419152 C>T maps to NM_017554.2 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:122419908 G>A maps to NM_017554.2 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:122419197 G>A maps to NM_017554.2 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:122437552 C>T maps to NM_017554.2 R1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:122447335 T>C maps to NM_017554.2 P1766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:122437032 G>T maps to NM_017554.2 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:122422731 A>G maps to NM_017554.2 T1075T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr3:122414492 A>G maps to NM_017554.2 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:122422731 A>G maps to NM_017554.2 T1075T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr3:122335946 T>C maps to NM_001113523.1 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:122335937 T>C maps to NM_001113523.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr3:122345680 C>T maps to NM_001113523.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:122334666 C>A maps to NM_001113523.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr14:20811814 G>A maps to NM_005484.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:51981822 A>G maps to NM_001003931.2 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr13:25029206 C>T maps to NM_006437.3 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr13:25052350 G>A maps to NM_006437.3 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr13:25029206 C>T maps to NM_006437.3 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr13:25060370 T>C maps to NM_006437.3 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr13:25043206 G>A maps to NM_006437.3 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr13:25051837 C>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:25008760 G>A maps to NM_006437.3 G1506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:72549730 G>A maps to NM_020214.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:72533876 G>A maps to NM_020214.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:50084394 C>T maps to ENST00000505697 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr5:50093021 G>A maps to ENST00000505697 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr3:122274754 C>T maps to NM_031458.2 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:122247426 T>C maps to NM_031458.2 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:55223918 C>A maps to NM_152268.3 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:12540053 G>A maps to NM_018222.4 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr11:12499395 A>G maps to NM_018222.4 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr22:44527476 C>T maps to NM_001003828.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr22:44559770 C>T maps to NM_001003828.1 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr22:44543765 C>T maps to NM_001003828.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:44543760 C>T maps to NM_001003828.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr22:44602299 G>A maps to NM_001137606.1 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:44586473 G>A maps to NM_001137606.1 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr22:44579283 A>G maps to NM_001137606.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr22:44592276 G>A maps to NM_001137606.1 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr22:44602261 C>T maps to NM_001137606.1 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:150842506 C>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:150840915 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:150840104 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:150842456 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:150840068 G>A did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:150832661 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:150789968 T>G did not map to a codon.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr23:150840984 C>A did not map to a codon.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr23:150793954 T>C did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:150842514 T>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:150780203 T>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:150840155 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:150842507 T>C did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:150842507 T>C did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:150842505 A>G did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:150844560 G>A did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:150793954 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:150844536 C>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:242051704 A>T maps to ENST00000358649 T1168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:242076661 C>T maps to ENST00000358649 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:242051704 A>T maps to ENST00000358649 T1168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:242063381 G>A maps to ENST00000358649 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:125618594 C>T maps to NM_138294.2 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr11:125647871 A>T maps to NM_212555.2 C34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:125647339 C>T maps to NM_212555.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr11:125647297 G>T maps to NM_212555.2 C107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr11:59410432 G>A maps to NM_152716.2 R657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:31741261 G>A maps to NM_014323.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr22:31741324 C>T maps to NM_014323.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr20:21689939 C>T maps to NM_006192.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr20:21687490 C>T maps to NM_006192.3 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:102509545 C>T maps to NM_003987.3 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:223160250 C>T maps to NM_181459.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:223066852 G>A maps to NM_181459.3 Y410Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:223085050 G>A maps to NM_181459.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr2:223066852 G>A maps to NM_181459.3 Y410Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr2:223161822 G>A maps to NM_181459.3 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr2:223160264 G>A maps to NM_181459.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr2:223086069 G>A maps to NM_181459.3 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:223066669 A>G maps to NM_181459.3 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:36966595 G>A maps to NM_016734.1 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:37020742 C>T maps to NM_016734.1 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:31816184 C>T maps to NM_001604.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr11:31812351 C>T maps to NM_001604.4 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:31822329 A>G maps to NM_001604.4 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr11:31824262 G>A maps to NM_001604.4 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:19062331 G>A maps to NM_002584.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:18962812 C>T maps to NM_002584.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:19062163 G>A maps to NM_002584.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr1:18962857 C>T maps to NM_002584.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr1:19018281 G>A maps to NM_002584.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:19018312 C>T maps to NM_002584.2 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr1:19062355 C>T maps to NM_002584.2 Y462Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:113999285 G>T maps to NM_003466.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:113984830 G>A maps to NM_003466.3 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr14:37132540 G>A maps to NM_006194.3 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:154760248 C>T maps to NM_007349.3 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:154768016 G>A maps to NM_007349.3 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr7:154759591 A>G maps to NM_007349.3 C609C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr10:70043969 A>G maps to NM_022129.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr3:52678789 T>A maps to ENST00000296302 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr3:52588776 C>T maps to ENST00000296302 P1524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:52610605 T>C maps to ENST00000296302 E1214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:52712579 G>A maps to ENST00000296302 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:52678726 G>A maps to ENST00000296302 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:52582237 G>A maps to ENST00000296302 D1637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr3:52712579 G>A maps to ENST00000296302 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr3:52651405 C>A maps to ENST00000296302 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:164790778 T>C maps to NM_002585.2 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:164761761 A>G maps to NM_002585.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:32156512 G>T maps to NM_002586.4 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:32154613 G>A maps to NM_002586.4 N363N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:128509818 T>C maps to ENST00000373487 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:128510864 G>A maps to ENST00000373487 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:128725381 T>G did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:128692038 C>T maps to ENST00000373487 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr19:19675817 C>T maps to NM_025245.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr19:19675817 C>A maps to NM_025245.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr19:19675817 C>T maps to NM_025245.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:19675817 C>A maps to NM_025245.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:154924333 G>A maps to NM_020524.2 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:66617581 C>T maps to NM_022172.2 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr11:66617210 A>G maps to NM_022172.2 D1006D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:66616462 C>T maps to NM_022172.2 V1148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:66620290 G>A maps to NM_022172.2 N510N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr11:66618549 T>C maps to NM_022172.2 E728E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr11:66618549 T>C maps to NM_022172.2 E728E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:66620245 C>T maps to NM_022172.2 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr11:66618549 T>C maps to NM_022172.2 E728E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:70315060 C>T maps to NM_006196.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr12:53856284 G>A maps to NM_005016.5 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr21:47360026 C>T maps to NM_020528.2 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr21:47360065 G>A maps to NM_020528.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:47321008 C>T maps to NM_020528.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr21:47361601 C>T maps to NM_020528.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:51992235 G>A maps to NM_033010.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:51992097 C>T maps to NM_033010.2 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr13:101180005 G>A maps to NM_000282.3 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr13:101077939 G>A maps to NM_000282.3 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:101077903 G>A maps to NM_000282.3 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:101077924 G>A maps to NM_000282.3 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:136002776 G>A maps to NM_001178014.1 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:141243141 G>T maps to NM_032420.2 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:141244088 G>A maps to NM_032420.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr5:141243375 C>T maps to NM_032420.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:141244308 A>G maps to NM_032420.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr5:141244785 A>G maps to NM_032420.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:141248433 A>G maps to NM_032420.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:141233819 C>T maps to NM_032420.2 A1167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:141248322 C>T maps to NM_032420.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:134084409 C>T maps to NM_032961.1 R1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:134072677 G>A maps to NM_032961.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr4:134072449 C>T maps to NM_032961.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:134073004 C>T maps to NM_032961.1 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr4:134073877 C>T maps to NM_032961.1 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:134072677 G>A maps to NM_032961.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:134072827 C>T maps to NM_032961.1 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:134072935 C>T maps to NM_032961.1 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:134071834 C>T maps to NM_032961.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:134073703 G>T maps to NM_032961.1 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:134072887 C>T maps to NM_032961.1 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:134075508 C>T maps to NM_032961.1 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:134072098 C>T maps to NM_032961.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:134072872 C>T maps to NM_032961.1 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr4:134072497 G>A maps to NM_032961.1 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:134071393 C>T maps to NM_032961.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:134071865 C>A maps to NM_032961.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:134072404 C>T maps to NM_032961.1 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr4:134073508 G>A maps to NM_032961.1 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:134071930 A>G maps to NM_032961.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:134072743 C>T maps to NM_032961.1 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr4:134071954 G>T maps to NM_032961.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr23:91131975 A>G did not map to a codon.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr23:91133857 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:91090551 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:91090522 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:91134242 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:91132829 G>T did not map to a codon.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr23:91133055 C>T did not map to a codon.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr23:91131800 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:91873510 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:91090593 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:91873779 A>G did not map to a codon.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr23:91091026 A>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:91133213 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:91456439 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:91873863 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:91090854 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:91132719 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:91132868 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:91133833 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:91133906 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:91456391 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:91873588 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:91132906 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:91133092 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:91134135 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:91873859 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:91134076 T>A did not map to a codon.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr23:91132408 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:91091031 G>A did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr23:91456393 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:91091031 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:91873316 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:91132377 T>G did not map to a codon.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr23:91873678 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:91090729 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:91131988 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:91134211 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:91873852 G>A did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:91134160 C>A did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:91134048 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:91133205 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr23:91456393 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr23:91133030 G>T did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:91133711 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:91134264 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:91873369 G>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:91090523 G>A did not map to a codon.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr24:4967287 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr24:4967845 G>A did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr24:4967116 C>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr24:4966400 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr24:4966984 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr24:4925167 G>A did not map to a codon.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr24:4967267 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr24:5605402 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr24:4925461 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:4925233 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:4967204 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:4967292 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr24:4925409 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr24:4967297 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr24:4968549 G>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr24:5605576 C>T did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr24:4966472 A>G did not map to a codon.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr24:5605513 C>T did not map to a codon.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr5:141336009 C>T maps to NM_016580.2 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:141335043 G>A maps to NM_016580.2 V791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr5:141335496 A>G maps to NM_016580.2 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:141335532 C>T maps to NM_016580.2 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:141336573 G>A maps to NM_016580.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:141336357 G>A maps to NM_016580.2 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:55912863 G>A maps to NM_001142763.1 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:56424015 G>A maps to NM_001142763.1 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr10:55582503 G>T maps to NM_001142763.1 S1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr10:55582280 G>A maps to NM_001142763.1 A1742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:55587238 C>T maps to NM_001142763.1 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:55826639 T>C maps to NM_001142763.1 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:55581706 C>A maps to NM_001142763.1 E1934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:55568490 C>T maps to NM_001142769.1 S1778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:55626440 G>A maps to NM_001142763.1 D1231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr10:55912942 G>A maps to NM_001142763.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr10:55955526 A>T maps to NM_001142763.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:55582543 C>A maps to NM_001142763.1 E1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:55944905 A>C maps to NM_001142763.1 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr10:55626400 C>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:55566509 C>T maps to ENST00000373965 A1628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr10:55996664 C>T maps to NM_001142763.1 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:55566701 C>T maps to ENST00000373965 T1564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:55912942 G>A maps to NM_001142763.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:55582610 C>T maps to NM_001142763.1 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr13:58208566 C>T maps to NM_001040429.2 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr13:58207249 C>A maps to NM_001040429.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr13:58207012 C>T maps to NM_001040429.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr13:58207402 G>A maps to NM_001040429.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr13:58206997 C>T maps to NM_001040429.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr13:58208641 C>T maps to NM_001040429.2 D654D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr13:58299161 T>C maps to NM_001040429.2 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:58208362 G>A maps to NM_001040429.2 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:58208647 G>A maps to NM_001040429.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:58208650 C>A maps to NM_001040429.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr13:58208161 G>C maps to NM_001040429.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr13:58208599 G>A maps to NM_001040429.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr13:58207609 C>T maps to NM_001040429.2 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr13:58206937 C>A maps to NM_001040429.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr13:58208227 C>T maps to NM_001040429.2 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr13:58298963 C>T maps to NM_001040429.2 R1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr13:58208428 C>T maps to NM_001040429.2 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr13:58208284 C>T maps to NM_001040429.2 Y535Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:58207012 C>T maps to NM_001040429.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:138442590 G>A maps to NM_019035.3 S1000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:138442722 C>T maps to NM_019035.3 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:138452071 G>A maps to NM_019035.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr4:138450956 C>T maps to NM_019035.3 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:138442404 A>G maps to NM_019035.3 F1062F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:138452690 G>A maps to NM_019035.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:138452429 C>T maps to NM_019035.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:138451484 T>C maps to NM_019035.3 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:138451931 A>G maps to NM_019035.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:138451214 G>T maps to NM_019035.3 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:138452882 A>C maps to NM_019035.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:138442680 G>A maps to NM_019035.3 D970D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr4:138442850 C>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:138442608 C>T maps to NM_019035.3 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:99662936 C>T did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:99662740 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:99662989 C>T did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:99662738 C>T did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:99661800 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:99551848 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:99663000 C>T did not map to a codon.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr23:99662748 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:99657799 T>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:99661800 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr23:99551463 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:99662412 G>A did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:99662512 G>A did not map to a codon.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr23:99662953 G>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:99663217 C>T did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:99661807 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:99662496 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:99551631 C>T did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:99551677 A>G did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr13:61986809 C>A maps to NM_022843.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr13:61987742 G>A maps to NM_022843.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr13:61986809 C>T maps to NM_022843.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3517-01A-01W-0831-10 chr13:61987742 G>A maps to NM_022843.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr13:61986610 C>A maps to NM_022843.3 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr13:61987586 C>T maps to NM_022843.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:61986209 G>A maps to NM_022843.3 V674V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:61987454 G>A maps to NM_022843.3 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr13:61986875 C>T maps to NM_022843.3 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr13:61986434 T>C maps to NM_022843.3 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:61986610 C>A maps to NM_022843.3 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr13:61986434 T>C maps to NM_022843.3 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:61987616 G>A maps to NM_022843.3 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:30724696 C>T maps to NM_001173523.1 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:30724555 C>A maps to NM_001173523.1 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr4:30725437 T>C maps to NM_001173523.1 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:30724564 G>A maps to NM_001173523.1 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:30724558 C>T maps to NM_001173523.1 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:30724844 C>T maps to NM_001173523.1 Q601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:30726070 C>T maps to NM_001173523.1 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:53418988 G>A maps to NM_002590.2 N973N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr13:67205462 C>T maps to NM_203487.2 P1073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:66879004 C>A maps to NM_203487.2 E1166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr13:67802287 T>C maps to NM_203487.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr13:67205435 G>A maps to NM_203487.2 H1082H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr13:67802542 A>G maps to NM_203487.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr13:67477704 A>G maps to NM_203487.2 P1023P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:67801792 A>G maps to NM_203487.2 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:67800975 C>A maps to NM_203487.2 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr13:67801774 G>A maps to NM_203487.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr13:67800079 G>A maps to NM_203487.2 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:67205540 C>T maps to NM_203487.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr13:67801645 A>T maps to NM_203487.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:67800523 G>T maps to NM_203487.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr13:67802446 G>A maps to NM_203487.2 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr13:66879065 A>G maps to NM_203487.2 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr13:67801687 G>A maps to NM_203487.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr13:67801237 C>T maps to NM_203487.2 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr13:67800825 C>A maps to NM_203487.2 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr13:67802199 G>A maps to NM_203487.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr5:140167758 G>A maps to NM_018900.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:140166906 T>C maps to NM_018900.2 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:140167126 C>T maps to NM_018900.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:140166588 C>T maps to NM_018900.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:140167737 G>A maps to NM_018900.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:140166324 G>A maps to NM_018900.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140167170 G>A maps to NM_018900.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140167383 G>A maps to NM_018900.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140389299 A>G maps to NM_018909.2 K877K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:140167212 C>T maps to NM_018900.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:140167383 G>A maps to NM_018900.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr5:140237129 C>T maps to NM_018901.2 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr5:140237330 G>A maps to NM_018901.2 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr5:140236080 C>T maps to NM_018901.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:140237891 G>A maps to NM_018901.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140236529 A>G maps to NM_018901.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:140237684 C>T maps to NM_018901.2 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr5:140236811 G>A maps to NM_018901.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:140236424 C>T maps to NM_018901.2 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr5:140249746 C>T maps to NM_018902.3 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:140248963 C>T maps to NM_018902.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr5:140249716 C>T maps to NM_018902.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr5:140250832 G>T maps to NM_018902.3 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr5:140250709 G>A maps to NM_018902.3 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140249365 T>C maps to NM_018902.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr5:140250496 C>T maps to NM_018902.3 N603N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr5:140249911 G>T maps to NM_018902.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:140250400 C>T maps to NM_018902.3 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:140250184 C>T maps to NM_018902.3 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:140249482 C>T maps to NM_018902.3 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr5:140249362 C>T maps to NM_018902.3 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:140250193 G>A maps to NM_018902.3 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr5:140250862 G>T maps to NM_018902.3 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:140255188 C>T maps to NM_018903.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:140256919 G>A maps to NM_018903.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr5:140256772 C>T maps to NM_018903.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:140256859 C>T maps to NM_018903.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140256955 G>A maps to NM_018903.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:140256445 C>T maps to NM_018903.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr5:140256664 C>T maps to NM_018903.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:140263778 G>A maps to NM_018904.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr5:140263205 C>T maps to NM_018904.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:140263832 G>A maps to NM_018904.2 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:140262933 G>T maps to NM_018904.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140263502 G>A maps to NM_018904.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr5:140263244 G>T maps to NM_018904.2 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:140263694 G>A maps to NM_018904.2 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140263751 G>A maps to NM_018904.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr5:140263637 C>T maps to NM_018904.2 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:140263514 C>T maps to NM_018904.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:140263220 G>A maps to NM_018904.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr5:140262614 C>T maps to NM_018904.2 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:140263646 C>T maps to NM_018904.2 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr5:140176315 C>T maps to NM_018905.2 H589H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:140174932 C>T maps to NM_018905.2 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:140176510 C>T maps to NM_018905.2 H654H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr5:140176360 C>T maps to NM_018905.2 N604N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr5:140175901 C>T maps to NM_018905.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr5:140176420 G>A maps to NM_018905.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:140176216 G>A maps to NM_018905.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr5:140175901 C>T maps to NM_018905.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr5:140176747 G>A maps to NM_018905.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr5:140182629 C>T maps to NM_018906.2 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr5:140182137 G>A maps to NM_018906.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr5:140180865 C>T maps to NM_018906.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:140182224 C>T maps to NM_018906.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:140182695 C>T maps to NM_018906.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr5:140182953 C>T maps to NM_018906.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:140182566 C>T maps to NM_018906.2 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:140188133 G>A maps to NM_018907.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr5:140188016 C>A maps to NM_018907.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:140189142 G>T maps to NM_018907.2 E791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:140187197 C>T maps to NM_018907.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:140188448 C>T maps to NM_018907.2 N559N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:140188277 C>T maps to NM_018907.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:140188700 G>A maps to NM_018907.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:140188379 C>T maps to NM_018907.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr5:140202637 G>A maps to NM_018908.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:140203408 G>A maps to NM_018908.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:140202739 C>T maps to NM_018908.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:140203735 C>A maps to NM_031501.1 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:140201765 G>T maps to NM_018908.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:140202910 C>T maps to NM_018908.2 Y517Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:140202550 G>A maps to NM_018908.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:140202967 G>A maps to NM_018908.2 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr5:140209877 G>A maps to NM_018909.2 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:140209211 G>A maps to NM_018909.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr5:140209208 C>T maps to NM_018909.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr5:140208482 G>T maps to NM_018909.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:140209184 G>A maps to NM_018909.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:140207972 C>T maps to NM_018909.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:140215527 G>A maps to NM_018910.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr5:140215890 C>T maps to NM_018910.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:140215245 C>T maps to NM_018910.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:140215326 G>A maps to NM_018910.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:140214111 C>T maps to NM_018910.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:140215581 C>T maps to NM_018910.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:140214138 G>A maps to NM_018910.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr5:140215911 G>T maps to NM_018910.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr5:140215374 G>A maps to NM_018910.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr5:140215305 C>T maps to NM_018910.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:140215329 G>A maps to NM_018910.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:140222486 G>A maps to NM_018911.2 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:140223023 G>A maps to NM_018911.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr5:140222267 G>A maps to NM_018911.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:140221064 G>A maps to NM_018911.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140222060 G>A maps to NM_018911.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:140222243 C>T maps to NM_018911.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr5:140222201 G>A maps to NM_018911.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr5:140221619 T>C maps to NM_018911.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:140222825 G>A maps to NM_018911.2 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr5:140229432 C>T maps to NM_031857.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr5:140230371 G>A maps to NM_031857.1 K764K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:140230083 G>A maps to NM_031857.1 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:140229573 G>A maps to NM_031857.1 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:140229375 G>A maps to NM_031857.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:140230125 G>A maps to NM_031857.1 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:140229249 G>A maps to NM_031857.1 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:140230607 A>G maps to NM_014005.3 *843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr5:140229204 C>T maps to NM_031857.1 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr5:140229342 C>T maps to NM_031857.1 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr5:140228289 C>G maps to NM_031857.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr5:140229441 G>A maps to NM_031857.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:140229636 G>A maps to NM_031857.1 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:140228439 C>T maps to NM_031857.1 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:140307634 G>A maps to NM_018898.3 Q386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr5:140308810 C>T maps to NM_018898.3 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr5:140307835 C>T maps to NM_018898.3 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:140306929 C>T maps to NM_018898.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:140307976 G>A maps to NM_018898.3 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr5:140307758 C>T maps to NM_018898.3 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140307835 C>T maps to NM_018898.3 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:140308501 G>A maps to NM_018898.3 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:140346875 C>T maps to NM_018899.5 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr5:140346836 G>A maps to NM_018899.5 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr5:140347635 C>T maps to NM_018899.5 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr5:140348165 C>T maps to NM_018899.5 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140346929 C>T maps to NM_018899.5 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:140346483 C>T maps to NM_018899.5 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr5:140347070 G>A maps to NM_018899.5 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140346878 C>T maps to NM_018899.5 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:140346425 A>G maps to NM_018899.5 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr5:140346905 C>T maps to NM_018899.5 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:140432458 G>A maps to NM_013340.2 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr5:140432842 C>T maps to NM_013340.2 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr5:140432176 G>A maps to NM_013340.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:140431762 C>T maps to NM_013340.2 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:140431927 G>A maps to NM_013340.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr5:140431240 C>T maps to NM_013340.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr5:140431990 T>C maps to NM_013340.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140432602 G>A maps to NM_013340.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:140431183 G>A maps to NM_013340.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:140431522 C>T maps to NM_013340.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140573600 G>A maps to NM_018930.3 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:140573501 C>T maps to NM_018930.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:140573825 C>T maps to NM_018930.3 N567N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:140573768 C>T maps to NM_018930.3 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:140573636 C>A maps to NM_018930.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:140572253 C>T maps to NM_018930.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr5:140573600 G>A maps to NM_018930.3 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr5:140573714 C>T maps to NM_018930.3 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:140573453 C>T maps to NM_018930.3 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:140573816 G>A maps to NM_018930.3 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:140574260 G>A maps to NM_018930.3 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr5:140573213 G>A maps to NM_018930.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:140573573 C>T maps to NM_018930.3 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:140581714 C>T maps to NM_018931.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:140580525 A>T maps to NM_018931.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:140581572 C>T maps to NM_018931.2 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140579643 C>T maps to NM_018931.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140581248 C>T maps to NM_018931.2 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:140580438 G>T maps to NM_018931.2 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140581470 C>T maps to NM_018931.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr5:140579766 A>G maps to NM_018931.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:140590275 C>T maps to NM_018932.3 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140590119 G>A maps to NM_018932.3 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr5:140589129 C>T maps to NM_018932.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr5:140589705 G>A maps to NM_018932.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr5:140589015 C>T maps to NM_018932.3 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:140588661 G>A maps to NM_018932.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140589057 G>A maps to NM_018932.3 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:140589987 G>T maps to NM_018932.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:140588601 C>T maps to NM_018932.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr5:140590590 G>A maps to NM_018932.3 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:140588661 G>A maps to NM_018932.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:140589894 C>T maps to NM_018932.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:140594498 G>A maps to NM_018933.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:140595353 C>T maps to NM_018933.2 D553D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:140594624 C>T maps to NM_018933.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:140595593 C>T maps to NM_018933.2 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:140595314 G>A maps to NM_018933.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:140595818 C>T maps to NM_018933.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140595782 G>A maps to NM_018933.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:140594618 C>T maps to NM_018933.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:140595572 C>T maps to NM_018933.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:140595824 G>A maps to NM_018933.2 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:140595368 G>A maps to NM_018933.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr5:140595170 G>A maps to NM_018933.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:140605125 C>A maps to NM_018934.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr5:140605329 C>T maps to NM_018934.2 Y751Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr5:140605444 C>T maps to NM_018934.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:140603649 C>T maps to NM_018934.2 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140604129 G>A maps to NM_018934.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:140604666 C>T maps to NM_018934.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr5:140603463 C>T maps to NM_018934.2 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:140604693 G>A maps to NM_018934.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:140627269 C>T maps to NM_018935.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140626855 G>T maps to NM_018935.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr5:140626891 G>A maps to NM_018935.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr5:140626825 C>T maps to NM_018935.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:140626753 C>T maps to NM_018935.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr5:140626675 C>T maps to NM_018935.2 N510N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:140626301 C>T maps to NM_018935.2 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140626049 C>T maps to NM_018935.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:140562797 C>T maps to NM_020957.1 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:140563060 C>T maps to NM_020957.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:140562928 C>T maps to NM_020957.1 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:140564171 C>T maps to NM_020957.1 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr5:140564290 G>A maps to NM_020957.1 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:140564227 G>A maps to NM_020957.1 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140563060 C>T maps to NM_020957.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:140475639 C>A maps to NM_018936.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr5:140475252 G>A maps to NM_018936.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140475975 C>T maps to NM_018936.2 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:140476513 C>A maps to NM_018936.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr5:140475678 C>T maps to NM_018936.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr5:140475900 C>T maps to NM_018936.2 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:140475058 C>T maps to NM_018936.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:140475570 T>C maps to NM_018936.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:140474754 C>T maps to NM_018936.2 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:140475414 G>A maps to NM_018936.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:140474985 C>T maps to NM_018936.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr5:140476044 C>T maps to NM_018936.2 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr5:140475990 C>A maps to NM_018936.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr5:140480499 A>G maps to NM_018937.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140482377 G>A maps to NM_018937.2 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr5:140481861 C>T maps to NM_018937.2 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:140481753 C>T maps to NM_018937.2 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr5:140480940 C>T maps to NM_018937.2 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:140480274 C>A maps to NM_018937.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr5:140481573 C>T maps to NM_018937.2 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:140480874 G>A maps to NM_018937.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr5:140481561 C>T maps to NM_018937.2 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:140481489 T>C maps to NM_018937.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr5:140481786 G>A maps to NM_018937.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr5:140481786 G>A maps to NM_018937.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:140482287 G>A maps to NM_018937.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr5:140481088 G>T maps to NM_018937.2 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr5:140481312 G>A maps to NM_018937.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:140481786 G>A maps to NM_018937.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140503547 G>A maps to NM_018938.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr5:140503790 C>T maps to NM_018938.2 D737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr5:140503268 G>A maps to NM_018938.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:140502953 C>T maps to NM_018938.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:140502261 C>T maps to NM_018938.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:140503700 C>T maps to NM_018938.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140502383 A>C maps to NM_018938.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr5:140503139 C>T maps to NM_018938.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:140501643 T>C maps to NM_018938.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:140501934 G>T maps to NM_018938.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:140502917 C>T maps to NM_018938.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:140501732 G>T maps to NM_018938.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr5:140503025 C>T maps to NM_018938.2 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140516479 G>A maps to NM_015669.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140516638 C>T maps to NM_015669.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:140516393 C>T maps to NM_015669.2 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr5:140516095 G>A maps to NM_015669.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:140517109 G>A maps to NM_015669.2 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:140517265 C>T maps to NM_015669.2 Y750Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:140517247 A>G maps to NM_015669.2 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr5:140517046 G>A maps to NM_015669.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr5:140517382 G>T maps to NM_015669.2 R789R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr5:140515489 G>A maps to NM_015669.2 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:140516632 G>A maps to NM_015669.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:140516632 G>A maps to NM_015669.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr5:140530308 C>T maps to NM_018939.2 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr5:140530653 G>A maps to NM_018939.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:140530653 G>A maps to NM_018939.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr5:140530473 C>T maps to NM_018939.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:140531208 C>T maps to NM_018939.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr5:140530017 G>A maps to NM_018939.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140531676 C>T maps to NM_018939.2 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr5:140531172 C>T maps to NM_018939.2 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:140531784 G>A maps to NM_018939.2 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:140532099 G>A maps to NM_018939.2 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr5:140530137 G>A maps to NM_018939.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:140553129 C>T maps to NM_018940.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr5:140552928 C>A maps to NM_018940.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr5:140553787 C>T maps to NM_018940.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr5:140554089 G>A maps to NM_018940.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:140554605 T>C maps to NM_018940.2 F730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:140552499 C>T maps to NM_018940.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr5:140552970 C>T maps to NM_018940.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140554359 C>T maps to NM_018940.2 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:140553576 C>T maps to NM_018940.2 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:140554449 G>A maps to NM_018940.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr5:140553903 G>A maps to NM_018940.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140553915 C>T maps to NM_018940.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:140553333 A>G maps to NM_018940.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr5:140553813 C>T maps to NM_018940.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr5:140553438 C>T maps to NM_018940.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr5:140554722 C>T maps to NM_018940.2 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr5:140558958 C>T maps to NM_019120.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr5:140559168 G>A maps to NM_019120.2 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:140558490 T>G maps to NM_019120.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:140559198 C>T maps to NM_019120.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr5:140557623 C>T maps to NM_019120.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr5:140559172 C>T maps to NM_019120.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr5:140559171 G>A maps to NM_019120.2 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr5:140559225 C>T maps to NM_019120.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr5:140559639 G>A maps to NM_019120.2 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:140568556 G>A maps to NM_019119.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:140568472 G>A maps to NM_019119.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:140569046 C>A maps to NM_019119.3 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:140568364 C>T maps to NM_019119.3 C491C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr5:140712437 A>G maps to NM_018912.2 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr5:140712482 C>T maps to NM_018912.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr5:140712389 G>A maps to NM_018912.2 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr5:140712440 C>T maps to NM_018912.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:140712476 C>T maps to NM_018912.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:140712341 G>A maps to NM_018912.2 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:140711177 C>T maps to NM_018912.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:140711897 C>T maps to NM_018912.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140710436 C>T maps to NM_018912.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:140712482 C>T maps to NM_018912.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:140711918 C>T maps to NM_018912.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr5:140712215 C>T maps to NM_018912.2 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:140711777 C>T maps to NM_018912.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:140711918 C>T maps to NM_018912.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:140712215 C>A maps to NM_018912.2 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:140711537 T>A maps to NM_018912.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:140793111 G>T maps to NM_018913.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:140794892 G>A maps to NM_018913.2 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:140794295 G>A maps to NM_018913.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr5:140792813 C>T maps to NM_018913.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:140794967 G>A maps to NM_018913.2 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:140792804 C>T maps to NM_018913.2 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:140802114 C>T maps to NM_018914.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:140802632 C>T maps to NM_018914.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:140802134 C>T maps to NM_018914.2 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140803007 G>A maps to NM_018914.2 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr5:140801147 C>T maps to NM_018914.2 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr5:140801231 C>T maps to NM_018914.2 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:140803301 G>A maps to NM_032091.1 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:140811648 C>T maps to NM_003735.2 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr5:140812767 C>A maps to NM_032094.1 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:140812197 C>T maps to NM_003735.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr5:140812209 G>A maps to NM_003735.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:140812608 G>T maps to NM_003735.2 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140810877 T>C maps to NM_003735.2 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:140810709 C>T maps to NM_003735.2 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr5:140811075 C>T maps to NM_003735.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr5:140720259 C>T maps to NM_018915.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr5:140720316 G>A maps to NM_018915.2 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr5:140720952 G>A maps to NM_018915.2 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140720425 C>T maps to NM_018915.2 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr5:140719020 C>T maps to NM_018915.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:140719020 C>T maps to NM_018915.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140720676 G>A maps to NM_018915.2 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:140720931 C>T maps to NM_018915.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:140720634 G>A maps to NM_018915.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr5:140718759 C>T maps to NM_018915.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:140720769 C>T maps to NM_018915.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140725882 G>A maps to NM_018916.3 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:140724692 G>T maps to NM_018916.3 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:140724706 C>T maps to NM_018916.3 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr5:140723926 G>T maps to NM_018916.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr5:140725861 C>T maps to NM_018916.3 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140735051 C>A maps to NM_018917.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr5:140735748 C>T maps to NM_018917.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr5:140735384 G>A maps to NM_018917.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:140743998 G>A maps to NM_018918.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:140746122 C>T maps to NM_018918.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:140744289 G>A maps to NM_018918.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:140744886 C>T maps to NM_018918.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr5:140745873 G>A maps to NM_018918.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:140744157 G>A maps to NM_018918.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:140744502 C>T maps to NM_018918.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:140755770 C>T maps to NM_018919.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr5:140755383 G>A maps to NM_018919.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr5:140754996 G>A maps to NM_018919.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140753997 T>G maps to NM_018919.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr5:140753715 G>A maps to NM_018919.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140755521 C>T maps to NM_018919.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr5:140754769 C>T maps to NM_018919.2 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:140755290 A>G maps to NM_018919.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:140754207 C>T maps to NM_018919.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:140755533 G>T maps to NM_018919.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:140755509 C>T maps to NM_018919.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:140755074 T>C maps to NM_018919.2 N475N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr5:140755557 C>T maps to NM_018919.2 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr5:140755848 G>A maps to NM_018919.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr5:140753670 T>C maps to NM_018919.2 H7H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:140763529 C>A maps to NM_018920.2 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140764118 C>T maps to NM_018920.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:140763266 C>T maps to NM_018920.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr5:140762825 C>T maps to NM_018920.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140772932 G>T maps to NM_032088.1 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr5:140772679 G>A maps to NM_032088.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:140772434 C>T maps to NM_032088.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr5:140772922 C>T maps to NM_032088.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:140784199 G>T maps to NM_018921.2 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:140731008 G>A maps to NM_018922.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:140730078 C>T maps to NM_018922.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:140730765 G>A maps to NM_018922.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:140730928 C>T maps to NM_018922.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:140730135 C>T maps to NM_018922.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140730216 C>T maps to NM_018922.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:140730021 G>T maps to NM_018922.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:140730057 G>A maps to NM_018922.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr5:140740469 G>A maps to NM_018923.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140741228 G>A maps to NM_018923.2 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140740019 C>T maps to NM_018923.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr5:140741729 C>T maps to NM_018923.2 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:140741030 C>T maps to NM_018923.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:140741360 C>T maps to NM_018923.2 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:140750221 C>T maps to NM_018924.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:140751685 C>T maps to NM_018924.2 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140750237 G>T maps to NM_018924.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:140750260 G>A maps to NM_018924.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:140751913 G>A maps to NM_018924.2 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr5:140750323 G>C maps to NM_018924.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr5:140751754 G>T maps to NM_018924.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:140751607 C>T maps to NM_018924.2 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:140751673 C>T maps to NM_018924.2 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr5:140751298 C>T maps to NM_018924.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:140769103 C>T maps to NM_003736.2 D551D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:140769223 G>A maps to NM_003736.2 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr5:140769655 C>T maps to NM_003736.2 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:140779658 G>A maps to NM_018925.2 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:140778884 G>A maps to NM_018925.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:140789193 C>T maps to NM_018926.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:140788033 C>T maps to NM_018926.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140788608 C>A maps to NM_018926.2 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr5:140788791 C>T maps to NM_018926.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:140790021 T>G maps to NM_018926.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr5:140789112 C>T maps to NM_018926.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:140789313 C>T maps to NM_018926.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:140797440 C>T maps to NM_018927.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:140797653 C>T maps to NM_018927.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:140798973 G>A maps to NM_018927.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:140799267 C>T maps to NM_018927.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:140855706 C>T maps to NM_002588.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:140856225 G>A maps to NM_002588.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:140855949 C>T maps to NM_002588.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr5:140856435 G>A maps to NM_002588.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:140856282 C>T maps to NM_002588.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:140856666 C>T maps to NM_002588.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:140865411 C>T maps to NM_018928.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:140866237 C>T maps to NM_018928.2 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:140865528 G>A maps to NM_018928.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr5:140864907 G>A maps to NM_018928.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:140866863 C>T maps to NM_018928.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:140864883 C>T maps to NM_018928.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:140866345 C>T maps to NM_018928.2 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr5:140865198 G>A maps to NM_018928.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:140870213 G>T maps to NM_018929.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr5:140869388 G>T maps to NM_018929.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr5:140870954 C>A maps to NM_018929.2 C716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:140870415 C>T maps to NM_018929.2 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr5:140869727 C>T maps to NM_018929.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr5:140870972 C>T maps to NM_018929.2 D722D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr2:120404569 C>T maps to NM_001029996.3 D468D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr2:120383253 G>A maps to NM_001029996.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:120404536 C>T maps to NM_001029996.3 C457C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:120362808 C>A maps to NM_001029996.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:82879674 G>A maps to NM_015885.3 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:82874869 G>A maps to NM_015885.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:82880626 C>T maps to NM_015885.3 Q1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:82881021 T>C maps to NM_015885.3 I1215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:82895846 C>T maps to NM_015885.3 R1527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:36891757 G>A maps to NM_007144.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:36895837 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:93011046 A>G did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr13:113833327 G>A maps to ENST00000246505 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:113834545 C>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr20:44574916 C>T maps to NM_022104.3 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr20:44575768 C>T maps to NM_022104.3 C557C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr20:44569839 C>T maps to NM_022104.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:44573589 G>A maps to NM_022104.3 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:56137878 G>A maps to NM_002591.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:56139619 G>A maps to NM_002591.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:56140138 C>A maps to NM_002591.3 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr14:24567559 C>T maps to NM_004563.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:24569453 T>C maps to NM_001018073.1 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:82764963 C>T maps to NM_033026.5 E634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr7:82585561 A>G maps to NM_033026.5 A1569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:82545960 G>A maps to NM_033026.5 R3781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:82595751 G>A maps to NM_033026.5 Q1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:82764221 G>A maps to NM_033026.5 R882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr7:82583035 A>G maps to NM_033026.5 P2411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:82387899 T>C maps to NM_033026.5 Q5140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:82785302 C>T maps to NM_033026.5 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr7:82586017 T>A maps to NM_033026.5 L1417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:82389989 G>A maps to NM_033026.5 R5085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:82579562 C>A maps to NM_033026.5 T3447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:82451892 G>A maps to NM_033026.5 S4903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:82580447 C>T maps to NM_033026.5 T3152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:82595506 T>C maps to NM_033026.5 K1199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:82595776 G>A maps to NM_033026.5 C1109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr7:82785599 G>A maps to NM_033026.5 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:82584622 T>C maps to NM_033026.5 K1882K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:82544079 C>A maps to NM_033026.5 E4408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:82544368 G>A maps to NM_033026.5 S4311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:82785547 C>A maps to NM_033026.5 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:82544335 T>C maps to NM_033026.5 E4322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:82544197 G>T maps to NM_033026.5 G4368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:82579568 T>C maps to NM_033026.5 V3445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr7:82784066 C>T maps to NM_033026.5 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:82508760 T>G maps to NM_033026.5 R4516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:82784429 G>T maps to NM_033026.5 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:82595804 T>C did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:82584604 T>C maps to NM_033026.5 T1888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr7:82545649 A>T maps to NM_033026.5 P3884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:17813021 C>A maps to NM_006197.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:17822079 G>A maps to NM_006197.3 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:17796494 G>T maps to NM_006197.3 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:17817533 A>C maps to NM_006197.3 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr8:17804813 T>C maps to NM_006197.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr8:17812988 A>G maps to NM_006197.3 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:17869233 T>C maps to NM_006197.3 N1803N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr8:17822262 G>A maps to NM_006197.3 K947K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:17817620 T>C maps to NM_006197.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr20:62891515 G>A maps to NM_018257.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr20:62904718 C>A maps to NM_018257.2 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr3:101298667 T>C maps to NM_020357.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr21:47831620 C>T maps to NM_006031.5 D1878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr21:47863774 A>C maps to NM_006031.5 P3251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr21:47851714 C>T maps to NM_006031.5 C2779C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr21:47773207 G>A maps to NM_006031.5 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr21:47847576 G>T maps to NM_006031.5 L2454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr21:47746418 C>T maps to NM_006031.5 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:47767387 T>C maps to NM_006031.5 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr21:47850065 C>T maps to NM_006031.5 S2611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr21:47766901 A>G maps to NM_006031.5 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr21:47773039 G>A maps to NM_006031.5 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:47766899 G>T maps to NM_006031.5 G322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr21:47786816 C>G maps to NM_006031.5 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr21:47831132 G>T maps to NM_006031.5 E1716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr21:47766901 A>G maps to NM_006031.5 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr21:47746367 G>A maps to NM_006031.5 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr21:47776922 C>T maps to NM_006031.5 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr21:47841956 G>A maps to NM_006031.5 V2366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:47801751 G>A maps to NM_006031.5 Q1103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr14:71444949 C>T maps to NM_014982.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr14:71575381 C>G maps to NM_014982.2 A2121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:71517430 A>G maps to NM_014982.2 T1467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:71435781 C>T maps to NM_014982.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:71540386 C>T maps to NM_014982.2 R1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:71575520 C>T maps to NM_014982.2 R2168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr14:71443977 T>C maps to NM_014982.2 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:71492844 T>C maps to NM_014982.2 R1065R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr14:71514553 T>C maps to NM_014982.2 G1397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:233135110 G>A maps to NM_014801.3 C1781C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:233394380 G>A maps to NM_014801.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr1:233231606 G>A maps to NM_014801.3 L1280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:233231576 G>A maps to NM_014801.3 V1290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:233134042 G>A maps to NM_014801.3 G1915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:233393963 A>G maps to NM_014801.3 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:233394782 C>T maps to NM_014801.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:233134042 G>A maps to NM_014801.3 G1915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr1:233120088 G>A maps to NM_014801.3 D2125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:233394056 C>T maps to NM_014801.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:65393481 G>A maps to NM_032223.2 Q1112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:65396166 C>T maps to NM_032223.2 A1268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:65394447 C>T maps to NM_032223.2 P1151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:65390988 C>T maps to NM_032223.2 F795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:65391790 G>A maps to NM_032223.2 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:65388395 C>T maps to NM_032223.2 Q732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:65403955 G>A maps to NM_032223.2 Q1896Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:65386335 C>T maps to NM_032223.2 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:65386338 T>C maps to NM_032223.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr11:65394450 C>T maps to NM_032223.2 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:65404346 C>A maps to NM_032223.2 A2001A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:100203328 C>T maps to NM_002593.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr3:142539837 G>A maps to NM_013363.3 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:142607675 C>T maps to NM_013363.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:142606612 A>C maps to NM_013363.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:142542455 A>G maps to NM_013363.3 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr21:41300963 A>G maps to NM_006198.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr21:41300975 G>T maps to NM_006198.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:95735706 G>A maps to NM_000439.4 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:95748195 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:95751802 C>A maps to NM_000439.4 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:17462333 G>A maps to NM_002594.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr20:17434529 C>T maps to NM_002594.2 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr20:17462522 C>T maps to NM_002594.2 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:17208061 T>C maps to NM_002594.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr20:17208108 C>T maps to NM_002594.2 H53H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr20:17446187 C>T maps to NM_002594.2 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr20:17434424 C>T maps to NM_002594.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr9:78638758 G>T maps to NM_001190482.1 G173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:78711017 C>T maps to NM_001190482.1 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr9:78784683 G>T maps to NM_001190482.1 E562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:78686646 C>T maps to NM_001190482.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr9:78804076 G>A maps to NM_001190482.1 Q816Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:101929721 G>T maps to NM_002570.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:101910676 G>A maps to NM_002570.3 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:117099033 G>A maps to NM_004716.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:117097897 G>A maps to NM_004716.2 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:55523739 G>T maps to NM_174936.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:55521825 C>T maps to NM_174936.3 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:53844701 G>T maps to NM_021213.3 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:53828571 C>A maps to NM_021213.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:53851224 G>A maps to NM_021213.3 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:70504236 G>T maps to NM_016297.3 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:148743641 C>T maps to NM_024028.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:148747691 G>A maps to NM_024028.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:195974267 C>T maps to NM_005017.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:195968926 G>T maps to NM_005017.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr3:195997348 C>T maps to NM_005017.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr3:195997363 C>T maps to NM_005017.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:195984686 A>T maps to NM_005017.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:195965636 A>C maps to NM_005017.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:195975174 A>T maps to NM_005017.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:24608139 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:24608207 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:24580515 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:24580416 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:24597509 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr7:98995496 C>A maps to NM_014891.6 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:242793419 G>A maps to NM_005018.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:242794772 C>A maps to NM_005018.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr2:242794404 G>A maps to NM_005018.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:167405482 T>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:167405481 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:105194615 C>T maps to NM_014976.1 N1243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:105194591 C>T maps to NM_014976.1 G1235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr10:105203721 A>G maps to NM_014976.1 K1725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr10:105164789 C>T maps to NM_014976.1 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:105185267 C>T maps to NM_014976.1 D1097D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:105203065 C>A maps to NM_014976.1 I1700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:105178279 C>A maps to NM_014976.1 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr10:105200272 C>T maps to NM_014976.1 Q1459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr10:105178279 C>T maps to NM_014976.1 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:105177546 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr10:105193703 G>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr9:5549452 T>C maps to NM_025239.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:170886684 C>A maps to NM_002598.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:34904689 T>C maps to NM_032346.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:34916904 G>A maps to NM_032346.1 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr19:34900209 C>A maps to NM_032346.1 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr10:112649379 G>A maps to NM_014456.4 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr19:33076809 G>A maps to NM_004708.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:306875 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:306798 C>T maps to NM_013232.3 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:33907950 G>A maps to NM_001162429.1 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:33906775 G>A maps to NM_001162429.1 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr3:33855079 T>G maps to NM_001162429.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:56422792 T>C maps to NM_152401.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr4:56447028 A>G maps to NM_152401.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr2:101188060 C>G maps to NM_024065.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr6:165827120 G>A maps to NM_001130690.1 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:165809903 C>T maps to NM_001130690.1 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:165829675 C>T did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr6:165749682 G>A maps to NM_001130690.1 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:178684953 T>C maps to NM_016953.3 Q523Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:178494179 T>G maps to NM_016953.3 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr2:178879076 C>A maps to NM_016953.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:178936707 G>A maps to NM_016953.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:178762793 G>A maps to NM_016953.3 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:178762793 G>A maps to NM_016953.3 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:178879088 A>G maps to NM_016953.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr2:178879076 C>T maps to NM_016953.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:178936303 A>G maps to NM_016953.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:178705079 G>A maps to NM_016953.3 Y466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:183387019 C>T maps to NM_005019.3 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:183053748 T>C maps to NM_005019.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr12:54966470 C>T maps to NM_000924.3 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr12:54966942 G>A maps to NM_000924.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:54964023 G>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:54963336 C>A maps to NM_000924.3 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:54962967 G>A maps to NM_000924.3 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr12:54960853 C>A maps to NM_000924.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr7:31864483 G>T maps to NM_001191057.1 S468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr7:31918637 G>A maps to NM_001191057.1 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:31864482 C>T maps to NM_001191057.1 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:31890334 C>T maps to NM_001191057.1 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:31887711 T>G did not map to a codon.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:32091173 C>T maps to NM_001191057.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:72295715 C>T maps to NM_002599.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:72301615 G>A maps to NM_002599.3 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:72295763 C>T maps to NM_002599.3 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:72300238 G>A maps to NM_002599.3 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:72307654 G>A maps to NM_002599.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:20801671 T>C maps to NM_000921.3 A872A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:20783022 A>G maps to NM_000921.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:20522790 G>A maps to NM_000921.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:20803483 G>T maps to NM_000921.3 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr12:20766426 C>T maps to NM_000921.3 H354H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:20522733 G>A maps to NM_000921.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr12:20787834 G>A did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr12:20799874 T>C maps to NM_000921.3 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:20522415 C>T maps to NM_000921.3 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr12:20799874 T>C maps to NM_000921.3 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:14839811 G>T maps to NM_000922.3 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:14808116 T>C maps to NM_000922.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:14865556 T>C maps to NM_000922.3 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:14880793 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:14854366 C>A maps to NM_000922.3 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:14882806 G>A maps to NM_000922.3 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:14825498 C>T maps to NM_000922.3 C475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:10568598 C>T maps to NM_001111307.1 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:10572326 C>T maps to NM_001111307.1 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:10556977 C>T maps to NM_001111307.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:10578041 C>T maps to NM_001111307.1 F802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:10578146 G>A maps to NM_001111307.1 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:10574587 C>T maps to NM_001111307.1 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:66713280 C>T maps to NM_001037341.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:66458708 T>C maps to NM_001037340.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:66833735 C>T maps to NM_001037341.1 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:66379008 C>T maps to NM_001037341.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:66834624 A>G maps to NM_001037341.1 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:18321822 G>T maps to NM_000923.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:18343779 C>T maps to NM_000923.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:18327630 G>A maps to NM_000923.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:18327676 G>A maps to NM_000923.3 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr19:18333053 G>A maps to NM_000923.3 Q108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr19:18327664 C>T maps to NM_000923.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:18332982 C>T maps to NM_000923.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:58272188 G>A maps to NM_001104631.1 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:144859981 G>T maps to NM_014644.4 A2034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:144881457 G>A maps to NM_014644.4 N1246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:144912153 G>A maps to NM_014644.4 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:144866679 C>T maps to NM_014644.4 L1854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr1:144879282 C>T maps to NM_014644.4 S1389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:144877084 G>A maps to NM_014644.4 L1534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:144856899 C>T maps to NM_014644.4 A2195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:144854563 G>A maps to NM_014644.4 N2302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:144881505 G>A maps to NM_014644.4 L1230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:144931699 C>T maps to NM_001002811.1 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr1:144915579 C>T maps to NM_014644.4 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr1:144868059 G>A maps to NM_014644.4 T1793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:144882799 G>A maps to NM_014644.4 I1073I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr1:144856832 C>A maps to NM_014644.4 E2218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:144879282 C>T maps to NM_014644.4 S1389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:144874012 C>T maps to NM_014644.4 S1648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr1:145075757 G>A maps to NM_022359.5 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr1:144866595 T>C maps to NM_014644.4 G1882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:144912273 C>T maps to NM_014644.4 V667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:145075751 C>T maps to NM_022359.5 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr1:144879269 T>A maps to NM_014644.4 R1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:144879282 C>T maps to NM_014644.4 S1389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:145075751 C>T maps to NM_022359.5 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:120432288 T>C maps to NM_001083.3 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:120446850 C>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr4:120488257 G>A maps to NM_001083.3 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:120527934 C>A maps to NM_001083.3 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr5:149247665 G>A maps to NM_000440.2 Q731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:149278949 C>T maps to NM_000440.2 E417E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr5:149324191 C>T maps to NM_000440.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:149278946 C>T maps to NM_000440.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr5:149245741 G>A maps to NM_000440.2 F783F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:149264055 G>A maps to NM_000440.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr4:661769 G>A maps to NM_000283.3 E826E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:652778 C>T maps to NM_000283.3 C480C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:656371 C>T maps to NM_000283.3 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:660381 C>T maps to NM_000283.3 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr4:619516 G>A maps to NM_000283.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:658004 C>T maps to NM_000283.3 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr4:649788 C>T maps to NM_000283.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:657984 G>T maps to NM_000283.3 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:95372505 C>T maps to NM_006204.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:95372505 C>T maps to NM_006204.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:95381721 G>T maps to NM_006204.3 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr10:95395364 A>T maps to NM_006204.3 K461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:95386564 G>A maps to NM_006204.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:95394660 C>A maps to NM_006204.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:95380444 G>A maps to NM_006204.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:232601991 G>A maps to NM_002601.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr8:66637116 G>T maps to ENST00000401827 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:66647076 G>A maps to ENST00000401827 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:66631528 G>T maps to ENST00000401827 S482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr6:136472383 C>T maps to NM_018945.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:136512842 C>T maps to NM_018945.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:136500167 C>A maps to NM_018945.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:136500260 C>T maps to NM_018945.3 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:136512923 C>T maps to NM_018945.3 H433H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:136512767 C>T maps to NM_018945.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr15:85632613 A>C maps to NM_002605.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr15:85669545 C>T maps to NM_002605.2 R732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:85634392 C>A maps to NM_002605.2 S278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr15:85656641 G>A maps to NM_002605.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:85664165 C>T maps to NM_002605.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr15:85610339 T>G maps to NM_002605.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr15:85669589 A>G maps to NM_002605.2 E746E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr15:85610363 G>T maps to NM_002605.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr15:85666363 G>A maps to NM_002605.2 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:76621398 C>T maps to NM_003719.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr5:76627247 G>A maps to NM_003719.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:76700599 G>A maps to NM_003719.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:76714109 C>T maps to NM_003719.3 D656D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:76621419 C>T maps to NM_003719.3 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr21:44152187 G>T maps to NM_002606.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr22:39621781 C>A maps to NM_002608.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr22:39621796 G>A maps to NM_002608.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr4:157732156 T>A maps to NM_016205.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr11:103797792 C>T maps to NM_025208.4 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:103870794 C>A maps to NM_025208.4 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:103814345 A>G maps to NM_025208.4 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr11:103814345 A>G maps to NM_025208.4 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:55155211 G>A maps to ENST00000507166 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr4:55144171 A>G maps to ENST00000507166 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr4:55141036 C>A maps to NM_006206.4 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr4:55144171 A>G maps to ENST00000507166 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:55141054 A>G maps to NM_006206.4 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr4:55129855 T>C maps to NM_006206.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr4:55141096 T>C maps to ENST00000507166 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr4:55156637 C>T maps to ENST00000507166 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr4:55155244 G>A maps to ENST00000507166 E708E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:55144635 G>T maps to ENST00000507166 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:55161378 C>T maps to ENST00000507166 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr4:55141033 G>A maps to NM_006206.4 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:55127460 G>A maps to NM_006206.4 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:55133596 G>T maps to NM_006206.4 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:55133777 G>T maps to NM_006206.4 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:55133832 G>A maps to NM_006206.4 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr4:55153643 C>T maps to ENST00000507166 N630N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr4:55156586 G>A maps to ENST00000507166 E756E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:55141012 G>T maps to NM_006206.4 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr4:55156586 G>A maps to ENST00000507166 E756E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr4:55129855 T>C maps to NM_006206.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr4:55133529 C>T maps to NM_006206.4 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr4:55129855 T>C maps to NM_006206.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr4:55131086 A>G maps to NM_006206.4 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr4:55133832 G>A maps to NM_006206.4 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:55161333 C>T maps to ENST00000507166 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:55141096 T>C maps to ENST00000507166 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:149512404 C>T maps to NM_002609.3 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr5:149515340 G>A maps to NM_002609.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:149515304 C>T maps to NM_002609.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:149497260 G>A maps to NM_002609.3 N1019N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr5:149516598 C>T maps to NM_002609.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:149500489 T>C maps to NM_002609.3 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:149514438 G>A maps to NM_002609.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:149505038 C>T maps to NM_002609.3 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr5:149505047 A>G maps to NM_002609.3 Y589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:149495376 C>T maps to NM_002609.3 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:19367442 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:19372682 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:19373599 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:19371228 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:19367457 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:19373477 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr23:19369485 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:19367443 G>A did not map to a codon.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr23:19367442 T>C did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:19367443 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:19367474 A>G did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr4:96762221 A>G maps to NM_005390.4 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:96762327 G>T maps to NM_005390.4 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:96761891 G>A maps to NM_005390.4 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr4:96761324 C>T maps to NM_005390.4 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:96761891 G>A maps to NM_005390.4 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:96761960 T>C maps to NM_005390.4 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:96761756 T>C maps to NM_005390.4 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr4:96761324 C>T maps to NM_005390.4 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:96761471 G>A maps to NM_005390.4 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:58413784 T>C maps to NM_000925.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:58414284 G>A maps to NM_000925.3 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:336444 C>T maps to NM_006849.2 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:333195 G>A maps to NM_006849.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr15:44058124 T>C maps to NM_005313.4 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr15:44048948 G>T maps to NM_005313.4 G117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:148700993 G>A maps to NM_004911.4 D610D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:122843154 G>A maps to NM_006810.3 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:122835133 C>T maps to NM_006810.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:122835105 G>A maps to NM_006810.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:122849377 C>T maps to NM_006810.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:10929026 A>G maps to ENST00000381611 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:10933245 G>A maps to ENST00000381611 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:10930937 G>A maps to ENST00000381611 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:10929898 G>A maps to ENST00000381611 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:26448657 G>T maps to NM_152835.3 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:26448761 C>A maps to NM_152835.3 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:26448761 C>A maps to NM_152835.3 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr16:20370763 G>A maps to NM_174924.1 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr16:20396087 G>A maps to NM_174924.1 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:20380897 G>A maps to NM_174924.1 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:20396087 G>A maps to NM_174924.1 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:20387497 G>A maps to NM_174924.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:20396018 C>T maps to NM_174924.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr16:20376793 C>T maps to NM_174924.1 K395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr16:20386197 G>T maps to NM_174924.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:24537110 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:24544329 A>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:24557251 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr23:24537110 A>G did not map to a codon.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr23:24552053 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:24521457 T>A did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:24552051 T>A did not map to a codon.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr23:24537110 A>G did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:24552051 T>C did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:95224434 G>A maps to NM_002612.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:95214966 C>A maps to NM_002612.3 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:95225560 G>A maps to NM_002612.3 N15N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:97023763 C>T maps to NM_020992.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:22451335 G>A maps to NM_021630.5 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr8:22438968 G>A maps to NM_021630.5 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr8:22442906 C>T maps to NM_021630.5 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:186429652 A>G maps to NM_014476.4 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:186446181 T>C maps to NM_014476.4 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:131598426 C>T maps to NM_003687.3 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:131607852 G>A maps to NM_003687.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:131607547 G>A maps to NM_003687.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:95578684 C>T maps to NM_006457.3 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:95561460 T>G maps to NM_006457.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:176919420 C>T maps to NM_005451.3 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:176910876 G>A maps to NM_005451.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:94934763 C>A maps to NM_001161778.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:94935249 A>G maps to NM_001161778.1 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr8:94934583 A>T maps to NM_001161778.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr8:94934355 T>C maps to NM_001161778.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr16:66918453 C>T maps to NM_020786.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:66919135 C>T maps to NM_020786.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:66919258 G>T maps to NM_020786.2 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr16:2607960 C>T maps to NM_002613.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr16:2647125 T>C maps to NM_002613.3 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:13910572 G>A maps to NM_006474.4 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:13936988 C>T maps to NM_006474.4 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:70162927 C>T maps to NM_017990.3 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:70177480 C>T maps to NM_017990.3 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:30534338 C>T maps to NM_030815.2 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr4:39905807 G>A maps to NM_001100399.1 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:39868614 T>C maps to NM_001100399.1 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:39875956 T>G maps to NM_001100399.1 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:39905697 T>C maps to NM_001100399.1 K449K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:39915327 G>A maps to NM_001100399.1 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr13:33330034 G>A maps to ENST00000400481 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr13:33281085 A>G maps to ENST00000400481 Q624Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr13:33309355 A>G maps to ENST00000400481 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:33258136 A>T maps to ENST00000400481 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr13:33344296 C>T maps to ENST00000400481 P1221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:33306318 G>A maps to ENST00000400481 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:33349184 C>T maps to ENST00000400481 R1448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:33232410 G>A maps to ENST00000400481 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr13:33232410 G>A maps to ENST00000400481 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr13:33232410 G>T maps to ENST00000400481 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:33338733 T>C did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr10:27013021 C>T maps to NM_014317.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:27012796 T>C maps to NM_014317.3 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:27024209 C>T maps to NM_014317.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:107531648 G>A maps to NM_020381.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr6:107566784 T>A maps to NM_020381.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:107595388 A>G maps to NM_020381.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr16:15129963 G>A maps to NM_015027.2 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:15125601 T>C maps to NM_015027.2 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:15092214 T>C maps to NM_015027.2 N38N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr21:45170383 A>G maps to NM_003681.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr22:38061644 G>T maps to ENST00000442465 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:1961061 C>T maps to NM_024411.4 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr20:1963673 T>G maps to NM_024411.4 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:1961136 G>A maps to NM_024411.4 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:69508006 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:69508352 T>C did not map to a codon.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr23:69508314 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:69506956 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:32072370 G>A maps to NM_178140.2 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:32087987 C>G maps to NM_178140.2 G1478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:32010497 G>A maps to NM_178140.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr5:32074103 C>T maps to NM_178140.2 C964C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:32088389 G>A maps to NM_178140.2 S1612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:32090399 G>A maps to NM_178140.2 P2282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:32088607 C>A maps to NM_178140.2 S1685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:32087577 G>T maps to NM_178140.2 G1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:32087963 C>T maps to NM_178140.2 C1470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr5:32090054 G>A maps to NM_178140.2 L2167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr5:32088542 C>T maps to NM_178140.2 S1663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:31799708 C>T maps to NM_178140.2 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr5:31799444 G>A maps to NM_178140.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr5:32074106 C>T maps to NM_178140.2 Y965Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:32087363 G>A maps to NM_178140.2 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:32074304 G>T maps to NM_178140.2 S1031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr5:31983405 C>T maps to NM_178140.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:32089286 G>A maps to NM_178140.2 T1911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:119058746 A>G maps to ENST00000392817 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:119057264 C>T maps to ENST00000392817 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:153069232 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:153068995 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:153068961 T>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:153069636 C>T did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:153070325 G>A did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:153068988 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:102789820 G>A maps to NM_001195263.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr10:102789820 G>A maps to NM_001195263.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:102783748 C>G maps to NM_001195263.1 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:102789778 G>A maps to NM_001195263.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:102789808 G>A maps to NM_001195263.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr10:102783745 G>A maps to NM_001195263.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:102780377 G>A maps to NM_001195263.1 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr10:102782087 G>A maps to NM_001195263.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:73432698 C>T maps to NM_015009.1 Q1006Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:73657780 C>A maps to NM_015009.1 G260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:73433787 G>A maps to NM_015009.1 C643C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:73433889 G>A maps to NM_015009.1 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:73433313 G>A maps to NM_015009.1 Y801Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:73433028 C>T maps to NM_015009.1 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:73453540 G>A maps to NM_015009.1 N308N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:73433091 C>A maps to NM_015009.1 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:73433010 C>T maps to NM_015009.1 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:73433850 G>A maps to NM_015009.1 N622N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:73433052 C>T maps to NM_015009.1 Q888Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr3:73433697 G>A maps to NM_015009.1 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr12:41949528 C>T maps to NM_001164595.1 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:41966258 G>T maps to NM_001164595.1 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr12:41957402 C>T maps to NM_001164595.1 N473N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr12:41967226 T>C maps to NM_001164595.1 C882C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:41957373 C>T maps to NM_001164595.1 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:41961653 G>T maps to NM_001164595.1 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:41966267 C>T maps to NM_001164595.1 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr12:41966458 A>G maps to NM_001164595.1 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:41967295 C>T maps to NM_001164595.1 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr1:156878530 T>C maps to NM_001080471.1 H400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:156873762 G>A maps to NM_001080471.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:156876651 C>T maps to NM_001080471.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr1:156883779 C>A maps to NM_001080471.1 P950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:22570885 G>A maps to NM_144962.2 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:22777723 C>T maps to NM_144962.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr8:22785140 C>T maps to NM_144962.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:4130795 T>C maps to ENST00000380120 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr6:4116218 T>C maps to NM_206836.2 E358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr7:94294963 G>A maps to NM_001172437.1 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:94293250 G>A maps to NM_001172437.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr7:94294753 C>T maps to NM_001172437.1 F704F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr7:94293991 C>A maps to NM_001172437.1 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr19:57328027 A>G maps to NM_006210.2 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr19:57327049 G>A maps to NM_006210.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:57326566 C>T maps to NM_006210.2 Q1081Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:57327526 C>T maps to NM_006210.2 K761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:57328863 C>A maps to NM_006210.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:57327379 G>A maps to NM_006210.2 F810F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr19:57328826 G>T maps to NM_006210.2 S328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:57325891 A>G maps to NM_006210.2 N1306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:57326314 A>G maps to NM_006210.2 C1165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:57328372 G>A maps to NM_006210.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:57328705 C>A maps to NM_006210.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr19:57328027 A>G maps to NM_006210.2 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr19:57325378 T>C maps to NM_006210.2 G1477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr19:57325378 T>C maps to NM_006210.2 G1477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr19:57335015 G>A maps to NM_006210.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:64327529 A>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:64322048 T>C maps to NM_020651.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:64335390 A>G maps to NM_020651.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:64322048 T>C maps to NM_020651.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:56763571 C>T maps to NM_021255.2 H317H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr14:56757044 C>T maps to NM_021255.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr14:56763461 C>A maps to NM_021255.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:66241210 C>T maps to NM_145065.2 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr5:52096722 G>A maps to NM_015946.4 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:52096302 C>T maps to NM_015946.4 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:4575444 T>C maps to ENST00000301396 E1091E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:4576308 G>T maps to ENST00000301396 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:4578651 C>T maps to ENST00000301396 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:4575327 C>T maps to ENST00000301396 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:4575909 G>A maps to ENST00000301396 P936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:57353998 G>T maps to NM_001135690.1 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr8:57353860 T>C maps to NM_001135690.1 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:33904509 G>A maps to NM_000285.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:34002016 G>A maps to NM_000285.3 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr19:33980957 G>A maps to NM_000285.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr19:33980957 G>A maps to NM_000285.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:8049786 A>G maps to NM_002616.2 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:8050603 G>A maps to NM_002616.2 N531N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:8044574 C>T maps to NM_002616.2 L1228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:8049375 G>A maps to NM_002616.2 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr17:8049357 C>G maps to NM_002616.2 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr2:239162194 C>T maps to NM_022817.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:239162194 C>T maps to NM_022817.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:239179989 C>T maps to NM_022817.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:7845513 C>T maps to ENST00000377532 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:7880237 T>C maps to ENST00000377532 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr1:7880237 T>C maps to ENST00000377532 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr22:30985242 C>T maps to NM_014303.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:30977517 C>T maps to NM_014303.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr4:152637170 C>T maps to NM_004564.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:152609906 G>A maps to NM_004564.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:152637227 C>T maps to NM_004564.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:92147473 C>T maps to NM_000466.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr7:92122278 C>A maps to NM_000466.2 S1065S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:92123644 G>A maps to NM_000466.2 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:92146640 A>G maps to NM_000466.2 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:92129068 T>C maps to NM_000466.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:92131267 A>G maps to NM_000466.2 F784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:92130987 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr7:92146931 G>A maps to NM_000466.2 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:92147523 G>A maps to NM_000466.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr15:90227159 C>A maps to NM_003847.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:90226808 T>C maps to NM_003847.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:7546965 C>T maps to NM_080662.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:33903142 G>T maps to NM_000286.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr2:61259021 T>A maps to NM_002618.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:61272930 A>G maps to NM_002618.3 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:61272859 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:10689884 C>T maps to NM_004565.2 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:10678449 A>C maps to NM_004565.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr1:10689897 G>T maps to NM_004565.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:10689653 G>A maps to NM_004565.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:160253412 G>A maps to NM_002857.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:77895523 G>A maps to NM_001172087.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr8:77895574 A>G maps to NM_001172087.1 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr22:18567977 C>T maps to NM_017929.5 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr22:18567980 G>C maps to NM_017929.5 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:143793348 G>T maps to NM_003630.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:143793362 C>T maps to NM_003630.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:143792700 A>G maps to NM_003630.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:7351700 C>T maps to NM_001131023.1 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:7360316 G>C maps to NM_001131023.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:7360670 G>A maps to NM_001131023.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:7361750 C>T maps to NM_001131023.1 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:179519747 A>G maps to NM_016559.1 H583H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:179525598 G>A maps to NM_016559.1 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:179525469 G>A maps to NM_016559.1 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:179593214 G>A maps to NM_016559.1 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr3:179592211 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:179576912 G>A maps to NM_016559.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr6:42932201 C>T maps to NM_000287.3 E938E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:42933084 G>A maps to NM_000287.3 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:42942644 G>A maps to NM_000287.3 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr17:8159850 G>A maps to NM_012393.2 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:8157547 G>A maps to NM_012393.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr5:139680110 T>G maps to NM_002622.4 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:139680080 C>T maps to NM_002622.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:161070588 C>A maps to NM_012394.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:52830979 G>T maps to NM_002623.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:53689706 C>T maps to NM_002624.3 L53L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3811-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr23:54989790 G>A did not map to a codon.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr23:54987294 G>T did not map to a codon.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr23:54984792 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:55020432 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:54971877 C>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:54986260 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:54959878 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:54971894 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:54960257 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:54989722 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:54975648 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:54985297 C>A did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:54971930 G>A did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:54959871 A>G did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:54982593 T>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:207240954 G>A maps to NM_006212.2 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:207243647 G>A maps to NM_006212.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:207236529 C>T maps to NM_006212.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:207245601 G>A maps to NM_006212.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr1:207236505 G>A maps to NM_006212.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:6261542 C>A maps to NM_004566.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:6265969 G>A maps to NM_004566.3 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:6262753 C>A maps to NM_004566.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr10:6261542 C>A maps to NM_004566.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:6264840 C>T maps to NM_004566.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr3:48561152 G>A maps to NM_004567.2 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr21:45733535 C>T maps to NM_002626.4 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr21:45732044 C>A maps to NM_002626.4 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:45738450 G>A maps to NM_002626.4 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr12:48539484 C>T maps to NM_001166686.1 A850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:3176773 G>T maps to NM_002627.3 G708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:3158978 C>T maps to NM_002627.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:3146058 C>T maps to NM_002627.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:3155601 C>T maps to NM_002627.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:3176688 T>C maps to NM_002627.3 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr3:149683983 G>A maps to ENST00000423691 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:24342446 C>A maps to NM_199346.1 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:61017218 C>T maps to ENST00000422676 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:44102512 C>T maps to NM_000290.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:44102455 C>T maps to NM_000290.3 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:197777636 A>G maps to NM_024989.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:197712710 T>A maps to NM_024989.3 K638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr11:3845150 C>T maps to NM_014489.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:37829820 G>A maps to NM_033419.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr17:37829374 C>T maps to NM_033419.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:28253416 G>A maps to NM_032507.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:28269934 T>C maps to NM_032507.3 D768D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:28269485 C>T maps to NM_032507.3 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:28268872 C>T maps to NM_032507.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:28251934 A>G maps to NM_032507.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:28269964 C>T maps to NM_032507.3 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:28269964 C>T maps to NM_032507.3 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr6:28269536 T>C maps to NM_032507.3 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr1:249210978 C>T maps to NM_170725.2 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:249211970 T>C maps to NM_170725.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:50725027 C>A maps to ENST00000515869 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:50723414 T>C maps to ENST00000515869 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:34395547 A>G maps to NM_152595.4 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr15:34395494 C>T maps to NM_152595.4 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:230492909 C>T maps to ENST00000321327 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr1:230513277 G>A maps to ENST00000321327 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:230472878 C>T maps to ENST00000321327 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:41712165 C>T maps to NM_002630.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:10477467 A>G maps to NM_002631.2 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:10477467 A>G maps to NM_002631.2 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:77378798 T>C did not map to a codon.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr23:77365404 A>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:77378736 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:77359879 A>G did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:77381287 T>G did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr6:49753790 A>G maps to NM_138733.4 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr6:49754501 T>C maps to NM_138733.4 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr6:49753712 G>A maps to NM_138733.4 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr6:49754594 T>C maps to NM_138733.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr6:49754594 T>C maps to NM_138733.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr6:49754594 T>C maps to NM_138733.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr6:49754491 C>A maps to NM_138733.4 G137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr19:17622687 C>T maps to NM_012088.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:46526054 C>T maps to NM_005091.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:15586514 G>A maps to NM_052890.3 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr19:15586370 C>T maps to NM_052890.3 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:153271670 C>T maps to NM_052891.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:64104427 C>T maps to NM_002633.2 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr1:64101903 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:64097430 C>T maps to NM_002633.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr1:64101993 G>A maps to NM_002633.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:37857284 C>T maps to NM_018290.3 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr4:37839219 G>A maps to NM_018290.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:37863133 T>C maps to NM_018290.3 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:37846146 G>A maps to NM_018290.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr4:37851850 C>T maps to NM_018290.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr4:37851852 A>G maps to NM_018290.3 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr4:37851852 A>G maps to NM_018290.3 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:74056675 G>A maps to NM_173582.3 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr6:83889624 A>T maps to ENST00000416472 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr9:71094428 C>T maps to NM_021965.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:71002415 C>A maps to NM_021965.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:71006621 T>C maps to NM_021965.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr9:71114162 G>A maps to NM_021965.3 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:70993152 G>A maps to NM_021965.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:99511763 C>T maps to NM_001102612.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr15:99511877 G>A maps to NM_001102612.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:99514384 C>T maps to NM_001102612.2 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:100920698 C>A maps to NM_000926.4 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:100912815 G>A maps to NM_000926.4 R836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:100912714 A>G maps to NM_000926.4 R869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:100912737 C>A maps to NM_000926.4 G862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr11:100933298 A>G maps to NM_000926.4 D697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:100999690 C>T maps to NM_000926.4 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:118370650 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:118370543 T>G did not map to a codon.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr4:129193673 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:76392417 C>T maps to NM_024419.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:76399751 C>T maps to NM_024419.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:13228095 G>A maps to NM_030948.1 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:13182904 C>A maps to NM_030948.1 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr6:13053735 C>T maps to NM_030948.1 S130S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AD-6963-01A-11D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr6:13273091 G>A maps to NM_030948.1 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr6:13286392 G>T maps to NM_030948.1 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:13053753 G>A maps to NM_030948.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:144095199 T>G maps to NM_001100164.1 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr6:144081565 G>A maps to NM_001100164.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr20:58381231 C>T maps to NM_080672.3 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr20:58330339 C>T maps to NM_080672.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:58349408 C>T maps to NM_080672.3 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:58318177 G>A maps to NM_080672.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:58381132 C>T maps to NM_080672.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr20:58348373 C>T maps to NM_080672.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:58349435 C>T maps to NM_080672.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:125960529 C>A maps to NM_032177.3 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:125960424 G>A maps to NM_032177.3 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:9070287 C>T maps to ENST00000433083 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:9074288 A>T maps to ENST00000433083 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:9089482 C>T maps to ENST00000433083 C895C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:9090430 G>T maps to ENST00000433083 E974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr12:9089551 C>T maps to ENST00000433083 C918C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:33820576 G>A maps to ENST00000419414 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:33841077 G>A maps to ENST00000419414 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:33794644 A>G maps to ENST00000419414 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:33836632 C>T maps to ENST00000419414 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:33832921 G>A maps to ENST00000419414 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:169846606 C>T maps to NM_024947.3 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr3:169846608 G>A maps to NM_024947.3 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:22112109 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:22051208 G>A did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr23:22239857 A>C did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:22244607 C>A did not map to a codon.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr23:22151683 G>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:22051204 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:22065194 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:22051146 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:22095779 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:22132623 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:22186503 G>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:22112103 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:22129652 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:22239744 A>C did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:22094567 C>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:22132673 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:22112162 C>A did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:22129652 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:33380093 A>G maps to NM_024165.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr6:170117955 T>C maps to NM_018288.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr6:170117955 T>C maps to NM_018288.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr6:170117955 T>C maps to NM_018288.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr6:170117955 T>C maps to NM_018288.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr6:170117955 T>C maps to NM_018288.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:170105739 A>C maps to NM_018288.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:170117955 T>C maps to NM_018288.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:170115887 A>G maps to NM_018288.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:50080831 C>T maps to NM_001040443.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr17:27250948 C>G maps to NM_001033561.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr17:27248743 G>A maps to NM_001033561.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr17:27235831 G>A maps to NM_001033561.1 N809N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:6681570 C>A maps to NM_153812.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr7:11022177 A>T maps to ENST00000303905 K98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:11076684 T>C maps to ENST00000303905 N649N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr7:11076699 T>C maps to ENST00000303905 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr7:11080330 C>G maps to ENST00000303905 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr7:11076699 T>C maps to ENST00000303905 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:133909448 C>T maps to ENST00000448712 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:133896568 C>T maps to ENST00000448712 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:133896553 C>T maps to ENST00000448712 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:46918112 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:46898413 C>T did not map to a codon.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr4:129778563 G>A maps to NM_199320.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:129764114 A>G maps to NM_199320.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:129770254 T>C maps to NM_199320.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:129783196 G>A maps to NM_199320.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:129764178 C>T maps to NM_199320.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:123636950 C>T maps to NM_015651.1 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr9:96411464 C>T maps to NM_005392.3 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:96422496 G>A maps to NM_005392.3 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr9:96415577 C>T maps to NM_005392.3 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:96422667 C>A maps to NM_005392.3 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:96418258 C>T maps to NM_005392.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr9:96438991 A>T maps to NM_005392.3 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:96425263 C>T maps to NM_005392.3 R592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:96422562 G>A maps to NM_005392.3 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr20:34487475 G>A maps to NM_016436.4 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr20:34457454 C>A maps to NM_016436.4 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:133848921 C>T maps to ENST00000395386 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:133848921 C>T maps to ENST00000395386 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr8:133837584 G>A maps to ENST00000395386 K572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:133854874 G>T maps to ENST00000395386 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:133826883 G>A maps to ENST00000395386 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr8:133854966 G>A maps to ENST00000395386 K866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:133816881 A>G maps to ENST00000395386 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:133826883 G>A maps to ENST00000395386 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr8:133807001 T>C maps to ENST00000395386 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr11:45992870 G>A maps to ENST00000257821 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:45955596 G>A maps to ENST00000257821 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr11:45992798 G>A maps to ENST00000257821 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:45975086 C>T maps to ENST00000257821 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr11:45967554 C>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:45312243 G>A maps to NM_138415.3 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:45279084 G>A maps to NM_138415.3 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:7139954 G>T maps to NM_024297.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:7139477 C>T maps to NM_024297.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:7139698 G>A maps to NM_024297.2 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:7139488 C>A maps to NM_024297.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:7139477 C>T maps to NM_024297.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:64421545 G>A maps to NM_015153.2 Q1354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:64423126 G>A maps to NM_015153.2 P1881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:64416111 A>G maps to NM_015153.2 P1187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:64422952 T>C maps to NM_015153.2 F1823F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:64394046 C>T maps to NM_015153.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:64416645 T>C maps to NM_015153.2 V1197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr6:64421566 T>C maps to NM_015153.2 T1361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:64389952 T>C maps to NM_015153.2 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr22:41856440 G>A maps to NM_032758.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr23:133547638 C>T did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:133511765 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:52448584 C>T maps to ENST00000454052 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:54019232 C>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:54022169 C>T did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr23:54013587 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:54028602 G>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:54040972 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:54049272 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:54011659 G>A did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:54011432 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:54048788 G>A did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:54069221 A>G did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:54014374 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:54069083 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:54011471 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:120279852 C>T maps to NM_006623.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:120277270 C>T maps to NM_006623.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr6:79698054 A>G maps to NM_017934.5 H777H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr6:79650558 G>A maps to NM_017934.5 R1773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr6:79664551 C>T maps to NM_017934.5 P1344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:79675690 A>G maps to NM_017934.5 P1096P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:79680569 G>A maps to NM_017934.5 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:79692616 C>A maps to NM_017934.5 E919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:79665400 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:79680569 G>A maps to NM_017934.5 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:79752672 G>A maps to NM_017934.5 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr6:79650574 T>C maps to NM_017934.5 R1767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr6:79664551 C>T maps to NM_017934.5 P1344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr6:79735743 A>G maps to NM_017934.5 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:79650574 T>C maps to NM_017934.5 R1767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr6:79655098 T>C maps to NM_017934.5 E1582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr6:79770436 T>C maps to NM_017934.5 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:71822045 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:71932664 C>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:71802396 G>A did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:71822974 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:71856206 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:71800893 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:71864322 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:71855007 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:71823001 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:71872498 G>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:71856222 T>C did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:71856222 T>C did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:71856224 T>A did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:18944692 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:18954182 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:18970647 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:18936799 T>C did not map to a codon.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr23:18924895 G>A did not map to a codon.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr23:18926932 A>C did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:18911678 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:18924857 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:18936841 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:18966933 G>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:18961839 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:18918807 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:18943833 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:18936848 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:18919690 G>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:18972421 T>C did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:18915315 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:18959750 C>A did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:18924864 C>T did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:18961882 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:18924630 G>A did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:47614262 C>T maps to NM_000293.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr16:47581456 G>A maps to NM_000293.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr16:47533769 C>T maps to NM_000293.2 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:47698873 A>G maps to NM_000293.2 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr16:47703298 A>G maps to NM_000293.2 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr16:47703298 A>G maps to NM_000293.2 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:47623000 A>G maps to NM_000293.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:30762429 A>G maps to NM_000294.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:76425011 C>T maps to NM_007350.3 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:76424918 C>T maps to NM_007350.3 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:201437674 G>A maps to NM_012396.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:118513087 C>T maps to NM_015157.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:118527415 C>T maps to NM_015157.2 F1339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:118486783 A>G maps to NM_015157.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr11:118516173 A>T maps to NM_015157.2 A1074A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:118498961 C>A maps to NM_015157.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:118516458 T>C maps to NM_015157.2 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:118498951 G>A maps to NM_015157.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:111688734 C>T maps to NM_001134438.1 R1172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:111667903 C>T maps to NM_001134438.1 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:111603770 C>T maps to NM_001134438.1 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr18:60562355 C>T maps to NM_194449.2 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr18:60646021 C>T maps to NM_194449.2 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:60646021 C>T maps to NM_194449.2 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:71712660 A>C maps to NM_015020.2 L422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:71724466 A>G maps to NM_015020.2 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:71686758 G>T maps to NM_015020.2 V917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr16:71703182 G>A maps to NM_015020.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr16:71689260 G>A maps to NM_015020.2 R823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:41750393 G>A maps to NM_003924.3 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:139745254 A>T maps to NM_014172.4 K112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:601664 A>G maps to ENST00000264555 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:591434 C>A maps to ENST00000264555 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:607393 G>A maps to ENST00000264555 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:605709 C>T maps to ENST00000264555 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:608863 G>A maps to ENST00000264555 K1136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:114248658 A>G maps to NM_006608.2 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr1:114247311 C>T maps to NM_006608.2 W593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:114249242 C>T maps to NM_006608.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:114249244 A>G maps to NM_006608.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:77572031 C>T maps to ENST00000427986 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:13336520 C>T maps to NM_006214.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:13336481 C>T maps to NM_006214.3 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr9:131702681 G>A maps to NM_001100876.1 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:131696065 C>T maps to NM_001100876.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr8:22078877 G>A maps to NM_014759.3 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:22084442 G>A maps to NM_014759.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:60998463 C>T maps to NM_032439.3 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:61005210 G>T maps to NM_032439.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr8:75761445 T>C maps to NM_015886.3 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:75757494 G>A maps to NM_015886.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:36930894 T>C maps to NM_153370.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr10:99426276 G>A maps to ENST00000416867 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr10:99416702 G>A maps to ENST00000416867 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr10:99416702 G>A maps to ENST00000416867 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr4:25256743 A>T maps to NM_018323.3 K161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:25265388 T>C maps to NM_018323.3 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr22:21073045 C>T maps to NM_058004.2 A1669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:21083749 T>C maps to NM_058004.2 S1453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:21073102 G>A maps to NM_058004.2 I1650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr22:21072001 G>A maps to NM_058004.2 Q1713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:21084261 G>A maps to NM_058004.2 V1384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr22:21119208 G>A maps to NM_058004.2 I810I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr22:21107403 C>T maps to NM_058004.2 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:21159268 G>A maps to NM_058004.2 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:151288456 A>G maps to NM_002651.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:151288762 G>A maps to NM_002651.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:151280085 G>T maps to NM_002651.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:151276078 A>G maps to NM_002651.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr15:68378932 C>A maps to NM_016166.1 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:68468921 G>T maps to NM_016166.1 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr15:68379020 G>A maps to NM_016166.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr15:68434290 C>T maps to NM_016166.1 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr15:68434290 C>T maps to NM_016166.1 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:44470621 A>G maps to NM_004671.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr1:145584538 G>A maps to NM_006099.3 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:145578474 C>T maps to NM_006099.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr19:4028782 C>T maps to NM_015897.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:4037380 G>A maps to NM_015897.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr11:85692180 A>G maps to ENST00000393343 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:85689111 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:38468556 C>T maps to NM_012407.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:229890416 G>A maps to NM_017933.4 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:229890416 G>A maps to NM_017933.4 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:229890560 G>A maps to NM_017933.4 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:15349875 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:15349628 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:15339704 G>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:15349974 G>C did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:55632952 C>A maps to ENST00000164305 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:172411333 A>C maps to NM_153747.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:527698 G>A maps to NM_001127178.1 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr4:514923 A>G maps to NM_001127178.1 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:517504 C>T maps to NM_001127178.1 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr14:68060618 A>G maps to NM_004569.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:77627340 G>A maps to NM_005482.2 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:77620285 A>G maps to NM_005482.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:16216925 G>T maps to NM_004278.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:160000818 C>T maps to NM_145167.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr18:59821801 A>G maps to NM_176787.4 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr18:59774019 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:35091321 G>A maps to NM_032634.2 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:35092617 C>T maps to NM_032634.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:35092698 C>T maps to NM_032634.2 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr9:35091444 C>T maps to NM_032634.2 E813E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr9:35091594 C>T maps to NM_032634.2 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr9:35092410 C>G maps to NM_032634.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:633117 C>T maps to NM_148920.1 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:633552 C>T maps to NM_148920.1 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:207112485 A>G maps to NM_002644.3 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:207107960 G>T maps to NM_002644.3 C503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:26890502 C>T maps to NM_033198.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr17:26887159 A>G maps to NM_033198.3 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:44052991 G>A maps to NM_015937.4 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr20:44054402 A>C maps to NM_015937.4 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:44045257 C>A maps to NM_015937.4 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:33222464 G>T maps to NM_080476.4 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr20:33169391 G>T maps to NM_080476.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:27121712 C>T maps to NM_017837.2 C396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:27121241 C>T maps to NM_017837.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:27121256 G>A maps to NM_017837.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:27121256 G>A maps to NM_017837.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr1:27120800 C>T maps to NM_017837.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:27120707 C>T maps to NM_017837.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr17:34893147 T>C maps to NM_178517.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr17:34893858 C>T maps to NM_178517.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:89443160 C>A maps to NM_032906.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:196678887 T>C maps to NM_025163.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr19:49952834 G>A maps to NM_017916.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:49950637 G>A maps to NM_017916.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:111941987 A>G maps to NM_138789.3 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:98380243 C>T maps to NM_152309.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr10:98369595 G>A maps to NM_152309.2 H681H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr10:98412535 C>A maps to NM_152309.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:98355384 C>T maps to NM_152309.2 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:98469552 G>A maps to NM_152309.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:98380134 G>A maps to NM_152309.2 R639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:98408568 C>T maps to NM_152309.2 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:98469504 G>T maps to NM_152309.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:17135985 T>C maps to NM_002645.2 R1081R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:17124219 G>A maps to NM_002645.2 G1280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:17126786 C>A maps to NM_002645.2 G1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:204429047 G>A maps to NM_002646.3 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:204401507 G>A maps to NM_002646.3 G1325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:204415136 C>T maps to NM_002646.3 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:204412577 C>T maps to NM_002646.3 Q1005Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:204393980 C>T maps to NM_002646.3 *1635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr1:204393979 T>C maps to NM_002646.3 *1635W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr1:204393979 T>C maps to NM_002646.3 *1635W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:18552754 A>G maps to NM_004570.4 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:18650659 T>C maps to NM_004570.4 C957C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr12:18800926 G>T maps to NM_004570.4 E1435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:18800944 G>T maps to NM_004570.4 G1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:18435081 G>T maps to NM_004570.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:18443803 T>G maps to NM_004570.4 Y259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:18446935 G>T maps to NM_004570.4 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:18715693 A>G maps to NM_004570.4 T1175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:18439782 A>G maps to NM_004570.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:18443908 T>C maps to NM_004570.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr12:18573883 T>C maps to NM_004570.4 D734D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:18446935 G>T maps to NM_004570.4 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr12:18443908 T>C maps to NM_004570.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr12:18435299 A>G maps to NM_004570.4 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr12:18443908 T>C maps to NM_004570.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr12:18573883 T>C maps to NM_004570.4 D734D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:39647365 C>T maps to ENST00000398870 F847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:39637994 G>A maps to ENST00000398870 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr18:39576651 T>C maps to ENST00000398870 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr3:178917643 T>C maps to NM_006218.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:178922364 T>C maps to NM_006218.2 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:178927975 A>G maps to NM_006218.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:178951888 G>T maps to NM_006218.2 E982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr3:178951980 A>G maps to NM_006218.2 E1012E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:178951905 T>C maps to NM_006218.2 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr3:178936071 T>C maps to NM_006218.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr3:178927981 T>C maps to NM_006218.2 C420C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr3:178936074 T>C maps to NM_006218.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:178927975 A>G maps to NM_006218.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:178951909 C>T maps to NM_006218.2 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:178951969 G>T maps to NM_006218.2 G1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:178936074 T>C maps to NM_006218.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:178936096 G>T maps to NM_006218.2 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr3:178952037 T>C maps to NM_006218.2 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr3:178916948 C>T maps to NM_006218.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr3:178951968 T>C maps to NM_006218.2 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:178947851 C>T maps to NM_006218.2 F909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:178951911 A>G maps to NM_006218.2 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:178916837 A>G maps to NM_006218.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:178921489 A>T maps to NM_006218.2 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:178948092 T>G maps to NM_006218.2 V955V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr3:178936074 T>C maps to NM_006218.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr3:178952067 A>G maps to NM_006218.2 K1041K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr3:178951989 T>C maps to NM_006218.2 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr3:178951968 T>C maps to NM_006218.2 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr3:178919180 T>C maps to NM_006218.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:178916924 A>G maps to NM_006218.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:178952091 T>C maps to NM_006218.2 G1049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:178952058 T>C maps to NM_006218.2 Y1038Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:178952130 T>A maps to NM_006218.2 I1062I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:178916853 G>T maps to NM_006218.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:178947827 T>C maps to NM_006218.2 C901C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr3:178936116 T>C maps to NM_006218.2 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:178917643 T>G maps to NM_006218.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:178936074 T>C maps to NM_006218.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:178936074 T>C maps to NM_006218.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:178916726 T>C maps to NM_006218.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:178938935 A>G maps to NM_006218.2 E726E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:178951980 A>G maps to NM_006218.2 E1012E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr3:178937807 A>G maps to NM_006218.2 Q661Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr3:178927981 T>C maps to NM_006218.2 C420C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr3:178952100 A>G maps to NM_006218.2 T1052T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr3:178916792 A>G maps to NM_006218.2 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr3:178927975 A>G maps to NM_006218.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:178938860 C>T maps to NM_006218.2 H701H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr3:178922325 A>G maps to NM_006218.2 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr3:178951980 A>G maps to NM_006218.2 E1012E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr3:178952044 G>T maps to NM_006218.2 E1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr3:178917496 A>G maps to NM_006218.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr3:178952082 A>G maps to NM_006218.2 A1046A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr3:178952151 A>G maps to NM_006218.2 *1069W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:178921543 C>A maps to NM_006218.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:178927981 T>C maps to NM_006218.2 C420C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:178951980 A>G maps to NM_006218.2 E1012E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr3:178936071 T>C maps to NM_006218.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr3:178916942 A>G maps to NM_006218.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr3:178921549 G>A maps to NM_006218.2 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr3:178952130 T>A maps to NM_006218.2 I1062I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:178952049 T>C maps to NM_006218.2 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:178916924 A>G maps to NM_006218.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:178916948 C>A maps to NM_006218.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:178937393 A>G maps to NM_006218.2 K594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr3:178916936 T>C maps to NM_006218.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr3:178917643 T>C maps to NM_006218.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr3:178922364 T>C maps to NM_006218.2 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr3:178927975 A>G maps to NM_006218.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr3:178952061 C>T maps to NM_006218.2 F1039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr3:178952004 A>G maps to NM_006218.2 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr3:178952058 T>C maps to NM_006218.2 Y1038Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr3:178952058 T>C maps to NM_006218.2 Y1038Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr3:178951911 A>G maps to NM_006218.2 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr3:178951977 A>G maps to NM_006218.2 P1011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr3:178936056 A>G maps to NM_006218.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr3:178928080 A>G maps to NM_006218.2 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr3:178936071 T>C maps to NM_006218.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr3:178937753 A>G maps to NM_006218.2 Q643Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr3:178917478 T>C maps to NM_006218.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr3:178951980 A>G maps to NM_006218.2 E1012E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr3:178937751 C>T maps to NM_006218.2 Q643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr3:178952049 T>C maps to NM_006218.2 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr3:178928068 T>C maps to NM_006218.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr3:178916792 A>G maps to NM_006218.2 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:178936017 C>T maps to NM_006218.2 D520D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr3:178916729 G>A maps to NM_006218.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr3:178952067 A>G maps to NM_006218.2 K1041K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:178917604 T>C maps to NM_006218.2 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:178922322 A>G maps to NM_006218.2 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:178936023 A>G maps to NM_006218.2 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr3:178928072 G>T maps to NM_006218.2 G451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr3:178951977 A>G maps to NM_006218.2 P1011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:178951989 T>C maps to NM_006218.2 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:178952061 C>T maps to NM_006218.2 F1039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:178947827 T>A maps to NM_006218.2 C901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr3:178951971 A>G maps to NM_006218.2 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr3:178952011 C>T maps to NM_006218.2 R1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr3:178927975 A>G maps to NM_006218.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr3:178928092 C>T maps to NM_006218.2 N457N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr3:178951977 A>G maps to NM_006218.2 P1011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr3:178936074 T>C maps to NM_006218.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr3:178927975 A>G maps to NM_006218.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:178922322 A>G maps to NM_006218.2 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:178927975 A>G maps to NM_006218.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr3:178951911 A>G maps to NM_006218.2 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr3:178952096 G>A maps to NM_006218.2 W1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr3:178951995 T>C maps to NM_006218.2 D1017D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr3:178936116 T>C maps to NM_006218.2 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr3:178951911 A>G maps to NM_006218.2 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr3:178936081 G>T maps to NM_006218.2 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr3:178916876 A>G maps to NM_006218.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr3:178951965 C>A maps to NM_006218.2 G1007G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr3:178951995 T>C maps to NM_006218.2 D1017D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:178952139 T>C maps to NM_006218.2 H1065H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:178928080 A>G maps to NM_006218.2 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:178936074 T>C maps to NM_006218.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:178951968 T>C maps to NM_006218.2 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr3:178952085 T>C maps to NM_006218.2 H1047H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:178952022 A>G maps to NM_006218.2 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr3:178952049 T>C maps to NM_006218.2 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr3:178952124 C>T maps to NM_006218.2 H1060H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:178922364 T>C maps to NM_006218.2 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:178951890 G>A maps to NM_006218.2 E982E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:178917643 T>C maps to NM_006218.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr3:178928226 A>G maps to NM_006218.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:178917496 A>G maps to NM_006218.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:178936023 A>G maps to NM_006218.2 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:178936068 A>G maps to NM_006218.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr3:138409963 A>G maps to NM_006219.1 Y638Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:9775729 C>T maps to ENST00000361110 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:9780915 A>G maps to ENST00000361110 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr1:9770518 C>T maps to ENST00000361110 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr1:9770518 C>T maps to ENST00000361110 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr7:106508629 G>A maps to NM_002649.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:106509676 G>A maps to NM_002649.2 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:106523499 C>T maps to NM_002649.2 D884D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:106508854 C>T maps to NM_002649.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:106508497 C>T maps to NM_002649.2 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:106509478 A>G maps to NM_002649.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr7:106509340 C>A maps to NM_002649.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:106509947 C>T maps to NM_002649.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr7:106508092 G>A maps to NM_002649.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:106509536 G>T maps to NM_002649.2 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr7:106520025 C>T maps to NM_002649.2 A818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr7:106508821 G>A maps to NM_002649.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr7:106545830 A>C maps to NM_002649.2 *1103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:106545828 C>T maps to NM_002649.2 A1102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr7:106509010 C>T maps to NM_002649.2 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr7:106508791 C>T maps to NM_002649.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr7:106508854 C>T maps to NM_002649.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr22:31679234 A>G maps to NM_052880.4 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr5:67589663 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:67522656 G>T maps to ENST00000396611 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:67576437 G>A maps to ENST00000396611 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:67588129 C>T maps to ENST00000396611 N320N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:67589617 C>T maps to ENST00000396611 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:67576820 A>G maps to ENST00000396611 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:67589619 A>G maps to ENST00000396611 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:67522656 G>T maps to ENST00000396611 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:67588186 G>A maps to ENST00000396611 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:67589613 A>G maps to ENST00000396611 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr5:67591086 C>T maps to ENST00000396611 D560D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:67591098 C>T maps to ENST00000396611 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr5:67589619 A>G maps to ENST00000396611 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr5:67592109 A>G maps to ENST00000396611 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr5:67591128 A>G maps to ENST00000396611 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr5:67589633 T>G maps to ENST00000396611 L466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:67589663 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr5:67588950 C>A maps to ENST00000396611 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr5:67590420 G>T maps to ENST00000396611 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:67591245 A>G did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:18273018 G>A maps to NM_005027.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr19:18271373 G>A did not map to a codon.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr1:46509494 G>T maps to NM_001114172.1 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:46509356 C>T maps to NM_001114172.1 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:130398194 A>G maps to NM_014602.2 T1347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr3:130463543 A>G maps to NM_014602.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:130435308 A>G maps to NM_014602.2 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:130425800 A>C maps to NM_014602.2 T904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:130452911 C>T maps to NM_014602.2 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr3:130447403 A>T maps to NM_014602.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:130447355 A>G maps to NM_014602.2 N586N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr3:130424528 T>A maps to NM_014602.2 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:130463543 A>G maps to NM_014602.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr3:130442411 G>A maps to NM_014602.2 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:8808157 A>G maps to NM_001142633.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:8784027 C>T maps to NM_001142633.1 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:8796940 C>T maps to NM_001142633.1 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:8791963 G>A maps to NM_001142633.1 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:8738736 C>T maps to NM_001010855.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:8740141 G>A maps to NM_001010855.2 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr17:8736311 G>A maps to NM_001010855.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:8741907 G>A maps to NM_001010855.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:209165749 G>A maps to NM_015040.3 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:209218726 C>T maps to NM_015040.3 R1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:209216127 C>T maps to NM_015040.3 L1888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:209190264 C>A maps to NM_015040.3 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:209195375 G>A maps to NM_015040.3 Q1307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:209179084 T>C maps to NM_015040.3 H588H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:209218726 C>T maps to NM_015040.3 R1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:209190375 G>A maps to NM_015040.3 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:209191041 T>C maps to NM_015040.3 P1169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:209219350 G>T maps to NM_015040.3 G2055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr2:209163421 A>G maps to NM_015040.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr2:209218728 A>G maps to NM_015040.3 R1984R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:209190291 T>C maps to NM_015040.3 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:209167031 C>T maps to NM_015040.3 H425H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr2:209138356 G>A maps to NM_015040.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr2:209216085 T>C maps to NM_015040.3 F1874F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:99971859 G>A maps to NM_013439.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:99956478 C>T maps to ENST00000413850 H182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:99964981 G>A maps to ENST00000413850 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr6:37141785 T>C maps to ENST00000373507 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:37140889 C>T maps to ENST00000373507 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:48772310 T>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr22:50356457 G>A maps to NM_001001852.3 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:71416723 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:71401606 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:71401613 C>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:20964360 G>A maps to NM_032409.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:10692282 G>T maps to ENST00000354846 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr8:10689193 G>A maps to ENST00000354846 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:10623186 C>T maps to NM_017884.4 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr8:10623132 C>T maps to NM_017884.4 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:76990177 C>G maps to NM_017439.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:77010630 T>C maps to NM_017439.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:76991951 C>T maps to NM_017439.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:76984730 A>G maps to NM_017439.3 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:76955546 C>T maps to NM_017439.3 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:76991933 T>C maps to NM_017439.3 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr7:76991933 T>C maps to NM_017439.3 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:142832313 C>T maps to NM_002652.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:142836629 C>T maps to NM_002652.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:142836253 A>G maps to NM_002652.2 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr10:22830871 C>T maps to NM_005028.4 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:22828899 G>A maps to NM_005028.4 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:23003180 C>T maps to NM_005028.4 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:22830772 G>A maps to NM_005028.4 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:36936824 A>G maps to NM_003559.4 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:36934041 C>T maps to NM_003559.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr17:36927474 G>A maps to NM_003559.4 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:36927504 G>T maps to NM_003559.4 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:57987836 G>A maps to NM_024779.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:151210669 C>A maps to NM_001135638.1 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr1:151205166 A>G maps to NM_001135638.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:71509352 C>T maps to NM_003558.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:3651849 G>A maps to NM_012398.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr9:130684332 G>T maps to NM_001135219.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:130684340 G>A maps to NM_001135219.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr17:27380439 C>T maps to NM_016518.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr17:27371894 C>T maps to NM_016518.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr17:27380495 G>T maps to NM_016518.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:15415585 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:15403214 C>A did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:15497902 T>C did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr22:32017781 C>T maps to ENST00000422296 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:32017667 C>T maps to ENST00000422296 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:1451626 G>A maps to ENST00000313486 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:28306974 C>T maps to NM_012399.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:28254425 C>T maps to NM_012399.3 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:28292578 G>A maps to NM_012399.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr22:28292560 T>C maps to NM_012399.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:28306974 C>T maps to NM_012399.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr17:65529042 C>T maps to NM_012417.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:67260979 C>T maps to NM_004910.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:67266197 C>T maps to NM_004910.2 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:67265774 G>A maps to NM_004910.2 H501H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:67269790 G>A maps to NM_004910.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:123498508 G>A maps to NM_020845.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:123474409 G>C maps to NM_020845.2 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:123497160 G>A maps to NM_020845.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:123480120 G>A maps to NM_020845.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:123474376 G>A maps to NM_020845.2 G896G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:123489799 C>T maps to NM_020845.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:123471093 G>A maps to NM_020845.2 H1205H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:6382037 G>A maps to NM_031220.3 H202H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:6428679 A>G maps to NM_031220.3 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:6387057 C>T maps to NM_031220.3 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:3189406 A>G maps to ENST00000380989 D758D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:3212379 C>T maps to ENST00000380989 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:3182951 G>A maps to ENST00000380989 R901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:3202074 T>C maps to ENST00000380989 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr10:3193507 G>A maps to ENST00000380989 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:3182922 G>A maps to ENST00000380989 G910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:111553634 G>A maps to NM_153426.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr4:111553531 T>A maps to NM_153426.1 K51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:111543538 G>T maps to NM_000325.5 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:103991527 A>G maps to NM_005029.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:103991515 G>A maps to NM_005029.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:130847611 C>T maps to NM_004764.4 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:130831095 G>A maps to NM_004764.4 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:130839527 C>T maps to NM_004764.4 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:130830410 G>T maps to NM_004764.4 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:130845840 G>A maps to NM_004764.4 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr12:130845925 G>A did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr12:130827214 G>A did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr12:130833913 C>T maps to NM_004764.4 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:130855801 C>T maps to NM_004764.4 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr12:130834472 C>T maps to NM_004764.4 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:22163438 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr8:22173834 A>G maps to NM_001135721.1 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr8:22173774 C>T maps to NM_001135721.1 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:22173828 C>T maps to NM_001135721.1 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:22211846 C>A maps to NM_001135721.1 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr8:22162368 T>C maps to NM_001135721.1 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr22:25144891 G>A maps to NM_001008496.2 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:25145392 C>A maps to NM_001008496.2 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:25120969 C>T maps to NM_001008496.2 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:25124335 A>G maps to NM_001008496.2 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr22:25145446 C>A maps to NM_001008496.2 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:25120972 T>C maps to NM_001008496.2 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr22:25150089 G>T maps to NM_001008496.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:94340780 C>T maps to NM_152431.2 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:94328517 T>G maps to NM_152431.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr23:68382323 T>C did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:68381406 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:68382109 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:68381405 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:68382053 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:68382386 C>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:68382314 A>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:108714626 G>A maps to NM_014819.4 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:108714955 C>T did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr5:108717297 T>C maps to NM_014819.4 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:2161153 G>A maps to NM_001009944.2 T1338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:2153666 G>A maps to NM_001009944.2 G2797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:2153672 G>A maps to NM_001009944.2 C2795C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:2161759 G>A maps to NM_001009944.2 G1136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:2147398 C>T maps to NM_001009944.2 A3442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:2156272 G>A maps to NM_001009944.2 L2508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr16:2160502 T>G maps to NM_001009944.2 A1555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:2158573 C>T maps to NM_001009944.2 P2198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:2161105 C>T maps to NM_001009944.2 T1354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:2143883 G>A maps to NM_001009944.2 G3583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:47840390 T>C maps to NM_138295.3 T2683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr7:47884660 C>T maps to NM_138295.3 A1723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:47894616 C>T maps to NM_138295.3 T1574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr7:47849109 G>A maps to NM_138295.3 G2549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:47886664 G>T maps to NM_138295.3 A1655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:47854976 G>T maps to NM_138295.3 G2348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:47835622 T>C maps to NM_138295.3 T2773T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr7:47872769 G>T maps to NM_138295.3 A2085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:47897217 G>A maps to NM_138295.3 S1525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:47842891 G>A maps to NM_138295.3 C2626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:47898366 G>A maps to NM_138295.3 L1422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:47925608 G>A maps to NM_138295.3 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:47945458 A>G maps to NM_138295.3 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:47930195 G>A maps to NM_138295.3 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:47892815 C>T maps to NM_138295.3 E1623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr7:47944081 C>T maps to NM_138295.3 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr7:47874628 C>T maps to NM_138295.3 P2021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr7:47842891 G>A maps to NM_138295.3 C2626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:81232564 C>T maps to NM_052892.3 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:81213273 C>A maps to NM_052892.3 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:81150977 C>T maps to NM_052892.3 E2256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:81253840 G>A maps to NM_052892.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:81190481 G>A maps to NM_052892.3 D1369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr16:81145824 G>A maps to NM_052892.3 G2308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:81232552 G>A maps to NM_052892.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:81194438 C>T maps to NM_052892.3 L1183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:81164208 G>A maps to NM_052892.3 Y1966Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:81236191 G>A maps to NM_052892.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:88989097 C>T maps to NM_000297.2 R803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr4:88989097 C>T maps to NM_000297.2 R803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr4:88996074 G>A maps to NM_000297.2 R878R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:88959428 G>A maps to NM_000297.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr10:102056748 C>T maps to NM_016112.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr10:102056750 G>A maps to NM_016112.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:102050167 C>A maps to NM_016112.2 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:102058488 G>A maps to NM_016112.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:102054769 G>A maps to NM_016112.2 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:102051057 C>T maps to NM_016112.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:102052784 C>T maps to NM_016112.2 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:102051057 C>T maps to NM_016112.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:102050210 C>T maps to NM_016112.2 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:137244496 C>A maps to ENST00000230643 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr22:46656102 G>A maps to NM_006071.1 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr22:46657212 A>G maps to NM_006071.1 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:46658366 T>G maps to NM_006071.1 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr22:46658493 G>A maps to NM_006071.1 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr22:46655628 G>A maps to NM_006071.1 Y1197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:46656824 G>A maps to NM_006071.1 R799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:46654848 C>T maps to NM_006071.1 A1457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:46656804 G>A maps to NM_006071.1 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr22:46654626 C>A maps to NM_006071.1 P1531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:46655469 G>T maps to NM_006071.1 V1250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr22:46657413 A>G maps to NM_006071.1 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr22:46653645 A>G maps to NM_006071.1 Y1858Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr6:51712675 A>G maps to NM_138694.3 C2668C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:51930828 T>C maps to NM_138694.3 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:51640663 G>A maps to NM_138694.3 A2832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:51524600 A>G maps to NM_138694.3 F3441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:51612633 C>T maps to NM_138694.3 W3260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:51732830 T>C maps to NM_138694.3 A2521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:51524672 G>A maps to NM_138694.3 S3417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:51882350 A>G maps to NM_138694.3 C1819C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr6:51613094 G>A maps to NM_138694.3 R3107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:51524752 C>A maps to NM_138694.3 E3391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:51611556 T>C maps to NM_138694.3 K3320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:51929756 C>T maps to NM_138694.3 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr6:51890746 C>T maps to NM_138694.3 V1287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr6:51512898 G>T maps to NM_138694.3 S3776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:51947260 G>T maps to NM_138694.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:51732830 T>C maps to NM_138694.3 A2521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:51720864 C>T maps to NM_138694.3 A2579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:51732697 C>A maps to NM_138694.3 G2566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:51889504 A>G maps to NM_138694.3 V1701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:51586807 C>T maps to NM_170724.2 E3389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:51732830 T>C maps to NM_138694.3 A2521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:51890701 T>C maps to NM_138694.3 V1302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:51909808 T>C maps to NM_138694.3 G890G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr6:51732830 T>C maps to NM_138694.3 A2521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:51497504 A>G maps to NM_138694.3 A3841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:51890343 G>T maps to NM_138694.3 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:51920408 G>T maps to NM_138694.3 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr6:51890437 C>A maps to NM_138694.3 R1390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:51619696 G>A maps to NM_138694.3 D2894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:51889737 G>T maps to NM_138694.3 R1624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:51889737 G>T maps to NM_138694.3 R1624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr6:51889737 G>T maps to NM_138694.3 R1624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:51612933 A>G maps to NM_138694.3 H3160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:110477370 G>A maps to ENST00000426474 W2770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:110502179 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr8:110408274 T>G maps to ENST00000426474 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr8:110471910 C>A maps to ENST00000426474 Y2364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:110447458 A>G maps to ENST00000426474 G1127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr8:110431379 G>A maps to ENST00000426474 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr8:110498940 G>A maps to ENST00000426474 L3257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:110503206 G>T maps to ENST00000426474 E3331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:110520467 C>T maps to ENST00000426474 G3791G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr8:110477190 C>T maps to ENST00000426474 V2710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:110408290 C>T maps to ENST00000426474 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:110416852 C>T maps to ENST00000426474 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:110447417 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:110539070 T>G maps to ENST00000426474 T4182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr8:110394690 G>A did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr8:110474073 C>T maps to ENST00000426474 C2440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:110457743 C>T maps to ENST00000426474 C1882C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:110420435 G>T did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr8:110534995 G>A maps to ENST00000426474 R4070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr8:110457125 C>T maps to ENST00000426474 S1676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr8:79510669 A>T maps to NM_181839.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr8:79510669 A>G maps to NM_181839.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr6:123039058 C>T maps to ENST00000368446 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr6:123038956 A>C maps to ENST00000368446 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr20:43243235 C>A maps to NM_181805.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:155263246 C>T maps to ENST00000423816 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:155265308 T>C maps to ENST00000423816 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr1:155263258 G>A maps to ENST00000423816 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:155265484 G>A maps to ENST00000423816 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:155264937 G>A maps to ENST00000423816 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:72509839 G>A maps to ENST00000419739 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:72502011 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:72511381 G>A maps to ENST00000419739 H93H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:14582526 C>T maps to NM_213560.1 D926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:14574646 G>A maps to NM_213560.1 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:14574646 G>A maps to NM_213560.1 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:89299049 T>G maps to NM_006256.2 T958T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr1:89273247 C>T maps to NM_006256.2 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:89299056 C>T maps to NM_006256.2 R961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:131482722 G>A maps to NM_013355.3 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:131482103 T>C maps to NM_013355.3 G755G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr9:131477727 C>T maps to NM_013355.3 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr9:131481968 C>T maps to NM_013355.3 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:44430204 T>C maps to NM_004571.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:44450174 C>T maps to NM_004571.3 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr11:125237799 C>A maps to NM_022062.2 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr11:125267927 C>A maps to NM_022062.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:201294926 C>T maps to NM_000299.3 D710D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:201286872 A>G maps to NM_000299.3 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:201286875 C>T maps to NM_000299.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr12:33031216 G>T maps to NM_004572.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:32977083 A>G maps to NM_004572.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:33030994 C>T maps to NM_004572.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr12:32949047 G>A maps to NM_004572.3 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr12:33021893 G>A maps to NM_004572.3 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr11:403706 G>A maps to NM_007183.2 Q671Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:159530236 A>G maps to NM_003628.3 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:159519840 C>T maps to NM_003628.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:159526421 C>T maps to NM_003628.3 G973G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:159481877 C>T maps to NM_003628.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:159433883 C>T maps to NM_003628.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:159514663 C>A maps to NM_003628.3 S644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:159490705 G>T maps to NM_003628.3 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr2:159517859 G>T maps to NM_003628.3 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:159519827 A>G maps to NM_003628.3 K816K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:159517859 G>T maps to NM_003628.3 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:119334937 C>T maps to NM_015900.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:119336939 C>T maps to NM_015900.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr3:119348263 C>T maps to NM_015900.2 N440N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr3:119343986 G>A maps to NM_015900.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr10:74714398 C>A maps to NM_032562.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr16:68293130 G>A maps to NM_012320.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr1:20501549 G>A maps to NM_001105572.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:20501585 C>T maps to NM_001105572.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:20246898 C>T maps to NM_014589.1 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:20246841 A>G maps to NM_014589.1 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:20470045 C>T maps to NM_022819.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:20469990 C>T maps to NM_022819.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:20471081 C>T maps to NM_022819.3 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr22:31536148 C>T maps to NM_015715.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr1:186925232 G>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:186901917 T>C maps to NM_024420.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:186946808 C>T maps to NM_024420.2 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr19:48607852 T>G maps to NM_003706.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:48578123 G>A maps to NM_003706.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr19:48551632 C>T maps to NM_003706.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr19:48551632 C>T maps to NM_003706.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:42278089 G>A maps to NM_001080490.1 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr15:42294860 G>A maps to NM_001080490.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:42280306 G>A maps to NM_001080490.1 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:42442838 G>A maps to ENST00000397272 H246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:38512100 C>T maps to NM_003560.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr22:38509551 C>T maps to NM_003560.2 W715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:160806287 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:160876667 C>T maps to NM_007366.4 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:160843840 T>C maps to NM_007366.4 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr2:160804043 A>G maps to NM_007366.4 L1246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:160843828 T>G maps to NM_007366.4 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:160840520 C>A maps to NM_007366.4 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:160833793 C>T did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:160813087 C>T maps to NM_007366.4 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:26905910 A>C maps to NM_001031689.2 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr9:26913895 G>A maps to NM_001031689.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:26926409 G>T maps to NM_001031689.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr23:133700504 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:133700529 G>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:133700349 G>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr11:59812238 C>T maps to NM_173801.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr4:84026173 C>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:145465116 G>A maps to NM_001029869.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:145483829 A>G maps to NM_001029869.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr8:57079488 T>C maps to NM_002655.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:57079935 G>A maps to NM_002655.2 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:57079944 C>T maps to NM_002655.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr8:57079500 C>T maps to NM_002655.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr8:57080585 C>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:30784812 T>C maps to NM_002657.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:42038126 G>A maps to NM_000930.3 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr8:42038189 C>A maps to NM_000930.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:42038120 C>T maps to NM_000930.3 W324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:42037581 G>A maps to NM_000930.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:42045469 G>A maps to NM_000930.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr8:42038189 C>A maps to NM_000930.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:75672057 C>T maps to NM_002658.3 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:75673382 G>T maps to NM_002658.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr10:75673800 G>A maps to NM_002658.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:75672057 C>T maps to NM_002658.3 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:75673513 C>T maps to NM_002658.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr19:44156386 G>T maps to NM_002659.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:44160745 G>T maps to NM_002659.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:28805312 C>T maps to NM_153021.4 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:28812543 A>G maps to NM_153021.4 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:28755048 C>A maps to NM_153021.4 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:28855866 C>T maps to NM_153021.4 R1353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:28764629 C>T maps to NM_153021.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:28802540 C>T maps to NM_153021.4 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:28805312 C>T maps to NM_153021.4 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:28808636 T>C maps to NM_153021.4 C581C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:28762030 C>T maps to NM_153021.4 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:28828751 A>G maps to NM_153021.4 P998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:14706284 T>C maps to NM_024829.5 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr12:113825635 C>T maps to NM_173542.3 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr12:113823016 C>T maps to NM_173542.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr20:8696934 G>A maps to NM_015192.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:8755221 G>T maps to NM_015192.2 T989T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr20:8639247 G>A maps to NM_015192.2 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr20:8745795 A>G maps to NM_015192.2 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr20:8713903 T>C maps to NM_015192.2 N636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr20:8705304 G>T maps to NM_015192.2 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr20:8717739 T>C maps to NM_015192.2 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:8698361 T>A maps to NM_015192.2 Y460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:40591068 C>T maps to NM_004573.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:40590555 C>T maps to NM_004573.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr15:40586535 C>T maps to NM_004573.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:40588557 C>T maps to NM_004573.2 E545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:40581113 C>T maps to NM_004573.2 Q1120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr15:40582996 C>T maps to NM_004573.2 A1026A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:40588569 C>T maps to NM_004573.2 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr15:40591420 G>A maps to NM_004573.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr15:40591420 G>A maps to NM_004573.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr15:40590102 G>A maps to NM_004573.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:40582785 G>A maps to NM_004573.2 A1067A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr11:64032810 C>T maps to NM_000932.2 R958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:64024129 C>T maps to NM_000932.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:64029897 C>T maps to NM_000932.2 N686N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:64026056 C>A maps to NM_000932.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:64029468 C>T maps to NM_000932.2 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr11:64034910 G>A maps to NM_000932.2 P1196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr11:64030130 C>T maps to NM_000932.2 Q736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr20:9371201 C>T maps to NM_001172646.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:9438094 G>T maps to NM_001172646.1 E1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:38050062 G>A maps to NM_001130964.1 N617N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:38050805 C>T maps to NM_001130964.1 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:43190016 C>T maps to NM_133373.3 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:219498440 A>G maps to ENST00000432688 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:96014737 C>T maps to ENST00000371380 A1162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:96018577 G>A maps to ENST00000371380 W1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:95892085 C>T maps to ENST00000371380 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:95791064 G>T maps to ENST00000371380 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:96025669 G>A maps to ENST00000371380 T1412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:95791948 G>A maps to ENST00000371380 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:96005757 G>T maps to ENST00000371380 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:96058274 T>C maps to ENST00000371380 C1769C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:95791612 T>C maps to ENST00000371380 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr10:95791030 G>A maps to ENST00000371380 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr20:39791857 G>A maps to NM_002660.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr20:39801223 C>T maps to NM_002660.2 Y1023Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:39802798 G>A maps to NM_002660.2 T1227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:39792605 C>A maps to NM_002660.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:39795226 C>T maps to NM_002660.2 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr20:39801405 G>A maps to NM_002660.2 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:39797438 C>T maps to NM_002660.2 A804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr20:39793964 T>C maps to NM_002660.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr20:39792437 T>C maps to NM_002660.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr16:81969921 C>T maps to NM_002661.2 Y997Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr16:81902828 C>T maps to NM_002661.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:81968077 C>T maps to NM_002661.2 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:81990341 A>C maps to NM_002661.2 R1205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:81902828 C>T maps to NM_002661.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:81944262 C>T maps to NM_002661.2 C624C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:155198846 G>A maps to ENST00000340059 H1664H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:155200505 A>G maps to ENST00000340059 G1111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:155199254 G>A maps to ENST00000340059 G1528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:155200757 G>A maps to ENST00000340059 S1027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:155282899 C>T maps to ENST00000340059 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:155200025 C>T maps to ENST00000340059 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:155282899 C>T maps to ENST00000340059 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:155241748 C>T maps to ENST00000340059 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:2418633 C>T maps to NM_014638.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:198948798 G>A maps to NM_006226.3 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:198950749 G>T maps to NM_006226.3 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:198949572 C>T maps to NM_006226.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:198949386 G>A maps to NM_006226.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:198949563 C>T maps to NM_006226.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:198950754 C>T maps to NM_006226.3 H838H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:198949645 C>T maps to NM_006226.3 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:198953767 C>T maps to NM_006226.3 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:198948720 T>C maps to NM_006226.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:198948810 T>C maps to NM_006226.3 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:198950700 G>A maps to NM_006226.3 Q820Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:198950031 C>T maps to NM_006226.3 Y597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr2:199011536 G>T maps to NM_006226.3 E1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr3:17052313 T>C maps to NM_001144382.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr3:17051488 G>A maps to NM_001144382.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr3:17051284 C>T maps to NM_001144382.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:17053468 C>T maps to NM_001144382.1 H873H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:17052745 G>A maps to NM_001144382.1 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:17052409 C>A maps to NM_001144382.1 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:17053453 T>C maps to NM_001144382.1 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr23:205422 T>G did not map to a codon.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr3:111426851 C>T maps to ENST00000312791 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:111564707 A>C maps to NM_153268.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr5:41382360 C>A maps to NM_001005473.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:41382160 G>T maps to NM_001005473.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr5:41382430 G>T maps to NM_001005473.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:41382519 G>T maps to NM_001005473.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr5:41313736 T>C maps to NM_001005473.2 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:18841082 C>A maps to ENST00000266505 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:18876251 G>A maps to ENST00000266505 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr12:18876436 C>A maps to ENST00000266505 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:18837162 C>A maps to ENST00000266505 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr12:18836223 A>G maps to ENST00000266505 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:171395395 G>A maps to NM_002662.3 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:171431714 C>T maps to NM_002662.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:171455801 G>A maps to NM_002662.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:171455715 G>A maps to NM_002662.3 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:171455387 C>T maps to NM_002662.3 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr3:171453333 T>G maps to NM_002662.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:171451242 A>G maps to NM_002662.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:4721851 C>A maps to NM_002663.3 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:4712400 C>T maps to NM_002663.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr19:40883709 C>T maps to NM_012268.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:40877593 C>T maps to NM_012268.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:105399138 G>A maps to NM_138790.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:242253344 T>C maps to NM_152666.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:242383292 T>G maps to NM_152666.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:242451789 T>C maps to NM_152666.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:242253176 T>A maps to NM_152666.2 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:242451723 C>T maps to NM_152666.2 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:242253158 T>C maps to NM_152666.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr1:242277235 G>A maps to NM_152666.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:242383412 G>A maps to NM_152666.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:242383367 C>A maps to NM_152666.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:242264039 T>C maps to NM_152666.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:242253161 G>A maps to NM_152666.2 N535N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr1:242264039 T>C maps to NM_152666.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:242264039 T>C maps to NM_152666.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:17106257 G>A maps to NM_178836.3 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:45895357 T>C maps to NM_012388.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:144997127 C>T maps to NM_201380.2 T2460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:144992884 G>A maps to NM_201380.2 Q3839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:145009241 G>A maps to NM_201380.2 Y391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:144995852 A>G maps to NM_201380.2 V2849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:144992561 G>A maps to NM_201380.2 I3946I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:144995513 G>A maps to NM_201380.2 P2962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:144993272 G>A maps to NM_201380.2 I3709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:144996422 G>A maps to NM_201380.2 D2659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr8:144994711 C>A maps to NM_201380.2 E3230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:145049519 A>G maps to NM_000445.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:145004701 G>A maps to NM_201380.2 D906D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr8:144997423 G>A maps to NM_201380.2 Q2362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:145007152 G>A maps to NM_201380.2 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr8:144994961 G>A maps to NM_201380.2 D3146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr8:144993272 G>A maps to NM_201380.2 I3709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:145006874 C>T maps to NM_201380.2 Q718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:68608010 C>T maps to NM_002664.2 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:68609716 G>T maps to NM_002664.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:124152794 C>T maps to NM_021622.4 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:179358717 T>G did not map to a codon.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr19:49363611 G>A maps to NM_020904.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:49362822 G>A maps to NM_020904.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr12:19427824 C>T maps to ENST00000429027 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:19427629 A>G maps to ENST00000429027 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr12:19422723 G>A maps to ENST00000429027 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr12:19511301 C>T maps to ENST00000429027 I1088I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:19475493 G>T maps to ENST00000429027 E781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr12:19518903 A>G maps to ENST00000429027 Q1200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr1:204192651 G>A maps to ENST00000367191 P1051P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr1:204217948 C>T maps to ENST00000367191 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr1:204197346 G>A maps to ENST00000367191 N985N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:204236636 G>A maps to ENST00000367191 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:204226531 G>T maps to ENST00000367191 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:204226500 G>A maps to ENST00000367191 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:16847989 C>T maps to ENST00000448080 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr11:16872785 G>A maps to ENST00000448080 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:16848055 G>A maps to ENST00000448080 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:16838490 A>G maps to ENST00000448080 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:16872755 G>A maps to ENST00000448080 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr12:45567092 G>A maps to ENST00000256692 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:45567851 C>T maps to ENST00000256692 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:45568090 C>A maps to ENST00000256692 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:73361655 G>A maps to NM_021200.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:131904258 T>A maps to ENST00000409158 Y202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:131904258 T>C maps to ENST00000409158 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:30164901 G>A maps to ENST00000436066 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr8:96166686 A>T maps to NM_024613.3 K139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr6:151140836 T>C maps to NM_001029884.1 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr6:151152742 C>T maps to NM_001029884.1 S832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr6:151152256 A>G maps to NM_001029884.1 K670K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:151152598 T>C maps to NM_001029884.1 F784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:39913544 G>A maps to NM_022835.2 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:39914970 C>T maps to NM_022835.2 G1066G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:39913400 C>T maps to NM_022835.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:39914099 C>T maps to NM_022835.2 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:39913899 G>T maps to NM_022835.2 E736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr19:39915252 C>A maps to NM_022835.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr19:39908600 A>G maps to NM_022835.2 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr19:39914135 G>A maps to NM_022835.2 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr19:39913400 C>A maps to NM_022835.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr16:67319276 C>T maps to NM_001129729.1 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr16:67320722 C>T maps to NM_001129729.1 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:67318905 C>T maps to NM_001129729.1 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr5:174193 G>A maps to NM_052909.3 R1105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:157001 G>A maps to NM_052909.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:163435 G>A maps to NM_052909.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr5:161983 C>T maps to NM_052909.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:155043 C>T maps to NM_052909.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:174142 G>A maps to NM_052909.3 S1088S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr5:156921 C>T maps to NM_052909.3 R439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr5:140562 C>T maps to NM_052909.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr5:182434 C>A maps to NM_052909.3 A1271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:163234 G>A maps to NM_052909.3 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:6556594 G>A maps to NM_198681.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:6528285 C>T maps to NM_198681.2 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:6529205 C>T maps to NM_198681.2 E792E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:6435607 G>A maps to NM_001144856.1 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr12:6426534 C>A maps to NM_001144856.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr12:93162792 C>T maps to NM_001004330.2 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:93147942 A>G maps to NM_001004330.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:43953500 C>T maps to NM_172069.3 R878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:43973006 T>C maps to NM_172069.3 I1186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:43958672 G>T maps to NM_172069.3 G959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:43937436 A>T maps to NM_172069.3 K728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:43971005 G>T maps to NM_172069.3 E1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:43921626 G>T maps to NM_172069.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr2:43939485 T>C maps to NM_172069.3 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:40822001 G>C maps to NM_024927.4 Y649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:40823034 G>A maps to NM_024927.4 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:40821935 C>T maps to NM_024927.4 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:43522954 C>T maps to NM_014798.2 A906A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr17:43552788 C>T maps to NM_014798.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:43531192 C>T maps to NM_014798.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:16053631 C>T maps to ENST00000420314 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:16053507 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:208811180 A>G maps to NM_001080475.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:208795844 T>C did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:908275 C>T maps to ENST00000379409 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:905685 A>G maps to ENST00000379409 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:150123205 T>C maps to ENST00000443480 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr1:150123229 C>G maps to ENST00000443480 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:161137790 C>A maps to NM_000301.3 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr6:161134080 C>T maps to NM_000301.3 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:161157917 G>A did not map to a codon.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr6:161143599 G>A did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr6:161155094 C>T maps to NM_000301.3 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr6:161152256 C>T maps to NM_000301.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:4852136 C>T maps to NM_005817.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:4512414 G>A maps to NM_001080400.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:4511574 C>G maps to NM_001080400.1 V785V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:4512660 G>A maps to NM_001080400.1 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:4510797 A>G maps to NM_001080400.1 S1044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr19:4511330 G>A maps to NM_001080400.1 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:4504887 G>A maps to NM_001080400.1 D1244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:4529878 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr16:23692346 C>T maps to NM_005030.3 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr16:23698842 C>T maps to NM_005030.3 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr16:23691500 C>T maps to NM_005030.3 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:23692346 C>T maps to NM_005030.3 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:23698842 C>T maps to NM_005030.3 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:23701326 T>C maps to NM_005030.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:23692316 C>T maps to NM_005030.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:21142688 C>T maps to NM_018474.4 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:21143503 C>T maps to NM_018474.4 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:21143059 G>A maps to NM_018474.4 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:57752401 C>A maps to NM_006622.2 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr5:57754913 G>A maps to NM_006622.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:45271008 G>A maps to NM_004073.2 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:45267415 C>T maps to NM_004073.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:45269604 T>C maps to NM_004073.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:128807142 C>T maps to NM_014264.4 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:128814699 A>C maps to NM_014264.4 I785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr4:128816106 G>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:128807019 T>C maps to NM_014264.4 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:128811162 A>G maps to NM_014264.4 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:128812290 G>A maps to NM_014264.4 K625K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:12016983 G>T maps to ENST00000376369 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:12018652 C>T maps to ENST00000376369 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:12032996 T>C maps to ENST00000376369 H704H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:145806450 A>G maps to NM_182943.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:145841965 G>A maps to NM_182943.2 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:100849570 G>A maps to NM_001084.4 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr7:100855810 G>A maps to NM_001084.4 N335N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:100859236 G>A maps to NM_001084.4 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:100860503 G>A maps to NM_001084.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr7:100856462 A>G maps to NM_001084.4 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr7:100853372 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:100853418 G>A maps to NM_001084.4 H546H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:103042881 T>C did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:103041610 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:103041611 G>A did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:103041612 G>T did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:103041611 G>T did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:103041612 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:103041544 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:49029590 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:49028406 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:49031024 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:49029508 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:155461790 C>T maps to NM_002669.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:142405142 T>C maps to NM_001172312.1 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr3:142405193 T>C maps to NM_001172312.1 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:142430383 A>C maps to NM_001172312.1 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:142408635 C>T maps to NM_001172312.1 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:142422793 G>T maps to NM_001172312.1 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:142396956 T>C did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:114880797 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:114871267 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:114877785 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:114879418 C>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:114871267 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:114863572 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr23:114863570 A>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:146243389 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:146322993 G>T maps to NM_001085420.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:44539854 G>A maps to NM_006227.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr20:31828116 G>A maps to NM_130852.2 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:31825963 T>C maps to NM_130852.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr20:31828047 C>T maps to NM_130852.2 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:31825972 G>T maps to NM_130852.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:37262188 C>T maps to NM_020405.4 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:37239767 G>A maps to NM_020405.4 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr10:20290767 C>T maps to NM_032812.7 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:20534331 C>T maps to NM_032812.7 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr10:20432305 C>T maps to NM_032812.7 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:20432299 C>T maps to NM_032812.7 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr10:20432305 C>T maps to NM_032812.7 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr10:20453401 T>A maps to NM_032812.7 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr10:20357163 C>A maps to NM_032812.7 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr10:20465932 C>T maps to NM_032812.7 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:126710378 C>T maps to NM_032242.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:126740972 C>T maps to NM_032242.3 L1362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:126707729 G>A maps to NM_032242.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:126707993 C>T maps to NM_032242.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:126708062 C>T maps to NM_032242.3 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:126733334 G>A maps to NM_032242.3 T873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:208383663 G>A maps to NM_025179.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:208252613 T>C maps to NM_025179.3 Q859Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:208212317 G>A maps to NM_025179.3 C1504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:208213106 G>A maps to NM_025179.3 C1453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:208219402 G>A maps to NM_025179.3 D1105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:153692405 C>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:153695474 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:153699468 G>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:153689699 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:153695785 T>C did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:153695018 G>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:153694763 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:153693479 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:153694399 G>A did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr23:153694823 A>G did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr23:153688773 G>A did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr23:153689840 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:153694062 G>A did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:153696707 C>T did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:153689487 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:153692832 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:153688562 G>A did not map to a codon.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr7:132192759 C>T maps to NM_020911.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr7:132192441 G>A maps to NM_020911.1 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr7:131895860 G>A maps to NM_020911.1 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:131866295 G>A maps to NM_020911.1 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr7:132192891 C>T maps to NM_020911.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr7:131833327 G>A maps to NM_020911.1 R1580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr7:131853118 G>A maps to NM_020911.1 A1410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:132192576 G>T maps to NM_020911.1 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:131866379 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:131866891 C>T maps to NM_020911.1 Q1072Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:131878901 C>T maps to NM_020911.1 Q925Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr7:131895902 C>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:132192312 C>T maps to NM_020911.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:48465621 C>T maps to NM_001130082.1 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:48462360 G>A maps to NM_001130082.1 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:48451133 G>C maps to NM_001130082.1 T1928T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:48465317 G>T maps to NM_001130082.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:48463099 G>A maps to NM_001130082.1 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr3:48456354 T>C maps to NM_001130082.1 E1354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:48461246 C>A maps to NM_001130082.1 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:50718979 C>T maps to NM_012401.2 T1371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:50728599 G>A maps to NM_012401.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:50719057 G>A maps to NM_012401.2 R1345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr22:50716088 G>A maps to NM_012401.2 D1709D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr22:50724511 C>A maps to NM_012401.2 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:50728404 G>A maps to NM_012401.2 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:153036049 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:153038805 C>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:153039915 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:153035338 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:153034414 G>T did not map to a codon.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr23:153043461 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:153037337 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:153035797 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:153036087 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:153041815 C>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:153043030 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:153032930 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:153042727 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:153032859 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:153035843 C>A did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:153042995 A>C did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:153043859 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:153033175 C>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:153040482 C>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:153032367 T>C did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:153035272 A>G did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:153041103 G>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:153041469 C>T did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:153035272 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:153043757 C>T did not map to a codon.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr12:94673352 G>T maps to NM_005761.1 E1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr12:94563056 C>T maps to NM_005761.1 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:94641680 C>A maps to NM_005761.1 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:94634368 T>G maps to NM_005761.1 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:94692457 A>G maps to NM_005761.1 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr12:94575220 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:94563011 C>A maps to NM_005761.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:129292539 G>A maps to NM_015103.2 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr3:129291750 T>C maps to NM_015103.2 P957P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:129275970 C>T maps to NM_015103.2 P1847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr3:129289974 G>A maps to NM_015103.2 L1170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:129275480 G>A maps to NM_015103.2 Y1880Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:129291732 G>A maps to NM_015103.2 T963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:129290351 C>T maps to NM_015103.2 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:129291459 C>T maps to NM_015103.2 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:129308229 C>T maps to NM_015103.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:129289673 C>T maps to NM_015103.2 S1235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:129284278 G>A maps to NM_015103.2 A1475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:129285408 G>T maps to NM_015103.2 S1384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr3:129304821 G>T maps to NM_015103.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:129292498 G>A maps to NM_015103.2 H925H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:129324774 G>A maps to NM_015103.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:205797786 G>A maps to NM_152491.4 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr1:205819056 G>A maps to NM_152491.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:205819185 G>A maps to NM_152491.4 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr6:89864488 A>T maps to NM_001010853.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr6:89858997 A>T maps to NM_001010853.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:56227531 T>C maps to NM_020182.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr20:56227420 G>A maps to NM_020182.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:156203489 A>G maps to NM_007221.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr16:72174373 C>T maps to NM_031293.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:72156820 G>A maps to NM_031293.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:72198796 C>A maps to NM_031293.2 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr15:74317243 C>T maps to NM_033238.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr15:74315195 G>T maps to NM_033238.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:74290415 G>A maps to NM_033238.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr15:74326825 C>T maps to NM_033238.2 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:74324938 C>T maps to NM_033238.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr15:74290565 G>A maps to NM_033238.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:74290565 G>T maps to NM_033238.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:41974861 G>A maps to NM_002676.2 F166F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AY-4071-01A-01W-1073-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr22:41974861 G>A maps to NM_002676.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr16:8905022 C>T maps to NM_000303.2 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:15162501 G>A maps to NM_000304.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:102949502 G>A maps to NM_004279.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:190718999 G>A maps to NM_000534.4 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:190708797 G>T maps to NM_000534.4 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:190660634 T>C maps to NM_000534.4 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:190719517 C>A maps to NM_000534.4 S507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr2:190682749 T>C maps to NM_000534.4 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr2:190719154 C>A maps to NM_000534.4 S386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:190682749 T>C maps to NM_000534.4 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr7:6027153 G>A maps to NM_000535.5 D414D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr7:6038762 G>A maps to NM_000535.5 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:6027134 G>A maps to NM_000535.5 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:6029581 G>A maps to NM_000535.5 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:6022501 G>A maps to NM_000535.5 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:6017317 G>A maps to NM_000535.5 D782D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:6038812 G>A maps to NM_000535.5 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:6038783 G>A maps to NM_000535.5 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:152936436 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:152937071 T>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:152935984 T>A did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:152936001 C>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:219188037 C>T maps to NM_022572.4 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:219136266 G>A maps to NM_015488.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:219205489 C>T maps to NM_015488.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:50365980 C>T maps to NM_007254.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr6:160234670 C>T maps to NM_173516.1 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr6:160234664 G>A maps to NM_173516.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:160238184 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:160240106 C>T maps to NM_173516.1 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:160224994 A>C did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr10:118314736 C>T maps to NM_000936.2 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:118315539 C>T maps to NM_000936.2 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:118354249 C>T maps to NM_006229.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:118220556 C>T maps to NM_001011709.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:118202577 G>A maps to NM_001011709.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:118236292 A>G maps to NM_001011709.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr10:118236235 T>C maps to NM_001011709.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:74179997 G>A maps to NM_006029.4 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:74179997 G>T maps to NM_006029.4 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:74180278 A>G maps to NM_006029.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:26365670 C>A maps to NM_007257.5 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr8:26365887 G>A maps to NM_007257.5 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:152226361 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:152226173 T>G did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr23:152225594 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:152225552 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:152226462 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:152226156 G>T did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr23:152226156 G>T did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:152159575 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:152158960 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:152160129 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:152159252 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:152159024 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:152159399 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:152159298 G>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:152159857 G>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:152159761 G>A did not map to a codon.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr19:46973170 G>A maps to NM_018215.3 Y374Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:46973218 G>A maps to NM_018215.3 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:46974169 C>T maps to NM_018215.3 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:46973368 C>T maps to NM_018215.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr19:46997339 C>T maps to NM_020709.1 A461A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AZ-4315-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:46997645 C>T maps to NM_020709.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr19:46997182 C>A maps to NM_020709.1 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr19:46997471 G>C maps to NM_020709.1 T417T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G4-6588-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:46997969 G>A maps to ENST00000377652 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:39646852 T>C maps to NM_002687.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:39650941 G>T maps to NM_002687.3 G677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:39645300 C>T maps to NM_002687.3 L45L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AZ-6608-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:28196672 G>T maps to NM_006228.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr14:20943359 G>T maps to NM_000270.3 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:36238409 C>T maps to ENST00000457797 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr6:36260863 G>A maps to ENST00000457797 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:36259307 G>A maps to ENST00000457797 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:44328792 C>A maps to NM_025225.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr22:44333039 G>A maps to NM_025225.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:44335928 C>T maps to NM_025225.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:44340649 C>T maps to NM_025225.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:7890116 T>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:7625589 C>A maps to NM_001166111.1 V1262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:7606888 A>G maps to NM_001166111.1 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:7621349 G>A maps to NM_001166111.1 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr19:7621563 C>T maps to NM_001166111.1 N1088N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:140358857 C>T maps to NM_001098537.1 T1030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr9:140373537 G>A maps to NM_001098537.1 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr9:140437096 G>A maps to NM_001098537.1 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:140437195 A>G maps to NM_001098537.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:140374874 G>T maps to NM_001098537.1 I823I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:140395258 C>T maps to NM_001098537.1 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:140391641 G>A maps to NM_001098537.1 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:108155050 C>T maps to NM_015723.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:108137133 G>A maps to NM_015723.2 R507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:55906921 G>A maps to NM_033109.3 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:55867797 C>T maps to NM_033109.3 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr3:52183890 C>T maps to NM_015426.4 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:52159188 G>T maps to NM_015426.4 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:89818991 G>A maps to NM_172240.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr12:89819117 A>C maps to NM_172240.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:89864200 A>G maps to NM_172240.2 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:75008687 C>T maps to NM_001099271.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:74981103 G>A maps to NM_001099271.1 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:74998519 G>A maps to NM_001099271.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:74970364 C>T maps to NM_001099271.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr1:53546512 C>T maps to NM_153703.4 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:53544291 G>A maps to NM_153703.4 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:14047234 G>A maps to NM_024825.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:14048618 G>A maps to NM_024825.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:14046541 C>T maps to NM_024825.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:131194201 G>A maps to NM_001018111.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:131194327 C>T maps to NM_001018111.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:131189174 C>T maps to NM_001018111.2 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr3:127379786 T>C maps to NM_015720.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:84561309 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:84561223 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:84614598 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:84558472 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:84561207 C>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:84563164 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:46698080 G>A maps to NM_133635.4 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:46698028 C>A maps to NM_133635.4 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr21:46687509 G>A maps to NM_133635.4 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:166818509 C>T maps to NM_017542.3 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr1:166819441 A>G maps to NM_017542.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:166819441 A>G maps to NM_017542.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:151380716 C>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:151378051 C>T maps to NM_015100.3 G1153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:151380600 G>A maps to NM_015100.3 R784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr1:151396564 G>A maps to NM_015100.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:151380988 G>A maps to NM_015100.3 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:151378488 G>A maps to NM_015100.3 R1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:24766429 T>C did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:24745992 G>A did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:24759516 T>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:24732753 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:24861720 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:24744171 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:24767005 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:24733283 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:24759523 A>G did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:24721401 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:24721417 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:24732733 C>T did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:24721400 G>T did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:24721401 A>G did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:24906153 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:65057325 T>C maps to NM_002689.2 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:65034979 T>C maps to NM_002689.2 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:42227444 T>G maps to NM_002690.1 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr19:50906748 G>A did not map to a codon.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr19:50919912 C>T maps to ENST00000391817 G1026G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:50917111 G>A maps to ENST00000391817 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:50905322 C>T maps to ENST00000391817 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:50909764 C>T maps to ENST00000391817 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:50912774 G>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:50902140 C>T maps to ENST00000391817 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:50905894 C>T maps to ENST00000391817 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:50918718 C>T maps to ENST00000391817 H889H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:44156466 G>A maps to NM_006230.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr7:44155451 G>A maps to NM_006230.2 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:44155841 G>A maps to NM_006230.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:44156511 G>A maps to NM_006230.2 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr11:74347268 C>T maps to NM_006591.1 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:74329821 G>A maps to NM_006591.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:74329759 G>T maps to NM_006591.1 G191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:74347267 A>G maps to NM_006591.1 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr11:74347267 A>G maps to NM_006591.1 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr11:74347267 A>G maps to NM_006591.1 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr12:133244145 G>A maps to ENST00000455752 Y757Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:133202347 C>T maps to ENST00000455752 A2183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:133218934 G>A maps to ENST00000455752 F1670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr12:133214670 G>A maps to ENST00000455752 N1872N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:133241997 G>A maps to ENST00000455752 G789G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:50136310 G>T maps to NM_002692.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:50133107 C>T maps to NM_002692.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:116171959 A>G maps to NM_017443.4 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:89864052 C>T maps to NM_002693.2 Q975Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr15:89862559 G>A maps to NM_002693.2 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:89861809 G>A maps to NM_002693.2 R1148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr15:89864377 G>A maps to NM_002693.2 D904D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr15:89868781 C>T maps to NM_002693.2 E616E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:89876736 C>T maps to NM_002693.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:43582003 C>T maps to NM_006502.2 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr6:43565574 G>A maps to NM_006502.2 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:43565580 A>G maps to NM_006502.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr6:43581825 C>A maps to NM_006502.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr18:51813782 T>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:51820201 G>T maps to NM_007195.2 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:51820531 G>T maps to NM_007195.2 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr18:51809297 A>G maps to NM_007195.2 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr5:74848304 A>G maps to NM_016218.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr5:74872702 T>C maps to NM_016218.2 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:74842934 G>T maps to NM_016218.2 G30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:103342588 G>A maps to NM_013274.3 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:44118407 C>T maps to NM_013284.2 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:2172414 T>A maps to NM_181808.2 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:2200384 G>A maps to NM_181808.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr4:2172408 T>C maps to NM_181808.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr4:2097653 A>G maps to NM_181808.2 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr4:2172441 C>T maps to NM_181808.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:121200502 G>A maps to ENST00000393672 R2179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:121248578 A>G maps to ENST00000393672 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:121203936 A>G maps to ENST00000393672 G2044G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:121178980 A>G maps to ENST00000393672 A2492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:121248600 C>T maps to ENST00000393672 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:121187159 G>T maps to ENST00000393672 P2415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:121203966 G>T maps to ENST00000393672 T2034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr3:121208693 C>T maps to ENST00000393672 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr3:121191008 G>A maps to ENST00000393672 D2318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr3:121228533 T>C maps to ENST00000393672 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr3:121186431 C>A maps to ENST00000393672 E2437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:121186366 T>C maps to ENST00000393672 P2458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:86266530 G>A maps to NM_015425.3 S1265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:86308731 C>T maps to NM_015425.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:86269163 G>A maps to NM_015425.3 A1140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:86302212 G>A maps to NM_015425.3 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr2:86258685 G>A maps to NM_015425.3 R1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr2:86274383 T>C maps to NM_015425.3 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:113332591 G>A maps to NM_019014.4 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:113332471 C>T maps to NM_019014.4 D858D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:28239939 G>C maps to NM_152705.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:37486112 T>G maps to NM_022490.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:37501826 G>A maps to NM_022490.1 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:7416219 A>G maps to NM_000937.4 S1578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:7415278 C>T maps to NM_000937.4 H1417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:7411769 C>T maps to NM_000937.4 S1147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:7404317 G>T maps to NM_000937.4 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:7399877 C>T maps to NM_000937.4 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:7417426 G>A maps to NM_000937.4 S1948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:57865796 T>C maps to NM_000938.1 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:57897135 G>A maps to NM_000938.1 P1169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:57877003 G>T maps to NM_000938.1 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:57881714 G>A maps to NM_000938.1 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:57888375 G>T maps to NM_000938.1 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr4:57865796 T>C maps to NM_000938.1 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:57504230 G>A maps to NM_032940.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:38352788 C>T maps to ENST00000407936 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr10:79767528 G>A maps to NM_007055.3 R669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:79769710 G>A maps to NM_007055.3 R561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:79764536 G>A maps to NM_007055.3 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:79781348 T>C maps to NM_007055.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:79769415 C>T maps to NM_007055.3 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:106838339 T>C maps to NM_018082.5 Y685Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:106838300 C>T maps to NM_018082.5 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:106848400 T>G maps to NM_018082.5 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr12:106890684 C>T maps to NM_018082.5 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:106890600 G>A maps to NM_018082.5 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:145608556 G>A maps to NM_006468.6 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:22107967 C>T maps to NM_001722.2 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:22105448 C>T maps to NM_001722.2 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr8:22106743 C>A maps to NM_001722.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:22106743 C>A maps to NM_001722.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr8:22105766 C>A maps to NM_001722.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr16:22320325 C>T maps to NM_018119.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr16:22337250 C>T maps to NM_018119.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:22337208 G>A maps to NM_018119.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:22335864 C>A maps to NM_018119.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:22344963 G>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:18461119 G>A maps to NM_006466.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:619020 G>C maps to NM_005035.3 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:630124 C>T maps to NM_005035.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:621774 G>A maps to NM_005035.3 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr19:622707 C>T maps to NM_005035.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:623504 G>A maps to NM_005035.3 C413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr7:72413699 C>T maps to ENST00000434423 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:75053446 G>T maps to ENST00000257665 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:75051188 G>A maps to ENST00000257665 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr7:75051155 G>C maps to ENST00000257665 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:53103780 C>T maps to NM_182595.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:53104197 C>T maps to NM_182595.3 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr7:53103576 G>A maps to NM_182595.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr2:25384060 C>T maps to NM_001035256.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:25383985 G>A maps to NM_001035256.1 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:25384183 G>A maps to NM_001035256.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:46660029 G>A maps to ENST00000371986 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:29252184 C>T maps to NM_015932.5 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:134379709 C>A maps to NM_007171.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:134394818 G>A maps to NM_007171.3 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr9:134385418 C>G maps to NM_007171.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:134381575 G>A maps to NM_007171.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:94937380 G>A maps to NM_000446.5 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:94953781 C>T maps to NM_000446.5 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:94940803 C>T maps to NM_000446.5 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:94947700 G>A maps to NM_000446.5 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:95040969 A>G maps to NM_000305.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:95019483 C>T maps to NM_000940.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:95001560 T>C maps to NM_000940.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr7:95001617 C>T maps to NM_000940.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr7:94993254 A>G maps to NM_000940.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:99135615 T>C maps to NM_015029.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:99162834 G>A maps to NM_015029.2 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr8:99140702 C>T maps to NM_015029.2 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:30106274 G>T maps to NM_006627.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:119379072 C>T maps to NM_022135.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:119378907 C>T maps to NM_022135.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr3:119379138 G>T maps to NM_022135.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:119379054 G>T maps to NM_022135.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:105609451 C>T maps to NM_022361.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:105607672 G>A maps to NM_022361.4 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr23:48374144 T>C did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:48369709 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:48372642 C>T did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr23:48374144 T>C did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:48374144 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:48370835 G>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:48371086 C>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr13:38162096 G>A maps to NM_006475.2 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr13:38164595 G>A maps to NM_006475.2 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr13:38154780 G>A maps to NM_006475.2 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:38154718 A>C maps to NM_006475.2 L503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr7:124493039 C>T maps to NM_015450.2 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:124493039 C>A maps to NM_015450.2 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:43152505 T>C maps to NM_001005365.2 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:43147773 C>T maps to NM_001005365.2 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr8:43152267 T>C maps to NM_001005365.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:14537861 C>A maps to ENST00000444806 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr18:14542797 G>A maps to ENST00000444806 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:15013818 G>T maps to NM_174981.3 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr21:14982902 C>T maps to NM_174981.3 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:14982917 C>T maps to NM_174981.3 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr2:131976343 C>T maps to NM_001083538.1 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:130878061 C>T maps to NM_001099771.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:19574194 G>T maps to NM_001005356.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr14:19553823 T>C maps to NM_001005356.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr14:19553823 T>C maps to NM_001005356.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr22:16287420 G>T maps to NM_001136213.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr22:16287537 G>A maps to NM_001136213.1 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr22:16287579 G>A maps to NM_001136213.1 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:16287792 G>T maps to NM_001136213.1 C31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:87322562 C>A maps to NM_001122757.1 G76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:87310420 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:111229511 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:111228277 G>A maps to NM_006235.2 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:167385013 G>A maps to NM_002697.3 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:167343355 G>A maps to NM_002697.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:167381208 C>T maps to NM_002697.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:167343433 C>T maps to NM_002697.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr11:120178197 G>A maps to NM_014352.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr11:120180222 A>G maps to NM_014352.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:120176390 C>T maps to NM_014352.2 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:99283615 G>A maps to NM_005604.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:105473035 G>A maps to NM_006236.1 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr2:105472984 G>A maps to NM_006236.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr23:82763638 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:82763440 C>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:82764036 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:82764390 A>C did not map to a codon.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr23:82764089 A>G did not map to a codon.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr23:82763391 G>A did not map to a codon.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr23:82763850 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:82763971 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:82763420 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:82763691 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:82763830 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:82764243 C>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:82763667 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:82763464 G>A did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr23:82763724 C>A did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:82763391 G>A did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:82763710 A>G did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:82763970 C>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:82764399 A>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:82763517 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:79177386 C>T maps to NM_006237.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr13:79175558 G>T maps to NM_006237.3 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr13:79176542 C>T maps to NM_006237.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:147561755 C>T maps to NM_004575.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:147561224 C>A maps to NM_004575.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:147561455 G>A maps to NM_004575.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:145719439 C>T maps to NM_002700.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr5:145719481 G>A maps to NM_002700.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr5:145719994 G>A maps to NM_002700.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:145719403 G>A maps to NM_002700.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:145719541 G>A maps to NM_002700.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr5:145719544 C>T maps to NM_002700.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:31138370 G>A maps to NM_002701.4 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:31138322 C>T maps to NM_002701.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:31138166 C>T maps to NM_002701.4 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:93076992 G>A maps to NM_153216.1 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:51584191 A>G maps to NM_002702.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:51584191 A>G maps to NM_002702.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:51584191 A>G maps to NM_002702.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:39379455 C>T maps to NM_007252.3 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr7:39379595 G>A maps to NM_007252.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr7:39247113 G>T maps to NM_007252.3 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:71977618 C>T maps to NM_021129.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr4:106345353 A>G maps to ENST00000357415 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:54721738 G>A maps to NM_176895.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:54721147 C>T maps to NM_176895.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:54721126 A>G maps to NM_176895.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr5:54771164 A>G maps to NM_003711.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:54763899 G>T maps to NM_176895.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:54721084 C>T maps to NM_176895.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr1:57002638 A>T maps to NM_003713.4 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:281390 G>T maps to NM_177543.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:288136 G>A maps to NM_177543.1 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:288136 G>A maps to NM_177543.1 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr10:122334685 C>A maps to NM_001030059.1 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:122216870 C>T maps to NM_001030059.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr10:122278387 T>A maps to NM_001030059.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:122348818 C>A maps to NM_001030059.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr9:134183373 C>T maps to NM_032728.3 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:134183529 C>T maps to NM_032728.3 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr22:46611088 G>A maps to NM_001001928.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:35393612 G>A maps to NM_006238.4 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr6:35389613 G>A maps to NM_006238.4 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr6:35392305 C>T maps to NM_006238.4 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:12393165 A>T maps to NM_015869.4 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:12421422 G>A maps to NM_015869.4 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr4:23830041 C>T maps to NM_013261.3 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:23830128 G>A maps to NM_013261.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:23830034 G>A maps to NM_013261.3 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:23833221 A>G maps to NM_013261.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:23815521 C>T maps to NM_013261.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:149212317 C>T maps to NM_133263.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:149225388 C>T maps to NM_133263.3 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:149212352 T>C maps to NM_133263.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:149109979 G>A maps to NM_133263.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr4:57301625 C>T maps to NM_002703.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:74853304 T>G maps to NM_002704.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr23:18842158 C>T did not map to a codon.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr23:18807255 A>C did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:18748396 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:18843897 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:18822153 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:18800495 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:18748332 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:18768005 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:18775798 A>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:18800499 G>T did not map to a codon.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr23:18751912 T>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:18802073 G>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr4:76809421 C>T maps to NM_006239.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:76805898 C>T maps to NM_006239.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:76787440 C>T maps to NM_006239.2 W607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:76797529 G>A maps to NM_006239.2 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:76797625 G>A maps to NM_006239.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:70224137 T>C maps to NM_003626.2 D1129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:70189941 G>A maps to NM_003626.2 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:70189941 G>A maps to NM_003626.2 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr11:70221129 G>A maps to NM_003626.2 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:81733021 C>A maps to NM_003625.2 G829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:82147876 T>G maps to NM_003625.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr12:81675059 A>C maps to NM_003625.2 L1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr12:81719599 G>T maps to NM_003625.2 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:81734930 A>C maps to NM_003625.2 T773T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr12:81671099 T>A maps to NM_003625.2 I1102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:81747070 T>C maps to NM_003625.2 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr12:81747070 T>C maps to NM_003625.2 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr12:81747070 T>C maps to NM_003625.2 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:81688675 G>A maps to NM_003625.2 R955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:49631647 C>T maps to NM_003660.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr19:49643052 G>A maps to NM_003660.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr19:49642998 C>A maps to NM_003660.2 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr19:49651434 G>A maps to NM_003660.2 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:49633843 C>T maps to NM_003660.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:49632181 C>A maps to NM_003660.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:203029508 A>G maps to ENST00000367238 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:203029424 G>T maps to ENST00000367238 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:203044856 G>A maps to ENST00000367238 P1161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:203036880 C>T maps to ENST00000367238 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:27835402 T>C maps to NM_003622.3 H710H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:27826712 C>T maps to NM_003622.3 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:27809550 T>C maps to NM_003622.3 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:27830004 C>T maps to NM_003622.3 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:27799017 C>T maps to NM_003622.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr12:27829529 T>G maps to NM_003622.3 L527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:27809550 T>C maps to NM_003622.3 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr11:7631577 G>C maps to NM_003621.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr11:7654129 G>A maps to NM_003621.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr11:7663546 A>G maps to NM_003621.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:7618835 C>A maps to NM_003621.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:7655750 C>T maps to NM_003621.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:7669615 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:42839890 G>A maps to NM_016488.6 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:42745781 T>G maps to NM_016488.6 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:42792724 G>T maps to NM_016488.6 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:42792657 G>A maps to NM_016488.6 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:42835142 C>T maps to NM_016488.6 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:64448278 G>T maps to NM_000942.4 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:122359632 C>T maps to NM_000943.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:159631930 C>A maps to NM_005038.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:159640378 C>A maps to NM_005038.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:40214722 C>T maps to NM_006112.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:170493493 C>T maps to NM_004792.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:170493051 C>T maps to NM_004792.2 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr22:22035645 T>C maps to NM_148175.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:22020408 A>G maps to NM_148175.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr22:22041232 C>T maps to NM_148175.2 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:22039198 C>T maps to NM_148175.2 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:149862652 A>G did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:50081138 T>C maps to NM_152329.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr14:50074350 T>C maps to NM_152329.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr14:50081024 T>C maps to NM_152329.3 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr14:50074350 T>C maps to NM_152329.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:109757378 G>A maps to NM_001111298.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:109757344 C>A maps to NM_001111298.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:109748350 G>A maps to NM_001111298.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:43851023 G>T maps to NM_001130858.2 R1118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:43873472 C>T maps to NM_001130858.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr15:43827408 G>A maps to NM_001130858.2 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr5:102469239 G>C maps to ENST00000451606 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:102465316 C>T maps to ENST00000451606 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:102483690 A>G maps to ENST00000451606 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:102469329 T>C maps to ENST00000451606 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:4940235 G>T maps to NM_002705.4 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:4934991 G>A maps to NM_002705.4 R1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:4934449 C>T maps to NM_002705.4 Q1402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:4940286 G>A maps to NM_002705.4 R737R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr16:4934344 G>A maps to NM_002705.4 A1437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:4934950 G>T maps to NM_002705.4 V1235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:4935679 G>A maps to NM_002705.4 Y992Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:4953942 C>T maps to NM_002705.4 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:4953962 G>A maps to NM_002705.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr16:4940196 C>A maps to NM_002705.4 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:4934728 C>T maps to NM_002705.4 A1309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:4949082 T>C maps to NM_002705.4 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr16:4949082 T>C maps to NM_002705.4 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:4934991 G>A maps to NM_002705.4 R1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:4940826 G>A maps to NM_002705.4 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr14:60756566 T>C maps to NM_177952.2 H405H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr17:58678152 G>A maps to NM_003620.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:57033105 G>A maps to NM_014906.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:56833438 C>T maps to NM_014906.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr17:57033120 G>A maps to NM_014906.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:57057996 G>T maps to NM_014906.3 E625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr17:56833453 G>A maps to NM_014906.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr17:56833456 G>C maps to NM_014906.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr17:57058103 G>T maps to NM_014906.3 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:57058283 G>A maps to NM_014906.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr17:57058103 G>T maps to NM_014906.3 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr17:57043168 C>A maps to NM_014906.3 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr22:22294002 G>A maps to NM_014634.3 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr22:22277563 G>A maps to NM_014634.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr22:22293946 T>C maps to NM_014634.3 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:27607617 A>G maps to NM_177983.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:27609129 C>T maps to NM_177983.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:63042351 G>T maps to NM_020700.1 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr12:63195907 C>T maps to NM_020700.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:113253653 A>G maps to NM_005167.5 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:113255587 G>T maps to NM_005167.5 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr4:89199645 G>A maps to NM_152542.3 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr4:89199468 T>C maps to NM_152542.3 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:89199444 G>A maps to NM_152542.3 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr3:160783242 C>T maps to NM_139245.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:160786804 C>T maps to NM_139245.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:160786804 C>T maps to NM_139245.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:160783284 C>T maps to NM_139245.2 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:46005309 G>A maps to NM_001080401.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:161136985 A>C maps to NM_001122764.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:67166195 G>A maps to NM_001008709.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:67166083 C>T maps to NM_001008709.1 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr2:29016823 A>G maps to NM_002709.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr2:29016733 G>A maps to NM_002709.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:29001807 A>G maps to NM_002709.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr6:30571993 A>G maps to NM_002714.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:30572800 T>C maps to NM_002714.2 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:30037016 G>A maps to NM_021959.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:80214689 T>C maps to NM_001143885.1 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:80202303 T>C maps to NM_001143885.1 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr12:80203745 T>C maps to NM_001143885.1 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr12:80192315 T>C maps to NM_001143885.1 K683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr12:80199974 C>G maps to NM_001143885.1 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr12:80190721 C>T maps to NM_001143885.1 Q767Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:202464771 C>T maps to ENST00000367270 R804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:202406995 T>C maps to ENST00000367270 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr1:202406995 T>C maps to ENST00000367270 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:202457751 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:55604236 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:55604177 G>A maps to NM_017607.2 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:55606057 C>T maps to NM_017607.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:104202438 G>A maps to NM_015316.2 D1044D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr14:104245134 G>A maps to NM_015316.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:45899614 C>T maps to NM_001142502.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:45901283 C>T maps to NM_001142502.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:49377201 G>T maps to NM_014330.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:204380040 A>G maps to NM_032833.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:145726613 G>A maps to NM_032902.5 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:145725481 C>T maps to NM_032902.5 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:145724316 C>T maps to NM_032902.5 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr8:145726928 G>A maps to NM_032902.5 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:37464765 C>T maps to NM_015568.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:37546993 C>T maps to NM_015568.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:37531332 C>T maps to NM_015568.2 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:37534658 C>T maps to NM_015568.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:54982250 G>A maps to NM_006741.3 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:182981983 G>T maps to ENST00000280295 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:195256659 C>T maps to NM_006241.4 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr7:113517840 A>G maps to NM_002711.3 V1102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr7:113519406 A>G maps to NM_002711.3 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr7:113558685 T>C maps to NM_002711.3 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:113518302 C>T maps to NM_002711.3 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:113518904 C>A maps to NM_002711.3 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:113519406 A>G maps to NM_002711.3 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:113518271 C>A maps to NM_002711.3 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:113520056 C>A maps to NM_002711.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:113517840 A>G maps to NM_002711.3 V1102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:113519484 C>T maps to NM_002711.3 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:113518188 A>G maps to NM_002711.3 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr7:113558790 A>G maps to NM_002711.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr7:113518500 A>G maps to NM_002711.3 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr7:113558583 T>C maps to NM_002711.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:113518602 G>T maps to NM_002711.3 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr7:113519907 T>C maps to NM_002711.3 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr7:113558763 C>T maps to NM_002711.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr7:113518302 C>A maps to NM_002711.3 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr7:113519406 A>G maps to NM_002711.3 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:8998966 G>A maps to NM_024607.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:58514113 G>A maps to NM_006242.3 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:49143041 G>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:49142646 C>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:49142521 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:49142390 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:49126719 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:49138516 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:49142862 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:49142349 A>C did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:49143087 A>G did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:49143089 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:49127237 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:49127331 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:242102704 C>T maps to NM_002712.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr7:94827709 T>C maps to NM_001166160.1 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:94827711 G>A maps to NM_001166160.1 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:94915573 C>T maps to NM_001166160.1 S1222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:94539734 G>T maps to NM_001166160.1 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:94540568 G>T maps to NM_001166160.1 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:94540144 T>G maps to NM_001166160.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:94540744 G>A maps to NM_001166160.1 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:133536762 G>T maps to NM_002715.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:133537661 T>C maps to NM_002715.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr5:133537661 T>C maps to NM_002715.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:133536738 C>T maps to NM_002715.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:133541779 G>A maps to NM_002715.2 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr19:52714553 G>A maps to NM_014225.5 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr19:52716221 G>A maps to NM_014225.5 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:52722999 T>C maps to NM_014225.5 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr19:52714601 G>A maps to NM_014225.5 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:111612830 A>G maps to NM_181699.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:26196443 G>T maps to NM_001177591.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:26220314 T>A maps to NM_001177591.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:26212048 A>G maps to NM_001177591.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:26218602 A>C maps to NM_001177591.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:26217718 G>A maps to NM_001177591.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:146030182 G>A maps to ENST00000394414 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:146435259 T>C maps to ENST00000394414 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:145980012 C>T maps to ENST00000394414 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:146030185 G>A maps to ENST00000394414 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:6382804 G>A maps to NM_181876.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:6330986 A>G did not map to a codon.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr4:6331041 G>A maps to NM_181876.2 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:133769199 C>T maps to ENST00000455566 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:133761122 C>A maps to ENST00000455566 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr3:135721378 C>T maps to NM_002718.4 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr3:135722028 C>A maps to NM_002718.4 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:135797264 G>A maps to NM_002718.4 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:135722040 C>A maps to NM_002718.4 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:135722028 C>T maps to NM_002718.4 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr14:35554882 G>A maps to NM_017917.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:35554939 G>T maps to NM_017917.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:35564331 T>C maps to NM_017917.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr14:35564331 T>C maps to NM_017917.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:35564331 T>C maps to NM_017917.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:131899913 C>T maps to NM_178001.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:102391599 C>T maps to NM_002719.3 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr14:102384281 C>T maps to NM_002719.3 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:102356579 T>C maps to NM_002719.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:102368093 C>T maps to NM_002719.3 H297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:42976110 C>A maps to NM_006245.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:42975153 C>T maps to NM_006245.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr14:63920523 C>T maps to ENST00000422769 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr14:63888722 C>T maps to ENST00000422769 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr4:102015056 C>A maps to NM_000944.4 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:102030182 G>A maps to NM_000944.4 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:102019595 C>T maps to NM_000944.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:102030194 C>T maps to NM_000944.4 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:75239210 G>A maps to NM_001142353.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:75227338 C>T maps to NM_001142353.1 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:75206289 G>A maps to NM_001142353.1 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:75198056 A>G maps to NM_001142353.1 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:75198020 C>T maps to NM_001142353.1 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:75198026 G>A maps to NM_001142353.1 H517H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:22368600 C>T maps to ENST00000397775 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr8:22380171 C>T maps to ENST00000397775 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr9:104357062 C>T maps to NM_147180.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:104356768 A>G maps to NM_147180.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr9:104356945 G>T maps to NM_147180.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:30094989 C>T maps to NM_002720.1 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:30096340 G>T maps to NM_002720.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr16:30094134 C>T maps to NM_002720.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr18:9577074 C>A maps to NM_001042388.1 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr18:9549239 G>A maps to NM_001042388.1 R882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:9547906 C>T maps to NM_001042388.1 E911E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr18:9550350 A>G maps to NM_001042388.1 Y779Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr18:9577156 A>T maps to NM_001042388.1 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:9563387 G>A maps to NM_001042388.1 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:9559584 C>T maps to NM_001042388.1 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr18:9583189 A>T maps to NM_001042388.1 C281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:73112848 C>T maps to NM_174907.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr14:94700905 C>T maps to NM_058237.1 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:94708735 C>A maps to NM_058237.1 C419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:94674875 G>A maps to NM_058237.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:94700959 C>T maps to NM_058237.1 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:94642399 G>T maps to NM_058237.1 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:94699988 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:94708198 G>T maps to NM_058237.1 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr14:94640825 C>A maps to NM_058237.1 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr19:46878952 C>T maps to NM_006247.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:46890389 C>T maps to NM_006247.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:46890449 C>T maps to NM_006247.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:127911966 C>T maps to NM_001123355.1 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:127911966 C>T maps to NM_001123355.1 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr9:127920556 A>G maps to NM_001123355.1 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr9:127916196 G>T maps to NM_001123355.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:244868958 G>A maps to NM_016076.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:244849970 G>T maps to NM_016076.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:244868958 G>A maps to NM_016076.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:103907144 C>T maps to NM_015062.3 R1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr10:103901279 C>A maps to NM_015062.3 A1005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:103898410 G>A maps to NM_015062.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:103899833 T>C maps to NM_015062.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:103897626 G>A maps to NM_015062.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr10:103897626 G>T maps to NM_015062.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr10:103897626 G>A maps to NM_015062.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr10:103899089 C>T maps to NM_015062.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:103909006 G>A maps to NM_015062.3 L1604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr10:103897626 G>T maps to NM_015062.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:110989597 C>T maps to NM_139283.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:110989696 C>T maps to NM_139283.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:64872833 T>C maps to NM_015342.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr5:64878978 C>T maps to NM_015342.2 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr23:48755809 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:48759296 G>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:48759745 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr18:77703383 C>T maps to NM_025078.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:19651141 C>T maps to NM_017765.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:19653800 C>T maps to NM_017765.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:19651237 T>C maps to NM_017765.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:19653906 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:11315127 T>C maps to NM_152391.3 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:48929656 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:48929636 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:48930137 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:48929637 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:48930138 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:8563815 G>A maps to NM_032152.4 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:8564205 C>T maps to NM_032152.4 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:22892529 A>G maps to NM_206954.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:22892320 A>G maps to NM_206954.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:12854348 G>A maps to NM_023013.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:12856054 G>A maps to NM_023013.2 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:12854615 C>T maps to NM_023013.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr1:12854423 C>T maps to NM_023013.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:12837669 C>T maps to NM_001080830.1 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr1:12837390 C>T maps to NM_001080830.1 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr1:12835961 A>T maps to NM_001080830.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:12918905 G>A maps to NM_023014.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:12921195 C>T maps to NM_023014.1 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:12919079 G>A maps to NM_023014.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr1:13036686 C>T maps to NM_001100631.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr1:12943041 C>T maps to NM_001009611.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:135165853 C>T maps to ENST00000423766 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:135165618 T>C maps to ENST00000423766 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:11506529 G>T maps to NM_005039.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:11506283 A>C maps to NM_005039.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr12:11420516 C>T maps to NM_006249.4 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:11420483 G>T maps to NM_006249.4 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr12:11420320 C>T maps to NM_006249.4 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr12:11420903 T>C maps to NM_006249.4 P93P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CK-6746-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:11461280 A>G maps to NM_002723.3 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:11461280 A>G maps to NM_002723.3 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr15:91513684 T>C maps to NM_003981.2 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr15:91513738 G>A maps to NM_003981.2 N489N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr15:91524881 C>T maps to NM_003981.2 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:91510387 G>A maps to NM_003981.2 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:91519979 G>A maps to NM_003981.2 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr15:91522411 G>T maps to NM_003981.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:156756509 G>A maps to NM_005973.4 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:156737853 C>T maps to NM_005973.4 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:82549606 C>A maps to NM_199418.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr6:106536284 A>G maps to NM_001198.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:106553333 C>T maps to NM_001198.3 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr6:106554883 G>A maps to NM_001198.3 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:106555108 C>T maps to NM_001198.3 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr6:106552788 G>T maps to NM_001198.3 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:129814884 C>T maps to NM_020228.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:129800940 G>T maps to NM_020228.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:129784871 G>A maps to NM_020228.2 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:129812496 C>A maps to NM_020228.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr11:129814728 A>G maps to NM_020228.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:129827802 C>T maps to NM_020228.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:129793295 C>T maps to NM_020228.2 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:129782003 G>A maps to NM_020228.2 T990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:129785593 G>A maps to NM_020228.2 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:129785608 G>A maps to NM_020228.2 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:45245900 A>G maps to NM_020229.2 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:45204586 C>T maps to NM_020229.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr11:45204514 G>A maps to NM_020229.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:133543669 C>T maps to NM_021619.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:133540258 C>T maps to NM_021619.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:100062532 G>A maps to ENST00000359773 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:100062292 G>A maps to ENST00000359773 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:70981552 A>G maps to NM_024504.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:70981792 C>T maps to NM_024504.2 W101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr8:70967603 A>G maps to NM_024504.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:70982068 G>A maps to NM_024504.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr21:43282099 C>T maps to NM_022115.3 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:43222907 G>A maps to NM_022115.3 G1335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:43246401 G>A maps to NM_022115.3 R881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:43277344 G>A maps to NM_022115.3 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:43277406 G>A maps to NM_022115.3 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:43258155 G>T maps to NM_022115.3 I662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr1:3347519 C>T maps to NM_022114.3 D1123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:3328479 G>T maps to NM_022114.3 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:3327993 G>A maps to NM_022114.3 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:3328008 C>T maps to NM_022114.3 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:3328656 C>T maps to NM_022114.3 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:3313155 C>T maps to NM_022114.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:3342714 C>T maps to NM_022114.3 D1070D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr1:3102869 C>T maps to NM_022114.3 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:3328440 C>T maps to NM_022114.3 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:3328644 C>T maps to NM_022114.3 D628D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:3329094 G>A maps to NM_022114.3 K778K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:14106290 T>C maps to NM_012231.4 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:14057565 G>A maps to NM_012231.4 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:14107172 G>A maps to NM_012231.4 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:14142939 G>A maps to NM_012231.4 A1685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr1:14108530 C>A maps to NM_012231.4 S1414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:14106983 C>T maps to NM_012231.4 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:14108954 G>A maps to NM_012231.4 Q1555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:14104961 G>A maps to NM_012231.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:14107151 C>A maps to NM_012231.4 P954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:14106824 A>G maps to NM_012231.4 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:14108282 C>T maps to NM_012231.4 T1331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:108128013 C>T maps to NM_012406.3 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:121739565 C>A maps to NM_018699.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr16:90128463 C>A maps to NM_001098173.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr16:90128868 G>A maps to NM_001098173.1 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:81121317 C>T maps to NM_001099403.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:81122494 T>C maps to NM_001099403.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:81124632 G>T maps to NM_001099403.1 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr4:81124595 G>C maps to NM_001099403.1 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr5:23522837 G>T maps to NM_020227.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:23522453 C>T maps to NM_020227.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:23517993 A>G maps to NM_020227.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:23526486 C>A maps to NM_020227.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:23521173 G>T maps to NM_020227.2 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:23526840 G>T maps to NM_020227.2 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:23527534 G>T maps to NM_020227.2 E780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:23526568 G>T maps to NM_020227.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:23527860 C>T maps to NM_020227.2 Y888Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:23522453 C>T maps to NM_020227.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:23526664 G>T maps to NM_020227.2 G490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr5:23526511 C>T maps to NM_020227.2 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr23:23700556 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:64087312 T>C maps to NM_012094.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:173455495 C>T maps to NM_004905.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:203453229 G>A maps to NM_201348.1 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:203455927 G>A maps to NM_201348.1 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr1:203452395 C>T maps to NM_201348.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr1:203455840 C>T maps to NM_201348.1 N327N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:203453088 C>T maps to NM_201348.1 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr1:203452956 C>T maps to NM_201348.1 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:105726111 G>A maps to NM_002726.4 H680H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:105729685 G>A maps to NM_002726.4 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:105733370 C>T maps to NM_002726.4 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:105736640 G>T maps to NM_002726.4 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr6:105736640 G>T maps to NM_002726.4 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:105845745 G>A maps to NM_002726.4 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:44586755 G>A maps to NM_001171603.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:44571725 C>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr20:47267996 G>A maps to NM_020820.3 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:47262498 G>A maps to NM_020820.3 S1134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr20:47259003 G>T maps to NM_020820.3 R1209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr20:47292799 A>G maps to NM_020820.3 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr20:47247298 C>T maps to NM_020820.3 T1520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr20:47251244 G>T maps to NM_020820.3 S1412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr20:47260995 G>T maps to NM_020820.3 T1184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:47267557 G>A maps to NM_020820.3 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr20:47266678 C>T maps to NM_020820.3 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr20:47305232 C>T maps to NM_020820.3 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:47246045 C>T maps to NM_020820.3 S1569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr20:47253042 G>A maps to NM_020820.3 G1375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:69033154 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr8:69012053 T>C maps to NM_024870.2 C897C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr8:69017410 G>A maps to NM_025170.4 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr8:68950459 G>T maps to NM_024870.2 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:69129901 C>T maps to NM_024870.2 H1552H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr8:69021744 C>G maps to NM_024870.2 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr8:68972958 T>C maps to NM_024870.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:69002889 G>A maps to NM_024870.2 E730E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:69104697 C>A maps to NM_024870.2 S1514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:68981358 C>T maps to NM_024870.2 D477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr8:68989672 T>C maps to NM_024870.2 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:68995594 A>C maps to NM_024870.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:68956820 C>T maps to NM_024870.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr8:68992729 G>A maps to NM_024870.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr8:69020465 T>G maps to NM_024870.2 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr8:69129898 C>T maps to NM_024870.2 S1551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:68989672 T>C maps to NM_024870.2 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:69005931 G>A maps to NM_024870.2 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr10:72360295 C>T maps to NM_005041.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr10:72357889 C>A maps to NM_005041.4 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:72358861 G>A maps to NM_005041.4 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:72360580 G>A maps to NM_005041.4 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr10:72360295 C>T maps to NM_005041.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:57156734 A>G maps to NM_002728.4 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:186266074 C>A maps to NM_005807.3 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:186277994 G>A maps to NM_005807.3 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:186277151 A>G maps to NM_005807.3 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:186275672 G>A maps to NM_005807.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:186275945 G>A maps to NM_005807.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:186270757 C>T maps to NM_005807.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:11035669 G>A maps to NM_006250.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:11082878 G>T maps to NM_001110213.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:62195617 G>A maps to NM_001037335.2 R1519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:62191320 A>G maps to NM_001037335.2 N2595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr20:62193173 A>G did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:62195545 G>A maps to NM_001037335.2 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr20:62196544 C>T maps to NM_001037335.2 T1210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr20:62197345 G>A maps to NM_001037335.2 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr20:62191906 G>A maps to NM_001037335.2 H2475H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:42858859 G>A maps to NM_153026.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:42858962 A>G maps to NM_153026.2 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:42853610 T>C maps to NM_153026.2 *832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr12:42860179 T>G maps to NM_153026.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:64084954 G>A maps to NM_198859.3 F769F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:64132809 G>A maps to NM_198859.3 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr3:64085176 G>A maps to NM_198859.3 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:64133202 G>T maps to NM_198859.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:64084735 G>T maps to NM_198859.3 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:64133058 T>C maps to NM_198859.3 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr3:64085269 G>T maps to NM_198859.3 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:49034730 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:49034778 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:49033534 C>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:49032451 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:49034396 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:41754788 T>C maps to NM_013397.5 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:57140613 G>A maps to NM_000946.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr6:57189025 C>T maps to NM_000947.2 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:94245528 G>T maps to NM_178013.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr5:40798228 C>T maps to NM_206907.3 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:40777677 A>G maps to NM_206907.3 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:40777688 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:57159483 C>T maps to NM_006252.3 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:57159516 C>T maps to NM_006252.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr1:57173244 T>C maps to NM_006252.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr1:57173244 T>C maps to NM_006252.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:57173253 C>T maps to NM_006252.3 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:120110170 C>A maps to NM_006253.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:146638125 G>A maps to NM_005399.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:146639481 G>A maps to NM_005399.3 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:14217583 G>A maps to NM_002730.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:14208432 G>A maps to NM_002730.3 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:84649718 G>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:84668406 A>G maps to NM_182948.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:71628408 G>A maps to NM_002732.3 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr9:71628402 G>C maps to NM_002732.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:71628978 G>A maps to NM_002732.3 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:49398781 G>T maps to NM_002733.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:151292526 T>C maps to NM_016203.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:151372616 G>T maps to NM_016203.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:219694811 G>A maps to NM_017431.2 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:219692574 A>G maps to NM_017431.2 H267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:219694796 G>T maps to NM_017431.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:219692577 T>C maps to NM_017431.2 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:66521920 C>T maps to NM_212472.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr17:66511602 C>T maps to NM_212472.1 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr17:66526059 G>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:751130 C>T maps to NM_002735.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:720251 G>A maps to NM_002735.2 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:48789131 G>A maps to NM_004157.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:106797672 C>T maps to NM_002736.2 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:106786831 G>T maps to NM_002736.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:64738868 C>T maps to NM_002737.2 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:64785021 G>A maps to NM_002737.2 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:64637477 C>T maps to NM_002737.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:64784983 C>T maps to NM_002737.2 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:64637477 C>A maps to NM_002737.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:64734895 C>T maps to NM_002737.2 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:64637477 C>T maps to NM_002737.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr17:64641504 C>T maps to NM_002737.2 C135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr16:24166124 C>T maps to NM_002738.6 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:23999907 C>T maps to NM_002738.6 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:24192239 C>T maps to NM_002738.6 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:23847588 G>A maps to NM_002738.6 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:24226094 C>A maps to NM_002738.6 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:24226001 C>T maps to NM_002738.6 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:24196836 C>T maps to NM_002738.6 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr16:24166138 G>A maps to NM_002738.6 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:53223210 G>A maps to NM_212539.1 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:53213608 G>A maps to NM_212539.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:53226260 C>T maps to NM_212539.1 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:53212455 C>T maps to NM_212539.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:53215467 C>T maps to NM_212539.1 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr3:53223175 G>T maps to NM_212539.1 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:53213677 C>T maps to NM_212539.1 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:6340746 G>T maps to NM_145040.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr19:54410064 C>T maps to NM_002739.3 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:54401295 G>A maps to NM_002739.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:54406391 G>A maps to NM_002739.3 E547E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:54401761 C>T maps to NM_002739.3 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:54385825 G>A maps to NM_002739.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:54395021 G>A maps to NM_002739.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:54387472 C>T maps to NM_002739.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr19:54401301 A>G maps to NM_002739.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr19:54394976 T>C maps to NM_002739.3 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:54410013 G>A maps to NM_002739.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:54392932 C>T maps to NM_002739.3 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:170009652 G>A maps to NM_002740.5 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:169998013 G>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:169998103 T>A maps to NM_002740.5 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:169981206 A>G maps to NM_002740.5 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:170013720 C>T maps to NM_002740.5 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:169981206 A>G maps to NM_002740.5 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr3:169981206 A>G maps to NM_002740.5 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:169981206 A>G maps to NM_002740.5 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr10:6470303 G>A maps to NM_006257.2 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr10:6483995 G>A maps to NM_006257.2 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:6504266 G>A maps to NM_006257.2 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:11558372 A>G maps to ENST00000436195 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:11559764 G>A maps to ENST00000436195 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:2116138 T>C did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:1986897 C>T maps to NM_002744.4 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:2082230 C>T maps to NM_002744.4 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:1986918 C>T maps to NM_002744.4 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:30133033 T>C maps to NM_002742.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:30100050 G>A maps to NM_002742.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr14:30066718 G>T maps to NM_002742.2 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr14:30105545 G>A maps to NM_002742.2 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr14:30046613 C>A maps to NM_002742.2 E857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:30105512 G>A maps to NM_002742.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:30194877 G>A maps to NM_002742.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:30046617 G>A maps to NM_002742.2 I855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:30107996 C>T maps to NM_002742.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr14:30107996 C>T maps to NM_002742.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr14:30108046 C>A maps to NM_002742.2 G254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr14:30100023 C>T maps to NM_002742.2 W532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr19:47181776 G>A maps to ENST00000449438 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:47177911 C>T maps to ENST00000449438 V845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:47197381 C>T maps to ENST00000449438 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:47207522 C>T maps to ENST00000449438 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:37516507 G>T maps to NM_005813.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr2:37516507 G>A maps to NM_005813.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr2:37516582 A>G maps to NM_005813.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr2:37516507 G>T maps to NM_005813.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:37516582 A>G maps to NM_005813.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:48761937 A>G did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:48691356 G>A maps to NM_006904.6 G3860G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:48746883 A>C maps to NM_006904.6 S2674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr8:48706924 G>C maps to NM_006904.6 P3531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr8:48845642 G>A maps to NM_006904.6 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:48809736 G>A maps to NM_006904.6 F1194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:48762031 C>T maps to NM_006904.6 A2345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:48794517 G>A maps to NM_006904.6 L1638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:48811030 G>A maps to NM_006904.6 R1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:48794073 G>T maps to NM_006904.6 S1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:48772220 G>T maps to NM_006904.6 S2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:48801609 T>C maps to NM_006904.6 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:48774661 G>A maps to NM_006904.6 I1981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:48790379 A>G maps to NM_006904.6 P1755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr8:48846523 C>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:48842410 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:48846614 T>G maps to NM_006904.6 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:48694806 A>C maps to NM_006904.6 L3801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:48869804 C>A maps to NM_006904.6 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr8:48746757 T>C maps to NM_006904.6 K2716K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:48716019 T>A maps to NM_006904.6 K3256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr8:48772312 A>G maps to NM_006904.6 P2021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr8:48841675 A>C maps to NM_006904.6 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:48690330 G>A maps to NM_006904.6 H3985H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:48840345 G>A maps to NM_006904.6 Y748Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr8:48744476 G>T maps to NM_006904.6 G2720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr8:48811085 G>A maps to NM_006904.6 R1136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr8:48746757 T>C maps to NM_006904.6 K2716K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr8:48794003 A>G maps to NM_006904.6 A1679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr8:48842568 C>T maps to NM_006904.6 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr8:48846523 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr10:53822298 A>G maps to NM_001098512.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:54048726 T>C maps to NM_001098512.1 N608N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr10:54050007 A>G maps to NM_001098512.1 E625E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:53921667 G>T maps to NM_001098512.1 G326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr4:82125931 T>A maps to NM_006259.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:82096076 A>G maps to NM_006259.1 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:82065387 C>T maps to NM_006259.1 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr4:82056365 G>T maps to NM_006259.1 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr4:82125795 G>A maps to NM_006259.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr4:82125877 C>T maps to NM_006259.1 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr4:82065432 T>C maps to NM_006259.1 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr4:82065432 T>C maps to NM_006259.1 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:179300970 G>A maps to NM_003690.4 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:179296855 G>A maps to NM_003690.4 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr2:179308054 T>C maps to NM_003690.4 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr2:179308054 T>C maps to NM_003690.4 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr2:179300870 C>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:179308056 C>A maps to NM_003690.4 G151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:102040047 C>A maps to NM_024653.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:76062797 G>A maps to NM_004705.2 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:76063234 A>C maps to NM_004705.2 L320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:76063308 G>A maps to NM_004705.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:3592723 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:3533926 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:3533910 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:3592724 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:3573392 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:22290545 G>A maps to ENST00000397199 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:22294637 G>A maps to ENST00000397199 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:22294775 C>T maps to ENST00000397199 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:238475293 T>C maps to NM_015893.1 H26H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr10:120353838 G>A maps to NM_004248.2 H306H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:120353877 C>T maps to NM_004248.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:120353835 G>A maps to NM_004248.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr10:120354471 C>T maps to NM_004248.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr5:35089685 G>A maps to NM_000949.4 L13L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CM-5864-01A-01D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:11374865 G>T maps to NM_002761.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:11370098 G>T maps to ENST00000435245 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:50187292 C>A maps to NM_001536.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:50185258 C>T maps to NM_001536.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr19:50185288 T>C maps to NM_001536.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr4:148591816 C>T maps to NM_138364.2 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr4:148579081 A>T maps to NM_138364.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:148579068 C>A maps to NM_138364.2 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:148605057 C>A maps to NM_138364.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:148575156 C>A maps to NM_138364.2 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:148594195 G>A maps to NM_138364.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr4:148575061 A>G maps to NM_138364.2 D662D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr4:148594892 A>G maps to NM_138364.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr21:48069572 C>T maps to NM_206962.1 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr11:20424503 C>T maps to NM_005788.3 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr11:20424473 C>T maps to NM_005788.3 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:23394138 G>T maps to NM_006109.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:23394129 G>T maps to NM_006109.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:107599375 C>G maps to NM_018137.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:107599777 A>G maps to NM_018137.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:107599897 C>A maps to NM_018137.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:107599879 C>T maps to NM_018137.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:107600333 C>T maps to NM_018137.2 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:107600356 G>A maps to NM_018137.2 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr1:107600299 G>A maps to NM_018137.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr16:68373382 C>T maps to NM_019023.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:3686079 C>T maps to NM_019854.3 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:3600841 G>A maps to NM_019854.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:3678728 C>T maps to NM_019854.3 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:3662818 C>T maps to NM_019854.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr12:3692261 G>A maps to NM_019854.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr20:4705652 C>T maps to NM_012409.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:4705274 G>A maps to NM_012409.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr20:4680468 C>T maps to NM_001080123.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr20:4680288 C>T maps to NM_001080123.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:27031808 C>T maps to ENST00000415329 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:27031031 C>T maps to ENST00000415329 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr20:33764133 C>A maps to NM_006404.3 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:33764232 C>T maps to NM_006404.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr22:18918567 G>A maps to NM_016335.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr22:18904464 G>A maps to NM_016335.4 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:36303770 C>T maps to NM_021232.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr19:36303629 G>A maps to NM_021232.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:110996680 C>T maps to NM_032414.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:110996642 C>T maps to NM_032414.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:68873204 C>T maps to NM_138964.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr2:68882419 G>A maps to NM_138964.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:68882254 C>T maps to NM_138964.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:68882143 C>T maps to NM_138964.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:68882131 C>T maps to NM_138964.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr2:68882176 C>T maps to NM_138964.2 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:68882077 C>T maps to NM_138964.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:68882254 C>A maps to NM_138964.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr20:5282946 A>G maps to NM_144773.2 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr20:5294760 G>T maps to NM_144773.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr4:71275251 A>G maps to NM_021225.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:71275428 T>C maps to NM_021225.4 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr4:71275273 C>T maps to NM_021225.4 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr4:71275251 A>G maps to NM_021225.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr4:71275722 C>A maps to NM_021225.4 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:16034997 T>G maps to NM_006017.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr4:15992901 G>A maps to NM_006017.2 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:15985957 C>T maps to NM_006017.2 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr4:16010627 G>A maps to NM_006017.2 N415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr4:15992901 G>A maps to NM_006017.2 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr4:15992901 G>T maps to NM_006017.2 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:95952586 C>A maps to NM_144707.2 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:95945718 C>T maps to NM_144707.2 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:95940474 C>A maps to NM_144707.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:95945631 C>T maps to NM_144707.2 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:95945745 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:95941835 C>T maps to NM_144707.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:95940437 G>A maps to NM_144707.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:177421250 C>T maps to NM_006261.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:93646114 G>T maps to NM_000313.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:93619764 C>A maps to NM_000313.3 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:93593244 A>G maps to NM_000313.3 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:93646240 C>T maps to NM_000313.3 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:214178536 G>A maps to NM_002763.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:214209053 C>T maps to NM_002763.3 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr1:214171515 C>T maps to NM_002763.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:214171554 C>T maps to NM_002763.3 C559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:214171554 C>T maps to NM_002763.3 C559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:113826076 C>T maps to ENST00000342783 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr13:113826334 G>A maps to ENST00000342783 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr13:113826017 G>T maps to ENST00000342783 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:13642284 G>A maps to NM_003675.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr10:13652103 C>T maps to NM_003675.3 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr11:60658670 G>A maps to NM_014502.4 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:60665369 C>T maps to NM_014502.4 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:150297543 C>T maps to NM_004698.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr1:150318497 C>T maps to NM_004698.2 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:54627238 C>A maps to NM_015629.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:109242473 T>C maps to NM_018061.2 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:109238328 G>A maps to NM_018061.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:116038952 G>A maps to NM_004697.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr9:116045416 G>A maps to NM_004697.3 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:116053296 G>A did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:116038035 C>T maps to NM_004697.3 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:116050499 G>A maps to NM_004697.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr9:116045693 C>T maps to NM_004697.3 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:116053804 G>A maps to NM_004697.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:116053843 C>T maps to NM_004697.3 H491H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr2:153533259 G>A maps to ENST00000410080 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:50025206 A>C maps to NM_001031698.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:50037534 G>A maps to NM_001031698.1 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:4057422 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:4032668 G>A maps to NM_003913.4 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr6:4057315 T>C maps to NM_003913.4 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr20:62616297 C>A maps to NM_012469.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:62630971 C>T maps to NM_012469.3 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:62658399 C>T maps to NM_012469.3 C698C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:1576725 G>A maps to NM_006445.3 C1194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:1559772 G>A maps to NM_006445.3 F1902F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr17:1565306 G>C maps to NM_006445.3 S1305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr17:1563791 G>A maps to NM_006445.3 L1573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:1559772 G>A maps to NM_006445.3 F1902F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:1577959 C>T maps to NM_006445.3 T1025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:1564594 C>T maps to NM_006445.3 W1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:49690677 C>T maps to ENST00000451891 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:49690216 C>T maps to ENST00000451891 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:42672324 C>T maps to NM_000322.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr6:42672303 G>A maps to NM_000322.4 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:106888483 A>G did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:106890855 C>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:106888530 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:106885618 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:106888483 A>G did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:106888483 A>G did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:106888531 T>C did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:106888531 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:106888530 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:18066475 G>T maps to NM_175886.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:18067213 G>A maps to NM_175886.2 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:12827403 G>T did not map to a codon.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr23:12838885 G>T did not map to a codon.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr23:12817461 G>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:12817489 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:12828248 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:12837762 C>T did not map to a codon.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr23:12838892 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:74326631 T>C maps to NM_002766.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:18827293 C>T maps to NM_002767.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:57270932 C>T maps to NM_018304.3 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:50105135 C>T maps to NM_020719.1 D1578D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:50103031 G>A maps to NM_020719.1 L1394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:50128734 C>A maps to NM_020719.1 G1994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:30666046 C>T maps to NM_024031.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr16:30667433 T>C maps to NM_024031.2 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:30666088 G>T maps to NM_024031.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:30664261 C>T maps to NM_024031.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:120021767 G>A maps to NM_016644.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:120022337 G>A maps to NM_016644.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:120021785 T>G maps to NM_016644.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:42814421 G>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:5783579 G>A maps to NM_001134316.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr19:5783213 G>A maps to NM_001134316.1 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:138724474 T>C maps to NM_001134659.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:138724951 G>A maps to NM_001134659.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:138763087 G>A maps to NM_001134657.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:138762949 T>C maps to NM_001134657.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:138762970 C>T maps to NM_001134657.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:855636 G>A maps to NM_001013638.1 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:30530208 C>T maps to NM_025263.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr12:10999789 G>A maps to NM_007244.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:10999789 G>A maps to NM_007244.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr22:45182361 G>T maps to ENST00000352766 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:176882785 G>A maps to NM_001174101.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:126860496 G>A maps to ENST00000330542 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:37312474 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:37312850 C>T did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:37285168 A>G did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:37285130 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr23:37312394 T>C did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:37285166 A>G did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:150869277 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:150868494 C>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:150869276 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:150869301 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:150869190 A>G did not map to a codon.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr23:150869436 G>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:150869330 C>T did not map to a codon.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr11:32858355 G>T maps to NM_024081.4 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:32874925 G>A maps to NM_024081.4 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr6:32118648 C>T maps to NM_030651.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:32118192 C>T maps to NM_030651.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:9991196 G>A maps to NM_207351.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:9990857 G>A maps to NM_207351.3 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:9989229 G>A maps to NM_207351.3 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:132482933 C>T maps to NM_016307.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:132481651 C>T maps to NM_016307.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:142459798 C>T maps to ENST00000486171 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:119237392 A>G maps to NM_003619.3 C412C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:119239565 C>A maps to NM_003619.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:27220714 C>T maps to NM_005865.3 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr6:27216930 A>G maps to NM_005865.3 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:27219656 G>A maps to NM_005865.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:27220720 C>T maps to NM_005865.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:27222622 T>C maps to NM_005865.3 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:2868785 G>A maps to NM_006799.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:2871109 C>T maps to NM_006799.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:86518862 G>T maps to NM_007173.4 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:2765789 G>A maps to NM_031948.3 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr6:84233342 G>A maps to NM_153362.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:84234053 G>A maps to NM_153362.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr6:84234347 C>T maps to NM_153362.2 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:84233480 G>A maps to NM_153362.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:84234335 T>C maps to NM_153362.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:31153079 C>A maps to NM_173502.3 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:31152853 G>A maps to NM_173502.3 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:31152812 C>T maps to NM_173502.3 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:31151822 G>T maps to NM_173502.3 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr16:31160545 G>A maps to NM_173502.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:141537729 G>A maps to NM_001008270.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:141537834 G>A maps to NM_001008270.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:228003839 G>A maps to NM_183062.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr1:228003878 C>T maps to NM_183062.2 Y79Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:58318583 G>A maps to NM_001080492.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:58314352 C>T maps to NM_001080492.1 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:58327693 C>T maps to NM_001080492.1 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:58314586 G>A maps to NM_001080492.1 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr16:58314145 G>A maps to NM_001080492.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr8:10388960 C>T maps to NM_198464.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:10396128 C>T maps to NM_198464.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:10387143 C>T maps to NM_198464.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:31144701 G>A maps to NM_002773.3 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr19:694911 G>A maps to NM_214710.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:691950 C>T maps to NM_214710.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:55965737 C>T maps to NM_173814.4 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:55965575 G>A maps to NM_173814.4 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:55971481 A>G did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr15:55965590 C>T maps to NM_173814.4 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:56032846 C>A maps to NM_173814.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr15:55974600 G>A maps to NM_173814.4 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr15:55974688 A>G maps to NM_173814.4 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:151006577 G>A maps to NM_021222.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:151006577 G>A maps to NM_021222.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:79322929 G>A maps to NM_015225.2 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:79259688 G>T maps to NM_015225.2 V2898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:79253133 C>T maps to NM_015225.2 A2933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:79461485 C>T maps to NM_015225.2 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:79322442 C>A maps to NM_015225.2 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:79323565 A>G maps to NM_015225.2 N1208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:79319713 A>C maps to NM_015225.2 S2492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr9:79321309 C>T maps to NM_015225.2 Q1960Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:79270372 G>A maps to NM_015225.2 G2774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr19:40902611 C>T maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr19:40903808 G>A maps to NM_181882.2 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:40900016 C>T maps to NM_181882.2 R1414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:40902611 C>T maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr19:40902965 C>A maps to NM_181882.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:40899941 G>A maps to NM_181882.2 S1439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr19:40902611 C>G maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:40900052 G>A maps to NM_181882.2 P1402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:40902611 C>G maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr19:40902611 C>G maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:40902611 C>G maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:73579480 A>T maps to ENST00000373120 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr10:73579612 C>A maps to ENST00000373120 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr10:73581659 A>G maps to ENST00000373120 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr10:104171502 G>A maps to NM_002779.3 R635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:104171502 G>A maps to NM_002779.3 R635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr10:104171956 C>T maps to NM_002779.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:139216446 C>T maps to NM_032289.2 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:139193235 G>A maps to NM_032289.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr5:139218290 C>T maps to NM_032289.2 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr5:139193007 C>T maps to NM_032289.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:18393372 C>T maps to ENST00000440756 S1010S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:18413828 T>A maps to ENST00000440756 K942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:113943595 G>A maps to NM_012455.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr2:113953762 G>A maps to NM_012455.2 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:113953762 G>A maps to NM_012455.2 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr2:113958986 C>T maps to NM_012455.2 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr2:113950109 C>T maps to NM_012455.2 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr2:113940416 C>T maps to NM_012455.2 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:227083195 G>A maps to ENST00000391872 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr1:227077739 C>T maps to ENST00000391872 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:227071563 C>T maps to ENST00000391872 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:227071479 G>A maps to ENST00000391872 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:227076733 C>T maps to ENST00000391872 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr19:36237708 G>A maps to NM_172341.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr19:36237685 C>A maps to NM_172341.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:43372256 G>A maps to NM_006905.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:43382149 C>T maps to NM_006905.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:43528842 G>A maps to ENST00000306308 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:43585207 G>A maps to ENST00000449000 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:43585114 G>A maps to ENST00000449000 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr19:43576056 T>A maps to NM_031246.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:43233278 G>T maps to NM_021016.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:43708377 C>T maps to NM_002780.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:43708212 G>A maps to NM_002780.3 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr19:43679415 G>A maps to ENST00000270059 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:43420601 G>A maps to NM_002782.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr19:43411113 A>C maps to NM_002782.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr19:43414858 C>T maps to NM_002782.3 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr19:43430715 G>A maps to NM_002783.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:43268067 G>A maps to NM_182707.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:43268242 G>A maps to NM_182707.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:43268100 C>A maps to NM_182707.2 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:43762594 G>A maps to NM_002784.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr19:43766249 G>A maps to NM_002784.3 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr9:15466798 G>A maps to NM_001128217.1 N493N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr9:15468733 T>C maps to NM_001128217.1 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:87060822 C>T maps to ENST00000276616 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr8:87076289 T>A maps to ENST00000276616 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:14535994 G>A maps to NM_148976.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr7:42961509 T>C maps to NM_002787.4 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr7:42964386 C>T maps to NM_002787.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr14:58737186 C>G maps to NM_002788.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:78839017 T>C maps to NM_002789.4 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:78841256 G>T maps to NM_002789.4 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:109955743 A>G maps to NM_002790.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:109954764 A>G maps to NM_002790.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:23758808 C>T maps to NM_144662.2 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:23724531 C>T maps to NM_144662.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr6:170846363 T>C maps to NM_002793.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:170858119 C>T maps to NM_002793.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr16:67969882 C>T maps to NM_002801.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr16:67969530 A>G maps to NM_002801.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:23511931 C>T maps to NM_001099780.1 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:36070881 A>G maps to NM_002794.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:151372582 A>G maps to NM_002796.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr1:151372580 C>A maps to NM_002796.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:23504084 C>T maps to NM_002797.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr14:23495356 G>A maps to NM_002797.3 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:23502760 G>A maps to NM_002797.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:4701075 C>T maps to NM_002798.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:4700982 A>G maps to NM_002798.1 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:32810026 G>A maps to NM_148919.3 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:32809440 C>T maps to NM_148919.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:32825851 C>T maps to NM_002800.4 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:103008410 T>C maps to NM_002803.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr11:47444452 T>C maps to NM_002804.4 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:40729484 G>A maps to NM_016556.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:61906924 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr17:61906876 A>G maps to NM_002805.5 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:61909088 G>A maps to NM_002805.5 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:61909273 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:53175043 G>T maps to NM_002806.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:232018348 C>T maps to NM_002807.3 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:231927366 T>C maps to NM_002807.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:231943446 T>C maps to NM_002807.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:107328301 C>A did not map to a codon.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr23:107332064 A>G did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:107331190 T>C did not map to a codon.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr23:107328299 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr23:107328301 C>A did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr17:30791553 T>C maps to NM_002815.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:30806354 G>A maps to NM_002815.2 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:30791553 T>C maps to NM_002815.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr17:65362551 T>A maps to NM_002816.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:65346353 G>A maps to NM_002816.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:247371 A>G maps to NM_002817.3 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:247371 A>G maps to NM_002817.3 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr2:162242081 G>A maps to NM_005805.4 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:184026512 C>A maps to NM_002808.3 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:184020169 C>T maps to NM_002808.3 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:184025224 C>T maps to NM_002808.3 N705N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:184020259 A>G maps to NM_002808.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:151236494 C>T maps to ENST00000368881 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:151237889 G>T maps to ENST00000368881 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr9:123595613 A>T maps to NM_005047.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:123589061 G>A maps to NM_005047.2 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:64008050 G>A maps to ENST00000492933 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:64005105 C>T maps to ENST00000492933 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:63996421 C>T maps to ENST00000492933 W417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:64004299 A>G maps to ENST00000492933 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:74339390 C>T maps to NM_002811.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:74338232 C>T maps to NM_002811.3 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr16:74335474 G>A maps to NM_002811.3 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:38869972 G>A maps to NM_002812.4 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:38866831 C>T maps to NM_002812.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr12:122326901 T>C did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:122353844 G>A maps to NM_002813.4 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:24606927 G>T maps to NM_176783.1 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:24606745 A>G maps to NM_176783.1 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr17:40991327 C>T maps to NM_176863.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr17:40990153 C>T maps to NM_176863.1 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:54159885 A>G maps to NM_014614.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:54115119 A>C maps to NM_014614.2 L1465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:54122777 C>A maps to NM_014614.2 E1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr21:40555245 C>T maps to NM_003720.2 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr21:40552306 A>G maps to NM_003720.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:1608924 G>A maps to NM_001134340.1 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:31107549 C>A maps to NM_014068.2 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:31105880 C>T maps to NM_014069.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:20304417 C>T maps to NM_001042414.1 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:20315768 C>A maps to NM_001042414.1 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:56084927 G>A maps to NM_004577.3 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr7:56079455 T>C maps to NM_004577.3 *226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:6375830 G>A maps to NM_004158.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:124740212 T>C did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:77320233 G>A maps to NM_003978.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:77328146 C>A maps to NM_003978.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:43591166 G>A maps to NM_024430.3 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:28476872 C>T maps to NM_001164721.1 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:72338239 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:806462 G>T maps to NM_002819.4 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:808666 C>T maps to NM_002819.4 Y456Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:804929 C>T maps to NM_002819.4 H236H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:805176 C>T maps to NM_002819.4 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:97235265 T>C maps to ENST00000370197 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr7:99030963 C>T maps to NM_001198879.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:99027399 G>A maps to NM_001198879.1 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:99017679 C>T maps to NM_001198879.1 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:71630867 C>T maps to NM_024754.3 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:71654185 C>T maps to NM_024754.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr9:98248085 A>G maps to NM_000264.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr9:98244269 C>T maps to NM_000264.3 W236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr9:98268696 C>T maps to NM_000264.3 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:98240450 G>A maps to NM_000264.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr9:98229536 G>T maps to NM_000264.3 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr9:98220429 G>A maps to NM_000264.3 N1011N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr9:98209655 A>T maps to NM_000264.3 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr9:98229452 T>C maps to NM_000264.3 E835E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr9:98231266 C>T maps to NM_000264.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:98221987 G>A maps to NM_000264.3 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:98229461 G>T maps to NM_000264.3 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:98231320 C>T maps to NM_000264.3 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:98229497 G>A maps to NM_000264.3 Y820Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:98212179 A>G maps to NM_000264.3 V1164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:98221903 G>T maps to NM_000264.3 Y955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr9:98242752 A>G maps to NM_000264.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr9:98242782 C>T maps to NM_000264.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:98231209 G>T maps to NM_000264.3 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:98231248 G>A maps to NM_000264.3 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:98240432 T>C maps to NM_000264.3 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:98241403 G>A maps to NM_000264.3 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:98248145 T>C maps to NM_000264.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:98248103 T>C maps to NM_000264.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:98231176 T>C maps to NM_000264.3 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr9:98248103 T>C maps to NM_000264.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr9:98242752 A>G maps to NM_000264.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr9:98248085 A>G maps to NM_000264.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:98221882 T>C maps to NM_000264.3 R962R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr9:98248103 T>C maps to NM_000264.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:98209661 G>A maps to NM_000264.3 S1292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:98231232 C>A maps to NM_000264.3 E684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:98239879 T>C maps to NM_000264.3 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr9:98242752 A>G maps to NM_000264.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr9:98241300 C>T maps to NM_000264.3 W399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr9:98231233 G>T maps to NM_000264.3 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr9:98231350 G>T maps to NM_000264.3 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr9:98244265 T>C maps to NM_000264.3 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:98231209 G>T maps to NM_000264.3 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr9:98239130 T>C maps to NM_000264.3 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr9:98242752 A>G maps to NM_000264.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr9:98248147 G>A maps to NM_000264.3 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr9:98244310 A>G maps to NM_000264.3 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr9:98231107 G>A maps to NM_000264.3 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:98215758 C>T did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr9:98248147 G>A maps to NM_000264.3 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr9:98220408 C>T maps to NM_000264.3 W1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr9:98231074 A>G maps to NM_000264.3 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr9:98212179 A>G maps to NM_000264.3 V1164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr9:98248145 T>C maps to NM_000264.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr9:98209619 G>T maps to NM_000264.3 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr9:98248025 G>T maps to NM_000264.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr9:98231200 C>T maps to NM_000264.3 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr9:98241415 G>A maps to NM_000264.3 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:98229623 C>T maps to NM_000264.3 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:98231233 G>T maps to NM_000264.3 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr9:98239130 T>C maps to NM_000264.3 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr9:98248145 T>A maps to NM_000264.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr9:98241430 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:98231272 G>A maps to NM_000264.3 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:45293541 G>A maps to NM_003738.4 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:23398362 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:23411371 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:23411858 A>G did not map to a codon.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr23:23412187 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:23411019 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:23412222 A>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:23411076 A>G did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:23411059 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:23411303 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:23411471 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:23412043 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr23:23397821 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:23410662 G>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:23411384 C>T did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:23411675 G>A did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:23411775 C>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:23410772 G>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:23411371 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:23411775 C>T did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:23411775 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:23397859 G>A did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:23410995 C>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:23397937 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:23411676 T>C did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:23397857 C>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:11589913 G>A maps to NM_020780.1 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:11596517 C>T maps to NM_020780.1 F1318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:11589889 G>T maps to NM_020780.1 V992V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:27702774 G>A maps to NM_001034842.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:27702555 G>A maps to NM_001034842.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr10:27688020 A>G maps to NM_001034842.3 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:27687465 G>T maps to NM_001034842.3 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:27702369 G>A maps to NM_001034842.3 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr10:27702945 C>T maps to NM_001034842.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr10:27702717 G>A maps to NM_001034842.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:42893186 C>T maps to NM_138296.2 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:42893065 C>T maps to NM_138296.2 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:97307441 C>T maps to NM_014754.1 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:97321793 C>T maps to NM_014754.1 Y339Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:97299301 C>T maps to NM_014754.1 F123F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CM-6675-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:489685 C>T maps to NM_030783.1 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:490035 G>A maps to NM_030783.1 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:489906 G>A maps to NM_030783.1 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr10:89692896 A>G maps to NM_000314.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr10:89653839 C>A maps to NM_000314.4 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr10:89692911 T>C maps to NM_000314.4 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr10:89717736 A>G maps to NM_000314.4 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr10:89692890 A>G maps to NM_000314.4 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr10:89692902 A>G maps to NM_000314.4 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr10:89717655 C>A maps to NM_000314.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:89624270 A>G maps to NM_000314.4 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:89653782 T>C maps to NM_000314.4 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:89717727 T>C maps to NM_000314.4 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:89720661 T>C maps to NM_000314.4 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr10:89692896 A>G maps to NM_000314.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr10:89692962 A>G maps to NM_000314.4 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr10:89717755 C>T maps to NM_000314.4 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr10:89717713 T>C maps to NM_000314.4 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr10:89720823 T>C maps to NM_000314.4 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr10:89692857 A>G maps to NM_000314.4 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr10:89624244 G>T maps to NM_000314.4 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr10:89720727 A>G maps to NM_000314.4 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr10:89692839 T>C maps to NM_000314.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr10:89725108 T>C maps to NM_000314.4 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr10:89717688 C>T maps to NM_000314.4 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr10:89692776 A>G maps to NM_000314.4 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr10:89692959 A>G maps to NM_000314.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:89717664 A>G maps to NM_000314.4 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:89711888 C>T maps to NM_000314.4 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:89717662 G>T maps to NM_000314.4 G230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:89690838 T>C maps to NM_000314.4 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:89692963 G>T maps to NM_000314.4 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr10:89692893 T>C maps to NM_000314.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:89685308 C>A maps to NM_000314.4 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr10:89711897 G>A maps to NM_000314.4 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:89720743 G>T maps to NM_000314.4 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr10:89717712 G>A maps to NM_000314.4 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr10:89720823 T>C maps to NM_000314.4 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr10:89624243 A>G maps to NM_000314.4 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr10:89692839 T>C maps to NM_000314.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr10:89692854 T>C maps to NM_000314.4 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:89720876 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr10:89692908 T>C maps to NM_000314.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:89692969 C>T maps to NM_000314.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:89692995 C>A maps to NM_000314.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:89711948 A>G maps to NM_000314.4 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:89653863 A>G maps to NM_000314.4 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:89717733 C>A maps to NM_000314.4 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr10:89624255 C>T maps to NM_000314.4 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:89711993 A>G maps to NM_000314.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr10:89692959 A>G maps to NM_000314.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr10:89692929 T>C maps to NM_000314.4 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr10:89692881 T>C maps to NM_000314.4 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr10:89692788 A>G maps to NM_000314.4 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr10:89720760 C>T maps to NM_000314.4 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:89692836 T>C maps to NM_000314.4 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:89692848 G>A maps to NM_000314.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:89692855 G>T maps to NM_000314.4 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:89720760 C>T maps to NM_000314.4 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr10:89653818 A>G maps to NM_000314.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr10:89717679 A>G maps to NM_000314.4 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr10:89692824 C>A maps to NM_000314.4 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr10:89692890 A>G maps to NM_000314.4 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr10:89717661 A>T maps to NM_000314.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr10:89692998 A>G maps to NM_000314.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:89717776 G>T did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr10:89653818 A>G maps to NM_000314.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr10:89720661 T>C maps to NM_000314.4 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr10:89725162 C>T maps to NM_000314.4 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:89653780 G>T did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:89653809 A>G maps to NM_000314.4 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr10:89711948 A>G maps to NM_000314.4 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr10:89720661 T>C maps to NM_000314.4 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr10:89720719 G>T maps to NM_000314.4 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:89692839 T>C maps to NM_000314.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:89692998 A>G maps to NM_000314.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr10:89720775 A>G maps to NM_000314.4 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr10:89653860 A>G maps to NM_000314.4 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr10:89692902 A>G maps to NM_000314.4 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr10:89653815 T>C maps to NM_000314.4 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr10:89720775 A>G maps to NM_000314.4 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr10:89692848 G>A maps to NM_000314.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:89692830 T>C maps to NM_000314.4 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:89717628 C>A maps to NM_000314.4 C218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr10:89653857 T>C maps to NM_000314.4 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr10:89711885 T>C maps to NM_000314.4 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:89685272 T>C maps to NM_000314.4 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:89692881 T>C maps to NM_000314.4 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr10:89653857 T>C maps to NM_000314.4 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr10:89653857 T>C maps to NM_000314.4 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr10:89692863 C>T maps to NM_000314.4 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr10:89653807 G>T maps to NM_000314.4 G36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr10:89653833 C>T maps to NM_000314.4 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr10:89711900 C>T maps to NM_000314.4 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr10:89653815 T>C maps to NM_000314.4 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr10:89692857 A>G maps to NM_000314.4 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr10:89692857 A>G maps to NM_000314.4 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr10:89720673 A>T maps to NM_000314.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr10:89692911 T>C maps to NM_000314.4 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr10:89653819 G>T maps to NM_000314.4 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr10:89653818 A>G maps to NM_000314.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr10:89692998 A>G maps to NM_000314.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:89624270 A>G maps to NM_000314.4 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:89717661 A>G maps to NM_000314.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr10:89717679 A>G maps to NM_000314.4 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr10:89624270 A>G maps to NM_000314.4 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr10:89692830 T>C maps to NM_000314.4 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr10:89692902 A>G maps to NM_000314.4 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr10:89720772 T>A maps to NM_000314.4 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr10:89692959 A>G maps to NM_000314.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr10:89624244 G>T maps to NM_000314.4 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr10:89720710 G>T maps to NM_000314.4 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr10:89720743 G>T maps to NM_000314.4 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr10:89720862 T>C maps to NM_000314.4 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr10:89624276 A>G maps to NM_000314.4 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr10:89692839 T>C maps to NM_000314.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr10:89692933 T>C maps to NM_000314.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr10:89624292 T>C maps to NM_000314.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr10:89653863 A>T maps to NM_000314.4 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr10:89725162 C>A maps to NM_000314.4 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr10:89692836 T>C maps to NM_000314.4 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr10:89692983 G>A maps to NM_000314.4 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr10:89692953 A>G maps to NM_000314.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr10:89720727 A>G maps to NM_000314.4 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr10:89720876 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:89720692 G>T maps to NM_000314.4 G282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr10:89725210 A>G maps to NM_000314.4 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr10:89692839 T>C maps to NM_000314.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr10:89717608 G>T did not map to a codon.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr10:89692843 C>T maps to NM_000314.4 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr10:89624273 T>C maps to NM_000314.4 Y16Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr10:89725051 G>A maps to NM_000314.4 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr10:89720673 A>G maps to NM_000314.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr10:89692899 G>A maps to NM_000314.4 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr10:89653818 A>G maps to NM_000314.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:89690832 A>G maps to NM_000314.4 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:89692896 A>G maps to NM_000314.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr10:89692893 T>C maps to NM_000314.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr10:89692983 G>A maps to NM_000314.4 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr10:89692812 A>G maps to NM_000314.4 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr10:89624244 G>T maps to NM_000314.4 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr10:89717664 A>G maps to NM_000314.4 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr10:89717608 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:89720649 G>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:89720661 T>C maps to NM_000314.4 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:89692980 T>C maps to NM_000314.4 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr10:89711912 T>C maps to NM_000314.4 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr10:89720862 T>A maps to NM_000314.4 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr10:16528557 C>T maps to NM_030664.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:16547114 C>T maps to NM_030664.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:16528505 T>C maps to NM_030664.3 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:23482747 C>T maps to NM_178161.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:23481500 C>T maps to NM_178161.2 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr14:52734923 G>A maps to NM_000953.2 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:52734923 G>A maps to NM_000953.2 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr14:52734923 G>A maps to NM_000953.2 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr14:52734923 G>A maps to NM_000953.2 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:139874449 C>T maps to ENST00000224167 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:71512609 G>A maps to ENST00000354608 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:71418654 C>A maps to NM_198718.1 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:40681127 C>A maps to NM_000958.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:130883507 G>A maps to NM_025072.5 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:78958622 G>A maps to NM_000959.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:79002107 T>A maps to NM_000959.3 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:117492111 G>A maps to NM_020440.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr1:117484583 C>T maps to NM_020440.2 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr1:117509632 G>A maps to NM_020440.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:117491874 C>A maps to NM_020440.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:117492009 G>A maps to NM_020440.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:117484373 G>A maps to NM_020440.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:117487547 C>T maps to NM_020440.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:117484439 C>T maps to NM_020440.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:117484610 C>T maps to NM_020440.2 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr20:48166608 G>T maps to NM_000961.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr20:48129709 G>A maps to NM_000961.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:48129636 C>A maps to NM_000961.3 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:48129709 G>A maps to NM_000961.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr9:114348375 C>T maps to NM_001146108.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr9:114348285 G>A maps to NM_001146108.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr9:114348381 C>T maps to NM_001146108.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr9:114341159 G>A maps to NM_001146108.1 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr9:125143818 C>A maps to NM_000962.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:125140781 C>T maps to NM_000962.2 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr9:125154672 C>T maps to NM_000962.2 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:125140223 C>A maps to NM_000962.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr9:125140731 C>A maps to NM_000962.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr1:186647483 G>T maps to NM_000963.2 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:186648219 G>A maps to NM_000963.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:186644504 T>C maps to NM_000963.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr11:13513969 A>T maps to NM_000315.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr11:13513969 A>T maps to NM_000315.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr11:13513969 A>T maps to NM_000315.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:46940794 G>A maps to NM_000316.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:49925726 A>G maps to NM_178449.3 *101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:209353742 G>T maps to NM_005048.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:209315504 T>G maps to NM_005048.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:209307187 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:209307091 G>T maps to NM_005048.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:209358128 G>A maps to NM_005048.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:28122397 G>A maps to ENST00000354417 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr8:141711061 T>C maps to NM_005607.4 E831E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:141771319 G>A maps to NM_005607.4 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr8:141711016 G>A maps to NM_005607.4 R846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:141810585 C>T maps to NM_005607.4 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr8:141727777 T>C maps to NM_005607.4 Q709Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr8:141711061 T>C maps to NM_005607.4 E831E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:141696771 G>A maps to NM_005607.4 R863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr8:141774360 A>G maps to NM_005607.4 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr8:141829028 G>A maps to NM_005607.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr8:141771319 G>A maps to NM_005607.4 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr8:27296584 G>T maps to NM_004103.3 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:27300394 C>T maps to NM_004103.3 D681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:27297898 C>T maps to NM_004103.3 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:27288487 C>T maps to NM_004103.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:43111254 C>A maps to NM_002821.3 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:43111212 C>T maps to NM_002821.3 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:43099777 A>G maps to NM_002821.3 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:6879329 A>G maps to NM_002824.4 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:50357982 C>T maps to NM_017432.3 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:50363247 C>T maps to NM_017432.3 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:64286868 G>A maps to NM_003463.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:96847537 T>C maps to ENST00000434261 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr10:17636321 G>A maps to NM_014241.3 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr15:65849120 G>A maps to NM_016395.2 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:65855133 A>C maps to NM_016395.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr9:21026622 G>T maps to NM_001010915.3 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr20:49197975 C>T maps to NM_002827.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr12:112926885 A>G maps to ENST00000392596 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:112926852 C>A maps to ENST00000392596 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:112924355 C>T maps to ENST00000392596 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr12:112888202 T>C maps to ENST00000392596 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr12:112888163 T>C maps to ENST00000392596 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr12:112888203 T>C maps to ENST00000392596 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr12:112888139 C>T maps to ENST00000392596 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:112888202 T>C maps to ENST00000392596 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr12:112888172 T>C maps to ENST00000392596 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr12:112926852 C>A maps to ENST00000392596 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:112891007 T>C maps to ENST00000392596 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:112888214 G>A maps to ENST00000392596 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr12:112926852 C>T maps to ENST00000392596 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr12:112915743 T>C maps to ENST00000392596 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr7:77268031 A>G maps to NM_002835.3 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr7:77268031 A>G maps to NM_002835.3 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:77265142 C>T maps to NM_002835.3 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:77214877 C>T maps to NM_002835.3 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:87706486 C>T maps to NM_080685.2 N2079N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:87655895 T>C maps to NM_080685.2 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:87728797 C>T maps to NM_080685.2 F2282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:87731070 C>T maps to NM_080685.2 G2416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:87653800 C>T maps to NM_080685.2 N580N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:87614799 C>T maps to NM_080685.2 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:87728978 C>T maps to NM_080685.2 R2343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:87692601 T>C maps to NM_080685.2 H1699H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:87692448 C>T maps to NM_080685.2 C1648C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:87724988 A>C maps to NM_080685.2 G2216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:87728797 C>T maps to NM_080685.2 F2282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:87686567 C>T maps to NM_080685.2 V1395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:87672194 G>A maps to NM_080685.2 A1028A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:87731088 C>T maps to NM_080685.2 T2422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr4:87680197 C>T maps to NM_080685.2 I1175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:87672007 A>C maps to NM_080685.2 A1012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:87728749 C>T maps to NM_080685.2 G2266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr4:87655895 T>A maps to NM_080685.2 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:214557901 G>A maps to NM_005401.4 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:214543009 G>A maps to NM_005401.4 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:214543009 G>A maps to NM_005401.4 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:214557180 C>A maps to NM_005401.4 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:214567074 G>A maps to NM_005401.4 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:214588069 C>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:214557490 G>T maps to NM_005401.4 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:214557997 C>T maps to NM_005401.4 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:214543009 G>A maps to NM_005401.4 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr1:214638038 C>T maps to NM_005401.4 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:214557412 C>T maps to NM_005401.4 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:131127348 G>A maps to NM_014369.3 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:131128830 C>T maps to NM_014369.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:12830940 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:12817258 C>A maps to NM_002828.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:88946361 C>T maps to NM_007039.3 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr14:88935310 A>G maps to NM_007039.3 T1115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr14:88935990 C>T maps to NM_007039.3 T1029T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr14:88935845 A>G maps to NM_007039.3 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr14:88946328 G>T maps to NM_007039.3 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:88935346 C>T maps to NM_007039.3 P1103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:88935843 T>C maps to NM_007039.3 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:88935310 A>C maps to NM_007039.3 T1115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr14:88945352 G>T maps to NM_007039.3 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:114380674 T>C maps to NM_015967.5 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr1:114372634 A>G maps to NM_015967.5 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:114377566 C>T maps to NM_015967.5 W620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr1:114401686 C>T maps to NM_015967.5 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:47446242 C>T maps to NM_015466.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr3:47452785 G>A maps to NM_015466.2 E1166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:47454432 C>T maps to NM_015466.2 Q1557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:47453361 C>T maps to NM_015466.2 T1326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr9:112144673 G>A maps to NM_002829.3 H812H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:112199204 C>T maps to NM_002829.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr9:112225660 C>A maps to NM_002829.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:112182812 C>A maps to NM_002829.3 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:112185043 C>A maps to NM_002829.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:112144728 T>G did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:112182878 G>A maps to NM_002829.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:120692534 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:120692412 C>T maps to NM_002830.2 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:120643418 T>C maps to NM_002830.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:120640133 T>C maps to NM_002830.2 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr2:120567545 T>C maps to NM_002830.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr2:120567545 T>C maps to NM_002830.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:120684185 A>G maps to NM_002830.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:18754171 C>T maps to NM_032781.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr11:18762158 C>T maps to NM_032781.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:7069508 G>A maps to ENST00000416215 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:7067209 C>T maps to ENST00000416215 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:7069308 G>A maps to ENST00000416215 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr12:7069323 G>A maps to ENST00000416215 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:7069092 C>T maps to ENST00000416215 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:7064536 G>A maps to ENST00000416215 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:202121701 G>A maps to ENST00000309017 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr15:75816632 G>T maps to NM_002833.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:75766052 G>T maps to NM_002833.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:75816632 G>A maps to NM_002833.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr15:75761307 C>T maps to NM_002833.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr15:75816632 G>A maps to NM_002833.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr15:75816632 G>T maps to NM_002833.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:75816632 G>A maps to NM_002833.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr20:3007782 G>A maps to NM_002836.3 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:2985770 C>T maps to NM_002836.3 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:2996517 C>T maps to NM_002836.3 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:3002007 T>C maps to NM_002836.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:2985781 C>T maps to NM_002836.3 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr12:70929803 C>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:70981005 C>A maps to NM_001109754.1 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:70963548 C>T maps to NM_001109754.1 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:70990063 C>T maps to NM_001109754.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr12:71016382 C>T maps to NM_001109754.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr12:70928615 G>A maps to NM_001109754.1 C2067C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:70956846 G>A maps to NM_001109754.1 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:198725091 C>T maps to ENST00000271610 Q1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:198721463 T>G maps to ENST00000271610 T1098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:198721736 A>G maps to ENST00000271610 R1115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:198687382 C>T maps to ENST00000271610 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:198675999 G>T maps to ENST00000271610 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:198718662 T>C maps to ENST00000271610 N1019N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:198725165 T>G maps to ENST00000271610 A1259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr1:198697499 A>G maps to ENST00000271610 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:198701436 G>A maps to ENST00000271610 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr1:198665961 T>C maps to ENST00000271610 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:198701654 G>A maps to ENST00000271610 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr1:198671561 A>T maps to ENST00000271610 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr9:8504330 A>G maps to NM_002839.3 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:8341947 G>A maps to NM_002839.3 I1564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:8375973 A>G maps to NM_002839.3 C1541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:8341701 G>A maps to NM_002839.3 L1646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:8465648 G>A maps to NM_002839.3 R1177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:8376626 G>A maps to NM_002839.3 R1496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:8500811 A>G maps to NM_002839.3 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:8504330 A>G maps to NM_002839.3 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr9:8636826 G>A maps to NM_002839.3 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr9:8636824 T>C maps to NM_002839.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:8485271 C>T maps to NM_002839.3 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr9:8341106 A>G maps to NM_002839.3 S1703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr9:8504330 A>G maps to NM_002839.3 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr9:8504330 A>G maps to NM_002839.3 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:129866448 C>G maps to NM_006504.4 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr10:129871626 C>T maps to NM_006504.4 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr10:129866397 C>T maps to NM_006504.4 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr10:129864424 C>T maps to NM_006504.4 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr10:129866517 C>T maps to NM_006504.4 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr10:129867991 C>T maps to NM_006504.4 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:129869124 G>A maps to NM_006504.4 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:44063652 G>A maps to NM_002840.3 W683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:44071226 T>C maps to NM_002840.3 I1139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:44044511 C>T maps to NM_002840.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:44064520 G>A maps to NM_002840.3 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:44063554 C>T maps to NM_002840.3 D650D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:44071268 A>G maps to NM_002840.3 T1153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr1:44086564 C>T maps to NM_002840.3 G1807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:44083443 C>T maps to NM_002840.3 I1411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:44070931 C>T maps to NM_002840.3 P1069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:44069402 C>T maps to NM_002840.3 A860A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr1:44071268 A>G maps to NM_002840.3 T1153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:44057078 G>A maps to NM_002840.3 W462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:62278131 T>A maps to NM_002841.3 L1364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr3:62189577 C>T maps to NM_002841.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:62257135 G>T maps to NM_002841.3 G1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:62204615 C>T maps to NM_002841.3 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:62254807 T>C maps to NM_002841.3 V991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr3:62248478 C>T maps to NM_002841.3 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:62189577 C>T maps to NM_002841.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:62189577 C>T maps to NM_002841.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr3:62189577 C>T maps to NM_002841.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:62189577 C>T maps to NM_002841.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr3:62189577 C>T maps to NM_002841.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:62189577 C>T maps to NM_002841.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:62189598 C>T maps to NM_002841.3 D710D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:55699454 G>A maps to NM_002842.3 D822D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:55716853 C>G maps to NM_002842.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:55710170 G>T maps to NM_002842.3 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:55713469 C>T maps to NM_002842.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr19:55699454 G>A maps to NM_002842.3 D822D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr19:55716808 T>C maps to NM_002842.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr19:55716808 T>C maps to NM_002842.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:48177416 C>T maps to NM_002843.3 N1098N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:48161170 G>A maps to NM_002843.3 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:48188813 C>A maps to NM_002843.3 S1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr11:48171647 A>G maps to NM_002843.3 K1017K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:48158675 A>G maps to NM_002843.3 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr11:48166554 T>C maps to NM_002843.3 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:48157624 C>T maps to NM_002843.3 Y550Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr11:48142553 G>T did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr11:48171646 G>T did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr11:48166554 T>C maps to NM_002843.3 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:48166554 T>C maps to NM_002843.3 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:48166554 T>C maps to NM_002843.3 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:128403760 G>T maps to ENST00000368210 S533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr6:128561245 C>T maps to ENST00000368210 G209G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3684-01A-02W-0900-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr6:128297858 A>G maps to ENST00000368210 S1322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:128298079 G>A maps to ENST00000368210 V1295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:128561244 G>A maps to ENST00000368210 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr6:128298166 T>C maps to ENST00000368210 T1266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr6:128505595 G>T maps to ENST00000368210 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr18:7906516 G>T maps to NM_001105244.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr18:7955389 C>T maps to NM_001105244.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr18:8378282 C>T maps to NM_001105244.1 H1161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr18:8384677 C>T maps to NM_001105244.1 A1346A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3672-01A-01W-0900-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:8253225 T>C maps to NM_001105244.1 D856D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:8384590 A>G maps to NM_001105244.1 V1317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:8253246 C>T maps to NM_001105244.1 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr18:7955225 C>T maps to NM_001105244.1 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:8394503 C>T maps to NM_001105244.1 C1413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr18:8069961 C>T maps to NM_001105244.1 Q471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr18:7906516 G>T maps to NM_001105244.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:7888177 G>T maps to NM_001105244.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr18:8387113 C>A maps to NM_001105244.1 G1363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:8069838 C>T maps to NM_001105244.1 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:7906516 G>T maps to NM_001105244.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr18:7906516 G>T maps to NM_001105244.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:220167153 G>A maps to NM_002846.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:220168553 C>A did not map to a codon.
Alternatively spliced codon TCGA-AA-3977-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:220172562 G>A maps to NM_002846.3 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr7:157931091 G>A maps to NM_002847.3 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:157929348 C>A maps to NM_002847.3 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:157874038 C>A maps to NM_002847.3 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:157341693 G>A maps to NM_002847.3 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:157926523 G>A maps to NM_002847.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr7:157985120 G>A maps to NM_002847.3 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:157449099 G>T maps to NM_002847.3 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr7:157449098 C>A maps to NM_002847.3 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:15734687 G>T maps to NM_030667.1 E1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr12:15742430 G>A maps to NM_030667.1 R1151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:15733641 A>G maps to NM_030667.1 S1003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:15636960 A>G maps to NM_030667.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:15654587 C>T maps to NM_030667.1 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:15636951 C>T maps to NM_030667.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:15650185 A>G maps to NM_030667.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr12:15650185 A>G maps to NM_030667.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:15722368 C>T maps to NM_030667.1 D922D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:71286695 C>T maps to NM_002849.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:71056272 A>G did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:71139682 G>A maps to NM_002849.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr12:71286551 G>A maps to NM_002849.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr19:5265109 G>A maps to NM_002850.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:5238981 C>T maps to NM_002850.3 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:5245841 G>A maps to NM_002850.3 C311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:5225783 G>A maps to NM_002850.3 G816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:5244386 G>A maps to NM_002850.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr19:5214664 C>T maps to NM_002850.3 P1467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:5223174 C>T maps to NM_002850.3 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr19:5238957 G>A maps to NM_002850.3 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:40877349 G>A maps to ENST00000373198 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:41306740 C>T maps to ENST00000373198 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr20:41419951 G>A maps to ENST00000373198 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr20:41306583 G>A maps to ENST00000373198 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:41306638 G>A maps to ENST00000373198 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr20:40979284 G>A maps to ENST00000373198 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:41100924 C>A maps to ENST00000373198 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:40709551 G>A maps to ENST00000373198 Y1453Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:40730858 G>A maps to ENST00000373198 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:40944416 G>T maps to ENST00000373198 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr20:41306530 G>A maps to ENST00000373198 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:40730798 C>A maps to ENST00000373198 E1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:40730781 G>T maps to ENST00000373198 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr20:40770603 G>A maps to ENST00000373198 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:41420101 A>C maps to ENST00000373198 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr20:41101119 G>A maps to ENST00000373198 Y412Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr20:40979350 G>A maps to ENST00000373198 Y594Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr20:40730913 A>G maps to ENST00000373198 R1210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr20:40713353 G>A maps to ENST00000373198 D1390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr20:41306602 G>A maps to ENST00000373198 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr20:40714430 G>A maps to ENST00000373198 F1325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr20:41514489 A>G maps to ENST00000373198 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:29647291 C>A maps to NM_005704.4 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:29644432 C>T maps to NM_005704.4 D1239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:29630523 G>A maps to NM_005704.4 T888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:29602120 C>T maps to NM_005704.4 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr1:29606125 C>T maps to NM_005704.4 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr1:29618534 C>A maps to NM_005704.4 R835R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:29650300 G>A did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:29581850 C>A maps to NM_005704.4 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:29630460 G>A maps to NM_005704.4 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:121637956 A>G maps to NM_002851.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:121653521 A>G maps to NM_002851.2 S1474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:121623806 A>G maps to NM_002851.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:121616229 C>T maps to NM_002851.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:121624142 C>T maps to NM_002851.2 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:121679536 T>C maps to NM_002851.2 D1844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr7:121699878 C>A maps to NM_002851.2 S2248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:121650566 C>T maps to NM_002851.2 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr7:121651100 A>G maps to NM_002851.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr7:121699878 C>T maps to NM_002851.2 S2248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr7:121651970 T>G maps to NM_002851.2 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr7:121699878 C>T maps to NM_002851.2 S2248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr17:40556740 C>T maps to NM_012232.5 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:40557352 C>T maps to NM_012232.5 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:57775225 C>A maps to ENST00000409433 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:112104157 G>A maps to NM_000317.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:37962072 C>T maps to NM_006607.2 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr3:157154772 C>T maps to NM_002852.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:31414865 C>T maps to ENST00000373741 Q1069Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:31426699 G>A maps to ENST00000373741 R854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr1:31409522 C>T maps to ENST00000373741 A1170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:31465298 G>A maps to ENST00000373741 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr1:31437644 G>A maps to ENST00000373741 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:31438943 G>A maps to ENST00000373741 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:31423065 G>A maps to ENST00000373741 R958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:31454165 C>T maps to ENST00000373741 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:31532194 G>A maps to ENST00000373741 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:20482862 G>T maps to ENST00000361078 S522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:20463197 G>A maps to ENST00000361078 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:20511271 G>A maps to ENST00000361078 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:20508295 A>G maps to ENST00000361078 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr7:44924341 G>A maps to NM_033224.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:132426356 G>A maps to NM_025215.5 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:132425852 G>A maps to NM_025215.5 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr2:61236078 T>C maps to NM_144709.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr2:61175176 C>T did not map to a codon.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr2:61175308 G>A maps to NM_144709.2 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:61236062 G>A maps to NM_144709.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:61192222 T>G maps to NM_144709.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:61236053 C>A maps to NM_144709.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:61236066 T>C maps to NM_144709.2 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr11:125765153 C>T maps to NM_031307.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:125765153 C>T maps to NM_031307.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:125765153 C>T maps to NM_031307.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:105103128 G>A maps to NM_019042.3 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:105105784 G>A maps to NM_019042.3 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:105103128 G>A maps to NM_019042.3 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr7:105111212 G>T maps to NM_019042.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:105098263 C>T maps to NM_019042.3 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:44148690 C>A maps to NM_031292.3 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr12:44130333 G>T maps to NM_031292.3 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:44124289 C>T maps to NM_031292.3 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr22:37209708 G>A maps to NM_002854.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:37209690 G>A maps to NM_002854.2 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:45150553 C>T maps to NM_006505.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:45153204 C>T maps to NM_006505.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:45150789 C>T maps to NM_006505.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:45150789 C>T maps to NM_006505.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:45150498 C>T maps to NM_006505.3 D28D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:119535675 G>A maps to NM_002855.4 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:119549446 G>A maps to NM_002855.4 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:119535588 G>A maps to NM_002855.4 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr11:119545974 G>A maps to NM_002855.4 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:119549131 C>T maps to NM_002855.4 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:119510690 A>G maps to NM_203285.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr19:45375164 G>A maps to NM_001042724.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:45375335 G>A maps to NM_001042724.1 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:45381540 A>G maps to NM_002856.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:45377643 C>T maps to NM_001042724.1 H317H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:45377694 C>T maps to NM_001042724.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr1:161042549 G>T maps to NM_030916.2 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr12:108105907 C>T maps to NM_007062.1 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:108098455 C>T maps to NM_007062.1 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr12:108102885 A>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr21:45534114 C>T maps to NM_005049.2 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:45540239 G>A maps to NM_005049.2 W400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:159520909 G>A maps to NM_001130864.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:159520032 C>A maps to NM_001130864.1 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:159520203 C>A maps to NM_001130864.1 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:134219628 C>A maps to NM_138499.3 S542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:1670091 G>A maps to NM_012293.1 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:1653181 G>A maps to NM_012293.1 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:1670091 G>A maps to NM_012293.1 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:1653433 G>A maps to NM_012293.1 N706N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr2:1664677 C>T maps to NM_012293.1 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr2:1653211 G>T maps to NM_012293.1 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:1664725 G>A maps to NM_012293.1 D588D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr2:1653118 G>A maps to NM_012293.1 D811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:1648499 G>A maps to NM_012293.1 I1211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:1667422 G>T maps to NM_012293.1 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:1652413 C>T maps to NM_012293.1 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:1652482 A>C maps to NM_012293.1 G1023G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:1652525 C>T maps to NM_012293.1 W1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:1670016 G>A maps to NM_012293.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:1684045 G>A maps to NM_012293.1 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:52321347 G>A maps to NM_144651.4 R946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:52384826 C>T maps to NM_144651.4 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr8:52252312 C>T maps to NM_144651.4 R1339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr8:52384838 C>T maps to NM_144651.4 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr8:52258472 C>T maps to NM_144651.4 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:52396228 A>G maps to NM_144651.4 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr8:52321234 C>T maps to NM_144651.4 T983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:52567294 C>A maps to NM_144651.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr8:52321990 G>A maps to NM_144651.4 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr8:52321669 G>A maps to NM_144651.4 N838N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:58389597 C>T maps to NM_017771.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:58395270 C>T maps to NM_017771.3 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:58368239 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr12:133281251 C>A maps to NM_018663.1 Y189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:120651776 G>A maps to NM_001080855.1 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr12:120660681 C>T maps to NM_001080855.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:120661576 A>G maps to NM_001080855.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:120659536 G>T maps to NM_001080855.1 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr12:120652726 G>A maps to NM_001080855.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:120650170 C>T maps to NM_001080855.1 K574K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:79892924 C>A maps to ENST00000432920 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:226109704 G>A maps to NM_013328.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:144688645 G>A maps to NM_023078.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:25273099 C>T maps to NM_002862.3 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr20:25269058 A>T did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr20:25255238 C>T maps to NM_002862.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr14:51379779 A>G maps to NM_002863.4 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:51372217 G>A maps to NM_002863.4 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:51378514 G>A maps to NM_002863.4 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:51382067 G>A maps to NM_002863.4 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:51372172 G>A maps to NM_002863.4 N827N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:55838558 G>A maps to NM_015617.1 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr15:55841164 T>C maps to NM_015617.1 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr1:154931835 G>A maps to NM_138300.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr1:158906750 C>A maps to NM_152501.3 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:158912053 A>G maps to NM_152501.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr1:158912077 G>A maps to NM_152501.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr1:158913765 C>T maps to NM_152501.3 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:21593345 T>G maps to NM_024854.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:21620425 G>A maps to NM_024854.3 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:21598303 C>T maps to NM_024854.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:21621540 A>G maps to NM_024854.3 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr10:100152251 C>T maps to NM_032709.2 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:100152235 G>A maps to NM_032709.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:100148156 T>C maps to NM_032709.2 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:100152746 C>T maps to NM_032709.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:100146972 G>A maps to NM_032709.2 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:100167721 G>A maps to NM_032709.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr12:9317938 T>C maps to NM_002864.2 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:9313658 C>A maps to NM_002864.2 E948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:9307349 C>T maps to NM_002864.2 V1212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:9318649 C>A maps to NM_002864.2 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:9309951 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:9349278 A>G maps to NM_002864.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:9353539 T>C maps to NM_002864.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:9312607 C>T maps to NM_002864.2 Q1021Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:9353512 C>T maps to NM_002864.2 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:9313020 C>A maps to NM_002864.2 E980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:9313658 C>A maps to NM_002864.2 E948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:9316305 C>T maps to NM_002864.2 E898E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:9334623 C>A maps to NM_002864.2 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:9311144 G>A maps to NM_002864.2 F1055F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:3146697 A>G maps to NM_014731.2 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr20:3147731 G>A maps to NM_014731.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:49133506 G>T maps to NM_005051.1 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:49136422 C>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:49135789 G>A maps to NM_005051.1 R694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr4:17493949 G>A maps to NM_000320.2 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:17503360 A>G maps to NM_000320.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr4:17493916 G>A maps to NM_000320.2 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:163836317 G>T maps to ENST00000361752 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:163876419 G>A maps to ENST00000361752 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:163983019 G>T maps to ENST00000361752 G191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr6:163987825 A>G maps to ENST00000361752 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:163876441 G>T maps to ENST00000361752 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:163984713 A>G maps to ENST00000361752 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:163983102 T>C did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr6:163984626 A>G maps to ENST00000361752 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:37594508 G>A maps to NM_012413.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:37594502 G>A maps to NM_012413.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr9:133769099 G>A maps to NM_198180.1 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:122254054 C>A maps to NM_198179.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr4:122301739 C>T maps to NM_198179.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr3:49114312 C>T maps to NM_198880.1 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr3:49084574 T>C maps to NM_198880.1 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:49094840 C>T maps to NM_198880.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr3:49069659 T>C maps to NM_198880.1 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:74287231 C>T maps to NM_032134.1 T1026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr17:74274185 C>T maps to NM_032134.1 K1501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:74289937 G>A maps to NM_032134.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:74287750 G>A maps to NM_032134.1 Y853Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:74276794 A>G maps to NM_032134.1 G1301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr17:74288242 A>G maps to NM_032134.1 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:74289831 G>A maps to NM_032134.1 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:107096992 C>T maps to NM_018292.4 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr11:32954225 T>G maps to NM_001076786.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:32956115 C>T maps to NM_001076786.1 G975G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:32953928 C>T maps to NM_001076786.1 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr11:32956226 A>G maps to NM_001076786.1 R1012R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:32955638 T>C maps to NM_001076786.1 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:32996804 C>T maps to NM_001076786.1 V1661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:32994981 C>T maps to NM_001076786.1 R1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:32997955 G>A maps to NM_001076786.1 W1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:32975655 C>T maps to NM_001076786.1 S1348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:180159620 G>A maps to NM_002826.4 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr1:180153053 C>A maps to NM_002826.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:180147955 G>A maps to NM_002826.4 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:180151397 C>T maps to NM_002826.4 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:180165604 A>G maps to NM_002826.4 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:139110638 C>T maps to NM_181701.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:113785108 G>T maps to ENST00000485050 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr3:113795759 C>T maps to ENST00000485050 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:136409478 A>T maps to ENST00000409606 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:136481597 C>T maps to ENST00000409606 G1013G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr12:57651848 G>A maps to ENST00000438036 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr12:57651896 G>A maps to ENST00000438036 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr12:57662722 A>G maps to ENST00000438036 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:57648611 G>A maps to ENST00000438036 R1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr12:57663178 A>G maps to ENST00000438036 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr20:42979341 G>A maps to NM_178491.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr15:66170172 C>A maps to ENST00000435304 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:66169842 C>T maps to ENST00000435304 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:8464744 A>G did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr19:8467068 C>T maps to NM_004218.3 H112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:37729778 G>A maps to NM_001002814.2 N847N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr8:37729814 G>T maps to NM_001002814.2 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr8:37732319 A>G maps to NM_001002814.2 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:37729271 G>A maps to NM_001002814.2 G1016G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr10:119800044 G>A maps to ENST00000369199 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:119805635 G>C maps to ENST00000369199 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:119805350 G>T maps to ENST00000369199 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:560767 G>A maps to NM_014700.3 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:532544 C>T maps to NM_014700.3 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:553006 C>T maps to NM_014700.3 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr16:570793 C>T maps to NM_014700.3 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:29761130 C>T maps to NM_032932.3 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:29848318 C>T maps to NM_032932.3 C233C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:29761062 C>T maps to NM_032932.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:29850574 C>T maps to NM_032932.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:73316061 G>A maps to NM_015470.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:73316352 G>A maps to NM_015470.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:73302804 G>A maps to NM_015470.2 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr2:238486709 G>A maps to NM_022449.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:27822870 C>T maps to NM_021252.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:65315713 A>G maps to NM_004161.4 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:66039306 C>T maps to NM_030981.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr13:111176074 T>C maps to NM_017817.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:56928355 C>T maps to NM_020673.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:56928585 C>T maps to NM_020673.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr20:56929289 G>A maps to NM_020673.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:57072465 A>G maps to NM_016277.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr6:57058661 C>T maps to NM_016277.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:156038195 C>T maps to NM_020387.2 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:156039471 A>T maps to NM_020387.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:55497903 C>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr18:52556547 G>A maps to NM_004163.3 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr18:52556571 T>C maps to NM_004163.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr4:13383171 C>A maps to NM_004249.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr4:13383173 G>T maps to NM_004249.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr8:61533315 C>T maps to NM_002865.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:61496777 A>G maps to NM_002865.1 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr14:21931901 C>T maps to NM_032846.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:21929444 A>G maps to NM_032846.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr14:21931832 T>C maps to NM_032846.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr18:9814045 A>G maps to NM_006868.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:146875593 T>C maps to NM_006834.3 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr23:129318594 G>T did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr4:140394210 T>C maps to NM_031296.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:27041903 C>A maps to NM_001144943.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr22:23487623 G>A maps to NM_004914.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:72736929 C>T maps to NM_001006638.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr23:154493535 A>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:154490501 G>A did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:154493545 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:18311198 A>G maps to NM_002866.4 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:18308288 G>A maps to NM_002866.4 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr5:58021920 A>G maps to NM_138453.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr5:57913495 C>T maps to NM_138453.2 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:58021920 A>G maps to NM_138453.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:135848569 T>C maps to NM_001172435.1 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:135870738 C>T maps to NM_001172435.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:135922169 G>T maps to NM_001172435.1 V871V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:220330641 G>A maps to ENST00000358951 T1175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:220330740 T>C maps to ENST00000358951 E1142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:220344362 G>A maps to ENST00000358951 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:220383752 G>A maps to ENST00000358951 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:220366636 G>A maps to ENST00000358951 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:220375681 T>C maps to ENST00000358951 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr1:220344446 A>G maps to ENST00000358951 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:61673991 G>A maps to NM_013401.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr11:61669972 G>A maps to NM_013401.2 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr11:61675747 C>T maps to NM_013401.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr12:70194020 G>A maps to NM_175623.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:102755101 G>T did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:102755639 G>C did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr23:102755507 G>A did not map to a codon.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr23:102193052 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:102192984 T>C did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:102192429 C>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:102192300 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:102192406 C>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:69504462 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:69503867 C>T did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:69503396 A>G did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:69502165 A>G did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:69502165 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:69504159 A>G did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:128840145 G>A maps to NM_198490.1 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:41292840 C>T maps to ENST00000419646 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr19:41292666 T>G did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:20017558 A>G maps to NM_004162.4 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr17:40280684 G>C maps to NM_201434.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:73427339 A>G maps to NM_198896.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:133557065 C>A maps to NM_016577.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:133558426 G>A maps to NM_016577.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:133553478 G>A maps to NM_016577.3 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:133560230 G>A maps to NM_016577.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:133553478 G>T maps to NM_016577.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr2:130737699 C>T maps to NM_032144.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:130738047 C>A maps to NM_032144.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:130737986 C>A maps to NM_032144.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr2:130737717 G>A maps to NM_032144.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:205740626 C>T maps to NM_003929.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:205739490 G>T maps to NM_003929.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:205740626 C>T maps to NM_003929.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr1:205740626 C>T maps to NM_003929.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:205740626 C>T maps to NM_003929.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:16240377 C>T maps to NM_005370.4 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:13727373 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:13727203 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:13727255 C>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:103080334 T>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:42462441 G>T maps to NM_006423.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr17:5286418 G>A maps to NM_004703.4 V830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr16:28917478 C>T maps to NM_024816.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:127995022 A>G maps to NM_005833.3 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:127996036 T>C maps to NM_005833.3 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:127982923 C>T maps to NM_005833.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:125777870 T>C maps to NM_012197.3 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:125852089 A>G maps to NM_012197.3 E826E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr9:125852555 G>A maps to NM_012197.3 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:125746912 C>T maps to NM_012197.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr9:125751632 C>T maps to NM_012197.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:174188378 T>C maps to NM_014857.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:174221711 G>T maps to NM_014857.3 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:174668742 C>T maps to NM_014857.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:174190162 A>G maps to NM_014857.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:174190162 A>G maps to NM_014857.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr1:174190162 A>G maps to NM_014857.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr1:174190126 T>C maps to NM_014857.3 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr7:66274189 A>G maps to ENST00000451741 Q682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:76257951 A>G maps to NM_004582.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:76260328 G>A maps to NM_004582.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:114398993 C>T maps to ENST00000409875 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr7:100958528 T>C maps to NM_022777.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:100959804 C>T maps to NM_022777.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:100958414 C>T maps to NM_022777.2 *186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:6441614 T>G maps to NM_018890.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:37622790 G>A maps to NM_002872.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:37628840 C>T maps to NM_002872.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr22:37627355 G>A maps to NM_002872.3 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:79991636 G>T maps to NM_005052.2 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr12:50390950 G>T maps to NM_013277.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:50387973 G>A maps to NM_013277.3 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:50399154 A>G maps to NM_013277.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr12:50390948 C>G maps to NM_013277.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:34911899 G>A maps to NM_002853.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:34914826 C>T maps to NM_002853.3 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:68710029 C>T maps to NM_133339.1 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:68682025 C>T maps to NM_133339.1 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr3:8923061 T>C maps to NM_020165.3 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:8932134 A>G maps to NM_020165.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:8977605 C>A maps to NM_020165.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr3:9005033 G>A maps to NM_020165.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:8983367 C>A maps to NM_020165.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:9005024 G>A maps to NM_020165.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:117859878 G>A maps to NM_006265.2 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr8:117869683 T>A maps to NM_006265.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr8:117862982 T>C maps to NM_006265.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:117869653 G>A maps to NM_006265.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr8:117864857 G>A maps to NM_006265.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:13058786 C>T maps to NM_005053.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:13059151 G>A maps to NM_005053.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:13056782 C>T maps to NM_005053.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr5:131976488 T>C maps to NM_005732.3 A1248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr5:131924496 A>G maps to NM_005732.3 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:131951754 G>T maps to NM_005732.3 E1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:131976488 T>C maps to NM_005732.3 A1248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:131976488 T>C maps to NM_005732.3 A1248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:41023336 C>T maps to NM_002875.4 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr15:41011043 C>T maps to NM_002875.4 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr12:4665537 T>C maps to NM_001130862.1 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:17698249 C>T maps to NM_001099218.2 W478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr2:17692184 C>A maps to NM_001099218.2 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:17697660 A>G maps to NM_001099218.2 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:33445524 A>G maps to NM_002878.3 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:1023605 C>A maps to NM_134424.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:1025528 C>T maps to NM_134424.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr8:95403905 G>T maps to NM_012415.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:95470619 A>G maps to NM_012415.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:95404067 A>G maps to NM_012415.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr8:95411725 C>A maps to NM_012415.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr8:95470592 A>G maps to NM_012415.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr8:95470592 A>G maps to NM_012415.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr8:95419895 C>A maps to NM_012415.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr8:95470592 A>G maps to NM_012415.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:46739341 T>C maps to NM_003579.3 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:46725756 G>A maps to NM_003579.3 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:46738352 C>A maps to NM_003579.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:51696445 C>T maps to NM_015106.2 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:51673505 C>T maps to NM_015106.2 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:51697105 G>A maps to NM_015106.2 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:51696568 T>C maps to NM_015106.2 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr12:110960200 T>C maps to NM_152442.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr12:110960200 T>C maps to NM_152442.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:110960200 T>C maps to NM_152442.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:4855922 C>T maps to NM_018059.4 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:4917281 C>T maps to NM_018059.4 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:4917239 C>T maps to NM_018059.4 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr7:4917281 C>T maps to NM_018059.4 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:4917440 G>A maps to NM_018059.4 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr20:55929765 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:150209666 C>T maps to NM_139165.1 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:150211210 C>T maps to NM_139165.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:150240410 T>A maps to NM_001001788.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:150240235 C>A maps to NM_001001788.2 G192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:150342173 T>C maps to NM_130900.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:12626680 G>A maps to ENST00000415519 I556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:12650746 G>A maps to ENST00000415519 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr11:36596671 A>G maps to NM_000448.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:36595450 C>T maps to NM_000448.2 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:36596789 G>T maps to NM_000448.2 E646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr11:36595135 C>T maps to NM_000448.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:36596422 G>A maps to NM_000448.2 Q523Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:36596383 G>A maps to NM_000448.2 E510E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:36596846 G>T maps to NM_000448.2 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:36596671 A>G maps to NM_000448.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr11:36596671 A>G maps to NM_000448.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:36596671 A>G maps to NM_000448.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr11:36597196 G>C maps to NM_000448.2 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr1:155109408 G>T maps to NM_018845.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:155110531 C>A maps to NM_018845.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr11:36614563 A>G maps to NM_000536.3 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr11:36614563 A>G maps to NM_000536.3 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr11:36614563 A>G maps to NM_000536.3 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:36614563 A>G maps to NM_000536.3 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr14:102717310 A>T maps to NM_014226.1 L143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:102717153 G>A maps to NM_014226.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:102695670 C>T maps to NM_014226.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:102717198 C>T maps to NM_014226.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr14:102698966 T>C maps to NM_014226.1 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr14:102695697 A>G maps to NM_014226.1 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr17:17700968 T>C maps to ENST00000395776 D1569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr17:17699399 G>A maps to ENST00000395776 R1046R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:34812009 A>T maps to NM_001145521.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:34830833 C>T maps to NM_001145521.1 I969I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr5:34823884 C>T maps to NM_001145521.1 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:34824361 G>A maps to NM_001145521.1 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:34757700 C>T maps to NM_001145521.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:34812036 C>A maps to NM_001145521.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:34824013 C>T maps to NM_001145521.1 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr5:34824277 T>C maps to NM_001145521.1 A777A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:34823453 C>T maps to NM_001145521.1 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:34823759 C>T maps to NM_001145521.1 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:17819599 C>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:17819907 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:17818710 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:17818797 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:17819893 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:17819213 G>A did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:17819225 A>G did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:17819335 G>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:17818711 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:39745748 C>T maps to NM_005402.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:39730052 C>T maps to NM_005402.2 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:121043634 C>A maps to NM_002881.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:121043610 G>T maps to NM_002881.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:9522378 G>T maps to NM_006788.3 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:9535781 G>A maps to NM_006788.3 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr18:9535901 G>A maps to NM_006788.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr14:36096534 T>C maps to NM_194301.2 G1700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:36142117 T>C maps to NM_194301.2 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:36190906 C>T maps to NM_194301.2 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr14:36074913 G>T maps to NM_194301.2 R1805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr14:36074911 T>C maps to NM_194301.2 R1805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:36159209 C>A did not map to a codon.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr14:36039875 T>C maps to NM_194301.2 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr14:36074911 T>C maps to NM_194301.2 R1805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr14:36096534 T>A maps to NM_194301.2 G1700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr14:36217915 G>A maps to NM_194301.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:20505115 G>T maps to NM_020343.3 P1278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:20620526 C>A maps to NM_020343.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr20:20596796 T>C maps to NM_020343.3 E526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:20569980 C>T maps to NM_020343.3 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:20620526 C>A maps to NM_020343.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:20392719 G>A maps to NM_020343.3 F1856F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:20596823 C>T maps to NM_020343.3 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr20:20569959 A>G maps to NM_020343.3 P797P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr20:37117116 T>C maps to NM_020336.2 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr20:37154596 T>C maps to NM_020336.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr20:37187089 C>T maps to NM_020336.2 N1175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:37186987 G>A maps to NM_020336.2 T1141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr20:37179742 T>A maps to NM_020336.2 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:135979679 G>A maps to NM_006266.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:135978224 C>T maps to NM_006266.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr9:135975676 C>T maps to NM_006266.2 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr9:135984183 A>G maps to NM_006266.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr9:135982060 A>G maps to NM_006266.2 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:135985846 A>G maps to NM_006266.2 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr9:129974454 G>A maps to NM_014636.2 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr9:129974997 C>T maps to NM_014636.2 H482H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:129831517 C>T maps to NM_014636.2 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:129928448 C>T maps to NM_014636.2 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr9:129957370 T>C maps to NM_014636.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:178854286 G>A maps to NM_152663.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:178802615 G>T maps to NM_152663.3 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:178846705 A>G maps to NM_152663.3 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:178858783 C>T maps to NM_152663.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr20:32664575 C>T maps to NM_016732.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:32665038 C>T maps to NM_016732.1 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr20:32663784 C>T maps to NM_016732.1 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr20:32661420 A>G maps to NM_016732.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:85774627 G>T maps to NM_001100391.1 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:85799986 C>T maps to NM_001100391.1 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:238785974 G>A maps to NM_005855.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr17:40914460 C>T maps to ENST00000456272 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:45216914 T>C maps to NM_005856.2 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:20114574 A>C maps to NM_002882.2 *202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr22:20109855 C>T maps to NM_002882.2 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:67763280 G>C maps to NM_020850.1 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:67760461 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr16:67765390 G>A maps to NM_020850.1 S291S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-F4-6570-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:67762413 G>A maps to NM_020850.1 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:67761239 G>A maps to NM_020850.1 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr5:170336708 C>A maps to NM_022897.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:170725861 A>G maps to NM_022897.3 *1089W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr5:170692763 C>A maps to NM_022897.3 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:109389334 G>T maps to NM_006267.4 E2709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr2:109368069 C>A maps to NM_006267.4 C514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:109380967 G>T maps to NM_006267.4 E1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr2:109382688 T>C maps to NM_006267.4 F1898F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:109380591 G>A maps to NM_006267.4 A1199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:109368356 A>G maps to NM_006267.4 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:5917853 G>A maps to NM_007322.2 D537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:36265605 A>C maps to NM_001161429.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr5:36301479 A>G maps to NM_001161429.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr9:6014638 T>G maps to NM_012416.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:6014812 A>G maps to NM_012416.2 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:6014542 A>C maps to NM_012416.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr9:6014608 A>G maps to NM_012416.2 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:6013702 G>A maps to NM_012416.2 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:13622656 T>C maps to NM_005493.2 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr6:13625894 A>G maps to NM_005493.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr6:13632709 A>G maps to NM_005493.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr6:13625894 A>G maps to NM_005493.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:21952805 G>C maps to NM_001145658.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr1:21924944 A>G maps to NM_001145658.1 Y673Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:2898741 C>A maps to NM_015085.4 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:2867169 G>A maps to NM_015085.4 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:2929730 C>T maps to NM_015085.4 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:2909313 G>A maps to NM_015085.4 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:2894625 G>A maps to NM_015085.4 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:2930338 G>A maps to NM_015085.4 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr17:2861060 G>A maps to NM_015085.4 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr17:2921365 C>T maps to NM_015085.4 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:2929350 C>T maps to NM_015085.4 Q601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr17:2861054 G>A maps to NM_015085.4 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:99214583 G>A maps to NM_001100426.1 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:99325730 T>C maps to NM_001100426.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:131348286 T>C did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:131348287 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:134471751 G>A maps to NM_198679.1 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:134477491 C>T maps to NM_198679.1 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:134477458 G>A maps to NM_198679.1 D662D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:134465322 G>A maps to NM_198679.1 R771R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:160271427 T>C maps to NM_014247.2 S1123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:160235804 C>T maps to NM_014247.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:160251634 G>A maps to NM_014247.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:160273990 C>T maps to NM_014247.2 I1179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:160235903 G>A maps to NM_014247.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr4:160264475 A>G maps to NM_014247.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:48144928 G>A maps to NM_001098531.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:48151768 G>A maps to NM_001098531.2 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr2:173659771 G>T maps to NM_007023.3 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:173855584 C>A maps to NM_007023.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:173659804 G>T maps to NM_007023.3 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:173883385 C>T maps to NM_007023.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:173882185 C>T maps to NM_007023.3 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:173891814 C>T maps to NM_007023.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:173885422 C>T maps to NM_007023.3 R745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:173850189 T>A maps to NM_007023.3 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:173885385 G>A maps to NM_007023.3 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr2:173782564 T>C maps to NM_007023.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:22184699 T>C maps to ENST00000344041 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:22184701 G>A maps to ENST00000344041 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr7:22184699 T>C maps to ENST00000344041 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:22196434 C>T maps to ENST00000344041 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr7:22165267 G>A maps to ENST00000344041 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:22184767 G>A maps to ENST00000344041 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr5:130766996 T>C maps to ENST00000514667 S1390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:130940387 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:38340594 C>A maps to ENST00000456989 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:38345550 G>A maps to ENST00000456989 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:38346908 G>A maps to ENST00000456989 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:204309641 G>A maps to ENST00000374493 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:204354321 C>T maps to ENST00000374493 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:204304954 A>G maps to ENST00000374493 G1038G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:204304228 C>T maps to ENST00000374493 T1280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:47469684 G>A maps to NM_005055.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:47469603 G>A maps to NM_005055.3 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr11:47469684 G>A maps to NM_005055.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr11:47469636 G>A maps to NM_005055.3 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr17:38487496 G>A maps to NM_001145301.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr17:38508716 C>A maps to NM_001145301.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:25622054 C>T maps to NM_000965.3 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:25636009 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:25542759 C>T maps to NM_000965.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:25636096 C>T maps to NM_000965.3 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:25611372 T>G maps to NM_000965.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:25636096 C>T maps to NM_000965.3 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:53607427 G>A maps to NM_000966.4 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr12:53621310 G>A maps to NM_000966.4 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:53621310 G>A maps to NM_000966.4 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:150036161 C>T maps to NM_002889.3 R96R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CA-5797-01A-01D-1650-10. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CM-6168-01A-11D-1650-10. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-DM-A1DA-01A-11D-A152-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:167933824 A>G maps to NM_002887.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:167929029 T>A maps to NM_002887.3 L326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:167937621 C>T maps to NM_002887.3 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:167922408 C>T maps to NM_002887.3 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:88255352 G>A maps to NM_020320.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:86672711 G>A maps to NM_002890.1 K733K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:86564678 G>A maps to NM_002890.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:86659262 G>T maps to NM_002890.1 G518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr5:86668002 C>T maps to NM_002890.1 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:86645040 C>G maps to NM_002890.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:86629107 C>T maps to NM_002890.1 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:141259373 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:141272710 C>T maps to ENST00000452898 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:141328312 A>G maps to ENST00000452898 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:141328312 A>G maps to ENST00000452898 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr3:141231095 T>C maps to ENST00000452898 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr3:141328312 A>G maps to ENST00000452898 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr13:114793339 C>T maps to ENST00000389544 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr13:114782805 T>C maps to ENST00000389544 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr12:113545928 C>T maps to NM_001193520.1 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:113543527 A>G maps to NM_001193520.1 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr12:113537856 G>A maps to NM_001193520.1 V766V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:113559441 C>T maps to NM_001193520.1 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:113565674 G>A maps to NM_001193520.1 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:113542004 G>A maps to NM_001193520.1 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:178411892 C>T maps to ENST00000263528 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr1:178411892 C>T maps to ENST00000263528 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:15566919 G>T maps to NM_022904.1 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:15565691 C>T maps to NM_022904.1 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr22:35947670 G>A maps to NM_014310.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr9:85611924 A>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:85611949 G>A maps to NM_152573.2 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr10:43693559 G>A maps to ENST00000374459 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:179564944 T>C maps to NM_175062.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr15:79339113 G>A maps to NM_002891.4 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr15:79284127 G>A maps to NM_002891.4 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:79265680 C>T maps to NM_002891.4 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:79324548 G>A maps to NM_002891.4 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:79284085 G>A maps to NM_002891.4 I1042I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr15:79277531 A>T maps to NM_002891.4 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:79292250 G>A maps to NM_002891.4 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:79310180 C>T maps to NM_002891.4 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:79310204 G>A maps to NM_002891.4 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:79350693 G>A maps to NM_002891.4 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:79350759 G>A maps to NM_002891.4 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:79277480 G>A maps to NM_002891.4 I1110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr15:79296342 G>A maps to NM_002891.4 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr15:79298658 C>T maps to NM_002891.4 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr15:79356805 G>A maps to NM_002891.4 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr15:79282539 G>A maps to NM_002891.4 H1085H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr15:79310180 C>T maps to NM_002891.4 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:79320146 G>A maps to NM_002891.4 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr15:79310180 C>T maps to NM_002891.4 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr15:79310180 C>T maps to NM_002891.4 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr5:80388680 G>A maps to NM_006909.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr5:80390757 T>C maps to NM_006909.1 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr5:80408626 G>T maps to NM_006909.1 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:80497208 C>T maps to NM_006909.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:80256721 G>A maps to NM_006909.1 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr5:80409416 C>A maps to NM_006909.1 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:80382666 G>T maps to NM_006909.1 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:80497208 C>T maps to NM_006909.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:80497249 G>A maps to NM_006909.1 A965A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr5:80409566 C>T maps to NM_006909.1 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:80497208 C>T maps to NM_006909.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:38803828 C>T maps to NM_005739.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:38791087 G>A maps to NM_005739.3 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:38786738 A>G maps to NM_005739.3 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr15:38786825 G>A maps to NM_005739.3 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:38852025 A>C maps to NM_005739.3 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:64494773 T>A maps to ENST00000320253 *671Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3864-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:64508448 C>T maps to ENST00000320253 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr2:33752229 C>A maps to NM_170672.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:33745022 C>T maps to NM_170672.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:33752337 C>T maps to NM_170672.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:33768655 T>C maps to NM_170672.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr2:33759418 T>C maps to NM_170672.2 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr2:33740210 C>A maps to NM_170672.2 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:38901633 G>A maps to ENST00000405332 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:38903338 A>G maps to ENST00000405332 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:38912741 G>A maps to ENST00000405332 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:38903605 G>A maps to ENST00000405332 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:49228139 C>T maps to NM_017805.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr19:49228040 C>T maps to NM_017805.2 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr17:34062284 G>T maps to NM_033315.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:27847219 C>T maps to NM_206827.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:27847384 C>T maps to NM_206827.1 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr4:53729460 C>T maps to NM_023940.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr3:50368841 G>T maps to NM_170714.1 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:50368839 C>T maps to NM_170714.1 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:50369008 G>A maps to NM_170714.1 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:4764962 G>A maps to NM_014737.2 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:4766953 G>A maps to NM_014737.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:65004480 C>T maps to NM_178169.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:45477988 C>T maps to NM_032023.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:206680982 A>C maps to NM_182663.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:206757864 C>A maps to NM_182663.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:206757783 G>A maps to NM_182663.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:74450914 T>C maps to NM_201431.1 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:74464383 C>T maps to NM_201431.1 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:562379 G>T maps to NM_003475.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:26217572 G>A maps to NM_001164747.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:86198989 A>G maps to NM_005447.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:86198721 C>A maps to NM_005447.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr12:86199133 G>A maps to NM_005447.3 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:86198721 C>A maps to NM_005447.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:10439539 A>G maps to NM_133452.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:65273153 A>G maps to ENST00000294428 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:65243318 A>G maps to ENST00000294428 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:65243522 T>C maps to ENST00000294428 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr1:65243411 T>C maps to ENST00000294428 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr13:48955549 C>T maps to NM_000321.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr13:49030360 T>C maps to NM_000321.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr13:48955551 A>G maps to NM_000321.2 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr13:48923112 T>C maps to NM_000321.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr13:49037877 T>C maps to NM_000321.2 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr13:48919332 A>G maps to NM_000321.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr13:48953759 C>A maps to NM_000321.2 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr13:48955381 G>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:48923112 T>C maps to NM_000321.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr13:49039373 C>A maps to NM_000321.2 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:48937017 G>A maps to NM_000321.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:48916842 G>T maps to NM_000321.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:48937069 G>T maps to NM_000321.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr13:48881439 A>G maps to NM_000321.2 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:48955549 C>T maps to NM_000321.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr13:49037877 T>C maps to NM_000321.2 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr13:48934195 G>A maps to NM_000321.2 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:49033839 T>C maps to NM_000321.2 Y659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:49039373 C>T maps to NM_000321.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr13:48881430 A>G maps to NM_000321.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr13:48919306 T>C maps to NM_000321.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:48955428 A>G maps to NM_000321.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr13:48955380 A>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:48947597 A>G maps to NM_000321.2 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:49037928 C>A maps to NM_000321.2 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr13:48955580 T>A did not map to a codon.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr13:48936996 A>G maps to NM_000321.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr13:49047507 A>G maps to NM_000321.2 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr13:48947577 T>C maps to NM_000321.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr13:48936982 C>T maps to NM_000321.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr13:49047522 C>T maps to NM_000321.2 F839F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr13:49030486 T>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr13:48955480 G>T maps to NM_000321.2 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr13:48936982 C>T maps to NM_000321.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr13:48953759 C>T maps to NM_000321.2 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr13:48955381 G>T did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr13:48919332 A>G maps to NM_000321.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr13:48942684 C>A maps to NM_000321.2 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr13:48881523 A>G maps to NM_000321.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr13:49039338 A>G did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr13:48919284 A>G maps to NM_000321.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr13:48941656 G>T maps to NM_000321.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr13:49030387 T>C maps to NM_000321.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr13:48919245 A>G maps to NM_000321.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr13:49033968 A>G maps to NM_000321.2 Q702Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr13:49030360 T>A maps to NM_000321.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr13:48936996 A>G maps to NM_000321.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr13:48955380 A>T did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr13:48936984 A>G maps to NM_000321.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr13:49033915 C>T maps to NM_000321.2 Q685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:49033915 C>T maps to NM_000321.2 Q685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:49037864 A>T did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr13:48941652 C>T maps to NM_000321.2 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr13:49039375 A>G maps to NM_000321.2 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr13:48881439 A>G maps to NM_000321.2 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr13:49027202 T>C maps to NM_000321.2 C590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr13:49030360 T>C maps to NM_000321.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr13:49037877 T>C maps to NM_000321.2 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr13:48941647 C>T maps to NM_000321.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:48881437 G>T maps to NM_000321.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:48921999 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:48955571 G>A maps to NM_000321.2 W563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:48955503 C>T maps to NM_000321.2 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:49027167 C>A maps to NM_000321.2 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr13:48936982 C>T maps to NM_000321.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr13:49037864 A>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:53555083 T>C maps to NM_014781.4 E1388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr8:53555083 T>C maps to NM_014781.4 E1388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:53555016 C>A maps to NM_014781.4 G1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr8:53536371 C>T maps to NM_014781.4 V1585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr8:53555083 T>C maps to NM_014781.4 E1388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr8:53555086 T>C maps to NM_014781.4 E1387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:53555086 T>C maps to NM_014781.4 E1387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr7:5103890 A>G maps to NM_021163.3 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:5105132 C>T maps to NM_021163.3 N682N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:5104320 C>T maps to NM_021163.3 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr7:5103356 A>G maps to NM_021163.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr7:5104674 C>T maps to NM_021163.3 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:205064085 C>T maps to NM_005057.3 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:205065975 G>A maps to NM_005057.3 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr16:24560271 A>G maps to NM_006910.4 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr16:24581211 G>C maps to NM_006910.4 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:24573230 G>A maps to NM_006910.4 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr16:24578490 C>T maps to NM_006910.4 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr16:24578490 C>T maps to NM_006910.4 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr16:24578490 C>T maps to NM_006910.4 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr16:24578490 C>T maps to NM_006910.4 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr23:16870193 G>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:16870929 T>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:16876897 G>A did not map to a codon.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr23:16863188 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:16870936 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:16870699 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:16870936 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:16870189 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:16887316 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:16870678 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:16876897 G>A did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:16870702 A>G did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:16870947 G>A did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:16870702 A>G did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:16870700 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:18470506 T>C maps to NM_006606.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:28050493 T>C maps to NM_022128.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:28050589 G>A maps to NM_022128.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:28004631 T>C maps to NM_022128.1 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:35646735 C>A maps to NM_002895.2 E890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:35627263 G>A maps to NM_002895.2 I1035I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:35696530 C>A maps to NM_002895.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr20:35651204 A>G maps to NM_002895.2 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr20:35672554 C>T maps to NM_002895.2 W568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:35696492 A>G maps to NM_002895.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr20:35695219 T>A maps to NM_002895.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr20:35690600 T>C maps to NM_002895.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr20:35690600 T>C maps to NM_002895.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr20:35690600 T>C maps to NM_002895.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr20:35690600 T>C maps to NM_002895.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr20:35635837 G>T maps to NM_002895.2 Y949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:35661223 A>G maps to NM_002895.2 N742N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr16:53498217 T>C maps to NM_005611.3 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:53495698 G>T maps to NM_005611.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr16:53488675 G>A maps to NM_005611.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr16:53476701 C>A maps to NM_005611.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:47044516 A>G did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:47039843 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:47039852 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:47039373 G>A did not map to a codon.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr23:47044718 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:47030584 T>G did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:47030587 G>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:47039842 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:47028738 C>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:47039844 C>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:47040646 T>C did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:34242083 G>A maps to NM_001198838.1 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:34242569 C>T maps to NM_001198838.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr20:34240745 G>A maps to NM_001198838.1 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr20:34242047 T>C maps to NM_001198838.1 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:94746316 C>T maps to NM_203390.2 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:94747242 G>A maps to NM_203390.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:94746982 C>T maps to NM_203390.2 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:94747012 A>G maps to NM_203390.2 H542H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:94747072 A>G maps to NM_203390.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr11:66391808 G>T maps to NM_006328.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:66392855 C>A maps to NM_006328.3 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:110883997 T>C maps to NM_022768.4 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:110883715 T>C maps to NM_022768.4 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:51429445 C>T maps to NM_013286.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:51430450 C>A maps to NM_013286.4 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:51430506 C>T maps to NM_013286.4 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:155114051 G>A maps to NM_014892.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:155152161 C>T maps to NM_014892.3 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:155152086 G>A maps to NM_014892.3 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr6:155153496 G>A maps to NM_014892.3 P928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:155126565 G>A maps to NM_014892.3 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:155154226 G>T maps to NM_014892.3 E1172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:155154013 G>T maps to NM_014892.3 E1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr6:155109054 C>T maps to NM_014892.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:155123172 A>G maps to NM_014892.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:6139039 C>T maps to NM_001145547.1 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:6146946 C>T maps to NM_001145547.1 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr10:6155545 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:6146891 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:125014160 G>A maps to NM_033117.3 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr12:114261091 G>A maps to NM_016196.3 D940D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr12:114383677 G>A maps to NM_016196.3 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr12:114386716 G>A maps to NM_016196.3 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:114393004 T>C maps to NM_016196.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:150078094 A>G maps to NM_018047.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:23375465 C>T maps to NM_001077351.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:17292124 A>T maps to NM_001143942.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:17292148 T>C maps to NM_001143942.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:17292139 C>T maps to NM_001143942.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr14:73543066 T>C maps to NM_021239.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:73538420 G>A maps to NM_021239.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr14:73566388 T>C maps to NM_021239.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr14:73572648 C>T maps to NM_021239.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:79929464 C>A maps to ENST00000438737 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:79894756 C>A maps to ENST00000438737 *1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:79946026 T>C maps to ENST00000438737 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:79942955 G>A maps to ENST00000438737 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr13:79933777 T>C maps to ENST00000438737 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr13:79915341 G>A maps to ENST00000438737 D817D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:145603075 G>T maps to NM_018989.1 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:145641278 G>A maps to NM_018989.1 Q700Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr5:145664252 A>G maps to NM_018989.1 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:145641215 G>A maps to NM_018989.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr5:145631427 T>A maps to NM_018989.1 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:145610235 G>A maps to NM_018989.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr5:145613208 A>T maps to NM_018989.1 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr5:145616994 C>T maps to NM_018989.1 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:145651140 C>T maps to NM_018989.1 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:145631307 T>A maps to NM_018989.1 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr7:127964699 C>T maps to NM_018077.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr7:127975663 G>A maps to NM_018077.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:127953308 T>C maps to NM_018077.2 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:127955001 T>C maps to NM_018077.2 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr7:127953308 T>C maps to NM_018077.2 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr7:127953308 T>C maps to NM_018077.2 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:127961435 G>A maps to NM_018077.2 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr7:127953308 T>C maps to NM_018077.2 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:127953308 T>C maps to NM_018077.2 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:48434785 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:155530817 A>G maps to NM_053043.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:155499701 C>A maps to NM_053043.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:155534568 G>A maps to NM_053043.2 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:155504075 C>A maps to NM_053043.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:155537745 T>G maps to NM_053043.2 L810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:155530324 G>A maps to NM_053043.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:155530970 G>A maps to NM_053043.2 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:235295029 A>C maps to NM_015014.2 *431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:55967807 C>T maps to NM_017495.4 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:34293194 A>G maps to NM_184234.1 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:66411263 G>A maps to NM_001198845.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:66411371 T>A maps to NM_001198845.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:106331756 G>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:106359246 T>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:106312567 C>T did not map to a codon.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr19:36128413 C>G maps to NM_024321.3 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:152108129 C>A maps to NM_198557.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:238725760 G>T maps to NM_001080504.2 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:238737911 G>T maps to NM_001080504.2 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:238726545 T>C maps to NM_001080504.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:238732982 G>A maps to NM_001080504.2 E791E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:238728987 T>G maps to NM_001080504.2 L637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:238729897 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:178981056 C>A maps to ENST00000456670 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:155720057 A>G maps to NM_144979.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr4:155720154 C>T maps to NM_144979.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:155720060 G>A maps to NM_144979.3 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:155718975 A>G maps to NM_144979.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr4:155718981 A>G maps to NM_144979.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:40440670 G>A maps to NM_001098634.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:66444439 G>A maps to NM_031492.2 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr3:50150913 C>T maps to NM_005778.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:50131247 C>T maps to NM_005778.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:50141718 C>T maps to NM_005778.2 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:50005160 G>A maps to NM_005777.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:50095922 C>T maps to NM_005777.2 N686N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:50085676 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:50091790 C>T maps to NM_005777.2 H552H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:50005641 C>T maps to NM_005777.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:114276459 C>A maps to NM_016090.2 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:114278226 C>T maps to NM_016090.2 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr11:114278226 C>T maps to NM_016090.2 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:114278226 C>T maps to NM_016090.2 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr22:36140241 T>A maps to ENST00000338644 *389C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:36164390 G>A maps to NM_001082578.1 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:36164336 T>C maps to NM_001082578.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:36142521 G>A maps to NM_001082578.1 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr22:36156077 A>G maps to NM_001082578.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:161174692 C>T maps to NM_016836.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:161135121 G>A maps to NM_016836.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:161143586 C>A maps to NM_016836.3 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:56956280 A>C maps to NM_002898.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:29476353 C>T maps to NM_001003793.2 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:29476406 G>A did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:29941230 C>T maps to NM_001003793.2 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr3:29781311 T>C maps to NM_001003793.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:29781311 T>C maps to NM_001003793.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr23:135957726 T>C did not map to a codon.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr23:135957726 T>C did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:135956526 C>T did not map to a codon.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr23:135956466 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:135957535 T>C did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:135957724 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:135961520 T>G did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:135957724 T>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:135957724 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:135957726 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr23:135957726 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:129543286 A>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:129546483 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:129546564 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:129546355 A>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:129546358 A>G did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:129543261 C>T did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:129546358 A>G did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr23:129543286 A>G did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:129543285 A>G did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:129543286 A>G did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr1:89448768 A>G maps to NM_019610.5 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:89448606 C>T maps to NM_019610.5 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:89448768 A>G maps to NM_019610.5 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr11:7110494 G>A maps to NM_014469.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:7111367 C>G maps to NM_014469.4 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr11:7111124 C>T maps to NM_014469.4 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:139180989 G>A maps to NM_004164.2 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:48390166 G>A maps to NM_002900.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:48386037 C>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:48390265 G>T maps to NM_002900.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr10:48389287 G>A maps to NM_002900.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:48383856 G>A maps to NM_002900.2 H1125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:48390484 G>A maps to NM_002900.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:48389437 G>A maps to NM_002900.2 H480H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:95360174 G>A maps to NM_006744.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:7280883 T>C maps to NM_031491.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:7280919 G>A maps to NM_031491.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:7281299 T>C maps to NM_031491.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:10067761 G>T maps to ENST00000377192 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:26426100 T>C maps to NM_005349.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:26426251 G>A did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:26426278 G>T maps to NM_005349.2 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr4:26432337 C>A maps to NM_005349.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:43942708 G>A maps to NM_014276.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr20:43943132 G>A maps to NM_014276.2 Q316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr20:43945565 G>A maps to NM_014276.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr20:43945346 C>T maps to NM_014276.2 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr20:43940883 G>T maps to NM_014276.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr20:43945358 C>T maps to NM_014276.2 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:43942214 C>T maps to NM_014276.2 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:30361946 G>T maps to NM_001008712.1 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:65040722 G>T maps to NM_194272.1 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:173916540 A>G maps to NM_172071.2 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:173950024 T>G maps to NM_172071.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:173950101 C>A maps to NM_172071.2 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:173951862 A>G did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr1:173953672 A>G maps to NM_172071.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:173930349 G>A maps to NM_172071.2 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr1:173962093 A>G maps to NM_172071.2 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:173962057 G>A maps to NM_172071.2 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:125611950 G>A maps to NM_001100588.1 N1177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:125612076 C>T maps to NM_001100588.1 P1135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:125621108 G>A maps to NM_001100588.1 R708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:125622277 A>G maps to NM_001100588.1 Y589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:24861730 G>A maps to NM_013441.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:24861703 G>A maps to NM_013441.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr13:50134089 G>T maps to NM_018191.3 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:50115896 G>A maps to NM_018191.3 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:49086906 G>T maps to NM_001268.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:49064377 C>A maps to NM_001268.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:49089838 A>G maps to NM_001268.2 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr13:49089739 G>A maps to NM_001268.2 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr13:49089362 T>C maps to NM_001268.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:49076884 G>A maps to NM_001268.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:28858744 G>T maps to NM_001048194.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:28864404 C>T maps to NM_001048194.2 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:28858369 C>T maps to NM_001048194.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr1:28863289 T>C maps to NM_001048194.2 Y354Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:17736523 C>T maps to NM_018715.2 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:17749252 G>A maps to NM_018715.2 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:17749312 C>T maps to NM_018715.2 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:66613394 C>T maps to NM_005133.2 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr11:66613553 C>A maps to NM_005133.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr4:76407851 G>A maps to NM_015436.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:32118782 C>A maps to NM_002901.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr15:77236184 G>A maps to ENST00000320963 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:50042437 T>G did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:103174920 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:103173722 C>T maps to NM_015156.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:63682285 C>T maps to NM_173587.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:63683826 G>A maps to NM_173587.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:63682168 G>T maps to NM_173587.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:63680190 G>A maps to NM_173587.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr11:63681554 T>C maps to NM_173587.3 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:211486899 G>A maps to NM_001136223.1 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:167666934 C>T maps to NM_052862.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:167666377 C>T maps to NM_052862.3 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:167666517 C>A maps to NM_052862.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr17:9808239 G>A maps to NM_002903.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:9804369 G>A maps to NM_002903.2 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:9808161 G>A maps to NM_002903.2 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:9808278 G>A maps to NM_002903.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr17:9808338 G>A maps to NM_002903.2 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:211652575 C>T maps to NM_183059.2 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:211654727 G>A maps to NM_183059.2 N10N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:31922407 C>T maps to ENST00000375425 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:74235195 G>T maps to NM_172037.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr14:68145067 A>G maps to NM_016026.3 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr14:68192801 G>A maps to NM_152443.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:18736569 C>A maps to NM_020905.3 G300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:57345950 C>A maps to NM_003708.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:56115524 A>G maps to NM_002905.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:10132251 C>T maps to NM_015725.2 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:10127856 T>C maps to NM_015725.2 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr19:10127889 G>A maps to NM_015725.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:10132391 C>T maps to NM_015725.2 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:10127887 C>T maps to NM_015725.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:34247202 G>A maps to NM_145654.3 H247H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr17:34257226 G>A maps to NM_145654.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:110143338 G>A maps to ENST00000405097 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:24648319 T>C maps to NM_005132.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr14:24646683 G>T maps to NM_005132.2 G250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:24647331 C>T maps to NM_005132.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr14:24648821 G>A maps to NM_005132.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:36112443 T>C maps to NM_021111.2 C677C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:36121660 C>T maps to NM_021111.2 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr9:36121660 C>T maps to NM_021111.2 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:21629860 T>C maps to NM_032941.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:145738993 G>A maps to ENST00000428558 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:145742878 T>C maps to ENST00000428558 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:145740397 G>T maps to ENST00000428558 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:145739891 C>T maps to ENST00000428558 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr8:145741707 G>A maps to ENST00000428558 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:73623510 G>T maps to NM_004259.5 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:86479142 A>G maps to NM_022912.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:86479187 G>A maps to NM_022912.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:137780987 C>T maps to ENST00000378339 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:137780130 C>T maps to ENST00000378339 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:65380580 C>T maps to NM_001001330.2 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:21997473 A>G did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr5:112214530 C>T maps to NM_005669.4 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:112256906 G>T maps to NM_005669.4 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:1496351 C>T maps to ENST00000395479 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr2:79312651 A>G maps to NM_006507.3 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr2:79314023 G>A maps to NM_006507.3 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr2:79314021 T>C maps to NM_006507.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:79384369 G>T maps to NM_138937.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:79255401 G>T maps to NM_001008387.1 *176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:79254221 C>A maps to NM_001008387.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:79253279 C>T maps to NM_001008387.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr1:120337248 G>A maps to NM_032044.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:61144036 T>C maps to NM_002908.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:61128172 G>T maps to NM_002908.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:61147239 T>C maps to NM_002908.2 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:61121548 A>G maps to NM_002908.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr2:61144021 A>G maps to NM_002908.2 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:61144152 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:65422199 C>T maps to NM_021975.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:65427642 C>A maps to NM_021975.3 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:45537748 G>A maps to ENST00000221452 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:45528975 C>T maps to ENST00000221452 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:37636666 G>A maps to NM_001085399.1 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:37636636 G>A maps to NM_001085399.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:37651072 C>T maps to NM_001085399.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr7:103629638 C>T maps to ENST00000428762 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:103244809 G>A maps to ENST00000428762 C1043C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:103113285 T>C maps to ENST00000428762 R3452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:103138555 C>T maps to ENST00000428762 A2937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:103207054 C>T maps to ENST00000428762 P1580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr7:103159777 A>G maps to ENST00000428762 S2618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr7:103162528 T>C maps to ENST00000428762 G2536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:103197579 G>A maps to ENST00000428762 L1881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:103338437 T>C maps to ENST00000428762 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:103214552 G>A maps to ENST00000428762 D1499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr7:103368565 G>A maps to ENST00000428762 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:103191674 G>A maps to ENST00000428762 F2047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr7:103294580 C>A maps to ENST00000428762 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:103193928 C>T maps to ENST00000428762 E2017E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:103252242 C>A maps to ENST00000428762 G904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr7:103126723 G>A maps to ENST00000428762 Y3301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:103179558 G>A maps to ENST00000428762 F2382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:103183274 G>A maps to ENST00000428762 R2192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:103175932 T>C did not map to a codon.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr7:103113285 T>C maps to ENST00000428762 R3452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr7:103214612 A>G maps to ENST00000428762 D1479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr7:103191623 G>A maps to ENST00000428762 H2064H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr7:103124185 G>T maps to ENST00000428762 V3365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:103162501 G>A maps to ENST00000428762 A2545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr7:103214612 A>G maps to ENST00000428762 D1479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr11:73103391 C>T maps to NM_152222.1 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr14:23355273 C>T maps to NM_173527.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr14:23354086 C>A maps to NM_173527.2 S103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr14:23354517 G>T maps to NM_173527.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr14:23354207 C>T maps to NM_173527.2 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:204131191 C>T maps to NM_000537.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:153209823 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:153209595 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:153209400 A>G did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:153209774 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr12:27850070 G>A maps to NM_001029874.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:150069991 C>T maps to NM_001099695.1 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:139226220 G>A maps to ENST00000367663 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:139269017 A>G maps to ENST00000367663 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:139266437 G>A maps to ENST00000367663 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr6:139242174 G>A maps to ENST00000367663 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:17165583 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:17024394 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:17072947 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:17080577 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:8419853 T>C maps to NM_012102.3 R1196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:8419859 C>T maps to NM_012102.3 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:8555164 G>A maps to NM_012102.3 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:8716050 A>G maps to NM_012102.3 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:8617491 G>A maps to NM_012102.3 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:8415651 G>T maps to NM_012102.3 P1498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:8716140 C>T maps to NM_012102.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr1:8418946 G>A maps to NM_012102.3 R1216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:8419841 G>A maps to NM_012102.3 R1200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:15262228 C>A maps to NM_032918.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:18238610 C>T maps to NM_024730.2 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:57797298 G>T maps to NM_005612.4 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:43595950 C>T maps to NM_020975.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:43623704 G>A maps to NM_020975.4 T1111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr10:43615623 A>G maps to NM_020975.4 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr10:43597938 C>A maps to NM_020975.4 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:43608299 G>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:43609020 G>T maps to NM_020975.4 G593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr10:43608316 C>T maps to NM_020975.4 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr10:43613843 C>T maps to NM_020975.4 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr10:43597886 A>T maps to NM_020975.4 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:43606722 C>A maps to NM_020975.4 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:43597940 G>T maps to NM_020975.4 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:43601906 G>A maps to NM_020975.4 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:43617419 A>G maps to NM_020975.4 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr10:43619214 C>T maps to NM_020975.4 T966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr10:43615003 C>T maps to NM_020975.4 Y806Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr10:43615552 A>T maps to NM_020975.4 R878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr10:43604492 C>A maps to NM_020975.4 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr10:43617431 T>C maps to NM_020975.4 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:43617431 T>C maps to NM_020975.4 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr10:43617419 A>G maps to NM_020975.4 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr10:43623707 T>C maps to NM_020975.4 F1112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr10:43622072 C>T maps to NM_020975.4 D1030D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:43622096 A>G maps to NM_020975.4 T1038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:108475400 C>T maps to NM_032579.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:85576684 A>G maps to NM_017750.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:100021023 G>A maps to NM_016316.2 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:100019197 G>A maps to NM_016316.2 G1150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr2:100019561 C>T maps to NM_016316.2 K1058K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:100020954 C>T maps to NM_016316.2 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:100046381 C>T maps to NM_016316.2 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr2:100037985 C>T maps to NM_016316.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:100017813 G>A maps to NM_016316.2 L1216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:100019357 T>C maps to NM_016316.2 K1126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:100055282 C>T maps to NM_016316.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:111696145 C>A maps to NM_002912.3 E1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:111737565 G>T maps to NM_002912.3 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr6:111628730 G>T maps to NM_002912.3 R3029R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr6:111693941 A>G maps to NM_002912.3 P1872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:111631244 G>A maps to NM_002912.3 Y2951Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:111695093 A>G maps to NM_002912.3 P1488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:111688582 G>T maps to NM_002912.3 S2136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:111665170 G>A maps to NM_002912.3 R2499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:111689122 G>A maps to NM_002912.3 F1956F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:111698970 A>G maps to NM_002912.3 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:111688950 C>A maps to NM_002912.3 E2014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:111693992 T>C maps to NM_002912.3 S1855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:111737483 A>G did not map to a codon.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:111710342 A>G maps to NM_002912.3 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr6:111634647 A>G maps to NM_002912.3 G2837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:111696197 G>A maps to NM_002912.3 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:1827791 G>A maps to NM_020695.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:1827902 C>T maps to NM_020695.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:1828199 G>A maps to NM_020695.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr9:136278031 G>A maps to NM_020385.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:136277473 G>A maps to NM_020385.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:136277527 G>A maps to NM_020385.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:39291538 C>A maps to ENST00000381897 E1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:39324980 A>G maps to ENST00000381897 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:39328260 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:39322990 G>A maps to ENST00000381897 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr4:39328197 A>G maps to ENST00000381897 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr4:39297373 A>G maps to ENST00000381897 I939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:39304182 A>G maps to ENST00000381897 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:39293291 G>A maps to ENST00000381897 G1046G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr4:39328197 A>G maps to ENST00000381897 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:39318545 C>A maps to ENST00000381897 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:34404003 C>A maps to NM_002915.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:34405482 T>C maps to NM_002915.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:186508044 C>A did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:186522457 C>T maps to NM_181573.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:186509516 G>A maps to NM_181573.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:118457549 G>T maps to NM_007370.4 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr12:118467630 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:118467595 C>T maps to NM_007370.4 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr12:118463632 G>A maps to NM_007370.4 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr12:118456906 T>C maps to NM_007370.4 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:94990044 G>T maps to NM_001131065.1 G115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:33339130 A>G maps to NM_001017368.1 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr17:33343447 C>T maps to NM_001017368.1 W276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:80008638 G>A maps to NM_002917.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr22:32587274 G>A maps to NM_001098527.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:32586803 G>A maps to NM_001098527.2 N364N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr22:32756593 G>A maps to NM_001098535.1 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:112671030 G>T maps to NM_001013734.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:53164397 G>A maps to NM_052859.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:53139706 A>G maps to NM_052859.3 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:16419323 C>A maps to NM_015150.1 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:16358511 C>T maps to NM_015150.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr3:16358604 T>C maps to NM_015150.1 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr3:16358727 T>C maps to NM_015150.1 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr3:16358604 T>C maps to NM_015150.1 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:198480649 G>A maps to NM_144629.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:198498519 C>A maps to NM_144629.2 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:198511351 G>A maps to NM_144629.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:198480649 G>A maps to NM_144629.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:198508895 C>A maps to NM_144629.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:176012865 G>A maps to NM_022457.5 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:175996717 G>A maps to NM_022457.5 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr16:74662416 C>T maps to NM_018124.3 E634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:74662491 A>G maps to NM_018124.3 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr19:14094034 C>T maps to NM_002918.4 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:14076456 G>A maps to NM_002918.4 D698D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:6007158 G>A maps to NM_000635.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:6047438 C>T maps to NM_000635.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr19:6040250 G>A maps to NM_000635.3 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:6016272 G>A maps to NM_000635.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:6016189 C>T maps to NM_000635.3 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:3225113 G>A maps to NM_134428.1 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:3270470 G>A maps to NM_134428.1 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:3263050 G>A maps to NM_134428.1 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:3293119 T>G maps to NM_134428.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr9:3257112 G>A maps to NM_134428.1 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr12:106995089 C>T maps to ENST00000357881 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:107048083 C>T maps to ENST00000357881 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:107090149 C>T maps to ENST00000357881 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:107103189 C>T maps to ENST00000357881 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:107078608 C>T maps to NM_032491.4 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:107103203 C>T maps to ENST00000357881 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:151316198 G>A maps to NM_000449.3 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:151315314 G>A maps to NM_000449.3 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:151315327 T>C maps to NM_000449.3 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:151318693 G>A maps to NM_000449.3 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:117250036 C>T maps to NM_173560.3 H838H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:117245848 C>T maps to NM_173560.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:117250118 C>T maps to NM_173560.3 R866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:117248469 C>T maps to NM_173560.3 T722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:117237470 T>G maps to NM_173560.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:117241470 A>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:56387063 G>A maps to NM_022841.5 P954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:56387066 T>A maps to NM_022841.5 T953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:56388764 G>A maps to NM_022841.5 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:19309476 G>A maps to NM_003721.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:19308408 C>T maps to NM_003721.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr13:37394093 G>A maps to NM_000538.3 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:101284410 T>C maps to NM_017819.2 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:101284410 T>C maps to NM_017819.2 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:100480405 C>T maps to NM_001134666.1 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr4:100470294 G>A maps to NM_001134666.1 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:100479276 G>A maps to NM_001134666.1 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr4:100472126 C>T maps to NM_001134666.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr4:100470493 T>C maps to NM_001134666.1 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr4:100479307 T>C maps to NM_001134666.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr4:100470493 T>C maps to NM_001134666.1 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr4:100470495 C>A maps to NM_001134666.1 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr4:100470493 T>C maps to NM_001134666.1 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:37776403 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:37763635 C>A maps to NM_144964.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:37762572 G>T did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:109693923 G>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:109697083 G>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:109693885 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:109694877 G>A did not map to a codon.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr23:109694633 G>A did not map to a codon.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr23:109695868 C>T did not map to a codon.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr23:109697206 C>T did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:109695688 C>A did not map to a codon.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr23:109695667 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:109695332 G>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:109694611 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:109697345 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:109697438 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:109696015 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:109697088 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:109697438 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:109696926 T>C did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:109697357 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:109697554 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:71350090 G>A did not map to a codon.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr23:71349793 G>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:71350665 C>T did not map to a codon.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr23:71350454 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:71350437 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:71350531 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:71349759 C>T did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:71350665 C>T did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:71350139 T>G did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:71350455 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:183876196 G>A maps to NM_015149.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr1:183881359 C>A maps to NM_015149.3 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:183876196 G>A maps to NM_015149.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:183867012 G>C maps to NM_015149.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:183895353 G>A maps to NM_015149.3 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:183895365 G>A maps to NM_015149.3 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr1:183849845 T>C maps to NM_015149.3 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:183816731 A>T maps to NM_015149.3 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:183849845 T>C maps to NM_015149.3 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:11513172 C>T maps to NM_001161616.1 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:11526751 C>T maps to NM_001161616.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:93588419 G>A maps to NM_020211.2 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr15:93588422 G>A maps to NM_020211.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:98128901 C>T maps to NM_001012761.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:98129407 T>A maps to NM_001012761.2 L463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:98128958 C>T maps to NM_001012761.2 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:46940592 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:46949334 C>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:73179621 C>T maps to NM_001080479.2 R990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr5:73163755 C>T maps to NM_001080479.2 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:107041115 C>A maps to ENST00000304514 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:86008713 C>T maps to ENST00000358110 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:86008737 G>A maps to ENST00000358110 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:86012655 C>T maps to ENST00000358110 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:192545026 C>T maps to NM_002922.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:192544927 C>T maps to NM_002922.3 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:121285602 C>A maps to NM_001005339.1 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:323531 C>T maps to NM_183337.1 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr4:3318001 G>A maps to NM_198229.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:3416493 G>T maps to NM_198229.2 E736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:3318055 G>T maps to NM_198229.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:3430377 G>T maps to NM_198229.2 E1169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr4:3319126 C>T maps to NM_198229.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:3319264 G>A maps to NM_198229.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:3419209 G>A maps to NM_198229.2 S901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr1:192628484 G>C maps to NM_144766.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:176794498 G>T maps to ENST00000398128 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr5:176793941 G>A maps to ENST00000398128 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:153345449 C>A maps to NM_012419.4 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:153347611 C>T maps to NM_012419.4 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:153365045 G>A maps to NM_012419.4 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:153332709 T>C maps to NM_012419.4 *211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr1:192150458 A>G maps to NM_130782.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:192127872 G>T maps to NM_130782.2 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr20:62705325 G>A maps to NM_005873.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr20:62705340 G>A maps to NM_005873.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr20:62705622 G>A maps to NM_005873.2 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:62705328 G>A maps to NM_005873.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:192778204 C>T maps to NM_002923.3 Q2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:192780123 A>G maps to NM_002923.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr8:54852158 G>A maps to NM_170587.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:54866662 C>T maps to NM_170587.2 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr8:54791852 C>T maps to NM_170587.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:192335064 C>T maps to NM_001039152.3 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr8:100999754 A>G maps to NM_015668.3 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:101065032 G>A maps to NM_015668.3 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:101052207 G>A maps to NM_015668.3 C682C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:101075774 A>G maps to NM_015668.3 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr8:101117619 A>T maps to NM_015668.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:101051196 C>A maps to NM_015668.3 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:101083706 C>A maps to NM_015668.3 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr8:100999754 A>G maps to NM_015668.3 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:101075774 A>T maps to NM_015668.3 Y407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:116359175 C>A maps to NM_144488.4 L1180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:116353677 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:116246461 G>A maps to NM_144488.4 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:116276867 G>A maps to NM_144488.4 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:116269629 A>C maps to NM_144488.4 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:116279900 C>T maps to NM_144488.4 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr1:163044229 C>T maps to NM_001102445.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:163044313 A>G maps to NM_001102445.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr14:72941365 C>T maps to NM_004296.4 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:72939654 G>A maps to NM_004296.4 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:72985127 C>A maps to NM_004296.4 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:72431579 C>T maps to NM_004296.4 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:240975294 G>A maps to ENST00000407727 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:63871639 T>G maps to NM_001029875.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:63871724 C>T maps to NM_001029875.1 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr1:182617328 C>T maps to NM_033345.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:182636088 G>A maps to NM_033345.2 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:63204095 T>A maps to NM_003835.3 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:33167873 C>T maps to NM_207391.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr6:49583358 G>A maps to NM_000324.2 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:227779032 C>T maps to NM_001167608.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:75517426 C>A maps to NM_001040456.1 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:29656137 G>A maps to NM_012265.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:108353 G>A maps to NM_022450.3 D851D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:111225 C>T maps to NM_022450.3 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:108362 G>A maps to NM_022450.3 Y848Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:74467938 G>A maps to NM_024599.5 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:39361718 A>G maps to ENST00000372985 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:39361730 G>A maps to ENST00000372985 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:30647998 C>T maps to NM_138328.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:30648025 C>A maps to NM_138328.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr1:156347170 C>T maps to NM_020407.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr1:156348107 G>T maps to NM_020407.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr1:156351673 G>A maps to NM_020407.3 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:156348062 C>T maps to NM_020407.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:25735325 G>A maps to NM_020485.4 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:25712263 C>T maps to NM_020485.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:25718593 G>A maps to NM_020485.4 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr15:90023597 G>A maps to NM_016321.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:151164246 G>A maps to NM_005614.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:151167703 C>A maps to NM_005614.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr7:151167703 C>A maps to NM_005614.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:129251530 T>C maps to NM_000539.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:129251162 C>T maps to NM_000539.3 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr3:129247761 C>T maps to NM_000539.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:129251141 G>A maps to NM_000539.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:129252482 C>T maps to NM_000539.3 C323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:129251141 G>A maps to NM_000539.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr3:129247884 C>T maps to NM_000539.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:49412865 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:49412973 C>A maps to NM_001664.2 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr3:49412973 C>A maps to NM_001664.2 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:49412973 C>A maps to NM_001664.2 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr2:20647264 C>T maps to NM_004040.2 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:62648342 G>A maps to NM_014836.4 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:62671288 G>A maps to NM_014836.4 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:62631979 G>T maps to NM_014836.4 C628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:62671216 C>T maps to NM_014836.4 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:62647976 C>T maps to NM_014836.4 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:22865167 T>C maps to NM_001160036.1 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr5:95067646 G>C maps to NM_014899.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:113246328 C>T maps to NM_175744.4 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:66834209 G>T maps to NM_014578.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:40245119 C>T maps to NM_004310.3 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:40245026 C>T maps to NM_004310.3 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:40245059 C>A maps to NM_004310.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:40245251 C>T maps to NM_004310.3 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:63757597 C>T maps to NM_020663.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:63671698 C>T maps to NM_020663.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:63747756 C>T maps to NM_020663.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:63671658 T>C maps to NM_020663.3 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr14:63735846 C>A maps to NM_020663.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr14:63671715 C>T maps to NM_020663.3 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:46770310 C>A maps to NM_012249.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr2:46803716 C>T maps to NM_012249.3 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr2:46803227 A>G maps to NM_012249.3 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:46770896 C>T maps to NM_012249.3 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr17:30526525 G>T maps to NM_001033568.1 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr17:30510233 C>T maps to NM_001033568.1 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:30534038 G>A maps to NM_001033568.1 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:30533948 G>A maps to NM_001033568.1 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:30509869 G>T maps to NM_001033568.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr17:30526010 A>G maps to NM_001033568.1 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr17:30529840 G>A maps to NM_001033568.1 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr16:718513 C>G maps to NM_138769.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:722986 C>T maps to NM_138769.1 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:228879270 G>A maps to NM_021205.4 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:228879192 G>A maps to NM_021205.4 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:41166148 A>G maps to NM_133639.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr23:119243189 C>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:119249449 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:119246780 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:119211113 G>A did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:119293303 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:119293135 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:144463884 C>T maps to ENST00000422773 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:144464047 G>T maps to ENST00000422773 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:33482728 C>T maps to NM_033103.4 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:33498944 G>A maps to NM_033103.4 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr19:33482728 C>A maps to NM_033103.4 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:53457376 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:53456905 G>A did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr22:45821832 C>T maps to NM_015653.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr11:8132316 C>T maps to ENST00000309737 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr11:8132394 A>G maps to ENST00000309737 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:12852557 C>T maps to NM_014859.4 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:12893373 G>A maps to NM_014859.4 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:12819215 G>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:12847416 G>A maps to NM_014859.4 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr17:12862146 G>T maps to NM_014859.4 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr5:38991080 G>A maps to ENST00000296782 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:38982100 T>C maps to ENST00000296782 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:38991156 G>T maps to ENST00000296782 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr2:152322492 T>C maps to NM_018151.4 P2153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr2:152292056 A>G maps to NM_018151.4 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:152314272 A>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:152314272 A>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:152321409 T>C maps to NM_018151.4 H1792H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:152314403 C>T maps to NM_018151.4 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:152322276 C>T maps to NM_018151.4 D2081D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr2:152296637 G>C maps to NM_018151.4 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:152320360 C>T maps to NM_018151.4 R1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:152319990 A>G maps to NM_018151.4 E1319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:152322492 T>A maps to NM_018151.4 P2153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:152267798 G>T maps to NM_018151.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr2:152293857 T>C maps to NM_018151.4 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:152319990 A>G maps to NM_018151.4 E1319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:152321385 A>G maps to NM_018151.4 E1784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr2:152314272 A>G did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr2:152321385 A>G maps to NM_018151.4 E1784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:152314272 A>T did not map to a codon.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr2:152273105 G>A maps to NM_018151.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:152322492 T>C maps to NM_018151.4 P2153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr2:152319990 A>G maps to NM_018151.4 E1319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:152308130 C>T maps to NM_018151.4 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:152322114 C>T maps to NM_018151.4 G2027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr2:152314272 A>G did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:152314272 A>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:152314272 A>G did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr2:152314272 A>T did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr2:152321898 C>T maps to NM_018151.4 D1955D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr12:123970319 G>A maps to NM_178314.3 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:123907700 G>T maps to NM_145058.1 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:130922972 C>T maps to NM_015347.4 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr12:130892306 G>A maps to NM_015347.4 Y963Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:130941155 G>A maps to NM_015347.4 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:130892273 G>A maps to NM_015347.4 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr12:130929759 C>T maps to NM_015347.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:130922972 C>T maps to NM_015347.4 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr12:130926987 G>A maps to NM_015347.4 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr12:130923032 G>A maps to NM_015347.4 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr12:130926672 C>T maps to NM_015347.4 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:20460134 G>A maps to NM_015672.1 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:42880158 C>T maps to NM_173642.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:42875718 C>T maps to NM_173642.3 H182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:8904625 G>A maps to NM_020734.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:8906505 C>T maps to NM_020734.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr6:73000444 C>A maps to NM_014989.4 V1206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:72806711 G>A maps to NM_014989.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:72960940 G>A maps to NM_014989.4 A856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:73043537 G>T maps to NM_014989.4 E1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:72947555 C>T maps to NM_014989.4 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:72943542 G>A maps to NM_014989.4 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:73110380 G>T maps to NM_014989.4 E1682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr6:72962468 C>T maps to NM_014989.4 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:73000540 G>A maps to NM_014989.4 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:72960765 C>T maps to NM_014989.4 Q839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:72806726 C>T maps to NM_014989.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:72892268 G>A maps to NM_014989.4 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:72952101 A>G maps to NM_014989.4 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:72889448 C>T maps to NM_014989.4 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:73043434 T>C maps to NM_014989.4 G1421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:72984117 G>A maps to NM_014989.4 A1155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:73107964 G>T maps to NM_014989.4 G1545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:73016970 A>C maps to NM_014989.4 V1287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr6:73000417 A>T maps to NM_014989.4 A1197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr6:73043343 C>A maps to NM_014989.4 S1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr6:73043378 G>T maps to NM_014989.4 G1403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:72984117 G>A maps to NM_014989.4 A1155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr6:72952107 T>A maps to NM_014989.4 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr6:72968727 T>C maps to NM_014989.4 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr6:73108724 C>A maps to NM_014989.4 R1597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:72678731 A>C maps to NM_014989.4 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:72943512 G>A maps to NM_014989.4 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:104897786 C>T maps to NM_001100117.2 Y320Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr8:104948920 C>T maps to NM_001100117.2 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:104898224 A>G maps to NM_001100117.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr8:104898168 T>C maps to NM_001100117.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:104928655 G>T maps to NM_001100117.2 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:104948862 C>T maps to NM_001100117.2 H820H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:104778624 G>A maps to NM_001100117.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr8:104948920 C>T maps to NM_001100117.2 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:104927793 A>G maps to NM_001100117.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:104897849 T>C maps to NM_001100117.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:105263915 C>T maps to NM_001100117.2 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr8:105025714 A>G maps to NM_001100117.2 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:104948946 C>T maps to NM_001100117.2 G848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr8:105025714 A>G maps to NM_001100117.2 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:105263972 C>A maps to NM_001100117.2 T1325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:104954999 G>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr8:104928759 T>A maps to NM_001100117.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr8:104954998 A>G did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr8:105257201 C>T maps to NM_001100117.2 A1131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr8:105263381 A>G maps to NM_001100117.2 K1274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr8:105010466 C>T maps to NM_014677.4 H825H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr8:104897618 C>T maps to NM_001100117.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr8:105025713 C>A maps to NM_001100117.2 S1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:41098747 T>C maps to NM_014747.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr20:43384801 G>A maps to NM_182970.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:43385613 G>A maps to NM_182970.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr11:66100001 G>A maps to NM_004292.2 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:19977392 G>A maps to ENST00000255006 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:19956306 C>T maps to ENST00000255006 C595C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:19972914 C>G maps to ENST00000255006 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:19956237 G>T maps to ENST00000255006 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:19955559 C>T maps to ENST00000255006 N346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:93125734 C>A maps to NM_024832.3 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr14:93118320 T>C maps to NM_024832.3 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr14:93118392 G>A maps to NM_024832.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr14:93118833 C>T maps to NM_024832.3 N480N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr14:93118332 C>A maps to NM_024832.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:39360270 C>T maps to NM_001195833.1 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr7:105187425 A>G maps to NM_021930.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr7:105207742 T>A maps to NM_021930.4 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:105182890 C>T maps to NM_021930.4 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:105189009 A>G maps to NM_021930.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:105183036 T>A maps to NM_021930.4 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr7:105183036 T>C maps to NM_021930.4 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr5:96507040 A>G maps to NM_018343.2 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr18:21043043 G>A did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr18:21044582 A>G maps to NM_003831.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr18:21044582 A>G maps to NM_003831.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr18:21044582 A>G maps to NM_003831.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:3105896 A>G maps to NM_003804.3 K396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr6:3083443 C>A maps to NM_003804.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:3111038 G>T maps to NM_003804.3 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:3111145 G>A maps to NM_003804.3 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:3083464 C>T maps to NM_003804.3 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:3104497 C>T maps to NM_003804.3 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr8:90782050 C>T maps to NM_003821.5 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr8:90802508 C>T maps to NM_003821.5 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:24806109 C>T maps to NM_006871.3 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:24808394 G>A maps to NM_006871.3 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:24808382 C>T maps to NM_006871.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr21:43176891 G>A maps to ENST00000352483 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr21:43161480 G>A maps to ENST00000352483 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr21:43161930 C>T maps to ENST00000352483 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr21:43161867 G>A maps to ENST00000352483 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr21:43162011 C>T maps to ENST00000352483 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr21:43161930 C>T maps to ENST00000352483 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:106146490 A>G did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:40503694 G>A maps to NM_002930.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr18:40503563 G>A maps to NM_002930.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:89760453 C>T maps to NM_000326.4 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr15:89761828 C>T maps to NM_000326.4 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:89758307 C>A maps to NM_000326.4 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:89760441 C>T maps to NM_000326.4 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:40701949 A>C maps to NM_012421.3 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:40704282 G>A maps to NM_012421.3 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:40703415 C>A maps to NM_012421.3 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:40688256 C>T maps to NM_012421.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:40703130 T>C maps to NM_012421.3 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr1:40703592 A>G maps to NM_012421.3 K1073K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr23:73812055 C>T did not map to a codon.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr23:73811989 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:73812149 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:73812800 T>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:73814189 T>C did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:73812798 T>C did not map to a codon.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr23:73812800 T>C did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:73811648 A>G did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:73811646 T>C did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:5339731 G>A maps to NM_006911.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:14139048 G>T maps to NM_080864.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:67691193 C>T maps to NM_001013838.1 L1390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:67683045 G>A maps to NM_001013838.1 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:67685911 G>A did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr16:67688411 C>T maps to NM_001013838.1 G1133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:67688351 A>G maps to NM_001013838.1 P1113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:67682617 G>A maps to NM_001013838.1 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:86615993 T>C maps to NM_024945.2 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:86616009 G>T maps to NM_024945.2 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:86617157 G>A maps to NM_024945.2 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:86617346 T>C maps to NM_024945.2 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:151743690 A>G maps to NM_017909.2 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:86992258 C>T maps to NM_022780.3 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:177570681 C>T maps to NM_022762.3 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:177569977 C>T maps to NM_022762.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr14:21270034 G>A maps to NM_198235.2 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr14:20978830 G>A maps to ENST00000430083 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:21052500 C>A maps to NM_145250.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:21052171 T>C maps to NM_145250.3 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr14:21052114 A>G maps to NM_145250.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr14:21052066 C>T maps to NM_145250.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:21424040 G>A maps to NM_002934.2 W37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr14:21511531 C>T maps to NM_032572.3 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr13:51509076 C>T maps to NM_024570.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:182545517 C>A maps to NM_021133.3 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:182555097 C>A maps to NM_021133.3 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:182555659 C>T maps to NM_021133.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr5:31526595 A>G maps to NM_013235.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:31483703 G>A maps to NM_013235.4 C676C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:31504712 G>A maps to NM_013235.4 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:31515282 C>A maps to NM_013235.4 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:31511211 G>A maps to NM_013235.4 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:31526816 G>A maps to NM_013235.4 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:31449418 T>C maps to NM_013235.4 R930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:49254797 C>T maps to NM_014470.3 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:49251876 G>A maps to NM_014470.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:49254797 C>T maps to NM_014470.3 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr17:41180095 G>T maps to NM_005440.4 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:41179233 C>A maps to NM_005440.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr12:120984349 C>T maps to ENST00000458409 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:59383325 A>G maps to ENST00000434298 R913R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr15:59368181 T>C maps to ENST00000434298 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:59323266 G>A maps to ENST00000434298 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr15:59368257 C>T maps to ENST00000434298 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr15:59359140 T>C maps to ENST00000434298 H515H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr15:59383325 A>G maps to ENST00000434298 R913R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr15:59383325 A>G maps to ENST00000434298 R913R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr17:19318123 A>G maps to NM_007148.4 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:119004605 C>G did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:119005317 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr13:98828962 G>A maps to NM_178861.4 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:98828574 C>A maps to NM_178861.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr1:145663166 C>T maps to NM_014455.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:145688205 C>T maps to NM_014455.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:71701645 C>A maps to NM_018320.4 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr3:49740091 G>A maps to NM_022064.2 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:49751584 C>T maps to NM_022064.2 D996D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:49736970 C>T maps to NM_022064.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:648205 A>G maps to ENST00000340092 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:105970347 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:106031158 T>C did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr23:106038928 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:106038845 C>A did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:105970196 C>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:105970370 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:106028342 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:149678776 C>T maps to NM_007282.4 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:149629767 C>T maps to NM_007282.4 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:149613279 A>G maps to NM_007282.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr3:149613279 A>G maps to NM_007282.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr3:149613279 A>G maps to NM_007282.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:179393926 G>A maps to NM_018434.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:179440132 A>G maps to NM_018434.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr5:179393926 G>A maps to NM_018434.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr5:179467636 A>G maps to NM_018434.4 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:122338123 A>G maps to NM_139175.1 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:122338675 C>T maps to NM_139175.1 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr17:29314969 T>C maps to NM_032322.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:29693799 C>A maps to NM_001191324.1 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:141358277 G>A maps to NM_183399.1 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:7160637 G>A maps to NM_014746.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr5:158588426 G>A maps to NM_144726.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr5:158588273 C>T maps to NM_144726.2 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr5:158603756 A>G maps to NM_144726.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:127608259 C>T maps to ENST00000368314 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:127608354 C>T maps to ENST00000368314 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:127608468 T>C maps to ENST00000368314 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr7:122341982 T>C maps to NM_198085.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:122342705 G>A maps to NM_198085.1 N33N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:101902592 G>A maps to NM_173647.3 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:142053581 C>T maps to NM_020724.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:142053773 G>A maps to NM_020724.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:141888827 G>T maps to NM_020724.1 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:141889013 G>A maps to NM_020724.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:141832469 G>A maps to NM_020724.1 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:141789414 T>G maps to NM_020724.1 *439C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:141832469 G>A maps to NM_020724.1 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:59483513 A>G maps to NM_173557.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr18:59483390 C>T maps to NM_173557.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr21:30318544 C>T maps to NM_015565.2 E1230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr21:30332977 G>A maps to NM_015565.2 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr21:30324513 A>G maps to NM_015565.2 D1150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr21:30354657 A>G maps to NM_015565.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr21:30303488 A>G maps to NM_015565.2 H1788H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:30325698 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr21:30331797 C>A maps to NM_015565.2 E905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr21:30303488 A>G maps to NM_015565.2 H1788H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr18:44013333 G>A maps to NM_152470.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:196199141 C>A maps to NM_152617.3 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:196214326 C>T maps to NM_152617.3 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr11:74547323 T>G maps to NM_001098638.1 L559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr11:74546904 G>A maps to NM_001098638.1 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:74546799 C>A maps to NM_001098638.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr11:74547039 A>G maps to NM_001098638.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr13:25418895 C>T maps to ENST00000381927 R1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:25433164 G>T maps to ENST00000381927 E1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:25448297 G>A maps to ENST00000381927 A1547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:25373591 G>T maps to ENST00000381927 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr13:25374503 A>G maps to ENST00000381927 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr13:25374501 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:42711333 G>A maps to NM_030954.3 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:42742905 G>A maps to NM_030954.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:154633694 G>A maps to ENST00000274068 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr5:63510247 G>A maps to NM_001113561.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:63509762 G>T maps to NM_001113561.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr5:63509803 C>A maps to NM_001113561.1 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr6:13977775 G>A maps to NM_001165033.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:13977385 T>A maps to NM_001165033.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr6:13977721 G>A maps to NM_001165033.1 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr6:13977523 A>G maps to NM_001165033.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr6:13977523 A>G maps to NM_001165033.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr6:13977478 T>C maps to NM_001165033.1 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr6:13977523 A>G maps to NM_001165033.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr6:13977478 T>C maps to NM_001165033.1 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:20141576 G>T maps to NM_019062.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr8:101299931 A>G maps to NM_183419.1 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:101271191 C>T maps to NM_183419.1 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr8:101299868 T>C maps to NM_183419.1 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr8:101299868 T>C maps to NM_183419.1 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:33407932 G>A maps to NM_153341.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:104309212 C>T maps to NM_019592.5 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr9:104309233 G>T maps to NM_019592.5 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr9:104314838 C>T maps to NM_019592.5 R569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr9:104314844 C>T maps to NM_019592.5 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:104316388 T>C did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr9:104312931 A>G maps to NM_019592.5 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:6278396 C>T maps to NM_207396.2 H567H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:6269553 C>T maps to NM_207396.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:1079710 G>T maps to NM_001131034.3 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:78363846 G>A maps to NM_020914.4 A5156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr17:78363858 G>T maps to NM_020914.4 P5160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:78346490 C>T maps to NM_020914.4 L4285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr17:78350234 T>C maps to NM_020914.4 D4489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:78348280 C>A maps to NM_020914.4 G4371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:78318749 C>T maps to NM_020914.4 C2254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr17:78314013 C>T maps to NM_020914.4 F1998F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:78321545 C>T maps to NM_020914.4 R3186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr17:78332234 T>C maps to NM_020914.4 S3719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:78320270 G>A maps to NM_020914.4 P2761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:78272294 G>A maps to NM_020914.4 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr17:78261891 A>G maps to NM_020914.4 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:78320162 C>T maps to NM_020914.4 T2725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr17:78363858 G>A maps to NM_020914.4 P5160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:78324166 C>T maps to NM_020914.4 I3434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr17:78358915 C>T maps to NM_020914.4 N4849N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:117150668 C>T maps to NM_207343.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:117150910 G>T maps to NM_207343.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:5780603 C>A maps to NM_207111.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:5754797 G>A maps to NM_207111.2 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr7:5662730 G>A maps to NM_207111.2 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr7:5680883 T>C maps to NM_207111.2 R761R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:5756344 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:125397988 C>T maps to NM_152553.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr13:79219012 A>G maps to NM_024546.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:79190281 G>T maps to NM_024546.3 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:79190473 A>G maps to NM_024546.3 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:79213203 G>A maps to NM_024546.3 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr13:79219012 A>G maps to NM_024546.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr13:79219012 A>G maps to NM_024546.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:79209252 T>C maps to NM_024546.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr13:79219012 A>G maps to NM_024546.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:79233246 C>T maps to NM_024546.3 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:44878203 C>A maps to ENST00000453887 C145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:45115565 G>A maps to ENST00000453887 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr1:45101823 T>C maps to ENST00000453887 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:44877904 C>T maps to ENST00000453887 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr1:44878362 C>T maps to ENST00000453887 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:3914787 T>C maps to NM_001134338.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:119205972 G>A maps to NM_032015.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr11:119207118 C>T maps to NM_032015.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr14:24619653 T>A maps to NM_017999.4 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr14:24626605 C>T maps to NM_017999.4 N867N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:24629073 C>A maps to NM_017999.4 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:24619653 T>C maps to NM_017999.4 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr14:24617531 C>T maps to NM_017999.4 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr14:24626801 C>T maps to NM_017999.4 R894R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr14:24619653 T>C maps to NM_017999.4 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:156447396 C>T maps to NM_001184997.1 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:156447391 G>T maps to NM_001184997.1 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:121858085 T>C maps to NM_194271.1 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:121858088 C>T maps to NM_194271.1 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr9:36369715 C>T maps to NM_022781.4 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr9:36356446 C>T maps to NM_022781.4 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr4:2502465 G>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:30773985 C>T maps to NM_014771.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:30776587 C>T maps to NM_014771.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:30777866 C>T maps to NM_014771.2 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:30780625 A>G maps to NM_014771.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:56604295 C>T maps to NM_194359.1 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr17:56435860 G>A maps to NM_017763.4 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr17:56436149 A>T maps to NM_017763.4 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:56440903 G>A maps to NM_017763.4 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:175956092 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:175957654 T>C maps to NM_014901.4 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:32147528 C>A maps to NM_006913.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr13:26788644 A>G maps to NM_005977.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr13:26789646 A>G maps to NM_005977.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr13:26789646 A>G maps to NM_005977.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr13:26788841 G>A maps to NM_005977.3 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr13:26789646 A>G maps to NM_005977.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:37358516 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:37358530 C>T maps to NM_003958.3 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:58033866 T>C maps to NM_016125.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:117187654 C>T maps to NM_001109903.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:117274038 C>T maps to NM_001109903.1 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr12:117271724 C>T maps to NM_001109903.1 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:117274038 C>T maps to NM_001109903.1 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr12:117271709 G>T maps to NM_001109903.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:89638916 C>A maps to NM_003800.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:89600293 C>T maps to NM_003800.3 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:89324035 G>A maps to NM_003800.3 Q529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:494899 G>A maps to NM_203389.1 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:90342923 G>A maps to NM_001031709.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:90122342 G>A maps to NM_001031709.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr18:13731884 T>C maps to NM_003799.1 T123T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3977-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:685764 A>G maps to NM_018146.2 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:691202 A>G did not map to a codon.
Multiple mappings detected for codon TCGA-CM-5349-01A-21D-1719-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CM-6171-01A-11D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:201958635 G>T maps to NM_020216.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:201972383 G>A maps to NM_020216.3 W482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr1:201970504 C>T maps to NM_020216.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:241515961 C>T maps to NM_018226.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:241512669 C>T maps to NM_018226.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:241513565 C>T maps to NM_018226.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:241514445 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr1:156027789 C>T maps to NM_014017.3 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:79638980 A>T maps to NM_002941.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:78708922 G>A maps to NM_002941.3 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:78708882 G>A maps to NM_002941.3 Q799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:78666950 G>A maps to NM_002941.3 N1372N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:78676637 T>C maps to NM_002941.3 E1236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:78666881 G>T maps to NM_002941.3 G1395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr3:78708889 A>T maps to NM_002941.3 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr3:78667088 C>T maps to NM_002941.3 A1326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:78795907 T>C maps to NM_002941.3 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr3:78685121 C>T maps to NM_002941.3 L1058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr3:78689014 C>T maps to NM_002941.3 A972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:78766435 C>A maps to NM_002941.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:78655952 A>G maps to NM_002941.3 N1558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:78685139 G>T maps to NM_002941.3 T1052T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:78710342 T>C maps to NM_002941.3 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:78676577 G>A maps to NM_002941.3 S1256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:78700891 A>G maps to NM_002941.3 G934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:78649270 C>A maps to NM_002941.3 E1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:78666965 C>T maps to NM_002941.3 T1367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:78767029 G>A maps to NM_002941.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr3:78719377 G>A maps to NM_002941.3 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr3:77671488 C>T maps to ENST00000332191 D1222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:77645843 T>C maps to ENST00000332191 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:77147466 C>T maps to ENST00000332191 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:77645884 A>C maps to ENST00000332191 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:77666772 C>T maps to ENST00000332191 R1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr3:77147279 G>A maps to ENST00000332191 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:77147474 G>A maps to ENST00000332191 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:77638009 G>A maps to ENST00000332191 W870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr3:77147310 C>T maps to ENST00000332191 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr3:77629225 T>C maps to ENST00000332191 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr3:77666780 G>A maps to ENST00000332191 V1137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr3:77671488 C>T maps to ENST00000332191 D1222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr3:77638009 G>A maps to ENST00000332191 W870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr3:77666777 C>T maps to ENST00000332191 G1136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:77693936 A>G maps to ENST00000332191 G1400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:124739491 G>T maps to NM_022370.3 G212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:124745143 G>A maps to NM_022370.3 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:124742832 C>T maps to NM_022370.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:124743267 C>T maps to NM_022370.3 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr11:124750425 C>T maps to NM_022370.3 G1357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:124744798 C>A maps to NM_022370.3 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:124739439 G>A maps to NM_022370.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:124766902 G>A maps to NM_019055.5 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:124754958 G>A maps to NM_019055.5 H993H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:124764163 G>A maps to NM_019055.5 C417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr11:124764106 G>A maps to NM_019055.5 C436C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:124756657 G>A maps to NM_019055.5 S832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr18:18608855 A>G maps to NM_005406.2 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr18:18564450 G>A maps to NM_005406.2 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr18:18548759 G>A maps to NM_005406.2 I992I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr18:18540138 T>C maps to NM_005406.2 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:18547037 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:18619492 C>A maps to NM_005406.2 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr18:18535139 A>G maps to NM_005406.2 P1193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr18:18540141 T>C maps to NM_005406.2 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr18:18540141 T>C maps to NM_005406.2 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr18:18534812 G>A maps to NM_005406.2 R1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr18:18603598 G>A maps to NM_005406.2 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:11355714 C>T maps to NM_004850.3 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:11334407 G>T maps to NM_004850.3 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:11341472 C>A maps to NM_004850.3 E896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:11364467 G>A maps to NM_004850.3 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:11337662 C>A maps to NM_004850.3 E1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr2:11334407 G>A maps to NM_004850.3 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:4850534 G>A maps to NM_024589.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr11:62381310 T>C maps to NM_000327.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:123688068 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:125702095 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:10461309 G>A maps to NM_031916.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:10461438 G>A maps to NM_031916.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr5:10448468 G>T maps to NM_031916.3 G77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:64608331 C>T maps to NM_005012.2 C391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr1:64643424 A>G maps to NM_005012.2 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:64605876 C>T maps to NM_005012.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:64644234 G>A maps to NM_005012.2 Q837Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:64515591 C>T maps to NM_005012.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:94487059 C>T maps to NM_004560.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:94486393 C>T maps to NM_004560.2 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr9:94487152 G>A maps to NM_004560.2 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr9:94486153 G>A maps to NM_004560.2 V874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr9:94493225 G>A maps to NM_004560.2 N383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr9:94486426 G>A maps to NM_004560.2 N783N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr9:94519713 C>T maps to NM_004560.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:60803545 A>G maps to NM_134260.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr9:77257573 C>T maps to ENST00000396204 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr9:77300485 G>A maps to ENST00000396204 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr9:77282722 G>C maps to ENST00000396204 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:77282782 C>T maps to ENST00000396204 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr9:77286723 A>G maps to ENST00000396204 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr9:77286723 A>G maps to ENST00000396204 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:77257633 A>G maps to ENST00000396204 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr9:77286723 A>G maps to ENST00000396204 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr9:77257633 A>G maps to ENST00000396204 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr9:77286723 A>G maps to ENST00000396204 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr9:77286723 A>G maps to ENST00000396204 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr9:77257522 C>T maps to ENST00000396204 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr9:77286723 A>G maps to ENST00000396204 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr9:77257528 C>T maps to ENST00000396204 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:151789712 C>T maps to ENST00000392697 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:151786066 G>T maps to ENST00000392697 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr6:117609654 T>A maps to NM_002944.2 *2348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:117609954 G>T maps to NM_002944.2 G2248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:117715375 A>G maps to NM_002944.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:117710594 G>T maps to NM_002944.2 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:117609954 G>A maps to NM_002944.2 G2248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr6:117658404 A>G maps to NM_002944.2 N1726N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:117715865 T>A maps to NM_002944.2 K298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:117686782 A>G maps to NM_002944.2 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:117686878 A>G maps to NM_002944.2 V946V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr6:117704572 G>C maps to NM_002944.2 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:117658373 C>A maps to NM_002944.2 E1737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:117662699 C>A maps to NM_002944.2 E1589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:117622268 C>A maps to NM_002944.2 E2201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:117647429 A>G maps to NM_002944.2 F1838F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:117708061 T>C maps to NM_002944.2 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:117631359 G>T maps to NM_002944.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr6:117715378 A>G maps to NM_002944.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr6:117665426 T>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:117704647 C>T maps to NM_002944.2 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr8:55537420 C>T maps to NM_006269.1 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:55538475 G>A maps to NM_006269.1 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr8:55541259 A>T maps to NM_006269.1 T1606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:55533669 C>T maps to NM_006269.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr8:55538688 C>T maps to NM_006269.1 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr8:55533672 C>T maps to NM_006269.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:55534128 G>A maps to NM_006269.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr8:55541187 C>A maps to NM_006269.1 C1582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr8:55534723 G>A maps to NM_006269.1 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr8:55537422 A>G maps to NM_006269.1 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr8:55538952 A>G maps to NM_006269.1 Q837Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:55537410 T>A maps to NM_006269.1 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr8:55537422 A>G maps to NM_006269.1 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr8:55537422 A>G maps to NM_006269.1 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:10465859 C>T maps to NM_178857.5 Q1916Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr8:10470689 G>A maps to NM_178857.5 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:10465037 C>T maps to NM_178857.5 Q2190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:10480618 C>T maps to NM_178857.5 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:10466420 C>A maps to NM_178857.5 G1729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:10467947 G>A maps to NM_178857.5 D1220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:10464662 T>C maps to NM_178857.5 E2315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:10467545 C>T maps to NM_178857.5 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:10470380 C>T maps to NM_178857.5 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr8:10464587 G>A maps to NM_178857.5 A2340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr8:10469906 C>T maps to NM_178857.5 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr8:10467947 G>A maps to NM_178857.5 D1220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr8:10467947 G>A maps to NM_178857.5 D1220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr8:10466663 G>A maps to NM_178857.5 G1648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr8:10467947 G>A maps to NM_178857.5 D1220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr8:10467947 G>A maps to NM_178857.5 D1220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr8:10467560 C>T maps to NM_178857.5 Q1349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:46712983 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:46713108 T>C did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr7:33136123 G>A maps to NM_203288.1 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:33136123 G>A maps to NM_203288.1 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr17:1800366 C>T maps to NM_002945.3 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:1798389 G>A did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:28223617 C>T maps to ENST00000313433 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:28233504 G>A maps to ENST00000313433 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:7678723 C>A maps to NM_002947.3 G51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:7677504 G>A maps to NM_002947.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:96140021 C>T did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:96139489 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:96139901 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:96139864 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:96139370 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:41813996 C>A maps to NM_015540.2 G993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:41827710 C>T maps to NM_015540.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:41828338 C>T maps to NM_015540.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:92765757 A>G maps to NM_024813.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:92811446 T>G maps to NM_024813.2 L555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:48063987 A>G maps to NM_024604.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr1:68904680 G>A maps to NM_000329.2 H314H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:68897189 G>A maps to NM_000329.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr1:68897202 G>A maps to NM_000329.2 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:68904888 G>T maps to NM_000329.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:68895611 T>C did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr1:68904933 A>C maps to NM_000329.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:68904680 G>A maps to NM_000329.2 H314H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:68906677 A>G maps to NM_000329.2 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:111320968 T>C maps to NM_032194.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr6:111320914 T>C maps to NM_032194.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:38160585 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:38145721 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:38178170 C>A did not map to a codon.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr23:38182661 A>G did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:38145703 C>T did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:38182661 A>G did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr14:21794061 C>T maps to NM_020366.3 R814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr14:21762956 T>C maps to NM_020366.3 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:21790086 T>A maps to NM_020366.3 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:21795962 C>T maps to NM_020366.3 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr14:21785911 G>T maps to NM_020366.3 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr14:21819341 T>C maps to NM_020366.3 I1276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr14:21792903 G>A maps to NM_020366.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:21796599 T>C maps to NM_020366.3 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:53686794 G>A maps to NM_015272.2 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr16:53726238 T>A maps to NM_015272.2 K90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr16:53726199 C>A maps to NM_015272.2 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr16:53635999 G>A maps to NM_015272.2 D1312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:113307562 G>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:113314484 C>T maps to NM_001143854.1 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr12:113328799 C>T maps to NM_001143854.1 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:113303309 C>T maps to NM_001143854.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr12:113321168 C>T maps to NM_001143854.1 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:171187 G>T maps to NM_006987.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:63695 G>A maps to NM_006987.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:89036159 C>T maps to NM_144563.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:153626875 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:153628248 T>C did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr14:47120303 C>T maps to NM_080746.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:47120840 G>T maps to NM_080746.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr9:130213587 C>A maps to NM_000976.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr9:130210155 G>A maps to NM_000976.2 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr16:89627459 T>G maps to NM_033251.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr19:49994984 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:40503581 G>A maps to NM_001034996.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:23960024 T>A maps to NM_002948.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr13:27828378 T>C maps to NM_000982.3 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:27830353 T>A maps to NM_000982.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:6257792 G>C maps to NM_000983.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:37006675 G>A maps to NM_000978.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:27050612 T>C maps to ENST00000394938 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr22:39711401 G>A maps to NM_000967.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:101635497 T>C maps to NM_001098577.2 *129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr17:72205952 G>A maps to NM_001035258.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:72205347 G>A maps to NM_001035258.1 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:118923916 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:118923946 G>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:118923898 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:186839007 A>G maps to NM_052969.1 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr16:2004053 C>T maps to NM_005061.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr15:66793327 G>A maps to NM_000968.2 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:112844628 A>G maps to NM_001024662.1 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:74204971 G>A maps to ENST00000396470 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:42852359 C>T maps to NM_198486.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:146015855 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:39458095 C>T maps to NM_000661.4 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr4:39456556 A>C maps to NM_000661.4 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr12:120635196 A>G maps to NM_053275.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:128341087 C>T maps to NM_002950.3 E520E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:128363790 T>C maps to NM_002950.3 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr3:128363790 T>C maps to NM_002950.3 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr3:128363790 T>C maps to NM_002950.3 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr20:35862445 C>A maps to NM_002951.3 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:35854147 C>T maps to NM_002951.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr20:35862472 G>A maps to NM_002951.3 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr10:92638842 G>A maps to ENST00000458617 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:4995341 A>G maps to NM_006638.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:4995491 C>T maps to NM_006638.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:33573149 G>A maps to NM_018170.3 H301H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr18:33606958 C>A maps to NM_018170.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr18:33606958 C>T maps to NM_018170.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr20:36685932 G>C did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:150445386 G>A maps to NM_015203.3 V1321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:150445638 C>T maps to NM_015203.3 D1405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:150337330 G>A maps to NM_015203.3 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:150443646 G>A maps to NM_015203.3 K741K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:154334899 C>T maps to NM_019845.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:50001264 C>T maps to NM_001015.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:17098742 G>T maps to NM_001017.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr19:39924367 G>A maps to NM_001020.4 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:2013209 C>T maps to NM_002952.3 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:81572041 A>G maps to NM_001025.4 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:56437177 A>G maps to NM_001029.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:56437900 A>G did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr12:56437900 A>G did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:8386867 G>A maps to ENST00000449223 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:71492547 T>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:71495494 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:71493690 C>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:71495556 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:58905931 C>T maps to NM_001009.3 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:19376647 A>G maps to NM_001010.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr9:19378871 G>A maps to NM_001010.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:26881655 G>A maps to NM_001006665.1 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:26888000 T>C maps to NM_001006665.1 Y488Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr1:26897998 C>T maps to NM_001006665.1 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:26881682 C>T maps to NM_001006665.1 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:166912106 G>A maps to ENST00000510118 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr6:166902390 C>T maps to ENST00000510118 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:166836895 G>A maps to ENST00000510118 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr6:166843952 G>T maps to ENST00000510118 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:166827304 G>A maps to ENST00000510118 R710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:166872961 G>A maps to ENST00000510118 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr6:166912094 C>T maps to ENST00000510118 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:166862226 G>A maps to ENST00000510118 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:166921747 G>A maps to ENST00000510118 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:166862263 G>T maps to ENST00000510118 S452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:20185713 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:20193366 A>G did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:20193367 G>A did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:20213248 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:20181082 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:20212319 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:20183030 A>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:20190969 A>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:20193366 A>G did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:20190968 A>G did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:20185859 A>G did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:20181098 G>T did not map to a codon.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr23:20195147 T>C did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:20193366 A>G did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:20190970 T>C did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:20194554 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:20190969 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:20185859 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:64127719 G>A maps to NM_003942.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:64137815 C>A maps to NM_003942.2 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr11:64135608 C>T maps to NM_003942.2 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr14:91356839 G>A maps to NM_004755.2 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr14:91386566 G>T maps to NM_004755.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr14:91338629 G>A maps to NM_004755.2 Q733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr23:83402038 T>C did not map to a codon.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr23:83360832 G>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:83351265 C>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:83360857 A>G did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:83357081 A>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:83362044 G>T did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr23:83360857 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:83411161 T>C did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:83401988 A>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:83372072 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:83374909 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:83361438 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:83360881 G>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:83351264 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:83357099 C>A did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:83374909 A>G did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:83351222 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:83360858 G>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:58013622 C>T maps to NM_003161.2 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:58018207 G>A maps to NM_003161.2 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:58011613 G>T maps to NM_003161.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr17:58011881 A>G maps to NM_003161.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:67200477 C>T maps to NM_003952.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:67200474 C>T maps to NM_003952.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:67202072 G>A maps to NM_003952.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:67202510 G>A maps to NM_003952.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr1:213436134 A>G maps to NM_012424.3 E1022E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:213436134 A>G maps to NM_012424.3 E1022E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr1:213436134 A>G maps to NM_012424.3 E1022E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:213414699 A>G maps to NM_012424.3 E627E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:213415444 C>T maps to NM_012424.3 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:213436134 A>G maps to NM_012424.3 E1022E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:213436134 A>G maps to NM_012424.3 E1022E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr1:213436134 A>G maps to NM_012424.3 E1022E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr1:213224754 T>A maps to NM_012424.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr14:75388085 C>T maps to NM_031464.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr14:75373758 A>G maps to NM_031464.3 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr14:75376468 A>G maps to NM_031464.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr14:75386559 G>C maps to NM_031464.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:3624213 C>T maps to NM_001011.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:45241775 G>C maps to NM_001012.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:152127240 G>A maps to NM_001122965.1 D778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:152129261 G>A maps to NM_001122965.1 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:78867579 C>T maps to NM_020761.2 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:78921116 C>T maps to NM_020761.2 N1077N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:78857693 C>T maps to NM_020761.2 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr17:78919563 C>T maps to NM_020761.2 A1041A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:78857630 C>T maps to NM_020761.2 N567N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr17:78519554 C>T maps to NM_020761.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr17:78882647 A>G maps to NM_020761.2 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr17:78931501 G>A maps to NM_020761.2 W1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:40865788 G>T maps to NM_152260.1 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr3:9885233 G>A maps to NM_173659.3 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:126073477 G>A maps to NM_032795.2 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:219449403 T>A maps to NM_005444.1 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr2:219447752 C>T maps to NM_005444.1 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr16:66956122 G>A maps to NM_004165.2 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:19049683 G>A maps to NM_006570.4 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:55783755 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:55782280 C>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:55757892 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:55784747 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:55782303 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:55784743 G>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:55779879 A>G did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:55753776 T>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:55782316 G>T did not map to a codon.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr1:39317318 G>A maps to NM_022157.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr6:90088990 C>A maps to NM_021244.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:90097154 G>A maps to NM_021244.4 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:90077896 G>T maps to NM_021244.4 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:17616198 C>T maps to ENST00000377813 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:17614128 G>A maps to ENST00000377813 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:17597382 G>A maps to ENST00000377813 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:17601422 G>A maps to ENST00000377813 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr4:110758685 C>G maps to NM_006583.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:103231119 A>G maps to NM_015713.4 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr16:15168712 T>C maps to NM_018427.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:15186471 C>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:99150242 G>A maps to NM_015179.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:99131877 G>A maps to NM_015179.3 D765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:99130757 G>T maps to NM_015179.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:99130025 G>A maps to NM_015179.3 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:99116900 G>A maps to NM_015179.3 R1282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:99148098 C>T maps to NM_015179.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:218504324 G>A maps to NM_016052.3 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr1:218504431 A>G maps to NM_016052.3 *283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:218504324 G>A maps to NM_016052.3 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr21:45094566 C>T maps to NM_015056.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:45107406 C>A maps to NM_015056.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr21:45079586 G>A maps to NM_015056.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:42910753 G>A maps to NM_015703.4 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:42910142 G>A maps to NM_015703.4 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:42910159 C>A maps to NM_015703.4 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:6623319 G>A maps to NM_015324.2 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr11:6621799 T>C maps to NM_015324.2 K389K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr11:6621802 C>T maps to NM_015324.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr8:67342361 G>C maps to NM_015169.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:18660226 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:18660226 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:18674836 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:18675768 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:18690149 G>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:18662575 A>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:18660144 C>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:18665358 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:48560711 C>T maps to NM_018346.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:48557384 G>A maps to NM_018346.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr17:48559558 A>G maps to NM_018346.1 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:7023646 G>A maps to NM_080657.4 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:7027240 C>T maps to NM_080657.4 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:7030431 C>T maps to NM_080657.4 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr1:114354653 T>C maps to NM_018364.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:77402578 C>T maps to NM_198467.2 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:15987164 C>T maps to NM_006511.1 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:15986665 C>T maps to NM_006511.1 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:15986578 T>C maps to NM_006511.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:77436719 A>G maps to NM_016578.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:77387927 G>A maps to NM_016578.3 R1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:77409716 G>A maps to NM_016578.3 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:77386194 G>A maps to NM_016578.3 R1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:77383146 G>A maps to NM_016578.3 R1231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:77412074 G>A maps to NM_016578.3 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:77412269 G>T maps to NM_016578.3 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:77413220 G>A maps to NM_016578.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr11:77386123 A>G maps to NM_016578.3 D1173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr11:77383213 C>T maps to NM_016578.3 R1208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr16:11931682 T>C maps to NM_015659.2 K478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr21:43913126 G>A maps to NM_080860.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr21:43906509 G>T maps to NM_080860.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr21:43913131 G>A maps to NM_080860.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:43913093 G>A maps to NM_080860.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr21:43896047 C>T maps to NM_080860.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:6797508 C>T maps to NM_173565.3 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr7:6797514 T>C maps to NM_173565.3 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr6:159401922 C>A maps to NM_031924.4 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:159414905 G>A maps to NM_031924.4 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr6:159401968 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:159401922 C>A maps to NM_031924.4 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr6:159401922 C>A maps to NM_031924.4 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:116938308 G>T maps to NM_001010892.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:116949177 A>G maps to NM_001010892.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:116953393 C>A maps to NM_001010892.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:46307941 T>C maps to NM_030785.3 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:46317831 G>A maps to NM_030785.3 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr19:46307767 C>T maps to NM_030785.3 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:43613038 C>T maps to NM_152732.4 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:43638592 C>T maps to NM_152732.4 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr6:43623375 C>T maps to NM_152732.4 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr8:108972905 A>G maps to NM_178565.4 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr8:108970479 A>G maps to NM_178565.4 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr8:108972905 A>G maps to NM_178565.4 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:108970479 A>G maps to NM_178565.4 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr6:127476477 C>T maps to ENST00000368317 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:948662 G>A maps to NM_001029871.3 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:57264686 C>T maps to NM_133368.1 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:57265192 C>T maps to NM_133368.1 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr16:57261339 T>C maps to NM_133368.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:158261227 C>A maps to NM_016625.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:157839923 G>T maps to NM_016625.2 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:123003482 G>A maps to NM_023012.5 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr12:122999722 G>A maps to NM_023012.5 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:123001774 G>A maps to NM_023012.5 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:122992980 T>G maps to NM_023012.5 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr10:16806405 G>T maps to NM_012425.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:16635455 C>T maps to NM_012425.3 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr19:12940706 T>A maps to NM_031429.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr19:12940628 C>A maps to NM_031429.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:12936726 G>A maps to NM_031429.1 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:12936603 G>T maps to NM_031429.1 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr20:62290784 C>T maps to ENST00000482936 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr20:62319036 C>T maps to ENST00000482936 H465H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:62294195 T>C maps to ENST00000482936 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:62294196 A>T maps to ENST00000482936 K165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:62324610 G>T maps to ENST00000482936 R989R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:62327177 C>T maps to ENST00000482936 S1290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:41730571 G>A maps to NM_015138.4 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:74655846 G>A maps to NM_001015055.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr2:74657770 G>C maps to NM_001015055.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:74657485 G>A maps to NM_001015055.1 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:74653594 C>T maps to NM_001015055.1 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:64022543 G>A maps to NM_145307.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr10:64000900 G>A maps to NM_145307.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:101350132 G>A maps to NM_001134888.2 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr14:101351104 G>A maps to NM_001134888.2 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:101348158 G>A maps to NM_001134888.2 G989G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr14:101350608 G>A maps to NM_001134888.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:101350009 G>A maps to NM_001134888.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:101347525 G>A maps to NM_001134888.2 F1200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:101350575 G>A maps to NM_001134888.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:101347456 G>A maps to NM_001134888.2 H1223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr14:101347411 G>A maps to NM_001134888.2 D1238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:60212465 G>A maps to NM_021136.2 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:60193673 G>A maps to NM_021136.2 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:60193883 G>A maps to NM_021136.2 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:60212897 G>T maps to NM_021136.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:60074022 G>A maps to NM_021136.2 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr14:60193844 C>T maps to NM_021136.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:63488088 C>T maps to ENST00000377819 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:63525744 T>C maps to NM_201430.1 *242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:55254492 C>A maps to NM_020532.4 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr2:55253658 C>A maps to NM_020532.4 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr2:55254060 G>A maps to NM_020532.4 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:55253124 C>A maps to NM_020532.4 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:55253530 A>G maps to NM_020532.4 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr2:55214835 T>A did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr2:55252690 A>G maps to NM_020532.4 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:55214835 T>A did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr2:55252690 A>G maps to NM_020532.4 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr6:107019899 G>A maps to NM_032730.4 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:107070839 A>G maps to NM_032730.4 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr17:1840059 C>T maps to NM_178568.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr17:1840143 G>A maps to NM_178568.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr17:1840968 C>T maps to NM_178568.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr3:186915362 C>T maps to NM_153708.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:186917437 C>T maps to NM_153708.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:186917374 G>A maps to NM_153708.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr3:186917760 C>A maps to NM_153708.2 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr3:186917437 C>T maps to NM_153708.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:187416657 C>T maps to NM_001004312.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr3:187416387 G>A maps to NM_001004312.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr3:187416387 G>A maps to NM_001004312.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:67864861 G>A maps to NM_173630.3 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr18:67725025 G>A maps to NM_173630.3 L1661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr18:67864859 C>T maps to NM_173630.3 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:67795702 A>G maps to NM_173630.3 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr18:67741141 C>T maps to NM_173630.3 T1551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr18:67795700 C>T maps to NM_173630.3 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr18:67795702 A>G maps to NM_173630.3 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:178994485 G>A maps to NM_025158.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:179016621 C>T maps to NM_025158.3 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr5:178996398 C>A maps to NM_025158.3 C267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:178994480 C>T maps to NM_025158.3 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:70136607 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:71659517 C>T maps to NM_001037442.2 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:71634278 C>T maps to NM_001037442.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:218939911 C>T maps to NM_198483.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:218939997 C>T maps to NM_198483.3 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:218941229 G>A maps to NM_198483.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:218939911 C>T maps to NM_198483.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:41143141 A>G maps to NM_173079.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr16:12093166 T>C maps to NM_032167.2 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:42389992 C>T maps to NM_001144825.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:87339911 C>T maps to NM_138290.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:87407125 G>T maps to NM_138290.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:87407140 C>T maps to NM_138290.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:87329836 A>G maps to NM_138290.2 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:87459245 G>A maps to NM_138290.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr21:36231828 T>C maps to NM_001754.4 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr21:36206727 G>A maps to NM_001754.4 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr21:36252875 C>T maps to NM_001754.4 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr21:36252899 C>T maps to NM_001754.4 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr21:36231828 T>C maps to NM_001754.4 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr21:36259148 G>A maps to NM_001754.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr21:36231828 T>C maps to NM_001754.4 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr21:36259262 G>A maps to NM_001754.4 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr21:36231780 T>C maps to NM_001754.4 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr21:36252901 G>A maps to NM_001754.4 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr21:36252920 A>T maps to NM_001754.4 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr21:36252914 T>C maps to NM_001754.4 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr21:36252977 A>G maps to NM_001754.4 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr21:36171606 G>T maps to NM_001754.4 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr21:36231861 A>G maps to NM_001754.4 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr21:36252875 C>T maps to NM_001754.4 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr21:36231860 G>A maps to NM_001754.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr8:92998412 G>A maps to NM_175634.2 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:93023297 C>A maps to NM_175634.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:92999179 C>A maps to NM_175634.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr8:92988169 C>T maps to NM_175634.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:92982957 C>T maps to NM_175634.2 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:92998468 C>A maps to NM_175634.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:93004109 C>A maps to NM_175634.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr8:92983011 C>A maps to NM_175634.2 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:92972562 G>A maps to NM_175634.2 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr8:93026956 G>T maps to NM_175634.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr6:45514855 G>A maps to ENST00000359524 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr6:45514678 C>T maps to ENST00000359524 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr1:25291053 C>T maps to NM_001031680.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:25228900 G>A maps to NM_001031680.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:25254125 G>A maps to NM_001031680.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:25254142 G>A maps to NM_001031680.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:155295670 C>T maps to NM_001105203.1 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:155297958 G>A maps to NM_001105203.1 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:155292262 A>G maps to NM_001105203.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr9:35560422 G>A maps to NM_001135999.1 W1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:35558360 A>G maps to NM_001135999.1 T1076T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:35547105 A>G maps to NM_001135999.1 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:35547570 C>T maps to NM_001135999.1 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:35557929 C>T maps to NM_001135999.1 N1001N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:49514546 C>T maps to NM_006666.1 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:49513770 G>T maps to NM_006666.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:95710079 G>A maps to NM_015485.4 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:184562606 G>T maps to ENST00000326397 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr4:184572199 C>T maps to ENST00000326397 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr4:184572201 A>G maps to ENST00000326397 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:159559165 T>G maps to ENST00000440678 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:32366914 C>T maps to NM_130806.3 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr13:32371377 T>C maps to NM_130806.3 Y609Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr13:32349469 C>T maps to NM_130806.3 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr13:32335912 C>T maps to NM_130806.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr13:32367139 T>C maps to NM_130806.3 Y567Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr13:32363295 C>T maps to NM_130806.3 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:33937450 C>T maps to NM_016568.3 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr5:33938065 C>T maps to NM_016568.3 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:33937912 G>A maps to NM_016568.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr5:33937246 C>T maps to NM_016568.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:33937315 C>T maps to NM_016568.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:33937519 C>T maps to NM_016568.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:33937558 G>A maps to NM_016568.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:155912121 A>C maps to NM_181885.2 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr1:155912408 C>T maps to NM_181885.2 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:137300014 C>T maps to NM_002957.4 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:137300026 C>T maps to NM_002957.4 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:33162584 A>G maps to ENST00000374685 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:33162506 G>A maps to ENST00000374685 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr6:33163372 T>C maps to ENST00000374685 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:165380233 A>C maps to NM_006917.4 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:165378918 C>A maps to NM_006917.4 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:165378811 G>A maps to NM_006917.4 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:165398129 G>A maps to NM_006917.4 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:133928665 C>T maps to ENST00000296084 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr19:38964339 G>A maps to NM_000540.2 A1363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr19:39003122 C>T maps to NM_000540.2 L3158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:38942432 C>T maps to NM_000540.2 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:38954160 C>T maps to NM_000540.2 Y892Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:39062777 C>T maps to NM_000540.2 G4622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr19:39052072 C>T maps to NM_000540.2 R4201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:39062777 C>T maps to NM_000540.2 G4622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:38994861 C>T maps to NM_000540.2 L2643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:39055627 C>T maps to NM_000540.2 F4218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:39068822 C>T maps to NM_000540.2 F4781F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:38948870 C>T maps to NM_000540.2 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr19:38976646 C>T maps to NM_000540.2 A1784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr19:38991283 C>T maps to NM_000540.2 R2454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:38968360 C>T maps to NM_000540.2 S1435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:39076753 C>T maps to NM_000540.2 I4964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr19:38976508 G>A maps to NM_000540.2 T1738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:38979833 C>T maps to NM_000540.2 G1855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:38980732 G>A maps to NM_000540.2 E1944E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:39062660 C>A maps to NM_000540.2 V4583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:39037098 C>T maps to NM_000540.2 I4009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:38956880 C>T maps to NM_000540.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:38985016 C>T maps to NM_000540.2 H2100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr19:38993555 C>T maps to NM_000540.2 R2624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:38943503 C>T maps to NM_000540.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:39076774 G>A maps to NM_000540.2 T4971T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:38976628 G>A maps to NM_000540.2 S1778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:38974016 C>T maps to NM_000540.2 L1599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:38959643 C>T maps to NM_000540.2 R1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:38996495 T>C maps to NM_000540.2 I2817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr19:38964030 C>T maps to NM_000540.2 D1260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr19:38968462 G>T maps to NM_000540.2 R1469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr19:38976757 C>T maps to NM_000540.2 D1821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr19:39023321 G>A maps to NM_000540.2 L3735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:39019688 G>A maps to NM_000540.2 T3711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr19:38964222 G>A maps to NM_000540.2 A1324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:39026021 C>T maps to NM_000540.2 Q3836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr1:237958597 C>T maps to NM_001035.2 P4641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:237806694 A>G maps to NM_001035.2 G2430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr1:237711847 G>A maps to NM_001035.2 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:237656273 A>G maps to NM_001035.2 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:237824139 G>T maps to NM_001035.2 E2777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:237756831 C>T maps to NM_001035.2 G1444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:237819185 T>C maps to NM_001035.2 P2677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:237948079 C>T maps to NM_001035.2 A4356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:237550594 C>T maps to NM_001035.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:237758866 T>C maps to NM_001035.2 N1502N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:237791327 C>T maps to NM_001035.2 L2130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:237875083 G>T maps to NM_001035.2 E3424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:237936914 A>G maps to NM_001035.2 K3914K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:237947446 C>T maps to NM_001035.2 I4145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:237804241 G>A maps to NM_001035.2 A2387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:237806637 C>T maps to NM_001035.2 A2411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:237949283 G>T maps to NM_001035.2 E4426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:237982394 C>T maps to NM_001035.2 I4831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:237778026 G>T maps to NM_001035.2 E1867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:237935369 C>A maps to NM_001035.2 I3872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:237982394 C>T maps to NM_001035.2 I4831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:237494213 C>T maps to NM_001035.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:237758806 C>T maps to NM_001035.2 R1482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:237947095 G>A maps to NM_001035.2 S4028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:237947122 C>A maps to NM_001035.2 P4037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:237780780 G>T maps to NM_001035.2 E1971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:237947122 C>A maps to NM_001035.2 P4037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:237550618 C>T maps to NM_001035.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:237604645 G>T maps to NM_001035.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:237753189 A>G maps to NM_001035.2 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:237774205 C>T maps to NM_001035.2 R1610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:237777866 T>C maps to NM_001035.2 T1813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:237957187 C>T maps to NM_001035.2 R4602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:237961381 G>T maps to NM_001035.2 E4668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:237753202 G>T maps to NM_001035.2 E1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:237870321 C>T maps to NM_001035.2 I3218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:237947545 C>T maps to NM_001035.2 N4178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:237494209 T>C maps to NM_001035.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:237758818 T>C maps to NM_001035.2 Y1486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:237777626 G>A maps to NM_001035.2 T1733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr1:237947293 C>T maps to NM_001035.2 I4094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:237777821 T>C maps to NM_001035.2 A1798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:237819143 A>G maps to NM_001035.2 K2663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr1:237802399 A>G maps to NM_001035.2 E2338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:237947122 C>T maps to NM_001035.2 P4037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:237732464 C>A maps to NM_001035.2 G1148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:237774129 G>A maps to NM_001035.2 P1584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:237863534 G>T maps to NM_001035.2 V3045V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr1:237811894 G>A maps to NM_001035.2 A2498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr1:237550597 C>T maps to NM_001035.2 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr1:237778085 C>A maps to NM_001035.2 G1886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:237794807 C>A maps to NM_001035.2 V2174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:237890470 C>A maps to NM_001035.2 R3604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr15:34032067 T>C maps to NM_001036.3 P2564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:33938643 C>A maps to NM_001036.3 I1286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr15:33938601 G>A maps to NM_001036.3 T1272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:33872279 C>T maps to NM_001036.3 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr15:33954587 G>A maps to NM_001036.3 K1619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr15:34113536 G>T maps to NM_001036.3 E3628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:34015015 C>A maps to NM_001036.3 L2240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:33916125 G>T maps to NM_001036.3 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:33988554 G>A maps to NM_001036.3 A1999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:34130255 C>T maps to NM_001036.3 F4025F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:34110876 G>A maps to NM_001036.3 T3566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr15:34152814 C>T maps to NM_001036.3 F4773F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:34130951 G>A maps to NM_001036.3 E4257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:33954809 G>A maps to NM_001036.3 T1693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:33991958 C>T maps to NM_001036.3 R2102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:34129120 C>T maps to NM_001036.3 I3861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:34064333 G>A maps to NM_001036.3 Q3010Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:34129830 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:33922197 G>T maps to NM_001036.3 E913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:34113778 C>T maps to NM_001036.3 N3657N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:34129120 C>T maps to NM_001036.3 I3861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:34130807 C>A maps to NM_001036.3 I4209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr15:33893730 C>T maps to NM_001036.3 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr15:34134208 G>C maps to NM_001036.3 G4394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr15:33993250 G>T maps to NM_001036.3 A2151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr15:33878214 G>A maps to NM_001036.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr15:34080587 C>T maps to NM_001036.3 D3253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr15:34014979 C>T maps to NM_001036.3 F2228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr15:34049782 A>G maps to NM_001036.3 K2897K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:33858919 A>C maps to NM_001036.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:33923485 G>T maps to NM_001036.3 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:34130069 G>A maps to NM_001036.3 L3963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:153587809 G>T maps to NM_020672.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:153516351 G>A maps to NM_002961.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:153516252 C>T maps to NM_002961.2 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:153507755 G>A maps to NM_014624.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:153507755 G>A maps to NM_014624.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:153390686 C>T maps to NM_176823.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:153409590 G>T maps to NM_001045479.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:153410739 T>C maps to NM_001045479.1 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:16669198 C>A did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:16672580 A>G did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:16669165 A>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:33321591 C>T maps to NM_022753.2 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:101705418 G>A maps to NM_001400.4 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:91616258 C>A maps to NM_005226.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr9:91617086 C>T maps to NM_005226.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:91616471 C>T maps to NM_005226.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:91616282 G>A maps to NM_005226.2 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr9:91617086 C>T maps to NM_005226.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr19:3179689 G>A maps to NM_003775.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr19:10624865 G>A maps to NM_001166215.1 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:10624718 G>A maps to NM_001166215.1 C323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:18267010 C>T maps to NM_030754.4 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:18253135 C>T maps to NM_006512.3 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:18108756 T>C maps to NM_138421.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:64812054 G>A maps to ENST00000301885 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:64811985 G>A maps to ENST00000301885 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:45785049 C>A maps to NM_014016.3 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:45780150 T>C maps to NM_014016.3 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr13:23904817 A>G maps to NM_014363.4 T4399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:23932516 G>A maps to NM_014363.4 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:23907075 C>A maps to NM_014363.4 E3647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:23913387 C>A maps to NM_014363.4 E1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr13:23932525 A>G maps to NM_014363.4 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr13:23911659 G>A maps to NM_014363.4 R2119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr13:23911438 G>A maps to NM_014363.4 I2192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:23911375 G>A maps to NM_014363.4 I2213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr13:23908777 A>C maps to NM_014363.4 L3079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr13:23908264 A>G maps to NM_014363.4 F3250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:23910438 C>A maps to NM_014363.4 E2526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr13:23915581 A>G maps to NM_014363.4 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:23913576 C>A maps to NM_014363.4 E1480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:23929712 C>T maps to NM_014363.4 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:23912322 C>A maps to NM_014363.4 E1898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr13:23911438 G>T maps to NM_014363.4 I2192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr13:23910865 G>A maps to NM_014363.4 R2383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:23907633 C>A maps to NM_014363.4 E3461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:23912371 G>T maps to NM_014363.4 G1881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr13:23915782 T>G maps to NM_014363.4 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr13:23909212 G>A maps to NM_014363.4 F2934F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:23905661 G>T maps to NM_014363.4 S4118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:23908824 C>A maps to NM_014363.4 E3064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:23910786 C>A maps to NM_014363.4 E2410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:23906767 G>A maps to NM_014363.4 I3749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:23911948 T>C maps to NM_014363.4 K2022K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:23942606 C>T maps to NM_014363.4 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr13:23911138 C>A maps to NM_014363.4 L2292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr13:23949320 T>C maps to NM_014363.4 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr13:23908465 G>T maps to NM_014363.4 S3183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr13:23909359 G>A maps to NM_014363.4 G2885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr13:23911438 G>T maps to NM_014363.4 I2192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr13:23911438 G>T maps to NM_014363.4 I2192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:47712418 C>T maps to NM_005500.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:47658418 C>T maps to NM_005500.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:5641839 C>T maps to ENST00000433404 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:5654189 C>T maps to ENST00000433404 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:5653241 G>A maps to ENST00000433404 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:5595388 G>A maps to NM_014649.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:5598854 C>T maps to NM_014649.2 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr19:5616304 G>A maps to NM_014649.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:5594107 G>T maps to NM_014649.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:134991045 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:134990328 C>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:134992619 C>T did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:134991131 T>G did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:134988608 A>G did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:134993367 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:134992710 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:134988658 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:134988658 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:134993402 G>A did not map to a codon.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr23:134992667 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:134987500 T>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:134989129 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:134994096 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:134992667 T>C did not map to a codon.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr23:134991923 G>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:134990737 C>A did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:134989177 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:134993765 G>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:134988627 T>C did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:134988658 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:134989560 A>G did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:134992667 T>C did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:134989535 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr16:51171196 G>A maps to ENST00000251020 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:51175649 G>A maps to ENST00000251020 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:51173804 C>T maps to ENST00000251020 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:51173918 G>T maps to ENST00000251020 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:51175913 G>A maps to ENST00000251020 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr16:51174818 C>T maps to ENST00000251020 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:51173897 C>T maps to ENST00000251020 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr16:51171247 G>A maps to ENST00000251020 N1250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:51176000 G>T maps to ENST00000251020 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr16:51175781 G>A maps to ENST00000251020 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:51175919 A>C maps to ENST00000251020 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:51171055 G>A maps to ENST00000251020 F1314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:51173828 G>A maps to ENST00000251020 C768C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr16:51173975 G>A maps to ENST00000251020 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr16:51171244 C>T maps to ENST00000251020 E1251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr16:51173557 C>A maps to ENST00000251020 E859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr16:51175127 G>A maps to ENST00000251020 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:51175481 G>A maps to ENST00000251020 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr14:21992436 C>T maps to NM_005407.1 K475K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:21991326 G>A maps to NM_005407.1 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr14:22005024 G>A maps to NM_005407.1 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr14:22004983 G>A maps to NM_005407.1 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr18:76754513 C>T maps to NM_171999.2 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr18:76753313 G>A maps to NM_171999.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr18:76753463 G>A maps to NM_171999.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:76757081 C>T maps to NM_171999.2 N1221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr18:76752098 C>T maps to NM_171999.2 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr18:76753904 C>T maps to NM_171999.2 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr20:50408409 G>A maps to NM_020436.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:50407863 G>A maps to NM_020436.3 Y386Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:50407749 G>A maps to NM_020436.3 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:50406765 A>G maps to NM_020436.3 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:48193454 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:130505304 G>A maps to ENST00000457563 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:130497110 G>A maps to ENST00000457563 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:130476161 A>G maps to ENST00000457563 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr6:130476161 A>G maps to ENST00000457563 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:55236866 C>T maps to NM_015589.4 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr14:55236925 T>A maps to NM_015589.4 Y566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:55236926 C>T maps to NM_015589.4 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:55226910 G>A maps to NM_015589.4 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:55034771 G>A maps to NM_015589.4 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:39860433 A>G maps to NM_018028.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:147885570 G>A maps to NM_001030060.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr3:169644596 C>T maps to NM_182610.2 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:169644796 C>T maps to NM_182610.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:169644769 G>A maps to NM_182610.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:169639113 C>A maps to NM_182610.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr7:92734432 T>C maps to NM_017654.3 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:92732343 C>A maps to NM_017654.3 G1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:92735035 C>T maps to NM_017654.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:92731164 G>A maps to NM_017654.3 R1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:92732284 T>C maps to NM_017654.3 E1042E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:92731747 A>G maps to NM_017654.3 N1221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr7:92731861 C>T maps to NM_017654.3 P1183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr7:92733457 A>G maps to NM_017654.3 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:92733271 T>C maps to NM_017654.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr7:92734434 G>A maps to NM_017654.3 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr7:92733457 A>G maps to NM_017654.3 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr7:92733037 G>A maps to NM_017654.3 Y791Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3517-01A-01W-0831-10 chr7:92761753 G>A maps to NM_152703.2 T1177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr7:92761120 A>T maps to NM_152703.2 I1388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:92761258 T>C maps to NM_152703.2 G1342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:92761053 G>A maps to NM_152703.2 R1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:92762985 A>G maps to NM_152703.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:92763595 A>C maps to NM_152703.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:92761039 T>C maps to NM_152703.2 Q1415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:92763519 G>A maps to NM_152703.2 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr20:35575183 G>A maps to NM_015474.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr22:44372005 G>A maps to NM_015380.4 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr22:44372011 G>A maps to NM_015380.4 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:44385027 C>T maps to NM_015380.4 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr21:15889329 T>C maps to ENST00000285670 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr21:15873050 T>C maps to ENST00000285670 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr21:15873050 T>C maps to ENST00000285670 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr21:15873050 T>C maps to ENST00000285670 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr2:128753925 G>A maps to NM_001145928.1 N477N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr2:128699654 G>A maps to NM_001145928.1 D1059D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr2:128700017 G>A maps to NM_001145928.1 R1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:128757315 G>A maps to NM_001145928.1 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:128747329 G>A maps to NM_001145928.1 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:128767913 A>C maps to NM_001145928.1 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:128712908 G>A maps to NM_001145928.1 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:128757351 G>A maps to NM_001145928.1 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr17:73699910 G>A maps to NM_013260.6 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr17:73698615 C>T maps to NM_013260.6 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr17:73698615 C>T maps to NM_013260.6 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr17:73698615 C>T maps to NM_013260.6 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:55753844 G>A maps to ENST00000443936 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr19:55748027 G>C maps to ENST00000443936 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:50853117 C>T maps to ENST00000216061 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:68326037 G>T maps to NM_001164160.1 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:68367905 G>A maps to NM_001164160.1 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:68369411 G>A maps to NM_001164160.1 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:68343481 G>T maps to NM_001164160.1 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr11:68305207 G>T maps to NM_001164160.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:68305183 G>T maps to NM_001164160.1 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:68305201 C>T maps to NM_001164160.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr11:68338542 T>A maps to NM_001164160.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr11:68337365 G>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:68305203 G>A maps to NM_001164160.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr5:133948387 A>G maps to NM_016103.3 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr9:136596540 C>T maps to NM_007101.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:136597565 G>A maps to NM_007101.3 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:136555641 A>G maps to NM_007101.3 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:136578195 G>A maps to NM_007101.3 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:136573486 G>A maps to NM_007101.3 Y464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:26711398 C>T maps to ENST00000379061 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:26722979 C>T maps to ENST00000379061 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:26722979 C>T maps to ENST00000379061 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:109778615 C>T maps to ENST00000369923 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:109756719 C>T maps to ENST00000369923 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:39406347 G>A maps to NM_017827.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:39406676 C>A maps to NM_017827.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:39412676 C>T maps to NM_001145901.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr11:65745240 C>A maps to NM_005146.4 I681I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:108954660 C>T maps to NM_014706.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr12:108932757 G>A maps to NM_014706.3 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:108931958 C>T maps to NM_014706.3 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:108920208 C>T maps to NM_014706.3 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:108936928 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:108941765 C>T maps to NM_014706.3 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:148865800 C>T maps to NM_015278.3 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:148865062 C>T maps to NM_015278.3 C819C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:148865269 C>T maps to NM_015278.3 V888V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:148808781 G>A maps to NM_015278.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr6:148865776 G>A maps to NM_015278.3 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:148795285 C>T maps to NM_015278.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:128926641 G>T did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:128927082 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:128926732 G>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:128926709 C>T did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:128927741 C>T did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:100584579 G>T maps to NM_194292.1 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:100572524 C>A maps to NM_194292.1 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:100576039 C>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:100550988 G>A maps to NM_194292.1 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:100571379 C>T maps to NM_194292.1 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr3:18419721 T>C maps to ENST00000332610 E507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:18419721 T>C maps to ENST00000332610 E507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr3:18436274 A>C maps to ENST00000332610 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:18436061 C>T maps to ENST00000332610 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:18391029 G>A maps to ENST00000332610 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:18419723 C>A maps to ENST00000332610 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:18391147 C>T maps to ENST00000332610 Q636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:18462302 G>A maps to ENST00000332610 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr3:18436301 C>T maps to ENST00000332610 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:200233355 T>C maps to NM_001172509.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:200298196 G>A maps to NM_001172509.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:200137317 C>T maps to NM_001172509.1 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:200246525 T>G maps to NM_001172509.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr23:84362584 A>G did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:84362693 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:84362784 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:84362582 T>C did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:84362344 G>A did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr7:66456234 G>A maps to NM_016038.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr22:50903103 G>A maps to ENST00000337034 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr22:50902871 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:50898583 C>T maps to ENST00000337034 S1106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:50903149 G>T maps to ENST00000337034 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr22:50905847 G>A maps to ENST00000337034 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr22:50893254 G>A maps to ENST00000337034 P1610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:9868552 G>A maps to NM_030962.3 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr11:9983575 G>A maps to NM_030962.3 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:10052670 A>C maps to NM_030962.3 L109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:9853948 G>A maps to NM_030962.3 V1158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr11:9878252 A>G maps to NM_030962.3 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:9861067 G>A maps to NM_030962.3 N1144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr11:10051404 G>T maps to NM_030962.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:28330478 C>T maps to NM_001024401.2 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr19:56042596 G>A maps to NM_001101401.2 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr12:123782660 G>A maps to NM_001167856.1 C1301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:123815832 T>G maps to NM_001167856.1 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:123800132 T>G maps to NM_001167856.1 R1004R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:123808312 A>C maps to NM_001167856.1 L680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:123780455 C>T maps to NM_001167856.1 *1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:123800151 A>G maps to NM_001167856.1 S997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr12:123829844 C>T maps to NM_001167856.1 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:1108236 G>A maps to NM_014963.2 G1361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:1109747 G>A maps to NM_014963.2 Y1019Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:1127683 C>T maps to NM_014963.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:36018889 G>T maps to NM_001166034.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:36019071 G>A maps to NM_001166034.1 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:166263023 C>T maps to NM_006745.3 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:121174257 C>T maps to NM_001024956.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr17:39964133 C>A maps to NM_006455.2 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr19:50156576 G>A maps to NM_021228.2 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:50148366 G>A maps to NM_021228.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr9:127828303 T>C maps to NM_173690.4 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:127791927 C>T maps to NM_173690.4 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:127733947 A>G did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr9:127757210 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:127789127 G>A maps to NM_173690.4 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:77755078 C>A maps to NM_004866.4 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:77717694 G>A maps to NM_004866.4 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:75144410 A>G maps to NM_005697.3 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:155230151 C>T maps to NM_005698.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:155230399 T>C maps to NM_005698.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:155226554 C>T maps to NM_005698.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:155227152 G>A maps to NM_005698.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr19:1923149 C>T maps to NM_079834.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:1918144 C>T maps to NM_079834.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr6:28543014 A>T maps to NM_052923.1 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr6:28543515 T>C maps to NM_052923.1 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:28543835 C>A maps to NM_052923.1 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:28540142 G>A maps to NM_052923.1 R1175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:28540282 G>T maps to NM_052923.1 S1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr6:28554442 C>A maps to NM_052923.1 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:47467021 A>C maps to NM_012235.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:47458672 G>A maps to NM_012235.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:47484369 T>C maps to NM_012235.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:47460152 C>T maps to NM_012235.2 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr15:77057313 T>C maps to ENST00000324767 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:76668544 G>A maps to ENST00000324767 I1271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:77064114 C>A maps to ENST00000324767 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:76958033 T>A maps to ENST00000324767 K869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:77134236 C>T maps to ENST00000324767 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr15:77057313 T>C maps to ENST00000324767 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:27528480 C>T maps to NM_016240.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:27528636 T>C maps to NM_016240.2 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:27528549 T>C maps to NM_016240.2 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr8:27516580 C>T maps to NM_016240.2 H298H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr8:27528519 C>T maps to NM_016240.2 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr8:27528702 G>A maps to NM_016240.2 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr8:27528702 G>A maps to NM_016240.2 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:27779195 C>A maps to NM_173833.5 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:27767182 G>A maps to NM_173833.5 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr12:125279774 G>A maps to NM_005505.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:125302127 C>T maps to NM_005505.4 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:125302136 G>A maps to NM_005505.4 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:125292346 G>A maps to NM_005505.4 C323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr4:77100780 G>C maps to NM_005506.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:77091127 G>A maps to NM_005506.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:77082895 C>T maps to NM_005506.2 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr4:77084440 C>G maps to NM_005506.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:1538675 C>T maps to NM_003693.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:1538588 A>G maps to NM_003693.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:1538675 C>T maps to NM_003693.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr22:20781709 G>A maps to NM_153334.4 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:20784813 G>A maps to NM_153334.4 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:102107858 G>A maps to NM_005063.4 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:83582160 C>T maps to NM_024906.2 W213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:83626507 C>T maps to NM_001037582.2 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:83626507 C>T maps to NM_001037582.2 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr13:78178496 A>G maps to NM_144777.2 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr13:78178496 A>G maps to NM_144777.2 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:78214894 T>C maps to NM_144777.2 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:31091558 G>A maps to ENST00000311943 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:31142520 G>T maps to ENST00000311943 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:31177241 G>T maps to ENST00000311943 G542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr14:31185182 C>T maps to ENST00000311943 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:53773653 G>A maps to NM_152540.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr4:53751931 C>A maps to NM_152540.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:224462370 C>A maps to NM_003469.4 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:224462353 C>T maps to NM_003469.4 E549E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:224463700 G>A maps to NM_003469.4 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:224462202 C>A maps to NM_003469.4 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:224463790 A>G maps to NM_003469.4 H70H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:224462818 G>T maps to NM_003469.4 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:224463751 A>G maps to NM_003469.4 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:224463948 A>G maps to NM_003469.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:51991600 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:51980523 C>T maps to NM_013243.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr11:61976227 C>T maps to NM_002407.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr11:62038449 C>T maps to NM_002411.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr5:147261172 C>T maps to NM_054023.4 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr6:25691321 G>T maps to NM_006998.3 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr6:25670235 C>T maps to NM_006998.3 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr6:25670237 A>G maps to NM_006998.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr6:25670235 C>T maps to NM_006998.3 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:25670235 C>A maps to NM_006998.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr3:159614530 A>T maps to NM_001197113.1 K554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:12664720 C>T maps to NM_001112706.2 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr4:129878242 C>A maps to NM_144643.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:129964612 A>G maps to NM_144643.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:129925016 A>C maps to NM_144643.2 L102*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3678-01A-01W-0900-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr2:238990350 G>A maps to NM_016510.4 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:238990798 C>T maps to NM_016510.4 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:238976751 G>A maps to NM_016510.4 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr2:238990407 C>T maps to NM_016510.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:239003058 A>G did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:239003058 A>C did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:239002527 C>T maps to NM_016510.4 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:238991893 T>C maps to NM_016510.4 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr1:41514527 G>A maps to NM_001031694.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:41514431 G>A maps to NM_001031694.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:41493969 G>A maps to NM_001031694.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:17768362 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:17770043 T>G did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:17768147 T>C did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:17768146 G>A did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:17768199 T>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:18342067 C>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:18260564 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:18342198 A>G did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:18275011 C>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:18343060 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:18276312 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:18264925 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:18276342 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:18265951 T>G did not map to a codon.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr23:18338493 T>C did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:18265965 C>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:18276180 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:18260604 G>A did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr6:108029192 C>T maps to NM_198081.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:108029108 T>C maps to NM_198081.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:108093489 G>T maps to NM_198081.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr6:108068058 C>T maps to NM_198081.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr6:108070990 G>T maps to NM_198081.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:38739289 G>A maps to NM_006514.2 F1807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr3:38770223 G>A maps to NM_006514.2 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:38739154 G>A maps to NM_006514.2 D1852D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:38770206 C>T maps to NM_006514.2 A822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr3:38766792 G>A maps to NM_006514.2 Q1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:38743471 C>T maps to NM_006514.2 T1505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr3:38755504 G>A maps to NM_006514.2 R1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:38781050 G>A maps to NM_006514.2 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:38739574 G>A maps to NM_006514.2 I1712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:38770188 G>T maps to NM_006514.2 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:38739838 G>A maps to NM_006514.2 F1624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:38743435 G>A maps to NM_006514.2 A1517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:38770212 G>T maps to NM_006514.2 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:38770332 G>A maps to NM_006514.2 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:38830490 A>G maps to NM_006514.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr3:38802215 T>C maps to NM_006514.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:38770223 G>A maps to NM_006514.2 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:38888838 G>A maps to ENST00000302328 C1574C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr3:38962576 C>T maps to ENST00000302328 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr3:38888268 G>A maps to ENST00000302328 N1764N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr3:38936098 C>T maps to ENST00000302328 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:38986960 G>A maps to ENST00000302328 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:38888327 G>A maps to ENST00000302328 R1745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:38949501 A>G maps to ENST00000302328 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:38991700 C>T maps to ENST00000302328 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:38951637 C>T maps to ENST00000302328 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:166852582 G>A maps to NM_001165963.1 Y1507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:166859104 G>A maps to NM_001165963.1 I1387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr2:166870321 G>A maps to NM_001165963.1 R1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr2:166894606 C>T maps to NM_001165963.1 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr2:166848282 C>T maps to NM_001165963.1 A1834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr2:166894531 G>A maps to NM_001165963.1 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:166892599 C>T maps to NM_001165963.1 T1129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:166848897 G>A maps to NM_001165963.1 F1629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:166904177 G>A maps to NM_001165963.1 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr2:166900217 C>T maps to NM_001165963.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:166929910 G>T maps to NM_001165963.1 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:166848834 G>A maps to NM_001165963.1 I1650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:166859185 A>G maps to NM_001165963.1 I1360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:166900451 G>A maps to NM_001165963.1 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:166900483 G>A maps to NM_001165963.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr2:166900217 C>A maps to NM_001165963.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:166903293 G>A maps to NM_001165963.1 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:166900235 C>T maps to NM_001165963.1 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:166895998 C>T maps to NM_001165963.1 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr2:166848050 G>A maps to NM_001165963.1 R1912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:166892743 T>C maps to NM_001165963.1 G1081G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:35524975 C>T maps to NM_199037.3 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:166245157 G>C maps to NM_001040142.1 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:166229739 A>G maps to NM_001040142.1 S1285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:166188041 G>A maps to NM_001040142.1 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr2:166187993 C>T maps to NM_001040142.1 C768C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr2:166201269 G>A maps to NM_001040142.1 W923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:166166893 C>A maps to NM_001040142.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:166201316 C>T maps to NM_001040142.1 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:166243299 C>A maps to NM_001040142.1 V1532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr2:166152458 G>A maps to NM_001040142.1 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:166223835 C>T maps to NM_001040142.1 F1210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr2:166187936 A>G maps to NM_001040142.1 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr2:166170588 C>T maps to NM_001040142.1 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr2:166245634 G>A maps to NM_001040142.1 A1773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:165969559 T>C maps to NM_006922.3 E1226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:166012355 G>T maps to NM_006922.3 Y363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:165987840 G>T maps to NM_006922.3 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:165986560 G>A maps to NM_006922.3 F937F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:166020345 G>T maps to ENST00000360093 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:165984233 G>A maps to NM_006922.3 T1100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:165997321 G>A maps to NM_006922.3 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:165947358 C>A maps to NM_006922.3 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:166012310 T>C maps to NM_006922.3 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:165947801 G>A maps to NM_006922.3 R1621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr2:166020179 C>T maps to NM_006922.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:165946673 C>A maps to NM_006922.3 E1997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:165947051 G>A maps to NM_006922.3 R1871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:165947562 G>T maps to NM_006922.3 I1700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:166025335 G>T did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr2:166012310 T>C maps to NM_006922.3 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr2:166012310 T>C maps to NM_006922.3 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:165997321 G>A maps to NM_006922.3 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr2:165952155 A>G maps to NM_006922.3 V1432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr2:165986590 G>A maps to NM_006922.3 N927N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:165947358 C>T maps to NM_006922.3 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:123508916 G>A maps to NM_018400.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:62018877 G>A maps to NM_000334.4 I1588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:62028843 G>A maps to NM_000334.4 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr17:62018678 T>A maps to NM_000334.4 K1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr17:62034638 G>A maps to NM_000334.4 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:62019084 G>A maps to NM_000334.4 F1519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:62026822 G>A maps to NM_000334.4 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:62038708 C>T maps to NM_000334.4 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr17:62019222 G>A maps to NM_000334.4 F1473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr17:62034806 C>T maps to NM_000334.4 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr17:62018451 G>A maps to NM_000334.4 C1730C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:62034788 C>T maps to NM_000334.4 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:118014719 G>A maps to NM_174934.3 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:38639270 C>T maps to NM_001099404.1 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:38622487 T>C maps to NM_001099404.1 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:38592825 G>A maps to NM_001099404.1 F1679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr3:38595857 A>G maps to NM_001099404.1 C1575C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:38601826 G>A maps to NM_001099404.1 G1352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:38663937 G>A maps to NM_001099404.1 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:38651294 G>A maps to NM_001099404.1 N288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:38622442 C>T maps to NM_001099404.1 T1069T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:38595794 G>A maps to NM_001099404.1 F1596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:38592408 G>A maps to NM_001099404.1 A1818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:38592882 G>A maps to NM_001099404.1 I1660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:38595794 G>A maps to NM_001099404.1 F1596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:38592864 G>A maps to NM_001099404.1 L1666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr3:38591964 G>T maps to NM_001099404.1 S1966S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:38598024 G>T maps to NM_001099404.1 I1448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:38622616 C>T maps to NM_001099404.1 P1011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr3:38618161 G>A maps to NM_001099404.1 C1167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:38595794 G>A maps to NM_001099404.1 F1596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr3:38592255 G>A maps to NM_001099404.1 D1869D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr3:38640529 C>T maps to NM_001099404.1 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr2:167273291 G>A maps to NM_002976.2 N1113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:167334137 C>T maps to NM_002976.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:167322356 G>A maps to NM_002976.2 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:167285764 G>T maps to NM_002976.2 S871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr2:167266217 C>T maps to NM_002976.2 A1313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:167300161 C>A maps to NM_002976.2 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:167262611 G>A maps to NM_002976.2 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:167284441 G>A maps to NM_002976.2 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr2:167301466 C>T maps to NM_002976.2 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:52093513 C>T maps to NM_014191.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:52180432 G>A maps to NM_014191.2 A1350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:52145172 C>T maps to NM_014191.2 C722C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:52093399 G>A maps to NM_014191.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:52080895 T>C maps to NM_014191.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:52080229 G>A maps to NM_014191.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:52115400 G>A maps to NM_014191.2 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:52200078 A>G maps to NM_014191.2 A1603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:52159696 C>A maps to NM_014191.2 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:52159714 G>T maps to NM_014191.2 G935G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr12:52115445 G>A maps to NM_014191.2 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr12:52115529 C>T maps to NM_014191.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:167085265 G>A maps to ENST00000303354 R1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:167159789 A>T maps to ENST00000303354 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:167056252 C>A maps to ENST00000303354 T1633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:167055199 G>A maps to ENST00000303354 S1984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:167056174 G>A maps to ENST00000303354 Y1659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:167128971 G>A maps to ENST00000303354 S1097S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr2:167134678 C>A maps to ENST00000303354 G831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:167084212 C>T maps to ENST00000303354 T1410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr2:167055664 C>T maps to ENST00000303354 L1829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:167145006 C>T maps to ENST00000303354 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr2:167168171 G>C maps to ENST00000303354 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:167142905 G>A maps to ENST00000303354 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr2:167138261 C>T maps to ENST00000303354 E678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:167056038 G>A maps to ENST00000303354 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:167060576 A>G maps to ENST00000303354 F1555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:167145041 C>A maps to ENST00000303354 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:167163066 G>A maps to ENST00000303354 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:167134663 G>A maps to ENST00000303354 R836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr2:167056252 C>T maps to ENST00000303354 T1633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr2:167160795 G>T maps to ENST00000303354 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr2:167168206 A>T maps to ENST00000303354 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:167162408 A>G maps to ENST00000303354 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:167133596 G>A maps to ENST00000303354 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr1:151139645 G>A maps to NM_024041.2 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:6464500 G>T maps to NM_001159576.1 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:6458341 C>T maps to NM_001159576.1 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:23391448 G>T maps to ENST00000307331 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:23364253 A>G maps to ENST00000307331 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr16:23387066 T>C maps to ENST00000307331 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:23359982 G>A maps to ENST00000307331 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:23387157 C>A maps to ENST00000307331 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:1221640 T>A maps to NM_001130413.2 C200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:1219401 G>A maps to NM_001130413.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:23200706 C>T maps to NM_001039.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:23197639 C>T maps to NM_001039.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr16:23205521 T>C maps to NM_001039.3 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:23197735 C>T maps to NM_001039.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr16:23208639 C>A maps to NM_001039.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr16:23197645 G>A maps to NM_001039.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr16:23208729 C>A maps to NM_001039.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:10596105 C>T maps to NM_004589.2 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:10590090 T>G maps to NM_004589.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:53446175 G>T maps to NM_002979.4 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:53516321 T>A maps to NM_002979.4 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:53427242 T>C maps to NM_002979.4 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:55079463 T>C maps to NM_021626.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:55074372 G>A maps to NM_021626.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:144891741 G>A maps to NM_182706.3 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:144895080 C>T maps to NM_182706.3 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:144895638 C>T did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr7:30008593 C>A maps to NM_001145514.1 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:29980460 C>T maps to NM_001145514.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:29983635 C>T maps to NM_001145514.1 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:45916169 C>T maps to NM_138355.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:145559753 G>A maps to NM_031309.4 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:145557056 C>T maps to NM_031309.4 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:145556951 C>T maps to NM_031309.4 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:644596 G>A maps to NM_033129.3 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:120252039 G>A maps to NM_002980.2 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:120236465 G>A maps to NM_002980.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:120219573 C>T maps to NM_002980.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:120252084 G>A maps to NM_002980.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:43614261 G>A maps to NM_173050.2 C630C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:43616480 G>A maps to NM_173050.2 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr22:43604225 A>G maps to NM_173050.2 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr22:43658795 C>T maps to NM_173050.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:9077456 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:9096133 G>A maps to ENST00000457346 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:9047345 G>A maps to ENST00000457346 I919I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:9048977 G>A maps to ENST00000457346 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr11:9087444 C>G maps to ENST00000457346 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:9047357 G>A maps to ENST00000457346 Y915Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:9051470 C>T maps to ENST00000457346 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:9068987 G>A maps to ENST00000457346 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:9074688 G>A maps to ENST00000457346 D468D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:9049064 A>G maps to ENST00000457346 I849I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:9047360 G>T maps to ENST00000457346 T914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:35201028 C>T maps to ENST00000394681 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:35213144 G>T maps to ENST00000394681 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:35216472 C>A maps to ENST00000394681 P1007P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:35196415 T>C maps to ENST00000394681 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr6:35211773 G>A maps to ENST00000394681 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr6:35209601 G>A maps to ENST00000394681 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:65293112 G>A maps to NM_020680.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:100732746 C>T maps to NM_017988.4 Q863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:100732406 T>C maps to NM_017988.4 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:100704945 C>A maps to NM_017988.4 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:100685391 C>T maps to NM_017988.4 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr12:100732734 C>T maps to NM_017988.4 Q859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr12:100732406 T>C maps to NM_017988.4 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:169823668 C>T maps to NM_181093.2 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:169857938 C>A maps to NM_181093.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:169823674 G>A maps to NM_181093.2 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:169831765 G>T maps to NM_181093.2 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:76881296 C>A maps to NM_018115.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:76881222 A>G maps to NM_018115.2 D493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr2:20403630 C>T maps to NM_001006946.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr8:97621772 G>A maps to NM_002998.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:97620627 C>T maps to NM_002998.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr8:97620630 A>G maps to NM_002998.3 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:31349782 G>T maps to NM_014654.3 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:31349809 G>A maps to NM_014654.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr1:31349817 C>A maps to NM_014654.3 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr20:43964467 G>A maps to NM_002999.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr8:59488595 A>T maps to NM_005625.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr20:1293004 G>A maps to NM_080489.4 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr20:1293259 G>A maps to NM_080489.4 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr20:1293007 C>T maps to NM_080489.4 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr20:1291460 G>A maps to NM_080489.4 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:50295464 C>T maps to NM_004713.3 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:50307551 T>G maps to NM_004713.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:50295439 C>A maps to NM_004713.3 G440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:50298973 C>A maps to NM_004713.3 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr14:50295788 A>G maps to NM_004713.3 H405H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr14:50272786 A>C maps to NM_004713.3 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr9:139302276 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:243437879 T>C maps to NM_006642.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:243434337 G>A maps to NM_006642.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:243419540 G>A maps to NM_006642.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:21998439 C>A maps to NM_022044.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:1159230 G>T maps to NM_016176.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:1158663 G>A maps to NM_016176.3 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:224546 C>T maps to NM_004168.2 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:235369 C>T maps to NM_004168.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:235426 C>T maps to NM_004168.2 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:61205544 C>T maps to NM_017841.2 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr11:61205105 C>T maps to NM_017841.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:161326488 G>A maps to NM_003001.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:4285376 C>T maps to NM_152744.3 G2107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr7:4189018 C>T maps to NM_152744.3 R1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:4277366 C>T maps to NM_152744.3 F2027F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:4002470 C>T maps to NM_152744.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr7:4011110 C>T maps to NM_152744.3 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr7:4014069 C>T maps to NM_152744.3 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:4260967 G>A maps to NM_152744.3 T1933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:4009042 G>A maps to NM_152744.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:3658862 C>T maps to NM_152744.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr7:4008985 C>T maps to NM_152744.3 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr7:4198112 G>T maps to NM_152744.3 L1553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:4056976 G>A maps to NM_152744.3 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:4277372 C>T maps to NM_152744.3 L2029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:4185414 C>T maps to NM_152744.3 V1430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr7:4002460 C>A maps to NM_152744.3 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr7:4026856 T>G maps to NM_152744.3 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr7:3991466 G>A maps to NM_152744.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr7:4189093 A>T maps to NM_152744.3 R1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:4153691 C>T maps to NM_152744.3 N1203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:4218192 C>T maps to NM_152744.3 P1691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr17:71354290 G>A maps to NM_001144952.1 I1840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr17:71364699 G>A maps to NM_001144952.1 L1671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:71397285 G>A maps to NM_001144952.1 N948N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr17:71415390 G>A maps to NM_001144952.1 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:71364615 G>A maps to NM_001144952.1 S1699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr17:71410866 C>T maps to NM_001144952.1 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:71437036 G>A maps to NM_001144952.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr17:71443796 G>A maps to NM_001144952.1 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:71334935 C>T maps to NM_001144952.1 T2103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr17:71420137 C>T maps to NM_001144952.1 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr2:192711270 C>T maps to NM_004657.5 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:192711321 C>T maps to NM_004657.5 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr2:192700687 G>A maps to NM_004657.5 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:192711384 G>A maps to NM_004657.5 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:192711441 G>A maps to NM_004657.5 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr14:24909578 G>A maps to NM_020195.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:24909407 G>A maps to NM_020195.2 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr16:82033809 G>A maps to NM_145168.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:82033147 C>T maps to NM_145168.2 Q250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr12:57324050 G>A maps to NM_148897.2 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:57327778 C>T maps to NM_148897.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:57327751 G>A maps to NM_148897.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:113873142 C>T maps to NM_138432.2 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr12:113873169 A>C maps to NM_138432.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr12:113874588 C>T maps to NM_138432.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:56822989 G>T maps to NM_033280.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr3:10357075 G>A maps to ENST00000343726 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:10343027 G>A maps to ENST00000343726 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:10342986 G>A maps to ENST00000343726 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr3:10346794 C>T maps to ENST00000343726 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:75199739 C>T maps to NM_001039573.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr17:75202898 C>T maps to NM_001039573.2 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:75202890 C>T maps to NM_001039573.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:75208084 G>A maps to NM_001039573.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr17:75202454 C>A maps to NM_001039573.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr22:30856115 G>A maps to NM_174975.4 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:30857435 G>A maps to NM_174975.4 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr22:30858105 A>G maps to NM_174975.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr22:30858105 A>G maps to NM_174975.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr22:30891941 C>T maps to NM_174977.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr22:30887831 G>T maps to NM_174977.3 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:30890139 G>A maps to NM_174977.3 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:30887894 C>T maps to NM_174977.3 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:30888130 G>A maps to NM_174977.3 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr22:30890942 G>T maps to NM_174977.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:5041891 G>A maps to NM_014692.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:5041933 T>C maps to NM_014692.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:5009351 C>T maps to NM_014692.1 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:5046379 G>A maps to NM_014692.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:139354290 C>T maps to NM_014866.1 P1703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:139360441 G>A maps to NM_014866.1 A1425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:139350202 G>A maps to NM_014866.1 Q1903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:139371398 C>T maps to NM_014866.1 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:139369517 C>T maps to NM_014866.1 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:139369517 C>T maps to NM_014866.1 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:139357509 G>T maps to NM_014866.1 P1574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:139370039 G>T maps to NM_014866.1 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr1:177917070 C>A maps to NM_033127.2 G518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr1:177909777 T>A maps to NM_033127.2 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:177930758 G>T maps to NM_033127.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:177928010 C>T maps to NM_033127.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:177917068 T>C maps to NM_033127.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr1:177917068 T>C maps to NM_033127.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:177917068 T>C maps to NM_033127.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:177917070 C>A maps to NM_033127.2 G518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:122928175 A>T maps to NM_012430.4 K38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:122964828 C>T maps to NM_012430.4 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:122964828 C>T maps to NM_012430.4 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:42610408 G>A maps to NM_032970.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr14:39510022 C>T maps to NM_006364.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:39512076 C>A did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr14:39514453 A>G maps to NM_006364.2 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr14:39565307 C>T maps to NM_006364.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:18531785 T>C maps to NM_001172745.1 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr20:18505625 A>G maps to NM_001172745.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:18505198 G>A maps to NM_001172745.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr10:121685733 G>T maps to NM_007190.2 G770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:121675362 G>A maps to NM_007190.2 W502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:121677365 T>G maps to NM_007190.2 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr10:121685735 A>G maps to NM_007190.2 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:121692641 G>T maps to NM_007190.2 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr10:121685735 A>G maps to NM_007190.2 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr10:121685735 A>G maps to NM_007190.2 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:133996827 G>A maps to NM_021982.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:110427525 T>C maps to NM_006323.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr4:110415909 C>A maps to NM_006323.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:75528786 T>C maps to NM_198597.1 F767F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:75530508 C>T maps to NM_198597.1 R1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr10:75506595 C>T maps to NM_198597.1 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:119726997 C>A maps to ENST00000379735 G306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:119660424 C>T maps to ENST00000379735 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:119754818 C>T maps to ENST00000379735 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:83778104 C>T maps to ENST00000505472 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr4:83788062 A>G maps to ENST00000505472 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:83763464 G>T maps to ENST00000505472 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:83778872 A>G maps to ENST00000505472 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:102256017 A>C maps to NM_015490.3 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr10:102258465 T>A maps to NM_015490.3 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:127783784 C>T maps to ENST00000464451 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:127783741 C>A maps to ENST00000464451 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr10:12206305 T>C maps to NM_018144.3 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr6:108227961 A>G maps to NM_007214.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:108224045 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:108192972 C>A maps to NM_007214.4 E740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr6:108227961 A>G maps to NM_007214.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr6:108227961 A>G maps to NM_007214.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr6:108227961 A>G maps to NM_007214.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:108246054 T>C maps to NM_007214.4 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr9:91943767 A>G maps to NM_024077.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr9:91943767 A>G maps to NM_024077.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:91934685 G>A maps to NM_024077.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr9:91947845 C>T maps to NM_024077.3 N275N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:91956350 C>T maps to NM_024077.3 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:91940837 G>A maps to NM_024077.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr15:49325258 C>T maps to NM_001193489.1 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:49293294 C>A did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr15:49284713 C>T maps to NM_001193489.1 V1011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:12986899 G>A maps to NM_001013437.1 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr14:82000057 G>A maps to NM_005065.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:81965997 G>T maps to NM_005065.4 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr14:81964334 A>G maps to NM_005065.4 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr14:81943417 G>A maps to NM_005065.4 Y761Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr20:13850179 G>A maps to NM_025229.1 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:13850834 G>A maps to NM_025229.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:13894460 G>T maps to NM_025229.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr20:13867032 C>T maps to NM_025229.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr20:13868463 T>C maps to NM_025229.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:25848931 C>T maps to NM_015187.3 Q239Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:25821486 C>A maps to NM_015187.3 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:25806267 G>A maps to NM_015187.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:25780792 C>T maps to NM_015187.3 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:169701084 T>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:169698773 G>A maps to NM_000450.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:169702041 T>G maps to NM_000450.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:169697295 A>G maps to NM_000450.2 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr1:151342219 G>C maps to ENST00000435071 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:151337075 G>A maps to ENST00000435071 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr22:50648716 C>T maps to NM_031454.1 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:50655146 G>A maps to NM_031454.1 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr22:50649110 G>A maps to NM_031454.1 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr22:50649089 C>T maps to NM_031454.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:50655255 C>T maps to NM_031454.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr22:50655493 C>T maps to NM_031454.1 Y594Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr22:50655147 C>T maps to NM_031454.1 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:169580733 A>G maps to NM_003005.3 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:169586593 G>T maps to NM_003005.3 Y51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:169586338 G>T maps to NM_003005.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:109017078 G>A maps to ENST00000228463 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:101815492 C>T maps to NM_018445.4 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:40005923 G>A maps to NM_182704.1 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:83592583 C>T maps to NM_006080.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:83592640 A>G maps to NM_006080.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:83610680 A>G maps to NM_006080.2 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr7:83592559 A>G maps to NM_006080.2 Y607Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:83689832 G>T maps to NM_006080.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:83634712 A>G maps to NM_006080.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr7:83640538 C>T maps to NM_006080.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:50312301 G>A maps to NM_004636.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:50312355 C>T maps to NM_004636.2 H479H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:50308337 C>T maps to NM_004636.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:80433564 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:80432077 C>A maps to NM_006379.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr7:80432077 C>T maps to NM_006379.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr7:84636233 C>A maps to NM_152754.2 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:84694782 G>A maps to NM_152754.2 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:84642104 G>A maps to NM_152754.2 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr7:84727177 T>C maps to NM_152754.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:84751159 A>G maps to NM_152754.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:84727258 A>G maps to NM_152754.2 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:84671485 C>T did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr7:84636123 T>C maps to NM_152754.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr7:84685071 G>A maps to NM_152754.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:84644454 G>A maps to NM_152754.2 C541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr7:84651725 A>G maps to NM_152754.2 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:83029485 A>G maps to NM_012431.2 H408H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr7:82997216 C>T maps to NM_012431.2 E671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:83025988 C>A maps to NM_012431.2 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:83021977 G>A maps to NM_012431.2 D520D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr7:83025955 T>A maps to NM_012431.2 K486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr7:83119489 C>T maps to NM_012431.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:83032004 T>C maps to NM_012431.2 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr7:83119471 T>C maps to NM_012431.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr7:82997195 G>A maps to NM_012431.2 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr3:50225202 C>T maps to NM_004186.3 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr3:52469642 C>T maps to NM_020163.1 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:52475405 G>A maps to NM_020163.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:52474774 G>A maps to NM_020163.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:52469618 C>A maps to NM_020163.1 *783Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr15:90771235 C>T maps to NM_198925.2 N625N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:90764257 C>G maps to NM_198925.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr15:90768363 C>T maps to NM_198925.2 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr2:97527532 G>A maps to NM_017789.4 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:92006181 G>A maps to NM_006378.3 C257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:92002511 G>A maps to NM_006378.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr9:91994491 C>T maps to NM_006378.3 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:91994518 C>T maps to NM_006378.3 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:92002451 G>A maps to NM_006378.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:92002316 G>T maps to NM_006378.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:92017869 G>A maps to NM_006378.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:74900816 C>T maps to NM_004263.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:74906970 C>T maps to NM_004263.3 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr2:74885008 C>T maps to NM_004263.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr10:102738344 C>T maps to NM_017893.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:102740948 G>A maps to NM_017893.2 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:102740963 C>A maps to NM_017893.2 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr10:102739916 A>T maps to NM_017893.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:102743065 A>G maps to NM_017893.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:9054361 G>A maps to NM_003966.2 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:9136618 A>G maps to NM_003966.2 C532C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:9337843 C>A maps to NM_003966.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:9190439 G>A maps to NM_003966.2 H404H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:9066665 G>A maps to NM_003966.2 G722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:9197384 G>T maps to NM_003966.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:9066704 G>T maps to NM_003966.2 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:9043083 G>T maps to NM_003966.2 Y1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr5:9052033 C>T maps to NM_003966.2 G932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:9066557 G>A maps to NM_003966.2 D758D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr3:122645450 G>A maps to NM_001031702.2 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:122630881 G>A maps to NM_001031702.2 C977C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:122646799 G>A maps to NM_001031702.2 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:122647440 G>A maps to NM_001031702.2 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:122647429 G>A maps to NM_001031702.2 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:122632413 G>A maps to NM_001031702.2 C749C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:122631064 G>A maps to NM_001031702.2 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:122641162 G>A maps to NM_001031702.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr5:115818243 A>G maps to ENST00000257414 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:115815885 C>T maps to ENST00000257414 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr5:115827472 T>G maps to ENST00000257414 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:115815885 C>T maps to ENST00000257414 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:115811250 C>T maps to ENST00000257414 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:115782368 G>A maps to ENST00000257414 P1028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:115782314 A>G maps to ENST00000257414 C1046C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CA-6717-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:115803441 C>T maps to ENST00000257414 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:115782938 C>T maps to ENST00000257414 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr5:115824602 G>A maps to ENST00000257414 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:115815897 G>A maps to ENST00000257414 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:4555540 G>A maps to NM_032108.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr19:4555492 G>C maps to NM_032108.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:151108161 A>G maps to NM_001178061.1 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3856-01A-01W-0900-09 chr1:151109039 G>A maps to NM_001178061.1 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:151115000 G>A maps to NM_001178061.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:151115030 G>A maps to NM_001178061.1 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:48056503 T>A did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr15:48057208 C>T maps to NM_153618.1 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr15:48056924 T>C maps to NM_153618.1 H396H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr15:48058182 T>C maps to NM_153618.1 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:74703970 G>A maps to NM_003612.3 H501H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:43836660 G>A maps to NM_003007.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:43850524 A>G maps to NM_003008.2 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr20:43851701 C>T maps to NM_003008.2 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:48458871 T>C maps to ENST00000004980 E417E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:48491791 C>T maps to ENST00000004980 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:7468153 C>T maps to ENST00000321337 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr3:196612999 G>A maps to NM_152699.4 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:196626860 C>T maps to NM_152699.4 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:196613323 C>T maps to NM_152699.4 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:196626606 A>G maps to NM_152699.4 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:196630448 G>T maps to NM_152699.4 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:76376614 A>G maps to NM_015571.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:76369065 C>A maps to NM_015571.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr6:76412420 T>C maps to NM_015571.2 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:76412420 T>C maps to NM_015571.2 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr6:76412420 T>A maps to NM_015571.2 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:76405522 C>A maps to NM_015571.2 Y693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr3:101080582 T>C maps to NM_020654.3 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr3:101047325 G>A maps to NM_020654.3 R954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:101044795 G>A maps to NM_020654.3 S1048S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:101060566 G>A maps to NM_020654.3 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:101080582 T>C maps to NM_020654.3 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:101062706 A>G maps to NM_020654.3 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:101136587 G>A maps to NM_020654.3 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:101086676 C>T maps to NM_020654.3 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:101083675 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:101136588 T>A maps to NM_020654.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:87329249 G>A maps to NM_004261.3 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:13386893 C>T maps to NM_012247.4 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr10:13380770 G>A maps to NM_012247.4 H77H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:30455833 G>A maps to ENST00000478753 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:26127535 A>G maps to NM_020451.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:42801064 G>A maps to NM_001093726.1 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:25153614 C>T maps to NM_016955.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:30390792 C>T maps to NM_052838.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:30392465 G>T maps to NM_052838.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:110303753 C>A maps to ENST00000356688 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:110303729 C>A maps to ENST00000356688 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:110350672 C>T maps to ENST00000356688 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:110303685 A>G maps to ENST00000356688 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:77941689 C>T maps to ENST00000510515 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr16:4829783 G>T maps to NM_144605.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr16:4835842 C>T maps to NM_144605.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:4836083 G>T maps to NM_144605.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:4837544 A>G maps to NM_144605.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:242282465 A>G maps to ENST00000391972 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr2:242277168 T>C maps to ENST00000391972 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:42390328 C>T maps to NM_145733.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:42377840 G>A did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr22:42377667 G>A maps to NM_145733.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:19709429 C>T maps to NM_002688.5 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr22:19709995 C>T maps to NM_002688.5 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:118763418 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:118797584 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:118797584 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:118784020 G>A did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:118763418 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:118771107 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:35942756 T>C maps to NM_001788.4 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:35872496 G>A maps to NM_001788.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:75484811 G>A maps to NM_001113491.1 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:75398477 G>A maps to NM_001113491.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:75316431 T>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:48284381 C>A maps to NM_003009.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr6:158567892 G>A maps to NM_032861.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:67895869 T>C maps to NM_001018067.1 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:18029506 G>C maps to NM_012139.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:18017394 A>G maps to NM_012139.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:122777657 A>G maps to NM_020755.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr6:122775299 T>A maps to NM_020755.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:122768327 C>T maps to NM_020755.2 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr6:122768410 C>G did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr20:43142612 C>T maps to NM_006811.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr13:44948193 C>T maps to NM_001010897.1 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:94849052 G>A maps to NM_001127707.1 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr14:94849247 C>T maps to NM_001127707.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr14:94756420 C>T maps to NM_001100607.1 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:94756360 G>A maps to NM_001100607.1 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr14:94756360 G>A maps to NM_001100607.1 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:94914907 G>A maps to NM_001080451.1 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:94914786 C>A maps to NM_001080451.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:94908957 G>A maps to NM_001080451.1 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:94964398 A>G maps to NM_173850.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:94953640 T>C maps to NM_173850.2 *415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr14:94964398 A>G maps to NM_173850.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr14:95085772 C>T maps to ENST00000393080 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr14:95090123 C>T maps to ENST00000393080 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:95081023 C>T maps to ENST00000393080 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:95085610 G>A maps to ENST00000393080 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr14:95035829 C>T maps to NM_006215.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr14:95033337 G>A maps to NM_006215.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:95033475 C>T maps to NM_006215.2 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr14:95035766 T>C maps to NM_006215.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:95054238 G>A maps to NM_000624.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:95057091 C>T maps to NM_000624.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:95054133 C>T maps to NM_000624.4 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:95057223 G>A maps to NM_000624.4 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:94776242 G>A maps to NM_001756.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr14:94780519 A>G maps to NM_001756.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr14:94780517 C>T maps to NM_001756.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr14:94770787 G>A maps to NM_001756.3 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr23:105277623 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:105278334 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:105279361 G>A did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr14:94935805 G>A maps to NM_175739.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr14:94929474 G>A maps to NM_175739.3 D421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr18:61388081 G>A maps to NM_080475.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:61388132 G>A maps to NM_080475.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr18:61388072 T>C maps to NM_080475.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:61379836 C>T maps to NM_080475.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:61383354 G>A maps to NM_080475.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr18:61226857 G>A maps to ENST00000382768 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:61225623 G>T maps to ENST00000382768 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr18:61233906 C>A maps to ENST00000382768 S314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:61570322 G>A maps to NM_001143818.1 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:61570493 G>A maps to NM_001143818.1 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr18:61570322 G>A maps to NM_001143818.1 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:61328348 G>A maps to NM_006919.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:61324079 G>A maps to NM_006919.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:61324079 G>A maps to NM_006919.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:61323022 G>A maps to NM_006919.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr18:61326647 C>T maps to NM_006919.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:61325785 G>A maps to NM_006919.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr18:61305069 G>A maps to NM_002974.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr18:61305084 G>A maps to NM_002974.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:61306433 G>A maps to NM_002974.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr18:61463517 G>T maps to NM_001040147.1 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:61463558 G>A maps to NM_001040147.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:61471707 G>T maps to NM_001040147.1 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr18:61468155 T>C maps to NM_001040147.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:61654229 T>C maps to NM_198833.1 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:61645622 C>T maps to NM_198833.1 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:2892098 G>A maps to NM_004155.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:2890501 G>A maps to NM_004155.4 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:173873143 C>T maps to NM_000488.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:173873143 C>T maps to NM_000488.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr1:173878765 G>A maps to NM_000488.3 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:21138368 C>T maps to NM_000185.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr22:21133650 G>A maps to NM_000185.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:100773741 G>A maps to NM_000602.3 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:100773714 C>T maps to NM_000602.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr7:100773744 C>A maps to NM_000602.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:100776988 G>A maps to NM_000602.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:224856553 C>T maps to NM_001136530.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:224847476 T>C maps to NM_001136530.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:224849482 C>T maps to NM_001136530.1 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:224849620 C>A maps to NM_001136530.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:224847491 T>G maps to NM_001136530.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:51921299 G>T maps to NM_001101320.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr13:51918520 C>T maps to NM_001101320.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr17:1674326 G>T maps to NM_002615.4 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr17:1674326 G>T maps to NM_002615.4 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr11:57373501 C>A maps to ENST00000403558 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:57381951 C>A maps to ENST00000403558 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr11:57367464 C>T maps to ENST00000403558 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:57382014 C>T maps to ENST00000403558 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:75280083 C>T maps to NM_001235.2 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:75280164 T>C maps to NM_001235.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:167512516 T>C maps to NM_005025.4 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr3:167170742 G>A maps to NM_006217.3 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:167184933 T>C maps to NM_006217.3 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:167167158 C>T maps to NM_006217.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr3:167183402 C>A maps to NM_006217.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:40929339 C>T maps to NM_013376.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:64863645 G>A maps to NM_014755.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:64863393 G>A maps to NM_014755.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:64863429 C>T maps to NM_014755.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:40947705 G>T maps to NM_203344.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:40947648 C>T maps to NM_203344.2 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:210415264 C>T maps to NM_019605.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr6:109308758 G>T maps to NM_014454.1 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:109319840 C>A maps to NM_014454.1 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr6:109323513 T>C maps to NM_014454.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr1:28599954 C>T maps to NM_031459.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr1:28605721 C>A maps to NM_031459.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:94918637 C>A maps to NM_144665.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr11:94924585 C>T maps to NM_144665.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:179986644 G>A maps to NM_178123.4 Q432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr2:179982317 G>A maps to NM_178123.4 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:180036888 C>T maps to NM_178123.4 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:179989225 G>A maps to NM_178123.4 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:180008449 C>A maps to NM_178123.4 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:179997153 C>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:131455236 G>T maps to NM_001122821.1 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr18:42281763 G>A maps to NM_015559.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:42643083 C>T maps to NM_015559.2 I1404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:42530724 G>T maps to NM_015559.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:42532616 C>T maps to NM_015559.2 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr18:42530552 T>C maps to NM_015559.2 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr18:42643521 C>A maps to NM_015559.2 G1550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr16:30980936 C>T maps to NM_014712.1 D981D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:30990682 C>A maps to NM_014712.1 P1192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:30975575 C>A maps to NM_014712.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:30982720 G>A maps to NM_014712.1 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:30982822 C>G maps to NM_014712.1 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:30990643 G>A maps to NM_014712.1 P1179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:47108598 G>A maps to NM_014159.6 R2024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:47098426 G>A maps to NM_014159.6 Q2283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr3:47144859 A>G maps to NM_014159.6 C1631C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:47162621 A>G maps to NM_014159.6 V1168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:47155436 C>T maps to NM_014159.6 Q1548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:47163425 G>A maps to NM_014159.6 C900C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:47061294 G>T maps to NM_014159.6 T2462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:47143032 C>A maps to NM_014159.6 G1644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr3:47161979 A>G maps to NM_014159.6 A1382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:47158222 T>C maps to NM_014159.6 R1492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr3:47061324 C>T maps to NM_014159.6 S2452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:47144859 A>G maps to NM_014159.6 C1631C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr3:47161979 A>G maps to NM_014159.6 A1382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr3:47139489 T>C maps to NM_014159.6 A1699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr3:47158224 G>A maps to NM_014159.6 R1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:47143032 C>A maps to NM_014159.6 G1644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr3:47143030 T>C maps to NM_014159.6 G1644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr3:47144859 A>G maps to NM_014159.6 C1631C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr3:47158195 A>T maps to NM_014159.6 C1501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:47139489 T>C maps to NM_014159.6 A1699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr3:47161979 A>G maps to NM_014159.6 A1382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr14:99871678 G>A maps to NM_032233.2 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:99865105 G>T maps to NM_032233.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:99866493 C>T maps to NM_032233.2 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr14:99870618 C>A maps to NM_032233.2 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr21:37431156 C>T maps to NM_017438.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:37417909 C>T maps to NM_017438.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:9483365 G>A maps to ENST00000407969 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr3:9483901 C>T maps to ENST00000407969 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:9489428 G>A maps to ENST00000407969 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:9482159 G>A maps to ENST00000407969 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:9482138 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:9483410 G>T maps to ENST00000407969 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:9484994 C>T maps to ENST00000407969 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr3:9512489 A>G maps to ENST00000407969 G1043G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:58552064 A>G maps to NM_001160305.1 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:140441535 A>G maps to NM_030648.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr4:140439084 C>A maps to NM_030648.2 G292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:140454435 C>T maps to NM_030648.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:123889531 C>T maps to NM_020382.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr12:123892037 A>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:150900403 G>T maps to NM_001145415.1 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:150923398 C>T maps to NM_001145415.1 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr1:150923105 C>T maps to NM_001145415.1 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:150921736 C>A maps to NM_001145415.1 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:150936003 A>G did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr1:150916431 T>C maps to NM_001145415.1 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:50056924 C>T maps to NM_031915.2 N415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr13:50055232 A>G maps to NM_031915.2 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:4354904 G>A maps to NM_006515.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:4358833 C>T maps to NM_006515.3 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:4345149 C>T maps to NM_006515.3 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:4354874 C>T maps to NM_006515.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr9:135205301 C>T maps to ENST00000372169 K561K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr9:135204404 G>A maps to ENST00000372169 N860N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr9:135204029 C>T maps to ENST00000372169 S985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:135145088 T>C maps to ENST00000372169 G2400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:135205331 C>T maps to ENST00000372169 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:135173630 C>A maps to ENST00000372169 E1873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:135204421 C>A maps to ENST00000372169 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:135224713 G>A maps to ENST00000372169 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:135205040 T>C maps to ENST00000372169 E648E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:135139850 G>A maps to ENST00000372169 P2632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:135176136 A>G maps to ENST00000372169 L1810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:135204182 A>T maps to ENST00000372169 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:135204301 C>A maps to ENST00000372169 E895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr9:135221651 A>G maps to ENST00000372169 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:27308923 G>T maps to NM_178860.4 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:27296971 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr22:26688759 G>A maps to NM_021115.4 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3522-01A-01W-0831-10 chr22:26688786 G>A maps to NM_021115.4 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr22:26693011 C>T maps to NM_021115.4 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:26761392 C>T maps to NM_021115.4 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:26706725 C>T maps to NM_021115.4 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr22:26689065 C>A maps to NM_021115.4 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr22:26688852 G>A maps to NM_021115.4 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr22:26706755 G>A maps to NM_021115.4 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr22:26771574 G>A maps to NM_021115.4 G954G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr22:26736554 C>T maps to NM_021115.4 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr22:26771565 G>A maps to NM_021115.4 S951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:29908191 C>T maps to NM_201575.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:29907158 G>A maps to NM_201575.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:29889660 G>A maps to NM_201575.2 C553C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:64534510 C>T maps to NM_201995.2 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:64536546 C>T maps to NM_201995.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:64535711 C>A maps to NM_201995.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr11:64544045 T>C maps to NM_201995.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:64535619 G>A maps to NM_201995.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr11:64544045 T>C maps to NM_201995.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:30734846 C>T maps to NM_005877.4 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr22:30734825 G>A maps to NM_005877.4 N565N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr22:30742465 G>A maps to NM_005877.4 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr22:30735181 A>G maps to NM_005877.4 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:30752745 C>T maps to NM_005877.4 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr19:2248148 T>C maps to NM_007165.4 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr19:2248151 T>C maps to NM_007165.4 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr19:2248178 T>C maps to NM_007165.4 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr19:2248184 A>T maps to NM_007165.4 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr2:198257820 A>G maps to NM_012433.2 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:198257818 C>T maps to NM_012433.2 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:198257820 A>G maps to NM_012433.2 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr2:198266777 A>G maps to NM_012433.2 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr11:65827044 C>T maps to NM_006842.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr11:65829173 A>G maps to NM_006842.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:65835753 G>T maps to NM_006842.2 E856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr11:65827380 C>T maps to NM_006842.2 Y510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:65824821 G>A maps to NM_006842.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr11:65823019 G>A maps to NM_006842.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:65829167 C>T maps to NM_006842.2 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:65829411 A>G maps to NM_006842.2 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:65819905 G>A maps to NM_006842.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr16:70595627 G>A maps to NM_012426.4 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:149895736 G>A maps to NM_005850.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:19413117 C>T maps to NM_172231.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:19427280 C>T maps to NM_172231.2 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:31924835 G>T maps to NM_001007467.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:32007129 C>T maps to NM_001007467.1 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:32011126 G>T maps to NM_001007467.1 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr3:53003138 G>A maps to NM_016329.3 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:52941177 T>G maps to NM_016329.3 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:52941612 G>A maps to NM_016329.3 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:52945025 G>A maps to NM_016329.3 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:7218127 C>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:7239527 G>A maps to NM_001018039.1 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:7214510 G>A maps to NM_001018039.1 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:7290521 C>T maps to NM_001018039.1 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:7409782 C>T maps to NM_001018039.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:7244458 G>A maps to NM_001018039.1 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:7205773 G>A maps to NM_001018039.1 I881I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:7242374 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr10:7247879 A>T maps to NM_001018039.1 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:7269821 G>A maps to NM_001018039.1 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:7409782 C>T maps to NM_001018039.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr10:7412308 G>T maps to NM_001018039.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:7205746 G>A maps to NM_001018039.1 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:7205833 C>T maps to NM_001018039.1 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:7214078 G>A maps to NM_001018039.1 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr10:7214483 G>A maps to NM_001018039.1 A708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr10:7230586 T>A maps to NM_001018039.1 K603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr10:7239545 C>A maps to NM_001018039.1 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr1:35656181 T>C maps to NM_005066.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr8:41166261 C>T maps to NM_003012.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:154709639 C>T maps to NM_003013.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:154709558 G>A maps to NM_003013.2 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:154702675 G>T maps to NM_003013.2 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:154702737 G>A maps to NM_003013.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:37947182 G>A maps to ENST00000223214 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:37956091 C>T maps to ENST00000223214 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:37955716 G>T maps to ENST00000223214 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:37949281 C>T maps to ENST00000223214 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr7:37951761 G>T maps to ENST00000223214 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:56083269 A>G maps to NM_006924.4 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:56083245 G>A maps to NM_006924.4 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:56083764 T>G maps to NM_006924.4 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:70687460 C>T maps to NM_004768.3 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:70694125 A>G maps to NM_004768.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:70715641 C>T maps to NM_004768.3 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:70705148 C>A maps to NM_004768.3 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr1:70716466 A>G maps to NM_004768.3 E478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:65473410 T>C maps to NM_001077199.1 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:65440326 C>T maps to NM_001077199.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:65466526 T>C maps to NM_001077199.1 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr6:89808302 A>G maps to ENST00000452027 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:89816948 G>A maps to ENST00000452027 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:89816961 G>A maps to ENST00000452027 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:19105231 G>A maps to NM_001017392.3 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr19:19130026 G>A maps to NM_001017392.3 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:19106068 G>A maps to NM_001017392.3 F1004F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:19115277 G>A maps to NM_001017392.3 D876D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AU-6004-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:19105981 G>T maps to NM_001017392.3 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:19120808 A>G maps to NM_001017392.3 N731N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr21:33073397 A>G maps to NM_020706.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr21:33066562 G>A maps to NM_020706.2 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr21:33044506 C>T maps to NM_020706.2 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr21:33044575 C>T maps to NM_020706.2 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr21:33068949 T>G maps to NM_020706.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:33063260 G>A maps to NM_020706.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr21:33065708 G>A maps to NM_020706.2 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr21:33074088 C>T maps to NM_020706.2 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:99848574 G>T maps to NM_032870.2 G753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:99850448 C>A maps to NM_032870.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:99857199 T>C maps to NM_032870.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:46321422 C>T maps to NM_004719.2 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr12:46342314 T>C maps to NM_004719.2 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:46316730 C>T maps to NM_004719.2 S1371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:46320827 C>A maps to NM_004719.2 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:46342316 G>A maps to NM_004719.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:46316862 T>C maps to NM_004719.2 G1327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:46357887 A>G did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:29475709 G>T maps to NM_005626.4 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:29475268 G>A maps to NM_005626.4 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:29475256 G>A maps to NM_005626.4 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr1:29475703 G>T maps to NM_005626.4 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr1:29475710 G>A maps to NM_005626.4 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr1:29475713 C>T maps to NM_005626.4 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:29475257 C>T maps to NM_005626.4 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr20:42088723 C>T maps to NM_006275.5 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:42089364 C>T maps to NM_006275.5 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:42088848 C>T maps to NM_006275.5 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr20:42088723 C>T maps to NM_006275.5 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:132241091 G>A maps to NM_004592.2 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:132240011 C>T maps to NM_004592.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:132204074 C>T maps to NM_004592.2 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:132209987 G>A maps to NM_004592.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:132212935 G>A maps to NM_004592.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr12:132250831 G>A maps to NM_004592.2 E707E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr12:120907270 G>T maps to NM_003769.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:166741781 A>G maps to NM_145169.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:166743721 G>T maps to NM_145169.1 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr2:85893829 G>A maps to NM_198843.2 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr2:85892779 G>A maps to NM_198843.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:85892793 G>A maps to NM_198843.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:85895287 G>A maps to NM_198843.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:85892794 C>A maps to NM_198843.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr8:22020245 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:81697859 G>A maps to NM_003019.4 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr10:81701821 T>C maps to NM_003019.4 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:174938471 C>T maps to NM_022754.5 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:174938519 A>G maps to NM_022754.5 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:174937117 G>A maps to NM_022754.5 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:104491916 G>A maps to NM_178858.4 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:120923645 T>C maps to NM_213649.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr10:120920466 G>T maps to NM_213649.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:52894958 A>C maps to NM_000232.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:52895018 G>A maps to NM_000232.4 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr5:156186370 T>C maps to NM_000337.5 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr7:94228193 C>T maps to NM_001099401.1 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr7:94257614 G>A maps to NM_001099401.1 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:94248260 C>A maps to NM_001099401.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:94285385 G>A maps to NM_001099401.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:23894856 G>A maps to NM_000231.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr8:14095113 T>C maps to NM_139167.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:14181628 C>A maps to NM_139167.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr8:14181673 G>A maps to NM_139167.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:13947954 G>A maps to NM_139167.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:14412330 G>A maps to NM_139167.2 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:14022200 A>G maps to NM_139167.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:14412369 T>C maps to NM_139167.2 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr8:13965706 C>T maps to NM_139167.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:14095113 T>C maps to NM_139167.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:14181673 G>A maps to NM_139167.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr8:13948086 A>G maps to NM_139167.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr8:14095115 C>A maps to NM_139167.2 G137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr8:14412279 G>T maps to NM_139167.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr3:153840851 G>C maps to NM_015595.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:153839846 G>A maps to NM_015595.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:67207078 A>G maps to ENST00000237247 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:67195072 C>T maps to ENST00000237247 H654H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:67101673 G>A maps to NM_032291.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:67147792 C>A maps to ENST00000237247 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:67147567 C>T maps to ENST00000237247 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:67147651 T>G maps to ENST00000237247 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:67155970 C>A maps to ENST00000237247 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr1:67147567 C>T maps to ENST00000237247 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:67147567 C>T maps to ENST00000237247 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:134492160 G>A maps to NM_001143676.1 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:134492053 C>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:42958909 C>A maps to NM_032237.3 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:42958744 G>A maps to NM_032237.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:8175831 G>T maps to NM_001080826.1 I1351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:8176274 G>A maps to NM_001080826.1 Q1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr8:8233877 G>A maps to NM_001080826.1 Q681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:8233776 C>T maps to NM_001080826.1 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr8:8176050 G>A maps to NM_001080826.1 Y1278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr8:8176046 G>A maps to NM_001080826.1 Q1280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:8234931 G>A maps to NM_001080826.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:77473110 A>G maps to NM_024776.2 N386N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:77472801 G>A maps to NM_024776.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:77407193 G>A maps to NM_024776.2 C1515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:77471550 T>C maps to NM_024776.2 E906E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:77425853 G>A maps to NM_024776.2 I1190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr15:77425853 G>T maps to NM_024776.2 I1190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr8:67743527 A>G maps to NM_013257.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr8:67726104 C>T maps to NM_013257.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr8:67743525 G>T maps to NM_013257.3 G169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr8:67726109 A>G maps to NM_013257.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr8:67743527 A>G maps to NM_013257.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr17:26938786 T>A maps to NM_001174103.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:26939072 G>A maps to NM_001174103.1 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr17:26938786 T>C maps to NM_001174103.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr17:26940297 T>C maps to NM_001174103.1 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:26940520 C>T maps to NM_001174103.1 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr10:52103640 G>A maps to ENST00000361543 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:52103592 G>A maps to ENST00000361543 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr10:52103559 G>A maps to ENST00000361543 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:52066984 G>A maps to ENST00000361543 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:52071130 G>T maps to ENST00000361543 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:108816789 C>T maps to NM_152621.5 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:20202664 G>A maps to NM_001012410.3 R540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:20216353 G>A maps to NM_001012410.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr2:201437639 A>G maps to NM_152524.5 Q857Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:201436035 C>T maps to NM_152524.5 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr2:201437637 C>T maps to NM_152524.5 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:201407315 C>A maps to NM_152524.5 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr2:201437637 C>T maps to NM_152524.5 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:201437192 T>C maps to NM_152524.5 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:201437639 A>G maps to NM_152524.5 Q857Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:72633280 C>T maps to NM_003901.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:72630851 T>G maps to NM_003901.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:64152828 G>T maps to NM_030791.2 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:64152941 G>A maps to NM_030791.2 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr17:78184394 C>T maps to NM_000199.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr22:25282571 C>T maps to NM_001039948.2 Y604Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:25282667 C>T maps to NM_001039948.2 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr22:25308688 G>A maps to NM_001039948.2 T1021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:25301095 C>T maps to NM_001039948.2 I975I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:25243760 C>T maps to NM_001039948.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr22:25251357 C>T maps to NM_001039948.2 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr22:25251321 C>T maps to NM_001039948.2 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:2267462 C>T maps to NM_014853.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:2276698 G>A maps to NM_014853.2 Q664Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:2275733 C>G maps to NM_014853.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:2267889 C>T maps to NM_014853.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:2268519 C>T maps to NM_014853.2 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:2280047 C>T maps to NM_014853.2 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr22:40800324 C>T maps to NM_015705.4 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:40801717 C>T maps to NM_015705.4 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:2763718 G>A maps to NM_003021.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:2763718 G>A maps to NM_003021.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:64966132 C>T maps to NM_019072.2 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr5:65016556 C>A maps to NM_019072.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:28884921 C>T maps to NM_001145795.1 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr16:28880331 A>G maps to NM_001145795.1 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:101957771 G>C maps to ENST00000306803 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr23:123480540 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:123480510 T>C did not map to a codon.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr23:123480593 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:123480571 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:156779200 G>A maps to NM_001161441.1 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:156778992 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:156779562 C>A maps to NM_001161441.1 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:156784857 A>G maps to NM_001161441.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:6755237 G>A maps to NM_005490.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:6755141 A>G maps to NM_005490.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:6752645 G>A maps to NM_005490.2 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:130506880 G>T maps to NM_170600.2 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:19177184 G>T maps to NM_022071.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:19218775 G>T maps to NM_022071.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr8:19221584 C>T maps to NM_022071.3 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:19221751 T>C maps to NM_022071.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:85662116 C>A maps to NM_198482.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:85662107 G>A maps to NM_198482.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr15:78390826 C>T maps to NM_001101404.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr15:78393476 C>A maps to NM_001101404.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:80532663 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:80532492 A>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:80532533 G>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:80532533 G>A did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:80532534 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:80383404 A>G maps to NM_031469.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr22:38042922 G>A maps to NM_018957.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:38046678 G>A maps to NM_018957.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:235950042 G>A maps to NM_014521.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:235951090 C>T maps to NM_014521.2 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:235951131 C>A maps to NM_014521.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:235950999 C>T maps to NM_014521.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:235950544 C>T maps to NM_014521.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr2:235943744 G>A maps to NM_014521.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:235950999 C>T maps to NM_014521.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:235950042 G>A maps to NM_014521.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr3:15298362 G>A maps to NM_004844.3 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:249106371 G>A maps to NM_030645.1 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr4:152054381 T>C maps to NM_001009555.3 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:152054263 G>A maps to NM_001009555.3 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:152058913 G>A maps to NM_001009555.3 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:4365617 C>T maps to NM_003025.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:4363770 G>A maps to NM_003025.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:4365527 G>A maps to NM_003025.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:17761457 T>A maps to NM_003026.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:17795638 C>A maps to NM_003026.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:84245388 C>T maps to ENST00000434347 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:84116330 G>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:87185203 G>T maps to ENST00000482504 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:87185235 T>C maps to ENST00000482504 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:87185262 T>G maps to ENST00000482504 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr9:131770989 A>G maps to ENST00000372554 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:19587273 C>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:19702078 G>A did not map to a codon.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr23:19713826 G>A did not map to a codon.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr23:19713744 G>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:19606878 A>G did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:19606772 A>G did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:19817769 G>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:19564093 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:19554563 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:19764486 T>G did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:19568109 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:19764495 C>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr10:105420858 G>T maps to ENST00000369774 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:105361584 C>T maps to ENST00000369774 E1130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:171766095 C>T maps to NM_001017995.2 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:171766904 A>G maps to NM_001017995.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:171765984 G>A maps to NM_001017995.2 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3517-01A-01W-0831-10 chr4:170017729 G>T maps to NM_020870.3 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr4:170057675 G>A maps to NM_020870.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:170057630 C>T maps to NM_020870.3 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr4:170037691 G>A maps to NM_020870.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr5:145442060 G>T maps to NM_152550.3 G663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:145428790 C>T maps to NM_152550.3 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr5:145442110 G>A maps to NM_152550.3 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:109964329 G>A maps to NM_001099289.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:110048995 C>T maps to NM_001099289.1 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:110259085 C>T maps to NM_001099289.1 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:110065800 C>T maps to NM_001099289.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:110036026 G>A maps to NM_001099289.1 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:109746232 C>T maps to NM_001099289.1 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:8224590 T>C maps to NM_018986.3 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr4:8242591 C>T maps to NM_018986.3 F1307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr4:8220030 C>T maps to NM_018986.3 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:8229004 C>T maps to NM_018986.3 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:8228986 G>A maps to NM_018986.3 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:8206929 C>T maps to NM_018986.3 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:8216305 C>T maps to NM_018986.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:8224590 T>C maps to NM_018986.3 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr4:8235095 C>G maps to NM_018986.3 Y1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:148384345 C>T maps to NM_024577.3 L1265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:148388465 A>G maps to NM_024577.3 Y1142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:148420240 C>A did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr2:234161 T>C maps to NM_015677.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:249812 T>C maps to NM_015677.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:218857 G>A maps to NM_015677.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr2:231082 A>G maps to NM_015677.2 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:231082 A>G maps to NM_015677.2 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:51169456 C>T maps to ENST00000391814 Q1928Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:51165668 A>G maps to ENST00000391814 P2021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:51217445 A>G maps to ENST00000391814 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:51169567 G>A maps to ENST00000391814 G1891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:51214672 G>A maps to ENST00000391814 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:51165404 G>A maps to ENST00000391814 F2109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr19:51165521 G>A maps to ENST00000391814 S2070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr19:51170068 G>A maps to ENST00000391814 A1724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:51165434 G>A maps to ENST00000391814 G2099G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:51171781 G>A maps to ENST00000391814 A1153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:51165653 C>T maps to ENST00000391814 S2026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr19:51171694 G>T maps to ENST00000391814 G1182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:70653143 G>A maps to ENST00000338508 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr11:70332926 G>A maps to ENST00000338508 F1151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:70331579 G>A maps to ENST00000338508 G1600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:70805603 C>T maps to ENST00000338508 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:70332917 G>A maps to ENST00000338508 G1154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:70348311 G>A maps to ENST00000338508 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr11:70332191 A>G maps to ENST00000338508 D1396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:70319318 G>A maps to ENST00000338508 P1729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:70332608 C>T maps to ENST00000338508 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:70331471 C>T maps to ENST00000338508 P1636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:70333646 G>A maps to ENST00000338508 Y911Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr22:51133221 C>A maps to NM_001080420.1 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:51133275 G>A maps to NM_001080420.1 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr9:37956052 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:7533564 C>T maps to NM_001040.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:7533516 C>T maps to NM_001040.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:7533519 G>A maps to NM_001040.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:91653177 G>A maps to NM_016848.5 N462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr9:91652925 G>C maps to NM_016848.5 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:91657028 G>A maps to NM_016848.5 Y424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:91657076 C>T maps to NM_016848.5 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr15:49135722 G>A maps to NM_203349.3 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr15:49254792 G>A maps to NM_203349.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:49118290 G>A maps to NM_203349.3 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:49143442 A>G maps to NM_203349.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:49254726 C>T maps to NM_203349.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr15:49118233 G>A maps to NM_203349.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr15:49135645 T>C maps to NM_203349.3 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr15:49135645 T>C maps to NM_203349.3 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:46638234 C>T maps to NM_024745.4 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr16:46615796 G>T maps to NM_024745.4 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr16:46649859 G>T maps to NM_024745.4 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr19:4284814 C>T maps to NM_020209.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr1:154471693 A>G maps to NM_001010846.2 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:154474132 G>T maps to NM_001010846.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:154458461 G>A maps to NM_001010846.2 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr1:154471693 A>G maps to NM_001010846.2 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:154471627 G>A maps to NM_001010846.2 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr7:155604645 G>A maps to NM_000193.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:26620785 C>T maps to NM_001007538.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:26621037 G>T maps to NM_001007538.1 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr4:42403144 C>T maps to NM_001080505.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr4:42400249 C>A maps to NM_001080505.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr19:41089371 C>T maps to NM_138392.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:41086792 C>T maps to NM_138392.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:41083522 G>T maps to NM_138392.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:41096182 C>T maps to NM_138392.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:41096634 G>C did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:18232646 C>T maps to NM_004169.3 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:18250896 C>T maps to NM_004169.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:18257052 G>A maps to NM_004169.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:18250890 C>A maps to NM_004169.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr12:57626342 C>T maps to NM_005412.5 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:57626545 G>T maps to NM_005412.5 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:112724476 G>T maps to NM_007373.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:112760261 G>T maps to NM_007373.3 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:112724137 G>T maps to NM_007373.3 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:3514000 A>G maps to NM_013276.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:3514081 G>T maps to NM_013276.2 C403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:146264842 A>G maps to ENST00000367503 D558D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:146245969 G>A maps to ENST00000367503 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:146244872 C>A maps to ENST00000367503 E1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:146276106 C>A maps to ENST00000367503 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:146276212 T>C maps to ENST00000367503 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:146262866 G>A maps to ENST00000367503 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:72866455 A>G maps to NM_018130.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:72866505 G>A maps to NM_018130.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:72890311 C>A maps to NM_018130.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:72866455 A>G maps to NM_018130.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:72866455 A>G maps to NM_018130.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr3:72866455 A>G maps to NM_018130.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr3:72881524 A>G maps to NM_018130.2 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:72897485 C>G maps to NM_018130.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:9862710 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:9859070 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:9859070 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:9863198 G>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:9905319 A>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:9900448 T>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:9907299 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:9914829 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:9912767 G>A did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:9900520 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:9859050 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr23:9841819 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:9863763 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:9862655 C>A did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:9905320 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:9914859 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr23:9864520 C>T did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:9900271 T>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:9863020 G>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:9864506 C>T did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:9914972 A>C did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr23:9841753 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:9841798 C>T did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:9905319 A>G did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:9866295 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:9863107 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:77691897 C>T maps to NM_020859.3 S1823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:77661719 G>A maps to NM_020859.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:77631356 C>T maps to NM_020859.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr4:77662118 A>G maps to NM_020859.3 A931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:50350751 T>C did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:50377134 A>G did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:50377302 G>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:50378663 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:50376646 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:50350499 A>C did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:50339760 G>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:50377270 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:50377323 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:50350943 C>T did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr23:50378291 C>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:50350873 C>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:50378348 G>A did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:50376377 C>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:50376605 G>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:50378663 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr23:50378274 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:50350848 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:50345665 C>A did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:50377029 T>C did not map to a codon.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr3:164697178 C>A maps to NM_001041.3 E1819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr3:164712046 A>G maps to NM_001041.3 H1613H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:164758755 C>A maps to NM_001041.3 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:164737503 C>T maps to NM_001041.3 S1103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:164792333 T>C maps to NM_001041.3 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr3:164741455 G>A maps to NM_001041.3 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:164697166 C>A maps to NM_001041.3 E1823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:164767588 C>T maps to NM_001041.3 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:164714402 C>A maps to NM_001041.3 E1538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr3:164785144 T>C maps to NM_001041.3 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr3:164741405 A>G maps to NM_001041.3 T1017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr3:164741405 A>G maps to NM_001041.3 T1017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr16:48395625 C>T maps to NM_001006610.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:150460158 G>A maps to NM_005067.5 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:150460377 G>A maps to NM_005067.5 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr13:46357655 G>A maps to NM_198849.2 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:113327007 T>C maps to ENST00000393830 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:113329853 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:113342522 C>T maps to ENST00000393830 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:113320477 A>G maps to ENST00000393830 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr3:113342522 C>T maps to ENST00000393830 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr3:113300224 C>T maps to ENST00000393830 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:113342546 A>G maps to ENST00000393830 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:117064642 G>A maps to NM_001040455.1 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:117053476 C>T maps to NM_001040455.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:117056930 G>A maps to NM_001040455.1 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:117063580 C>T maps to NM_001040455.1 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:3677825 C>A maps to NM_023068.3 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr20:3670714 C>G maps to NM_023068.3 L1596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr19:51916977 C>T maps to NM_033130.4 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:51917070 C>T maps to NM_033130.4 K572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr19:51920142 C>T maps to NM_033130.4 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:51920686 G>A maps to NM_033130.4 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:51918486 G>A maps to NM_033130.4 H426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr19:51919320 T>C maps to NM_033130.4 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:50455577 G>A maps to NM_052884.2 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr19:50461972 G>A maps to NM_052884.2 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:50464028 T>C maps to NM_052884.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:52004720 A>G maps to NM_053003.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:52002860 C>T maps to NM_053003.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:52003465 A>G maps to ENST00000441969 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr19:52002734 C>T maps to NM_053003.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:52003582 C>T maps to NM_033329.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr19:52004720 A>G maps to NM_053003.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:52149191 C>A maps to NM_001098612.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr19:52149212 T>G maps to NM_001098612.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr19:52132297 G>A maps to ENST00000222107 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:52034450 G>A maps to NM_001245.5 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:52033188 G>A maps to NM_001245.5 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:52033995 A>G maps to NM_001245.5 C215C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr19:51647930 C>G maps to NM_014385.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:51647912 G>A maps to NM_014385.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr19:51645955 C>T maps to NM_014385.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr19:51645712 G>A maps to NM_014385.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr19:51961254 T>C maps to NM_014442.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr19:51957556 G>A maps to NM_014442.2 C387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr19:51961359 G>T maps to NM_014442.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr19:51957993 G>A maps to NM_014442.2 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:51955707 G>A maps to NM_014442.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr19:51957960 C>T maps to NM_014442.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr19:51955689 T>C maps to NM_014442.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr19:51955689 T>C maps to NM_014442.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:51628944 G>A maps to NM_014441.2 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr19:51633149 G>A maps to NM_014441.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:51629347 G>A maps to NM_014441.2 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:51630553 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr21:44838140 T>C maps to NM_173354.3 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr21:44841644 G>A maps to NM_173354.3 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr21:44840296 G>A maps to NM_173354.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr21:44841638 C>T maps to NM_173354.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr21:44845357 A>G maps to NM_173354.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:44841547 G>A maps to NM_173354.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr11:111571670 C>T maps to NM_015191.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:111473304 C>G maps to NM_015191.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:111594232 C>T maps to NM_015191.1 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:111594549 A>G maps to NM_015191.1 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:111592579 C>T maps to NM_015191.1 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:116728793 G>A maps to ENST00000445177 H1122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr11:116734488 A>G maps to ENST00000445177 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:116730132 G>A maps to ENST00000445177 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:116744653 G>A maps to ENST00000445177 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:116747013 G>T maps to ENST00000445177 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr11:116767011 G>A maps to ENST00000445177 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:116734488 A>G maps to ENST00000445177 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr11:116734488 A>G maps to ENST00000445177 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:116734488 A>G maps to ENST00000445177 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr11:116734488 A>G maps to ENST00000445177 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:116734506 C>A maps to ENST00000445177 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:116767059 G>A maps to ENST00000445177 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:138362600 A>G maps to ENST00000509534 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr12:56351303 G>A maps to NM_006928.3 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:56351426 G>A maps to NM_006928.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr6:100896061 G>A maps to ENST00000262901 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr6:100838914 C>T maps to ENST00000262901 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:100838455 G>T maps to ENST00000262901 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:100841486 C>T maps to ENST00000262901 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:100841711 G>A maps to ENST00000262901 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:100896494 G>A maps to ENST00000262901 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:100838860 A>G maps to ENST00000262901 H559H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr6:100897247 G>A maps to ENST00000262901 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:100841570 C>T maps to ENST00000262901 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:100841570 C>T maps to ENST00000262901 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:100838800 C>T maps to ENST00000262901 E579E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr6:100895244 C>T maps to ENST00000262901 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr6:100897473 G>A maps to ENST00000262901 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr6:100895289 C>T maps to ENST00000262901 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr6:100838722 A>G maps to ENST00000262901 C605C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr6:100841521 G>A maps to ENST00000262901 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr21:38117102 C>T maps to NM_005069.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr21:38081492 G>A maps to NM_005069.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr21:38115762 C>T maps to NM_005069.3 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr15:75668178 G>A maps to NM_001145357.1 R1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr15:75684802 T>C maps to NM_001145357.1 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:75699431 T>C maps to NM_001145357.1 K457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:75688615 A>G maps to NM_001145357.1 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:75668017 G>A maps to NM_001145357.1 L1193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:75703907 A>C maps to NM_001145357.1 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:75673042 G>A maps to NM_001145357.1 R1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr15:75702577 A>T maps to NM_001145357.1 L353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr15:75705231 G>A maps to NM_001145357.1 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr19:16986966 C>T maps to NM_015260.1 C930C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:16957794 C>T maps to NM_015260.1 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:16974594 C>T maps to NM_015260.1 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:16976444 C>T maps to NM_015260.1 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:16976225 C>T maps to NM_015260.1 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:16962257 G>A maps to NM_015260.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:65417250 C>T maps to NM_153253.29 G887G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:65410028 G>A maps to NM_153253.29 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr14:72128130 C>T maps to NM_015556.1 H734H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:72196974 G>A maps to NM_015556.1 P1627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr14:72055497 A>G maps to NM_015556.1 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr14:72055092 C>T maps to NM_015556.1 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr14:72190525 C>T maps to NM_015556.1 G1478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:72085486 T>C maps to NM_015556.1 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:72176111 C>T maps to NM_015556.1 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:72196968 G>A maps to NM_015556.1 S1625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:72117189 G>T maps to NM_015556.1 G653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:72152246 G>A maps to NM_015556.1 S1091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr14:72117174 C>T maps to NM_015556.1 R648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr14:72205811 C>T maps to NM_015556.1 S1783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:232581486 G>A maps to NM_020808.3 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:232596814 G>A maps to NM_020808.3 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:232551371 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:232601013 G>A maps to NM_020808.3 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:232650179 G>A maps to NM_020808.3 H302H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:232649837 A>G maps to NM_020808.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:232581366 G>A maps to NM_020808.3 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:232568024 C>T maps to NM_020808.3 P1408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:232649972 C>T maps to NM_020808.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:232600831 G>A maps to NM_020808.3 H858H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr1:232626619 C>A maps to NM_020808.3 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:232581314 G>A maps to NM_020808.3 R1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:38689131 C>T maps to NM_015073.1 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:38573512 C>T maps to NM_015073.1 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:38631841 C>T maps to NM_015073.1 Y1054Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr19:38573506 C>T maps to NM_015073.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:38610083 C>T maps to NM_015073.1 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:38573614 C>T maps to NM_015073.1 N470N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:1903079 C>T maps to ENST00000400068 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr20:1902266 C>T maps to ENST00000400068 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:1546836 G>A maps to NM_006065.3 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr20:1559125 C>T maps to NM_006065.3 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:1532436 G>T maps to ENST00000381621 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr20:1532451 G>T maps to ENST00000381621 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr20:1532451 G>T maps to ENST00000381621 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:1629803 G>A maps to NM_018556.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr19:39369890 C>T maps to NM_012237.3 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:218903 G>A maps to NM_012239.5 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:120741405 C>T maps to NM_012240.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:120750307 G>T maps to NM_012240.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:13597206 T>C maps to NM_012241.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:13599302 C>T maps to NM_012241.3 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr19:4175888 G>A maps to NM_016539.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr14:105225783 A>T maps to NM_006427.3 K164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr14:61115478 G>A maps to NM_005982.3 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:61115784 G>A maps to NM_005982.3 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr2:45233431 G>T maps to NM_016932.4 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:45235703 G>A maps to NM_016932.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr14:61180294 A>G maps to NM_017420.4 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:61180202 A>G maps to NM_017420.4 C756C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:61180412 C>T maps to NM_017420.4 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:61187156 T>C maps to NM_017420.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr14:61187156 T>C maps to NM_017420.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:61180400 A>G maps to NM_017420.4 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:60976653 C>T maps to ENST00000381716 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr14:60976475 G>A maps to ENST00000381716 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr14:60976610 C>T maps to ENST00000381716 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr13:21742533 G>A maps to NM_145061.5 H112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr13:21734097 T>C maps to NM_145061.5 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:46262209 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:46247979 G>A maps to NM_003726.3 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr17:46423315 G>A maps to NM_003726.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:46507443 G>A maps to NM_003726.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr7:26709784 T>C maps to NM_003930.3 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:2235320 C>T maps to NM_003036.3 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:2237598 C>T maps to NM_003036.3 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:170078895 C>T maps to NM_005414.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:170078895 C>T maps to NM_005414.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:170078895 C>T maps to NM_005414.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:31927863 G>A maps to NM_006929.4 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:31936527 G>A maps to NM_006929.4 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:31935072 C>T maps to NM_006929.4 N834N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:54662554 C>A maps to NM_015360.4 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:54603957 G>C maps to NM_015360.4 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:54618223 C>T maps to NM_015360.4 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:36168444 G>A maps to NM_005983.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr5:36166632 T>C maps to NM_005983.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr5:36166632 T>C maps to NM_005983.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr5:36166632 T>C maps to NM_005983.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr20:35262927 C>T maps to NM_032214.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:78335206 T>C maps to ENST00000389459 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:78334972 G>A maps to ENST00000389459 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:78318514 T>C maps to ENST00000389459 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:48424084 C>T maps to NM_020846.1 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr4:48380054 G>A maps to NM_020846.1 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr4:48371910 G>A maps to NM_020846.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:160607005 G>A maps to NM_003037.2 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:160616702 G>A maps to NM_003037.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:160616666 G>A maps to NM_003037.2 Y23Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:160719755 C>T maps to NM_021181.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr1:160720186 G>A maps to NM_021181.3 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:159799764 G>A maps to NM_020125.2 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:159796693 C>A maps to NM_020125.2 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:159922244 A>G maps to NM_033438.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:1696524 G>T maps to ENST00000318386 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:70263788 G>A maps to NM_003049.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr13:103701654 G>A maps to NM_000452.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr13:103701786 C>T maps to NM_000452.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr13:103718236 G>A maps to NM_000452.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr13:103703764 G>A maps to NM_000452.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:103698578 T>C maps to NM_000452.2 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr13:103718242 G>A maps to NM_000452.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:153716751 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:153716441 C>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:153716439 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:153716438 C>T did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:153716183 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:48486153 C>T maps to NM_152679.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:48490769 G>A maps to NM_152679.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:48487011 C>A maps to NM_152679.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:48485643 G>A maps to NM_152679.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr8:82606468 G>A maps to NM_001010893.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:82606304 G>A maps to NM_001010893.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:87744876 A>C maps to NM_197965.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:87744978 C>T maps to NM_197965.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:147214121 G>A maps to ENST00000507030 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:147215240 G>A maps to ENST00000507030 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:219259670 C>T maps to NM_000578.3 H522H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:51389533 G>A maps to NM_001174125.1 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr15:48536974 C>T maps to NM_000338.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr15:48541772 G>A maps to NM_000338.2 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:48519367 G>T maps to NM_001184832.1 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr15:48539535 T>G maps to NM_000338.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr5:127516686 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:127484532 T>C maps to NM_001046.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:127510234 G>T maps to NM_001046.2 E936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr5:127484532 T>C maps to NM_001046.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:127516605 G>A maps to NM_001046.2 T1044T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr5:127471438 C>T maps to NM_001046.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:127520165 T>C maps to NM_001046.2 D1136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:127469880 G>T maps to NM_001046.2 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:127448570 G>T maps to NM_001046.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:56913479 G>A maps to NM_000339.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:56906571 C>T maps to NM_000339.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr16:56920296 G>A maps to NM_000339.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:56904089 C>T maps to NM_000339.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:56914039 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:56936356 C>T maps to NM_000339.2 N940N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr16:67980938 G>A maps to NM_005072.4 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:67984299 G>A maps to NM_005072.4 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:67995475 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:67982037 G>A maps to NM_005072.4 F591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:67978820 G>A maps to NM_005072.4 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:67983704 G>T maps to NM_005072.4 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr16:67995579 C>T maps to NM_005072.4 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:67985076 G>T maps to NM_005072.4 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:67997906 G>A maps to NM_001145963.1 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:44680411 C>T maps to NM_001134771.1 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr20:44680390 C>T maps to NM_001134771.1 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr20:44673619 G>T maps to NM_001134771.1 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:44665417 G>A maps to NM_001134771.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr20:44664101 C>T maps to NM_001134771.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr20:44681716 C>T maps to NM_001134771.1 H856H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:44671864 C>T maps to NM_001134771.1 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr20:44673649 C>A maps to NM_001134771.1 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr15:34529712 G>A maps to NM_133647.1 A947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:34546763 G>T maps to NM_133647.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:34553200 G>A maps to NM_133647.1 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:34551141 C>A maps to NM_133647.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr15:34553219 G>A maps to NM_133647.1 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:34526134 G>A maps to NM_133647.1 R1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:34532915 A>G maps to NM_133647.1 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:1094345 C>A maps to NM_006598.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:1076828 G>A maps to NM_006598.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:1076903 G>A maps to NM_006598.2 N551N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:1057716 T>C maps to NM_006598.2 A965A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr5:1087122 C>A maps to NM_006598.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:1076884 G>A maps to NM_006598.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr5:1064196 C>T did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:1064242 G>A maps to NM_006598.2 D854D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:1075538 C>T maps to NM_006598.2 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:124826370 C>T maps to NM_001195483.1 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:124802766 G>A maps to NM_001195483.1 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:100453394 C>T maps to NM_020246.2 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:100457599 G>A maps to NM_020246.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:122787226 T>C maps to NM_022444.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:122809343 C>T maps to NM_022444.3 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr7:122809381 G>A maps to NM_022444.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:122763253 C>A maps to NM_022444.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr7:122809295 A>G maps to NM_022444.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr17:26821502 T>C maps to NM_001145975.1 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr17:26817533 C>T maps to NM_001145975.1 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:26818798 C>T maps to NM_001145975.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:26818762 C>T maps to NM_001145975.1 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:26820648 C>T maps to NM_001145975.1 C362C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr20:45212208 A>G did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr20:45221158 C>T maps to NM_022829.5 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:45194936 G>A maps to NM_022829.5 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr20:45221119 G>A maps to NM_022829.5 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr20:45242313 C>T maps to NM_022829.5 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:45188717 C>T maps to NM_022829.5 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:45221071 G>T maps to NM_022829.5 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:45221119 G>A maps to NM_022829.5 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:135378889 G>A maps to NM_012450.2 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:135370314 G>A maps to NM_012450.2 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:6616579 G>A maps to NM_177550.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:6607353 G>A maps to NM_177550.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr17:6606290 G>A maps to NM_177550.3 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:43328368 C>T maps to NM_001146037.1 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr18:43314250 A>G maps to NM_001146037.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr18:43243840 C>T maps to NM_007163.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:43219736 C>T maps to NM_007163.3 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:43212386 G>A maps to NM_007163.3 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:43247876 C>T maps to NM_007163.3 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:43207079 G>A maps to NM_007163.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:43252866 T>C maps to NM_007163.3 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:43219781 C>T maps to NM_007163.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr13:99379095 C>T did not map to a codon.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr13:99338445 G>A maps to NM_005073.3 Q645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:99337037 G>A maps to NM_005073.3 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:99378649 G>A maps to NM_005073.3 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr13:99337076 C>T maps to NM_005073.3 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr13:99361878 C>T maps to NM_005073.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:99361022 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr13:99338503 G>A maps to NM_005073.3 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr13:99364164 C>T maps to NM_005073.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:121643231 T>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:121642114 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:121634096 C>T maps to NM_021082.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr3:121643199 G>T maps to NM_021082.3 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:60704780 C>T maps to NM_016582.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr11:60711235 G>A maps to NM_016582.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:60714169 G>A maps to NM_016582.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:60706958 G>A maps to NM_016582.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr12:129299465 G>A maps to ENST00000376744 C232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:129283831 G>A maps to ENST00000376744 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:113471897 G>A maps to NM_003051.3 Y11Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:113464678 A>G maps to NM_003051.3 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:113456731 G>A maps to NM_003051.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr6:111498831 T>G maps to NM_018593.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:111498639 C>T maps to NM_018593.4 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:6945894 C>T maps to NM_153357.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:6945987 G>A maps to NM_153357.1 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:6945117 G>T maps to NM_153357.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr10:91195895 C>A maps to NM_213606.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:6942110 G>T maps to NM_201566.2 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr2:230911220 C>T maps to NM_152527.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr2:230911184 G>A maps to NM_152527.4 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:230911154 C>A maps to NM_152527.4 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr2:230911100 T>C maps to NM_152527.4 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:230911100 T>C maps to NM_152527.4 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:73751227 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:73744269 G>A did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr23:73751290 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr23:73751290 A>G did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:73641568 T>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:73740927 T>C did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr17:80196749 T>C maps to NM_001042423.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:110924343 A>G maps to NM_004696.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:110923601 A>G did not map to a codon.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr1:110921583 A>G maps to NM_004696.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:110921583 A>G maps to NM_004696.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:110921583 A>G maps to NM_004696.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr1:110921583 A>G maps to NM_004696.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:73096361 G>T maps to ENST00000450736 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:73096774 C>T maps to ENST00000450736 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:73096361 G>T maps to ENST00000450736 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr17:73100203 G>T maps to ENST00000450736 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:73102013 T>C maps to ENST00000450736 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:66267064 G>A maps to NM_004694.4 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:66267511 G>A maps to NM_004694.4 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr17:66270134 G>A maps to NM_004694.4 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:66267064 G>A maps to NM_004694.4 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:60168502 C>T maps to NM_004731.3 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr12:60165048 G>C maps to NM_004731.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:60173361 G>T maps to NM_004731.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:60173361 G>T maps to NM_004731.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:60169248 T>C maps to NM_004731.3 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:60173226 G>T maps to NM_004731.3 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr12:60168465 C>T maps to NM_004731.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:60169119 C>T maps to NM_004731.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:38478817 C>T maps to NM_013356.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr22:38474622 G>A maps to NM_013356.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr10:61413886 A>G maps to NM_194298.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr10:61413886 A>G maps to NM_194298.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:61413886 A>G maps to NM_194298.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr10:61413886 A>T maps to NM_194298.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:25813136 C>T maps to NM_005074.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:25813136 C>T maps to NM_005074.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr6:25811899 G>A maps to NM_005074.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:25913552 G>A maps to NM_005835.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr6:25916963 T>C maps to NM_005835.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:25769309 T>A maps to NM_005495.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr6:74304856 G>A maps to NM_012434.4 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:74320121 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:22397549 G>T maps to NM_020346.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr11:22384369 C>T maps to NM_020346.2 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:22384369 C>T maps to NM_020346.2 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:22397591 C>A maps to NM_020346.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:22363205 C>T maps to NM_020346.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:22363118 G>A maps to NM_020346.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:22360166 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:22360112 G>T maps to NM_020346.2 G12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:22399153 T>C maps to NM_020346.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr11:22387180 T>C maps to NM_020346.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:49934000 G>A maps to NM_020309.3 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:49936085 G>A maps to NM_020309.3 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:49934661 C>T maps to NM_020309.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr19:49933892 G>A maps to NM_020309.3 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr12:100787224 C>T maps to NM_139319.2 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:100751192 C>A maps to NM_139319.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:100790170 C>A maps to NM_139319.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:61595635 C>T maps to NM_022082.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr20:61598070 C>T maps to NM_022082.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:61594026 G>A maps to NM_022082.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:20005195 G>A maps to NM_001135691.2 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr8:20031926 T>A maps to NM_001135691.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr8:20036639 G>C maps to NM_001135691.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:20031893 T>A maps to NM_001135691.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:20007201 A>G maps to NM_001135691.2 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:119003704 C>T maps to NM_003054.4 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:119029636 C>T maps to NM_003054.4 H414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:119001290 G>A maps to NM_003054.4 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr10:119001215 C>T maps to NM_003054.4 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr10:119012957 C>T maps to NM_003054.4 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr10:50818989 C>T maps to NM_003055.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:50819670 C>T maps to NM_003055.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:50819925 C>T maps to NM_003055.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:50819322 C>T maps to NM_003055.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:50819241 C>T maps to NM_003055.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:50818899 C>T maps to NM_003055.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr10:50819358 C>T maps to NM_003055.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:50819241 C>T maps to NM_003055.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr1:169446644 C>T maps to NM_006996.2 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr1:169446650 T>A maps to NM_006996.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:169437362 C>A maps to NM_006996.2 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:169439226 G>A maps to NM_006996.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:228563685 G>A maps to NM_025243.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:228552262 T>A maps to NM_025243.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:228564157 G>T maps to NM_025243.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:228564082 G>A maps to NM_025243.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr2:228563704 C>T maps to NM_025243.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:4583073 C>T maps to NM_004170.5 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:4544618 G>A maps to NM_004170.5 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:4566089 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:4576640 C>T maps to NM_004170.5 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:4544612 T>C maps to NM_004170.5 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:4564341 A>G did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:35302436 C>A maps to NM_004171.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:35338924 A>G maps to NM_004171.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:36686236 C>T maps to NM_004172.4 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr5:36680670 C>T maps to NM_004172.4 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:65243615 C>T maps to NM_003038.4 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:65245676 A>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:15067394 G>A maps to NM_005071.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:15067487 A>G maps to NM_005071.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:15072847 C>A maps to NM_005071.1 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:53569180 A>G maps to NM_006671.4 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:53558242 C>T maps to NM_006671.4 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:53580524 G>T maps to NM_006671.4 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:53556440 C>A maps to NM_006671.4 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:53555485 G>A maps to NM_006671.4 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:53556363 C>T maps to NM_006671.4 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:113416889 C>T maps to NM_005415.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:113416958 C>T maps to NM_005415.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:113410370 A>G maps to NM_005415.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:113417306 T>C maps to NM_005415.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr8:42295090 T>C maps to NM_006749.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:42286314 G>A maps to NM_006749.3 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:42294775 G>A maps to NM_006749.3 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:160577037 G>A maps to NM_003057.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:160555145 G>A maps to NM_003057.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:63064805 T>C maps to NM_001039752.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:63072298 C>T maps to NM_001039752.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr11:63067101 G>T did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr11:63057878 C>A maps to NM_001039752.3 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr11:63057879 A>G maps to NM_001039752.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:64336163 C>A maps to NM_018484.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:64336208 C>A maps to NM_018484.2 C447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:64337234 C>T maps to NM_018484.2 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:64329514 G>A maps to NM_018484.2 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:64337297 G>A maps to NM_018484.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:64360333 G>A maps to NM_144585.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:64367273 G>C maps to NM_144585.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:64360258 C>T maps to NM_144585.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:64361005 C>T maps to NM_144585.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr3:38307446 T>C maps to NM_004256.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:38316484 G>T maps to NM_004256.3 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr3:38307446 T>C maps to NM_004256.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:38347681 C>T maps to NM_004803.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:38350514 G>A maps to NM_004803.3 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:38354564 C>T maps to NM_004803.3 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:38355271 C>T maps to NM_004803.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr3:38357898 C>T maps to NM_004803.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:116569565 A>G maps to NM_018420.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:116605410 C>T maps to NM_018420.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr1:116562222 A>G maps to NM_018420.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:116534698 G>A maps to NM_018420.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:110746108 C>T maps to NM_033125.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:110763561 C>T maps to NM_033125.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:110746251 A>G maps to NM_033125.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:23821264 G>T maps to NM_020372.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr14:23821249 C>T maps to NM_020372.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:23817423 G>A maps to NM_020372.2 R262*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G4-6588-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:160664607 A>G maps to NM_003058.3 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr11:64990014 A>G maps to ENST00000438990 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr11:64990014 A>G maps to ENST00000438990 E237E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3558-01A-01W-0831-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr6:3273558 G>A maps to ENST00000436008 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr6:3287144 G>A maps to ENST00000436008 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:3287186 G>A maps to ENST00000436008 C484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr11:62902165 T>C maps to NM_001136506.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:62863493 G>A maps to NM_001136506.1 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:62985140 G>A maps to NM_199352.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:62931430 G>T maps to NM_199352.3 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:62984849 G>A maps to NM_199352.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr11:62996893 G>T maps to NM_199352.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:160829921 C>T maps to ENST00000392145 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr6:160858027 G>T did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr6:160858026 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:160864691 G>C maps to ENST00000392145 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr6:160858026 A>C did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:160858026 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:131657892 C>G maps to NM_003059.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:131630647 C>T maps to NM_003059.2 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:131719910 G>A maps to ENST00000435065 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:62747338 G>T maps to NM_004790.3 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:62751069 G>A maps to NM_004790.3 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:62744654 C>T maps to NM_004790.3 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:43270466 C>T maps to ENST00000372585 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:43267760 C>T maps to ENST00000372585 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:43267376 G>T maps to ENST00000372585 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:43271898 G>A maps to ENST00000372585 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:43266165 C>T maps to ENST00000372585 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:62782318 G>A maps to ENST00000430500 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:62782277 C>T maps to ENST00000430500 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:63175653 T>G maps to NM_080866.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:63175656 T>C maps to NM_080866.2 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:138707799 G>A maps to NM_152685.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:138713127 G>A maps to NM_152685.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:138715647 A>G maps to NM_152685.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr20:4842633 G>A maps to NM_203327.1 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr20:4842648 C>T maps to NM_203327.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr20:4880286 G>A maps to NM_203327.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:4913124 C>T maps to NM_203327.1 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr20:4883155 G>A maps to NM_203327.1 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:4843469 C>T maps to NM_203327.1 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:4855281 C>T maps to NM_203327.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr20:4840030 C>T did not map to a codon.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr20:4854681 A>G maps to NM_203327.1 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:220034284 G>T maps to NM_001144890.1 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:65942955 T>C maps to NM_004727.2 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr15:65938034 C>T maps to NM_004727.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr15:65932006 G>A maps to NM_004727.2 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr9:19786270 G>A maps to NM_020344.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:19786468 T>C maps to NM_020344.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr9:19786174 G>T maps to NM_020344.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr9:19516185 C>A maps to NM_020344.2 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:19786012 G>A maps to NM_020344.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr9:19786213 G>T maps to NM_020344.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:19566118 C>T maps to NM_020689.3 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr20:19664856 C>T maps to NM_020689.3 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:19566088 C>A maps to NM_020689.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr20:19496165 C>T maps to NM_020689.3 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:92908506 G>A maps to NM_153646.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr14:92949081 C>T maps to NM_153646.3 C438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr14:92922899 G>A maps to NM_153646.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:92909063 C>T maps to NM_153646.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:92909805 C>T maps to NM_153646.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:92922791 G>A maps to NM_153646.3 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:92959938 C>T maps to NM_153646.3 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr14:92920370 C>T maps to NM_153646.3 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:48414090 G>A maps to NM_205850.2 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr15:48426723 C>T maps to NM_205850.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:113758439 G>A maps to NM_024959.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:113754411 G>A maps to NM_024959.2 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:19163732 G>A maps to NM_005984.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:172669987 C>T maps to NM_003705.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:172641846 C>T maps to NM_003705.3 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:95800819 T>C maps to NM_001160210.1 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:95813663 C>A maps to NM_001160210.1 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:95838170 C>T maps to NM_001160210.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:95818945 T>C maps to NM_001160210.1 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr7:95761172 C>T maps to NM_001160210.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr23:129474318 G>T did not map to a codon.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr23:129483310 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:129498702 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:129479159 A>G did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:129480554 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:129480555 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:129480617 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:129483309 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:129483309 C>T did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr13:41383802 A>G maps to NM_014252.3 *302W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr22:41175103 A>T maps to NM_006358.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr22:41188619 G>A maps to NM_006358.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr22:18070834 G>A maps to NM_031481.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:73279563 G>T maps to NM_021734.4 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr5:140682559 C>T maps to NM_031947.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr5:140682571 G>A maps to NM_031947.2 Y287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:140682570 C>A maps to NM_031947.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr3:48900020 A>G maps to NM_000387.4 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:37153042 T>C maps to NM_030631.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:794873 G>A maps to NM_001191061.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr19:6452331 G>T maps to NM_024103.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:6444237 G>A maps to NM_024103.2 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:6442162 G>A maps to NM_024103.2 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:108681766 A>G maps to NM_013386.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr9:130869348 C>T maps to ENST00000373069 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:130869357 C>T maps to ENST00000373069 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:130869548 G>A maps to ENST00000373069 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:66420957 C>T maps to NM_173471.3 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:66293730 G>T maps to NM_173471.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr10:101370692 G>A maps to NM_031212.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:101373552 G>A maps to NM_031212.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:101373516 G>A maps to NM_031212.3 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:101373552 G>A maps to NM_031212.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr14:100758796 G>A maps to NM_001039355.1 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:98995010 G>T maps to NM_213611.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr12:98995203 G>A maps to NM_213611.2 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:98993792 C>T maps to NM_213611.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr12:98995305 G>A maps to NM_213611.2 *362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:98995218 C>T maps to NM_213611.2 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr12:98989335 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:45973113 T>C maps to NM_001010875.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr13:45983190 A>T maps to NM_001010875.2 L28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:128694629 C>T maps to NM_031291.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:128651861 G>A maps to NM_031291.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:128694701 C>T maps to NM_031291.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:128694629 C>T maps to NM_031291.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:104413838 G>A maps to NM_030780.3 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:8193298 G>A maps to NM_201520.1 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:8198092 G>A maps to NM_201520.1 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:8198104 G>A maps to NM_201520.1 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:140695156 G>A maps to NM_001104647.1 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:23423718 C>A maps to NM_016612.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr8:23423811 C>T maps to NM_016612.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:39431017 C>T maps to NM_017875.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:42397485 T>C did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:186068076 C>T maps to NM_001151.3 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:186066192 C>A maps to NM_001151.3 C129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:186068076 C>T maps to NM_001151.3 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr4:186066369 A>G maps to NM_001151.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:87476264 T>C maps to NM_018843.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:87477212 C>A maps to NM_018843.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:6430169 G>T maps to NM_173637.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:6427386 G>A maps to NM_173637.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr19:19218741 A>G maps to NM_178526.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:118540507 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:118586876 G>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:65143937 G>T maps to NM_182556.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:65143978 C>A maps to NM_182556.2 G256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:65147400 C>T maps to NM_182556.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:110096915 C>T maps to NM_138773.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:118604884 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:118604435 T>C did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:118603950 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:118603828 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:118603843 T>G did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:118604372 C>A did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:118603983 G>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:118602568 C>T did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:118604439 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:973229 C>T maps to NM_134425.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:984138 G>A maps to NM_213613.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:58016410 C>T maps to NM_133489.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:58015534 G>A maps to NM_133489.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:78199682 G>A maps to NM_173626.3 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:78199640 G>A maps to NM_173626.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:78219973 G>A maps to NM_173626.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:149361099 T>G maps to NM_000112.3 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:149361243 C>T maps to NM_000112.3 N696N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:107432367 G>A maps to NM_000111.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr7:107416911 C>T maps to NM_000111.2 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:107414364 C>T maps to NM_000111.2 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:107432332 T>A maps to NM_000111.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr7:107414362 A>G did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr7:107334924 G>A maps to NM_000441.1 K447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:107323768 C>T maps to NM_000441.1 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:107340589 C>T maps to NM_000441.1 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:107342393 T>C maps to NM_000441.1 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:107342393 T>A maps to NM_000441.1 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr7:107342393 T>C maps to NM_000441.1 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr7:107350538 C>T maps to NM_000441.1 D710D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr7:107342417 T>C maps to NM_000441.1 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:107342417 T>C maps to NM_000441.1 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:103051902 G>A maps to ENST00000354356 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:103051977 T>G maps to ENST00000354356 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:103050846 G>T maps to ENST00000354356 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr7:103019694 G>A maps to ENST00000354356 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr3:48667387 C>A maps to NM_022911.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:48670482 G>A maps to NM_022911.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3517-01A-01W-0831-10 chr8:92378848 G>A maps to NM_134266.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:92401665 G>A maps to NM_134266.1 E592E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr8:92352762 C>A maps to NM_134266.1 S337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:92307867 C>T maps to NM_134266.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:92350434 G>T maps to NM_134266.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:92301362 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:92406079 G>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr8:92307792 C>T maps to NM_134266.1 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr8:92307792 C>T maps to NM_134266.1 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:35987295 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:35967769 A>G maps to NM_052961.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:35923015 C>T maps to NM_052961.3 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:35927505 A>G maps to NM_052961.3 H572H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr6:35945097 G>A maps to NM_052961.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:35980078 G>A maps to NM_052961.3 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr1:205904882 A>G maps to NM_134325.2 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr1:205897956 G>A maps to NM_134325.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:17597626 C>T maps to NM_198580.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:50474986 G>A maps to NM_003645.3 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:153751867 C>T maps to ENST00000271857 H726H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:131112645 C>T maps to NM_005094.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:59023238 A>G maps to NM_012254.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:128302091 A>C maps to NM_001017372.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:128351646 G>T maps to NM_001017372.1 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr15:85478409 A>G maps to NM_004213.3 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:85486698 G>A maps to NM_004213.3 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:85438638 G>A maps to NM_201651.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:85478724 C>T maps to NM_004213.3 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:85467223 T>G maps to NM_004213.3 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:45559871 A>G maps to NM_004212.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:45556920 T>G maps to NM_004212.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:45559862 G>T did not map to a codon.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr9:86900448 G>T maps to NM_022127.2 C486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:86909107 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr9:86903069 T>C maps to NM_022127.2 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:86893216 G>A maps to NM_022127.2 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:44197522 T>C maps to ENST00000313248 H182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr6:44199748 T>C maps to ENST00000313248 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:44201184 G>T maps to ENST00000313248 G510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:44201258 T>C maps to ENST00000313248 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:44199748 T>C maps to ENST00000313248 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr6:44199748 T>C maps to ENST00000313248 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:66136898 C>T maps to NM_001532.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:73121989 C>A maps to NM_018344.5 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:73121878 C>T maps to NM_018344.5 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr7:5330369 C>T maps to NM_153247.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr7:5340144 C>T maps to NM_153247.2 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr20:45354349 C>T maps to NM_030777.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:45354050 C>T maps to NM_030777.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr20:45362439 G>A maps to NM_030777.3 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr20:45354499 G>T maps to NM_030777.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr20:45354004 C>T maps to NM_030777.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr20:45354505 C>T maps to NM_030777.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:24224965 C>T maps to NM_030807.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:24220009 G>A maps to NM_030807.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:24219287 G>T maps to NM_030807.3 G163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr22:24219349 C>T maps to NM_030807.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr22:24219284 C>T maps to NM_030807.3 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:134312295 G>T maps to NM_145176.2 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:134312298 C>T maps to NM_145176.2 E616E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:134327977 G>A maps to NM_145176.2 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:134350401 G>A maps to NM_145176.2 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr12:40258655 G>T maps to NM_052885.3 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:40158310 G>A maps to NM_052885.3 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr12:7970483 G>A maps to NM_153449.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr12:7973852 G>A maps to NM_153449.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:170723085 G>A maps to NM_000340.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:170723777 G>T maps to NM_000340.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:170723135 G>A maps to NM_000340.1 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:170723097 A>G maps to NM_000340.1 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:170725020 G>A maps to NM_000340.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr3:170723097 A>G maps to NM_000340.1 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr12:8084023 T>C maps to NM_006931.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:8083088 C>T maps to NM_006931.2 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr12:8084023 T>C maps to NM_006931.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:8084023 T>C maps to NM_006931.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:7187882 T>C maps to NM_001042.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr17:7189058 G>C maps to NM_001042.2 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:7187642 C>T maps to NM_001042.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr1:9097839 G>A maps to NM_003039.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:9107723 G>A maps to NM_003039.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr1:9098907 G>T maps to NM_003039.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:9099610 G>A maps to NM_003039.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr1:9100029 G>A maps to NM_003039.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:136342330 G>A maps to NM_017585.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr9:136341410 C>T maps to NM_017585.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:9074847 G>A maps to NM_207420.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:9079298 G>T maps to NM_207420.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:9083080 G>A maps to NM_207420.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:9064867 G>A maps to NM_207420.2 D421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:9079298 G>A maps to NM_207420.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr9:130169526 G>A maps to NM_014580.3 *478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:130162196 C>T maps to NM_014580.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:9998463 G>A maps to NM_020041.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:9892307 T>A maps to NM_020041.2 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:9982320 G>A maps to NM_020041.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:9828062 G>A maps to NM_020041.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:211748957 C>T maps to NM_021194.2 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:211749178 C>A maps to NM_021194.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:220088928 G>A maps to NM_018713.2 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:220091717 A>T maps to NM_018713.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:220101512 G>A maps to NM_018713.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr1:26371515 G>A maps to NM_001004434.1 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:27479347 C>T maps to NM_003459.4 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:27479254 G>A maps to NM_003459.4 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:27478182 G>T maps to NM_003459.4 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:27479304 G>A maps to NM_003459.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:68396693 C>T maps to NM_022902.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:68396693 C>T maps to NM_022902.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:68417573 C>T maps to NM_022902.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr5:68419113 C>T maps to NM_022902.2 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:68414385 G>A maps to NM_022902.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:32445289 A>G maps to NM_001193513.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:32445305 C>T maps to NM_001193513.1 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:32396373 C>T maps to NM_001193513.1 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:101427386 T>G maps to NM_133496.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:101379279 T>C maps to NM_133496.4 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr8:118184799 T>C maps to NM_173851.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:118159335 G>A maps to NM_173851.2 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:118183324 C>T maps to NM_173851.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr8:118170071 G>T maps to NM_173851.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr8:118170071 G>A maps to NM_173851.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:42025372 T>C maps to NM_006345.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr4:42022493 T>C maps to NM_006345.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:42088116 C>T maps to NM_006345.3 R561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:42065035 G>A maps to NM_006345.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr4:42065134 A>G maps to NM_006345.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:42020144 G>T maps to NM_006345.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:37356885 T>C maps to NM_080552.2 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:37357098 C>T maps to NM_080552.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr20:37353747 C>T maps to NM_080552.2 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr20:37353696 C>T maps to NM_080552.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:37356276 C>T maps to NM_080552.2 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:37353441 C>T maps to NM_080552.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr20:37356909 C>T maps to NM_080552.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr20:37356948 C>T maps to NM_080552.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:155571417 T>C maps to NM_004733.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:155546118 A>G maps to NM_004733.3 Y510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:155560337 G>A maps to NM_004733.3 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:155571173 A>G maps to NM_004733.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:176813454 C>T maps to NM_003052.4 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr5:176825151 C>T maps to NM_003052.4 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr5:176812814 C>T maps to NM_003052.4 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:25677971 C>T maps to NM_006424.2 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:25678340 G>A maps to NM_006424.2 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:25672397 T>C maps to NM_006424.2 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:25677860 C>A maps to NM_006424.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr4:25677980 C>T maps to NM_006424.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:25664175 C>T maps to NM_006424.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:25673269 T>G maps to NM_006424.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr4:25671403 A>G maps to NM_006424.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:25676011 G>A maps to NM_006424.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr4:25671403 A>G maps to NM_006424.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:88210226 G>T maps to NM_006416.4 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:48767238 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:100487956 A>G maps to ENST00000370153 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:139947467 C>T maps to NM_080670.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:139946948 C>T maps to NM_080670.2 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:139947215 C>A maps to NM_080670.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr17:47785135 A>G maps to ENST00000415270 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:47780309 G>A maps to ENST00000415270 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:47785093 C>T maps to ENST00000415270 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:47780355 C>T maps to ENST00000415270 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:44224595 G>A maps to NM_178148.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:44223045 C>A maps to NM_178148.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:133979782 G>T maps to NM_032826.4 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:45832456 G>A maps to NM_018389.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:44986400 G>A maps to NM_173179.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr20:44986364 G>A maps to NM_173179.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr20:44984488 A>G maps to NM_173179.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:44984448 C>A maps to NM_173179.2 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:44980770 G>A maps to NM_173179.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:67518501 C>A maps to NM_015139.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr1:67486114 G>A maps to NM_015139.2 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr6:137245146 C>T maps to NM_001008783.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:137243790 G>A maps to NM_001008783.1 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:137243718 C>T maps to NM_001008783.1 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:137245416 G>A maps to NM_001008783.1 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:137245563 A>G maps to NM_001008783.1 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:16664711 G>A maps to NM_024881.4 Y337Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:16666006 G>A maps to NM_024881.4 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:16678866 C>T maps to NM_024881.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:1663893 T>C maps to NM_182838.2 *267W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:1597409 G>T maps to NM_001110781.1 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:1669811 G>A maps to NM_182838.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:1597289 T>A maps to NM_001110781.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr22:31042900 C>T maps to NM_001001479.2 Y312Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr22:31032769 A>G maps to NM_001001479.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:31032451 G>A maps to NM_001001479.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr22:31032919 A>G maps to NM_001001479.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr6:118598659 T>C maps to NM_001029858.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr11:107663427 G>A maps to NM_017515.4 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:107673876 C>A maps to NM_017515.4 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:234367292 C>T maps to NM_173508.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:234367433 C>T maps to NM_173508.2 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:234458949 G>A maps to NM_173508.2 Q478Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr1:234367388 G>A maps to NM_173508.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:234041391 G>A maps to NM_173508.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:234452364 C>T maps to NM_173508.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:234455842 G>T did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:234452418 C>T maps to NM_173508.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:234040849 C>T maps to NM_173508.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:234041350 T>C maps to NM_173508.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:234445005 C>T maps to NM_173508.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:58036530 G>T maps to NM_001080455.1 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:58056151 G>T maps to NM_001080455.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:58036514 G>A maps to NM_001080455.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:114476796 C>T maps to NM_025181.2 W477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:150847278 G>A maps to NM_078483.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:150867610 C>T maps to NM_078483.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:150726883 T>C maps to NM_181776.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:150704952 C>A maps to NM_181776.2 G302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:150701760 G>A maps to NM_181776.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr5:150714979 G>A maps to NM_181776.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr5:150726982 G>A maps to NM_181776.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr5:150657102 C>A maps to NM_001145017.1 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr5:150678159 G>A maps to NM_001145017.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr5:150666875 G>A maps to NM_001145017.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:150657118 G>A maps to NM_001145017.1 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:150663633 G>T maps to NM_001145017.1 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr5:150657102 C>A maps to NM_001145017.1 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:150663720 A>G maps to NM_001145017.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:150667991 G>A maps to NM_001145017.1 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr5:150660573 C>A did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr5:150667007 G>A maps to NM_001145017.1 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr5:150678186 C>A maps to NM_001145017.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr11:92901193 T>C maps to NM_152313.2 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr21:43959681 C>T maps to NM_018964.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:124949031 G>A maps to NM_198277.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:124951789 G>T maps to NM_198277.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:124952141 C>T maps to NM_198277.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:124950578 C>A maps to NM_198277.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:140045704 G>A maps to NM_207113.1 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:140035209 G>A maps to NM_032295.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:140058558 T>C maps to NM_207113.1 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:140051072 C>T maps to NM_207113.1 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:46598119 G>A maps to NM_030674.3 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr12:46591708 T>C maps to NM_030674.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:46623027 G>T maps to NM_030674.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:46601348 G>A maps to NM_030674.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:46591708 T>C maps to NM_030674.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:46582841 A>G maps to NM_030674.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:46591708 T>C maps to NM_030674.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:79220399 C>A maps to NM_001037984.1 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:165771643 C>T maps to ENST00000409662 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:165772467 G>A maps to ENST00000409662 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:165809227 G>T maps to ENST00000409662 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr2:165802217 C>T maps to ENST00000409662 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:165772428 G>A maps to ENST00000409662 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:46754962 C>T maps to NM_018976.4 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:50256121 G>A maps to NM_006841.4 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:50256253 C>T maps to NM_006841.4 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:50256333 G>A maps to NM_006841.4 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:47178415 C>T maps to NM_018018.4 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:47186827 G>T maps to NM_018018.4 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr23:48326261 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:48321366 T>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:48325401 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr23:48318119 A>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:48318119 A>G did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:48318118 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:48318146 G>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:48325228 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:84050788 A>C maps to NM_001080442.1 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr16:84067036 C>T maps to NM_001080442.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:54965611 G>A maps to NM_173514.2 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:153935037 G>A maps to NM_014437.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:153932900 G>A maps to NM_014437.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:153932741 C>T maps to NM_014437.3 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:196592994 T>C maps to NM_001127257.1 G753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:196545753 G>T maps to NM_001127257.1 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:70645342 G>A maps to NM_001159770.1 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:71027748 G>T maps to NM_001159770.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:18276411 C>T maps to NM_001145195.1 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:18276534 C>T maps to NM_001145195.1 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:18292109 C>T maps to NM_001145195.1 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr10:18289716 G>A maps to NM_001145195.1 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:18280222 A>G maps to NM_001145195.1 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:22267591 G>A maps to NM_015359.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:22277210 G>T maps to NM_001135153.1 *493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:2733354 C>T maps to NM_144564.4 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:2732910 C>T maps to NM_144564.4 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:145640662 G>A maps to NM_130849.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr18:33694255 G>A maps to NM_012319.3 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:33706246 C>A maps to NM_012319.3 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:33694126 G>A maps to NM_012319.3 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:33170433 G>A maps to NM_006979.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:33169599 C>A maps to NM_006979.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:103184217 C>A maps to NM_001135146.1 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:103189146 G>A maps to NM_001135146.1 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr14:69908981 C>T maps to NM_018375.3 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr14:69866160 C>A maps to NM_018375.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr14:69925186 C>T maps to NM_018375.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:69908888 G>A maps to NM_018375.3 Q103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:44539748 C>T maps to NM_000341.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:44528188 G>A maps to NM_000341.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:44531311 T>C maps to NM_000341.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr2:44503054 C>A maps to NM_000341.3 Y127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:44502754 T>C maps to NM_000341.3 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:190428310 G>A maps to NM_014585.5 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:190444541 A>G maps to NM_014585.5 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:190426660 G>A maps to NM_014585.5 C553C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:190437577 C>T maps to NM_014585.5 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:205779317 G>A maps to NM_173854.4 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:205767884 G>A maps to NM_173854.4 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:125725927 G>A maps to NM_017836.3 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:125786852 G>A maps to NM_001008485.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:125725957 G>A maps to NM_001008485.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:125775224 G>A maps to NM_001008487.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr11:57268686 G>A maps to NM_003627.5 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:57258812 G>A maps to NM_003627.5 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:57259276 G>T maps to NM_003627.5 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:1531045 C>T maps to ENST00000382147 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:1520019 C>T maps to ENST00000382147 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr11:57188793 G>T maps to ENST00000428603 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:57188507 C>T maps to ENST00000428603 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:57175327 G>A maps to ENST00000428603 F484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:57193509 G>A maps to ENST00000428603 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:57177424 C>T maps to ENST00000428603 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:57176719 C>T maps to ENST00000428603 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:108072051 A>G maps to NM_080546.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:108147779 G>A maps to NM_080546.3 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr9:108136922 C>T maps to NM_080546.3 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:108110696 T>G maps to NM_080546.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr19:10742576 C>T maps to NM_020428.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:10742728 C>A maps to NM_020428.3 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:10748716 A>G maps to NM_020428.3 K596K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:10745874 A>G maps to NM_020428.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:10745893 C>T maps to NM_020428.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:95360381 A>G maps to NM_001114106.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:95358033 A>T maps to NM_001114106.1 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:95290068 G>A maps to NM_001114106.1 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:31831439 G>A maps to NM_025257.2 N699N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:31833104 G>A maps to NM_025257.2 R583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr6:31832428 G>A maps to NM_025257.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:31837021 T>C maps to NM_025257.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:75681474 A>G maps to NM_152697.4 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:75669450 C>T maps to NM_001130058.1 K705K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:75683569 G>A maps to NM_152697.4 Y535Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:8403937 T>C maps to ENST00000377479 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:8384709 C>T maps to ENST00000377479 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:8386013 G>A maps to ENST00000377479 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:8390539 C>T maps to ENST00000377479 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:8399748 G>A maps to ENST00000377479 Q691Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:8397972 G>A maps to ENST00000377479 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr1:8384574 G>A maps to ENST00000377479 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr1:8386031 C>T maps to ENST00000377479 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:8384691 C>T maps to ENST00000377479 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:33984559 G>A maps to NM_016180.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr5:33944812 C>T maps to NM_016180.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr5:33963827 G>A maps to NM_016180.3 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:33984373 G>A maps to NM_016180.3 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr5:33944875 G>A maps to NM_016180.3 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:205628522 G>A maps to NM_033102.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:205631170 G>A maps to NM_033102.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:205631991 C>A maps to NM_033102.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:142228685 G>A maps to NM_001080431.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr8:142228495 G>T maps to NM_001080431.1 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:142228883 G>A maps to NM_001080431.1 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr8:142222397 C>T maps to NM_001080431.1 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:115652538 C>T maps to NM_033051.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:115652739 G>T maps to NM_033051.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:115648837 G>T maps to NM_033051.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr13:29291991 A>G maps to NM_001135919.1 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:29287374 G>A maps to NM_001135919.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:29287672 T>C maps to NM_001135919.1 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:19459314 C>T maps to ENST00000395585 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:19480670 G>A maps to ENST00000395585 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:19437293 G>A maps to ENST00000395585 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:19480787 G>A maps to ENST00000395585 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr17:19459362 C>A maps to ENST00000395585 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:19437386 G>A maps to ENST00000395585 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:42335952 C>A maps to NM_000342.3 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:42335964 A>G maps to NM_000342.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:42335366 G>A maps to NM_000342.3 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:42330615 G>T maps to NM_000342.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:42330663 G>A maps to NM_000342.3 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr17:42340072 C>A maps to NM_000342.3 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:162799394 C>T maps to NM_001178015.1 N697N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:162815046 A>G maps to NM_001178015.1 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr2:162813737 C>T maps to NM_001178015.1 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:162719519 C>A maps to NM_001178015.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr2:162813737 C>T maps to NM_001178015.1 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr2:162813737 C>T maps to NM_001178015.1 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:162711510 G>T maps to NM_001178015.1 G150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr20:3211399 C>T maps to NM_001174090.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:3215508 G>A maps to NM_001174090.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:3209853 C>T maps to NM_001174090.1 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr20:3215472 G>A maps to NM_001174090.1 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr20:3212029 C>T maps to NM_001174090.1 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:27910873 C>T maps to NM_018158.2 C730C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:27887995 C>T maps to NM_018158.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:150765113 C>T maps to NM_003040.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:150768866 C>A maps to NM_003040.3 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:150761823 G>A maps to NM_003040.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:150767154 G>A maps to NM_003040.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr7:150771301 G>A maps to NM_003040.3 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:220500521 G>A maps to NM_201574.2 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:220504377 C>T maps to NM_201574.2 A1093A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:220493275 C>T maps to NM_201574.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:220504356 G>A maps to NM_201574.2 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:220496745 C>A maps to NM_201574.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:220494375 G>A maps to NM_201574.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:220503474 G>A maps to NM_201574.2 S996S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr2:220500572 C>T maps to NM_201574.2 F744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:220493292 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:72412097 G>A maps to NM_001098484.2 W825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr4:72338473 C>T maps to NM_001098484.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:72399969 C>T maps to NM_001098484.2 F769F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr4:72363372 G>T maps to NM_001098484.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:72412179 C>T maps to NM_001098484.2 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:72420864 C>T maps to NM_001098484.2 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:74466641 T>C maps to NM_021196.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:74492354 G>A maps to NM_021196.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:74466593 G>A maps to NM_021196.3 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:74454960 G>T maps to NM_021196.3 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:74483008 G>A maps to NM_021196.3 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:74531614 C>T did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr2:74480207 G>A maps to NM_021196.3 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:74480207 G>A maps to NM_021196.3 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:27462219 G>A maps to ENST00000454389 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr3:27427502 T>C maps to ENST00000454389 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:27436606 C>T did not map to a codon.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr3:27472840 T>C maps to ENST00000454389 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr3:27472840 T>C maps to ENST00000454389 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr3:27477998 G>T maps to ENST00000454389 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr12:51888784 C>A maps to NM_001039960.1 I942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:51863397 G>A maps to NM_001039960.1 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:51853835 G>A maps to NM_001039960.1 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:139744112 T>C maps to ENST00000507527 D542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr22:32479100 G>A maps to NM_000343.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:32480498 T>C maps to NM_000343.3 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:32482279 C>A maps to NM_000343.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:18922780 C>T maps to NM_152351.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:18863862 C>T maps to NM_152351.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:18918398 G>A maps to NM_152351.3 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:18863919 C>A maps to NM_152351.3 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:24895427 G>T maps to NM_052944.2 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:24870050 C>T maps to NM_052944.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:24902340 G>T maps to NM_052944.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr16:24922823 C>T maps to NM_052944.2 C666C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr16:24881271 C>A maps to NM_052944.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:24921760 C>T maps to NM_052944.2 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr16:24895411 G>A maps to NM_052944.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr16:24902340 G>T maps to NM_052944.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:26725392 T>C maps to NM_178498.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:26743249 C>T maps to NM_178498.3 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:31501828 C>T maps to ENST00000431354 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:31500230 G>A maps to ENST00000431354 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:31499731 G>A maps to ENST00000431354 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:31500622 G>A maps to ENST00000431354 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:31500541 G>A maps to ENST00000431354 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr22:32630945 G>A maps to NM_014227.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr22:32626991 G>A maps to NM_014227.2 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr22:32616994 G>A maps to NM_014227.2 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr22:32625275 G>A maps to NM_014227.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:17988624 G>A maps to NM_000453.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:27423928 T>C maps to NM_021095.2 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:108618399 C>T maps to NM_021815.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:108626824 C>A maps to NM_021815.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:108622653 A>G maps to NM_021815.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:108626704 C>T maps to NM_021815.2 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:108608646 A>C maps to NM_021815.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:101603326 C>T maps to NM_145913.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:101577997 G>T maps to NM_145913.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:101577913 T>C maps to NM_145913.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr12:101603596 G>A maps to NM_145913.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:101581229 G>A maps to NM_145913.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:48701422 C>T maps to NM_001135181.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:48703420 C>T maps to NM_001135181.1 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:48688509 C>T maps to NM_001135181.1 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:48697274 A>G maps to NM_001135181.1 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:48697663 G>A maps to NM_001135181.1 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:11067965 C>T maps to NM_003042.3 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:11072876 C>T maps to NM_003042.3 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:11075337 C>T maps to NM_003042.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:11064045 C>T maps to NM_003042.3 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr3:11060284 C>T maps to NM_003042.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr3:10916710 G>A maps to NM_014229.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:10980003 G>T maps to NM_014229.1 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:10858057 G>A maps to NM_014229.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr3:10916710 G>A maps to NM_014229.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr3:10861168 C>T maps to NM_014229.1 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr3:10960055 C>T maps to NM_014229.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:10885970 C>T maps to NM_014229.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:10953836 C>T maps to NM_014229.1 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:300377 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:302538 C>T maps to NM_003044.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:319116 A>C maps to NM_003044.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:319119 C>T maps to NM_003044.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:304439 G>A maps to NM_003044.3 C460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:307154 C>T maps to NM_003044.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:300287 C>T maps to NM_003044.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:346365 G>T maps to NM_016615.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr23:115578012 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:115590084 A>C did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:115572241 G>T did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:115577961 G>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:115576093 C>T did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr12:85285809 A>G maps to NM_182767.4 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:85255749 T>C maps to NM_182767.4 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:85260838 A>G maps to NM_182767.4 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr12:85270338 G>A maps to NM_182767.4 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:85270386 C>A did not map to a codon.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr12:85279830 T>G maps to NM_182767.4 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:85266439 C>A maps to NM_182767.4 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr12:85285809 A>G maps to NM_182767.4 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr12:85285809 A>G maps to NM_182767.4 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr12:85255554 G>A maps to NM_182767.4 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr12:85255569 G>A maps to NM_182767.4 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:49812217 G>A maps to NM_014037.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:49794005 C>T maps to NM_014037.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:49813651 G>T maps to NM_014037.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:110740768 G>A maps to NM_001010898.2 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr1:110734757 G>A maps to NM_001010898.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:110734664 C>A maps to NM_001010898.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:110738283 C>T maps to NM_001010898.2 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:1244881 C>T maps to NM_182632.2 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr5:1243695 C>T maps to NM_182632.2 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:1243866 C>A maps to NM_182632.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:1213597 G>A maps to NM_001003841.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:1201812 G>A maps to NM_001003841.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:1213681 G>A maps to NM_001003841.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:1219196 G>A maps to NM_001003841.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:1217002 C>T maps to NM_001003841.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:1212499 C>T maps to NM_001003841.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:1221850 G>A maps to NM_001003841.2 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr5:1221331 C>T maps to NM_001003841.2 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr5:1221325 G>A maps to NM_001003841.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr5:1221850 G>A maps to NM_001003841.2 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:55725861 C>T maps to NM_001043.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:55690776 G>A maps to NM_001043.3 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr16:55719183 A>G maps to NM_001043.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr16:55706024 C>T maps to NM_001043.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr3:45801399 G>A maps to NM_020208.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:45812875 G>A maps to NM_020208.3 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:45823590 C>T maps to NM_020208.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:45814089 C>T maps to NM_020208.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:45823665 C>T maps to NM_020208.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr3:45801357 G>A maps to NM_020208.3 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:45801357 G>A maps to NM_020208.3 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr5:1416311 C>T maps to NM_001044.4 W311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:1443057 C>A maps to NM_001044.4 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr5:1409159 G>A maps to NM_001044.4 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr5:1411360 G>A maps to NM_001044.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr17:28536248 G>A maps to ENST00000394821 Y529Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr17:28536212 G>A maps to ENST00000394821 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:28548964 C>T maps to ENST00000394821 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr17:28539761 G>A maps to ENST00000394821 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:28548646 G>A maps to ENST00000394821 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr17:28530327 C>T maps to ENST00000394821 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:20625911 C>T maps to NM_004211.3 Y207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr11:20648387 G>T maps to NM_004211.3 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:20660027 T>G maps to NM_004211.3 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr11:20623021 G>A maps to NM_004211.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:20649561 T>C maps to NM_004211.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr11:20676317 C>T maps to NM_004211.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:20676383 G>T maps to NM_004211.3 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:20660030 G>T maps to NM_004211.3 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:20639297 G>A maps to NM_004211.3 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:14485309 C>T maps to NM_001134367.1 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:14518801 C>T maps to NM_001134367.1 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:14523234 C>T maps to NM_001134367.1 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:152958550 G>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:44463598 C>T maps to NM_201649.2 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr1:44463553 G>A maps to NM_201649.2 C633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:44463390 C>T maps to NM_201649.2 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:44468303 C>T maps to NM_201649.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:44463273 C>T maps to NM_201649.2 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:30097581 G>A maps to NM_003045.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr13:30097524 C>T maps to NM_003045.4 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr13:30098323 C>T maps to NM_003045.4 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr13:30096571 G>C maps to NM_003045.4 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr13:30091902 C>T maps to NM_003045.4 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr13:30097437 T>C maps to NM_003045.4 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr13:30096511 G>A maps to NM_003045.4 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:33702138 G>T maps to NM_019849.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:87242125 G>A maps to NM_138817.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:87242284 G>A maps to NM_138817.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:87226721 T>A maps to NM_138817.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:87229773 T>C maps to NM_138817.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:170216488 C>T maps to NM_020949.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:170185108 G>A maps to NM_020949.2 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:170185082 C>T maps to NM_020949.2 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:170216524 G>A maps to NM_020949.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr3:170219132 G>A maps to NM_020949.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:170204127 G>A maps to NM_020949.2 Y263Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr3:170198579 C>T maps to NM_020949.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr3:170184995 G>A maps to NM_020949.2 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:170185076 T>C maps to NM_020949.2 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr8:17418002 C>T maps to NM_001164771.1 Q529*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-A00N-01A-02W-A00E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:70145722 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:70148428 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:70146410 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:70147186 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:70147721 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:70147796 C>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:70147736 C>G did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:70149827 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr23:70146388 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:70147374 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr22:21385714 A>G maps to NM_004173.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:21383418 G>A maps to NM_004173.2 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:87885345 G>A maps to NM_003486.5 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:87874686 A>G maps to NM_003486.5 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr16:87871537 G>A maps to NM_003486.5 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:68308730 G>A maps to NM_003983.4 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr16:68308850 T>A maps to NM_003983.4 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr16:68330406 G>A maps to NM_003983.4 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr16:68330603 C>A maps to NM_003983.4 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:68325153 G>A maps to NM_003983.4 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:68325153 G>A maps to NM_003983.4 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:68344510 T>C maps to NM_032178.2 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr16:68338018 A>G maps to NM_032178.2 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr14:23282373 G>A maps to NM_001126106.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:23242877 C>A maps to NM_001126106.1 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr14:23243301 G>T maps to NM_001126106.1 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr14:23634554 C>T maps to NM_012244.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:23597261 C>T maps to NM_012244.2 W469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:23597360 G>A maps to NM_012244.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr14:23635657 C>T maps to NM_012244.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:33333093 C>A maps to NM_014270.4 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:33351530 C>A maps to NM_014270.4 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:33350824 C>T maps to NM_014270.4 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:33321531 A>G maps to NM_014270.4 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:40656676 G>A maps to NM_021097.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:40342410 G>T maps to NM_021097.2 C968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:40342493 G>T maps to NM_021097.2 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:40366565 G>A maps to NM_021097.2 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:40397448 C>T maps to NM_021097.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr2:40656621 G>A maps to NM_021097.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:40656621 G>T maps to NM_021097.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:40366679 C>T maps to NM_021097.2 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr2:40656621 G>A maps to NM_021097.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:47935622 C>A maps to NM_015063.2 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:47960488 C>T maps to NM_015063.2 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:47960452 C>T maps to NM_015063.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:47951364 G>A maps to NM_015063.2 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:47960437 G>A maps to NM_015063.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr14:70527577 C>T maps to NM_183002.1 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr14:70512963 G>A maps to NM_183002.1 N828N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:70515508 G>A maps to NM_183002.1 F794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3517-01A-01W-0831-10 chr14:70634134 C>T maps to NM_183002.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr14:70635087 G>A maps to NM_183002.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr14:70634935 A>T maps to NM_183002.1 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:70633795 G>A maps to NM_183002.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:70512792 C>T maps to NM_183002.1 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:70634646 G>A maps to NM_183002.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:70635054 G>T maps to NM_183002.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:70530570 G>A maps to NM_033262.3 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr14:70518706 C>T maps to NM_183002.1 K677K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr14:70634578 G>A maps to NM_183002.1 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:27434151 G>A maps to NM_003047.3 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:27436073 G>T maps to NM_003047.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:27436136 G>A maps to NM_003047.3 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:111927207 A>G maps to NM_183061.1 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:111899442 C>A maps to NM_183061.1 G906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr3:111888082 A>G maps to NM_183061.1 A1004A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:111927186 T>C maps to NM_183061.1 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:173556846 G>A maps to NM_178527.3 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:173503759 C>A maps to NM_178527.3 G613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:173502852 G>T maps to NM_178527.3 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:173567136 G>T maps to NM_178527.3 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:173545822 C>A maps to NM_178527.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:173545822 C>T maps to NM_178527.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:103318897 G>A maps to NM_003048.3 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:103274215 A>G maps to NM_003048.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr2:103274047 C>T maps to NM_003048.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:488469 G>A maps to NM_004174.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:476460 C>T maps to NM_004174.2 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:476448 G>A maps to NM_004174.2 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:476159 C>T maps to NM_004174.2 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:524281 C>T maps to NM_004174.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr5:482200 G>A maps to NM_004174.2 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr5:476690 C>T maps to NM_004174.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:482773 G>A maps to NM_004174.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:483527 G>A maps to NM_004174.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:483446 C>T maps to NM_004174.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:72764668 C>T maps to NM_004252.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:103095694 G>A maps to NM_001011552.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:103130572 C>T maps to NM_001011552.3 Y528Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:103148957 C>A maps to NM_001011552.3 Y736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr16:67299009 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:67286592 G>A maps to NM_004594.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:67286673 C>T maps to NM_004594.2 A139A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CM-6163-01A-11D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr16:67289029 T>C maps to NM_004594.2 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:135092701 C>G did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr23:135126868 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:135067765 C>T did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:135092706 G>C did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:135122337 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:135122282 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:135106493 C>T did not map to a codon.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr23:135122269 C>T did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:135092604 A>G did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:46539181 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:46508205 C>T did not map to a codon.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr23:46502695 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:46521555 A>G did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:46521493 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:46472752 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:46541841 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:46618243 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:46539127 T>C did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:46466592 C>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:46466493 T>C did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:46521552 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:46541845 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:46521555 A>G did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:48431592 C>T maps to ENST00000417961 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr20:48431625 G>A maps to ENST00000417961 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:48503377 C>T maps to ENST00000417961 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:48504385 C>A maps to ENST00000417961 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:48431625 G>A maps to ENST00000417961 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:143513859 G>T maps to NM_173653.3 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:21450404 G>T maps to NM_134431.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:21446931 G>A maps to NM_134431.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:21445207 G>A maps to NM_134431.3 C500C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:21453469 C>T maps to NM_134431.3 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:21450335 A>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:21377683 G>A maps to NM_006446.4 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:21355618 G>T maps to NM_006446.4 G444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:21370111 C>A maps to NM_006446.4 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:21350094 G>T maps to NM_006446.4 G315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr12:21358822 T>C maps to NM_006446.4 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr12:21329829 A>G maps to NM_006446.4 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr12:21294579 C>T maps to NM_006446.4 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:21353577 G>A maps to NM_006446.4 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:21036470 A>C maps to NM_019844.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:21054389 C>T maps to NM_019844.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:21028305 G>T maps to NM_019844.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:20876022 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:20903648 T>C maps to NM_017435.4 D613D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr12:20890097 C>T maps to NM_017435.4 C480C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:20868199 C>T maps to NM_017435.4 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:20890100 A>G maps to NM_017435.4 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:133670137 G>A maps to NM_005630.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:133667521 C>T maps to NM_005630.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:133672504 A>G did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:133653613 G>A maps to NM_005630.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:133698429 G>A maps to NM_005630.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:74904276 C>T maps to NM_007256.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:74876902 C>A maps to NM_007256.4 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr15:92706073 C>T maps to NM_013272.3 C614C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr15:92690347 C>T maps to NM_013272.3 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr15:92669417 C>T maps to NM_013272.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr15:92647677 C>T maps to NM_013272.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:92647689 C>T maps to NM_013272.3 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:92706214 C>T maps to NM_013272.3 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:61288354 G>T maps to NM_016354.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:61288393 C>T maps to NM_016354.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:101592850 C>T maps to NM_180991.4 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:101575030 A>G maps to NM_180991.4 D646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr5:101585436 G>A maps to NM_180991.4 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr5:101593746 A>C maps to NM_180991.4 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:70667761 A>C maps to NM_030958.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr8:70617288 G>A maps to NM_030958.2 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:70744356 G>A maps to NM_030958.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:70674018 A>G maps to NM_030958.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:70585202 G>A maps to NM_030958.2 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:101735296 A>G maps to NM_173488.3 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr5:101834416 G>A maps to NM_173488.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr5:101834473 C>T maps to NM_173488.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:101834422 C>T maps to NM_173488.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:101709109 T>C maps to NM_173488.3 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:101811420 C>T maps to NM_173488.3 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:101813431 T>C maps to NM_173488.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:33690642 G>A maps to NM_152270.3 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr17:33679959 G>T maps to NM_152270.3 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr17:33689794 G>A maps to NM_152270.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:33680076 G>A maps to NM_152270.3 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr17:33689935 G>T maps to NM_152270.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:33690346 G>T maps to NM_152270.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:33690153 C>A maps to NM_152270.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:33679695 C>T maps to NM_152270.3 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr17:33738647 T>C maps to NM_018042.3 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:33806544 C>T maps to ENST00000361112 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr17:33802295 A>C maps to ENST00000361112 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr17:33769243 A>G maps to NM_144682.5 H420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:33768059 C>A maps to NM_144682.5 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr17:33771751 C>A maps to NM_144682.5 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:33770901 C>T maps to NM_144682.5 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:33767694 C>T maps to NM_144682.5 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:33772632 C>A maps to NM_144682.5 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:33585841 C>T maps to NM_144975.3 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:33592111 C>T maps to NM_144975.3 C627C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr17:33591397 C>T maps to NM_144975.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr17:33592435 T>C maps to NM_144975.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:41483570 G>A maps to NM_144990.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:41483567 G>A maps to NM_144990.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:98763840 C>T maps to NM_003061.2 A1283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr10:98762597 G>A maps to NM_003061.2 C1339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr10:98808784 G>T maps to NM_003061.2 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:98803152 G>A maps to NM_003061.2 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:98823275 C>T maps to NM_003061.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:98823995 C>A maps to NM_003061.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr4:20258327 G>A maps to ENST00000273739 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:20541067 T>C maps to ENST00000273739 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:20597355 C>T maps to ENST00000273739 C1086C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:20255527 G>A maps to ENST00000273739 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:20270489 G>C maps to ENST00000273739 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:20525768 A>G maps to ENST00000273739 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:20620553 C>T maps to ENST00000273739 F1517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr4:20619085 C>T maps to ENST00000273739 P1400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:20258327 G>A maps to ENST00000273739 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:20512709 C>A maps to ENST00000273739 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:20512135 A>G maps to ENST00000273739 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr4:20619085 C>T maps to ENST00000273739 P1400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:20543105 C>T maps to ENST00000273739 N673N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr4:20530578 A>G maps to ENST00000273739 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:20469447 T>C did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:168199921 G>A maps to NM_003062.2 C441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:168123345 G>A maps to NM_003062.2 C1011C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr5:168233530 C>T maps to NM_003062.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr5:168111011 C>T maps to NM_003062.2 L1215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:168199873 G>A maps to NM_003062.2 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:168175367 G>A maps to NM_003062.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr5:168180900 G>A maps to NM_003062.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr5:168222515 G>A maps to NM_003062.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:168123345 G>A maps to NM_003062.2 C1011C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:168222552 G>A maps to NM_003062.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:168112760 G>A maps to NM_003062.2 F1162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:168199834 G>A maps to NM_003062.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:168119694 G>A maps to NM_003062.2 C1031C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:168139288 G>A maps to NM_003062.2 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:168123324 G>A maps to NM_003062.2 Y1018Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr5:168678453 G>A maps to NM_003062.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr5:168222515 G>A maps to NM_003062.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr5:168620499 C>T maps to NM_003062.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:168123333 G>A maps to NM_003062.2 I1015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:168096833 G>T maps to NM_003062.2 P1430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:168175367 G>A maps to NM_003062.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:168310307 C>T maps to NM_003062.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:168112799 G>A maps to NM_003062.2 F1149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:84455408 G>A maps to NM_052910.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr13:84455108 G>T maps to NM_052910.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr13:84455252 G>A maps to NM_052910.1 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr13:84455252 G>A maps to NM_052910.1 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:84455408 G>A maps to NM_052910.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:84454882 C>A maps to NM_052910.1 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr13:84453602 T>G maps to NM_052910.1 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr13:84454595 G>A maps to NM_052910.1 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:84454313 G>A maps to NM_052910.1 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr13:84455069 C>T maps to NM_052910.1 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr13:84453563 C>T maps to NM_052910.1 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr23:144906029 G>T did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:144904008 C>T did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:144905176 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:144905617 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:144904738 A>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:144905323 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:144905526 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:144904847 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:144905470 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:144904882 C>T did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:144906362 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:144904946 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:144905349 T>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:144905617 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:144905744 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:144905352 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:144905220 C>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:144906296 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:144904006 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:144903988 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:144904051 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:144905325 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:144905617 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:144904026 T>G did not map to a codon.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr23:144904007 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:144904686 G>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:144905477 A>G did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:144905052 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:144905478 A>G did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:144904232 G>T did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:144905635 G>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:164905959 G>A maps to NM_014926.2 R887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:164907976 T>C maps to NM_014926.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:164907220 G>A maps to NM_014926.2 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:164905714 T>C maps to NM_014926.2 E968E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:164906380 C>T maps to NM_014926.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:164906263 C>T maps to NM_014926.2 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:164908336 G>T maps to NM_014926.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:164906122 C>T maps to NM_014926.2 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr3:164905714 T>C maps to NM_014926.2 E968E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:164906122 C>T maps to NM_014926.2 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:164908528 C>T maps to NM_014926.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr3:164905714 T>C maps to NM_014926.2 E968E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:164906122 C>T maps to NM_014926.2 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:164908336 G>T maps to NM_014926.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr3:164907523 G>T maps to NM_014926.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:142718544 A>G did not map to a codon.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr23:142718313 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:142717670 T>A did not map to a codon.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr23:142717306 C>A did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:142717239 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:142718314 G>A did not map to a codon.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr23:142716863 A>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:142717078 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:142717274 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:142716640 A>C did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:142717582 G>A did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:142717610 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:142717953 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:142717190 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:142718257 G>A did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:142716451 G>C did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:142718734 G>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:142716782 A>G did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:142716782 A>G did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:142717783 T>C did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:142718306 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:142718308 C>A did not map to a codon.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr23:142717610 C>G did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:142717802 C>T did not map to a codon.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr23:142716782 A>G did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:142716782 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr13:88327684 T>C maps to NM_015567.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:88328828 C>T maps to NM_015567.1 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr13:88329424 G>A maps to NM_015567.1 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:88329601 C>T maps to NM_015567.1 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr13:88330252 C>T maps to NM_015567.1 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr13:88328683 G>A maps to NM_015567.1 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr13:88329445 C>T maps to NM_015567.1 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:88327834 C>T maps to NM_015567.1 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr13:88329445 C>A maps to NM_015567.1 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr13:88329538 G>A maps to NM_015567.1 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:88329883 C>T maps to NM_015567.1 H747H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr13:88329445 C>A maps to NM_015567.1 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr13:86368320 G>A maps to NM_032229.2 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:86370358 A>G maps to NM_032229.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr13:86370358 A>G maps to NM_032229.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:86368410 C>A maps to NM_032229.2 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:86370450 G>A maps to NM_032229.2 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr13:86370358 A>G maps to NM_032229.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr13:86368483 A>G maps to NM_032229.2 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr13:86369119 C>T maps to NM_032229.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:105763108 G>T maps to NM_014720.2 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:105761237 C>T maps to NM_014720.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:105768030 C>T maps to NM_014720.2 R901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:105762148 C>T maps to NM_014720.2 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:105762012 T>A maps to NM_014720.2 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:105763158 G>A maps to NM_014720.2 E741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:105762264 C>T maps to NM_014720.2 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr10:105768063 G>T maps to NM_014720.2 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:105762264 C>T maps to NM_014720.2 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:105763266 T>C maps to NM_014720.2 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:57817165 G>A maps to ENST00000428312 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:57882316 A>G maps to ENST00000428312 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr20:43883154 C>T maps to NM_003064.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:59179260 A>C maps to NM_024755.2 A916A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:59180630 C>T maps to NM_024755.2 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:59189385 A>G maps to NM_024755.2 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr15:59179263 G>A maps to NM_024755.2 G915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:59185150 A>G maps to NM_024755.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr15:59181648 G>A maps to NM_024755.2 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:159834978 C>A maps to NM_006425.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:146467906 C>T maps to NM_001003688.1 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr18:45374881 G>A maps to NM_001003652.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:45372031 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:45395709 C>A maps to NM_001003652.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr18:45372067 G>A maps to NM_001003652.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr18:45368210 G>T maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr18:45368210 G>C maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr18:45371711 G>A maps to NM_001003652.2 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr18:45368210 G>C maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr18:45368212 G>T maps to NM_001003652.2 C463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr18:45368210 G>T maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:67473577 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:67358558 C>T maps to NM_005902.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:67479736 C>T maps to NM_005902.3 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr15:67358638 C>T maps to NM_005902.3 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr18:48604776 C>T maps to NM_005359.5 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr18:48604698 A>G maps to NM_005359.5 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr18:48591864 C>A maps to NM_005359.5 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr18:48573512 G>T maps to NM_005359.5 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr18:48604735 G>T maps to NM_005359.5 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:48575101 G>A maps to NM_005359.5 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr18:48604650 T>G maps to NM_005359.5 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr18:48604768 C>A maps to NM_005359.5 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr18:48604716 C>G maps to NM_005359.5 Y513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr18:48575195 A>G maps to NM_005359.5 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr18:48604722 A>G maps to NM_005359.5 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr18:48573568 A>G maps to NM_005359.5 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr18:48591910 A>G maps to NM_005359.5 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr18:48604768 C>A maps to NM_005359.5 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr18:48593406 T>C maps to NM_005359.5 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr18:48604791 A>G maps to NM_005359.5 E538E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr18:48575151 C>T maps to NM_005359.5 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr18:48604768 C>A maps to NM_005359.5 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr18:48603031 C>A maps to NM_005359.5 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr18:48575671 A>T maps to NM_005359.5 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr18:48581197 G>T maps to NM_005359.5 G168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr18:48593508 T>C maps to NM_005359.5 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:48604689 T>C maps to NM_005359.5 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:48575210 A>G maps to NM_005359.5 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:48575070 G>T maps to NM_005359.5 G89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr18:48586236 G>A maps to NM_005359.5 W302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr18:48603021 T>C maps to NM_005359.5 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr18:48586272 T>C maps to NM_005359.5 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr18:48586254 T>C maps to NM_005359.5 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:48604689 T>C maps to NM_005359.5 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:48604722 A>G maps to NM_005359.5 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr18:48603031 C>T maps to NM_005359.5 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr18:48575671 A>T maps to NM_005359.5 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr18:48604768 C>A maps to NM_005359.5 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr18:48604698 A>G maps to NM_005359.5 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr18:48591904 T>C maps to NM_005359.5 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr18:48604689 T>C maps to NM_005359.5 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr18:48603021 T>C maps to NM_005359.5 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr18:48591808 T>C maps to NM_005359.5 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr18:48584567 A>G maps to NM_005359.5 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr18:48586261 C>T maps to NM_005359.5 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr18:48604650 T>C maps to NM_005359.5 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr18:48603021 T>C maps to NM_005359.5 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr18:48593496 A>G maps to NM_005359.5 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr18:48604768 C>A maps to NM_005359.5 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr18:48593472 T>C maps to NM_005359.5 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr18:48604650 T>C maps to NM_005359.5 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:48604698 A>G maps to NM_005359.5 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr18:48603146 G>C did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr18:48604656 T>C maps to NM_005359.5 D493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr18:48604722 A>G maps to NM_005359.5 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr18:48573505 A>G maps to NM_005359.5 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr18:48573532 A>G maps to NM_005359.5 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr18:48591889 T>C maps to NM_005359.5 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr18:48603033 A>G maps to NM_005359.5 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr18:48591820 C>T maps to NM_005359.5 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr18:48581228 C>A maps to NM_005359.5 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr18:48604722 A>G maps to NM_005359.5 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr18:48575111 T>C maps to NM_005359.5 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr18:48603033 A>G maps to NM_005359.5 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr18:48575111 T>C maps to NM_005359.5 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr18:48584827 T>C did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr18:48584504 C>T maps to NM_005359.5 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr18:48573568 A>G maps to NM_005359.5 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr18:48573538 A>G maps to NM_005359.5 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr18:48593496 A>G maps to NM_005359.5 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr18:48575671 A>T maps to NM_005359.5 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr18:48604653 T>C maps to NM_005359.5 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:48586236 G>A maps to NM_005359.5 W302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:135489589 T>C maps to NM_001001419.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr5:135510284 C>T maps to NM_001001419.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:135496779 T>C maps to NM_001001419.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr18:46448236 G>A maps to NM_005904.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:46476362 C>T maps to NM_005904.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr13:37439725 A>G maps to NM_001127217.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:37439875 G>A maps to NM_001127217.2 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:37427603 G>A maps to NM_001127217.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:37441422 C>T maps to NM_001127217.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:37453544 G>A maps to NM_001127217.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:71508370 A>G maps to NM_001044305.1 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:40879874 G>A maps to NM_022733.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:40881993 G>A maps to NM_022733.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:40879842 G>T maps to NM_022733.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr23:128630780 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:128641932 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:128624084 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:128650349 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr23:128599924 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:128605210 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:128605242 T>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:128599921 A>G did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:128645796 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:128645832 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:128599854 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:128649710 T>C did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr23:128630778 C>T did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:128645831 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr23:128640171 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:128615122 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:2047454 C>T maps to NM_003070.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:2181577 C>T maps to NM_003070.3 R1421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:2039820 G>A maps to NM_003070.3 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:2083394 G>A maps to NM_003070.3 V799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:11106968 C>T maps to NM_001128849.1 D558D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:11100019 T>C maps to NM_001128849.1 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:11136180 C>T maps to NM_001128849.1 I1055I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:11144501 A>G maps to NM_001128849.1 P1278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr19:11138567 C>T maps to NM_001128849.1 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr19:11132438 C>G maps to NM_001128849.1 R885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr19:11114030 G>A maps to NM_001128849.1 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr19:11138591 T>C maps to NM_001128849.1 F1116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr19:11138567 C>A maps to NM_001128849.1 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr19:11170838 T>C maps to NM_001128849.1 D1661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr19:11138567 C>A maps to NM_001128849.1 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr4:144459997 G>A maps to NM_003601.2 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:144445621 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:95155254 T>C maps to NM_001128429.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:95199764 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:95199662 G>T maps to NM_001128429.1 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr4:95202678 T>C maps to NM_001128429.1 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:217347483 C>T maps to NM_014140.3 Y883Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:217341881 C>T maps to NM_014140.3 S826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:217280978 G>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:217340050 C>A maps to NM_014140.3 C768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr2:217311805 G>A maps to NM_014140.3 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr2:217303198 G>A maps to NM_014140.3 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr2:217280023 T>C maps to NM_014140.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:24145583 A>G maps to NM_003073.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr22:24159023 G>A maps to NM_003073.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:24135749 C>T maps to NM_003073.3 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr22:24145517 C>T maps to NM_003073.3 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr22:24143192 T>A maps to NM_003073.3 L142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:24175792 C>A maps to NM_003073.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr22:24143191 T>C maps to NM_003073.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr22:24145581 C>T maps to NM_003073.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:24145581 C>T maps to NM_003073.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr22:24145586 C>T maps to NM_003073.3 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr22:24133992 C>A maps to NM_003073.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:47703941 A>C maps to NM_003074.3 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr3:47704052 G>A maps to NM_003074.3 N643N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:56558312 A>G maps to NM_003075.3 P1114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:56565664 G>A maps to NM_003075.3 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:56563641 G>A maps to NM_003075.3 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:56565714 C>A maps to NM_003075.3 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr12:56574854 A>G maps to NM_003075.3 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:56561897 G>T maps to NM_003075.3 I901I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr12:56561864 G>T maps to NM_003075.3 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr12:56575490 A>G maps to NM_003075.3 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:56565712 T>C maps to NM_003075.3 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr12:50483719 G>A maps to NM_003076.4 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr12:50492580 C>T maps to NM_003076.4 R493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:50484181 G>A maps to NM_003076.4 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr12:50484145 C>T maps to NM_003076.4 H332H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:61910490 G>A maps to NM_001098426.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:150939641 C>T maps to NM_003078.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:150937521 G>A maps to NM_003078.3 N329N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr17:38792251 G>A maps to NM_003079.4 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:38792664 G>A maps to NM_003079.4 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:53432008 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:53436065 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:53426612 C>T did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr23:53436388 G>A did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:53432458 C>T did not map to a codon.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr23:53432007 C>A did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:53436361 T>C did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:53432458 C>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:53436359 G>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:53436412 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:53432062 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:53407070 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:53439196 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:53440065 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:53409442 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:53439000 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:53432286 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:53409533 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:53436012 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:53432293 C>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:53440234 G>A did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:53407628 T>C did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:53436359 G>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:53432590 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:53440233 C>T did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:53436162 G>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:53423414 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:45798341 A>C maps to NM_148674.3 L242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr22:45782902 T>C maps to NM_148674.3 L585L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D5-6931-01A-11D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr9:106887379 A>G maps to NM_001042550.1 K815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:106862450 A>G maps to NM_001042550.1 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr9:106887379 A>G maps to NM_001042550.1 K815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:112350787 G>A maps to NM_005445.3 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr10:112362984 T>C maps to NM_005445.3 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:112343657 A>G maps to NM_005445.3 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:160142762 C>T maps to NM_005496.3 R812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:160122244 C>T maps to NM_005496.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:160141436 A>G maps to NM_005496.3 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:160151483 C>T maps to NM_005496.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:72965071 C>T maps to NM_015110.3 R978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:72893513 C>T maps to NM_015110.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr9:72939037 T>C maps to NM_015110.3 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:72965053 C>T maps to NM_015110.3 R972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr9:72929698 T>C maps to NM_015110.3 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr9:72939037 T>C maps to NM_015110.3 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr9:72939037 T>C maps to NM_015110.3 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr9:72939037 T>C maps to NM_015110.3 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:17906607 C>T maps to ENST00000381272 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr2:17881567 C>T maps to ENST00000381272 E793E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:17899367 C>T maps to ENST00000381272 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:2763696 C>T maps to NM_015295.2 G1543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:2743860 C>T maps to NM_015295.2 R1246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:2751360 G>A maps to NM_015295.2 L1417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr18:2724948 C>T maps to NM_015295.2 R886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:18166138 C>T maps to NM_148886.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:18221133 C>T maps to NM_144775.2 Y677Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:18226335 C>T maps to NM_144775.2 H922H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:18219408 C>A maps to NM_144775.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:91942288 G>A maps to ENST00000417249 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:91925106 G>T maps to ENST00000417249 S833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:55777079 C>T maps to NM_001122964.1 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:55842619 C>T maps to NM_001122964.1 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:18882776 T>C maps to ENST00000389467 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:18845567 A>G maps to ENST00000389467 S2841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:18908160 C>T maps to ENST00000389467 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:18841654 C>T maps to ENST00000389467 P2943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:18847355 C>T maps to ENST00000389467 P2652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:18859182 T>C maps to ENST00000389467 K1932K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:18856971 C>A maps to ENST00000389467 E2000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr16:18845567 A>G maps to ENST00000389467 S2841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:18853620 G>A maps to ENST00000389467 G2125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr16:18882776 T>C maps to ENST00000389467 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:18882776 T>C maps to ENST00000389467 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr16:18882776 T>C maps to ENST00000389467 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr16:18858826 G>A maps to ENST00000389467 Q1982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:156247747 C>A maps to NM_015327.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:156221248 C>A maps to NM_015327.2 E925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:156235986 C>T maps to NM_015327.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:156244427 C>T maps to NM_015327.2 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:156228858 G>A maps to NM_015327.2 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:156235779 G>T maps to NM_015327.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:156230307 C>T maps to NM_015327.2 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:156235779 G>A maps to NM_015327.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:156244414 G>A maps to NM_015327.2 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:2203353 G>A maps to NM_017575.4 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:2202207 C>T maps to NM_017575.4 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:2201186 A>G maps to NM_017575.4 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:2202266 G>A maps to NM_017575.4 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:2201318 A>G maps to NM_017575.4 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:183495819 G>A maps to ENST00000367537 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:183515465 G>A maps to ENST00000367537 P909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:183510187 A>G maps to ENST00000367537 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:183510178 A>G maps to ENST00000367537 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:183518341 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:128848636 C>T maps to NM_005631.4 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:128845581 C>T maps to NM_005631.4 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:128852087 A>C maps to NM_005631.4 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr7:128850838 G>A maps to NM_005631.4 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:128849190 C>T maps to NM_005631.4 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr14:70442469 C>T maps to NM_001034852.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr14:70478204 C>T maps to NM_001034852.1 Y287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:169053753 G>A maps to NM_022138.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr20:4163061 G>A maps to ENST00000443211 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr20:4164183 C>A maps to ENST00000443211 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:4163143 C>T maps to ENST00000443211 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr20:4155821 C>T maps to ENST00000443211 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr20:4168035 C>G maps to ENST00000443211 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:4163385 C>T maps to ENST00000443211 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:6415152 C>T maps to NM_000543.4 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:109763486 C>T maps to NM_003080.2 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr16:68404947 G>A maps to NM_018667.3 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr16:68405862 C>T maps to NM_018667.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:130912004 G>A maps to NM_017951.4 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr2:130930423 A>G maps to NM_017951.4 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:130925147 G>T maps to NM_017951.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr2:130912735 G>A maps to NM_017951.4 H501H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:123130270 G>A maps to NM_006714.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:28285132 C>T maps to NM_014474.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:28285066 C>T maps to NM_014474.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:21761874 A>G did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:21772399 C>T did not map to a codon.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr23:21755806 A>G did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:21755768 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:21755768 G>A did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:21772396 C>T did not map to a codon.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr4:71255516 C>A maps to NM_006685.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr4:71255495 G>T maps to NM_006685.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:21995186 C>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:21995259 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:22003278 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:21995312 C>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:21995348 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr22:31492767 G>A maps to ENST00000454496 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr22:31486965 C>T maps to ENST00000454496 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr22:31484885 C>T maps to ENST00000454496 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr11:57314065 C>T maps to ENST00000457912 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:57314068 A>G maps to ENST00000457912 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr11:57314065 C>T maps to ENST00000457912 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:33056218 A>G maps to NM_018225.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:33048118 C>T maps to NM_018225.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr9:33056108 A>C did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr9:33053231 G>A maps to NM_018225.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:98649879 C>T maps to NM_020429.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:62547794 T>C maps to NM_022739.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr17:62547794 T>C maps to NM_022739.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr17:62547794 T>G maps to NM_022739.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr17:62547794 T>C maps to NM_022739.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:62589630 C>T maps to NM_022739.3 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr17:62547794 T>A maps to NM_022739.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:88387386 G>A maps to NM_198274.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:88409901 A>G maps to NM_198274.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:88405893 T>C maps to NM_198274.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:88405959 C>A maps to NM_198274.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:88383882 C>T maps to NM_198274.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:88367481 C>T maps to NM_198274.3 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:214507644 G>T maps to NM_020197.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:214498039 G>A maps to NM_020197.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:214488172 C>A maps to NM_020197.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:245912888 G>A maps to NM_001167740.1 C421C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:245912893 C>A maps to NM_001167740.1 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:246498776 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:246518362 G>A maps to NM_001167740.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr17:1703856 C>T maps to NM_052928.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:73446038 C>T maps to NM_006062.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr8:49833764 G>A maps to NM_003068.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:49832626 G>A maps to NM_003068.3 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:49831547 C>A did not map to a codon.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr8:49831545 C>T maps to NM_003068.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:49831545 C>A maps to NM_003068.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr8:49831547 C>A did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr8:49831547 C>A did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr16:88747604 G>T maps to NM_178310.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:88747817 G>T maps to NM_178310.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:10273905 T>G maps to NM_130811.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr20:10265389 A>C maps to NM_130811.1 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr20:10273812 A>G maps to NM_130811.1 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr22:21242112 C>T maps to NM_004782.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:21237843 C>T maps to NM_004782.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:21224764 A>G maps to NM_004782.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:21242112 C>T maps to NM_004782.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:227935442 C>T maps to NM_053052.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:227935743 C>T maps to NM_053052.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:84366473 G>A maps to NM_014841.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:84303203 G>T maps to NM_014841.2 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:84303269 G>T maps to NM_014841.2 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:84417613 G>A maps to NM_014841.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr6:84350843 G>A maps to NM_014841.2 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:62244825 G>T maps to NM_003082.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:62245585 A>G maps to NM_003082.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:7986981 G>A maps to NM_003083.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:15444607 T>C maps to NM_001039697.1 H162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:15433621 C>T maps to NM_001039697.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:15423927 T>C maps to NM_001039697.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr9:139290204 G>A maps to NM_003086.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:139289305 G>A maps to NM_003086.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:139281956 G>A maps to NM_003086.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr9:139272501 T>C maps to NM_003086.2 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:139290159 A>G maps to NM_003086.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:139277946 C>T maps to NM_003086.2 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:139273440 G>T maps to NM_003086.2 T946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:121759109 C>T maps to ENST00000379533 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:121758833 T>C maps to ENST00000379533 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:121786272 A>G maps to ENST00000379533 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:121787094 C>T maps to ENST00000379533 N898N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:176056547 G>A maps to NM_003085.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:176056613 G>A maps to NM_003085.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:176048259 C>T maps to NM_003085.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:127342543 T>C maps to NM_014390.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr7:127725825 C>T maps to NM_014390.2 Y766Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:127344907 G>T maps to NM_014390.2 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:127727066 G>T maps to NM_014390.2 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr7:127484387 G>A maps to NM_014390.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:127727066 G>A maps to NM_014390.2 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:241992579 C>T maps to NM_001080437.1 C698C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:241973252 C>T maps to NM_001080437.1 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr2:241969903 C>T maps to NM_001080437.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:242004356 C>T maps to NM_001080437.1 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:242011288 A>G maps to NM_001080437.1 R1271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:38019740 C>T maps to NM_024700.2 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:38006254 G>A maps to NM_024700.2 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:1281256 G>A maps to ENST00000381876 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr20:1285647 C>T maps to ENST00000381876 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr20:1277866 C>T maps to ENST00000381876 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr20:1281256 G>A maps to ENST00000381876 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:43389955 G>A maps to NM_017719.4 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:43345159 G>A maps to NM_017719.4 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:43344718 T>C maps to NM_017719.4 Y8Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr3:43381974 C>T maps to NM_017719.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:96944057 G>A maps to NM_014014.3 R1843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:96945251 G>A maps to NM_014014.3 H1690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:96952492 G>A maps to NM_014014.3 F1254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:96964437 C>T maps to NM_014014.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:96957511 G>A maps to NM_014014.3 R763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:96953611 G>A maps to NM_014014.3 I1118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:96953638 G>A maps to NM_014014.3 D1109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:96952743 C>T maps to NM_014014.3 K1213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:96940752 A>G maps to NM_014014.3 D2136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:96952205 C>T maps to NM_014014.3 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:70122304 G>C maps to NM_006857.1 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:70123577 C>T maps to NM_006857.1 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:123950464 C>T maps to NM_180699.2 Y131Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:31762250 T>C maps to ENST00000446633 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr19:41265388 C>A maps to NM_004596.4 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:2448272 A>G maps to ENST00000339610 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr20:16712403 A>G maps to NM_198220.2 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:19203727 T>C maps to NM_006938.2 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:46191649 G>A maps to NM_004597.5 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:46191661 G>A maps to NM_004597.5 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:25223427 G>A maps to NM_022805.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr15:25223433 G>A maps to NM_022805.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:31997968 G>A maps to NM_003098.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr20:32005541 G>A maps to NM_003098.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr20:32000127 G>A maps to NM_003098.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr20:31996387 C>T maps to NM_003098.2 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:32000133 C>T maps to NM_003098.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr20:31996327 G>C maps to NM_003098.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr8:121644854 C>T maps to NM_021021.3 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr8:121561131 T>C maps to NM_021021.3 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr8:121561131 T>C maps to NM_021021.3 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr16:69333635 C>T maps to NM_006750.3 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr8:51569560 T>C maps to NM_018967.2 C314C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:51314771 A>C maps to NM_018967.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr8:51705268 C>T maps to NM_018967.2 C478C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr8:51617242 G>A maps to NM_018967.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr8:51705268 C>T maps to NM_018967.2 C478C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:51449257 G>A maps to NM_018967.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr8:51363273 T>A maps to NM_018967.2 C116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr8:51449243 T>C maps to NM_018967.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:1271264 C>T maps to NM_018968.3 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:1204904 G>A maps to NM_018968.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr2:1204808 G>A maps to NM_018968.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr2:1204904 G>A maps to NM_018968.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:1168826 C>A maps to NM_018968.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:1161256 C>T maps to NM_018968.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:1079205 G>A maps to NM_018968.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:1263161 G>A maps to NM_018968.3 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr2:1312324 G>A maps to NM_018968.3 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr2:1271213 G>A maps to NM_018968.3 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:1161295 G>A maps to NM_018968.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:1312321 C>T maps to NM_018968.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr2:1271163 C>T maps to NM_018968.3 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:75901980 A>G maps to ENST00000371091 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr15:25207279 C>T maps to NM_022804.2 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:25213165 G>A maps to NM_022804.2 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:78198866 G>A maps to NM_012245.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr14:78184619 G>A maps to NM_012245.2 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr15:64410998 G>T maps to NM_003099.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:46196129 C>T maps to NM_152244.1 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:70288093 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:70282758 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:70282762 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:70288021 C>T did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:70281779 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:17890017 G>A maps to ENST00000417048 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:17915105 C>A maps to ENST00000417048 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr7:17915405 C>A maps to ENST00000417048 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:17838645 G>A maps to ENST00000417048 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:17855897 T>C maps to ENST00000417048 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:17854474 T>C maps to ENST00000417048 K730K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:86256863 G>A maps to NM_153816.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:64802604 G>A maps to NM_013306.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr11:64802604 G>A maps to NM_013306.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:64799917 C>A maps to NM_013306.4 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:82727568 T>C maps to NM_152836.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr8:82736046 A>G maps to NM_152836.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:27599552 C>T maps to NM_014748.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:53814507 C>A maps to NM_052870.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:53815533 C>T maps to NM_052870.2 D584D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr5:53814681 G>A maps to NM_052870.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:53814993 C>T maps to NM_052870.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:53815026 C>T maps to NM_052870.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:53815137 C>T maps to NM_052870.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:53815269 C>T maps to NM_052870.2 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:130785608 G>A maps to NM_014758.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:122163130 C>T maps to NM_003100.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr5:122163275 C>T maps to NM_003100.2 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:122163130 C>T maps to NM_003100.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr16:50711380 G>A maps to NM_182854.2 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:50707907 G>A maps to NM_182854.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:50707904 C>T maps to NM_182854.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr20:44469555 G>A maps to NM_033421.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:44469708 C>T maps to NM_033421.2 H293H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:122337659 C>T maps to ENST00000395451 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr4:186188234 C>A maps to NM_031953.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:186180030 C>T maps to NM_031953.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr4:186263207 A>T maps to NM_031953.2 K545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr4:186267692 C>T maps to NM_031953.2 C566C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr4:186267692 C>T maps to NM_031953.2 C566C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:186267728 T>C maps to NM_031953.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:151641080 T>C maps to ENST00000458013 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:151611522 C>T maps to ENST00000458013 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:151665460 C>T maps to ENST00000458013 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:151665516 T>G did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:151633277 T>C maps to ENST00000458013 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:12371857 G>T maps to NM_001080530.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:115593108 G>A maps to NM_001012994.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:115593012 C>T maps to NM_001012994.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:65617467 C>A maps to NM_152760.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:65617941 G>T maps to NM_152760.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:125238944 G>A maps to NM_003794.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr20:17928268 G>A maps to NM_152227.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr14:35036889 A>G did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr1:99156719 A>G maps to NM_015976.4 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr7:2317863 C>T maps to NM_013321.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr7:2314849 C>T maps to NM_013321.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:158327171 T>C maps to NM_016224.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:179319495 C>T maps to NM_003101.4 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr1:179308681 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:179320539 C>A maps to NM_003101.4 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr6:107827551 A>G maps to NM_018013.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:107854661 G>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:107955184 G>A maps to NM_018013.3 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:107955295 G>A maps to NM_018013.3 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:55510448 C>T maps to NM_199421.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:46985950 C>T maps to NM_144949.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:46986985 C>T maps to NM_144949.2 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:46986014 C>T maps to NM_144949.2 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr18:67992803 G>A maps to NM_004232.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr17:36521263 A>C maps to NM_014598.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr21:33039669 C>T maps to NM_000454.4 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr9:138588563 C>T maps to NM_001101677.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr9:138588563 C>T maps to NM_001101677.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:36764117 G>T maps to ENST00000511166 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:36776095 A>G maps to ENST00000511166 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr13:36764147 C>T maps to ENST00000511166 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:598025 C>T maps to NM_005632.2 C396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:603485 C>T maps to NM_005632.2 V1077V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr21:34927314 T>C maps to NM_138927.1 S1926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr21:34923225 G>A maps to NM_138927.1 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:34925163 G>A maps to NM_138927.1 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:34921956 G>A maps to NM_138927.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:34925259 A>G maps to NM_138927.1 V1241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr21:34926744 G>A maps to NM_138927.1 P1736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr21:34923165 G>T maps to NM_138927.1 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr21:34923540 C>T maps to NM_138927.1 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr10:97096777 G>A maps to NM_001034954.1 R1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:97192277 C>T maps to NM_001034954.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:97174499 G>T maps to NM_001034954.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr4:186598549 T>G maps to NM_001145673.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:186583258 G>A maps to ENST00000355634 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:186545076 C>T maps to ENST00000355634 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:186536213 C>T maps to ENST00000355634 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:186548066 G>A maps to ENST00000355634 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:186599611 G>A maps to ENST00000355634 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr4:186548139 C>A maps to ENST00000355634 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:186544107 G>A maps to ENST00000355634 N921N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:22429301 C>A maps to NM_005775.4 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:108447982 C>T maps to NM_001013031.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:108337004 C>A maps to NM_001013031.1 E1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:108371698 G>A maps to NM_001013031.1 I1001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:108389017 G>A maps to NM_001013031.1 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:108536384 A>C maps to NM_001013031.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr10:108389098 G>A maps to NM_001013031.1 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:108357184 C>T maps to NM_001013031.1 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:108459099 C>A maps to NM_001013031.1 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:108339146 G>A maps to NM_001013031.1 F1117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:108459130 G>A maps to NM_001013031.1 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:108338999 C>T maps to NM_001013031.1 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr10:108337216 C>A maps to NM_052918.3 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr10:108434895 C>T maps to NM_001013031.1 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr10:108427541 T>A maps to NM_001013031.1 R736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:108338891 C>T maps to NM_001013031.1 R1163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr10:108459112 G>A maps to NM_001013031.1 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:108439064 G>A maps to NM_001013031.1 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:7730155 C>T maps to NM_020777.2 D983D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:7677886 C>T maps to NM_020777.2 Y424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr4:7668936 A>G maps to NM_020777.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:7666140 C>T maps to NM_020777.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:7705921 C>T maps to NM_020777.2 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr4:7716909 C>T maps to NM_020777.2 C708C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr4:7640152 C>T maps to NM_020777.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:106899244 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:107022208 T>C maps to NM_014978.1 P1188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr10:107022208 T>C maps to NM_014978.1 P1188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:106918669 G>A maps to NM_014978.1 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:107016626 C>T maps to NM_014978.1 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:106907397 C>T maps to NM_014978.1 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:106982991 C>T maps to NM_014978.1 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr10:106960987 C>A maps to NM_014978.1 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr10:106602581 C>T maps to NM_014978.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr10:106865179 C>T maps to NM_014978.1 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:107005319 C>T maps to NM_014978.1 S963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:107023092 C>T maps to NM_014978.1 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr10:107022106 C>T maps to NM_014978.1 N1154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr10:107022118 A>G maps to NM_014978.1 Q1158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr10:106959826 C>A maps to NM_014978.1 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:121459965 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:121476197 G>A maps to NM_003105.5 T1622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:121367604 T>C maps to NM_003105.5 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:121459995 T>C maps to NM_003105.5 C1325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:121429518 G>A maps to NM_003105.5 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr11:121491798 C>T maps to NM_003105.5 L1972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr11:121459965 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:121391558 G>A did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:121457024 T>C maps to NM_003105.5 D1267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:121424655 G>A maps to NM_003105.5 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:121457024 T>C maps to NM_003105.5 D1267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr11:121461818 C>T maps to NM_003105.5 Y1441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:121414435 G>A did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:109870187 G>A maps to NM_002959.4 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:109893591 T>C maps to NM_002959.4 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr1:109883373 G>A maps to NM_002959.4 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:109859530 G>A maps to NM_002959.4 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:109897102 A>G maps to NM_002959.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:39213108 G>A maps to NM_005633.3 S1286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:39250341 A>G maps to NM_005633.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:39250023 T>C maps to NM_005633.3 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:39281837 G>A maps to NM_005633.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:39222288 G>A maps to NM_005633.3 S1107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr14:50655255 G>A maps to NM_006939.2 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr14:50585241 T>C maps to NM_006939.2 R1273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:50606744 G>A maps to NM_006939.2 D900D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:50606687 T>C maps to NM_006939.2 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:41836049 T>C maps to NM_025237.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:16502568 G>A maps to ENST00000396652 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:16502438 C>A maps to ENST00000396652 G143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:38379437 C>T maps to NM_006941.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:38370167 C>T maps to NM_006941.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr22:38369570 G>T maps to NM_006941.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:5833131 C>T maps to NM_003108.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr2:5833162 C>A maps to NM_003108.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr2:5834086 G>T maps to NM_003108.3 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:5834031 G>A maps to NM_003108.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:5833971 G>A maps to NM_003108.3 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:306805 C>T maps to NM_006943.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:204095051 G>A maps to ENST00000367206 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr1:204092030 G>C maps to ENST00000367206 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:137484156 C>T maps to NM_004189.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:137484315 C>T maps to NM_004189.2 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:7492955 G>A maps to NM_006942.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:55370934 T>C maps to NM_022454.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr8:55370964 G>A maps to NM_022454.3 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:181430831 G>A maps to NM_003106.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:181430375 C>T maps to NM_003106.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr3:181430444 G>A maps to NM_003106.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr13:95364213 G>A maps to NM_007084.2 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr23:139587062 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:139587068 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:139586762 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:139586702 C>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:139586649 G>T did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:139586669 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:157073780 A>C maps to NM_178424.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:23757332 T>G maps to NM_006940.4 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:23728682 T>C maps to NM_006940.4 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr12:23687161 T>C maps to NM_006940.4 Q761Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:23818414 G>A maps to NM_006940.4 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr12:23728628 C>T maps to NM_006940.4 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr12:23757374 A>G maps to NM_006940.4 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:23893953 A>G maps to NM_006940.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr12:23696166 G>A maps to NM_006940.4 N583N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr12:24048939 T>C maps to NM_006940.4 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:23893815 C>T maps to NM_006940.4 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:15994564 T>C maps to NM_001145819.1 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr11:16340157 T>C maps to NM_001145819.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:16071312 C>A maps to NM_001145819.1 G488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr11:15994564 T>C maps to NM_001145819.1 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:10583418 G>A maps to ENST00000354846 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:10587766 C>T maps to NM_031439.2 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:10583340 G>A maps to ENST00000354846 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:1034884 C>T maps to NM_014587.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr16:1033886 C>T maps to NM_014587.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:1033871 C>T maps to NM_014587.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:70117875 G>A maps to NM_000346.3 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr17:70120243 C>T maps to NM_000346.3 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr17:70119733 C>T maps to NM_000346.3 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:70119049 C>T maps to NM_000346.3 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr17:70120177 C>T maps to NM_000346.3 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr17:70119682 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:53777101 G>A maps to NM_138473.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:53776891 A>G maps to NM_138473.2 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr2:231405596 G>A maps to NM_001080391.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:231077599 C>T maps to NM_080424.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:231036874 G>A maps to NM_080424.2 C574C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:231037654 G>A maps to NM_080424.2 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr2:231074723 C>G did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr2:231033860 G>T maps to NM_080424.2 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:231079698 G>T maps to NM_080424.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:231048327 T>C maps to NM_080424.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:231120170 C>T maps to NM_007237.4 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:231113640 G>T maps to NM_007237.4 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr2:231150494 C>A maps to NM_007237.4 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:231152655 T>C maps to NM_007237.4 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:231150482 C>T maps to NM_007237.4 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr2:231118029 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:45994015 C>T maps to NM_003110.5 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr17:46000486 C>T maps to NM_003110.5 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:174820363 G>T maps to NM_003111.4 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:174820615 A>G maps to NM_003111.4 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:174820114 C>T maps to NM_003111.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:174820615 A>G maps to NM_003111.4 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr2:174820615 A>G maps to NM_003111.4 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr2:174820591 G>T maps to NM_003111.4 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr7:21521628 A>G maps to NM_003112.3 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr7:21521626 C>T maps to NM_003112.3 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr7:21469763 T>C maps to NM_003112.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr7:21521628 A>G maps to NM_003112.3 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:21521628 A>G maps to NM_003112.3 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr7:21470025 C>T maps to NM_003112.3 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:171573412 C>T maps to NM_001003845.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:45925573 C>T maps to NM_199262.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:45925552 C>T maps to NM_199262.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:53722499 C>A maps to NM_001173467.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:53722298 C>T maps to NM_001173467.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:53722751 C>T maps to NM_001173467.1 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr11:124545186 C>T maps to NM_017425.3 H9H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr6:88769238 C>T maps to NM_030960.2 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:88776008 G>T maps to NM_030960.2 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:88769206 G>T maps to NM_030960.2 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr6:88763697 C>T maps to NM_030960.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr17:31322541 C>T maps to NM_173847.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:101237509 G>T maps to NM_003114.3 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr8:101237532 A>G maps to NM_003114.3 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr8:7308704 C>T maps to NM_016512.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:215274948 C>T maps to NM_024532.3 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:214215359 A>C maps to NM_024532.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:214354772 G>A maps to NM_024532.3 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:214794683 T>C maps to NM_024532.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:215013919 G>A maps to NM_024532.3 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr2:214228855 T>C maps to NM_024532.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:214149311 G>A maps to NM_024532.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:118548138 A>T maps to NM_206996.2 Y1558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:118624085 G>A maps to NM_206996.2 Q648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:118624161 C>T maps to NM_206996.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:118550747 G>A maps to NM_206996.2 I1502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:118537124 A>T maps to NM_206996.2 P1694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:118634559 T>A maps to NM_206996.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:118634278 G>A maps to NM_206996.2 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:118629317 G>A maps to NM_206996.2 H529H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:118658000 T>A maps to NM_206996.2 K127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:118509277 G>A maps to NM_206996.2 I2162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:118539037 C>A maps to NM_206996.2 E1670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:118598354 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:118598484 C>A maps to NM_206996.2 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr1:118548180 A>G maps to NM_206996.2 C1544C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr1:118506475 T>C maps to NM_206996.2 T2206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:118583458 G>A maps to NM_206996.2 H1020H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr1:118558644 T>C maps to NM_206996.2 R1410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr20:34205088 G>A maps to NM_003116.1 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:34208886 T>C maps to NM_003116.1 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:26906386 T>A maps to NM_006461.3 K1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr17:26919700 A>G maps to NM_006461.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:26907056 C>A maps to NM_006461.3 G923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr10:22657521 G>A maps to ENST00000376603 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:22699983 C>T maps to ENST00000376603 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:22690152 C>T maps to ENST00000376603 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr10:22634742 C>T maps to ENST00000376603 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:22678225 A>G maps to ENST00000376603 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr17:4864118 C>A maps to NM_004890.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:4862852 C>A maps to NM_004890.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:4862930 C>T maps to NM_004890.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:35810934 G>A maps to NM_001039592.1 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:35811027 G>A maps to NM_001039592.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:35811214 C>T maps to NM_001039592.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:49075926 T>C maps to ENST00000376407 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:49098615 G>A maps to ENST00000376407 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:49073973 G>A maps to ENST00000376407 D640D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr17:49072420 A>G maps to ENST00000376407 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:123594520 G>A maps to NM_001174046.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:123599569 G>A maps to NM_001174046.1 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr7:123599953 C>T maps to NM_001174046.1 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr23:140335817 C>T did not map to a codon.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr23:140335819 T>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:140785693 C>A did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:140785772 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:144337205 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:144337231 T>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:142795191 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:142795376 C>T did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:142795557 G>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:142596704 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr23:142596797 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:142596667 A>G did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:142596798 A>G did not map to a codon.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr23:142596667 A>G did not map to a codon.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr23:142596643 C>A did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:142596667 A>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:142596669 A>G did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:142596669 A>G did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:142596667 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:52825637 C>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:88416147 G>A maps to NM_004684.4 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:32362227 G>A maps to NM_014946.3 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:32379498 C>T maps to NM_014946.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:32339824 T>G maps to NM_014946.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr2:32353547 C>T maps to NM_014946.3 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:57107880 A>G maps to NM_181727.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr13:24863159 G>A maps to ENST00000424834 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr13:24868996 G>T maps to ENST00000424834 V1104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:24863309 T>C maps to ENST00000424834 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:24860488 C>T maps to ENST00000424834 R850R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:172642036 G>T maps to NM_031955.5 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:172835113 G>A maps to NM_031955.5 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr4:52938115 C>T maps to NM_145263.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:52926990 G>A maps to NM_145263.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:52928495 C>T maps to NM_145263.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:52951166 T>C did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr4:52936031 G>A maps to NM_145263.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr4:52948573 G>A maps to NM_145263.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:52951140 C>T maps to NM_145263.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr20:48522341 G>A maps to NM_006038.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr20:48522353 C>A maps to NM_006038.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:48628079 C>T maps to NM_022827.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:48627367 C>A maps to NM_022827.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:48629539 C>T maps to NM_022827.2 D652D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:48629482 C>T maps to NM_022827.2 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:16748428 A>G maps to NM_198546.1 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:16725318 T>C did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:16748428 A>G maps to NM_198546.1 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:16757836 C>T maps to NM_198546.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:3366053 G>T maps to NM_001170695.1 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:3343554 G>A maps to NM_001170695.1 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:89764260 C>T maps to NM_152339.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:177113910 C>T maps to NM_144644.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:177113910 C>T maps to NM_144644.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:123855352 T>C maps to NM_145207.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr4:123850244 G>A maps to NM_145207.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:123850275 A>C maps to NM_145207.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:123949433 C>T maps to NM_145207.2 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:123855774 G>A maps to NM_145207.2 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:45702646 C>T maps to NM_024063.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:45709474 G>T maps to NM_024063.2 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr15:45713329 G>A maps to NM_024063.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:48825367 C>T maps to NM_019073.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:48825412 G>A maps to NM_019073.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:48918740 A>G maps to NM_019073.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:48877207 C>T maps to NM_019073.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:88903904 C>T maps to NM_018418.4 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr14:88899544 A>G maps to NM_018418.4 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:88892661 T>G maps to NM_018418.4 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:88895774 T>C maps to NM_018418.4 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr15:97327424 C>T maps to NM_173499.3 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:97328235 T>C maps to NM_173499.3 C69C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:94994562 C>A maps to NM_031952.3 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:145095787 C>A maps to NM_198572.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:145094855 C>T maps to NM_198572.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:44344169 G>A maps to NM_145026.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:44329727 C>T maps to NM_145026.3 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:44344797 T>C maps to NM_145026.3 *301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:44344775 T>A maps to NM_145026.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:44320580 T>C maps to NM_145026.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr12:49918573 C>A maps to NM_023071.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:49888627 C>T maps to NM_023071.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:49912931 G>A maps to NM_023071.3 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:11258792 A>C maps to NM_182513.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:169733807 A>G maps to NM_020675.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:169733808 T>C maps to NM_020675.3 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr11:74676929 T>C maps to NM_014752.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr11:74688087 G>T maps to NM_014752.2 *227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr11:74676929 T>C maps to NM_014752.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:177249468 G>A maps to NM_021928.3 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr4:177248356 T>C maps to NM_021928.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:34512064 G>A maps to NM_012391.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr6:34511926 C>T maps to NM_012391.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:29052119 T>C maps to NM_182756.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:8660754 G>A maps to NM_001128076.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:8661640 C>T maps to NM_001128076.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:8656494 C>T maps to NM_001128076.1 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:3759094 C>T maps to NM_015417.4 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr20:3759902 C>T maps to NM_015417.4 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:35705870 G>T maps to NM_024867.3 E876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:35712933 G>T maps to NM_024867.3 E954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr5:35670224 G>T maps to NM_024867.3 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:35806919 G>T maps to NM_024867.3 E1708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr5:35654812 C>T maps to NM_024867.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:35700763 G>T maps to NM_024867.3 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:35644611 T>C maps to NM_024867.3 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:35705824 A>G maps to NM_024867.3 K860K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:35774025 T>C maps to NM_024867.3 P1327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:220353554 G>A maps to NM_005876.4 A2694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:220309646 G>A maps to NM_005876.4 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:220342057 C>T maps to NM_005876.4 C1540C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:220333405 C>T maps to NM_005876.4 F1083F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:220342429 C>T maps to NM_005876.4 V1583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:220355344 G>T maps to NM_005876.4 E3046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:220326766 C>A maps to NM_005876.4 P868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:220353307 G>A maps to NM_005876.4 K2649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr2:220337810 G>A maps to NM_005876.4 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr2:220315876 C>T maps to NM_005876.4 Y711Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:220332115 C>T maps to NM_005876.4 D1034D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:7323954 C>T maps to NM_199339.2 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:7324671 G>A maps to NM_199339.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:7324498 C>T maps to NM_199339.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:16245954 G>A maps to NM_015001.2 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:16262115 G>A maps to NM_015001.2 Q3127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr1:16258068 C>T maps to NM_015001.2 D1778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr1:16261134 G>A maps to NM_015001.2 A2800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:16257957 G>A maps to NM_015001.2 S1741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:16199370 T>C maps to NM_015001.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:16261623 C>A maps to NM_015001.2 P2963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:16199454 G>A maps to NM_015001.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:16237704 G>A maps to NM_015001.2 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:16258758 T>C maps to NM_015001.2 A2008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:16264037 A>C maps to NM_015001.2 P3469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:16255264 C>T maps to NM_015001.2 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr1:16257198 A>G maps to NM_015001.2 R1488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:46287372 C>T maps to NM_152719.1 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr13:46276587 G>A maps to NM_152719.1 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:46276586 G>A maps to NM_152719.1 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:69238505 C>T maps to NM_145658.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:44887651 G>T maps to NM_025137.3 A1480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr15:44891015 A>G maps to NM_025137.3 N1235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:44925802 T>G maps to NM_025137.3 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:44890523 C>A maps to NM_025137.3 E1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:44898281 G>T maps to NM_025137.3 S1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:44858183 C>T maps to NM_025137.3 Q2289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:44889052 C>A maps to NM_025137.3 E1364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:44941209 C>A did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:44861676 C>T maps to NM_025137.3 R2168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:36905691 C>T maps to NM_001142294.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr13:36909169 G>T maps to NM_001142294.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:36886585 G>A maps to NM_001142294.1 C504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:36878537 C>T maps to NM_001142294.1 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr13:36886521 T>A maps to NM_001142294.1 K526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:36888391 T>G maps to NM_001142294.1 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:65273308 G>A maps to NM_016630.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:89616971 C>T maps to NM_003119.2 H578H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:74382952 G>A maps to NM_182965.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr17:74382946 G>A maps to NM_182965.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:49132858 G>A maps to NM_020126.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:49131259 C>T maps to NM_020126.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:228884249 A>T maps to NM_001142644.1 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:228883301 C>T maps to NM_001142644.1 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr2:228884375 G>A maps to NM_001142644.1 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:228881600 G>T maps to NM_001142644.1 I1323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:228883465 G>A maps to NM_001142644.1 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr2:228882353 G>A maps to NM_001142644.1 G1072G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr2:228890169 T>C maps to NM_001142644.1 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:228884600 A>C maps to NM_001142644.1 Y323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr2:228884249 A>G maps to NM_001142644.1 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr2:228882998 G>A maps to NM_001142644.1 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:47376933 G>A maps to NM_001080547.1 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:50931346 C>T maps to NM_003121.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:101880434 C>A maps to ENST00000299272 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:91083294 C>T maps to NM_006717.2 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:57146365 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:57020706 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:57021343 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:57021288 T>G did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:57021238 T>C did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:57021243 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:62570410 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:62570023 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:62570401 C>T did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:62570402 T>C did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:62570557 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:57676321 G>A maps to ENST00000506738 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:147498001 C>T maps to NM_001127698.1 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr5:147493974 C>A maps to NM_001127698.1 C646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:147481450 C>T maps to NM_001127698.1 C470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:147465985 A>T maps to NM_001127698.1 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:147505094 C>T maps to NM_001127698.1 C916C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr20:44175992 C>A maps to ENST00000396669 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:44170791 G>A maps to NM_020398.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:38778555 G>A maps to NM_021102.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr20:44351107 T>C maps to NM_178455.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr20:44351107 T>C maps to NM_178455.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr20:44351107 T>C maps to NM_178455.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr18:12452384 C>T maps to NM_001128626.1 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr16:89922042 C>T maps to NM_032451.1 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:89920722 G>A maps to NM_032451.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr16:28990558 C>T maps to NM_032038.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr16:28994544 C>T maps to NM_032038.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:28992840 G>A maps to NM_032038.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr16:28990543 G>A maps to NM_032038.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:4434060 C>T maps to NM_001124758.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr17:4433991 C>T maps to NM_001124758.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:4381929 C>T maps to NM_182538.4 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:4349383 T>C maps to NM_182538.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:4337462 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:4350214 G>A maps to NM_182538.4 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:55909831 T>C maps to ENST00000371258 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:55909834 C>T maps to ENST00000371258 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:55908297 C>A maps to ENST00000371258 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:55908261 T>C maps to ENST00000371258 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:55908261 T>C maps to ENST00000371258 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr20:55908261 T>C maps to ENST00000371258 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:32280127 T>C maps to NM_144569.4 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:32257846 C>T maps to NM_144569.4 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:32256701 A>G maps to NM_144569.4 D1051D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr1:32256632 G>T maps to NM_144569.4 G1074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:32256383 C>T maps to NM_144569.4 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:136324303 G>T maps to NM_004598.3 C245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:136834163 G>A maps to NM_004598.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:136315105 G>A maps to NM_004598.3 C348C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:73828005 G>A maps to NM_014767.2 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:167810295 T>G maps to NM_016950.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr4:167675842 T>C maps to NM_016950.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr4:167656167 T>C maps to NM_016950.2 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:14157020 A>G maps to NM_006108.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:14276112 G>A maps to NM_006108.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:14280847 C>T maps to NM_006108.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:14282204 C>T maps to NM_006108.2 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:14284331 C>T maps to NM_006108.2 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:14284331 C>T maps to NM_006108.2 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr11:14282298 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:1164238 G>A maps to NM_012445.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr17:47684703 C>A maps to NM_003563.3 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:47679312 G>A maps to NM_003563.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:139310140 C>T maps to NM_001001664.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:88902727 C>T maps to NM_001040058.1 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:234969116 C>T maps to NM_006944.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr2:234959633 C>T maps to NM_006944.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr15:51040387 T>C maps to NM_032802.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:2340958 G>A maps to NM_152988.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:2343974 C>T maps to NM_152988.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:2339855 C>T maps to NM_152988.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:2338797 C>T maps to NM_152988.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:2337467 G>T maps to NM_152988.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr15:38643495 G>A maps to NM_152594.2 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:38631943 G>T maps to NM_152594.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:65540904 C>G maps to NM_181784.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:65540706 C>T maps to NM_181784.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:65541168 C>T maps to NM_181784.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:65540727 G>T maps to NM_181784.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:65540826 C>T maps to NM_181784.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:65561754 G>A maps to NM_181784.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:153029157 G>A maps to NM_005988.2 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:153066098 C>T maps to NM_001024209.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:153085149 C>T maps to NM_001014450.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:152975945 A>C maps to NM_005416.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:124323507 C>A maps to NM_199327.1 C254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:124322994 T>C maps to NM_199327.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr4:124323408 C>T maps to NM_199327.1 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr4:124323408 C>T maps to NM_199327.1 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr13:80911654 G>A maps to NM_005842.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:155004017 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:141694016 G>A maps to NM_030964.3 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:141693977 G>A maps to NM_030964.3 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:141693931 G>A maps to NM_030964.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:141694415 G>A maps to NM_030964.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:56863099 C>A maps to NM_207344.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr12:56863168 T>C maps to NM_207344.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr11:55659005 C>A maps to NM_032681.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:55655689 T>G maps to NM_032681.3 Y230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:55657417 G>A maps to NM_032681.3 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:55655681 G>T maps to NM_032681.3 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:55653128 C>T maps to NM_032681.3 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:1827784 G>A maps to NM_080861.3 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr16:1828595 G>A maps to NM_080861.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr3:140866108 T>C maps to NM_080862.1 *274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:140785518 C>T maps to NM_080862.1 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr1:158609791 T>C maps to NM_003126.2 Q1581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:158650501 T>C maps to NM_003126.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:158632602 G>A maps to NM_003126.2 R785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr1:158637648 T>C maps to NM_003126.2 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:158585094 G>A maps to NM_003126.2 Y2233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr1:158585118 G>A maps to NM_003126.2 D2225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:158615094 C>A maps to NM_003126.2 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:158626407 G>A maps to NM_003126.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:158622423 G>T maps to NM_003126.2 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:158585169 C>T maps to NM_003126.2 A2208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:158648200 G>A maps to NM_003126.2 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr1:158583524 A>G maps to NM_003126.2 A2325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr1:158592892 G>A maps to NM_003126.2 H2000H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr1:158606538 T>A maps to NM_003126.2 I1734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:158637648 T>C maps to NM_003126.2 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr9:131344062 G>A maps to NM_001130438.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:131353808 C>T maps to NM_001130438.2 Y1020Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr9:131367447 C>T maps to NM_001130438.2 L1285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:131371927 A>G did not map to a codon.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr9:131383492 C>T maps to NM_001130438.2 R1930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:131374039 C>T maps to NM_001130438.2 N1607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:131344998 C>T maps to NM_001130438.2 H559H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr9:131344155 G>A maps to NM_001130438.2 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:131346767 C>T maps to NM_001130438.2 R801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:131394743 G>T maps to NM_001130438.2 E2332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:131346163 G>A maps to NM_001130438.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:131369973 C>T maps to NM_001130438.2 R1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr9:131353799 G>A maps to NM_001130438.2 P1017P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:131353799 G>A maps to NM_001130438.2 P1017P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:131394991 G>A maps to NM_001130438.2 P2385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:131367423 C>T maps to NM_001130438.2 G1277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:131389747 C>T maps to NM_001130438.2 N2220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr9:131395552 C>T maps to NM_001130438.2 G2458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr9:131353799 G>A maps to NM_001130438.2 P1017P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr14:65267581 G>T maps to ENST00000389723 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr14:65252301 G>A maps to ENST00000389723 L1274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:65235817 G>A maps to ENST00000389723 Q1990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr14:65253655 G>T maps to ENST00000389723 A1013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:65237691 C>T maps to ENST00000389723 A1907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr14:65264521 G>A maps to ENST00000389723 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:65237802 A>G maps to ENST00000389723 Y1870Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:65251015 C>T maps to ENST00000389723 A1321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:65246495 G>A maps to ENST00000389723 L1478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:65220466 T>C maps to ENST00000389723 P2134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr14:65260196 C>T maps to ENST00000389723 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr14:65267479 G>A maps to ENST00000389723 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr14:65242040 C>T maps to ENST00000389723 A1552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr14:65239381 G>A maps to ENST00000389723 D1827D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr14:65261194 G>A maps to ENST00000389723 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:65289746 G>T maps to ENST00000389723 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:54876781 C>T maps to NM_003128.2 R1745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:54858240 G>A maps to NM_003128.2 A1019A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:54849603 C>T maps to NM_003128.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr2:54853340 C>G maps to NM_003128.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:54753704 T>A did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr2:54887105 C>T maps to NM_003128.2 N2130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr2:54870198 G>A maps to NM_003128.2 W1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:54874341 C>T maps to NM_003128.2 T1647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr2:54874341 C>A maps to NM_003128.2 T1647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:66472244 G>A maps to NM_006946.2 Y834Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:66475106 C>T maps to NM_006946.2 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:66455671 G>A maps to NM_006946.2 G2114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr11:66457736 G>A maps to NM_006946.2 D1861D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:66466884 A>G maps to NM_006946.2 I1256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:66478180 C>T maps to NM_006946.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr11:66473256 G>A maps to NM_006946.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr11:66455338 C>T maps to NM_006946.2 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr11:66456213 T>C maps to NM_006946.2 E2047E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:41012214 C>T maps to NM_020971.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr19:41021259 C>T maps to NM_020971.2 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:40995992 G>A maps to NM_020971.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:40978533 G>A maps to NM_020971.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:40978662 G>A maps to NM_020971.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr19:40978641 T>A maps to NM_020971.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr15:42149115 G>A maps to ENST00000320955 L2915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr15:42154471 G>A maps to ENST00000320955 A2468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:42144484 C>T maps to ENST00000320955 Q3493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:42162667 G>T maps to ENST00000320955 L1846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr15:42149131 C>T maps to ENST00000320955 V2909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:42149152 G>T maps to ENST00000320955 A2902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:42172471 G>A maps to ENST00000320955 F899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:42149155 G>A maps to ENST00000320955 D2901D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:94812350 T>C did not map to a codon.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr9:94821590 C>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr14:78043215 G>T maps to NM_004863.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:78021797 A>G maps to NM_004863.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:77978650 C>T maps to NM_004863.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr20:13107236 G>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:13053052 G>A maps to NM_018327.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:13107242 C>T maps to NM_018327.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:13145504 C>T maps to NM_018327.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:79616748 G>T maps to NM_032567.3 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:79616316 G>T maps to NM_032567.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:79616439 G>T maps to NM_032567.3 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr5:79616448 G>T maps to NM_032567.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr8:126011653 T>C maps to NM_003129.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr5:179250951 T>C maps to NM_003900.4 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:179251005 G>A maps to NM_003900.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:142738827 G>A maps to NM_001080415.1 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:142746041 G>A maps to NM_001080415.1 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:142746003 C>T maps to NM_001080415.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:142772568 G>T maps to NM_001080415.1 E903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:142731108 C>T maps to NM_001080415.1 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:45616571 T>C maps to NM_018079.4 K955K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:45832556 C>T maps to NM_018079.4 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:45774700 G>A maps to NM_018079.4 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr20:36026210 G>A maps to ENST00000373558 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr20:36024646 C>T maps to ENST00000373558 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr20:36022369 G>A maps to ENST00000373558 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr20:36022369 G>T maps to ENST00000373558 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr20:36024598 C>T maps to ENST00000373558 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:36024691 G>A maps to ENST00000373558 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:30732597 T>C maps to NM_006662.2 V1114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:30723462 G>A maps to NM_006662.2 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr16:30723189 T>C maps to NM_006662.2 D509D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr16:30748803 C>A maps to NM_006662.2 I2481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:30734467 T>C maps to NM_006662.2 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:30750246 C>T maps to NM_006662.2 S2962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:30724641 G>A maps to NM_006662.2 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:30747711 A>G maps to NM_006662.2 E2307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr16:30731532 T>C maps to NM_006662.2 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr16:30748866 T>C maps to NM_006662.2 P2502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr16:30750175 C>T maps to NM_006662.2 R2939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:30750657 C>T maps to NM_006662.2 S3099S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:30735856 G>A maps to NM_006662.2 T1704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr17:36720471 G>A maps to NM_025248.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:36734841 G>A maps to NM_025248.2 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:36719665 C>T maps to NM_025248.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:36720474 G>A maps to NM_025248.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:76026898 G>A maps to NM_080744.1 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:31758810 G>A maps to NM_000348.3 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:31758715 A>G maps to NM_000348.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr2:31805894 C>T maps to NM_000348.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:56230310 C>T maps to NM_024592.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:56230355 C>T maps to NM_024592.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:17722326 C>T maps to NM_001005291.2 K386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr22:42269954 C>T maps to NM_004599.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr22:42273417 C>T maps to NM_004599.2 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:42263036 A>G maps to NM_004599.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr22:42263036 A>G maps to NM_004599.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:42299077 A>G maps to NM_004599.2 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:42263243 G>A maps to NM_004599.2 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:42262989 G>T maps to NM_004599.2 G82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr22:42293061 C>T maps to NM_004599.2 F834F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr22:42269824 C>T maps to NM_004599.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr22:42276928 C>T maps to NM_004599.2 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr22:42269824 C>T maps to NM_004599.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr22:42271667 T>C maps to NM_004599.2 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:43144301 G>A maps to NM_003131.2 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:43146056 G>A maps to NM_003131.2 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:121354990 C>T maps to NM_152546.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr12:64377818 C>T maps to NM_020762.2 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:64536266 C>T maps to NM_020762.2 R1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:64536266 C>T maps to NM_020762.2 R1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:64485110 C>T maps to NM_020762.2 Q498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr12:64472796 A>G maps to NM_020762.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:64377731 C>T maps to NM_020762.2 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:64536211 G>A maps to NM_020762.2 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:64536334 C>T maps to NM_020762.2 G1047G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:206603534 G>A maps to ENST00000414359 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:206626582 C>T maps to ENST00000414359 Y662Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:206567030 G>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:9100069 G>A maps to NM_014850.2 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:9032477 G>A maps to NM_014850.2 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:9099961 G>A maps to NM_014850.2 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr3:9166566 A>G maps to NM_014850.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr3:9057382 G>A maps to NM_014850.2 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:87838693 G>A maps to NM_003130.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:4242237 G>A maps to ENST00000330063 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:4242647 C>A maps to ENST00000330063 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr16:4242675 C>T maps to ENST00000330063 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr16:4247872 C>T maps to ENST00000330063 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr16:4242675 C>A maps to ENST00000330063 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr16:4254546 G>A maps to ENST00000330063 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:11116778 G>A maps to NM_003132.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:11116799 G>T maps to NM_003132.2 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:62173561 G>T maps to NM_080823.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:62173660 G>T maps to NM_080823.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:35480861 T>G maps to NM_003136.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr14:35492182 A>G maps to NM_003136.3 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:74060086 G>A maps to NM_014230.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:74036541 A>G maps to NM_014230.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:57354130 A>G maps to NM_006947.3 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:57344669 G>A did not map to a codon.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr6:35837265 G>A maps to ENST00000361690 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:35858735 C>T maps to ENST00000361690 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:35837361 T>C maps to ENST00000361690 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr6:35840498 G>A maps to ENST00000361690 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:35858675 A>G maps to ENST00000361690 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr7:104783606 G>A maps to ENST00000336613 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr7:104782524 T>C maps to ENST00000336613 Q522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:104767452 A>T maps to ENST00000336613 Y634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:104844138 C>T maps to ENST00000336613 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:104844171 T>C maps to ENST00000336613 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:104758317 G>A maps to ENST00000336613 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr7:104782491 T>C maps to ENST00000336613 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:104909266 C>T maps to NM_182691.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:104782563 G>A maps to ENST00000336613 C509C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:153048469 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:153049765 A>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:153048415 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr11:126134282 G>A maps to NM_003139.3 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:126134414 G>A maps to NM_003139.3 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:133538555 C>T maps to NM_021203.3 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:133534490 T>C maps to NM_021203.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:38031268 A>G did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:38024105 C>T did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:38019294 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:38033498 C>T did not map to a codon.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr23:38019431 G>T did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr23:38031151 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:38031304 G>A did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:99917177 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:99925848 T>C did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:99905796 C>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:99919783 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:26887468 C>A maps to NM_001013694.2 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:26886014 G>A maps to NM_001013694.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:24975462 C>T maps to NM_005839.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr1:24977930 C>T maps to NM_005839.3 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:24995922 G>A maps to NM_005839.3 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:24987216 A>G maps to NM_005839.3 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:24997956 G>A maps to NM_005839.3 K827K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:24998031 T>C maps to NM_005839.3 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:24978037 T>C maps to NM_005839.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:2816873 C>T maps to NM_016333.3 S2115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:2819141 T>C maps to NM_016333.3 S2626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:2819045 T>C maps to NM_016333.3 R2594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr16:2818001 T>C maps to NM_016333.3 N2491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr16:2814597 G>T maps to NM_016333.3 G1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:119554805 C>T maps to NM_194286.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr12:119588836 G>A maps to NM_194286.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:119583424 C>T maps to NM_194286.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:119583358 C>T maps to NM_194286.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:119419785 C>T maps to NM_194286.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:119559877 C>A maps to NM_194286.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:119568488 C>T maps to NM_194286.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr7:100482978 C>T maps to NM_015908.5 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:100485672 A>G maps to NM_015908.5 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr7:100483959 G>A maps to NM_015908.5 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr20:629546 G>A maps to NM_080725.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr24:2655269 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr24:2655515 C>G did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr24:2655496 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr24:2655460 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:2655337 C>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr18:23619373 T>C maps to ENST00000415083 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:60736634 C>T maps to NM_198935.1 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:42635940 C>A maps to NM_016305.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:141445299 C>T maps to NM_003143.1 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:80911290 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:54708960 G>A maps to NM_145716.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:182787054 G>T maps to NM_001130445.1 G1197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:182761651 G>T maps to NM_001130445.1 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:182780760 G>A maps to NM_001130445.1 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:182784026 G>T maps to NM_001130445.1 E1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr12:109205075 G>T maps to NM_018984.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:109198939 T>C maps to NM_018984.3 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:109210872 G>A maps to NM_018984.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:109186271 G>A maps to NM_018984.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:109198954 A>G maps to NM_018984.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr12:109186130 G>A maps to NM_018984.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:109194613 C>A maps to NM_018984.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:27975193 T>C maps to NM_033389.2 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:28030073 G>A maps to NM_033389.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:27959511 G>A maps to NM_033389.2 F873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:27959511 G>A maps to NM_033389.2 F873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:27963145 G>T maps to NM_033389.2 S674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:27963759 G>A maps to NM_033389.2 H469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:28003847 G>A maps to NM_033389.2 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:27959208 T>C maps to NM_033389.2 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:67075397 C>A maps to NM_017857.3 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr11:67072309 A>G maps to NM_017857.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr12:26377302 T>C maps to NM_005086.4 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr12:26348802 C>T maps to NM_005086.4 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:149500638 C>T maps to NM_198455.2 G2681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:149500318 C>T maps to NM_198455.2 C2616C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr7:149476684 G>A maps to NM_198455.2 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:149500086 C>T maps to NM_198455.2 C2572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr7:149476735 C>A maps to NM_198455.2 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:149476708 C>T maps to NM_198455.2 C387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:149512401 C>T maps to NM_198455.2 S3577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr7:149486358 G>A maps to NM_198455.2 T1446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:149480388 G>A maps to NM_198455.2 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:149515018 C>A maps to NM_198455.2 S3806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr7:149493792 G>A maps to NM_198455.2 S2264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:7310232 C>A maps to ENST00000474597 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:155988059 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:57099242 G>T maps to NM_003146.2 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:57101944 G>A maps to NM_003146.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr11:57095242 C>T maps to NM_003146.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:57095242 C>A maps to NM_003146.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr14:38679631 C>T maps to NM_001049.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr14:38679541 C>T maps to NM_001049.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:38679628 C>T maps to NM_001049.2 N345N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:38679488 C>T maps to NM_001049.2 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:38679133 C>T maps to NM_001049.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:38679004 C>T maps to NM_001049.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr17:71165784 C>G maps to NM_001050.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr22:37603623 C>T maps to NM_001051.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr22:37603653 C>T maps to NM_001051.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:37602678 C>T maps to NM_001051.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:23016314 C>T maps to NM_001052.2 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr20:23016560 C>T maps to NM_001052.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr20:23016792 C>T maps to NM_001052.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:1129257 G>A maps to NM_001053.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:1129713 C>T maps to NM_001053.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:48125764 G>T did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr1:85124055 G>A maps to NM_001166417.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:85113244 A>G maps to NM_001166417.1 N572N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:85122087 G>A maps to NM_001166417.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:48211570 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:48207005 C>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:48214640 G>A did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:48209518 C>T did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:48209485 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:48049615 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:48047119 T>G did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:48054551 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:48054726 T>G did not map to a codon.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr23:48053629 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:52674516 G>A did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr22:41252523 G>A maps to NM_003932.3 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr11:130058082 G>A maps to NM_021978.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:130078532 C>T maps to NM_021978.3 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:130068299 C>T maps to NM_021978.3 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:130068938 C>T maps to NM_021978.3 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr8:53044590 C>A maps to NM_014682.2 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr8:53092682 T>C maps to NM_014682.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr8:53025885 C>A maps to NM_014682.2 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr8:53045827 G>A maps to NM_014682.2 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr8:53077785 C>G did not map to a codon.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr8:134474123 G>A maps to NM_173344.2 C281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:134474201 G>T maps to NM_173344.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:134478195 C>T maps to NM_173344.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr16:70432187 G>A maps to NM_006927.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr1:44290498 T>C maps to NM_174963.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:44363950 C>T maps to NM_174963.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:44290498 T>C maps to NM_174963.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:44290498 T>C maps to NM_174963.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:44395826 A>G maps to NM_174963.2 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:44386458 C>T maps to NM_174963.2 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr1:44290498 T>C maps to NM_174963.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:126278026 C>T maps to ENST00000356132 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr11:126276862 A>T maps to ENST00000356132 K43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr11:126276395 G>T maps to ENST00000356132 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:98492774 C>T maps to ENST00000493584 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:8729382 G>T maps to NM_005418.3 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:8719177 G>A maps to NM_005418.3 D982D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:8739296 C>T maps to NM_005418.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:8739338 C>T maps to NM_005418.3 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:8751516 A>G maps to NM_005418.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:8728724 G>T maps to NM_005418.3 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:8752604 G>A maps to NM_005418.3 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:186790725 T>C maps to NM_003032.2 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:186793531 G>T maps to NM_003032.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr3:186791960 G>T maps to NM_003032.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr2:107459974 G>A maps to NM_001142351.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:107449071 G>A maps to NM_001142351.1 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr17:74568774 T>A maps to NM_006456.2 K205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr1:76779491 A>G maps to NM_152996.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:76877919 G>A maps to NM_152996.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:76877854 C>T maps to NM_152996.2 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:76877880 T>C maps to NM_152996.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr1:76877829 A>G maps to NM_152996.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr1:77093235 C>A maps to NM_152996.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:130674839 C>T maps to NM_175039.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:77510001 C>T maps to NM_030965.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:77528884 G>T maps to NM_030965.1 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:116778505 T>C maps to ENST00000323984 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:116863015 T>C maps to NM_021908.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:113098528 C>A maps to NM_017744.4 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr12:22487106 C>T maps to NM_003034.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:22354545 G>A maps to NM_003034.3 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:92981822 C>T maps to NM_006011.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr15:93007368 C>A maps to NM_006011.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:92937377 C>T maps to NM_006011.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr15:92988057 C>T maps to NM_006011.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr15:92973338 T>C maps to NM_006011.3 N53N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:55024413 C>T maps to NM_015879.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr18:55024347 G>A maps to NM_015879.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr18:55024422 G>A maps to NM_015879.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:100192014 T>G maps to NM_005668.4 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:100231358 T>G maps to NM_005668.4 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:100191996 G>A maps to NM_005668.4 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:100222108 A>G maps to NM_005668.4 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr5:100192101 T>C did not map to a codon.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr5:100222273 T>C maps to NM_005668.4 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr18:44268779 G>A maps to NM_013305.4 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr18:44260370 G>A maps to NM_013305.4 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr18:44260277 C>T maps to NM_013305.4 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:44272208 C>T maps to NM_013305.4 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr18:44260298 C>T maps to NM_013305.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:17369026 G>A maps to NM_001004470.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:17363212 G>A maps to NM_001004470.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:17362950 C>A maps to NM_001004470.1 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:17401528 C>A maps to NM_001004470.1 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr10:17373466 G>A maps to NM_001004470.1 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr3:52553531 C>T maps to NM_015136.2 T1729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:52555386 C>T maps to NM_015136.2 G1973G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:52552007 C>T maps to NM_015136.2 R1584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:52554000 G>A maps to NM_015136.2 R1759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:52550138 T>C maps to NM_015136.2 H1343H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:52550713 G>A maps to NM_015136.2 V1431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:52538835 C>T maps to NM_015136.2 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:52537087 C>T maps to NM_015136.2 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:52556239 C>T maps to NM_015136.2 T2153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:52542329 G>A maps to NM_015136.2 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr3:52545694 C>T maps to NM_015136.2 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr12:104144469 C>T maps to NM_017564.9 D2184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:104155079 G>T maps to NM_017564.9 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:104131548 C>T maps to NM_017564.9 F1896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:104151977 C>T maps to NM_017564.9 R2340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:104100730 C>T maps to NM_017564.9 C1386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:104157304 G>A maps to NM_017564.9 K2508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:104142813 C>A maps to NM_017564.9 V2106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr12:104118856 C>T maps to NM_017564.9 R1596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr12:104083673 C>T maps to NM_017564.9 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:103984748 C>T maps to NM_017564.9 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:104083646 G>A maps to NM_017564.9 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr12:104126917 G>A maps to NM_017564.9 K1806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr12:104155079 G>T maps to NM_017564.9 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr12:104155079 G>T maps to NM_017564.9 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:104100745 C>T maps to NM_017564.9 Y1391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:104131482 C>T maps to NM_017564.9 A1874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr12:104078852 C>T maps to NM_017564.9 N996N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:104054122 T>C maps to NM_017564.9 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:36587687 C>A maps to NM_003149.1 C372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr3:36527668 C>T maps to NM_003149.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr3:36534719 C>T maps to NM_003149.1 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:37370511 G>A maps to NM_198993.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:37368556 C>T maps to NM_198993.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr17:37371454 G>A maps to NM_198993.3 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr12:57638345 G>T maps to NM_145064.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:57637918 G>T maps to NM_145064.1 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:57642941 C>T maps to NM_145064.1 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:136068198 T>C maps to NM_005862.2 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:136076580 G>A maps to NM_005862.2 R1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:136219114 G>A maps to NM_005862.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:136141286 G>A maps to NM_005862.2 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr3:136141316 G>A maps to NM_005862.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:136323296 G>T maps to NM_005862.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr23:123176442 G>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:123176452 G>A did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:123200088 G>T did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:123179101 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:123217380 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:123197836 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:123191803 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:123185020 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:123176434 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:123181255 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:123220539 G>A did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:123179101 G>T did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:123195092 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:123184054 C>A did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:123195092 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:123200090 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:123195633 G>A did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:99802311 C>T maps to NM_012447.2 I955I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:99796552 T>C maps to NM_012447.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:99796990 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:99796886 C>T maps to NM_012447.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr7:99786619 T>C maps to NM_012447.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:99795753 A>G maps to NM_012447.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr10:17747017 T>C maps to NM_003473.2 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:17756586 G>A maps to NM_003473.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:152977246 A>G maps to NM_005843.4 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:152988650 A>G maps to NM_005843.4 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr2:74086466 C>T maps to NM_213622.1 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr2:74076511 C>T maps to NM_213622.1 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:74072350 C>T maps to NM_213622.1 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:90676486 G>T maps to NM_020799.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:68458988 A>G maps to NM_012108.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr4:68447153 T>G maps to NM_012108.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:4325420 G>A maps to ENST00000314714 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr8:38006195 C>T maps to NM_000349.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr8:38003899 G>A maps to NM_000349.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:33684130 G>A maps to NM_178007.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:33704195 G>A maps to NM_178007.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:33680944 C>T maps to NM_178007.2 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:33703871 C>T maps to NM_178007.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr13:33739487 T>A maps to NM_178007.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:33686985 C>T maps to NM_178007.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:37809966 G>A maps to NM_006804.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:37815748 G>A maps to NM_006804.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:37809885 G>A maps to NM_006804.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:37815766 C>A maps to NM_006804.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:37819125 C>T maps to NM_006804.3 R435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:38256633 G>A maps to NM_032016.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:38256675 G>A maps to NM_032016.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:110835762 G>A maps to NM_139164.1 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:81616398 G>C maps to NM_181900.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr15:81605692 A>G maps to NM_181900.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr15:81610757 A>C maps to NM_181900.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:81610766 G>A maps to NM_181900.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:96858166 G>A maps to NM_020151.3 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:96852491 G>A maps to NM_020151.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:96852514 G>T maps to NM_020151.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:67943630 A>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:67943584 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:67935141 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:67942452 C>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:67938427 C>T did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:67938361 A>G did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:67937368 C>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:67942347 C>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:191843727 C>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:191850350 C>T maps to NM_007315.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr2:191847186 G>A maps to NM_007315.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:191847217 T>C maps to NM_007315.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr2:191847217 T>C maps to NM_007315.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:56737181 A>C maps to NM_005419.3 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:56742765 G>T maps to NM_005419.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:56737288 C>A maps to NM_005419.3 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:40485937 G>A maps to NM_139276.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:40485937 G>A maps to NM_139276.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr17:40476865 T>G did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr17:40481598 G>T maps to NM_139276.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:191922746 A>G maps to NM_003151.2 H401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:191937898 G>T maps to NM_003151.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr2:191929582 G>A maps to NM_003151.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr2:191922746 A>G maps to NM_003151.2 H401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:40458435 C>T maps to NM_003152.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr17:40452284 C>T maps to NM_003152.3 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:40459417 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:40456359 C>T maps to NM_003152.3 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:40368067 C>T maps to NM_012448.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:40369409 G>T maps to NM_012448.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr17:40359723 C>A maps to NM_012448.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:40371846 C>T maps to NM_012448.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:57493655 G>A maps to NM_003153.4 Y546Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:57492307 G>A maps to NM_003153.4 N713N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:57500574 C>A maps to NM_003153.4 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:47733749 G>A maps to NM_017453.2 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:47768211 A>G maps to NM_017453.2 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:47734529 A>G maps to NM_017453.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr8:74601018 C>T maps to NM_001164380.1 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:74529630 C>A maps to NM_001164380.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr8:74526004 T>A maps to NM_001164380.1 K289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:23711961 G>A maps to NM_003155.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr5:172755118 G>A maps to NM_003714.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:172752951 G>A maps to NM_003714.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:172745041 G>A maps to NM_003714.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:172745182 G>A maps to NM_003714.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:172750286 C>T maps to NM_003714.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:89790589 C>T maps to ENST00000433102 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:89854449 A>G maps to NM_152999.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:89859244 T>G maps to NM_152999.3 Y360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr2:120003323 G>A maps to NM_182915.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr2:120003146 C>T maps to NM_182915.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr2:120020871 G>A maps to NM_182915.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:87912273 G>A maps to NM_024636.2 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:87912273 G>A maps to NM_024636.2 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:87913313 C>A maps to NM_024636.2 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr17:44076725 C>T maps to NM_001007532.2 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:47746464 G>T maps to NM_001048166.1 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:47767291 C>A maps to NM_001048166.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:47746581 G>T maps to NM_001048166.1 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr1:47746506 A>T maps to NM_001048166.1 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:4107743 G>A maps to NM_003156.3 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:3877577 T>C maps to NM_003156.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr4:27010418 A>G maps to ENST00000382009 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:27024323 T>C maps to ENST00000382009 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:27003939 G>T maps to ENST00000382009 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr4:27010416 C>T maps to ENST00000382009 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr4:27010418 A>G maps to ENST00000382009 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr4:27010416 C>T maps to ENST00000382009 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:27010418 A>T maps to ENST00000382009 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr4:27010418 A>T maps to ENST00000382009 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:27010418 A>G maps to ENST00000382009 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr11:63961671 A>G maps to ENST00000358794 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:63963152 C>T maps to ENST00000358794 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:63965010 T>A maps to ENST00000358794 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:63967491 C>T maps to ENST00000358794 N415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:63967672 G>T maps to ENST00000358794 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr11:63962066 C>T maps to ENST00000358794 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:171517333 C>G maps to NM_005990.3 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr5:171534842 C>T maps to NM_005990.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr5:171523444 G>A maps to NM_005990.3 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:171484379 C>A maps to NM_005990.3 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:171491741 C>T maps to NM_005990.3 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr5:171517245 T>A maps to NM_005990.3 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr19:1207082 A>G maps to NM_000455.4 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr19:1221209 A>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:1207167 C>A maps to NM_000455.4 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:1226541 C>T maps to NM_000455.4 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:1207169 A>G maps to NM_000455.4 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:1207117 C>A maps to NM_000455.4 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:1206953 G>A maps to NM_000455.4 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:1206968 G>T maps to NM_000455.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:1207091 C>T maps to NM_000455.4 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:1222982 G>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:1207203 T>A did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:1226510 C>T maps to NM_000455.4 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:1220434 C>T maps to NM_000455.4 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:1206956 C>T maps to NM_000455.4 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:1219358 G>A maps to NM_000455.4 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr19:1221209 A>G did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr19:1221209 A>G did not map to a codon.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr19:1221209 A>G did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr19:1221209 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:1219343 C>T maps to NM_000455.4 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:220466107 T>C maps to NM_052902.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:220478596 T>C maps to NM_052902.2 C898C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr2:220113175 G>A maps to ENST00000409260 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:220111585 A>G maps to ENST00000409260 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:43663331 C>T maps to NM_004760.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:197002221 G>A maps to NM_004226.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:197021245 A>C maps to NM_004226.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr6:31940169 T>C maps to NM_032454.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr13:99118653 G>T maps to NM_003576.3 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:99127563 C>A maps to NM_003576.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr13:99127546 G>A maps to NM_003576.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr2:242435832 G>A maps to NM_006374.3 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:242440934 G>A maps to NM_006374.3 C73C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:242438731 G>A maps to NM_006374.3 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr2:242435922 G>A maps to NM_006374.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:242438436 G>A maps to NM_006374.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:99718859 A>G maps to ENST00000354930 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:99591933 A>G maps to ENST00000354930 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:99718795 C>A maps to ENST00000354930 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:23776604 G>T maps to NM_031414.3 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:23854761 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:23810667 T>C maps to NM_031414.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr7:23810667 T>C maps to NM_031414.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:23808682 A>T maps to NM_031414.3 K496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr5:146703580 C>A maps to NM_001112724.1 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:5418602 G>A maps to NM_018401.1 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr4:5170124 C>A maps to NM_018401.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr4:5461852 C>T maps to NM_018401.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr4:5469788 C>T maps to NM_018401.1 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:5333027 G>A maps to NM_018401.1 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:5170043 C>T maps to NM_018401.1 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:5458538 G>A maps to NM_018401.1 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:5468557 G>A maps to NM_018401.1 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:5500695 C>A maps to NM_018401.1 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:5053595 C>T maps to NM_018401.1 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr4:5418602 G>A maps to NM_018401.1 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:8478989 C>A maps to NM_030906.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr11:8483429 A>G maps to NM_030906.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr11:8474432 C>T maps to NM_030906.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr11:8414137 G>T maps to NM_030906.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:8457637 A>G maps to NM_030906.2 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:8435221 C>T maps to NM_030906.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr20:2097672 G>A maps to NM_080836.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:219538657 C>T maps to NM_015690.3 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr2:219559279 T>C maps to NM_015690.3 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr2:219563458 G>A maps to NM_015690.3 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:219538430 G>T maps to NM_015690.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr2:219563821 T>C maps to NM_015690.3 P1185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:36483213 C>T maps to NM_007271.2 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr6:36507889 A>G maps to NM_007271.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr12:27465525 T>C maps to NM_015000.3 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:27461279 A>G maps to NM_015000.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr12:27461381 A>G maps to NM_015000.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:168931675 A>G maps to NM_013233.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:169038577 A>C maps to NM_013233.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr20:43629840 C>T maps to NM_006282.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr1:36814406 C>A maps to ENST00000373130 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:36823911 C>A maps to ENST00000373130 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr8:80577063 G>A maps to NM_007029.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr20:62275629 G>A maps to NM_015894.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr8:27099213 C>T maps to NM_030795.2 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:39541000 G>A maps to NM_145286.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:48809589 A>G maps to NM_172311.2 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:48809430 G>C maps to NM_172311.2 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:48809254 G>T maps to NM_172311.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:48808876 G>T maps to NM_172311.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr2:48808143 G>T maps to NM_172311.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:81743302 G>A maps to NM_033104.2 Y784Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr14:81862319 C>T maps to NM_033104.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:70646060 G>T maps to NM_001130161.2 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:70644709 A>G maps to NM_001130161.2 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr4:184931031 C>T maps to NM_020225.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:184930804 C>A maps to NM_020225.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:184931442 C>T maps to NM_020225.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:184931052 C>T maps to NM_020225.1 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:74489765 T>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:74487990 A>G maps to NM_001142620.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr7:134927533 G>A maps to NM_182489.1 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:134943241 T>G maps to NM_182489.1 *331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:134927582 C>T maps to NM_182489.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr7:134925468 G>C did not map to a codon.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr17:61781385 C>A maps to NM_001003787.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:202340379 G>T maps to NM_018571.5 G155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:202343321 A>G maps to NM_018571.5 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:202343321 A>G maps to NM_018571.5 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:16042943 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:16036523 A>C maps to ENST00000025399 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr12:16050902 T>C maps to ENST00000025399 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:125895238 G>A maps to NM_018387.4 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr9:125920703 A>G maps to NM_018387.4 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr9:125920703 A>G maps to NM_018387.4 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:125887899 A>C maps to NM_018387.4 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:125895151 C>T maps to NM_018387.4 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:125920703 A>G maps to NM_018387.4 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr9:125920703 A>G maps to NM_018387.4 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr15:43900092 G>A maps to NM_153700.2 N1254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:43900288 G>A maps to NM_153700.2 R1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:43892846 G>C maps to NM_153700.2 L1626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:37126773 G>A maps to NM_003162.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:37129803 C>T maps to NM_003162.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:7252076 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:7175328 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:7177634 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:7177530 C>T did not map to a codon.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr23:7175298 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:7171330 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr23:7194043 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:7267956 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:7267968 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:7243377 A>C did not map to a codon.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr23:7268150 C>T did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:7223222 A>T did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:7175603 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:7223115 A>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr11:125484066 G>A maps to NM_152713.3 W547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:31663651 T>A maps to NM_178862.1 L464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:31656600 T>C maps to NM_178862.1 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:31661278 C>T maps to NM_178862.1 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr16:732018 G>T did not map to a codon.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr6:144508324 C>T maps to NM_003764.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:144508279 C>T maps to NM_003764.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:28146225 C>T maps to ENST00000373939 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:28146225 C>T maps to ENST00000373939 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:28120118 C>T maps to ENST00000373939 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr1:28146182 A>G maps to ENST00000373939 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr4:4421784 G>A maps to NM_016930.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:131293186 G>A maps to NM_194356.1 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:131291629 C>T maps to NM_194356.1 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr12:131297508 C>T maps to NM_194356.1 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:59562907 C>T maps to NM_004177.4 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:59556355 T>C maps to NM_004177.4 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:31050926 G>A maps to NM_004604.3 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:62594832 G>A maps to NM_003164.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:180959119 C>T maps to NM_005819.4 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:132796799 A>G maps to NM_003569.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:132793476 C>A maps to NM_003569.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:132793476 C>A maps to NM_003569.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:7706970 C>T maps to ENST00000441779 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:7704614 A>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:109321906 G>T did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr1:109325070 G>A maps to NM_007269.2 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr1:109315284 A>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:53237205 G>A maps to NM_178509.5 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:53156093 A>G maps to NM_178509.5 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:147660521 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:147525742 G>A maps to NM_001127715.1 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:147648353 T>G maps to NM_001127715.1 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:147684798 C>T maps to NM_001127715.1 C958C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:147704026 C>T maps to NM_001127715.1 R1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:120941990 G>A maps to NM_014980.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:121097678 C>T maps to NM_014980.2 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:120673815 C>T maps to NM_014980.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:10772760 G>A maps to NM_018423.2 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:53224042 G>T maps to NM_145251.3 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr13:48547445 C>A maps to NM_003850.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr13:48542865 A>G maps to NM_003850.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr13:48542865 A>G maps to NM_003850.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:84668526 A>C maps to NM_003849.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:67570980 G>A maps to NM_003848.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:67579539 A>C maps to NM_003848.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:67578594 C>T maps to NM_003848.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:67451203 T>C maps to NM_003848.3 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr3:151599308 A>G maps to NM_033050.4 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:118848934 C>A maps to NM_022491.2 C287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:104359301 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:104386942 C>T maps to NM_016169.3 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:53232567 C>A maps to NM_001130912.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr13:53237240 T>C maps to NM_001130912.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr8:70550791 T>C maps to NM_001128206.1 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr8:70533457 G>A maps to NM_001128206.1 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr8:70550806 G>A maps to NM_001128206.1 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:70515483 G>A maps to NM_001128206.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:70533398 G>T maps to NM_001128206.1 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:70541765 A>G maps to NM_001128206.1 K712K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:46365633 C>T maps to NM_001161841.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:46365452 G>T maps to NM_001161841.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr20:46365452 G>T maps to NM_001161841.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr20:46365450 C>A maps to NM_001161841.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr20:46365452 G>T maps to NM_001161841.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr20:46365633 C>T maps to NM_001161841.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr20:46365452 G>T maps to NM_001161841.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr20:46365452 G>T maps to NM_001161841.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr20:46365477 G>T maps to NM_001161841.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr20:46365452 G>T maps to NM_001161841.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:28617186 C>T maps to NM_177529.1 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:28619858 G>A maps to NM_177529.1 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:28604820 T>C maps to NM_001054.3 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr16:28604868 G>A maps to NM_001054.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:108921076 C>T maps to ENST00000437390 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:109002691 G>A maps to NM_006588.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:70721060 G>A maps to NM_005420.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:70721109 G>A maps to NM_005420.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:70721060 G>A maps to NM_005420.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:48386923 T>C maps to NM_003167.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:49090612 G>A maps to NM_177973.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr22:44229555 C>T maps to NM_014351.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr22:44229588 G>A maps to NM_014351.3 H178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:44224991 G>A maps to NM_014351.3 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:37406711 G>A maps to NM_001032377.1 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:37406711 G>A maps to NM_001032377.1 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr2:37398685 A>G maps to NM_001032377.1 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:37398685 A>G maps to NM_001032377.1 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr2:37398685 A>G maps to NM_001032377.1 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr2:37406691 T>A maps to NM_001032377.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:56132066 G>A maps to ENST00000395437 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr21:46233929 C>T maps to ENST00000411651 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:905625 C>T maps to ENST00000456758 Y823Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:893230 C>T maps to ENST00000456758 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:905655 T>C maps to ENST00000456758 F833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:892252 C>T maps to ENST00000456758 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:899820 C>T maps to ENST00000456758 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr22:39144766 C>T maps to ENST00000405018 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr22:39134711 G>A maps to ENST00000405018 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr22:39136370 G>A maps to ENST00000405018 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr22:39146275 G>A maps to ENST00000405018 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:48068433 G>A maps to NM_152782.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr7:48034019 G>A maps to NM_152782.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:48068418 C>T maps to NM_152782.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:48035666 A>G maps to NM_152782.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr7:48046773 C>T maps to NM_152782.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr7:48046773 C>T maps to NM_152782.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:31577456 G>T maps to NM_080675.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr20:31573703 G>A maps to NM_080675.3 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr12:56398447 C>G maps to NM_001032387.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:56397712 T>C maps to NM_001032387.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:21827735 C>T maps to NM_007192.3 T736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:21831293 T>G maps to NM_007192.3 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:44929546 G>A maps to NM_181356.1 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:44929546 G>A maps to NM_181356.1 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:44971494 T>C maps to NM_181356.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr6:44971496 T>A maps to NM_181356.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:44971494 T>C maps to NM_181356.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr6:44971494 T>C maps to NM_181356.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:44971494 T>C maps to NM_181356.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:44971503 C>T maps to NM_181356.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr17:56424895 G>A maps to NM_003168.1 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr19:39963691 C>A maps to NM_003169.3 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:39960838 C>T maps to NM_003169.3 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:39963908 G>A maps to NM_003169.3 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:39965026 G>A maps to NM_003169.3 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:39948327 G>A maps to NM_003169.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr19:39959441 G>T maps to NM_003169.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:27015218 G>A maps to NM_003170.3 T1039T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr17:27000472 T>C maps to NM_003170.3 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:27014203 C>T maps to NM_003170.3 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:27022440 C>T maps to NM_003170.3 R1282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:27011612 C>T maps to NM_003170.3 R747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:27011879 C>T maps to NM_003170.3 C796C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr17:27010323 T>G maps to NM_003170.3 Y639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:27024642 C>T maps to NM_003170.3 F1405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:27880451 G>A maps to NM_014860.1 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr10:70968637 A>G maps to NM_003171.3 R736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:70949118 A>G maps to NM_003171.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:70945749 A>C maps to NM_003171.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:136227993 C>T maps to NM_017503.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:136227276 C>T maps to NM_017503.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:136230467 G>A maps to NM_033161.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr9:136233510 G>A maps to NM_033161.2 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:136233543 G>A maps to NM_033161.2 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:136199078 G>A maps to NM_006753.4 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:136198935 G>A maps to NM_006753.4 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:114873964 C>T maps to NM_022486.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:114904606 A>G maps to NM_022486.3 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:114886579 G>A maps to NM_022486.3 C281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr22:24584247 G>A maps to NM_019601.3 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr22:24580146 G>T maps to NM_019601.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr22:24579055 C>T maps to NM_019601.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr22:24579055 C>T maps to NM_019601.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr9:95840269 C>A maps to NM_145006.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:223396759 C>T maps to NM_017982.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:223465961 G>A maps to NM_017982.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:223401039 C>T maps to NM_017982.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:33195088 A>G maps to NM_015551.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr3:33249324 G>C maps to NM_015551.1 Y128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:33195328 G>T maps to NM_015551.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:33194236 G>T maps to NM_015551.1 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr3:33216567 T>C did not map to a codon.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr23:48564663 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:48564954 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:48564735 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:48559091 G>A did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr23:48564908 G>C did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:48558949 C>T did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:48557329 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:14939185 C>T maps to NM_001193424.1 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:67926105 C>T maps to NM_017635.3 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:67939037 C>T maps to NM_017635.3 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:67925553 G>A maps to NM_017635.3 N753N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr11:67925529 C>T maps to NM_017635.3 K761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:67938554 C>A maps to NM_017635.3 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr11:67925802 A>G maps to NM_017635.3 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:67939031 A>G maps to NM_017635.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr11:67925802 A>G maps to NM_017635.3 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:67925802 A>G maps to NM_017635.3 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:55857660 C>T maps to NM_032701.3 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr17:30267330 C>T maps to NM_015355.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr17:30303571 C>T maps to NM_015355.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr1:149883482 A>G maps to NM_014849.3 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:149884971 G>A maps to NM_014849.3 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:149882229 G>T maps to NM_014849.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr1:149882489 G>A maps to NM_014849.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:149881363 G>A maps to NM_014849.3 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:149877580 G>A maps to NM_014849.3 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr1:149881105 C>T maps to NM_014849.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr1:149879664 G>A maps to NM_014849.3 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:149881352 T>C maps to NM_014849.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:91827398 G>T maps to NM_014848.4 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:91835780 G>A maps to NM_014848.4 *684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:91769648 T>C maps to NM_014848.4 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:91835652 A>G maps to NM_014848.4 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:75427679 C>T maps to NM_014979.1 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:75427934 G>A maps to NM_014979.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr9:113312288 C>T maps to ENST00000374463 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:113139553 C>A maps to ENST00000374463 E3504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:113168921 T>C maps to ENST00000374463 S2989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:113170424 G>A maps to ENST00000374463 H2488H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:113205879 G>A maps to ENST00000374463 I1528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:113192602 G>T maps to ENST00000374463 I1830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:113163283 A>G maps to ENST00000374463 D3227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr9:113208196 G>A maps to ENST00000374463 D1461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:113166813 C>T maps to ENST00000374463 T3156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:113173369 T>C maps to ENST00000374463 P2210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:113137743 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:113189926 G>T maps to ENST00000374463 V1976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:113166750 G>T maps to ENST00000374463 I3177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr9:113194309 G>A maps to ENST00000374463 V1749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr9:113265468 C>T maps to ENST00000374463 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr9:113341673 G>T maps to ENST00000374463 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr10:29839608 G>A maps to NM_021738.2 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:29822200 A>G maps to NM_021738.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr10:29818641 G>A maps to NM_021738.2 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:29754656 C>T maps to NM_021738.2 A2000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:29762862 G>A maps to NM_021738.2 C1811C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:29779941 C>T maps to NM_021738.2 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:29762862 G>A maps to NM_021738.2 C1811C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:29782171 G>A maps to NM_021738.2 F1330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr10:29813619 C>T maps to NM_021738.2 K789K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr10:29821007 A>G maps to NM_021738.2 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr10:29821007 A>G maps to NM_021738.2 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:29769679 C>T maps to NM_021738.2 T1721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:29822010 C>A maps to NM_021738.2 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:29747365 G>A maps to NM_021738.2 F2185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr10:29839779 G>A maps to NM_021738.2 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr10:29754533 C>T maps to NM_021738.2 A2041A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr10:29812601 G>T maps to NM_021738.2 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:109311851 T>C maps to NM_018711.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:138281212 G>A maps to NM_001139456.1 C472C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr11:9746380 T>A maps to NM_015055.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:9735173 T>C maps to NM_015055.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:16761841 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:16775420 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:110631116 C>T maps to NM_001099744.1 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:115489937 G>A maps to NM_003176.2 E773E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:115418730 G>A maps to NM_003176.2 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:115454107 A>G maps to NM_003176.2 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:115466094 G>T maps to NM_003176.2 E582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:115488941 C>T maps to NM_003176.2 D729D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:115430286 G>T maps to NM_003176.2 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr20:58448982 T>C maps to NM_014258.2 S1161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:58476773 G>A maps to NM_014258.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:58476793 C>A maps to NM_014258.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:58475831 C>T maps to NM_014258.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:58467200 C>T maps to NM_014258.2 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:58461867 C>A maps to NM_014258.2 E796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr20:58441386 T>C maps to NM_014258.2 K1427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr20:58441386 T>C maps to NM_014258.2 K1427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr20:58441386 T>C maps to NM_014258.2 K1427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr20:58441386 T>C maps to NM_014258.2 K1427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:10961773 T>A maps to NM_001040274.2 C799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:10903166 C>T maps to NM_001040274.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:10931722 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:10961613 G>T maps to NM_001040274.2 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:10912973 C>T maps to NM_001040274.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr6:10961755 T>C maps to NM_001040274.2 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr6:10928673 G>A maps to NM_001040274.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr6:10907805 G>A maps to NM_001040274.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr6:10930667 T>C maps to NM_001040274.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:10907805 G>A maps to NM_001040274.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:15220056 C>T maps to NM_033025.4 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:15224674 C>T maps to NM_033025.4 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:15220791 G>A maps to NM_033025.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:15224662 C>T maps to NM_033025.4 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:85648050 A>C maps to NM_032184.1 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:85665971 G>A maps to NM_032184.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:93624610 C>T maps to NM_003177.5 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr19:46345574 C>T maps to NM_004819.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr19:46334688 C>T maps to NM_004819.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:46332316 G>A maps to NM_004819.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:47435565 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:47466387 G>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:47435899 T>C did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:47435933 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:47464418 G>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:47434142 C>T did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:47433414 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:12187196 C>T maps to NM_133625.3 F181F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-A010-01A-01W-A00E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr3:12203086 C>T maps to NM_133625.3 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:33402392 C>T maps to NM_003490.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:32937578 C>A maps to NM_003490.3 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:86324791 G>A maps to NM_006372.4 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:86329125 G>A maps to NM_006372.4 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:86324965 A>C maps to NM_006372.4 Y460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:152527407 G>A maps to NM_182961.2 G7638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:152823836 G>T maps to NM_182961.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr6:152806046 G>A maps to NM_182961.2 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr6:152683343 C>T maps to NM_182961.2 A3420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:152623192 C>T maps to NM_182961.2 L5784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr6:152651647 C>T maps to NM_182961.2 A4724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr6:152615103 T>C maps to NM_182961.2 L5947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:152680527 G>A maps to NM_182961.2 G3455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr6:152541997 G>T maps to NM_182961.2 A7280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr6:152477148 G>A maps to NM_182961.2 D7958D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:152702374 G>T maps to NM_182961.2 A2925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr6:152711422 G>A maps to NM_182961.2 H2723H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr6:152469480 C>T maps to NM_182961.2 R8225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:152716765 C>A maps to NM_182961.2 E2533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr6:152652715 G>A maps to NM_182961.2 A4368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr6:152464859 G>T maps to NM_182961.2 G8339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:152655306 T>C maps to NM_182961.2 E4210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr6:152749407 G>A maps to NM_182961.2 Y1636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:152590403 C>T maps to NM_182961.2 K6197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:152651359 G>A maps to NM_182961.2 S4820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:152770769 A>C maps to NM_182961.2 S1134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:152614839 C>T maps to NM_182961.2 Q5965Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:152771896 C>T maps to NM_182961.2 V1086V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr6:152453310 G>T maps to NM_182961.2 T8680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:152605205 C>T maps to NM_182961.2 A6038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:152728312 C>A maps to NM_182961.2 E2187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:152861102 G>A maps to NM_182961.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr6:152558008 G>A maps to NM_182961.2 S6714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr6:152716781 C>A maps to NM_182961.2 L2527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:152631869 G>A maps to NM_182961.2 R5617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:152631995 C>A maps to NM_182961.2 E5575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:152651911 G>A maps to NM_182961.2 V4636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:152652873 C>A maps to NM_182961.2 E4316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:152545655 A>G maps to NM_182961.2 A7165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:152638049 G>A maps to NM_182961.2 V5548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:152646404 C>T maps to NM_182961.2 E5157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:152711566 A>G maps to NM_182961.2 G2675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:152774789 G>A maps to NM_182961.2 T986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:152782857 C>A maps to NM_182961.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:152831499 C>A maps to NM_182961.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:152841605 G>A maps to NM_182961.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:152461138 A>G maps to NM_182961.2 R8468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr6:152461264 G>A maps to NM_182961.2 A8426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr6:152565761 T>C maps to NM_182961.2 K6534K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:152639374 G>A maps to NM_182961.2 G5471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:152589224 G>A maps to NM_182961.2 Q6261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:152638049 G>T maps to NM_182961.2 V5548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:152683408 G>A maps to NM_182961.2 R3399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr6:152720817 T>C maps to NM_182961.2 E2390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:152552672 C>T maps to NM_182961.2 Q6964Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:152557360 G>T maps to NM_182961.2 S6759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr6:152762297 C>T maps to NM_182961.2 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:152589201 A>G maps to NM_182961.2 S6268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:152640072 A>C maps to NM_182961.2 A5438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:152642908 C>A maps to NM_182961.2 E5344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:152644800 C>T maps to NM_182961.2 S5243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:152652873 C>A maps to NM_182961.2 E4316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:152717919 C>A maps to NM_182961.2 E2516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:152754988 C>A maps to NM_182961.2 E1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:152762365 C>A maps to NM_182961.2 E1350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:152527407 G>A maps to NM_182961.2 G7638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:152697631 G>A maps to NM_182961.2 R3070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr6:152629718 G>A maps to NM_182961.2 Q5751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr6:152629718 G>A maps to NM_182961.2 Q5751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:152510428 G>A maps to NM_182961.2 R7753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr6:152738117 G>A maps to NM_182961.2 G1818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr6:152477048 G>A maps to NM_182961.2 L7992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr6:152763329 G>T maps to NM_182961.2 I1296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:152605133 C>T maps to NM_182961.2 S6062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:152674828 T>C maps to NM_182961.2 G3659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr6:152826407 G>A maps to NM_182961.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:152443750 G>A maps to NM_182961.2 R8738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr6:152541997 G>T maps to NM_182961.2 A7280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:152527367 C>A maps to NM_182961.2 E7652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:152665262 C>A maps to NM_182961.2 E4060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:152462374 G>T maps to NM_182961.2 G8403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:64589030 C>T maps to NM_182914.2 D4436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:64593398 C>T maps to NM_182914.2 G4597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr14:64489534 C>A maps to NM_182914.2 S1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:64488163 C>T maps to NM_182914.2 I1761I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:64669641 C>T maps to NM_182914.2 C6054C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:64681006 C>T maps to NM_182914.2 S6384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr14:64641825 G>A maps to NM_182914.2 E5800E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:64522759 C>A maps to NM_182914.2 P3281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:64537472 A>G maps to NM_182914.2 L3514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr14:64416698 T>C maps to NM_182914.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr14:64516547 G>T maps to NM_182914.2 E2533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:64596923 C>T maps to NM_182914.2 T4766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:64596827 C>T maps to NM_182914.2 F4734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr14:64586323 T>C maps to NM_182914.2 D4340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr14:64469652 A>G maps to NM_182914.2 T1334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:64557766 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:64689929 A>G maps to NM_182914.2 E6738E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr14:64516516 C>A maps to NM_182914.2 L2522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:64529564 G>A maps to NM_182914.2 S3388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:64453239 G>T maps to NM_182914.2 E740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:64483205 G>T maps to NM_182914.2 E1582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:64516567 G>A maps to NM_182914.2 L2539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:64519712 G>T maps to NM_182914.2 E3028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:64560099 G>T maps to NM_182914.2 E4004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr14:64632035 C>A maps to NM_182914.2 R5505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr14:64457274 A>G maps to NM_182914.2 K820K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:64518439 T>C maps to NM_182914.2 L2603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr14:64689908 A>G maps to NM_182914.2 Q6731Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr14:64604639 C>T maps to NM_182914.2 L4928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr14:64516516 C>A maps to NM_182914.2 L2522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr14:64461921 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:64564806 G>A maps to NM_182914.2 L4083L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr14:64516516 C>A maps to NM_182914.2 L2522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr14:64689908 A>G maps to NM_182914.2 Q6731Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr14:64457274 A>G maps to NM_182914.2 K820K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:64460566 T>C maps to NM_182914.2 I887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:64463846 G>A maps to NM_182914.2 Q1041Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:64676718 C>T maps to NM_182914.2 Y6200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr14:64680985 T>C maps to NM_182914.2 S6377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:33412219 G>A did not map to a codon.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr6:33408580 C>T maps to NM_006772.2 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:33419592 G>A maps to NM_006772.2 P1314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:39777879 C>T maps to NM_004711.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr22:39772090 C>T maps to NM_004711.4 C124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:76167860 C>T maps to NM_004710.3 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr17:76166902 C>T maps to NM_004710.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:76167905 C>T maps to NM_004710.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:2043015 G>A maps to NM_004209.5 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:48869126 C>T maps to NM_012451.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr21:34045775 G>A maps to NM_003895.3 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr21:34011411 G>A maps to NM_003895.3 L1280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr21:34072302 G>A maps to NM_003895.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:34045775 G>A maps to NM_003895.3 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:34012086 C>T maps to NM_003895.3 T1236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr21:34053868 G>A maps to NM_003895.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:34012086 C>T maps to NM_003895.3 T1236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:34072236 A>G maps to NM_003895.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr21:34030179 A>C maps to NM_003895.3 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr21:34038795 C>T maps to NM_003895.3 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr21:34011220 C>T maps to NM_003895.3 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr21:34067555 G>A maps to NM_003895.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr21:34058110 G>A maps to NM_003895.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr21:34011220 C>T maps to NM_003895.3 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr21:34004042 C>T maps to NM_003895.3 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:158438263 A>G maps to NM_003898.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:158490642 G>A maps to NM_003898.3 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:158454666 C>A maps to NM_003898.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:158490642 G>A maps to NM_003898.3 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:158505198 G>A maps to NM_003898.3 T1067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:158483160 C>T maps to NM_003898.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:158454576 C>T maps to NM_003898.3 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr15:99671579 C>G maps to ENST00000336292 V1004V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:99670217 G>A maps to ENST00000336292 Q550Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr15:99670385 C>T maps to ENST00000336292 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:99666942 G>T maps to ENST00000336292 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:99671358 G>T maps to ENST00000336292 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:99673043 G>A maps to ENST00000336292 A1492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:99670895 G>A maps to ENST00000336292 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr5:150028274 G>A maps to NM_001166209.1 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:150028109 G>A maps to NM_001166209.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:150029162 C>T maps to NM_001166209.1 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:119952995 G>A maps to NM_133477.2 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:119951678 C>T maps to NM_133477.2 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr4:119951285 C>T maps to NM_133477.2 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr4:119951127 C>T maps to NM_133477.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:119978888 A>C maps to NM_133477.2 R1196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr4:119952722 G>A maps to NM_133477.2 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:119951018 C>T maps to NM_133477.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:119951693 G>A maps to NM_133477.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:119948012 C>T maps to NM_133477.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr4:119952995 G>A maps to NM_133477.2 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr4:119958313 C>T maps to NM_001128934.1 Y1100Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:119948054 C>T maps to NM_133477.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:119947835 C>T maps to NM_133477.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:119952845 C>A maps to NM_133477.2 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:119951741 G>A maps to NM_133477.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr4:119948243 C>T maps to NM_133477.2 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr4:119948252 G>T maps to NM_133477.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr4:119952605 G>A maps to NM_133477.2 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:75408401 G>A maps to NM_001114133.1 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:75408419 C>G maps to NM_001114133.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr10:75413202 G>A maps to NM_001114133.1 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr10:75410675 C>T maps to NM_024875.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr17:35902212 C>A maps to NM_007247.4 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:35902212 C>T maps to NM_007247.4 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr17:35913745 A>G maps to NM_007247.4 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:35896148 G>A maps to NM_007247.4 Q1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:35902341 C>T maps to NM_007247.4 K978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:35921354 A>T maps to NM_007247.4 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:35902212 C>A maps to NM_007247.4 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr17:35902212 C>A maps to NM_007247.4 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr17:35902213 G>T maps to NM_007247.4 S1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:35899311 G>A maps to NM_007247.4 C1134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr17:35902212 C>T maps to NM_007247.4 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr17:35902212 C>A maps to NM_007247.4 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr23:49054292 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:49054199 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:49054187 G>A did not map to a codon.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr23:49049789 T>C did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:49049790 G>A did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr1:110019430 C>T maps to NM_001040709.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:110020564 C>A maps to NM_001040709.1 C194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:110022001 C>A maps to NM_001040709.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:110009709 G>A maps to NM_001040709.1 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr1:110019430 C>T maps to NM_001040709.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:43995655 C>T maps to NM_033542.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:79679573 G>A maps to NM_005639.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:79693258 C>T maps to NM_005639.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr12:79679693 G>T maps to NM_005639.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:79679630 T>C maps to NM_005639.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:79693162 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:33560220 C>A maps to NM_198992.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:33579260 A>T maps to NM_198992.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr12:33579431 T>A did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:155838164 T>C maps to NM_152280.4 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:66802239 G>A maps to NM_001177880.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:66807514 C>T maps to NM_001177880.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:66813320 C>A maps to NM_001177880.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:66802239 G>A maps to NM_001177880.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:45277388 G>A maps to NM_020826.2 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:45275827 G>A maps to NM_020826.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:45274157 G>T maps to NM_020826.2 T220T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A6-3809-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr1:210187083 C>T maps to NM_001146261.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr1:210334371 G>A maps to NM_001146261.1 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:210334158 T>C maps to NM_001146261.1 N544N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr1:210273757 A>G maps to NM_001146261.1 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr1:210334242 A>G maps to NM_001146261.1 K572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr1:210194567 T>C maps to NM_001146261.1 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr1:210329076 C>T maps to NM_001146261.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr10:46961993 C>T maps to NM_031912.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr10:46961978 C>T maps to NM_031912.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr10:46967614 C>T maps to NM_031912.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr14:62550996 G>A maps to NM_031914.2 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr14:62567224 C>T maps to NM_031914.2 Q580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr14:62463201 A>G maps to NM_031914.2 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:62462769 G>A maps to NM_031914.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:19191847 G>A maps to NM_016524.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr16:19191754 C>T maps to NM_016524.2 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:19191784 G>A maps to NM_016524.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:202566070 G>A maps to NM_177402.4 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr1:202568417 G>T maps to NM_177402.4 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:51135706 A>G maps to NM_001160329.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:51128801 G>A maps to NM_001160329.1 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:51128445 G>A maps to NM_001160329.1 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:40853909 C>A maps to NM_020783.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:40850374 C>T maps to NM_020783.3 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:40854303 G>T maps to NM_020783.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:40853588 C>A maps to NM_020783.3 G269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:55686626 G>A maps to NM_003180.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr19:55686337 G>A maps to NM_003180.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:55687088 G>T maps to NM_003180.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:55690400 C>T maps to NM_003180.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:114641765 C>T maps to ENST00000369545 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:114646337 G>A maps to ENST00000369545 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr1:114646298 C>G maps to ENST00000369545 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:61323668 C>T maps to NM_004200.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr11:61300522 G>T maps to NM_004200.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr11:1858193 C>T maps to NM_138567.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:1857138 G>A maps to NM_138567.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:1857728 G>A maps to NM_138567.3 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:7324621 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:7324273 C>T maps to NM_175733.3 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:7439293 C>A maps to NM_175733.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:7439225 C>T maps to NM_175733.3 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr11:7439230 G>A maps to NM_175733.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:27677361 C>T maps to NM_001193308.1 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr11:85429863 C>T maps to ENST00000359152 Q1374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr11:85435588 G>A maps to ENST00000359152 F1161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:85435180 C>T maps to ENST00000359152 S1297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:85436830 G>A maps to ENST00000359152 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr11:85445216 A>T maps to NM_001162953.1 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:85435180 C>T maps to ENST00000359152 S1297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:85445573 C>T maps to NM_001162953.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:85431934 G>T maps to ENST00000359152 S1355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:85435747 T>C maps to ENST00000359152 V1108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:85445348 C>T maps to NM_001162953.1 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:85436341 C>T maps to ENST00000359152 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr11:85436341 C>A maps to ENST00000359152 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr11:85436929 T>C maps to ENST00000359152 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr11:85425536 A>G maps to ENST00000359152 P1389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:85436020 C>T maps to ENST00000359152 T1017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:159166651 C>T maps to ENST00000297239 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:159184392 G>A maps to ENST00000297239 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:99943431 T>C did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:99956564 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:99934349 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:99943434 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:99941054 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:99942063 G>A did not map to a codon.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr23:99956962 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:99936279 A>C did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:99941007 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:99941135 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:99945568 T>G did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:99942147 T>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:99943431 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:99942101 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:37965869 G>A did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr23:37984552 A>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:37965868 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:37981338 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:37893201 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:37969599 A>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:37981402 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:37961664 G>A did not map to a codon.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr23:37893173 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:37981417 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:37935842 C>T did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:64897271 A>G maps to NM_172230.2 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:64896086 C>T maps to NM_172230.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:64897594 A>G maps to NM_172230.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:166580268 G>A maps to NM_003181.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:166572003 G>A maps to NM_003181.2 N369N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:166572039 G>A maps to NM_003181.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:166576058 A>C maps to NM_003181.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr6:166576019 C>T maps to NM_003181.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:166576058 A>C maps to NM_003181.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr6:166580283 G>T maps to NM_003181.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:166580244 C>T maps to NM_003181.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:132966988 T>A maps to NM_138327.1 K52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:132938816 G>A maps to NM_001033080.1 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr6:132938831 A>T maps to NM_001033080.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:132938299 C>A maps to NM_001033080.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr6:132910099 C>A maps to NM_003967.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:132910783 C>T maps to NM_003967.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:132910242 G>A maps to NM_003967.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:132910611 G>A maps to NM_003967.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr6:132910498 C>T maps to NM_003967.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr6:132891645 G>A maps to NM_175067.1 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:132891879 T>C maps to NM_175067.1 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:132891885 C>A maps to NM_175067.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:132892143 G>A maps to NM_175067.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:132891744 G>A maps to NM_175067.1 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr6:132892221 A>G maps to NM_175067.1 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:132873971 T>C maps to NM_053278.1 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:132860060 C>T maps to NM_175057.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:132859790 T>C maps to NM_175057.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:132859535 C>T maps to NM_175057.3 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:39811627 C>T maps to NM_006116.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr22:39822772 C>T maps to NM_006116.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:149700454 C>A maps to NM_015093.4 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:149718855 C>T maps to NM_015093.4 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr23:30873228 T>C did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:30873228 T>C did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:30877627 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:30870904 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:30873031 C>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:30852222 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:30873228 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:30872750 C>T did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:30873228 T>C did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:30873038 G>A did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:30873484 T>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:30872960 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr7:97369204 A>G maps to NM_003182.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr7:97363588 T>C maps to NM_003182.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:97363097 C>T maps to NM_003182.2 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr12:57406183 C>T maps to NM_013251.3 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:38646224 G>A maps to ENST00000379931 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:38646224 G>A maps to ENST00000379931 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr10:123844543 C>T maps to NM_206862.2 D843D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:123844408 G>A maps to NM_206862.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:123846859 C>T maps to NM_206862.2 P1615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr10:123847354 G>A maps to NM_206862.2 G1780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:123844195 T>C maps to NM_206862.2 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:123848028 G>A maps to NM_206862.2 S1832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr10:123847145 C>T maps to NM_206862.2 L1711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:123844192 T>C maps to NM_206862.2 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:123845209 C>T maps to NM_206862.2 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:123844171 G>A maps to NM_206862.2 E719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:123846055 A>G maps to NM_206862.2 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:1746534 G>A maps to NM_006342.1 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:1737015 G>A maps to NM_006342.1 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:1730382 C>T maps to NM_006342.1 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr4:1730511 C>T maps to NM_006342.1 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr4:1729572 C>T maps to NM_006342.1 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:1730262 G>A maps to NM_006342.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr2:75347719 C>T maps to NM_001058.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:75425880 G>A maps to NM_001058.3 H60H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:75347719 C>T maps to NM_001058.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:75347719 C>T maps to NM_001058.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:75347749 G>A maps to NM_001058.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:75347749 G>A maps to NM_001058.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:75425724 G>A maps to NM_001058.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:75425859 C>T maps to NM_001058.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:75276648 C>T maps to NM_001058.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:75276649 G>T maps to NM_001058.3 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:71176052 T>C maps to NM_001057.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr10:71166847 G>A maps to NM_001057.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:104640595 C>A maps to NM_001059.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr4:104640589 C>T maps to NM_001059.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:104640661 C>T maps to NM_001059.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr4:104640415 C>T maps to NM_001059.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr4:104510898 A>G maps to NM_001059.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr4:104511030 G>A maps to NM_001059.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr1:166831526 A>G maps to NM_053053.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr4:7056537 C>T maps to NM_152293.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:9827054 C>A maps to NM_006354.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:9825890 C>T maps to NM_006354.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:9825722 G>A maps to NM_006354.2 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr23:70597458 C>T did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:70603818 A>G did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:70679461 C>A did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:70679537 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:70613303 C>T did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:70679536 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:70679457 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:70683798 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:70601644 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:70598177 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:70608155 A>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:70618465 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:70678208 T>G did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:70607289 G>A did not map to a codon.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr23:70598795 A>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:70613189 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:70601608 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:70612785 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:70621582 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:70603963 G>T did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:70602947 T>C did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:70679538 A>G did not map to a codon.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr23:70603819 A>G did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:70601607 T>C did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:70603818 A>G did not map to a codon.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr23:70602945 G>T did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:70602947 T>C did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:70679538 A>G did not map to a codon.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr23:70627866 A>G did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:70601608 T>C did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:70679538 A>G did not map to a codon.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr23:70602945 G>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:70627445 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:70602945 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:70601606 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:70603818 A>G did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:70602947 T>C did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:70679489 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr6:34850806 T>C maps to NM_005643.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:28931966 G>A maps to NM_005644.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr1:28931966 G>A maps to NM_005644.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:109607294 A>G maps to NM_005645.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr1:109607185 G>A maps to NM_005645.3 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:34171823 T>C maps to NM_139215.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr2:10073947 T>C maps to NM_005680.2 N534N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr2:10050866 G>T maps to NM_005680.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr16:84216897 C>T maps to NM_005679.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:84213446 G>A maps to NM_005679.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:84212909 C>T maps to NM_005679.2 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:84214793 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:93471367 C>T maps to NM_024116.3 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr9:32632682 A>G maps to NM_153809.2 C965C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr9:32635436 T>C maps to NM_153809.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:32635358 C>A maps to NM_153809.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr9:32635358 C>T maps to NM_153809.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr9:32633680 G>A maps to NM_153809.2 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:32635565 G>A maps to NM_153809.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:32635316 A>G maps to NM_153809.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:32632481 A>G maps to NM_153809.2 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr9:32630105 G>A maps to NM_153809.2 H1824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:32630501 G>T maps to NM_153809.2 V1692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:32635358 C>A maps to NM_153809.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:32635436 T>C maps to NM_153809.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr9:32631451 G>A maps to NM_153809.2 R1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:32635451 G>A maps to NM_153809.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:32635307 G>A maps to NM_153809.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr9:32632682 A>G maps to NM_153809.2 C965C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr9:32635358 C>T maps to NM_153809.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:32632174 G>A maps to NM_153809.2 Q1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr9:32635436 T>C maps to NM_153809.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr9:32632682 A>G maps to NM_153809.2 C965C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:120774769 C>A maps to NM_003184.3 E815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr8:120772950 C>T maps to NM_003184.3 Q862Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:120797468 C>A maps to NM_003184.3 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr8:120810026 A>G maps to NM_003184.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:7866477 G>T maps to NM_031923.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:8007450 G>T maps to NM_031923.2 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr10:8006453 G>A maps to NM_031923.2 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:60572662 C>A maps to NM_003185.3 A1011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:60575613 C>A maps to NM_003185.3 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr20:60585122 G>A maps to NM_003185.3 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:60587936 C>T maps to NM_003185.3 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr18:23845164 G>A maps to ENST00000418698 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:23901112 C>T maps to ENST00000418698 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr18:23866114 T>G maps to ENST00000418698 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr18:23865899 C>T maps to ENST00000418698 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr18:23969974 G>A maps to ENST00000418698 *868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:105138144 G>A maps to NM_006951.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:105139436 G>T maps to NM_006951.3 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:229738235 G>A maps to NM_014409.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:99709847 C>T maps to ENST00000472509 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr7:99709350 G>A maps to ENST00000472509 Y357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:99704904 G>A maps to ENST00000472509 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:99707696 C>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr11:62545580 T>C maps to NM_006473.2 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:62554020 C>A maps to NM_006473.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:62549388 G>A maps to NM_006473.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:62549403 G>A maps to NM_006473.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr11:62545451 T>C maps to NM_006473.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr23:100531071 T>A did not map to a codon.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr23:100547927 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:100531345 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:100542484 A>C did not map to a codon.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr23:100531072 T>C did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:100531071 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:100536758 C>T did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:100531073 T>C did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:100531073 T>C did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:100531073 T>C did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:100532668 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr5:68661330 G>A maps to NM_001015892.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr5:68661387 G>A maps to NM_001015892.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:77387155 T>G did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:77394406 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:77393554 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:159461768 G>A maps to NM_054114.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr6:159456975 C>T maps to NM_054114.3 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr6:159457956 T>C maps to NM_054114.3 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr1:159888625 G>A maps to ENST00000368096 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:159890170 G>A maps to ENST00000368096 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:111732265 G>A maps to NM_001008272.1 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:47685460 C>T maps to ENST00000371883 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:108424992 G>A maps to NM_005421.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr11:760169 C>T maps to NM_006755.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr11:763909 C>T maps to NM_006755.1 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:160087102 G>A maps to NM_033394.2 P1722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:160050910 C>T maps to NM_033394.2 D962D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:160043534 G>A maps to NM_033394.2 K914K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:160042334 G>A maps to NM_033394.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:160028665 G>A maps to NM_033394.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:61482552 G>T maps to ENST00000389520 V1060V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:61176578 C>T maps to ENST00000389520 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:61497575 C>T maps to ENST00000389520 F1421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:61499297 C>T maps to ENST00000389520 F1995F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:61497365 C>T maps to ENST00000389520 F1351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr17:61499297 C>T maps to ENST00000389520 F1995F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:61499219 C>T maps to ENST00000389520 Y1969Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:61278205 C>T maps to ENST00000389520 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:61498967 C>T maps to ENST00000389520 T1885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:61278298 C>T maps to ENST00000389520 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:61498205 C>T maps to ENST00000389520 A1631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:162036190 C>T maps to NM_004180.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:162081147 T>C maps to NM_004180.2 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:27802704 T>C maps to NM_020791.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:27861258 C>T maps to NM_020791.2 R829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr17:27834911 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:27861258 C>T maps to NM_020791.2 R829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr16:29998274 A>T maps to NM_016151.2 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:29998922 T>C maps to NM_016151.2 G1110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:29994200 C>T maps to NM_016151.2 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:29994885 G>A maps to NM_016151.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:29994523 C>T maps to NM_016151.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:29998805 G>A maps to NM_016151.2 R1071R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr12:118619363 G>A maps to NM_016281.3 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:118599786 G>A maps to NM_016281.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:32821020 C>T maps to NM_000593.5 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr6:32815314 A>G maps to NM_000593.5 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:32813559 C>T maps to NM_000593.5 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr6:32821060 G>C maps to NM_000593.5 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:32818270 T>C maps to NM_000593.5 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:32818212 G>A maps to NM_000593.5 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:32800562 C>T maps to ENST00000452392 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:32805411 A>G maps to ENST00000452392 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:32797241 G>A maps to ENST00000452392 R623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:32803462 G>T maps to ENST00000452392 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:32798154 C>T maps to ENST00000452392 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:32798510 G>A maps to ENST00000452392 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:32803417 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:32797190 G>A maps to ENST00000452392 Q640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:33272928 G>T maps to NM_172208.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:16193007 G>A maps to NM_153365.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:16168367 C>T maps to NM_153365.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr1:234529518 C>T maps to NM_005646.3 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:234603258 C>A maps to NM_005646.3 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:234553940 A>G maps to NM_005646.3 A1198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:234582609 G>T maps to NM_005646.3 C691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:53898556 G>T maps to NM_134323.1 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:53897508 C>T maps to NM_134323.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:53898556 G>T maps to NM_134323.1 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:53899459 C>T maps to NM_134323.1 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr12:53898513 G>A maps to NM_134323.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:11073807 C>T maps to NM_007375.3 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:11080583 C>T maps to NM_007375.3 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr7:38305052 C>T maps to ENST00000443402 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:38305079 G>A maps to ENST00000443402 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:33467053 C>T maps to ENST00000455217 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:150463884 A>C maps to NM_025150.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:150479449 T>C maps to NM_025150.3 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr1:150463138 T>G maps to NM_025150.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:150471103 G>A maps to NM_025150.3 Q455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:150470119 C>T maps to NM_025150.3 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:150471112 C>T maps to NM_025150.3 D458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:150463183 C>T maps to NM_025150.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:150477164 G>A maps to NM_025150.3 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:102197160 G>A maps to NM_152334.2 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:102249073 T>G maps to NM_152334.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr15:102224307 G>A maps to NM_152334.2 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:6638809 G>A maps to NM_138697.3 E564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:6636587 A>G maps to NM_138697.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:6638855 C>T maps to NM_138697.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:19181081 A>C maps to NM_152232.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:19166911 G>A maps to NM_152232.2 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr1:19180922 C>T maps to NM_152232.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr1:19181039 C>T maps to NM_152232.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:19181312 G>A maps to NM_152232.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr1:19166377 G>A maps to NM_152232.2 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr1:19181468 G>A maps to NM_152232.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:1268408 C>T maps to NM_152228.1 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr1:1268976 G>A maps to NM_152228.1 W564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr5:9629976 A>T maps to NM_019599.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:9629346 A>G maps to NM_019599.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr5:9629457 A>T maps to NM_019599.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:10978246 G>A maps to NM_023921.1 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr12:10978096 G>A maps to NM_023921.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:11061156 A>G maps to NM_023920.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:11061747 G>T maps to NM_023920.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:11091629 A>C maps to NM_023922.1 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:11150144 G>A maps to NM_176889.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr7:141464185 T>C maps to NM_016943.2 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr7:141464551 C>A maps to NM_016943.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr12:11286357 C>T maps to NM_001097643.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:11286390 C>T maps to NM_001097643.1 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:11286167 T>A maps to NM_001097643.1 K226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:11183744 A>G maps to NM_176885.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:11183508 A>G maps to NM_176885.2 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr7:142880891 T>C maps to NM_176881.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:141478734 G>A maps to NM_016944.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:141478329 T>C maps to NM_016944.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:142919980 C>A maps to NM_176882.1 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:143175075 A>G maps to NM_176883.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:11338709 C>T maps to NM_181429.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr12:11244600 A>G maps to ENST00000422992 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:11214776 T>C maps to NM_176887.2 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr7:141490670 A>T maps to NM_018980.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr12:11139423 T>A maps to NM_176890.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:11138637 G>A maps to NM_176890.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr12:11139423 T>A maps to NM_176890.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr12:11139423 T>A maps to NM_176890.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:11138750 A>G maps to NM_176890.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:10954395 G>T maps to NM_023919.2 Y258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr12:10959264 G>T maps to NM_023918.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:10958814 G>T maps to NM_023918.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr12:10959141 A>G maps to NM_023918.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:10962437 G>A maps to NM_023917.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr20:13514768 A>T maps to NM_017714.2 L232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr20:13561563 C>T maps to NM_017714.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr20:13610607 G>A maps to NM_017714.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr20:13567965 C>A maps to NM_017714.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr20:13514768 A>T maps to NM_017714.2 L232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:13371018 G>A maps to NM_017714.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:13539708 T>C maps to NM_017714.2 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr20:13398139 C>T maps to NM_017714.2 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:13415763 G>A maps to NM_017714.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:71610149 G>A maps to NM_000353.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:71602061 C>T maps to NM_000353.2 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:71606507 A>G maps to NM_000353.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:71610261 G>A maps to NM_000353.2 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:71602112 C>A maps to NM_000353.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr16:71610309 T>C maps to NM_000353.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:125520867 G>A maps to NM_032026.3 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:10312639 G>T maps to NM_014760.3 G592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr7:27831746 G>A maps to ENST00000409980 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:27824918 C>T maps to ENST00000409980 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr7:27832791 A>G maps to ENST00000409980 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:27832789 C>T maps to ENST00000409980 Q457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr7:27832791 A>G maps to ENST00000409980 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr7:27831731 C>T maps to ENST00000409980 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:153648560 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:153649262 A>G did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:38097655 A>G maps to NM_015173.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:38020051 C>A maps to NM_015173.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:37903931 A>G maps to NM_015173.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:37904078 C>T maps to NM_015173.2 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr22:30690042 C>T maps to ENST00000403477 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr22:30695510 C>T maps to ENST00000403477 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:30688509 C>A maps to ENST00000403477 G468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr16:30369282 C>T maps to NM_015527.3 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:30376899 G>A maps to NM_015527.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:30369537 G>A maps to NM_015527.3 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:30369651 C>G maps to NM_015527.3 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr16:30370625 C>T maps to NM_015527.3 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr11:67173157 G>A maps to NM_198517.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr10:96260016 A>G maps to NM_015188.1 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:96269848 T>C maps to NM_015188.1 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:96162495 C>T maps to NM_015188.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:96282099 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:131568286 C>T maps to NM_018201.3 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr9:131553693 A>G maps to NM_018201.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr4:6925430 C>T maps to NM_001113361.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:6925638 G>T maps to NM_001113361.1 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:6925628 C>T maps to NM_001113361.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:72316794 G>A maps to NM_022771.4 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:72290488 G>A maps to NM_022771.4 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr17:77924302 G>A maps to NM_019020.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:77921557 C>T maps to NM_019020.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:77914678 G>A maps to NM_019020.2 D761D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:50391537 C>T maps to NM_024682.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr4:26744201 C>T maps to NM_018317.2 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr4:26737074 A>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:26622280 G>T maps to NM_018317.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:26661277 T>A maps to NM_018317.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:101006376 G>A maps to NM_018421.3 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:100961793 G>T maps to NM_018421.3 R875R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:100971149 G>T maps to NM_018421.3 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:100995716 G>C maps to NM_018421.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr9:100995793 G>A maps to NM_018421.3 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:100971113 G>A maps to NM_018421.3 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr9:100971347 T>C maps to NM_018421.3 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr9:101006373 A>G maps to NM_018421.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:419246 G>A maps to ENST00000246077 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:74173769 G>T maps to NM_153356.1 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr22:47193398 C>T maps to NM_014346.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr22:47307998 G>A maps to NM_014346.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr22:47507444 C>T maps to NM_014346.2 C457C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr22:47189739 T>C did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:37250120 C>T maps to NM_017772.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:37284921 C>T maps to NM_017772.2 Y443Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:37281659 G>A maps to NM_017772.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:100029347 T>G maps to ENST00000394144 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:100029266 A>G maps to ENST00000394144 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:2548322 G>A maps to ENST00000434757 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:2549913 G>T maps to ENST00000434757 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:2546445 G>A maps to ENST00000434757 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:48419241 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:48418569 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:48419279 C>T did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:48403396 G>A did not map to a codon.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr23:48418376 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:48417696 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:48399813 G>A did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:48417293 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:48418408 C>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:48417587 T>C did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:48419185 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:18541184 G>A maps to NM_001039397.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:28890412 G>A maps to NM_015594.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:78316665 G>A maps to NM_144572.1 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:75923378 A>G maps to ENST00000431480 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr13:75936233 T>C maps to ENST00000431480 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr13:75873654 C>A maps to ENST00000431480 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr13:75936167 G>A maps to ENST00000431480 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:75900508 C>T maps to ENST00000431480 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:75884107 G>A maps to ENST00000431480 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:75861155 A>G maps to ENST00000431480 A1224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:75863147 A>G maps to ENST00000431480 D1196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:75900472 G>A maps to ENST00000431480 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:17279703 C>T maps to NM_001134381.1 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:17279657 T>A maps to NM_001134381.1 K529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:17255827 G>A maps to NM_001134381.1 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:17418096 G>A maps to NM_001134381.1 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:17279702 G>A maps to NM_001134381.1 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:17333464 G>A maps to NM_001134381.1 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:17279666 G>A maps to NM_001134381.1 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr6:13306728 A>G maps to NM_016495.4 C232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:13327070 A>G maps to NM_016495.4 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:101643909 G>T maps to NM_001102426.1 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:101666932 G>A maps to NM_001102426.1 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:101652579 G>A maps to NM_001102426.1 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:101655075 C>T maps to NM_001102426.1 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:101627970 C>T maps to NM_001102426.1 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr23:106064217 A>G did not map to a codon.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:106064218 A>G did not map to a codon.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr23:106064147 G>A did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:106083994 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:106117177 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:106069424 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:106109244 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:106083350 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:106091523 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:106097472 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:106117067 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:106064218 A>G did not map to a codon.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr23:106064217 A>G did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:106083996 T>C did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:106064216 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:106064218 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:106070441 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:106064218 A>G did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:141578864 G>A maps to NM_015130.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:141590149 G>A maps to NM_015130.2 Y503Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr4:141543996 G>A maps to NM_015130.2 H1051H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr4:141607512 C>G maps to NM_015130.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr4:141598056 C>T maps to NM_015130.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:141590859 G>A maps to NM_015130.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:141598056 C>T maps to NM_015130.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr4:141622715 A>G maps to NM_015130.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:179320405 G>A maps to NM_198868.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:179331765 G>A maps to NM_198868.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:179290804 G>A maps to NM_198868.2 S1132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr5:179302134 C>T maps to NM_198868.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:179290948 G>A maps to NM_198868.2 D1084D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:179318426 G>A maps to NM_198868.2 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:179326188 G>A maps to NM_198868.2 H116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:77004064 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr5:77004069 C>T maps to NM_004607.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr19:36616596 C>T maps to NM_001281.2 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:36606545 C>T maps to NM_001281.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:186272227 G>A maps to NM_001134415.1 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:186272718 G>A maps to NM_001134415.1 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr3:186274243 T>G maps to NM_001134415.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:186281977 T>C maps to NM_001134415.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:186272137 G>T maps to NM_001134415.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:80888396 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:80865657 C>T maps to NM_005993.4 D648D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:80851493 T>C maps to NM_005993.4 C545C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:80828253 G>A maps to NM_005993.4 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:235611996 G>T maps to NM_003193.3 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr1:235612027 T>G maps to NM_003193.3 L512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:120930716 T>A maps to NM_152715.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:120929066 G>A maps to NM_152715.3 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:107173154 C>T maps to NM_001163436.1 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:107114775 G>A maps to NM_001163436.1 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:107115873 C>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr4:107016791 A>G maps to NM_001163436.1 I806I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr12:64878158 C>T maps to NM_013254.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr12:64890764 G>A maps to NM_013254.3 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr12:64889345 A>G maps to NM_013254.3 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:64875754 C>T maps to NM_013254.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:64860679 G>T did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:9659687 G>A did not map to a codon.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr23:9684277 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:9679794 C>T did not map to a codon.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr23:9683033 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:9679709 C>T did not map to a codon.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr23:9660259 C>T did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr23:9673061 A>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:9659626 G>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:9622288 G>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:9656109 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:176752058 C>A maps to NM_024665.4 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:176765105 T>C maps to NM_024665.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:176743291 C>T maps to NM_024665.4 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr24:6958127 A>G did not map to a codon.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr24:6938318 T>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr24:6954356 C>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:72992836 A>G maps to NM_012453.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:2026261 C>T maps to NM_006453.2 C413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:2026249 C>T maps to NM_006453.2 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:2024785 C>T maps to NM_006453.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:170870904 C>A maps to NM_003194.4 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:170871036 G>A maps to NM_003194.4 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:170880503 G>A maps to NM_003194.4 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:162280641 G>A maps to NM_006593.2 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:162273211 C>T maps to NM_006593.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr2:162273382 C>T maps to NM_006593.2 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr7:45143808 G>T maps to ENST00000404564 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:45148785 A>G maps to ENST00000404564 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:19748707 G>A maps to NM_080647.1 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr22:19770478 C>T maps to NM_005992.1 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr22:19751836 C>T maps to NM_080647.1 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:67400436 T>G maps to NM_005995.4 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:119427486 C>T maps to ENST00000369429 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:119466064 A>G maps to ENST00000369429 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:119428101 A>C maps to ENST00000369429 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:119467440 C>A did not map to a codon.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr1:119427486 C>T maps to ENST00000369429 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr1:119467433 C>T maps to ENST00000369429 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:85472341 C>T maps to NM_001080508.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:85446702 G>A maps to NM_001080508.1 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:85457709 G>A maps to NM_001080508.1 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:85446435 C>T maps to NM_001080508.1 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:85466460 G>A maps to NM_001080508.1 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:85457772 C>T maps to NM_001080508.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:85466568 C>T maps to NM_001080508.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr6:85446417 A>G maps to NM_001080508.1 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:85466415 A>G maps to NM_001080508.1 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr6:85446417 A>G maps to NM_001080508.1 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:168282170 G>A maps to NM_005149.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:168262443 C>A maps to NM_005149.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:168278109 G>A maps to NM_005149.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr1:168274405 G>A maps to NM_005149.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr1:168274366 G>A maps to NM_005149.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:59482791 C>T maps to NM_005994.3 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:35293183 G>A maps to NM_001077653.2 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:35244133 G>A maps to NM_001077653.2 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr7:35271119 C>A maps to NM_001077653.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:35244133 G>A maps to NM_001077653.2 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr7:35293183 G>A maps to NM_001077653.2 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:45820026 C>T maps to NM_013351.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr23:79278617 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:79283561 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:79282235 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:79282243 C>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:79282347 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:79282759 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:79281182 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:79286361 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:79283561 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:79283567 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:79283544 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:79286245 C>A did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:79277828 A>C did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:79283560 G>A did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:79281261 G>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:79277813 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:79277802 T>C did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:79283561 C>A did not map to a codon.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr12:115118888 A>T maps to NM_016569.3 L151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:115109672 C>T maps to NM_016569.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:115112443 C>T maps to NM_016569.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:115112131 G>A maps to NM_016569.3 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:115120674 C>A maps to NM_016569.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:59557454 G>T maps to ENST00000393853 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr17:59560685 C>T maps to ENST00000393853 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:59543269 C>T maps to ENST00000393853 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:59560462 C>T maps to ENST00000393853 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr12:114832608 C>T maps to NM_000192.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr12:114793375 G>A maps to NM_000192.3 H506H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:114823366 C>T maps to NM_000192.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:114832659 T>C maps to NM_000192.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr12:114836455 G>A maps to NM_000192.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:114836461 G>A maps to NM_000192.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:114841688 G>A maps to NM_000192.3 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:3600428 G>A maps to NM_201636.2 C68C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:3595781 G>A maps to NM_201636.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:3599996 G>A maps to NM_201636.2 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:3600542 G>A maps to NM_201636.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:139717620 C>T maps to NM_001166253.1 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:139719874 C>T maps to NM_001166253.1 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr7:139653249 C>A maps to NM_001166253.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:139706970 G>A maps to NM_001166253.1 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:139655320 C>T maps to NM_001166253.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:92268613 C>T maps to NM_001128596.1 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:92278731 A>G maps to NM_001128596.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:92258833 T>C maps to NM_001128596.1 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:62701930 G>A maps to NM_003195.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:23743853 C>A maps to NM_003196.1 G90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:23743760 G>A maps to NM_003196.1 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:102884878 C>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:102884959 C>T did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:102884960 G>A did not map to a codon.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr23:101381930 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:101382001 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:102842109 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:102841768 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:102842040 T>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:102841985 G>T did not map to a codon.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr23:102528901 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:102529120 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:102528983 A>G did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:102529120 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:102529287 A>G did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:102528901 T>C did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:101396190 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:101395942 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:101396176 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:102586578 T>G did not map to a codon.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr23:102508590 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:102508780 T>C did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:13681067 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:13681447 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:13681613 A>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:13681283 A>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:13681167 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:13681678 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:13680889 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:24077401 C>T maps to NM_003198.2 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:24078985 C>A maps to NM_003198.2 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr18:44560669 G>A maps to NM_016427.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:44561530 G>A maps to NM_016427.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:44560276 C>T maps to NM_016427.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr18:44560717 C>T maps to NM_016427.2 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr18:44560012 C>T maps to NM_016427.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr18:44560050 G>A maps to NM_016427.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr18:44559423 G>A maps to NM_016427.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:145847949 C>T maps to NM_006706.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:145834700 C>T maps to NM_006706.3 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:145859604 G>T maps to NM_006706.3 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr5:145838679 A>G maps to NM_006706.3 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:145834753 G>A maps to NM_006706.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:132896611 C>A maps to NM_174937.3 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:132915130 C>T maps to NM_174937.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:133106654 C>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:133058621 G>A maps to NM_174937.3 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:133058600 C>T maps to NM_174937.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr10:132944829 G>A maps to NM_174937.3 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr15:57545465 C>T maps to NM_207036.1 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr15:57525046 C>T maps to NM_207036.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:57544624 C>T maps to NM_207036.1 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:57356018 A>C maps to NM_207036.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr15:57543590 C>A maps to NM_207036.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:31130319 C>T maps to NM_007109.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr22:42607669 C>T maps to NM_005650.1 P1214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr22:42608914 A>G maps to NM_005650.1 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:42610027 A>G maps to NM_005650.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:42564697 C>T maps to NM_005650.1 A1948A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:42607755 C>A maps to NM_005650.1 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr22:42610543 A>G maps to NM_005650.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr22:42609745 G>T maps to NM_005650.1 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:42610600 A>T maps to NM_005650.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr6:134210720 G>A maps to NM_003206.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:27373166 C>T maps to NM_175769.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:89973661 G>A maps to NM_014972.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:1650214 G>A maps to NM_003200.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:1621936 A>G maps to NM_003200.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:1615740 C>T maps to NM_003200.2 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:1619834 G>A maps to NM_003200.2 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:53252541 A>C maps to ENST00000398339 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr5:133474705 G>A maps to ENST00000395029 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:133479302 G>A maps to ENST00000395029 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:85361007 G>A maps to NM_031283.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:85536428 C>T maps to NM_031283.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:85533597 A>G maps to NM_031283.2 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr10:114849292 T>C maps to NM_001146283.1 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr10:114901014 G>T maps to NM_030756.4 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:114911612 C>T maps to NM_030756.4 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr10:114925475 G>A maps to NM_030756.4 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr10:114912148 C>T maps to NM_030756.4 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr10:114903721 T>G maps to NM_030756.4 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr10:114920447 C>A maps to NM_001146274.1 C463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:114925412 G>A maps to NM_030756.4 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr10:114920393 G>A maps to NM_001146274.1 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr10:114910853 C>T maps to NM_030756.4 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr10:114905820 C>A maps to NM_030756.4 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr10:114920421 C>T maps to NM_001146274.1 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr10:114905823 C>A maps to NM_030756.4 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:61488982 C>T maps to NM_006602.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:61488886 G>A maps to NM_006602.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:61488886 G>A maps to NM_006602.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:61488918 G>A maps to NM_006602.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:152079944 G>A maps to NM_007113.2 G1916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:152081687 G>A maps to NM_007113.2 D1335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:152079878 T>C maps to NM_007113.2 R1938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:152083449 C>T maps to NM_007113.2 W748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:152080697 G>A maps to NM_007113.2 R1665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:152084147 G>A maps to NM_007113.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:152085485 G>A maps to NM_007113.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:152080307 T>C maps to NM_007113.2 R1795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr1:152060538 T>G maps to NM_001008536.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:152059464 G>T maps to NM_001008536.1 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:152057444 A>C maps to NM_001008536.1 *905G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:152057613 G>T maps to NM_001008536.1 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr12:110345417 G>T maps to NM_032300.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr12:110352294 C>T maps to NM_032300.4 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:110341816 G>A maps to NM_032300.4 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr12:110345398 G>A maps to NM_032300.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:67816598 C>T maps to NM_006019.3 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:67815432 C>T maps to NM_006019.3 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:67812540 C>T maps to NM_006019.3 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr14:96178091 T>C maps to NM_021966.2 *115W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:96157198 C>T maps to NM_004918.3 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:96157185 C>T maps to NM_004918.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:96157137 C>T maps to NM_004918.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr22:31011724 C>T maps to NM_000355.3 N297N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr22:31011694 C>A maps to NM_000355.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr22:31011709 G>C maps to NM_000355.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr22:31013428 C>T maps to NM_000355.3 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:149755423 G>A maps to ENST00000451292 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr6:167786656 T>C maps to NM_004610.3 *327W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr21:33954542 C>T maps to ENST00000431216 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:167594187 C>T maps to NM_001145121.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr6:167585649 C>T maps to NM_001145121.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:35086182 C>A maps to NM_001093728.1 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:35086093 G>A maps to NM_001093728.1 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:106715428 C>T maps to NM_152772.1 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr12:106715367 T>C maps to NM_152772.1 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr3:49452267 C>T maps to NM_022171.2 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:44253985 G>A maps to NM_182539.3 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:44247989 G>A maps to NM_182539.3 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:44254270 T>C did not map to a codon.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr6:44253952 C>T maps to NM_182539.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:44248037 G>A maps to NM_182539.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr6:44248003 G>A maps to NM_182539.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:44253790 G>A maps to NM_182539.3 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:170144361 C>T maps to NM_174910.1 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:67220431 C>T maps to NM_152665.2 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:45271761 G>A maps to NM_001013632.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr12:111079390 C>T maps to NM_001082538.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:124156102 C>T maps to NM_024809.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:124189190 G>A maps to NM_024809.3 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:124175172 G>T maps to NM_024809.3 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:97423972 G>A maps to ENST00000371217 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:97453541 G>A maps to ENST00000371217 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr10:97447399 G>A maps to ENST00000371217 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:97447399 G>A maps to ENST00000371217 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:104376703 T>C maps to NM_003211.4 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr12:104376703 T>C maps to NM_003211.4 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr4:156830040 C>G maps to NM_005651.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr4:156835521 G>A maps to NM_005651.2 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr14:90429604 C>T maps to NM_018319.3 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:90429970 C>A maps to NM_018319.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr14:90450919 G>A maps to NM_018319.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:24653318 A>G maps to NM_016614.2 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:115973337 G>T maps to NM_198795.1 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:115986981 C>T maps to NM_198795.1 V1109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:115962050 C>T maps to NM_198795.1 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:154515228 A>G maps to NM_001098475.1 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:154516507 C>T maps to NM_001098475.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:154516936 C>T maps to NM_001098475.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr13:61102777 G>A maps to NM_001146070.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr13:61013896 T>C maps to NM_001146070.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr13:61103153 C>T maps to NM_001146070.1 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr13:61102513 G>A maps to NM_001146070.1 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:61102910 G>T maps to NM_001146070.1 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr13:61141714 G>A maps to NM_001146070.1 Q725Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:61083901 T>C maps to NM_001146070.1 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:61103254 G>A maps to NM_001146070.1 K632K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:61034648 G>T maps to NM_001146070.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:61103093 C>T maps to NM_001146070.1 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:179631395 C>A maps to ENST00000444136 S827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr1:179608973 G>T maps to ENST00000444136 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr1:179631312 A>G maps to ENST00000444136 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr1:179659906 T>C maps to ENST00000444136 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr6:46660019 G>A maps to NM_001010870.2 V1385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:46659044 G>A maps to NM_001010870.2 K1060K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:46657457 T>C maps to NM_001010870.2 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr9:100257988 C>T maps to NM_014290.2 R1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:100222630 G>T maps to NM_014290.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr9:100237744 A>G maps to NM_014290.2 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:104481096 C>A maps to NM_153046.2 I714I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:104473537 G>A maps to NM_153046.2 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:104506667 C>T maps to NM_153046.2 V1284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr14:104457533 C>T maps to NM_153046.2 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr14:104394849 C>T maps to NM_153046.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr14:104488607 T>C maps to NM_153046.2 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:151751266 G>A maps to NM_001083965.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr1:151751671 G>A maps to NM_001083965.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:151747627 C>T maps to NM_001083965.1 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:12903466 C>A maps to NM_021961.5 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:12923503 C>T maps to NM_021961.5 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr11:12883804 G>T maps to NM_021961.5 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:49862705 G>T maps to NM_003598.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:49858415 C>T maps to NM_003598.1 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:49862705 G>A maps to NM_003598.1 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:35444119 C>A maps to ENST00000357281 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:35442925 C>T maps to ENST00000357281 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr4:48169970 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:48169969 G>A maps to NM_003215.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:48169936 C>A maps to NM_003215.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:48230565 C>T maps to NM_003215.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr4:48140804 T>C maps to NM_003215.2 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:48151685 C>T maps to NM_003215.2 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr4:48169967 T>C maps to NM_003215.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:97858423 G>A maps to ENST00000379795 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:97875401 G>T maps to ENST00000379795 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:97851776 C>T maps to ENST00000379795 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:97852316 C>T maps to ENST00000379795 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr7:97847039 G>A maps to ENST00000379795 H1118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:97852322 G>A maps to ENST00000379795 G971G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr7:97870520 G>A maps to ENST00000379795 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr14:102904390 C>A maps to NM_014844.3 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:102900785 C>T maps to NM_014844.3 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:102843129 G>A maps to NM_014844.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:102904453 C>T maps to NM_014844.3 G830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:102843108 C>T maps to NM_014844.3 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr14:102916015 G>A maps to NM_014844.3 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr14:102916186 C>T maps to NM_014844.3 V1099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:102898175 C>T maps to NM_014844.3 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:102964033 C>T maps to NM_014844.3 P1353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr14:102918905 G>T maps to NM_014844.3 T1194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:65170882 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:65274937 G>A maps to NM_001010874.4 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr11:121028626 G>A maps to NM_005422.2 P1461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:121032948 C>T maps to NM_005422.2 Y1714Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:121000406 C>T maps to NM_005422.2 R810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:121032948 C>T maps to NM_005422.2 Y1714Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:121058675 C>T maps to NM_005422.2 C2045C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:121000714 C>T maps to NM_005422.2 C912C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:120980005 C>T maps to NM_005422.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr11:121000406 C>T maps to NM_005422.2 R810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:120998617 C>T maps to NM_005422.2 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr11:121000621 C>T maps to NM_005422.2 F881F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:120980029 G>A maps to NM_005422.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:120996243 G>A maps to NM_005422.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:120980005 C>T maps to NM_005422.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:120998647 C>T maps to NM_005422.2 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:120996336 C>T maps to NM_005422.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:121059793 C>T maps to NM_005422.2 C2056C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr11:120998872 C>T maps to NM_005422.2 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr11:120998725 C>T maps to NM_005422.2 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:120998497 C>T maps to NM_005422.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:121016319 C>A maps to NM_005422.2 I1200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:121031010 C>T maps to NM_005422.2 C1619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr11:121008226 C>T maps to NM_005422.2 C1013C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr11:121031010 C>T maps to NM_005422.2 C1619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:120998635 C>T maps to NM_005422.2 C650C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:120989207 A>T maps to NM_005422.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr11:121000441 C>T maps to NM_005422.2 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr11:121032999 C>T maps to NM_005422.2 C1731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:120979960 C>T maps to NM_005422.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:121033038 C>T maps to NM_005422.2 F1744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr10:114063039 C>T maps to NM_058222.1 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr10:114059320 G>A maps to NM_058222.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:114059269 C>T maps to NM_058222.1 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr1:182369050 A>G maps to NM_172000.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:27180340 G>A maps to NM_000459.3 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr9:27157988 G>A maps to NM_000459.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr9:27158088 C>T maps to NM_000459.3 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:27158094 C>T maps to NM_000459.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:27157988 G>A maps to NM_000459.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:27220078 G>T maps to NM_000459.3 E1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:27192530 G>T maps to NM_000459.3 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:27158006 T>C maps to NM_000459.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr9:27203076 A>G maps to NM_000459.3 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:6718498 G>A maps to NM_053285.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:36553053 C>T maps to NM_014466.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:15234455 A>G maps to NM_031898.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:15234455 A>G maps to NM_031898.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:15231347 G>A maps to NM_031898.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:15234875 C>T maps to NM_031898.2 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:15234455 A>G maps to NM_031898.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:15234455 A>G maps to NM_031898.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:95540661 C>T maps to NM_144705.2 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:95542363 G>A maps to NM_144705.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr16:10788481 G>A maps to NM_144674.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:10788676 G>A maps to NM_144674.1 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr16:10783857 G>T maps to NM_144674.1 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:10775848 C>T did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr16:10721463 G>A maps to NM_144674.1 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:10788535 C>T maps to NM_144674.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:1550166 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:1549246 G>A maps to NM_016111.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:1550418 C>A maps to NM_016111.3 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:53453503 C>T maps to NM_170754.2 C693C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:53446251 G>A maps to NM_170754.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:53456220 G>A maps to NM_170754.2 L1243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr14:20854649 G>A maps to NM_007110.4 I939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr14:20846380 G>A maps to NM_007110.4 P1841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:20854323 C>T maps to NM_007110.4 E964E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr14:20840908 C>T maps to NM_007110.4 S2353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:20850835 C>T maps to NM_007110.4 P1362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr14:20864063 G>A maps to NM_007110.4 N568N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:20852600 C>A maps to NM_007110.4 G1096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr16:58019149 C>T maps to NM_199046.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr16:58019122 C>T maps to NM_199046.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:58019357 G>A maps to NM_199046.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr8:73926143 C>T maps to NM_017489.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr16:69390899 T>C maps to NM_005652.3 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr16:69400948 G>A maps to NM_005652.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:75688295 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:1272344 G>A maps to NM_198253.2 H779H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:1254510 G>A maps to NM_198253.2 Y1089Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:1278779 G>A maps to NM_198253.2 H754H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:1282593 G>T maps to NM_198253.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:1279444 C>A maps to NM_198253.2 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr7:115890507 G>A maps to NM_015641.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:115892391 T>C maps to NM_015641.2 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:35607376 C>T maps to NM_006285.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:35609690 C>T maps to NM_006285.2 H611H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:45810994 G>A maps to NM_007170.2 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr1:45813303 G>A maps to NM_007170.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:45811114 G>T maps to NM_007170.2 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:45812445 G>A maps to NM_007170.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr1:45887410 A>G maps to NM_007170.2 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:45812451 C>A did not map to a codon.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr10:70450874 C>T maps to NM_030625.2 G1905G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr10:70333343 G>T maps to NM_030625.2 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:70405743 G>A maps to NM_030625.2 S1086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:70426803 T>G maps to NM_030625.2 V1488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:70332955 G>A maps to NM_030625.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:70332409 G>A maps to NM_030625.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:70333141 C>T maps to NM_030625.2 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:70360757 G>A maps to NM_030625.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr10:70450886 T>C maps to NM_030625.2 P1909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:70405822 C>T maps to NM_030625.2 Q1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr10:70406304 C>T maps to NM_030625.2 N1273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:106156728 C>T maps to ENST00000513237 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:106157489 C>T maps to ENST00000513237 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:106157186 C>T maps to ENST00000513237 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:106162532 C>A maps to ENST00000513237 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:106158206 C>T maps to ENST00000513237 H1057H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:74328237 C>T maps to ENST00000409262 G1348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr2:74328439 C>T maps to ENST00000409262 R1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:74274282 G>A maps to ENST00000409262 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:74327682 C>T maps to ENST00000409262 S1163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:74328853 C>T maps to ENST00000409262 L1554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:103109102 C>A maps to NM_017746.3 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr9:103092363 A>G maps to NM_017746.3 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:103082639 T>C maps to NM_017746.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:103082639 T>C maps to NM_017746.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:103090147 G>A maps to NM_017746.3 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr19:43922404 C>A maps to NM_031451.4 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr23:69890309 A>G did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:69826840 T>C did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:69773167 A>G did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:69945167 A>G did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:69945139 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:70072985 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:69830356 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:70093093 T>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:69826838 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:69945179 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:69945178 A>G did not map to a codon.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr23:69826839 A>G did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:69811647 T>G did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:69826842 A>G did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:70072984 C>T did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:69960605 C>A did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr23:69945169 A>G did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:69749759 A>G did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:69826840 T>C did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:70053388 C>A did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:69945167 A>G did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:69749761 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:112040045 G>T maps to NM_031275.4 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:104464850 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:104464396 C>T did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr23:104463980 A>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:104464181 C>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:104464193 C>T did not map to a codon.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr23:104463700 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:104464290 T>C did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:107225128 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:107224737 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:107225315 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:107225315 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:107225260 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:107225094 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:56676755 T>C maps to ENST00000240361 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr17:56699084 G>T maps to ENST00000240361 Y160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr17:56643117 G>A maps to ENST00000240361 G1364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:56650659 C>T maps to ENST00000240361 T1177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:56676338 G>A maps to ENST00000240361 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr17:56676431 G>A maps to ENST00000240361 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:56679901 T>C maps to ENST00000240361 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:56679810 G>A maps to ENST00000240361 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:56688667 C>T maps to ENST00000240361 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:56679862 C>T maps to ENST00000240361 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:56707838 G>A maps to ENST00000240361 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr17:56690823 C>T maps to ENST00000240361 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr17:56688586 G>C maps to ENST00000240361 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr17:56693648 C>T maps to ENST00000240361 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr8:30704238 G>T maps to NM_031271.3 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:30704109 C>T maps to NM_031271.3 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3517-01A-01W-0831-10 chr8:30705384 C>T maps to NM_031271.3 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr8:30702747 C>T maps to NM_031271.3 A1262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr8:30694787 A>G maps to NM_031271.3 N2621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:30702104 T>G maps to NM_031271.3 R1477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:30700480 A>T maps to NM_031271.3 L2018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:30705873 A>G maps to NM_031271.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr8:30703341 C>T maps to NM_031271.3 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:30702045 G>T maps to NM_031271.3 I1496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:30701514 G>A maps to NM_031271.3 N1673N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:30703143 T>C maps to NM_031271.3 E1130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:30694475 G>A maps to NM_031271.3 G2725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:30706270 G>T maps to NM_031271.3 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:30695552 G>A maps to NM_031271.3 S2366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:30700329 G>T maps to NM_031271.3 V2068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:30702138 T>C maps to NM_031271.3 K1465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:30700596 A>G maps to NM_031271.3 N1979N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr8:30703197 A>G maps to NM_031271.3 S1112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:62238158 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:62271030 A>T maps to NM_018469.3 Y688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:62230401 C>A maps to NM_018469.3 E1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr17:62291304 C>T maps to NM_018469.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:62254682 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:62291283 C>G maps to NM_018469.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:51737896 C>T maps to NM_015926.4 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:51708388 C>A maps to NM_015926.4 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:56704615 A>G maps to NM_198524.1 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:56719817 G>T maps to NM_198524.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:56680709 G>T maps to NM_198524.1 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:133485146 G>A maps to NM_001063.3 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:133473406 C>T maps to NM_001063.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:133478064 G>A maps to NM_001063.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:133478057 G>A maps to NM_001063.3 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr3:133475799 C>T maps to NM_001063.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr3:133495909 C>T maps to NM_001063.3 N630N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:60154687 T>C maps to NM_003201.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr6:10407062 C>G maps to ENST00000379613 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr6:10410328 G>C maps to ENST00000379613 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:10400739 G>A maps to ENST00000379613 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:10404874 G>T maps to ENST00000379613 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:50805783 G>A maps to ENST00000263046 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:50810933 C>T maps to ENST00000263046 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:50805718 C>T maps to ENST00000263046 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:50810804 G>A maps to ENST00000263046 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:50810927 G>A maps to ENST00000263046 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:50803792 G>A maps to ENST00000263046 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr6:50803864 C>T maps to ENST00000263046 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr20:55206742 G>A maps to NM_003222.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr20:55206349 C>G maps to NM_003222.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:55206310 C>A maps to NM_003222.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr6:50682948 G>T maps to NM_172238.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr6:50683109 C>T maps to NM_172238.3 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr6:50718992 T>C maps to NM_172238.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:50682981 C>T maps to NM_172238.3 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:50683289 C>T maps to NM_172238.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:50718941 C>T maps to NM_172238.3 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:50682902 C>T maps to NM_172238.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr6:50682971 C>A maps to NM_172238.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:50740540 T>C maps to NM_172238.3 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr6:50740384 G>T maps to NM_172238.3 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:50718992 T>C maps to NM_172238.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:50740459 T>C maps to NM_172238.3 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr6:50740459 T>C maps to NM_172238.3 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr6:50683052 C>T maps to NM_172238.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:50718929 C>T maps to NM_172238.3 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr6:50718992 T>C maps to NM_172238.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr6:50682840 G>T maps to NM_172238.3 G18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:155619710 A>C maps to NM_016020.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr6:155581416 G>A maps to NM_016020.3 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:155606309 A>G maps to NM_016020.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:246719892 A>G maps to NM_022366.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:246704494 A>T maps to NM_022366.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr1:246704482 C>T maps to NM_022366.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:246711909 C>A did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:246704363 C>T maps to NM_022366.2 W387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:51511512 G>A maps to NM_005653.4 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:51502957 G>A maps to NM_005653.4 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:121997210 G>A maps to NM_014553.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:122004501 G>A maps to NM_014553.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:121995202 G>A maps to NM_014553.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:122006618 C>T maps to NM_014553.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr13:114288853 A>G maps to NM_007111.4 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr13:114288233 C>T maps to NM_007111.4 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr13:114285966 G>A maps to NM_007111.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr13:114265315 T>C maps to NM_007111.4 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr13:114265312 C>A maps to NM_007111.4 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr13:114265315 T>C maps to NM_007111.4 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr13:114288853 A>G maps to NM_007111.4 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr23:132351197 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:132351775 A>G did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:132351468 G>A did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:132351129 C>A did not map to a codon.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr23:132351858 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:132351290 C>T did not map to a codon.
Sequencing variant TCGA-AA-3532-01A-01W-0831-10 chr23:48896801 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:48889017 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:48896731 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:48895939 G>A did not map to a codon.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr23:48896791 G>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:48896752 G>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr6:41654895 G>A maps to ENST00000343317 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr6:41652690 G>T maps to ENST00000343317 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:41658481 G>A maps to ENST00000343317 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr6:41657519 A>G maps to ENST00000343317 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr7:115590926 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:115582008 C>A maps to NM_012252.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:115582051 C>A maps to NM_012252.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:115594696 C>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr21:43767607 C>T maps to NM_005423.4 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr21:43770113 G>A maps to NM_005423.4 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:100447605 C>T maps to NM_001007565.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr3:100463720 C>T maps to NM_001007565.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:100467074 T>G maps to NM_001007565.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:100432666 A>C maps to NM_001007565.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr22:26888032 G>A maps to NM_012143.2 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:26906061 C>T maps to NM_012143.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:26895204 G>A maps to NM_012143.2 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr22:26895443 C>A maps to NM_012143.2 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr2:188361752 C>T maps to NM_006287.4 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:188361689 G>A maps to NM_006287.4 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:188349643 A>C maps to NM_006287.4 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:93519503 G>A maps to NM_006528.2 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:54611368 T>C maps to NM_013342.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:54611506 C>T maps to NM_013342.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:54611470 C>T maps to NM_013342.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:100228539 G>A maps to NM_003227.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:100228530 G>A maps to NM_003227.3 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr7:100225547 A>G maps to NM_003227.3 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr7:100230623 C>T maps to NM_003227.3 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr7:100225247 G>T maps to NM_003227.3 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr7:100239099 C>T maps to NM_003227.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:195780387 T>C maps to NM_001128148.1 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:195779003 G>A maps to NM_001128148.1 R698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:195780354 T>C maps to NM_001128148.1 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:195780354 T>C maps to NM_001128148.1 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr3:195798992 A>G maps to NM_001128148.1 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:195798992 A>G maps to NM_001128148.1 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:133900727 T>C maps to NM_003235.4 H892H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr8:133911136 C>T maps to NM_003235.4 F1104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:134034345 C>T maps to NM_003235.4 I2329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:134030026 C>A maps to NM_003235.4 I2189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:133980075 G>A maps to NM_003235.4 E1908E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:134108556 C>T maps to NM_003235.4 V2504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr8:133883695 C>T maps to NM_003235.4 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr8:133919101 C>T maps to NM_003235.4 S1268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr8:133880411 G>A maps to NM_003235.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:133953755 C>T maps to NM_003235.4 C1734C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr8:133925454 G>T maps to NM_003235.4 S1441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr8:134107313 C>T maps to NM_003235.4 A2422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:133899371 C>T maps to NM_003235.4 I585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:133945818 C>T maps to NM_003235.4 D1610D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr8:133935682 T>C maps to NM_003235.4 C1543C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr8:133900727 T>C maps to NM_003235.4 H892H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr8:133984843 A>G maps to NM_003235.4 G2019G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr8:133894179 T>C maps to NM_003235.4 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:133900271 G>A maps to NM_003235.4 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:41850769 C>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:41848075 G>A maps to NM_000660.4 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:31484786 T>C maps to NM_001042454.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr1:218607442 T>G maps to NM_001135599.2 L205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:218520153 C>T maps to NM_001135599.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:218578616 C>A maps to NM_001135599.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr1:218520123 C>T maps to NM_001135599.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:218520159 G>A maps to NM_001135599.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:135388644 C>T maps to NM_000358.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:135388764 C>T maps to NM_000358.2 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:135385183 G>A maps to NM_000358.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr9:101909975 A>G maps to NM_004612.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:101904884 C>A maps to NM_004612.2 Y291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr9:101900288 G>A maps to NM_004612.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr9:101900288 G>A maps to NM_004612.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr9:101908872 C>T maps to NM_004612.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr9:101900288 G>A maps to NM_004612.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:30686326 T>C maps to NM_001024847.2 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr3:30732979 C>A maps to NM_001024847.2 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:30713623 T>C maps to NM_001024847.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:30686245 C>T maps to NM_001024847.2 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:30729967 C>T maps to NM_001024847.2 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:30713460 G>A maps to NM_001024847.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:30732940 T>A maps to NM_001024847.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr3:30713601 G>A maps to NM_001024847.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr3:30732940 T>C maps to NM_001024847.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr3:30729967 C>T maps to NM_001024847.2 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr3:30686362 C>T maps to NM_001024847.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr3:30732940 T>A maps to NM_001024847.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:30729882 A>G maps to NM_001024847.2 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr3:30686362 C>T maps to NM_001024847.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:30686326 T>C maps to NM_001024847.2 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:92224193 G>T maps to NM_003243.4 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr1:92174337 A>G maps to NM_003243.4 C723C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:92182145 G>A maps to NM_003243.4 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr1:92174304 G>A maps to NM_003243.4 D734D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:105883890 G>A maps to NM_004257.4 A844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr2:105924506 C>T maps to NM_004257.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:105886066 G>A maps to NM_004257.4 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr18:3456511 C>A maps to NM_170695.2 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr18:3457640 C>A maps to NM_170695.2 C303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:89177578 C>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:89177710 G>A did not map to a codon.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr23:89177765 G>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:89177665 G>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:89177438 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:89177408 C>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:89177636 G>A did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:89177588 A>G did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:89177100 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:3447793 G>T did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr24:3447302 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr14:24731363 G>T maps to NM_000359.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:24729842 A>G maps to NM_000359.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr14:24724030 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr20:36767991 G>A maps to NM_004613.2 Y388Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr20:36775176 G>A maps to NM_004613.2 H267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr20:36766731 G>T maps to NM_004613.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:36759571 C>T maps to NM_004613.2 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:36768051 C>T maps to NM_004613.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr20:36760864 G>A maps to NM_004613.2 Y551Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:36775233 G>A maps to NM_004613.2 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:2308803 C>T maps to NM_003245.3 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:2290333 G>T maps to NM_003245.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr20:2293605 T>C maps to NM_003245.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr20:2290333 G>T maps to NM_003245.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:2291772 C>T maps to NM_003245.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:44938214 C>T maps to NM_003241.3 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:44943411 C>T maps to NM_003241.3 H320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:44952833 T>C maps to NM_003241.3 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:44952865 G>A maps to NM_003241.3 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:44932150 C>T maps to NM_003241.3 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:44948492 C>A maps to NM_003241.3 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:44948516 C>T maps to NM_003241.3 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:44926848 C>T maps to NM_003241.3 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:43531051 C>T maps to NM_201631.3 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr15:43525400 G>A maps to NM_201631.3 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr15:43527907 A>T maps to NM_201631.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:43531054 G>A maps to NM_201631.3 D435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr20:2384320 C>T maps to NM_198994.2 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr20:2413192 C>T maps to NM_198994.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr20:2413183 C>A maps to NM_198994.2 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:2377209 C>T maps to NM_198994.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:2381051 C>T maps to NM_198994.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:2380295 C>T maps to NM_198994.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr20:2375888 G>A maps to NM_198994.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:2384311 G>A maps to NM_198994.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr15:43574081 G>A maps to NM_052955.2 D437D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:43569139 G>A maps to NM_052955.2 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr15:43577100 G>A maps to NM_052955.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr15:43571865 G>T maps to NM_052955.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:85555049 G>T maps to ENST00000409015 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:56737238 C>T maps to NM_024831.6 R847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:56715034 G>A maps to NM_024831.6 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr8:56723473 C>T maps to NM_024831.6 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr8:56699227 T>C maps to NM_024831.6 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr8:56699227 T>C maps to NM_024831.6 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr11:2193001 G>A maps to NM_199292.2 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:2185573 C>T maps to NM_199292.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:2191023 C>T maps to NM_199292.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:2186499 G>A maps to NM_199292.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:57564694 C>T maps to NM_198976.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr20:57567045 A>C maps to NM_198976.1 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:57566036 C>T maps to NM_198976.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:57566054 A>G maps to NM_198976.1 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr2:43802071 G>A maps to ENST00000330266 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:43458359 T>C maps to ENST00000330266 P1864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr2:43779371 T>G maps to ENST00000330266 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr2:43458179 T>C maps to ENST00000330266 G1924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:242545754 G>A maps to NM_015963.5 H458H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:242572691 G>A maps to NM_015963.5 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:108205017 C>A maps to NM_001130475.1 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr4:83839143 C>T maps to NM_024672.4 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr4:83827781 T>C did not map to a codon.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr20:23029136 C>T maps to NM_000361.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:23028938 C>T maps to NM_000361.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:23028479 G>A maps to NM_000361.2 C554C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:23028479 G>A maps to NM_000361.2 C554C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr20:23028707 G>A maps to NM_000361.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr15:39883510 T>C maps to NM_003246.2 N791N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:39876294 C>T maps to NM_003246.2 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:39881160 T>C maps to NM_003246.2 D549D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:39881530 C>T maps to NM_003246.2 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:39882016 C>T maps to NM_003246.2 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr15:39882721 T>C maps to NM_003246.2 N717N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr15:39885307 C>T maps to NM_003246.2 R959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr15:39880772 C>A maps to NM_003246.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr15:39885658 C>T maps to NM_003246.2 D1019D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr6:169640558 C>A maps to NM_003247.2 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr6:169621525 T>G maps to NM_003247.2 R1124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:169632131 G>A maps to NM_003247.2 D698D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr6:169626378 G>A maps to NM_003247.2 R812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:169632191 G>A maps to NM_003247.2 C678C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:169626361 G>A maps to NM_003247.2 Y817Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:169648841 G>A maps to NM_003247.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:169632191 G>A maps to NM_003247.2 C678C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr6:169648757 C>T maps to NM_003247.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:169648775 G>A maps to NM_003247.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:169648841 G>A maps to NM_003247.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr6:169625306 G>A maps to NM_003247.2 N902N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr6:169632191 G>A maps to NM_003247.2 C678C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:169640594 C>T maps to NM_003247.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:169626349 A>G maps to NM_003247.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr6:169625300 G>A maps to NM_003247.2 G904G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:169626325 G>A maps to NM_003247.2 D829D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr6:169625333 G>A maps to NM_003247.2 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr6:169650826 C>T did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:155172183 G>A maps to NM_007112.3 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:155166967 G>A maps to NM_007112.3 R846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:155169836 G>A maps to NM_007112.3 D592D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr1:155166947 A>G maps to NM_007112.3 T852T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr1:155168350 C>T maps to NM_007112.3 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr5:79374022 C>T maps to NM_003248.4 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr5:79368128 A>G maps to NM_003248.4 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:79366896 C>A maps to NM_003248.4 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:79378954 C>T maps to NM_003248.4 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:79355303 C>T maps to NM_003248.4 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:79335942 C>T maps to NM_003248.4 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:79374966 C>A maps to NM_003248.4 I799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:79361255 C>T maps to NM_003248.4 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:79368125 C>T maps to NM_003248.4 C582C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:375760 G>A maps to NM_016585.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr19:375838 G>A maps to NM_016585.3 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr19:375859 G>A maps to NM_016585.3 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr1:151823572 C>T maps to NM_182578.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr1:151820749 G>A maps to NM_182578.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr1:151823620 T>C maps to NM_182578.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:151823620 T>C maps to NM_182578.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:128150815 C>A maps to NM_001164685.1 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:128176310 T>C maps to NM_001164685.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:128134225 A>G maps to NM_001164685.1 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr6:128134714 G>A maps to NM_001164685.1 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:157161601 G>T maps to NM_017872.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:157161676 A>G maps to NM_017872.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:25313871 C>T maps to NM_024838.4 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:25313676 G>T maps to NM_024838.4 G509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr10:25312634 A>C maps to NM_024838.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:88474164 C>A maps to NM_018271.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:88485603 C>T maps to NM_018271.3 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:88482593 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:246321 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr18:214781 A>G maps to NM_005131.2 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr23:122755178 C>T did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:122747960 C>G did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:122747913 C>G did not map to a codon.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr23:122759793 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:122772820 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:122778657 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:122779201 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:122799602 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:122747989 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:122757734 T>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:122759894 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:122747495 C>T did not map to a codon.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr23:122802126 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:122757775 T>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:122758464 C>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:122753274 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:122778719 A>G did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:122765638 A>G did not map to a codon.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr23:122799677 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:29935451 C>A maps to NM_003678.4 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr22:29927829 C>T maps to NM_003678.4 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr16:3077074 G>A did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:63820830 T>C maps to NM_025075.2 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr3:63820830 T>C maps to NM_025075.2 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr3:63820830 T>C maps to NM_025075.2 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr3:63820830 T>C maps to NM_025075.2 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:2807710 C>T maps to NM_003249.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:2794858 C>T maps to NM_003249.3 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr19:2808363 G>A maps to NM_003249.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:2811638 C>T maps to NM_003249.3 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:184090432 T>C maps to NM_000460.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:184090804 G>T maps to NM_000460.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:184090465 A>G maps to NM_000460.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:38244661 C>T maps to NM_003250.5 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr1:36757055 C>T maps to NM_005119.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:36752131 C>T maps to NM_005119.3 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:36752131 C>T maps to NM_005119.3 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:36754720 C>T maps to NM_005119.3 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:36755227 T>C maps to NM_005119.3 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:36755143 C>T maps to NM_005119.3 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:36752736 C>T maps to NM_005119.3 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:24185090 C>T maps to NM_001128177.1 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:24185081 G>A maps to NM_001128177.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr3:24231690 G>A maps to NM_001128177.1 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr3:24188295 G>A maps to NM_001128177.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:77775154 G>A maps to NM_003251.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:77775043 C>T maps to NM_003251.2 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr13:52951815 C>T maps to NM_018676.3 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr13:52952406 C>T maps to NM_018676.3 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr13:52971790 A>G maps to NM_018676.3 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:72037556 C>A maps to NM_024817.2 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:71447237 C>T maps to NM_024817.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr15:72021062 C>T maps to NM_024817.2 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:11441506 C>T maps to ENST00000423059 Q1442Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:11676433 G>A maps to ENST00000423059 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:11632923 C>A maps to ENST00000423059 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr7:11676142 G>A maps to ENST00000423059 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:138030163 C>T maps to ENST00000272643 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:137814065 C>T maps to ENST00000272643 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr2:138417303 C>T maps to ENST00000272643 S1485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:137814056 T>C maps to ENST00000272643 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr2:137872774 G>A maps to ENST00000272643 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:137852668 G>T maps to ENST00000272643 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:138208413 G>T did not map to a codon.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr2:138434172 T>A maps to ENST00000272643 *1610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:138376052 A>C maps to ENST00000272643 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:137872774 G>A maps to ENST00000272643 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:20752968 G>A maps to ENST00000431224 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr16:20752991 G>A maps to ENST00000431224 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:39998697 A>C maps to NM_025264.4 L70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr3:9412892 T>C maps to NM_015453.2 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:134118352 C>T maps to NM_199298.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:70444050 G>A maps to NM_022173.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr2:70443373 G>A maps to NM_022173.2 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:27400961 G>A maps to NM_004740.3 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr10:121341477 T>C maps to NM_001033925.1 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:121337240 A>T maps to NM_001033925.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr21:32492771 C>A maps to NM_003253.2 G1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr21:32567573 G>A maps to NM_003253.2 H847H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr21:32508251 G>A maps to NM_003253.2 F1294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr21:32493119 G>T maps to NM_003253.2 R1448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:32595820 C>T maps to NM_003253.2 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:32508251 G>A maps to NM_003253.2 F1294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:32567611 C>A maps to NM_003253.2 E835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:32526693 G>T maps to NM_003253.2 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:32638717 C>A maps to NM_003253.2 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:32639242 C>A maps to NM_003253.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr21:32502558 C>T maps to NM_003253.2 A1339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr21:32617908 G>A maps to NM_003253.2 H493H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr21:32624445 G>A maps to NM_003253.2 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr21:32638802 C>T maps to NM_003253.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr21:32526657 C>T maps to NM_003253.2 G1026G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr21:32638664 G>A maps to NM_003253.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr21:32638778 G>A maps to NM_003253.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr21:32493036 G>A maps to NM_003253.2 P1475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr21:32638778 G>T maps to NM_003253.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:155574086 G>A maps to ENST00000456144 S1404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:155450635 G>A maps to ENST00000456144 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:155574086 G>A maps to ENST00000456144 S1404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:155574086 G>A maps to ENST00000456144 S1404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:155465848 G>A maps to ENST00000456144 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:155497955 G>T maps to ENST00000456144 E790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr6:155577954 C>T maps to ENST00000456144 D1631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:4817393 C>T maps to NM_182919.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr19:4817990 C>A maps to NM_182919.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:4817789 A>G maps to NM_182919.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:4817693 G>A maps to NM_182919.2 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:4817968 G>A maps to NM_182919.2 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:43775102 C>T maps to NM_005424.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:43783697 C>T maps to NM_005424.2 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:43778045 C>A maps to NM_005424.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:43770985 G>A maps to NM_005424.2 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:43779004 C>T maps to NM_005424.2 N709N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:43788359 C>T maps to NM_005424.2 Y1128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr1:43777417 G>A maps to NM_005424.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:113199404 A>G maps to NM_052864.2 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:90035301 G>T maps to NM_145715.2 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:90035033 G>A maps to NM_145715.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:65124265 C>T maps to NM_145719.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:153691109 T>C maps to NM_145720.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:153691348 G>A maps to NM_145720.2 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:153692075 G>A maps to NM_145720.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr4:153691680 G>T maps to NM_145720.2 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr4:153691679 C>T maps to NM_145720.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:149374932 G>A maps to NM_030953.2 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr16:3349696 G>A maps to NM_033208.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:3349495 G>T maps to NM_033208.3 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr16:3350314 G>A maps to NM_033208.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:114018495 G>A maps to ENST00000481065 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr3:114014632 C>T maps to ENST00000481065 N168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:114018492 C>T maps to ENST00000481065 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:156349137 G>A maps to NM_138379.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:156376728 G>A maps to NM_138379.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr5:156381462 G>A maps to NM_138379.2 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:156346506 C>T maps to NM_138379.2 Q366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr5:156378688 G>A maps to NM_138379.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr5:156353321 T>C maps to NM_138379.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr12:56814762 T>C maps to NM_003920.3 Q1008Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr12:56817081 A>G maps to NM_003920.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr12:56815226 G>A maps to NM_003920.3 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr12:56826203 C>T maps to NM_003920.3 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:56817203 G>A maps to NM_003920.3 Q716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:56822845 C>T maps to NM_003920.3 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:56817432 T>C maps to NM_003920.3 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr12:56824744 G>T maps to NM_003920.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:56824744 G>T maps to NM_003920.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:56827557 T>G maps to NM_003920.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr12:56822683 A>G maps to NM_003920.3 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr12:56818670 C>G maps to NM_003920.3 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:56822138 G>A maps to NM_003920.3 R487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr12:56824742 T>C maps to NM_003920.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:57296324 G>A maps to NM_012456.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:201934573 C>T maps to NM_006335.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:48754133 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:48751382 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:902116 G>T maps to NM_013337.2 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:51592610 G>A maps to NM_006327.2 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:8002997 C>A maps to NM_006351.3 E76*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-A010-01A-01W-A00E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr19:7992988 A>G maps to NM_006351.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr19:7999054 C>T maps to NM_006351.3 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:39976380 G>A maps to NM_001001563.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:100601574 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:47444679 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:54191605 A>G maps to NM_014464.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:54216167 G>T maps to NM_014464.3 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:54173578 G>A maps to NM_014464.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:54254623 G>A maps to NM_014464.3 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:54254645 C>T maps to NM_014464.3 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:54219309 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr6:54191630 G>T maps to NM_014464.3 G181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:54208097 C>T maps to NM_014464.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr1:32050496 C>T maps to NM_022164.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:24709839 G>T maps to NM_001099274.1 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr14:24710904 A>G maps to NM_001099274.1 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:24709941 C>T maps to NM_001099274.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr14:24710310 C>T maps to NM_001099274.1 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:156395882 C>T maps to NM_015508.4 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:126162999 T>C maps to NM_148910.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:126162459 A>T maps to NM_148910.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:126162684 C>T maps to NM_148910.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:126162852 C>T maps to NM_148910.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr15:29993875 G>A maps to NM_003257.3 Q1724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:30003071 C>T maps to NM_003257.3 A1445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr15:30025331 C>A maps to NM_003257.3 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr15:30001001 T>C maps to NM_003257.3 R1537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:29993840 G>A maps to NM_003257.3 L1735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:30065520 G>A maps to NM_003257.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr15:29996471 G>T maps to NM_003257.3 P1702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:30026544 G>A maps to NM_003257.3 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:30026577 G>A maps to NM_003257.3 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:30011998 C>T maps to NM_003257.3 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr15:30065520 G>A maps to NM_003257.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:71833173 G>T maps to NM_004817.3 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:3733755 C>T maps to NM_014428.1 N260N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:3736177 G>A maps to NM_014428.1 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr19:3731984 G>A maps to NM_014428.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:3738919 C>T maps to NM_014428.1 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:3746493 G>A maps to NM_014428.1 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:53274277 G>A maps to ENST00000423516 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr3:53263299 G>A maps to ENST00000423516 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:53260859 G>T maps to ENST00000423516 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:53263320 G>A maps to ENST00000423516 C421C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:153556025 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:153539196 T>G did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:153543570 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:153551556 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:153539469 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:153539361 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:153541031 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:153543584 C>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:153555937 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr23:153549204 A>G did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:153549204 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:164393536 G>A maps to NM_032136.4 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:164393325 C>A maps to NM_032136.4 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:84249120 C>T maps to NM_005077.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:84300588 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:84205955 A>G maps to NM_005077.3 N531N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:84208113 G>A maps to NM_005077.3 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr9:84205868 C>T maps to NM_005077.3 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:84200447 G>A maps to NM_005077.3 C700C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr9:84300629 A>G maps to NM_005077.3 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr19:3019711 C>T maps to NM_003260.4 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:3005843 G>A maps to NM_003260.4 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:2997866 G>A maps to NM_003260.4 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:3006465 G>A maps to NM_003260.4 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:70347552 C>T maps to NM_005078.2 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr15:70358527 G>A maps to NM_005078.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:70345574 G>A maps to NM_005078.2 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:70349944 G>A maps to NM_005078.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:70352873 G>A maps to NM_005078.2 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:82323586 C>T maps to ENST00000376537 N415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr9:82323593 C>T maps to ENST00000376537 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr9:82267605 C>T maps to ENST00000376537 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr9:82319727 C>T maps to ENST00000376537 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:82337412 G>T maps to ENST00000376537 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:2994022 G>A maps to NM_001143986.1 W515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:2991864 A>C maps to NM_001143986.1 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:2991957 T>C maps to NM_001143986.1 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:2989139 G>A maps to NM_001143986.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:2987723 G>A maps to NM_001143986.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:171911673 C>T maps to ENST00000360843 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:171906376 G>A maps to ENST00000360843 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:60657489 G>A maps to ENST00000326270 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:60601613 G>A maps to ENST00000326270 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:60657489 G>A maps to ENST00000326270 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:60654090 T>C maps to ENST00000326270 H403H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:60650612 G>T maps to ENST00000326270 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:166929129 G>T maps to ENST00000507499 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:166986902 C>T maps to ENST00000507499 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:167020624 C>A maps to ENST00000507499 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr4:166924626 T>C maps to ENST00000507499 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:166924702 A>C maps to ENST00000507499 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr4:166924626 T>C maps to ENST00000507499 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:166946570 C>A maps to ENST00000507499 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr4:166960564 C>T maps to ENST00000507499 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:98180804 A>G maps to NM_012465.3 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:98129914 A>G maps to NM_012465.3 V940V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:98145871 C>T maps to NM_012465.3 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:98129928 G>T maps to NM_012465.3 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr10:98145961 G>A maps to NM_012465.3 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:35711653 G>A maps to NM_006289.3 R1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:35699365 A>G maps to NM_006289.3 A2287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:35705809 G>A maps to NM_006289.3 F1850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:35706348 C>T maps to NM_006289.3 A1735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:35703798 A>G maps to NM_006289.3 A2110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr9:35703798 A>G maps to NM_006289.3 A2110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr9:35703798 A>G maps to NM_006289.3 A2110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:35715082 G>A maps to NM_006289.3 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:35719514 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:63089483 G>A maps to NM_015059.2 A2039A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr15:62991056 C>T maps to NM_015059.2 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr15:63031653 G>A maps to NM_015059.2 Q1265Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr15:63088447 G>A maps to NM_015059.2 A2002A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:63040639 C>T maps to NM_015059.2 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr15:62967498 C>T maps to NM_015059.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr15:63127964 C>T maps to NM_015059.2 D2386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:63131095 C>T maps to NM_015059.2 V2472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr15:62985082 C>T maps to NM_015059.2 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr15:62948194 C>T maps to NM_015059.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:38799381 A>G maps to NM_003263.3 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:38798316 G>T maps to NM_003263.3 Y712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:38799087 A>G maps to NM_003263.3 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr4:38799983 G>A maps to NM_003263.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:38775306 G>A maps to NM_030956.3 H635H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:38775201 G>A maps to NM_030956.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:38775803 C>A maps to NM_030956.3 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr4:38774784 A>G maps to NM_030956.3 D809D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:154625499 G>T maps to NM_003264.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:154625768 G>A maps to NM_003264.3 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:154626368 G>A maps to NM_003264.3 Q770Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr4:187004019 C>T maps to NM_003265.2 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:187000106 G>A maps to NM_003265.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:187004216 C>T maps to NM_003265.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:187004654 C>A maps to NM_003265.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr4:186997976 C>T maps to NM_003265.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr9:120475245 G>C maps to NM_138554.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:120476415 T>C maps to NM_138554.3 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:120475189 G>T maps to NM_138554.3 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr9:120470866 C>T maps to NM_138554.3 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:120470866 C>A maps to NM_138554.3 C40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:223285329 C>A maps to NM_003268.5 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:223285782 C>T maps to NM_003268.5 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr1:223286288 G>A maps to NM_003268.5 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr1:223285617 T>C maps to NM_003268.5 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:38829237 G>A maps to NM_006068.3 C619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:38829843 A>G maps to NM_006068.3 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:38830680 G>A maps to NM_006068.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:38830902 G>A maps to NM_006068.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr4:38829756 T>C maps to NM_006068.3 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:38829756 T>C maps to NM_006068.3 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:12906102 A>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:12904794 C>T did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:12906395 T>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:12904438 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:12905355 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:12906408 C>A did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:12905843 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:12903658 A>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:12905988 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:12906229 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:12904726 C>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:12904361 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:12904829 T>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:12906029 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:12904281 G>A did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:12939055 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:12938606 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:12940263 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:12937182 G>A did not map to a codon.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr23:12938218 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:12937552 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:12939794 T>C did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:12937960 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:12937471 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:12937479 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:12938348 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:12939504 T>C did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:12938880 A>G did not map to a codon.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr23:12937167 C>A did not map to a codon.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr23:12939894 C>T did not map to a codon.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr23:12938880 A>G did not map to a codon.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr23:12939056 C>T did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:12937803 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:12939843 C>T did not map to a codon.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr3:52257575 G>A maps to ENST00000494383 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:52255658 A>G maps to ENST00000494383 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:52255664 G>A maps to ENST00000494383 N1042N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:52255952 C>T maps to ENST00000494383 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:102849559 C>A maps to NM_001085398.1 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:74742010 C>T maps to NM_016170.4 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr5:170737325 G>A maps to NM_021025.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr3:149051100 G>T maps to NM_138786.3 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:196050735 A>G maps to NM_138461.2 H194H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:149205419 G>A maps to NM_004617.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:4685904 C>T maps to NM_003963.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:4684106 C>T maps to NM_003963.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:4685826 C>T maps to NM_003963.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:4686310 C>T maps to NM_003963.2 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:4685901 C>T maps to NM_003963.2 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:19381858 G>A maps to NM_001001524.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:19381058 G>A maps to NM_001001524.2 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr19:19380544 C>T maps to NM_001001524.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:64882446 G>A maps to NM_003273.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:64882419 C>T maps to NM_003273.2 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:27128553 G>T maps to NM_016551.2 S442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:27127080 C>T maps to NM_016551.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:27133505 C>T maps to NM_016551.2 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:27128432 A>C maps to NM_016551.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:27126963 T>C maps to NM_016551.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:105361113 G>T maps to NM_030788.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:105367115 T>C maps to NM_030788.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:105360851 C>T maps to NM_030788.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr8:105367328 A>G maps to NM_030788.2 Q418Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:105360821 T>C maps to NM_030788.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:24659701 G>A maps to NM_006405.5 N437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:24664180 C>T maps to NM_006405.5 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr14:24662163 C>T maps to NM_006405.5 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:24659701 G>A maps to NM_006405.5 N437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr14:24661884 G>A maps to NM_006405.5 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr13:100207864 A>G maps to NM_004800.1 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:98311093 C>A maps to NM_020123.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:98287047 T>G did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr10:98321865 C>A maps to NM_020123.3 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:30747883 C>T maps to NM_014742.3 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:219144058 G>T maps to NM_022152.4 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:66563647 C>T maps to ENST00000286424 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr12:66563680 G>A maps to ENST00000286424 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr9:75445567 C>T maps to NM_138691.2 R744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:75406941 C>T maps to NM_138691.2 Y455Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr20:2539321 C>T maps to NM_080751.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr20:2517921 C>T maps to NM_080751.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:2560593 A>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:2539195 C>T maps to NM_080751.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr20:2605003 C>T maps to NM_080751.2 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr20:2539195 C>T maps to NM_080751.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:2539195 C>T maps to NM_080751.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr15:81633788 T>G maps to ENST00000454937 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr15:81627239 C>T maps to ENST00000454937 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr15:81631048 C>A maps to ENST00000454937 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:81624894 G>A maps to ENST00000454937 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr15:81666382 G>A maps to ENST00000454937 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:81625545 T>C maps to ENST00000454937 T842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr15:81631768 G>A maps to ENST00000454937 R641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr15:81666358 G>A maps to ENST00000454937 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr15:81624849 C>T maps to ENST00000454937 P1074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:54664691 G>A maps to NM_001145303.1 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr19:54664066 C>A maps to NM_001145303.1 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:54664634 C>T maps to NM_001145303.1 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:54668262 A>G maps to NM_001145303.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr16:19498612 C>T maps to NM_001105248.1 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:19477555 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:19452149 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:19455572 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:76115096 G>A maps to NM_007267.6 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr17:76120802 G>C maps to NM_007267.6 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:76113679 G>T maps to NM_007267.6 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3869-01A-01W-0995-10 chr16:19058477 C>T maps to NM_024847.3 Y549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:129373846 G>A maps to NM_001017395.3 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:129373834 G>T maps to NM_001017395.3 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:205241038 G>A maps to NM_014858.3 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr1:205238112 C>T maps to NM_014858.3 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:205210817 C>T maps to NM_014858.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:205211105 T>C maps to NM_014858.3 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr1:205211153 C>T maps to NM_014858.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:205238151 C>T maps to NM_014858.3 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:94972273 G>A maps to NM_020698.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:165721336 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr1:165737453 T>C maps to NM_019026.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:165712408 G>A maps to NM_019026.3 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr1:165737453 T>C maps to NM_019026.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr13:114174958 C>T maps to NM_017905.4 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:114164668 G>A maps to NM_017905.4 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:114152658 A>G maps to NM_017905.4 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr13:114175030 C>T maps to NM_017905.4 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:20067315 G>A maps to NM_181719.4 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:20082257 C>T maps to NM_181719.4 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:20072046 C>A maps to NM_181719.4 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:20067330 G>T maps to NM_181719.4 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:20063945 G>A maps to NM_181719.4 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr15:38228541 G>A maps to NM_152453.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:140021523 G>A maps to ENST00000252100 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr5:140023382 C>T maps to ENST00000252100 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:68909186 C>T maps to NM_024562.1 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:68894273 A>G maps to NM_024562.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:68894132 C>T maps to NM_024562.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:68943157 T>C maps to NM_024562.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:10943829 C>T maps to NM_006858.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:75614381 C>T maps to NM_006827.5 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:124069273 G>T maps to NM_006815.3 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:79614462 G>A maps to NM_007364.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr15:79606253 C>T maps to NM_007364.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr7:44621354 G>A maps to NM_182547.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr7:44619208 G>A maps to NM_182547.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:69385563 C>T maps to NM_144676.3 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:114956343 G>A maps to NM_001164468.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:77808176 G>A maps to NM_213601.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr5:177022344 C>T maps to NM_017510.4 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:103334818 G>T maps to NM_001198812.1 G381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:192863794 G>A maps to NM_016192.2 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr17:53798212 C>T maps to NM_001099640.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:42089385 C>T maps to NM_032376.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:7339936 T>G maps to NM_178518.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:72781658 G>A maps to NM_017728.3 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr17:72832600 G>T maps to NM_017728.3 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:72832174 C>T maps to NM_017728.3 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:72786435 G>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:72832174 C>T maps to NM_017728.3 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr17:79287663 G>A maps to NM_178520.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:79287663 G>T maps to NM_178520.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:12270013 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:12271507 C>T maps to NM_018374.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:48359749 G>A maps to NM_001143842.1 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:133099121 C>T maps to NM_001136469.1 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr3:133099130 G>A maps to NM_001136469.1 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:133114794 C>T maps to NM_001136469.1 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:133099766 T>C maps to NM_001136469.1 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:60689553 C>T maps to NM_024092.2 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:21101732 C>T maps to NM_003876.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:52889425 A>G maps to ENST00000504329 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:10005794 G>A maps to NM_018447.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr3:10005794 G>A maps to NM_018447.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr3:50396125 A>G maps to NM_007024.4 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:112371792 C>A maps to NM_001193531.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:44338055 G>A maps to NM_032256.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:44781911 C>T maps to NM_032256.1 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr12:108985994 C>T maps to NM_181724.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:122208870 C>T maps to NM_001080825.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:43738980 C>A maps to NM_144626.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:43738959 C>A maps to NM_144626.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:43738818 G>A maps to NM_144626.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:43738713 C>A maps to NM_144626.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:43738821 G>A maps to NM_144626.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr11:85366722 T>C maps to NM_032273.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:85347143 G>A maps to NM_018480.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:85346748 C>T maps to NM_018480.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:96920586 G>A maps to NM_017849.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:4242184 G>A maps to ENST00000382753 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr4:4239631 C>T maps to ENST00000382753 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:1720312 C>T maps to NM_001127266.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr4:1722453 C>G maps to NM_001127266.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:98457887 G>A maps to NM_001134450.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:98457809 G>A maps to NM_001134450.1 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:98460787 G>T maps to NM_001134450.1 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr7:98460910 G>A maps to NM_001134450.1 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:98457803 G>A maps to NM_001134450.1 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr7:98449170 G>A maps to NM_001134450.1 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr7:98446237 G>T maps to NM_001134450.1 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr2:98430601 A>G maps to NM_015348.1 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:98412852 C>A maps to NM_015348.1 E1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr2:98392470 T>C maps to NM_015348.1 K1385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:98373723 G>A maps to NM_015348.1 G1830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:98504540 C>T maps to NM_015348.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:98392470 T>C maps to NM_015348.1 K1385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:98392470 T>C maps to NM_015348.1 K1385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:98392470 T>C maps to NM_015348.1 K1385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:98392470 T>C maps to NM_015348.1 K1385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:60698098 C>T maps to NM_017870.3 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:126138286 G>A maps to NM_052907.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:126004086 G>T maps to NM_052907.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:126139040 G>T maps to NM_052907.2 E1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:126139220 A>T maps to NM_052907.2 R1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr12:126138326 C>T maps to NM_052907.2 Q770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:125900175 G>A maps to NM_052907.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr12:129569097 G>A maps to NM_133448.2 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr12:129558986 T>C maps to NM_133448.2 K911K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:130015743 C>T maps to NM_133448.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr12:130185178 G>A maps to NM_133448.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:130387854 C>T maps to NM_133448.2 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr12:129558800 C>A maps to NM_133448.2 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:130184551 G>A maps to NM_133448.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:130184593 G>A maps to NM_133448.2 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:129569106 G>A maps to NM_133448.2 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:129558521 C>T maps to NM_133448.2 V1066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr12:130184521 G>A maps to NM_133448.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr12:129559151 C>T maps to NM_133448.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr12:129558986 T>C maps to NM_133448.2 K911K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:130184521 G>A maps to NM_133448.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:32956061 C>T maps to NM_207313.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:32964755 C>T maps to NM_207313.1 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr17:32963072 G>A maps to NM_207313.1 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr17:32964791 G>A maps to NM_207313.1 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr11:87032258 C>T maps to NM_022918.3 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:61136172 C>T maps to NM_016464.4 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:61133678 C>T maps to NM_016464.4 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:134849672 A>G maps to NM_018295.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr7:134849633 G>A maps to NM_018295.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:48866780 C>A maps to NM_018273.2 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:48863391 C>T maps to NM_018273.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr19:48866634 G>A maps to NM_018273.2 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr4:159154097 G>A maps to NM_018342.4 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr4:159136378 G>A maps to NM_018342.4 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr4:159165476 T>C maps to NM_018342.4 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:42819403 C>T maps to ENST00000406159 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr19:5778512 C>A maps to NM_152784.3 Y741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:5751779 C>T maps to NM_152784.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:5778449 C>A maps to NM_152784.3 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:5745964 C>T maps to NM_152784.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:5770953 G>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:5757852 G>T did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr19:5744461 G>T maps to NM_152784.3 G200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr19:5737147 G>T did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr19:5763258 G>A maps to NM_152784.3 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:36038288 G>A maps to NM_032635.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:36231923 C>A did not map to a codon.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr6:10751450 C>T maps to NM_030969.3 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr6:10726167 G>A maps to NM_016462.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:55831529 C>T maps to NM_001085488.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr19:55824409 G>A maps to NM_001085488.1 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:83411211 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:66061977 G>A maps to NM_153266.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:66062229 C>T maps to NM_153266.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:39000341 A>G maps to NM_024943.1 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:21190855 C>T maps to ENST00000451578 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr16:21185397 C>T maps to ENST00000451578 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:21185436 C>A maps to ENST00000451578 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:87501680 C>T maps to NM_153354.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr2:135309654 G>A maps to NM_030923.4 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr2:135308175 G>A maps to NM_030923.4 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:109416546 C>T did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:109416609 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:109310615 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:109416478 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:109388073 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:109247077 G>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:109247113 C>T did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:109247240 C>A did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:109247082 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:109416611 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:109388038 T>C did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:109247115 G>A did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr7:112424139 T>C maps to NM_022484.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:112424312 G>A maps to NM_022484.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr7:112424764 A>T maps to NM_022484.4 L39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr7:112424140 G>T maps to NM_022484.4 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr2:216960853 C>A maps to NM_138390.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:216960883 C>T maps to NM_138390.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr2:216960883 C>T maps to NM_138390.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:62729902 G>A maps to NM_198276.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:11575739 A>G maps to NM_001100829.1 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:138860833 G>A maps to NM_198282.2 Y107Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:72469177 G>A maps to NM_153217.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr5:72469177 G>T maps to NM_153217.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr4:949594 C>T maps to NM_032326.2 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:150498682 G>A maps to NM_018487.2 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:39934187 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr2:39944366 G>A maps to NM_152390.2 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:104230568 C>A maps to NM_024789.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:104230799 C>A maps to NM_024789.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:104230833 C>T maps to NM_024789.3 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr10:104231153 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:158994457 G>A maps to NM_020823.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:158994457 G>A maps to NM_020823.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:159046768 C>T maps to NM_020823.1 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:158994508 C>T maps to NM_020823.1 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr6:158994457 G>A maps to NM_020823.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:1589818 G>A maps to NM_001097620.1 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:1586725 G>A maps to NM_001097620.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:1589818 G>A maps to NM_001097620.1 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:38617478 G>A maps to NM_012264.4 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr22:38617526 G>A maps to NM_012264.4 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr4:148554110 G>A maps to NM_018241.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:148554926 C>T maps to NM_018241.2 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr23:148693048 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:148690344 A>G did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:148690458 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:148693007 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:148693134 A>G did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:8889913 C>T maps to NM_015421.3 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr16:8889847 A>G maps to NM_015421.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:153248161 T>C did not map to a codon.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr16:50063696 T>A maps to NM_153261.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr19:55889215 C>T maps to NM_139172.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:166009620 T>G maps to NM_001100389.1 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:15427041 C>A maps to NM_001004320.1 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:15405838 C>T maps to NM_001004320.1 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:19761718 C>A maps to NM_152774.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr2:220412345 C>T maps to NM_001005209.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:220414515 C>T maps to NM_001005209.1 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:220414512 G>A maps to NM_001005209.1 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:26687806 G>A maps to ENST00000457710 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:26685981 C>A maps to ENST00000457710 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr9:74315592 T>C maps to NM_013390.2 Q1114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr9:74360286 G>A maps to NM_013390.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:74349809 G>A maps to NM_013390.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:74360367 C>T maps to NM_013390.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:130762502 T>G maps to NM_052913.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:130762493 T>C maps to NM_052913.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr6:130762180 T>A maps to NM_052913.2 L205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:29447743 G>A maps to NM_001003682.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:5891882 G>T maps to NM_001080209.1 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:5891951 G>A maps to NM_001080209.1 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:5890222 C>A maps to NM_001080209.1 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:9657089 C>T maps to NM_001130924.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr15:72699529 G>A maps to NM_001080462.1 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:72691127 C>T maps to NM_001080462.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:72698943 T>A maps to NM_001080462.1 Y113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:140099470 G>T maps to NM_053045.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:1592019 C>T maps to NM_024600.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:11453690 G>A maps to NM_198536.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr1:212538673 G>T maps to NM_001198862.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:212558639 C>T maps to NM_001198862.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr1:212558648 G>A maps to NM_001198862.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr1:212548588 T>C maps to NM_001198862.1 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:190167562 C>T maps to NM_207316.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:190147395 T>C maps to NM_207316.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:67262278 T>C maps to NM_014187.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr2:27263668 C>T maps to NM_017727.4 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:27263266 C>T maps to NM_017727.4 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:27263358 A>G maps to NM_017727.4 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr9:32784369 C>T maps to NM_212558.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:32784243 C>T maps to NM_212558.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr11:61165381 C>A maps to NM_001173991.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr11:124971168 A>G maps to NM_001080546.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:136573556 T>C maps to NM_025246.2 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:136573865 A>C maps to NM_025246.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:67940541 G>A maps to NM_182526.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr14:67940154 G>A maps to NM_182526.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:75589734 C>T maps to NM_001077416.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:118404166 C>T maps to NM_032780.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr10:63170154 G>A maps to NM_178505.6 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:63170301 G>A maps to NM_178505.6 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:63188766 G>T maps to NM_178505.6 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:15646099 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:75969071 G>A maps to NM_018247.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:75974987 G>A maps to NM_018247.3 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:102968684 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:102968894 T>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:41937521 C>T maps to NM_018126.2 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:100349677 G>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:100349694 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:100333999 C>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:100334065 T>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:100349880 G>A did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:100349633 C>T did not map to a codon.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr23:100349856 C>A did not map to a codon.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:120194727 C>T maps to NM_183240.2 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:16791312 G>A maps to NM_024074.1 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:108456997 C>T maps to NM_018112.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:108484836 G>A maps to NM_018112.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr3:119153647 G>A maps to NM_018266.1 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:12779659 T>C maps to ENST00000431022 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr11:9304981 T>A maps to NM_015012.2 K289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:14176285 C>T maps to NM_024334.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:14174405 C>T maps to NM_024334.2 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr3:194325057 G>A maps to NM_001166305.1 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr3:194349177 C>T maps to NM_001166305.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:100287727 T>C maps to ENST00000403410 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:100287742 C>A maps to ENST00000403410 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:100275682 C>T maps to ENST00000403410 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr3:100287742 C>T maps to ENST00000403410 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:100287742 C>A maps to ENST00000403410 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr3:100275641 C>T maps to ENST00000403410 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr3:100287742 C>A maps to ENST00000403410 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr3:100287739 C>T maps to ENST00000403410 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:34657430 C>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:34657469 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:34675056 C>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:34675036 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:34648568 T>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:34675080 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:54291574 C>A maps to NM_018087.4 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:54252923 C>T maps to NM_018087.4 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:54266420 C>T maps to NM_018087.4 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:57812771 G>A maps to NM_030938.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:57917265 T>G maps to NM_030938.3 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr17:57812702 C>A maps to NM_030938.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr12:64199055 G>A maps to NM_014254.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:64202557 C>T maps to NM_014254.1 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr21:34832753 G>T maps to NM_006134.5 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr21:34832753 G>A maps to NM_006134.5 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:33363762 G>A maps to NM_033504.2 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:33363726 C>A maps to NM_033504.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr8:92032431 G>T maps to NM_018710.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:25815700 G>T maps to NM_018202.4 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr1:25773328 G>T maps to NM_018202.4 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:25783239 C>T maps to NM_018202.4 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:18729196 G>A maps to NM_012109.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:18727814 G>A maps to NM_012109.2 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:55451924 G>A maps to NM_182532.1 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr1:55457507 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:43438759 G>A maps to NM_024956.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr15:43438750 C>A maps to NM_024956.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:226054849 A>G maps to NM_014698.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:226059725 C>T maps to NM_014698.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:226034784 G>A maps to NM_014698.2 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:226034789 A>T maps to NM_014698.2 L792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:226034911 G>T maps to NM_014698.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:226055726 A>G maps to NM_014698.2 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr6:44107272 C>T maps to NM_018426.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:44115122 C>A maps to NM_018426.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:44116544 C>T maps to NM_018426.1 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:44122145 A>G maps to NM_018426.1 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr14:77710771 C>T maps to NM_020431.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:77712960 C>A maps to NM_020431.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:77715643 C>T maps to NM_020431.2 Y627Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr14:77723036 C>T maps to NM_020431.2 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:77715168 C>T maps to NM_020431.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr14:77706032 C>T maps to NM_020431.2 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr14:77685914 T>C maps to NM_020431.2 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:77715649 C>T maps to NM_020431.2 C629C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:77697948 C>T maps to NM_020431.2 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr8:91637910 G>A maps to NM_001008495.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr8:125335610 G>T maps to NM_194291.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:46159420 A>G maps to NM_016486.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr1:46159420 A>G maps to NM_016486.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:46159420 A>G maps to NM_016486.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:74893854 G>T maps to NM_017866.5 *261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:133764157 G>A maps to ENST00000395406 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr8:133740206 C>A maps to ENST00000395406 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr8:133740206 C>A maps to ENST00000395406 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr10:45430218 C>T maps to NM_001123376.1 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:45429138 C>T maps to NM_001123376.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:109796709 G>A maps to NM_153015.1 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr8:109796469 C>T maps to NM_153015.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr8:109797036 C>T maps to NM_153015.1 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr8:109796607 C>T maps to NM_153015.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:156255664 C>T maps to NM_032323.2 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:156255379 G>A maps to NM_032323.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:156255377 C>T maps to NM_032323.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:700161 A>G maps to ENST00000449452 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:16073398 G>A maps to NM_001013641.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr15:34520759 G>A maps to NM_016454.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:18723126 G>A maps to NM_153347.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:18723210 G>A maps to NM_153347.1 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:18723240 C>T maps to NM_153347.1 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:18722703 C>T maps to NM_153347.1 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:424795 G>A maps to NM_021259.2 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:426631 C>T maps to NM_021259.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr16:427515 T>C maps to NM_021259.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:424003 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr9:35842683 C>T maps to ENST00000360192 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr9:35842554 G>A maps to ENST00000360192 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr9:136380642 C>T maps to NM_001080483.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr9:136389831 C>T maps to NM_001080483.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr20:24524044 C>T maps to NM_024893.1 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr20:24524065 C>T maps to NM_024893.1 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:31263429 C>T maps to NM_015544.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:69084176 C>T maps to NM_007114.2 Q747Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:69074742 T>A maps to NM_007114.2 K994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:69097669 C>T maps to NM_007114.2 W62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:69088120 C>A maps to NM_007114.2 E623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr17:28656431 G>C maps to NM_206832.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:28656473 C>T maps to NM_206832.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr17:28651914 T>A maps to NM_206832.1 K187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:4294784 G>A maps to NM_144615.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:154754273 G>A did not map to a codon.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr23:154736636 C>G did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:154754253 A>G did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:154754253 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:100331208 T>C maps to NM_003275.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr9:100326386 A>G maps to NM_003275.3 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr15:52100642 C>T maps to NM_014548.3 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:52098675 C>T maps to NM_014548.3 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:52098713 C>T maps to NM_014548.3 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr15:52181328 A>G maps to NM_014547.4 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr15:52181328 A>G maps to NM_014547.4 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:98926685 A>G maps to NM_003276.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:98941581 C>T maps to NM_001032283.2 N437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:98927349 G>T maps to NM_003276.2 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:98938306 G>T maps to NM_001032283.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:68784829 G>A maps to NM_182606.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:68777137 A>G maps to NM_182606.3 C396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr4:68780303 A>T did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr4:69096979 G>T maps to NM_182502.3 Y209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:69107479 C>T maps to NM_182502.3 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:68725332 G>A maps to NM_004262.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:68708304 C>T maps to NM_004262.2 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:68703950 A>C maps to NM_004262.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:68692994 G>A maps to NM_004262.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr4:68925084 A>G maps to NM_207407.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr4:68964725 T>C maps to NM_207407.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:51281073 C>G maps to NM_182559.2 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:51236767 C>T maps to NM_182559.2 S7S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-A01P-01A-21W-A096-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr12:51237697 C>T maps to NM_182559.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr12:51236818 G>A maps to NM_182559.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:117785188 C>T maps to ENST00000413475 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:117789316 T>C maps to ENST00000413475 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr21:19647585 C>T maps to NM_002772.2 Q944Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr21:19687474 C>A maps to NM_002772.2 E674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr21:19642410 C>A maps to NM_002772.2 E979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr21:19775797 G>A maps to NM_002772.2 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:19770557 G>T maps to NM_002772.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:19732146 G>A maps to NM_002772.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:19770251 G>T maps to NM_002772.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:19685371 C>T maps to NM_002772.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:19770251 G>T maps to NM_002772.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:19666615 C>T maps to NM_002772.2 W819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr21:19737539 C>T maps to NM_002772.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr21:19642312 G>A maps to NM_002772.2 T1011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr21:19744603 A>C maps to NM_002772.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr21:19775813 T>A maps to NM_002772.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr21:42839671 G>A maps to NM_001135099.1 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr21:42845364 C>T maps to NM_001135099.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr21:43805636 C>T maps to ENST00000380399 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr21:43803175 G>A maps to ENST00000380399 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr21:43802180 C>T maps to ENST00000380399 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr11:113565198 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:113570377 G>A maps to NM_030770.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr11:113565237 C>T maps to NM_030770.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:111795731 T>C maps to ENST00000443106 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:111785323 C>T maps to ENST00000443106 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr3:111795731 T>C maps to ENST00000443106 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:2399121 C>A maps to NM_182973.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr19:2399141 C>T maps to NM_182973.1 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:2399129 G>A maps to NM_182973.1 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:101770059 T>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:103219129 A>G did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:103219128 A>G did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:103219129 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:15817111 A>G did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:91760140 C>T maps to NM_183049.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:91760140 C>T maps to NM_183049.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr12:29757202 G>A maps to NM_001193451.1 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:29904672 G>A maps to NM_001193451.1 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr12:29757133 C>T maps to NM_001193451.1 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr12:29725063 C>T maps to NM_001193451.1 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr12:83290315 T>C maps to NM_152588.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr12:83081385 C>T maps to NM_152588.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:83289947 G>T maps to NM_152588.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr12:83081385 C>T maps to NM_152588.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:83290351 T>G maps to NM_152588.1 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:88570067 C>T maps to NM_181783.3 Y468Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:101257340 G>T maps to NM_032813.2 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr13:101316542 G>A maps to NM_032813.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr17:42266938 C>T maps to NM_001076674.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:51710663 G>A maps to NM_030755.4 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr18:66367652 G>A maps to NM_019022.3 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr18:66348253 G>A maps to NM_019022.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr18:66369003 G>A maps to NM_019022.3 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr18:66354970 G>A maps to NM_019022.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr18:66378626 G>A maps to NM_019022.3 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr18:66377321 A>G maps to NM_019022.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:7963215 C>T maps to NM_021156.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr20:7963134 G>A maps to NM_021156.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:7963044 G>T maps to NM_021156.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr9:117849445 G>A maps to NM_002160.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr9:117826237 C>A maps to NM_002160.2 V1199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:117848659 G>A maps to NM_002160.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:117849229 G>A maps to NM_002160.2 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:117838828 T>C maps to NM_002160.2 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr9:117803271 G>A maps to NM_002160.2 I1780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:117798461 G>A maps to NM_002160.2 L1857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:117849420 G>A maps to NM_002160.2 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:117808755 G>A maps to NM_002160.2 Y1686Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr9:117783543 G>A maps to NM_002160.2 G2166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:117788870 G>A maps to NM_002160.2 S2091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:117838849 G>A maps to NM_002160.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr9:117853060 C>T maps to NM_002160.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:117786407 G>A maps to NM_002160.2 S2113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr9:117808872 G>A maps to NM_002160.2 F1647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:117848368 G>A maps to NM_002160.2 C547C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:117803361 A>G maps to NM_002160.2 G1750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:117848767 G>A maps to NM_002160.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:117827109 A>T maps to NM_002160.2 Y1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:117853171 T>C maps to NM_002160.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:117849552 C>T did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr9:117845003 A>G maps to NM_002160.2 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr9:117845003 A>G maps to NM_002160.2 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr9:117836029 G>T maps to NM_002160.2 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr9:117840405 G>A maps to NM_002160.2 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr9:117783441 C>T maps to NM_002160.2 R2200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr9:117849316 G>A maps to NM_002160.2 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr9:117825244 G>A maps to NM_002160.2 G1328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr9:117838854 C>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:117826074 C>A maps to NM_002160.2 E1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr9:117838852 G>A maps to NM_002160.2 G892G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr9:117825247 G>A maps to NM_002160.2 H1327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:31545088 C>T maps to NM_000594.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr6:31545064 C>T maps to NM_000594.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:103593921 C>T maps to NM_006291.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr6:138196108 C>A maps to NM_006290.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:138197202 T>C maps to NM_006290.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr6:138196108 C>T maps to NM_006290.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:138196150 G>A maps to NM_006290.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr6:138202410 C>T maps to NM_006290.2 N776N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:138196150 G>T maps to NM_006290.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr6:138192456 A>G maps to NM_006290.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:138197202 T>C maps to NM_006290.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:138201283 A>G maps to NM_006290.2 E661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:138199748 G>A maps to NM_006290.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr6:138192417 T>C maps to NM_006290.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr6:138199566 A>G did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:138199577 A>G maps to NM_006290.2 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr6:138198219 A>G maps to NM_006290.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr6:138192456 A>G maps to NM_006290.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr6:138201268 G>A maps to NM_006290.2 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr6:138200358 C>T maps to NM_006290.2 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:138202425 A>G maps to NM_006290.2 E781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr6:138199577 A>G maps to NM_006290.2 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr6:138199586 A>G maps to NM_006290.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:138202423 G>T maps to NM_006290.2 E781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr6:138196110 G>A maps to NM_006290.2 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr6:138192456 A>G maps to NM_006290.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr6:138198217 C>T maps to NM_006290.2 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr6:138199646 A>G maps to NM_006290.2 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2677-01A-01W-0831-10 chr2:152226603 C>T maps to NM_007115.3 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr2:152226744 C>T maps to NM_007115.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:51350428 G>A maps to NM_207381.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr15:51350203 G>A maps to NM_207381.2 H251H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr8:23049491 G>A maps to NM_003844.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:23049491 G>A maps to NM_003844.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr8:23060238 G>T maps to NM_003844.3 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:22880375 G>T maps to NM_003842.4 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:22886047 C>A maps to NM_003842.4 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:22974369 G>A maps to ENST00000356864 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr18:60033965 G>A maps to NM_003839.2 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr18:60033950 G>A maps to NM_003839.2 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:60051999 C>T maps to NM_003839.2 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr8:119936821 G>A maps to NM_002546.3 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr8:119945283 C>A maps to NM_002546.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr8:119936993 G>A maps to NM_002546.3 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:119945347 C>T maps to NM_002546.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:3071629 C>T maps to NM_016639.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:16843025 C>T maps to NM_012452.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr16:12061604 C>T maps to NM_001192.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:12060076 G>A maps to NM_001192.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:1139813 G>A maps to NM_004195.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr13:24242833 C>T maps to NM_018647.2 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:6442254 G>A maps to NM_001065.3 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:12253033 A>G maps to NM_001066.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:12267061 G>A maps to NM_001066.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:12253150 A>C maps to NM_001066.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:47200698 G>A maps to NM_014452.3 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:47202493 G>A maps to NM_014452.3 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:47202562 G>A maps to NM_014452.3 N527N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:47251812 G>A maps to NM_014452.3 C368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:47251815 C>A maps to NM_014452.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:6524762 C>T maps to ENST00000355862 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:1149109 G>A maps to NM_003327.3 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:62328741 C>T maps to NM_003823.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:62328828 C>G maps to NM_003823.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr20:62329702 G>A maps to NM_003823.2 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:12164484 C>T maps to NM_001243.3 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:12170187 C>A maps to NM_001243.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:12172071 G>A did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:12198390 G>T maps to NM_001243.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:12170211 G>T maps to NM_001243.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:7999985 T>C maps to NM_001561.5 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:172224434 C>T maps to ENST00000382750 W231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr13:43181002 G>A maps to NM_003701.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:43175019 G>A maps to NM_003701.3 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:43180897 G>A maps to NM_003701.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:43175017 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr13:43180766 C>T maps to NM_003701.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:43180775 G>T maps to NM_003701.3 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:7460158 C>T maps to NM_172089.3 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:7453447 C>T maps to NM_172089.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:7460432 G>A maps to NM_003809.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr13:108955873 G>T maps to NM_006573.3 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:108922765 G>T maps to NM_006573.3 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:108955897 C>T maps to NM_006573.3 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:6665209 G>A maps to NM_003807.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr19:6667145 G>T maps to NM_003807.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr19:6665254 G>T maps to NM_003807.3 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:117552800 G>A maps to NM_005118.2 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr9:117552902 G>A maps to NM_005118.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:173010806 G>A maps to NM_005092.3 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:173155705 G>A maps to NM_003326.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:173155690 A>G maps to NM_003326.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:117666528 C>T maps to NM_001244.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:6534701 G>A maps to NM_003811.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:170802111 G>A maps to NM_015028.2 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:170781734 G>A maps to NM_015028.2 R1340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:170884889 C>A maps to NM_015028.2 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:170825895 T>C maps to NM_015028.2 K780K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:171177843 G>A maps to NM_015028.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr3:170811741 T>C maps to NM_015028.2 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:170819311 G>A maps to NM_015028.2 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr5:150413339 A>G maps to NM_006058.3 H536H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:122075753 C>T maps to ENST00000509841 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:122053785 C>A maps to NM_001128843.1 *326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr4:122068295 G>A maps to ENST00000509841 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr4:122068295 G>A maps to ENST00000509841 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr17:7292366 C>A maps to NM_003985.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:7289890 G>A maps to NM_003985.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr3:195610181 T>C did not map to a codon.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:195611843 G>T maps to NM_001010938.1 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr3:195611886 T>C maps to NM_001010938.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:195608956 G>A maps to NM_001010938.1 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr8:9413683 C>T maps to NM_003747.2 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:9609159 A>G maps to NM_003747.2 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:9562211 C>T maps to NM_003747.2 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:9562211 C>T maps to NM_003747.2 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:57076914 A>G maps to NM_033396.2 F1090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:57080070 G>A maps to NM_033396.2 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr11:57081288 G>A maps to NM_033396.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr11:57077475 G>A maps to NM_033396.2 N903N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:57076080 G>A maps to NM_033396.2 G1368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:57077319 G>A maps to NM_033396.2 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:57076704 G>A maps to NM_033396.2 D1160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:57081342 G>T maps to NM_033396.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:57076215 G>T maps to NM_033396.2 T1323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr10:93619360 T>A maps to NM_025235.3 T1079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr10:93590702 T>C maps to NM_025235.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:93615385 C>T maps to NM_025235.3 R977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:93590702 T>C maps to NM_025235.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:93615385 C>T maps to NM_025235.3 R977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr10:93619360 T>C maps to NM_025235.3 T1079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr10:93590702 T>C maps to NM_025235.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr10:93586931 C>A maps to NM_025235.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:93605607 C>T maps to NM_025235.3 R757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:93619297 C>T maps to NM_025235.3 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr10:93619360 T>C maps to NM_025235.3 T1079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr10:93586931 C>T maps to NM_025235.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr10:93590901 T>C maps to NM_025235.3 N413N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr10:93590702 T>C maps to NM_025235.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:93608291 A>G maps to NM_025235.3 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:99854026 G>T did not map to a codon.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr23:99852576 A>G did not map to a codon.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr23:99840037 A>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:99854566 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:99854138 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:99849321 T>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:99854135 A>G did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:175046850 C>T maps to NM_022093.1 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:175067522 G>A maps to NM_022093.1 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr1:175067498 C>T maps to NM_022093.1 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:175092542 C>T maps to NM_022093.1 D886D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:175097761 C>T maps to NM_022093.1 C1070C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:175105026 G>A maps to NM_022093.1 W1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:175066799 T>C maps to NM_022093.1 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr1:175067561 C>T maps to NM_022093.1 Y650Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr1:175092740 C>T maps to NM_022093.1 H952H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr1:175048763 C>T maps to NM_022093.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:175046682 C>T maps to NM_022093.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:175067570 C>T maps to NM_022093.1 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:1861849 G>A maps to ENST00000381906 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:74715141 G>A did not map to a codon.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr1:75009633 C>T maps to NM_001112808.2 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:74797198 A>G maps to NM_001112808.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:74835095 C>T maps to NM_001112808.2 C599C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:74835260 G>A maps to NM_001112808.2 E654E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:74835123 C>T maps to NM_001112808.2 R609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:74701140 A>G maps to NM_015978.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr1:74905181 T>C maps to NM_001112808.2 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr1:74905181 T>C maps to NM_001112808.2 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:55652556 G>A maps to NM_003283.4 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:201334413 C>A maps to ENST00000421663 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:201328370 G>A maps to ENST00000421663 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:201334381 G>A maps to ENST00000421663 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr1:201336917 C>T maps to ENST00000421663 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:201334429 G>T maps to ENST00000421663 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr11:1955641 C>T maps to ENST00000397301 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:1953740 C>T maps to ENST00000397301 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:11363035 G>A maps to NM_005425.4 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:11362858 G>A maps to NM_005425.4 N87N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr5:72151676 T>C maps to NM_002270.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr5:72168474 T>C maps to NM_002270.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:72178953 C>T maps to NM_002270.3 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:72196845 A>G maps to NM_002270.3 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:72195907 G>A maps to NM_002270.3 W805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:72189280 C>T maps to NM_002270.3 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:12829981 C>T maps to NM_001136196.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:12821555 G>A maps to NM_001136196.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr19:12812441 C>T maps to NM_001136196.1 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:12826086 C>T maps to NM_001136196.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:12812580 C>T maps to NM_001136196.1 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr7:128655104 T>C maps to ENST00000471166 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:128655104 T>C maps to ENST00000471166 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr7:128641270 C>T maps to ENST00000471166 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:128640605 G>A maps to ENST00000471166 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr7:128612607 G>A maps to ENST00000471166 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr1:175334317 A>G maps to NM_003285.2 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:175372341 G>A maps to NM_003285.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr1:175331865 G>A maps to NM_003285.2 Y929Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:175332867 G>A maps to NM_003285.2 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:175372291 G>A maps to NM_003285.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:175375396 G>A maps to NM_003285.2 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:175299237 G>A maps to NM_003285.2 L1255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:175365848 G>T maps to NM_003285.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:175299255 G>A maps to NM_003285.2 S1249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr1:175331871 G>A maps to NM_003285.2 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr1:175375649 G>A maps to NM_003285.2 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr1:175331871 G>T maps to NM_003285.2 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr1:175331871 G>T maps to NM_003285.2 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr1:175299294 G>A maps to NM_003285.2 A1236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:175334217 C>A maps to NM_003285.2 E839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr1:175355234 G>A maps to NM_003285.2 Y570Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:175365878 G>A maps to NM_003285.2 D347D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:5347889 C>T maps to NM_001080495.2 S2918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr7:5352826 A>G maps to NM_001080495.2 S2565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:5391687 G>A maps to NM_001080495.2 D1744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:5391723 A>G maps to NM_001080495.2 N1732N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:5347802 G>A maps to NM_001080495.2 L2947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr7:5391705 G>A maps to NM_001080495.2 D1738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:5402370 C>T maps to NM_001080495.2 G1435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:5391705 G>A maps to NM_001080495.2 D1738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:5401343 G>A maps to NM_001080495.2 R1514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:5347913 G>A maps to NM_001080495.2 D2910D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:24804908 G>T maps to NM_014494.2 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr16:24762100 C>T maps to NM_014494.2 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:24804926 G>A maps to NM_014494.2 T1103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr16:24831664 C>T maps to NM_014494.2 D1762D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr22:40704528 C>T maps to ENST00000454349 G1392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr22:40697159 C>T maps to ENST00000454349 R1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:40717173 T>G maps to ENST00000454349 T1699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr22:40662370 C>T maps to ENST00000454349 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr22:40657950 C>T maps to ENST00000454349 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr22:40662359 G>A maps to ENST00000454349 W723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr22:40660896 C>A maps to ENST00000454349 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:40708930 G>A maps to ENST00000454349 S1550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr22:40706962 C>T maps to ENST00000454349 I1481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr22:40657987 G>T maps to ENST00000454349 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:76089761 C>T maps to NM_001142640.1 D1405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:76083031 C>A maps to NM_001142640.1 P1217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:76089785 T>C maps to NM_001142640.1 T1413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:76047371 C>T maps to NM_001142640.1 N743N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:76046513 C>T maps to NM_001142640.1 N457N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr17:76067219 A>T maps to NM_001142640.1 K942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr17:76071241 C>T maps to NM_001142640.1 D978D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:218683199 G>A maps to NM_022648.4 R1181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:218678465 G>A maps to NM_022648.4 Y1497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:218682803 G>T maps to NM_022648.4 G1313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:218678510 C>T maps to NM_022648.4 P1482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:218683268 C>T maps to NM_022648.4 P1158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr2:218683268 C>T maps to NM_022648.4 P1158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:218677935 A>G did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:218674974 C>T maps to NM_022648.4 G1596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:218699817 A>G maps to NM_022648.4 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr2:218677962 C>T maps to NM_022648.4 K1539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:218678531 C>T maps to NM_022648.4 A1475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:47408787 G>A maps to NM_022748.11 H485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr7:47479120 C>T maps to NM_022748.11 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:47344433 C>A maps to NM_022748.11 E940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:47407960 C>T did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr7:47440382 T>C maps to NM_022748.11 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:47342827 C>A maps to NM_022748.11 G1059G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:47384425 C>T maps to NM_022748.11 A859A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:47451347 G>A maps to NM_022748.11 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:47317778 C>A maps to NM_022748.11 T1411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:47317778 C>A maps to NM_022748.11 T1411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:38652434 C>T maps to NM_032865.5 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr6:32030090 G>T maps to ENST00000375244 Y2337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:32053671 C>T maps to ENST00000375244 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:32012951 G>A maps to ENST00000375244 F3586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:32052334 G>A maps to ENST00000375244 D1100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:32029225 A>G maps to ENST00000375244 Y2480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:32056709 G>A maps to ENST00000375244 A877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:32036718 C>A maps to ENST00000375244 G1928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:32063796 G>A maps to ENST00000375244 Y611Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:32041547 C>T maps to ENST00000375244 P1519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:32015688 G>A maps to ENST00000375244 F3382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:32020624 G>A maps to ENST00000375244 F2979F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:32017224 G>A maps to ENST00000375244 F3193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:32047095 G>A maps to ENST00000375244 G1363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr6:32046975 G>A maps to ENST00000375244 T1403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr6:32026147 G>A maps to ENST00000375244 D2504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:32025834 C>A maps to ENST00000375244 E2609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr6:32017059 G>A maps to ENST00000375244 T3248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr6:32041547 C>T maps to ENST00000375244 P1519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr6:32024393 G>A maps to ENST00000375244 R2704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:32064015 G>A maps to ENST00000375244 C538C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:32018012 G>A maps to ENST00000375244 T3067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr6:32010333 G>A maps to ENST00000375244 N4036N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:41832524 G>A maps to NM_016272.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr22:41832458 G>A maps to NM_016272.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:45808186 T>C maps to NM_025077.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:45808848 G>A maps to NM_025077.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:35729416 G>A maps to ENST00000451197 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:52991146 C>T maps to NM_005486.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:45404020 G>A maps to NM_006114.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:161197742 C>T maps to NM_032174.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr3:100093992 G>A maps to NM_014820.3 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr3:100105122 T>C maps to NM_014820.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:100084503 C>T maps to NM_014820.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:100105122 T>C maps to NM_014820.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr3:100105122 T>C maps to NM_014820.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr3:100105122 T>C maps to NM_014820.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr20:39708806 C>T maps to NM_003286.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:39690065 C>A maps to NM_003286.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr20:39708736 T>A maps to NM_003286.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:39750721 C>T maps to NM_003286.2 R708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:39706224 C>A maps to NM_003286.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:39721180 C>A maps to NM_003286.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr8:144398218 G>A maps to NM_052963.1 R470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:144400004 C>T maps to NM_052963.1 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:144391640 G>A maps to NM_052963.1 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:144403400 G>A maps to NM_052963.1 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:38552630 A>G maps to ENST00000357601 A1244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:38555153 G>A maps to ENST00000357601 N1144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:38552561 T>A maps to ENST00000357601 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:38569497 G>T maps to ENST00000357601 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:38546234 C>T maps to ENST00000357601 S1520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr17:38564821 G>A maps to ENST00000357601 Q458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:25678728 C>A maps to ENST00000264331 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:25666190 C>T maps to ENST00000264331 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:25679653 A>G did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr3:25675406 T>C maps to ENST00000264331 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:25662277 C>T maps to ENST00000264331 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr3:25656959 C>A maps to ENST00000264331 E1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:18208456 G>A maps to NM_004618.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:18208510 G>A maps to NM_004618.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:18181298 G>A maps to NM_004618.3 N839N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr17:18178142 G>T maps to NM_004618.3 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr17:18178241 C>T maps to NM_004618.3 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr22:22316801 G>A maps to NM_003935.3 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr22:22313017 C>T maps to NM_003935.3 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr3:133336128 T>A maps to NM_007027.3 K1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:133368389 G>A maps to NM_007027.3 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:133335748 A>C maps to NM_007027.3 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr3:133356881 A>G maps to NM_007027.3 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:133362899 T>C maps to NM_007027.3 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr3:133356881 A>G maps to NM_007027.3 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:133356881 A>G maps to NM_007027.3 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr3:133362899 T>C maps to NM_007027.3 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:32542176 G>A maps to NM_005802.4 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:32543328 C>T maps to NM_005802.4 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:32542374 G>A maps to NM_005802.4 Y716Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr9:32543483 G>A maps to NM_005802.4 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr9:32544138 T>C maps to NM_005802.4 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr9:32541756 C>T maps to NM_005802.4 E922E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:132580871 T>C maps to ENST00000437532 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:132576487 G>A maps to ENST00000437532 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:132584904 C>T maps to ENST00000437532 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:179858505 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:179858476 C>T maps to ENST00000398836 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:179887121 C>T maps to ENST00000398836 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr1:179858463 A>T maps to ENST00000398836 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr1:179815682 G>A maps to NM_145034.4 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:179820118 G>A maps to NM_145034.4 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:132569588 C>T maps to NM_014506.1 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:130494366 G>T maps to NM_001085347.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:179054949 C>T maps to NM_022371.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr8:59750747 A>G maps to NM_014729.2 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr8:59739455 A>G maps to NM_014729.2 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr20:42695443 C>T maps to ENST00000348077 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:42635368 A>G maps to ENST00000348077 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:42683105 C>T maps to ENST00000348077 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr20:42694569 A>G maps to ENST00000348077 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:21960728 T>C maps to NM_014828.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr14:21963445 C>A maps to NM_014828.2 S567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2674-01A-02W-0831-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr17:7577572 G>C maps to NM_001126112.1 Y236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr17:7579389 G>A maps to NM_001126112.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr17:7578221 T>C maps to NM_001126112.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:7577028 G>A maps to NM_001126112.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:7577587 G>T maps to NM_001126112.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr17:7577560 A>G maps to NM_001126112.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr17:7578260 T>C maps to NM_001126112.1 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr17:7579467 C>T maps to NM_001126112.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr17:7577084 C>A maps to NM_001126112.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:7578247 A>G maps to NM_001126112.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3553-01A-01W-0831-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:7578215 A>G maps to NM_001126112.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:7578254 T>C maps to NM_001126112.1 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:7577609 T>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:7578275 A>G maps to NM_001126112.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3673-01A-01W-0900-09 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr17:7578245 C>T maps to NM_001126112.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:7577052 A>T maps to NM_001126112.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr17:7578401 G>T maps to NM_001126112.1 C176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr17:7577141 C>A maps to NM_001126112.1 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:7572932 T>C maps to NM_001126112.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:7576882 T>C maps to NM_001126112.1 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr17:7579407 C>A maps to NM_001126112.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:7576891 T>C maps to NM_001126112.1 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr17:7576864 A>G maps to NM_001126112.1 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr17:7577037 G>A maps to NM_001126112.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr17:7579323 A>G maps to NM_001126112.1 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:7576882 T>C maps to NM_001126112.1 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr17:7578419 C>T maps to NM_001126112.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr17:7572980 A>G maps to NM_001126112.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr17:7579362 A>G maps to NM_001126112.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr17:7578369 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:7578191 G>T maps to NM_001126112.1 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr17:7577548 G>A maps to NM_001126112.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr17:7578242 A>G maps to NM_001126112.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr17:7577587 G>A maps to NM_001126112.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:7579405 G>T maps to NM_001126112.1 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr17:7576851 C>A did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr17:7579449 A>G maps to NM_001126112.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr17:7573982 C>T maps to NM_001126112.1 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr17:7578266 A>G maps to NM_001126112.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr17:7574021 A>G maps to NM_001126112.1 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr17:7578231 A>T maps to NM_001126112.1 L206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:7577070 G>A maps to NM_001126112.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr17:7579398 A>G maps to NM_001126112.1 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:7576882 T>C maps to NM_001126112.1 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr17:7578287 A>G maps to NM_001126112.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr17:7577115 A>G maps to NM_001126112.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr17:7579530 T>C maps to NM_001126112.1 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr17:7574000 T>C maps to NM_001126112.1 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr17:7579512 T>C maps to NM_001126112.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr17:7578239 C>A maps to NM_001126112.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr17:7573009 T>C did not map to a codon.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr17:7579425 T>C maps to NM_001126112.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr17:7576851 C>A did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr17:7577067 G>T maps to NM_001126112.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr17:7579388 G>A maps to NM_001126112.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr17:7576891 T>C maps to NM_001126112.1 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr17:7577533 C>T maps to NM_001126112.1 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr17:7578262 G>T maps to NM_001126112.1 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr17:7572971 G>A maps to NM_001126112.1 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr17:7577548 G>A maps to NM_001126112.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr17:7578272 C>T maps to NM_001126112.1 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr17:7578223 T>A maps to NM_001126112.1 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr17:7578287 A>G maps to NM_001126112.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr17:7578368 A>G did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:7578470 G>A maps to NM_001126112.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr17:7578221 T>C maps to NM_001126112.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr17:7579446 A>G maps to NM_001126112.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:7577578 G>A maps to NM_001126112.1 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr17:7578431 T>C maps to NM_001126112.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr17:7577016 A>C did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr17:7573981 C>A maps to NM_001126112.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr17:7579413 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr17:7574000 T>C maps to NM_001126112.1 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr17:7577052 A>T maps to NM_001126112.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr17:7579485 T>C maps to NM_001126112.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:7576927 T>C did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr17:7573994 C>T maps to NM_001126112.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr17:7577142 C>T maps to NM_001126112.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr17:7577518 G>A maps to NM_001126112.1 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr17:7578191 G>T maps to NM_001126112.1 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:7577509 C>T maps to NM_001126112.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr17:7578555 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:7579398 A>G maps to NM_001126112.1 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr11:128807692 C>T maps to NM_022112.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr15:43748294 C>T maps to NM_001141980.1 Q837Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:43724445 A>G maps to NM_001141980.1 S1207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:43784502 C>T maps to NM_001141980.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:43708557 C>A maps to NM_001141980.1 E1580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:43766965 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:43784495 C>A maps to NM_001141980.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:43784495 C>A maps to NM_001141980.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr15:43771605 T>C maps to NM_001141980.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr15:43712599 G>A maps to NM_001141980.1 Y1528Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr1:223980218 A>G maps to NM_001031685.2 D956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:223984041 G>A maps to NM_001031685.2 N733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:223986097 C>A maps to NM_001031685.2 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:223980130 G>A maps to NM_001031685.2 Q986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr1:223991095 C>A maps to NM_001031685.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:224002010 G>A maps to NM_001031685.2 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr1:223980218 A>G maps to NM_001031685.2 D956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:44959838 C>T maps to NM_006034.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:24300580 G>A maps to NM_147184.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:24300591 G>A maps to NM_147184.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:95942748 G>T maps to NM_033285.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:95952410 T>C maps to NM_033285.3 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:45315699 G>A maps to NM_033550.3 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:45315454 C>T maps to NM_033550.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr20:44002571 C>T maps to NM_014477.2 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:44004137 G>A maps to NM_014477.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:44003909 G>A maps to NM_014477.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:189597918 C>T maps to NM_001114979.1 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:189584510 G>A maps to NM_003722.4 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:189526182 C>T maps to NM_003722.4 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:189526071 G>A maps to NM_003722.4 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:189584499 C>T maps to NM_003722.4 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr3:189585725 C>T maps to NM_003722.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:189586485 C>T maps to NM_003722.4 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:189526266 C>T maps to NM_003722.4 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:189612027 C>T maps to NM_003722.4 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:189526188 G>A maps to NM_003722.4 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:189586505 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr3:189526134 C>T maps to NM_003722.4 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:3645961 G>A maps to NM_005427.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:3624243 C>T maps to NM_005427.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:3624255 G>A maps to NM_005427.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:3646581 G>A maps to NM_005427.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:113716623 G>A maps to NM_001143819.1 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr12:113707612 G>C maps to NM_001143819.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:113724815 C>T maps to NM_001143819.1 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:113733806 C>T maps to NM_001143819.1 Q865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:68840143 C>T maps to NM_139075.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:68840441 C>T maps to NM_139075.3 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:68830440 G>A maps to NM_139075.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:68846029 G>T maps to NM_139075.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:80950449 C>T maps to NM_001025252.1 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:80992547 A>G did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr6:125550287 C>T maps to NM_003287.2 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:62505151 C>T maps to NM_199360.1 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr20:62507183 T>C maps to NM_199360.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:6329011 G>A maps to NM_033516.5 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:18057662 G>A maps to ENST00000341556 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr12:72388224 A>G maps to ENST00000389376 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:72425354 A>C maps to ENST00000389376 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr12:72388224 A>G maps to ENST00000389376 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr12:72388224 A>G maps to ENST00000389376 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr12:72388224 A>G maps to ENST00000389376 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr7:144320300 G>A maps to NM_022445.3 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:63353065 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:35684534 C>A maps to ENST00000329305 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:35689808 G>A maps to ENST00000329305 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:35685081 G>A maps to NM_213674.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:154145397 A>G maps to NM_001043351.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:154155544 C>T maps to NM_001043351.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:154144502 A>G did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr19:16204510 A>G maps to NM_001145160.1 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr6:18149253 G>A maps to NM_000367.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr6:18134094 G>A maps to NM_000367.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:1418191 C>G maps to NM_000547.5 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:1481012 C>T maps to NM_000547.5 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:1544464 G>A maps to NM_000547.5 P906P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:1480919 C>T maps to NM_000547.5 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:1520658 C>T maps to NM_000547.5 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:1457561 C>T maps to NM_000547.5 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr2:1491665 C>T maps to NM_000547.5 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr2:1457576 C>T maps to NM_000547.5 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr11:6636210 T>C maps to ENST00000453338 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr11:6637258 G>A maps to ENST00000453338 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:6638238 A>G maps to ENST00000453338 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr13:103288596 C>T maps to ENST00000376052 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr13:103288707 C>T maps to ENST00000376052 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:103289482 C>A maps to ENST00000376052 S577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr13:103297359 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr13:103297359 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:103257168 C>T maps to ENST00000376052 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr13:103280241 T>C maps to ENST00000376052 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr13:103280241 T>C maps to ENST00000376052 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr13:103299675 C>T maps to ENST00000376052 G870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr13:103268786 G>A maps to ENST00000376052 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr5:665279 T>C maps to NM_007030.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr5:665294 A>G maps to NM_007030.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr5:677920 C>T maps to NM_007030.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:21499194 G>A maps to NM_173846.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:67424211 C>T maps to NM_016140.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr1:186332577 C>T did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr1:186312595 T>C maps to NM_003292.2 R1204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr1:186328959 A>G maps to NM_003292.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:186305628 A>G maps to NM_003292.2 A1568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:186306273 C>T maps to NM_003292.2 S1459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr1:186301458 A>G maps to NM_003292.2 S1824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:186344030 C>A maps to NM_003292.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:186310225 G>A maps to NM_003292.2 S1318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:186321203 A>G maps to NM_003292.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:186321203 A>G maps to NM_003292.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:186302434 A>G maps to NM_003292.2 S1758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr1:186332061 C>T maps to NM_003292.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr1:186302434 A>G maps to NM_003292.2 S1758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:186312595 T>C maps to NM_003292.2 R1204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr1:186301458 A>G maps to NM_003292.2 S1824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:186302434 A>G maps to NM_003292.2 S1758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:186325418 A>G maps to NM_003292.2 H629H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr3:188956656 C>A maps to NM_198485.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:3544147 C>T maps to NM_182752.3 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:3541659 G>T maps to NM_182752.3 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:3544082 C>T maps to NM_182752.3 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:140087029 C>T maps to NM_001128228.2 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr19:48305145 C>T maps to NM_198479.2 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:1291217 G>A maps to ENST00000461509 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:1306864 C>T maps to NM_012217.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:65705978 A>G maps to NM_003596.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr21:10951357 G>A maps to NM_199261.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr21:10951281 G>A maps to NM_199261.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:10916376 C>T maps to NM_199261.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:10970016 C>T maps to NM_199261.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr21:10951281 G>T maps to NM_199261.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr21:10941943 A>G maps to NM_199261.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr21:10906904 T>C maps to NM_199261.2 *552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr13:20067595 C>T maps to NM_199254.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:20067595 C>T maps to NM_199254.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr13:20012234 G>A maps to NM_199254.2 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr20:30380609 C>T maps to ENST00000340513 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:30354390 G>T maps to ENST00000340513 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:30381809 G>T maps to ENST00000340513 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr20:30371702 T>A maps to ENST00000340513 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr7:23545854 G>A maps to NM_013293.3 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:185643391 G>A maps to NM_004593.2 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:185643368 C>T maps to NM_004593.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:185643398 T>C maps to NM_004593.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr22:50635875 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:67190494 C>A maps to NM_003789.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr9:123667477 G>A maps to NM_001190945.1 H357H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:139814867 C>T maps to ENST00000359662 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:139794963 G>T maps to ENST00000359662 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr9:139820172 C>T maps to ENST00000359662 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:103352551 C>T maps to NM_145725.2 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:103371796 C>T maps to NM_145725.2 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:103371802 C>T maps to NM_145725.2 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:239253145 G>T maps to NM_015650.3 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:239237343 G>A maps to NM_015650.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr2:239264708 A>G maps to NM_015650.3 K559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr2:239229371 C>A maps to NM_015650.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:239253145 G>T maps to NM_015650.3 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr1:209955412 C>T maps to NM_025228.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:209951513 G>A maps to NM_025228.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:209955412 C>T maps to NM_025228.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:211533364 C>T maps to ENST00000427925 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr1:211534099 G>A maps to ENST00000427925 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:211534446 T>G maps to ENST00000427925 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr1:211533307 C>A maps to ENST00000427925 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:36511953 G>A maps to NM_145803.1 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:36520087 T>C maps to NM_145803.1 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr11:36511762 C>T maps to NM_145803.1 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr16:2225595 G>T maps to NM_032271.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:2221293 G>A maps to NM_032271.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:2220646 C>T maps to NM_032271.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:49879335 C>T maps to NM_005879.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr3:49881257 G>A maps to NM_005879.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:42264529 T>G maps to NM_001042646.1 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr3:42264856 C>T maps to NM_001042646.1 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:42264460 T>C maps to NM_001042646.1 C698C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr3:42226217 G>A maps to NM_001042646.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:42229575 C>T maps to NM_001042646.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:202251103 G>A maps to NM_015049.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:202260101 G>A maps to NM_015049.2 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr2:202245451 T>C maps to NM_015049.2 Q853Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:202263031 G>A maps to NM_015049.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:202245444 C>A maps to NM_015049.2 G856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:202252666 T>C maps to NM_015049.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:71499188 A>G maps to NM_014294.5 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr8:71510233 G>A maps to NM_014294.5 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:71520394 G>A maps to NM_014294.5 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:118005625 T>C maps to NM_152402.2 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:118005760 C>A maps to NM_152402.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr4:118005712 C>T maps to NM_152402.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:36898692 T>A maps to NM_014831.2 S796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:36874983 C>T maps to NM_014831.2 A1986A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr3:36896709 C>T maps to NM_014831.2 K1457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr3:36898484 G>A maps to NM_014831.2 R866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:36873918 C>T maps to NM_014831.2 G2341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:36898938 C>T maps to NM_014831.2 E714E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:36898404 C>T maps to NM_014831.2 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:36887856 G>A maps to NM_014831.2 I1647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:36899232 A>C maps to NM_014831.2 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:3708853 G>A maps to NM_016292.2 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr16:3708225 G>A maps to NM_016292.2 Y673Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3679-01A-02W-0900-09 chr21:45479027 C>T maps to NM_003274.4 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr21:45518386 G>A maps to NM_003274.4 E1106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr21:45483467 C>T maps to NM_003274.4 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr21:45452011 G>A maps to NM_003274.4 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr21:45511857 A>G maps to NM_003274.4 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr21:45451970 G>T did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr21:45452035 A>G maps to NM_003274.4 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:13734197 A>T did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:13734794 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:88926073 C>T maps to NM_016209.3 Y70Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:36603546 T>A maps to NM_014408.3 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:36603573 C>T maps to NM_014408.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:45667237 G>A maps to NM_024108.1 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr8:141370287 C>T maps to NM_031466.5 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:141449153 C>A maps to NM_031466.5 G341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:141461421 G>A maps to NM_031466.5 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:140744338 G>A maps to NM_031466.5 S1152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:141034089 A>G maps to NM_031466.5 H979H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:108572534 C>T maps to NM_016388.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:17195521 T>C maps to NM_004412.5 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:17204199 C>T maps to NM_004412.5 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr6:123892158 A>C maps to NM_006073.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:123588881 G>A maps to NM_006073.2 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr6:123892251 C>A maps to NM_006073.2 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr6:123869664 A>G maps to NM_006073.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:123869689 C>T maps to NM_006073.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:118530454 C>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:41250247 G>A maps to NM_018643.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:41243946 G>T maps to NM_018643.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:41248799 A>G maps to NM_018643.2 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:41121517 G>T maps to NM_178174.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr6:41166024 G>A maps to ENST00000373108 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr6:41196489 G>A maps to NM_198153.2 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr6:42231079 G>T maps to NM_033502.2 S621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:42224546 G>A maps to NM_033502.2 C833C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr6:42231258 C>T maps to NM_033502.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:42231078 C>T maps to NM_033502.2 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr6:42214280 A>G maps to NM_033502.2 G886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:152710634 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:72969284 C>T maps to NM_013381.2 R717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:72771777 C>T maps to NM_013381.2 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:73014953 G>T maps to NM_013381.2 G801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:72667154 G>A maps to NM_013381.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:72955973 T>C maps to NM_013381.2 N561N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:72969063 G>T maps to NM_013381.2 G676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:73056899 C>T maps to NM_013381.2 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr12:72667271 C>T maps to NM_013381.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr12:72893297 C>T maps to NM_013381.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:126445614 G>A maps to NM_025195.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:126448511 C>T maps to NM_025195.2 H306H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr8:126445776 C>T maps to NM_025195.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:12880832 G>A maps to NM_021643.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:12880481 C>T maps to NM_021643.3 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:12880874 G>A maps to NM_021643.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:12863669 C>T maps to NM_021643.3 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr2:12863462 C>A maps to NM_021643.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:12880721 G>A maps to NM_021643.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr20:376931 C>T maps to ENST00000422053 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr20:368851 C>T maps to ENST00000422053 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr20:372142 C>T maps to ENST00000422053 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr20:371971 T>C maps to ENST00000422053 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr6:30128593 G>T maps to NM_006778.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:30126364 G>A maps to NM_006778.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:30121958 G>A maps to NM_006778.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr13:50586658 C>T maps to NM_001007278.1 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:50587062 C>T maps to NM_001007278.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr9:100854208 G>A maps to NM_033219.1 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr9:100857227 G>A maps to NM_033219.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:30139753 G>A maps to NM_033229.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:30139771 C>A maps to NM_033229.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr6:30138322 C>T maps to NM_033229.2 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:15535913 C>T maps to ENST00000455584 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:15535017 G>A maps to ENST00000455584 D356D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr17:15532480 T>C maps to ENST00000455584 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr17:18630893 T>G maps to NM_001037330.1 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:228595961 C>A maps to NM_016102.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:228596897 C>T maps to NM_016102.3 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:228595961 C>T maps to NM_016102.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr1:228596798 C>T maps to NM_001134855.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:228602464 G>A maps to NM_016102.3 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:154249752 T>A maps to NM_015271.3 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr4:154216476 C>T maps to NM_015271.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:154216995 C>T maps to NM_015271.3 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:154243885 G>A maps to NM_015271.3 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:4411570 G>A maps to NM_003141.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:4406832 C>T maps to NM_003141.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:5719555 G>A maps to NM_006074.4 Q177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr5:64907522 A>G maps to NM_001656.3 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr5:64905201 T>C maps to NM_001656.3 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr5:64905201 T>C maps to NM_001656.3 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:64909987 T>C maps to NM_001656.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:64909987 T>C maps to NM_001656.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:138262237 C>T maps to NM_015905.2 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr7:138235836 T>C maps to NM_015905.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:138239455 C>T maps to NM_015905.2 I425I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CA-6718-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:138262237 C>T maps to NM_015905.2 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr7:138235836 T>C maps to NM_015905.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:138268671 C>T maps to NM_015905.2 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr7:138268671 C>A maps to NM_015905.2 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:138203956 C>T maps to NM_015905.2 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:54976524 A>G maps to NM_005082.4 H368H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr17:54969483 C>T maps to NM_005082.4 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr6:30153715 G>T maps to NM_003449.3 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:30166517 G>A maps to NM_003449.3 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:30164370 G>A maps to NM_003449.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr6:30166679 G>A maps to NM_003449.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:30154048 G>A maps to NM_003449.3 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:28891382 G>A maps to NM_006510.4 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr6:28872119 T>C maps to NM_006510.4 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:59060403 C>T maps to NM_005762.2 R487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr19:59061362 C>T maps to NM_005762.2 R718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr19:59061350 C>T maps to NM_005762.2 H714H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:119998259 C>T maps to NM_012101.3 E306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr11:6479489 C>T maps to NM_033278.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:6479468 C>T maps to NM_033278.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr11:6479366 G>A maps to NM_033278.2 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr11:6472625 G>A maps to NM_033278.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:30071564 G>A maps to NM_007028.3 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr6:30071891 C>T maps to NM_007028.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:119460675 C>T maps to NM_012210.3 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr9:119461659 G>T maps to NM_012210.3 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr9:119461598 C>A maps to NM_012210.3 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:114976294 C>T maps to NM_015906.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr1:114976300 T>C maps to NM_015906.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:114948206 G>A maps to NM_015906.3 R865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:114976243 C>T maps to NM_015906.3 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr1:114942231 C>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:5653755 T>C maps to NM_001003819.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:5653767 G>A maps to NM_001003819.3 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr11:5653740 T>A maps to NM_001003819.3 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:5663737 T>C did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr8:27145294 C>T maps to NM_171982.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr5:114499400 C>A maps to NM_018700.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr5:114469587 T>C maps to NM_018700.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr5:114469587 T>C maps to NM_018700.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:114483065 C>T maps to NM_018700.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr5:114480312 A>G maps to NM_018700.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:114513563 T>G maps to NM_001017398.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr5:114469587 T>C maps to NM_018700.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:114466326 T>C maps to NM_018700.3 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr5:114469587 T>C maps to NM_018700.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr5:114482960 T>C maps to NM_018700.3 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:114482962 C>A maps to NM_018700.3 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr5:114469803 A>G maps to NM_018700.3 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr17:57128676 A>G maps to NM_015294.3 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:57076782 G>A maps to NM_015294.3 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:57119243 A>G maps to NM_015294.3 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:57106033 G>A maps to NM_015294.3 R667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:57153051 C>A maps to NM_015294.3 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr17:57165758 G>C maps to NM_015294.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr17:57128676 A>G maps to NM_015294.3 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:30309924 C>A maps to NM_021253.3 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr6:30309621 C>T maps to NM_021253.3 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr6:30303706 C>T maps to NM_021253.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:30309621 C>T maps to NM_021253.3 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:99500889 C>T maps to NM_033017.3 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:180661969 T>G maps to NM_201627.1 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr5:180651184 G>A maps to NM_033549.3 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr3:140397100 A>G maps to NM_152616.4 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr3:140419801 C>T maps to NM_152616.4 Q720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:140401912 C>T maps to NM_152616.4 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:140401459 C>T maps to NM_152616.4 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr3:140406990 C>T maps to NM_152616.4 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:140407191 T>C maps to NM_152616.4 C556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:140401870 C>A maps to NM_152616.4 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr11:35747696 G>T maps to NM_017583.4 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:35685075 C>T maps to NM_017583.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:117659290 G>A maps to NM_025188.3 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:117658312 T>C did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr1:117660661 C>A maps to NM_025188.3 G406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr1:117661316 C>T maps to NM_025188.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:117663415 G>A maps to NM_025188.3 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:117658311 C>T did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr1:117659338 C>T maps to NM_025188.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr1:117656104 G>T maps to NM_025188.3 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:155150501 G>T maps to NM_025058.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:155154430 G>A maps to NM_025058.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:155151085 C>T maps to NM_025058.3 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:155154358 C>T maps to NM_025058.3 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:155149717 G>A maps to NM_025058.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr17:73871097 C>T maps to NM_033452.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:73870956 G>A maps to NM_033452.2 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:73870623 G>A maps to NM_033452.2 D619D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:55029785 C>T maps to NM_024114.3 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:89531756 G>T maps to NM_020358.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr11:89531783 C>A maps to NM_020358.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:5699634 G>T maps to NM_033034.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:5686248 A>C maps to NM_033034.2 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr7:72732997 G>A maps to NM_178125.2 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:72727342 G>A maps to NM_178125.2 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr7:72726958 G>A maps to NM_178125.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr5:180687439 T>C maps to NM_032765.2 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:27521439 G>A maps to NM_032546.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:27521452 C>T maps to NM_032546.3 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:27527861 A>G maps to NM_032546.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:67064759 G>A maps to NM_184085.1 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:67039671 G>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr7:100731738 C>T maps to NM_030961.1 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr7:100731111 C>T maps to NM_030961.1 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr1:248039701 T>C maps to NM_015431.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:248020703 C>T maps to NM_015431.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr1:248039220 C>T maps to NM_015431.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr1:248039701 T>C maps to NM_015431.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr1:248039415 C>A maps to NM_015431.3 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:248039701 T>C maps to NM_015431.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:160156158 C>T maps to ENST00000483754 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr3:160156617 A>C maps to ENST00000483754 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr11:5626617 C>T maps to NM_001003819.3 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:5631435 C>T maps to NM_001003819.3 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:5626617 C>T maps to NM_001003819.3 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:5653545 C>T maps to NM_001003819.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:5653545 C>T maps to NM_001003819.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:165961382 T>A maps to NM_152620.2 C53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:165962540 T>G maps to NM_152620.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:165961415 C>T maps to NM_152620.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr4:165962036 A>G maps to NM_152620.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:73886937 G>A maps to NM_173547.2 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr1:231349674 C>T maps to NM_001004342.3 H746H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr1:231342459 C>T maps to NM_001004342.3 Y581Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:231342435 C>T maps to NM_001004342.3 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:231298738 C>T maps to NM_001004342.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:231298858 G>A maps to NM_001004342.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:231342462 C>T maps to NM_001004342.3 N582N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:231337126 C>T maps to NM_001004342.3 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:231342462 C>T maps to NM_001004342.3 N582N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:231342438 T>C maps to NM_001004342.3 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr11:4621925 G>A maps to NM_018073.5 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:4621712 C>T maps to NM_018073.5 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr11:4622018 A>G maps to NM_018073.5 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr11:4622018 A>G maps to NM_018073.5 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:45047252 A>G maps to NM_182985.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr15:45059513 C>T maps to NM_182985.3 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:180625204 T>G maps to NM_203293.1 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:180622642 C>T maps to NM_203293.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:180622240 G>A maps to NM_203293.1 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:32859628 C>T maps to NM_001039111.1 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:32932352 C>T maps to NM_001039111.1 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:32933065 C>A maps to NM_001039111.1 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:32933285 C>T maps to NM_001039111.1 R864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr16:31230668 C>T maps to NM_001008274.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:31235535 G>A maps to NM_001008274.3 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:104416654 C>T maps to NM_030912.2 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:104416555 C>T maps to NM_030912.2 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:104416962 C>G maps to NM_030912.2 S503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:104416663 G>T maps to NM_030912.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:51561111 G>A maps to ENST00000338969 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr14:51446148 C>A maps to ENST00000338969 E757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:51467493 G>A maps to ENST00000338969 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:51561384 C>T maps to ENST00000338969 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr14:51560955 C>T maps to ENST00000338969 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr14:51444035 G>A maps to NM_015163.5 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr14:51475904 C>T maps to ENST00000338969 W400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr4:189067976 G>A maps to NM_178556.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr4:189065282 C>T maps to NM_178556.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr4:189060960 C>A maps to NM_178556.3 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:189012655 G>A maps to ENST00000326754 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr4:189012952 C>A maps to ENST00000326754 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr4:189013096 T>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:14387605 G>A maps to NM_007118.2 G1210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr5:14508131 C>T maps to NM_007118.2 L2965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr5:14497065 C>T maps to NM_007118.2 G2653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:14419939 C>T maps to NM_007118.2 N1671N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:14508200 C>T maps to NM_007118.2 G2988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:14508200 C>T maps to NM_007118.2 G2988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:14508110 C>T maps to NM_007118.2 F2958F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:14504648 C>T maps to NM_007118.2 V2853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:14508314 C>T maps to NM_007118.2 F3026F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr5:14358330 C>T maps to NM_007118.2 D697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr5:14358339 C>T maps to NM_007118.2 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:14487618 C>G maps to NM_007118.2 G2294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:14488222 C>T maps to NM_007118.2 R2496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr5:14297203 C>T maps to NM_007118.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr5:14487618 C>G maps to NM_007118.2 G2294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:14280431 T>C maps to NM_007118.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:14479449 C>A maps to NM_007118.2 T2078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr5:14387900 C>T maps to NM_007118.2 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:14465651 A>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr5:14492765 G>T maps to NM_007118.2 G2575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr5:14297299 G>A maps to NM_007118.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:14270946 C>T maps to NM_007118.2 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:14488128 G>A maps to NM_007118.2 A2464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:14508341 C>T maps to NM_007118.2 P3035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr5:14492767 A>G maps to NM_007118.2 G2575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr5:14358330 C>T maps to NM_007118.2 D697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:38121331 C>T maps to NM_001039141.2 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr22:38120428 T>C maps to NM_001039141.2 D622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr22:38120051 C>T maps to NM_001039141.2 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr22:38120129 C>T maps to NM_001039141.2 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr22:38120053 A>G maps to NM_001039141.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:6743777 G>A maps to ENST00000313244 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr14:92439175 T>C maps to NM_004239.3 L1868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr14:92472044 G>A maps to NM_004239.3 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr14:92472629 G>A maps to NM_004239.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr14:92442459 T>C maps to NM_004239.3 K1778K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:92471237 G>A maps to NM_004239.3 R1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:92471237 G>A maps to NM_004239.3 R1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr14:92480702 C>A maps to NM_004239.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr14:92441012 G>T maps to NM_004239.3 P1844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr14:92470680 C>T maps to NM_004239.3 K1213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr14:92480700 T>C maps to NM_004239.3 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr14:92439175 T>C maps to NM_004239.3 L1868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:230636318 G>A maps to ENST00000389044 G1881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:230657812 A>G maps to ENST00000389044 H1312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:230652241 T>C maps to ENST00000389044 A1631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:230693966 A>G maps to ENST00000389044 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:230661335 G>A maps to ENST00000389044 R1236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:230655918 A>G maps to ENST00000389044 G1461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:230662510 A>G maps to ENST00000389044 H1146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr2:230668350 A>C maps to ENST00000389044 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:230724268 A>G maps to ENST00000389044 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr2:230683208 T>A maps to ENST00000389044 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:230642129 T>C maps to ENST00000389044 S1783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:230643667 C>T maps to ENST00000389044 A1684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:230723677 C>T maps to ENST00000389044 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:230723869 C>T maps to ENST00000389044 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:230723851 A>G maps to ENST00000389044 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:230683208 T>A maps to ENST00000389044 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:230675920 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:230683208 T>C maps to ENST00000389044 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr2:230667083 T>C maps to ENST00000389044 G1003G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr15:64710831 A>G maps to NM_016213.4 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr15:64686192 T>C maps to NM_016213.4 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:100468232 T>C maps to NM_003302.2 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr7:100468283 A>G maps to NM_003302.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:40307571 G>T maps to ENST00000316891 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:40310220 G>A maps to ENST00000316891 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:13220805 C>T maps to NM_001136035.2 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:13216194 G>A maps to NM_001136035.2 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:13226228 G>A maps to NM_001136035.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr6:126317171 G>A maps to NM_001031712.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr6:126332472 T>C maps to NM_001031712.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:126319742 G>A maps to NM_001031712.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr6:126317169 C>A maps to NM_001031712.2 R66R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AZ-4315-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr23:100292051 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr23:100276090 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:100277037 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:100276969 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:61442540 C>A maps to NM_020810.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr14:61442481 G>A maps to NM_020810.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr14:61442481 G>A maps to NM_020810.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr20:5922604 G>A maps to NM_015939.3 N368N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:5924271 G>A maps to NM_015939.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr14:103999024 G>A maps to ENST00000299201 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:103996339 C>T maps to ENST00000299201 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:29087916 G>A maps to NM_017910.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:46749742 C>T maps to NM_018006.4 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:46751890 C>A maps to NM_018006.4 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr3:3189645 G>A maps to NM_182916.2 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:3189272 G>A maps to NM_182916.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:54952913 C>G did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:54957414 G>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:54949364 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:54956373 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:54950918 T>C did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:54950943 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:54954150 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:54955114 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:54956936 T>G did not map to a codon.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr23:54956130 G>A did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:54949796 C>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:54949438 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:54957194 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:54950943 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:54952045 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:54949670 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:54951126 T>C did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:54950145 T>A did not map to a codon.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr23:54952110 G>C did not map to a codon.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr23:54956878 G>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:54950034 C>T did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:54955076 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:54956091 T>G did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:49724193 C>G maps to NM_005480.3 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr12:49724344 G>T maps to NM_005480.3 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:193046158 T>A maps to NM_004600.5 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr8:72935335 A>G maps to NM_007332.2 T1055T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:72948635 C>T maps to NM_007332.2 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:72964988 A>G maps to NM_007332.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:72975036 C>A maps to NM_007332.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:72984051 C>T maps to NM_007332.2 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:72966059 G>A maps to NM_007332.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:72950286 A>T maps to NM_007332.2 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:72948575 A>G maps to NM_007332.2 C834C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:72981382 C>A maps to NM_007332.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr8:72935335 A>G maps to NM_007332.2 T1055T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:72948575 A>G maps to NM_007332.2 C834C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr8:72948575 A>G maps to NM_007332.2 C834C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr8:72975060 G>A maps to NM_007332.2 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr8:72948575 A>G maps to NM_007332.2 C834C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:72963012 C>T maps to NM_007332.2 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr8:72973969 A>G maps to NM_007332.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr3:142503847 A>G maps to ENST00000476941 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:142522906 G>T maps to ENST00000476941 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:142509969 C>A maps to ENST00000476941 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr3:142521186 G>A did not map to a codon.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr4:122825611 G>A maps to NM_001130698.1 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:122853605 G>A maps to NM_001130698.1 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr4:122846205 A>G maps to NM_001130698.1 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr4:122853578 G>A maps to NM_001130698.1 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr4:122854058 G>A maps to NM_001130698.1 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:122824165 G>T maps to NM_001130698.1 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:122872745 G>A maps to NM_001130698.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:122872778 C>T maps to NM_001130698.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr4:122824120 A>T maps to NM_001130698.1 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr4:122853986 G>A maps to NM_001130698.1 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr4:122853635 G>A maps to NM_001130698.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr13:38211558 C>T maps to NM_003306.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr13:38225428 T>C maps to NM_003306.1 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr13:38225515 A>T maps to NM_003306.1 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr13:38248373 T>C maps to NM_003306.1 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr13:38225545 A>G maps to NM_003306.1 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:38320331 G>A maps to NM_003306.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr13:38320285 C>A maps to NM_003306.1 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:38211381 G>T maps to NM_003306.1 I869I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:38229287 G>T maps to NM_003306.1 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr13:38225512 G>T maps to NM_003306.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr13:38266166 G>A maps to NM_003306.1 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:38225455 T>C maps to NM_003306.1 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr13:38266235 G>A maps to NM_003306.1 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr13:38225512 G>A maps to NM_003306.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr13:38320385 G>T maps to NM_003306.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr13:38225422 T>C maps to NM_003306.1 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:33592269 C>T maps to NM_015638.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr23:111020032 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:111022223 C>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:111090572 G>A did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:111019685 A>C did not map to a codon.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr23:111155753 C>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:111155730 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:111090572 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:111020010 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:111025268 G>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:111155846 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:111090572 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:111095569 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:111078327 G>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:111090507 G>A did not map to a codon.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr23:111078307 T>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:111078264 G>A did not map to a codon.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr11:101374889 G>A maps to NM_004621.5 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr11:101375147 C>T maps to NM_004621.5 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr11:101374889 G>A maps to NM_004621.5 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr11:101374889 G>A maps to NM_004621.5 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr11:101375048 G>T maps to NM_004621.5 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:101374889 G>T maps to NM_004621.5 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:135692319 T>C maps to NM_020389.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr5:135587337 G>A maps to NM_020389.2 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr5:135651371 G>A maps to NM_020389.2 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:135587448 G>A maps to NM_020389.2 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:135567122 G>A maps to NM_020389.2 Y653Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr5:135561021 G>C maps to NM_020389.2 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr15:31294624 C>T maps to NM_002420.4 T1404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr15:31295080 T>C maps to NM_002420.4 E1252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:31341661 G>A maps to NM_002420.4 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:31354786 C>A maps to NM_002420.4 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:31294540 A>G maps to NM_002420.4 C1432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:31295002 G>A maps to NM_002420.4 N1278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr15:31338436 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr15:31295263 A>G maps to NM_002420.4 N1191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:31294038 C>A maps to NM_002420.4 E1600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:31294276 G>A maps to NM_002420.4 R1520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr15:31330342 G>T maps to NM_002420.4 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr21:45786638 C>T maps to ENST00000397932 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr21:45786702 C>T maps to ENST00000397932 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr21:45855037 G>A maps to ENST00000397932 L1383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr21:45821662 C>T maps to ENST00000397932 F807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr21:45819242 C>T maps to ENST00000397932 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr21:45820224 G>A maps to ENST00000397932 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:73151345 G>A maps to ENST00000419692 D1515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:73461500 G>A maps to ENST00000419692 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr9:73477877 C>T maps to ENST00000419692 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:73477943 G>A maps to ENST00000419692 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:73218323 C>T maps to ENST00000419692 W864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr9:73235035 G>A maps to ENST00000419692 N649N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:73213484 G>A maps to ENST00000419692 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:73152212 G>A maps to ENST00000419692 I1226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr9:73151498 A>G maps to ENST00000419692 R1464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr9:73151498 A>G maps to ENST00000419692 R1464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:73167778 A>G maps to ENST00000419692 D1139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:73240406 G>T maps to ENST00000411705 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr9:73164493 G>C maps to ENST00000419692 S1178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr9:73235023 G>A maps to ENST00000419692 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:73426149 C>T maps to ENST00000419692 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr9:73426146 A>G maps to ENST00000419692 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr9:73426146 A>G maps to ENST00000419692 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr9:73426146 A>G maps to ENST00000419692 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:49671601 T>C maps to NM_017636.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:49692314 C>T maps to NM_017636.3 D662D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:49692022 C>T maps to NM_017636.3 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:49685971 G>A maps to NM_017636.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr19:49713616 C>T maps to NM_017636.3 R1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:49685965 C>T maps to NM_017636.3 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:49675264 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:49671946 C>A maps to NM_017636.3 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:49671838 C>T maps to NM_017636.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr11:2436437 G>A maps to ENST00000452833 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:2444212 C>T maps to ENST00000452833 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr9:77457186 A>G maps to NM_017662.4 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr9:77377202 C>A maps to NM_017662.4 E1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:77377434 A>G maps to NM_017662.4 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:77502748 C>T maps to NM_017662.4 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:77435335 G>A maps to NM_017662.4 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:77339596 C>A maps to NM_017662.4 E2001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr15:50920432 A>G maps to NM_017672.4 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:50884760 G>T maps to NM_017672.4 S1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:50884407 C>A maps to NM_017672.4 E1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:50886718 G>A maps to NM_017672.4 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:50923656 T>C maps to NM_017672.4 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr15:50902083 G>A maps to NM_017672.4 I785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:50866668 C>A maps to NM_017672.4 E1704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr15:50901804 T>C maps to NM_017672.4 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr15:50920432 A>G maps to NM_017672.4 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr15:50901804 T>C maps to NM_017672.4 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr15:50920432 A>G maps to NM_017672.4 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr15:50935714 G>A maps to NM_017672.4 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr15:50901775 A>G did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr15:50901804 T>C maps to NM_017672.4 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr15:50901804 T>C maps to NM_017672.4 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:234854585 C>T maps to NM_024080.4 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:234871930 G>A maps to NM_024080.4 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:234835190 T>C maps to NM_024080.4 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:234847745 C>T maps to NM_024080.4 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:234915581 C>T maps to NM_024080.4 N1072N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:234869448 G>A maps to NM_024080.4 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:234847769 G>A maps to NM_024080.4 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:234847745 C>A maps to NM_024080.4 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr8:116616926 A>G maps to NM_014112.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:116427306 G>C maps to NM_014112.2 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:116616593 C>T maps to NM_014112.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:116616404 C>T maps to NM_014112.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr8:116599476 C>T maps to NM_014112.2 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:116632162 C>T maps to NM_014112.2 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:116599710 G>A maps to NM_014112.2 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:116599371 C>T maps to NM_014112.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr8:116631433 A>G maps to NM_014112.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr8:116426721 C>T maps to NM_014112.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr8:116599404 C>T maps to NM_014112.2 R841R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr8:116616926 A>G maps to NM_014112.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:116616297 G>T maps to NM_014112.2 S633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr8:116616926 A>G maps to NM_014112.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr8:116427033 C>A maps to NM_014112.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr8:116599311 G>A maps to NM_014112.2 G872G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr8:116599302 C>T maps to NM_014112.2 K875K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr8:116426721 C>T maps to NM_014112.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr11:63992063 C>T maps to NM_001160393.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:3494309 C>T maps to ENST00000399756 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr17:3494360 G>A maps to ENST00000399756 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:3495377 G>A maps to ENST00000399756 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:3494357 G>A maps to ENST00000399756 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:3491574 G>A maps to ENST00000399756 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:16325985 G>A maps to NM_016113.4 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr17:3427613 A>G maps to ENST00000381913 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:3448483 G>T maps to ENST00000381913 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:3431411 C>T maps to ENST00000381913 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:3436223 C>T maps to ENST00000381913 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:3446879 C>T maps to ENST00000381913 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr12:110222190 G>A maps to NM_021625.4 N796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr12:110230483 C>T maps to NM_021625.4 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr7:142626622 A>G maps to NM_019841.4 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:142605754 A>G maps to NM_019841.4 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:142626580 G>T maps to NM_019841.4 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:142626550 G>A maps to NM_019841.4 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:142627462 G>A maps to NM_019841.4 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr7:142626634 A>C maps to NM_019841.4 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr7:142605796 G>A maps to NM_019841.4 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:142612048 A>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:142611834 A>C maps to NM_019841.4 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr7:142572321 G>A maps to NM_018646.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr7:142572363 G>T maps to NM_018646.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr7:142574922 G>T maps to NM_018646.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:98547351 C>T maps to ENST00000359863 R1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:98608993 C>T maps to ENST00000359863 R3711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr7:98524888 C>A maps to ENST00000359863 A1025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr7:98565206 C>T maps to ENST00000359863 F2459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:98533269 A>G maps to ENST00000359863 S1361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr7:98550867 G>T maps to ENST00000359863 E1841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr7:98552776 G>A maps to ENST00000359863 Q1922Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:98569468 G>T maps to ENST00000359863 T2573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:98609881 C>T maps to ENST00000359863 F3828F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:98545941 G>A maps to ENST00000359863 T1542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr7:98563472 C>A maps to ENST00000359863 I2370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:98574212 C>T maps to ENST00000359863 C2682C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:98547863 C>T maps to ENST00000359863 F1764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr7:98609761 C>T maps to ENST00000359863 D3788D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr7:98547743 T>G maps to ENST00000359863 R1724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:98540630 C>T maps to ENST00000359863 S1488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:98574581 G>A maps to ENST00000359863 A2749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:98608718 G>A maps to ENST00000359863 P3647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr7:98592277 G>A maps to ENST00000359863 V3358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:98569468 G>A maps to ENST00000359863 T2573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:98515220 G>A maps to ENST00000359863 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr7:98592469 G>A maps to ENST00000359863 T3422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:98524789 C>T maps to ENST00000359863 N992N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:98609103 G>A maps to ENST00000359863 P3747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr7:98555701 C>T maps to ENST00000359863 R2103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr7:98493412 A>G maps to ENST00000359863 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr7:98493412 A>G maps to ENST00000359863 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr9:135797256 A>G maps to NM_000368.4 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:135779130 C>T maps to NM_000368.4 E705E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr9:135801105 G>A maps to NM_000368.4 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:135782189 G>A maps to NM_000368.4 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr9:135779190 T>C maps to NM_000368.4 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:135804223 G>T maps to NM_000368.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:135772662 C>T maps to NM_000368.4 E961E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:135771795 G>A maps to NM_000368.4 D1107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr9:135798750 C>T maps to NM_000368.4 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:135781194 A>T maps to NM_000368.4 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:2105442 G>A maps to NM_000548.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr16:2122848 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:2115608 C>T maps to NM_000548.3 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr16:2104427 G>A maps to NM_000548.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:2129086 C>T maps to NM_000548.3 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:2132488 G>A maps to NM_000548.3 R1289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr13:45148203 G>A maps to NM_183422.2 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr13:45147954 T>C maps to NM_183422.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:45010692 A>C maps to NM_006022.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr3:150128153 T>C maps to NM_014779.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:150127970 G>A maps to NM_014779.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:107018481 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:106959996 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:106959139 C>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:100074937 G>A maps to NM_030935.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:184020999 C>T maps to NM_052965.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:12531404 G>T maps to NM_025265.3 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:12544850 G>A maps to NM_025265.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:12544850 G>A maps to NM_025265.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr3:12544790 G>A maps to NM_025265.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr3:12558135 A>G maps to NM_025265.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr3:12558135 A>G maps to NM_025265.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:12558135 A>G maps to NM_025265.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:73518238 C>T maps to NM_207346.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr17:73519782 T>C maps to NM_207346.2 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:18503413 G>A maps to NM_006292.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:99725895 G>A maps to NM_025244.2 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:99725402 C>A maps to NM_025244.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr2:99720473 G>A maps to NM_025244.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:99651690 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:65713271 G>A maps to NM_152762.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr7:130357605 A>G maps to NM_052933.2 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:115576114 C>T maps to NM_000549.3 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:115576075 C>T maps to NM_000549.3 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr14:81609346 G>T maps to NM_000369.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:81606160 T>G maps to NM_000369.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:81609502 C>T maps to NM_000369.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:81557427 T>C maps to NM_000369.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:81606172 C>T maps to NM_000369.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr14:81609916 C>T maps to NM_000369.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr14:81609694 C>T maps to NM_000369.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr14:81610270 C>T maps to NM_000369.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr14:81609337 A>G maps to NM_000369.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr14:81610287 T>A maps to NM_000369.2 L629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr18:72999857 G>A maps to NM_005786.4 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:72998900 G>A maps to NM_005786.4 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr18:72998702 G>A maps to NM_005786.4 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr18:73000343 C>T maps to NM_005786.4 G949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr18:72999683 G>A maps to NM_005786.4 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr18:72997583 C>T maps to NM_005786.4 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr18:72999956 C>T maps to NM_005786.4 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3527-01A-01W-0831-10 chr20:51872384 C>T maps to NM_173485.5 A796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr20:51870839 C>T maps to NM_173485.5 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr20:51871826 G>A maps to NM_173485.5 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:51871781 C>A maps to NM_173485.5 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02F-01A-01W-A00E-09 chr20:51870104 C>T maps to NM_173485.5 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:51872381 C>T maps to NM_173485.5 I795I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:51871889 C>T maps to NM_173485.5 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr20:51870468 C>T maps to NM_173485.5 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:51870965 C>T maps to NM_173485.5 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr20:51871043 C>T maps to NM_173485.5 N349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr20:51871889 C>T maps to NM_173485.5 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:31769384 C>A maps to NM_020856.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:31767626 C>T maps to NM_020856.2 P1024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr19:31770212 G>A maps to NM_020856.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr19:31769339 C>T maps to NM_020856.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:31770476 G>A maps to NM_020856.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr19:31768400 C>T maps to NM_020856.2 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr19:31769252 G>A maps to NM_020856.2 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:31770413 G>A maps to NM_020856.2 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr19:31770140 C>T maps to NM_020856.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:31770647 G>A maps to NM_020856.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:31768043 C>T maps to NM_020856.2 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr19:31767932 G>A maps to NM_020856.2 Y922Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:31769384 C>T maps to NM_020856.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:31768676 C>T maps to NM_020856.2 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr19:31770658 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr19:31768400 C>T maps to NM_020856.2 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3530-01A-01W-0995-10 chr19:50251422 G>A maps to NM_021733.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:50243050 G>A maps to NM_021733.1 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:50247576 G>A maps to NM_021733.1 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:50266447 C>A maps to NM_021733.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:50251645 G>A maps to NM_021733.1 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:50266447 C>A maps to NM_021733.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr11:76507574 G>A maps to NM_015516.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:76507118 G>A maps to NM_015516.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr11:76507397 G>A maps to NM_015516.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:76507586 C>T maps to NM_015516.3 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:110409261 C>T maps to NM_033035.4 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:110409277 G>T maps to NM_033035.4 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:122516311 G>T maps to NM_004622.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:122518993 G>A maps to NM_004622.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:122516343 A>G maps to NM_004622.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr2:122516343 A>G maps to NM_004622.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr2:122520632 A>G maps to NM_004622.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr2:122516343 A>G maps to NM_004622.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr2:122520632 A>G maps to NM_004622.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:143356158 C>A maps to ENST00000445818 G478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr1:231678341 C>T maps to NM_005999.2 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:67857537 G>T maps to ENST00000339830 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr16:67860109 C>T maps to ENST00000339830 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:67861862 T>C maps to ENST00000339830 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:79612160 C>T maps to NM_031945.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:79612442 T>C maps to NM_031945.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:31116849 C>T maps to NM_001080509.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:31135996 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:120428920 T>A maps to NM_012338.3 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:82269184 C>T maps to NM_030927.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:82275991 G>T maps to NM_030927.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:71265992 C>T maps to NM_012339.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:11417374 C>A maps to NM_012466.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr5:176083738 C>T maps to NM_012171.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr11:44940829 C>T maps to ENST00000425677 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr11:44941387 C>T maps to ENST00000425677 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr11:44941453 G>A maps to ENST00000425677 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:44940849 C>A maps to ENST00000425677 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr11:44941378 C>T maps to ENST00000425677 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:85423717 T>G maps to NM_001100917.1 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:115615560 G>T maps to NM_005725.4 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:115604773 C>T maps to NM_005725.4 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:115615580 T>C maps to NM_005725.4 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:77346611 C>A maps to NM_005724.5 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:58140002 C>A maps to NM_005981.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:99399876 G>A maps to NM_005723.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:99403202 G>T maps to NM_005723.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:99891685 C>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:99890198 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:99890689 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:99891632 A>G did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:99890587 A>C did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:99891619 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:99888991 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr23:99888434 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr23:99888435 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:38420869 T>C did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr23:38530639 T>C did not map to a codon.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr23:38535047 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:38530639 T>C did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:38546875 C>T did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr23:38533569 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:38525536 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:38540476 C>T did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:38530640 T>C did not map to a codon.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr23:38535028 C>T did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:71533489 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:71526595 G>A maps to NM_004616.2 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr12:71533629 T>C did not map to a codon.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr12:3387609 A>G maps to ENST00000407263 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr12:3390366 C>T maps to ENST00000407263 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:43558843 G>A maps to NM_000714.4 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:41011295 C>T maps to NM_001159726.1 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr24:6115427 T>C did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:53112276 G>T did not map to a codon.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr23:53112395 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:53116988 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:53111972 A>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:53114950 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:116574465 G>A maps to ENST00000368611 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:116573985 G>A maps to ENST00000368611 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:98288839 A>G maps to NM_033512.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:98289661 G>A maps to NM_033512.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:98289706 G>A maps to NM_033512.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:54482715 G>A maps to NM_001003937.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr2:54482772 G>A maps to NM_001003937.2 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:54483108 C>T maps to NM_001003937.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:54482706 C>T maps to NM_001003937.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:54482928 C>T maps to NM_001003937.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:54482130 G>A maps to NM_001003937.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:54482808 G>A maps to NM_001003937.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr17:2237777 G>A maps to NM_018128.4 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:2232664 G>A maps to NM_018128.4 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:2235463 G>A maps to NM_018128.4 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr17:2235485 G>A maps to NM_018128.4 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr17:2236407 C>T maps to NM_018128.4 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr17:2238853 C>T maps to NM_018128.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:54467206 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:3261113 C>T maps to ENST00000398659 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:3341854 C>T maps to ENST00000398659 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:112770527 G>A maps to NM_032028.3 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:112769507 A>G maps to NM_032028.3 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:112769819 C>T maps to NM_032028.3 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr5:112769903 G>A maps to NM_032028.3 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:112770419 C>T maps to NM_032028.3 A39A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A6-6780-01A-11D-1835-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-3966-01A-01W-1073-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AA-A010-01A-01W-A00E-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AU-6004-01A-11D-1719-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AZ-4315-01A-01D-1408-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:32829232 C>T maps to NM_052841.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:32829289 C>T maps to NM_052841.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:100368457 A>G maps to NM_139246.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:100367791 C>T maps to NM_139246.4 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr9:100364995 G>A maps to NM_139246.4 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr9:100368457 A>G maps to NM_139246.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr6:43227414 G>A maps to NM_032538.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:43220493 C>T maps to NM_032538.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr6:43251672 G>A maps to NM_032538.1 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:43225608 C>A maps to NM_032538.1 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr6:43220514 C>T maps to NM_032538.1 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:43251042 C>T maps to NM_032538.1 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr6:43222800 C>T maps to NM_032538.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:43164917 G>A maps to ENST00000263802 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:43067377 C>T maps to ENST00000263802 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:43170760 C>A maps to NM_173500.3 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr15:43044267 C>T maps to ENST00000263802 W1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:43045171 C>A maps to ENST00000263802 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:43044269 T>C maps to ENST00000263802 S1463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr15:43045187 T>C maps to ENST00000263802 Q1157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr5:159437636 T>C maps to NM_003314.1 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:113211440 C>T maps to NM_017868.3 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:113200679 G>T maps to NM_017868.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:113205734 C>T maps to NM_017868.3 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:113211428 C>A maps to NM_017868.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:231059669 G>A maps to NM_024525.4 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:231044528 G>A maps to NM_024525.4 D799D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:231044498 C>T maps to NM_024525.4 E809E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr1:231060660 C>T maps to NM_024525.4 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:231060660 C>A maps to NM_024525.4 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:180322347 T>C maps to NM_133462.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:180325448 G>T maps to NM_133462.3 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:180328303 G>T maps to NM_133462.3 E763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:180321069 G>T maps to NM_133462.3 G149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr3:180327537 G>A maps to NM_133462.3 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:3405663 C>T maps to NM_016030.5 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr2:3464058 T>C maps to NM_016030.5 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:3392389 C>T maps to NM_016030.5 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr2:3464058 T>C maps to NM_016030.5 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:130485453 G>A maps to NM_144965.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:130486542 G>A maps to NM_144965.1 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr11:43418345 C>T maps to NM_018259.5 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:43428932 G>T maps to NM_018259.5 E624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr11:43400784 G>T maps to NM_018259.5 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:43419594 A>G maps to NM_018259.5 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr11:43472791 C>T maps to NM_018259.5 R1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:75107951 G>A maps to NM_145170.3 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:75051169 G>A maps to NM_145170.3 R755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr10:75038038 G>A maps to NM_145170.3 Q836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:75037097 G>T maps to NM_145170.3 S877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:75051202 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:75069971 T>C maps to NM_145170.3 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:39166825 C>T maps to ENST00000301819 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:39161505 C>T maps to ENST00000301819 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:39153965 C>T maps to ENST00000301819 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:166786756 C>A maps to NM_024753.3 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:166786685 T>C maps to NM_024753.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:166731339 A>T maps to NM_024753.3 V1292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:166805993 G>A maps to NM_024753.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr2:166786687 G>A maps to NM_024753.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr2:166797565 A>G maps to NM_024753.3 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr2:166740360 T>C maps to NM_024753.3 Q1209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:55251699 G>A maps to NM_001114108.1 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr15:99768896 G>A maps to NM_022905.4 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:99740150 G>A maps to NM_022905.4 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:34850316 C>T maps to NM_144725.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:34840820 C>T maps to NM_144725.3 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:34850316 C>T maps to NM_144725.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:34850316 C>T maps to NM_144725.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:34864548 G>T maps to NM_144725.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:34867035 A>G maps to NM_144725.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:156556272 G>A maps to NM_001105669.2 W560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:156555792 G>A maps to NM_001105669.2 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:156553128 G>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:40117185 T>C maps to ENST00000377543 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:40113476 C>T maps to ENST00000377543 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr17:40091573 G>A maps to ENST00000377543 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:138845747 G>T maps to NM_024926.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:138831940 C>A maps to NM_024926.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:138863304 A>G maps to NM_024926.2 Q401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr2:33045890 T>C maps to NM_017735.4 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:33036135 C>T maps to NM_017735.4 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr2:33037596 C>A maps to NM_017735.4 Y741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr2:32983472 C>A maps to NM_017735.4 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr2:33007706 G>A maps to NM_017735.4 W598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:33045959 G>A maps to NM_017735.4 V829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr4:147860972 G>T maps to ENST00000513335 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:147795916 G>A maps to ENST00000513335 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:147824791 C>A maps to ENST00000513335 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr4:147830322 G>A maps to ENST00000513335 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr21:38522403 C>T maps to NM_003316.3 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr21:38460553 C>T maps to NM_003316.3 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:38460523 T>C maps to NM_003316.3 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr21:38467694 G>T maps to NM_003316.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr21:38524295 G>T maps to NM_003316.3 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:178482982 T>C maps to NM_152275.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr2:178481445 C>A maps to NM_152275.3 G662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:178482807 G>A maps to NM_152275.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:178483234 G>A maps to NM_152275.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:178481598 C>A maps to NM_152275.3 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:178482763 A>G maps to NM_152275.3 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:178416387 G>A maps to NM_152517.2 C368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:178416677 C>A maps to NM_152517.2 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:178416561 C>T maps to NM_152517.2 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:74720216 C>T maps to NM_022492.4 R478*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3872-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr2:74720209 A>T maps to NM_022492.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr5:40746924 C>A maps to NM_012382.2 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:40746897 A>G did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr5:40747035 C>A maps to NM_012382.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:109498787 C>T maps to NM_014673.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:94803569 G>A maps to NM_014639.3 D1540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr5:94857878 T>C maps to NM_014639.3 E630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:94857878 T>C maps to NM_014639.3 E630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr5:94859029 C>A maps to NM_014639.3 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr5:94839590 A>G maps to NM_014639.3 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:94863778 C>A maps to NM_014639.3 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:94838627 A>G maps to NM_014639.3 Y1099Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:94833130 G>A maps to NM_014639.3 R1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:94818242 T>G maps to NM_014639.3 P1382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:46669804 C>T maps to NM_017931.2 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr22:46684401 C>T maps to NM_017931.2 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr22:46668269 C>T maps to NM_017931.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr22:46685332 C>T maps to NM_017931.2 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:51787445 C>A maps to ENST00000447632 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:51753908 G>A maps to ENST00000447632 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:51767351 G>A maps to ENST00000447632 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:15189767 C>T maps to NM_152574.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:15214180 A>G maps to NM_152574.2 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:15267937 G>A maps to NM_152574.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr18:21660801 C>A maps to NM_001135993.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:55183318 C>A maps to NM_004623.4 Y128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:47184024 C>T maps to ENST00000394850 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:47184060 C>T maps to ENST00000394850 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:47177652 T>C maps to ENST00000394850 H112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:47233182 C>T maps to ENST00000394850 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr2:47278960 C>T maps to ENST00000394850 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr14:91007828 G>A maps to NM_001010854.1 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr14:91121400 C>T maps to NM_001010854.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:91077182 A>G maps to NM_001010854.1 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:91247234 C>A maps to NM_001010854.1 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr14:91007747 G>A maps to NM_001010854.1 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr14:91113317 G>A maps to NM_001010854.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr14:89337994 A>G maps to NM_144596.2 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr14:89307485 C>A maps to NM_144596.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:89305828 G>T maps to NM_144596.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr14:71134431 C>A maps to NM_015351.1 Y186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:62496478 A>G maps to NM_173810.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:135251364 C>T maps to NM_007344.2 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:135254497 A>G maps to NM_007344.2 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:135275461 G>A maps to NM_007344.2 Y517Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:117633246 T>C did not map to a codon.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr1:117620556 C>T maps to NM_003594.3 H531H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:117617694 C>T maps to NM_003594.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:117618192 G>A maps to NM_003594.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:117618264 C>T maps to NM_003594.3 D353D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:117635418 T>C maps to NM_003594.3 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:80751903 A>G maps to NM_003318.4 K853K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr6:80747706 A>G maps to NM_003318.4 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr6:80721178 A>G maps to NM_003318.4 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:80747706 A>G maps to NM_003318.4 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:113251867 G>T maps to NM_153712.4 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:113251878 C>T maps to NM_153712.4 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:113277948 T>C maps to NM_153712.4 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr22:43442423 G>A maps to NM_012263.4 Y378Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr22:43460272 C>T maps to NM_012263.4 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr1:1132065 C>A maps to NM_001130045.1 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:1132096 G>T did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr1:1115603 C>A maps to NM_001130045.1 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr1:1115603 C>T maps to NM_001130045.1 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:124751970 C>A maps to NM_001139442.1 G348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:124794079 C>T maps to NM_001139442.1 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:124751548 G>A maps to NM_001139442.1 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:124751545 C>T maps to NM_001139442.1 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr9:124751926 C>T maps to NM_001139442.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr9:124622634 G>A maps to NM_001139442.1 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:43570611 C>T maps to NM_015140.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr22:43579146 G>A maps to NM_015140.3 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr22:43575985 C>T maps to NM_015140.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr22:43564150 G>A maps to NM_015140.3 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:90801485 G>A maps to ENST00000438251 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:167755077 G>T maps to NM_031949.4 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:9871012 C>T maps to NM_001025930.3 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:9868894 G>A maps to NM_001025930.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:9867483 C>T maps to NM_001025930.3 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:9877043 C>T maps to NM_001025930.3 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:219616466 G>T maps to NM_014640.4 E972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:219603298 T>C maps to NM_014640.4 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr14:76165588 G>A maps to NM_015072.4 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr14:76249776 C>T maps to NM_015072.4 R964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:76349059 C>A maps to NM_015072.4 S1185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:76249776 C>T maps to NM_015072.4 R964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:76249664 C>T maps to NM_015072.4 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr14:76173431 T>C did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr17:46862383 A>G maps to NM_001130918.1 N647N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr17:46863546 G>A maps to NM_001130918.1 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:84394871 G>A maps to NM_024686.4 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr1:84394906 G>A maps to NM_024686.4 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:84372034 C>A maps to NM_024686.4 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:84403624 C>T maps to NM_024686.4 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr22:50470537 G>A maps to NM_001080447.1 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr2:179611405 C>A maps to ENST00000375038 E5243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:179666928 T>C maps to NM_133378.4 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr2:179438326 G>A maps to NM_133378.4 Q21610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr2:179453352 T>C maps to NM_133378.4 E18465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr2:179642180 G>T maps to NM_133378.4 G1537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:179407132 A>G maps to NM_133378.4 V29882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:179592035 G>A maps to NM_133378.4 R5442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:179400187 G>A maps to NM_133378.4 G31150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:179449075 G>T maps to NM_133378.4 I19166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:179457897 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:179469989 G>A maps to NM_133378.4 R15404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:179397589 A>G maps to NM_133378.4 L32016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:179434079 A>G maps to NM_133378.4 F23025F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr2:179452770 A>G maps to NM_133378.4 A18553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:179396620 G>T maps to NM_133378.4 I32339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:179455520 G>A maps to NM_133378.4 R17743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:179560960 C>A maps to NM_133378.4 E9036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:179594487 C>T maps to NM_133378.4 Q4920Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr2:179490117 G>T maps to NM_133378.4 V12242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr2:179648922 G>A maps to NM_133378.4 F883F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr2:179604135 T>A maps to NM_133437.3 I4437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:179431070 G>A maps to NM_133378.4 S24028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:179395462 T>C maps to NM_133378.4 K32725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:179396692 G>A maps to NM_133378.4 R32315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:179474561 T>C maps to NM_133378.4 R14628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:179495845 G>A maps to NM_133378.4 I12075I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:179575511 G>A maps to NM_133378.4 R8194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:179423275 G>A maps to NM_133378.4 G26402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:179468996 G>A maps to NM_133378.4 F15571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:179600699 C>A maps to NM_133378.4 E3581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:179612931 G>T maps to ENST00000375038 S4734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:179613531 A>C maps to ENST00000375038 L4534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr2:179598041 G>A maps to NM_133378.4 H4082H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr2:179612564 A>G maps to ENST00000375038 S4856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:179631233 G>A maps to NM_133378.4 R3193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr2:179636163 G>A maps to NM_133378.4 T2630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:179484510 T>C maps to NM_133378.4 Q12943Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:179647682 C>A maps to NM_133378.4 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:179395462 T>C maps to NM_133378.4 K32725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:179441839 G>T maps to NM_133378.4 S20506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:179494033 G>A maps to NM_133378.4 S12238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:179616385 G>A maps to ENST00000375038 L3583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:179635205 G>A maps to NM_133378.4 I2771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:179648446 C>T maps to NM_133378.4 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:179397570 G>A maps to NM_133378.4 R32023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:179426123 T>C maps to NM_133378.4 E25677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:179452470 C>A maps to NM_133378.4 G18621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:179466139 T>C maps to NM_133378.4 K15960K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:179606562 T>C maps to NM_133437.3 E3628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:179396491 C>T maps to NM_133378.4 S32382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:179418737 T>C maps to NM_133378.4 E27132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr2:179641514 A>G maps to NM_133378.4 G1692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:179456174 C>A maps to NM_133378.4 G17525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:179464485 C>T maps to NM_133378.4 P16146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:179498194 G>A maps to NM_133378.4 G11729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr2:179621398 G>A maps to NM_133437.3 Q3431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:179397814 A>T maps to NM_133378.4 L31941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:179466154 T>C maps to NM_133378.4 G15955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:179516632 T>C maps to NM_133378.4 P10685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:179538426 C>T maps to NM_133378.4 V10272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:179641025 C>A maps to NM_133378.4 G1855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr2:179644741 A>C maps to NM_133378.4 T1238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr2:179576941 C>T maps to NM_133378.4 P7961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr2:179397589 A>G maps to NM_133378.4 L32016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:179442500 A>G maps to NM_133378.4 P20316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:179458949 G>A maps to NM_133378.4 L16822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:179574311 C>T maps to NM_133378.4 T8334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:179595811 G>T maps to NM_133378.4 G4616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:179641994 G>A maps to NM_133378.4 V1565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr2:179407412 C>A maps to NM_133378.4 E29822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:179412413 G>A maps to NM_133378.4 T28745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:179494149 T>G maps to NM_133378.4 R12200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:179497756 A>G maps to NM_133378.4 I11799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:179433590 T>C maps to NM_133378.4 A23188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:179545032 G>A maps to NM_133378.4 V9878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:179425739 C>T maps to NM_133378.4 E25805E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:179446654 G>A maps to NM_133378.4 A19579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:179428361 G>T maps to NM_133378.4 T24931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:179466465 G>A maps to NM_133378.4 R15883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:179641310 G>A maps to NM_133378.4 C1760C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:179409090 C>T maps to NM_133378.4 Q29387Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:179425532 G>A maps to NM_133378.4 A25874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:179430413 G>A maps to NM_133378.4 Y24247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr2:179633625 G>A maps to NM_133378.4 N2979N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:179399239 G>A maps to NM_133378.4 F31466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:179427827 G>A maps to NM_133378.4 L25109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:179453600 C>A maps to NM_133378.4 E18383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:179577621 C>A maps to NM_133378.4 G7800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:179615266 C>A maps to ENST00000375038 E3956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:179636046 A>G maps to NM_133378.4 S2669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:179398381 G>A maps to NM_133378.4 I31752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:179585337 A>C maps to NM_133378.4 S6473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr2:179581903 G>T maps to NM_133378.4 G7275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:179666973 G>A maps to NM_133378.4 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:179396034 C>A maps to NM_133378.4 E32535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:179427832 C>A maps to NM_133378.4 E25108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:179495590 G>T maps to NM_133378.4 I12130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:179499207 G>T maps to NM_133378.4 I11532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:179569255 G>A maps to NM_133378.4 S8737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:179579172 G>A maps to NM_133378.4 I7532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:179640737 T>C maps to NM_133378.4 V1951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:179645913 C>A maps to NM_133378.4 E1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:179669351 C>T maps to NM_133378.4 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr2:179408002 G>A maps to NM_133378.4 R29665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179402066 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179418028 T>C maps to NM_133378.4 R27298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179425300 C>A maps to NM_133378.4 E25952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179427754 G>A maps to NM_133378.4 R25134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179429179 C>A maps to NM_133378.4 E24659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179430272 G>A maps to NM_133378.4 S24294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179486021 G>A maps to NM_133378.4 C12573C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179542485 G>A maps to NM_133378.4 L10141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179583912 G>A maps to NM_133378.4 C6824C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179595717 C>A maps to NM_133378.4 E4648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179599470 G>A maps to NM_133378.4 V3816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179613494 G>A maps to ENST00000375038 D4546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:179659915 G>T maps to NM_133378.4 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr2:179594835 G>T maps to NM_133378.4 A4853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:179440280 G>A maps to NM_133378.4 P20958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr2:179464575 G>A maps to NM_133378.4 C16116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:179421584 G>A maps to NM_133378.4 I26864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:179471891 G>A maps to NM_133378.4 Q15245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr2:179482763 G>T maps to NM_133378.4 R13204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:179428361 G>A maps to NM_133378.4 T24931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr2:179428618 G>A maps to NM_133378.4 R24846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr2:179477521 A>T maps to NM_133378.4 P14074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr2:179596187 C>A maps to NM_133378.4 E4525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr2:179665379 G>A maps to NM_133378.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:179542420 A>G maps to NM_133378.4 P10162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:179574311 C>A maps to NM_133378.4 T8334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr2:179458167 T>C maps to NM_133378.4 T17021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr2:179452692 G>A maps to NM_133378.4 A18579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr2:179474561 T>C maps to NM_133378.4 R14628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr2:179581821 C>A maps to NM_133378.4 E7303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:179404277 C>T maps to NM_133378.4 V30270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr2:179410757 G>A maps to NM_133378.4 D29167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr2:179611381 C>A maps to ENST00000375038 E5251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:179456503 T>C maps to NM_133378.4 V17446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:179453856 A>G maps to NM_133378.4 P18297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:179474031 G>A maps to NM_133378.4 R14767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:179391749 G>A maps to NM_133378.4 R33421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:179396617 A>G maps to NM_133378.4 F32340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:179426957 A>C maps to NM_133378.4 L25399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:179429821 G>A maps to NM_133378.4 R24445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:179474255 G>A maps to NM_133378.4 R14693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:179482119 G>A maps to NM_133378.4 R13330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:179486044 C>A maps to NM_133378.4 G12566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:179497034 C>T maps to NM_133378.4 W11961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:179569648 A>G maps to NM_133378.4 F8639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:179599629 G>A maps to NM_133378.4 G3763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr2:179575470 G>A maps to NM_133378.4 S8207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr2:179442016 C>T maps to NM_133378.4 A20447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:179498580 G>T maps to NM_133378.4 V11647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:179395462 T>C maps to NM_133378.4 K32725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr2:179414887 A>G maps to NM_133378.4 T27991T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr2:179441117 C>T maps to NM_133378.4 P20679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr2:179487395 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr2:179659185 T>A maps to NM_133378.4 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179399239 G>A maps to NM_133378.4 F31466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179404292 G>A maps to NM_133378.4 L30265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179419747 C>A maps to NM_133378.4 E26912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179422483 G>A maps to NM_133378.4 V26631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179424330 A>C maps to NM_133378.4 L26275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179430959 G>A maps to NM_133378.4 F24065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179432720 A>G maps to NM_133378.4 H23478H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179436326 G>T maps to NM_133378.4 Y22276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179454007 G>T maps to NM_133378.4 S18247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179496982 G>A maps to NM_133378.4 D11978D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179497445 A>G maps to NM_133378.4 C11861C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179500442 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179539105 G>T maps to NM_133378.4 S10247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179552846 C>A maps to NM_133378.4 E9524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179577514 G>A maps to NM_133378.4 F7835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179590149 G>A maps to NM_133378.4 C5683C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179616103 C>A maps to ENST00000375038 E3677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179622335 G>T maps to NM_133432.3 Y3491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179654730 C>A maps to NM_133378.4 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:179654778 C>A maps to NM_133378.4 E622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:179453262 A>G did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:179598351 A>C maps to NM_133378.4 L4011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:179615320 G>A maps to ENST00000375038 R3938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr2:179640869 T>C maps to NM_133378.4 T1907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr2:179399905 G>T maps to NM_133378.4 T31244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr2:179429240 A>G maps to NM_133378.4 I24638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:179453856 A>G maps to NM_133378.4 P18297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:179505979 T>A maps to NM_133378.4 K10973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr2:179429588 A>G maps to NM_133378.4 L24522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr2:179399905 G>T maps to NM_133378.4 T31244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr2:179407925 T>C maps to NM_133378.4 T29690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr2:179606562 T>C maps to NM_133437.3 E3628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:179413898 G>T maps to NM_133378.4 P28250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:179412920 C>G maps to NM_133378.4 R28576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:179414183 A>G maps to NM_133378.4 P28155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:179510752 A>G maps to NM_133378.4 P10866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:179410253 A>G maps to NM_133378.4 Y29293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:179629527 C>T maps to NM_133378.4 P3238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:179454190 C>T maps to NM_133378.4 W18186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:179474935 C>T maps to NM_133378.4 W14538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:179542873 T>C maps to NM_133378.4 K10080K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:179576878 G>A maps to NM_133378.4 C7982C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:179474015 G>T maps to NM_133378.4 R14773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:179478664 C>A did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:179497916 G>T maps to NM_133378.4 S11793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:179603001 A>G maps to NM_133378.4 A3482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:179395462 T>C maps to NM_133378.4 K32725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:179414887 A>G maps to NM_133378.4 T27991T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:179594553 G>A maps to NM_133378.4 D4898D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:179643638 C>A maps to NM_133378.4 P1390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr2:179590329 G>A maps to NM_133378.4 A5623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:179471844 A>G maps to NM_133378.4 L15260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:179593864 A>G maps to NM_133378.4 N5056N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:179621183 G>A maps to NM_133437.3 C3502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:179634898 G>T maps to NM_133378.4 V2843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr2:179400997 T>C maps to NM_133378.4 P30924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr2:179404664 T>C maps to NM_133378.4 R30141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr2:179397559 G>T maps to NM_133378.4 R32026R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr2:179593296 G>A maps to NM_133378.4 S5208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:179397805 C>T maps to NM_133378.4 P31944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:179399905 G>T maps to NM_133378.4 T31244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:179404664 T>C maps to NM_133378.4 R30141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:179458387 C>A maps to NM_133378.4 G16979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:179474561 T>C maps to NM_133378.4 R14628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:179489339 C>T maps to NM_133378.4 G12321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:179427758 T>C maps to NM_133378.4 K25132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr2:179434250 A>G maps to NM_133378.4 G22968G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr2:179428868 C>T maps to NM_133378.4 Q24762Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr2:179472551 C>T maps to NM_133378.4 P15086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr2:179510752 A>G maps to NM_133378.4 P10866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr2:179395462 T>C maps to NM_133378.4 K32725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr2:179641292 A>T maps to NM_133378.4 V1766V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr2:179650442 C>T maps to NM_133378.4 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr2:179453352 T>C maps to NM_133378.4 E18465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr2:179640869 T>C maps to NM_133378.4 T1907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:179600412 C>T maps to NM_133378.4 T3676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:179640848 C>T maps to NM_133378.4 A1914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr2:179517060 G>C maps to NM_133378.4 P10613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr2:179517069 A>T maps to NM_133378.4 P10610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr2:179482554 A>G maps to NM_133378.4 V13273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:179395462 T>C maps to NM_133378.4 K32725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:179486325 T>C maps to NM_133378.4 R12507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr2:179431313 G>A maps to NM_133378.4 G23947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr2:179640500 G>C maps to NM_133378.4 L2030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr2:179440586 T>C maps to NM_133378.4 K20856K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr2:179455962 G>A maps to NM_133378.4 A17595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:179621198 G>A maps to NM_133437.3 D3497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:179666955 G>A maps to NM_133378.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr2:179454190 C>T maps to NM_133378.4 W18186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr2:179500867 C>A maps to NM_133378.4 V11242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr2:179641514 A>G maps to NM_133378.4 G1692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:179494966 C>T did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr2:179437012 G>A maps to NM_133378.4 R22048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr2:179592835 C>A did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr2:179643656 A>G maps to NM_133378.4 A1384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:179404664 T>C maps to NM_133378.4 R30141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:179429954 G>T maps to NM_133378.4 I24400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:179437997 C>A maps to NM_133378.4 L21719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr2:179605791 G>T maps to NM_133437.3 P3885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:179452770 A>G maps to NM_133378.4 A18553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr2:179590681 C>T maps to NM_133378.4 P5545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr2:179458197 A>G maps to NM_133378.4 V17011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr2:179454009 T>C maps to NM_133378.4 R18246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:179404664 T>C maps to NM_133378.4 R30141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:179454190 C>T maps to NM_133378.4 W18186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr2:179403769 G>A maps to NM_133378.4 P30396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr2:179495649 G>A maps to NM_133378.4 R12111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr2:179435390 A>G maps to NM_133378.4 A22588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr2:179611634 G>A maps to ENST00000375038 S5166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr2:179604135 T>A maps to NM_133437.3 I4437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr2:179435390 A>G maps to NM_133378.4 A22588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr2:179454009 T>C maps to NM_133378.4 R18246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr2:179615282 T>C maps to ENST00000375038 Q3950Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:179593062 A>G maps to NM_133378.4 S5252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr2:179404664 T>C maps to NM_133378.4 R30141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr2:179641514 A>G maps to NM_133378.4 G1692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:179469927 G>A maps to NM_133378.4 G15424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:179666955 G>A maps to NM_133378.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:179453352 T>C maps to NM_133378.4 E18465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:179474935 C>T maps to NM_133378.4 W14538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:179435390 A>G maps to NM_133378.4 A22588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:179454009 T>C maps to NM_133378.4 R18246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:179460378 C>A maps to NM_133378.4 V16666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr2:179510752 A>G maps to NM_133378.4 P10866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:179440598 C>T maps to NM_133378.4 P20852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr2:179486325 T>C maps to NM_133378.4 R12507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr2:179599091 G>A maps to NM_133378.4 V3909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:179577182 G>A maps to NM_133378.4 Q7912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:179395462 T>C maps to NM_133378.4 K32725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:179635205 G>A maps to NM_133378.4 I2771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:179429981 G>A maps to NM_133378.4 G24391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:179453973 T>C maps to NM_133378.4 S18258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:179574431 A>G maps to NM_133378.4 S8294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr20:43108737 C>A maps to NM_024331.3 C33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr20:43108857 C>T maps to NM_024331.3 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr18:29175097 T>C maps to ENST00000432547 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr18:29175118 A>G maps to ENST00000432547 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr19:54930426 G>A maps to ENST00000391739 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:54946768 C>T maps to ENST00000391739 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:54930429 C>T maps to ENST00000391739 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:72233507 C>A maps to NM_032646.5 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:72246430 C>T maps to NM_032646.5 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr11:8123100 C>T maps to NM_003320.4 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr11:8060485 C>T maps to NM_003320.4 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr11:8120356 C>T maps to NM_003320.4 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr11:8118319 C>T maps to NM_003320.4 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr11:8117138 C>T maps to NM_003320.4 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:8120325 G>A maps to NM_003320.4 K395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:49580178 C>A maps to NM_006009.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr12:49579758 C>T maps to NM_006009.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:49580451 C>T maps to NM_006009.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:49521893 C>T maps to NM_006082.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr13:19752430 G>A maps to NM_006001.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:19753676 C>T maps to NM_006001.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr13:19751363 C>T maps to NM_006001.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr13:19751434 G>A maps to NM_006001.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr13:19752478 G>A maps to NM_006001.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr13:19748089 G>T maps to NM_006001.1 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:132238153 C>T maps to NM_080386.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr2:130953851 G>A maps to NM_207312.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr2:130953941 G>A maps to NM_207312.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:130949664 G>A maps to NM_207312.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:220115937 A>G maps to NM_006000.1 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:220116426 G>A maps to NM_006000.1 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:220115937 A>G maps to NM_006000.1 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr22:18607050 C>T maps to NM_018943.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:5436205 C>T maps to NM_024803.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:30691354 A>G maps to NM_178014.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:30691165 C>T maps to NM_178014.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:30692146 C>T maps to NM_178014.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:57599543 C>T maps to NM_030773.3 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:57599222 C>T maps to NM_030773.3 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr6:3154126 G>A maps to NM_001069.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr6:3226485 G>T maps to NM_178012.4 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr6:3225014 G>A maps to NM_178012.4 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:140137053 C>T maps to NM_006088.5 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:140137896 C>T maps to NM_006088.5 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr9:140137893 C>T maps to NM_006088.5 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr16:90001392 G>A maps to ENST00000304984 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr16:90001338 C>T maps to ENST00000304984 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:90001338 C>T maps to ENST00000304984 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:90001620 C>T maps to ENST00000304984 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr16:90001458 C>G maps to ENST00000304984 Y547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:6495414 C>T maps to NM_006087.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:6495276 G>A maps to NM_006087.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:6495447 G>A maps to NM_006087.2 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:6495627 G>A maps to NM_006087.2 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr19:6501535 G>A maps to NM_006087.2 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr19:6495336 G>A maps to NM_006087.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr18:12310999 C>T maps to NM_032525.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr18:12310963 C>T maps to NM_032525.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr18:12325768 C>T maps to NM_032525.1 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:12325114 C>T maps to NM_032525.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:94001 C>A maps to NM_177987.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr10:95151 G>A maps to NM_177987.2 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr17:57958428 G>A maps to NM_016261.3 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr17:57937775 A>G maps to NM_016261.3 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr17:57937775 A>G maps to NM_016261.3 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:112393215 G>A maps to NM_016262.4 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:112392704 A>C maps to NM_016262.4 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:112400841 C>A maps to NM_016262.4 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr6:112405394 T>C maps to NM_016262.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:40765684 C>A maps to NM_001070.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:40762210 T>C maps to NM_001070.4 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:40766938 C>T maps to NM_001070.4 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr17:40815056 C>T maps to NM_016437.2 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:40817718 C>T maps to NM_016437.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr17:40817778 G>T maps to NM_016437.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr10:135103367 C>T maps to NM_006659.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr10:135098641 G>A maps to NM_006659.2 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:135106711 G>A maps to NM_006659.2 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr10:135113047 C>T maps to NM_006659.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr10:135107109 C>T maps to NM_006659.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:113143917 G>A maps to NM_006322.4 R848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:113158399 G>A maps to NM_006322.4 H751H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:22842085 G>A maps to NM_052903.4 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:22841054 C>T maps to NM_052903.4 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:50656786 G>A maps to NM_020461.3 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr22:50659052 C>T maps to NM_020461.3 V1245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr22:50659598 G>A maps to NM_020461.3 V1063V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr22:50656992 G>C maps to NM_020461.3 G1626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:50660510 A>G maps to NM_020461.3 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr22:50664523 G>A maps to NM_020461.3 Y596Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr22:50658082 G>A maps to NM_020461.3 Y1435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr22:50657577 C>T maps to NM_020461.3 A1515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr22:50659790 C>T maps to NM_020461.3 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:28854369 G>T maps to NM_003321.4 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:28855387 G>A maps to NM_003321.4 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:28855324 G>A maps to NM_003321.4 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:151536435 G>A maps to NM_020127.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr6:35477676 C>T maps to NM_003322.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr6:35473866 C>T maps to NM_003322.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr6:35466229 A>T maps to NM_003322.3 Y501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr6:35479434 G>A maps to NM_003322.3 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr6:35479524 C>T maps to NM_003322.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr6:35479515 C>T maps to NM_003322.3 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:49387058 G>T maps to NM_003323.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:49391404 G>A maps to NM_003323.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:49391266 G>A maps to NM_003323.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:3047413 G>A maps to NM_001160408.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr6:158834140 G>A maps to NM_020245.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:158924660 C>T maps to NM_020245.3 T1322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:158923247 G>A maps to NM_020245.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr6:158915799 C>T maps to NM_020245.3 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:158924441 G>A maps to NM_020245.3 T1249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:158925068 G>T maps to NM_020245.3 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:158900824 C>T maps to NM_020245.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr6:158873190 A>G maps to NM_020245.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr6:158910755 A>G maps to NM_020245.3 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:15397998 G>A maps to NM_006765.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr8:15508206 C>T maps to NM_006765.2 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:15588188 G>A maps to NM_006765.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:15508235 G>A maps to NM_006765.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:15480587 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:15605905 C>T maps to NM_006765.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr8:15531302 T>C maps to NM_006765.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:15517146 G>A maps to NM_006765.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:1183438 G>A maps to NM_172367.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:1183561 C>T maps to NM_172367.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr11:62348622 A>G maps to NM_022830.2 C253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr11:62348622 A>G maps to NM_022830.2 C253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr11:62349044 C>A maps to NM_022830.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:44194315 C>T maps to NM_002822.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:44193220 G>A maps to NM_002822.3 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr12:44191531 T>C maps to NM_002822.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3520-01A-01W-0831-10 chr3:52269093 G>A maps to NM_007284.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr3:52265959 G>T maps to NM_007284.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:52263130 G>A maps to NM_007284.3 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:52263073 C>T maps to NM_007284.3 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr7:19156560 G>A maps to NM_000474.3 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:19156416 G>A maps to NM_000474.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr7:19738154 C>T maps to NM_001002926.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:48114498 G>A maps to NM_003328.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr4:48114447 G>A maps to NM_003328.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr4:48088601 G>A maps to NM_003328.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:32660717 G>A maps to NM_175852.3 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:32657916 C>T maps to NM_175852.3 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr6:139563911 C>T maps to ENST00000358430 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:139598052 C>A maps to ENST00000358430 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:139597981 C>T maps to ENST00000358430 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:139563812 G>A maps to ENST00000358430 C635C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:16850811 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:16857989 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:16855757 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:16850755 A>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:16859606 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:16847824 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:16836987 G>T did not map to a codon.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr23:16852425 A>C did not map to a codon.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr23:16859758 A>G did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr9:113013636 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:11791983 G>A maps to ENST00000356957 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:11773230 C>T maps to ENST00000356957 A926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:52490212 G>A maps to NM_015913.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr1:52486660 G>A maps to NM_015913.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:134229333 T>C maps to NM_024715.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:134229333 T>C maps to NM_024715.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr14:52948969 A>G maps to NM_020784.2 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:52907319 C>T maps to NM_020784.2 Q655Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:52899162 T>C maps to NM_020784.2 E779E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:52906084 G>T maps to NM_020784.2 I677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:6545106 T>A maps to NM_032731.3 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:9887393 C>T maps to NM_001098529.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr18:9888068 A>G maps to NM_001098529.1 E531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:9886890 G>T maps to NM_001098529.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:37890315 C>T maps to NM_016616.4 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr7:37934111 C>T maps to NM_016616.4 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:37923971 G>A maps to NM_016616.4 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:37927880 T>G maps to NM_016616.4 L417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr7:37916482 G>T maps to NM_016616.4 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:37901670 G>A maps to NM_016616.4 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:37903063 C>T maps to NM_016616.4 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:37905167 A>G maps to NM_016616.4 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr7:37901737 C>T maps to NM_016616.4 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:37901737 C>A maps to NM_016616.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:37934137 T>C maps to NM_016616.4 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr6:7904928 C>A maps to NM_030810.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:7904928 C>T maps to NM_030810.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr6:7891940 C>T maps to NM_030810.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr3:138037013 G>A maps to ENST00000333911 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:138025299 G>T maps to ENST00000333911 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr3:138022430 C>A maps to ENST00000333911 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:99944082 C>A maps to NM_005783.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr18:77733750 G>A maps to NM_006701.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:72120624 G>A maps to NM_001142318.1 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:72122959 T>C maps to NM_001142318.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:104713346 G>T maps to NM_001093771.1 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr12:104712833 G>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr22:19918586 G>A maps to NM_006440.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr22:19902796 A>G maps to NM_006440.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:10477139 G>A maps to NM_003331.4 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:50965644 C>A maps to ENST00000395681 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr18:669135 C>T maps to NM_001071.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr18:670770 G>A maps to NM_001071.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr18:670768 C>T maps to NM_001071.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:88911366 C>T maps to NM_000372.4 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:88911210 G>A maps to NM_000372.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr11:88911357 G>A maps to NM_000372.4 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr11:88911357 G>A maps to NM_000372.4 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:88924374 C>T maps to NM_000372.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:88961060 T>C maps to NM_000372.4 Y369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr15:41865580 T>C maps to NM_006293.3 R687R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:41865276 C>T maps to NM_006293.3 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:41870147 C>T maps to NM_006293.3 R783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr15:41865881 G>A maps to NM_006293.3 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr15:41853760 C>T maps to NM_006293.3 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:12704610 A>G maps to NM_000550.2 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:12698632 T>C maps to NM_000550.2 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:71902478 C>T maps to NM_173555.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:66548521 T>C maps to NM_018264.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:66548515 G>A maps to NM_018264.2 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:66582514 T>C maps to NM_018264.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:66563594 C>T maps to NM_018264.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:72277766 G>T maps to NM_001145440.1 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:75217983 G>A maps to NM_138467.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr1:75202278 A>G maps to NM_138467.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr1:75204423 A>T maps to NM_138467.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr1:75202278 A>G maps to NM_138467.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:75214493 A>G maps to NM_138467.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr21:44521491 C>T maps to NM_001025203.1 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:36235265 G>A maps to ENST00000412391 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:56171881 T>C maps to NM_007279.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr19:56179888 G>A maps to NM_007279.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:56180967 C>T maps to NM_007279.2 D401D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:70959686 A>G maps to NM_018003.2 V1112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr15:70960693 C>A maps to NM_018003.2 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:70959097 C>A maps to NM_018003.2 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:70975128 C>A maps to NM_018003.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:70961159 C>T maps to NM_018003.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr15:70979907 C>T maps to NM_018003.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:70959502 C>A maps to NM_018003.2 E1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr15:70959965 A>G maps to NM_018003.2 S1019S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr15:70959965 A>G maps to NM_018003.2 S1019S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr15:70959965 A>G maps to NM_018003.2 S1019S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr15:70959965 A>G maps to NM_018003.2 S1019S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:162560163 G>A maps to ENST00000367925 K407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5912-01A-11D-1650-10 chr1:162546747 T>A maps to ENST00000367925 Y154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:139974453 G>A maps to NM_207309.2 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:47070572 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:47072565 G>A did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:47070570 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:47065701 C>T did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:47060929 C>T did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:47062966 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:47070257 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:47061868 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:47072565 G>A did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:47065671 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:47069399 C>A did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:47061847 A>T did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:47070293 G>A did not map to a codon.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr23:47072408 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:34942895 G>A maps to NM_005499.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr3:69105767 T>G maps to NM_003968.3 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:69105825 A>G maps to NM_003968.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:69111276 A>T maps to NM_003968.3 C249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:69111276 A>T maps to NM_003968.3 C249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr3:132389865 T>C maps to NM_024818.3 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr3:132390645 G>A maps to NM_024818.3 W202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:68488928 G>T maps to NM_018227.5 S951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:68534356 A>G maps to NM_018227.5 H235H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:68544194 G>A maps to NM_018227.5 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr4:68543397 G>C maps to NM_018227.5 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:68501200 T>C maps to NM_018227.5 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr4:68490843 A>G maps to NM_018227.5 D860D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:138838169 C>T maps to NM_016172.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:100037483 C>T maps to NM_001144072.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr9:33953306 G>T maps to NM_018449.2 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:33924246 C>T maps to NM_018449.2 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:33944452 G>A maps to NM_018449.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:34017045 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:33923250 G>A maps to NM_018449.2 Y979Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr9:33948441 A>G maps to NM_018449.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr9:33927810 C>T maps to NM_018449.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr9:33944368 A>T maps to NM_018449.2 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:33935857 G>A maps to NM_018449.2 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr1:154199807 T>C maps to NM_014847.3 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:154215748 G>A maps to NM_014847.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr21:43838595 G>A maps to NM_018961.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr21:43863451 G>A maps to NM_018961.2 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr21:43862590 C>T maps to NM_018961.2 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:43867291 C>A maps to NM_018961.2 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr21:43863427 G>A maps to NM_018961.2 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr11:122650278 G>A maps to NM_032873.4 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:122526915 C>T maps to NM_032873.4 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:122678799 C>T maps to NM_032873.4 H576H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr12:125398020 G>A maps to NM_021009.5 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:125398023 G>A maps to NM_021009.5 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:125398308 G>T maps to NM_021009.5 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr12:125398161 A>G maps to NM_021009.5 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr12:125397693 C>T maps to NM_021009.5 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:118717176 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:118715494 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:118715489 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:118717114 A>C did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:133716429 G>T maps to NM_003337.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:44444066 A>G maps to NM_181799.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr6:83754182 C>T maps to NM_198920.1 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr6:83754350 C>T maps to NM_198920.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3529-01A-02W-0831-10 chr7:43990225 C>T maps to NM_015983.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr3:23930691 A>G maps to NM_003341.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:23541164 C>A maps to NM_152653.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:23631282 C>T maps to NM_152653.3 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:4186188 C>A maps to NM_003342.4 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:129479122 G>A maps to NM_003344.2 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:129474884 G>A maps to NM_003344.2 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:1364355 C>T maps to NM_194259.1 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:1374748 C>T maps to NM_194259.1 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr6:90052126 G>A maps to NM_016021.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr6:90039424 G>A maps to NM_016021.2 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:1190594 G>A maps to NM_194315.1 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr22:21965225 C>T maps to ENST00000458578 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr22:21947226 G>A maps to ENST00000458578 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr11:57319947 C>T maps to NM_004223.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr11:57321979 G>A maps to NM_004223.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr19:59068447 C>G maps to NM_003969.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:142967365 G>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:142967450 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:142967241 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:142967458 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:142967514 G>A did not map to a codon.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr23:142967376 C>G did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:142967299 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr17:74394413 A>G maps to NM_022066.3 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr17:74395693 C>T maps to NM_022066.3 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:74395758 C>A maps to NM_022066.3 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr17:74387882 C>T maps to NM_022066.3 R1054R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr17:74392665 G>A maps to NM_022066.3 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:74401379 C>T maps to NM_022066.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr1:154524881 G>A maps to NM_017582.6 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:154530762 C>T maps to NM_017582.6 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:76161347 T>C maps to NM_173469.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:202302436 G>A maps to NM_014176.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:202304773 G>A maps to NM_014176.3 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:64672450 A>G maps to ENST00000371077 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:48955656 C>T maps to NM_003350.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr8:74706351 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:74722771 T>G maps to NM_001001481.1 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr8:74717930 G>A maps to NM_001001481.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:25605574 C>A maps to NM_000462.2 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:25601840 G>A maps to NM_000462.2 H655H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr15:25616672 C>T maps to NM_000462.2 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr15:25616656 G>A maps to NM_000462.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:25585331 T>G maps to NM_000462.2 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:25616393 C>T maps to NM_000462.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:25620681 C>T maps to NM_000462.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:25585286 C>A maps to NM_000462.2 G818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr15:25601193 G>A maps to NM_000462.2 Q660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:109936078 C>T maps to NM_183415.1 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr12:109972568 G>A maps to NM_183415.1 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr12:109972418 C>T maps to NM_183415.1 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr12:109972400 C>T maps to NM_183415.1 T1007T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:109961916 C>A maps to NM_183415.1 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr7:156963053 C>T maps to NM_014671.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:156961750 C>T maps to NM_014671.2 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:156976674 C>A maps to NM_014671.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:157046760 C>T maps to NM_014671.2 C936C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:157000524 C>T maps to NM_014671.2 R569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr7:157046709 C>T maps to NM_014671.2 Y919Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr7:156976704 C>T maps to NM_014671.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:118247331 G>A maps to NM_004788.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:118242236 C>T maps to NM_004788.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:118252104 G>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:118255419 G>A maps to NM_004788.2 W763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:10163151 T>C did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:10166431 G>A maps to NM_001105562.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:10163146 G>T maps to NM_001105562.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:10192506 C>T maps to NM_001105562.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:10165688 T>C maps to NM_001105562.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr1:10190571 G>C maps to NM_001105562.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:10177612 C>T maps to NM_001105562.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:10221277 T>C maps to NM_001105562.2 S1044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr1:10192467 C>T maps to NM_001105562.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr16:23574050 G>T maps to ENST00000219638 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:23581802 G>A maps to ENST00000219638 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:11346049 C>A maps to NM_013319.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr15:74751133 C>T maps to NM_201265.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr15:74743156 G>A maps to NM_201265.1 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:74751079 C>T maps to NM_201265.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr5:158696922 T>G maps to NM_145049.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr5:158710264 G>T maps to NM_145049.3 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:158710264 G>T maps to NM_145049.3 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr16:4925323 C>T maps to NM_016936.3 G971G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr16:4920851 G>T maps to NM_016936.3 E480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:4924216 G>A maps to NM_016936.3 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:4930087 T>G maps to NM_016936.3 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr7:138946195 C>T maps to NM_173569.3 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:138946195 C>T maps to NM_173569.3 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:138946315 C>T maps to NM_173569.3 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:138944027 G>T maps to NM_173569.3 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr20:3102419 G>A maps to NM_014948.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:3103212 G>A maps to NM_014948.2 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr20:3102777 G>A maps to NM_014948.2 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:3102654 C>T maps to NM_014948.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:3102942 C>T maps to NM_014948.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:33450179 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:33431823 C>A maps to NM_001128161.1 *541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr9:86292717 A>G maps to NM_013438.4 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:86292714 G>A maps to NM_013438.4 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr9:86301034 A>G maps to NM_013438.4 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:86300962 A>G maps to NM_013438.4 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:86276754 C>A maps to NM_013438.4 G573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr9:86284177 C>A maps to NM_013438.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:86284097 A>G did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr9:86322495 C>T maps to NM_013438.4 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:56591231 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:56591457 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:56591116 A>G did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:56591171 G>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:56591151 C>T did not map to a codon.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr23:56590912 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:5529960 A>G maps to NM_017481.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:5530614 G>A maps to NM_017481.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr11:5529471 T>C maps to NM_017481.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:156006912 C>T maps to NM_020131.3 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:5537068 C>T maps to NM_145053.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:5536744 T>C maps to NM_145053.4 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:5537082 C>A maps to NM_145053.4 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr11:5536504 G>A maps to NM_145053.4 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr11:5536837 A>G maps to NM_145053.4 N278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr11:5536732 T>C maps to NM_145053.4 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr15:43317089 C>T maps to NM_174916.2 R892R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr15:43252850 G>A maps to NM_174916.2 T1583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:43244543 G>A maps to NM_174916.2 N1646N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr15:43367257 A>G maps to NM_174916.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:42629982 T>C maps to NM_015255.2 C1168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:42631103 C>T maps to NM_015255.2 C1215C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:42615887 C>T maps to NM_015255.2 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr6:42573530 T>C maps to NM_015255.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr6:42573530 T>C maps to NM_015255.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:42609390 C>T maps to NM_015255.2 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:170780643 A>G maps to ENST00000442603 E661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr2:170728829 T>C maps to ENST00000442603 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:170912048 C>T maps to ENST00000442603 S1609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:170814948 C>T maps to ENST00000442603 R1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr1:19490880 T>C maps to ENST00000375267 A1522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr1:19481545 G>C maps to ENST00000375267 G2108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:19443905 A>G maps to ENST00000375267 Y3544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr1:19480386 C>A maps to ENST00000375267 E2169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:19479891 G>A maps to ENST00000375267 N2245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:19491450 G>A maps to ENST00000375267 G1451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:19408021 C>T maps to ENST00000375267 L5018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:19440524 G>A maps to ENST00000375267 R3748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:19472308 G>A maps to ENST00000375267 F2641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:19472401 C>T maps to ENST00000375267 P2610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:19455498 G>A maps to ENST00000375267 G2992G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:19483401 G>A maps to ENST00000375267 L1926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:19414330 G>A maps to ENST00000375267 C4841C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr1:19493577 A>G maps to ENST00000375267 R1349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:19479818 G>A maps to ENST00000375267 R2270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:19488358 A>C maps to ENST00000375267 T1663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:19504098 C>T maps to ENST00000375267 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:19503999 A>G maps to ENST00000375267 Y864Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:19480329 G>A maps to ENST00000375267 L2188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:19513100 G>A maps to ENST00000375267 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:19473347 C>T maps to ENST00000375267 T2592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr1:19491471 C>T maps to ENST00000375267 P1444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:19480386 C>A maps to ENST00000375267 E2169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr1:19442127 T>C maps to ENST00000375267 P3609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr1:19447842 C>G maps to ENST00000375267 L3327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:19465664 G>A maps to ENST00000375267 T2881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:103292690 G>A maps to NM_015902.4 R1978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:103372381 C>T maps to NM_015902.4 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr8:103327017 C>T maps to NM_015902.4 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr8:103300406 G>A maps to NM_015902.4 Q1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr8:103311188 T>C maps to NM_015902.4 T1071T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:103297373 G>A maps to NM_015902.4 R1893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr8:103354748 A>G maps to NM_015902.4 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr8:103292688 T>A maps to NM_015902.4 R1978R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr8:103292688 T>C maps to NM_015902.4 R1978R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr8:103307430 C>T did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:103292691 C>T maps to NM_015902.4 T1977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr8:103277449 A>G maps to NM_015902.4 D2493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr8:103277496 G>A maps to NM_015902.4 R2478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr8:103292688 T>C maps to NM_015902.4 R1978R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr8:103354748 A>G maps to NM_015902.4 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr8:103323532 A>G maps to NM_015902.4 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr8:103277449 A>G maps to NM_015902.4 D2493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr14:93688695 C>T maps to NM_175748.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr10:99327782 C>T maps to NM_024954.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:171638917 G>A maps to NM_152277.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:171661227 C>A maps to NM_152277.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr17:42293039 C>T maps to NM_014233.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:42284923 G>A maps to NM_014233.2 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:42284959 G>A maps to NM_014233.2 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr11:62445514 C>T maps to NM_015853.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3858-01A-01W-0900-09 chr1:26612397 G>A maps to NM_183008.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr2:24199876 C>T maps to NM_181713.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr8:59352254 T>C maps to NM_001077619.1 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:136513167 G>T maps to NM_014607.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:136528143 G>T maps to NM_014607.3 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr2:136513160 G>A maps to NM_014607.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:4445551 G>T maps to NM_025241.2 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:196096306 A>G maps to NM_015562.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr3:196118686 T>C maps to NM_015562.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:196134256 A>G maps to NM_015562.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr3:196094994 A>G maps to NM_015562.1 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr3:196118688 C>A maps to NM_015562.1 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr4:41263915 C>T maps to NM_004181.4 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:41266138 G>A maps to NM_004181.4 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr4:41262788 C>A maps to NM_004181.4 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:192998522 G>A maps to ENST00000367450 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr1:193018904 G>A maps to ENST00000367450 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:134404348 G>A maps to NM_031432.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:165859538 T>C maps to NM_012474.4 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:165859445 C>A maps to NM_012474.4 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:165859445 C>T maps to NM_012474.4 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:62577830 C>T maps to NM_017859.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr20:62577830 C>T maps to NM_017859.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr20:62575922 G>A maps to NM_017859.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:13271629 G>A maps to NM_145314.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:13275592 C>T maps to NM_145314.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr10:13276216 G>A maps to NM_145314.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:141489826 T>C maps to NM_021833.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr4:141484517 C>T maps to NM_021833.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr11:73688929 C>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr11:73716850 G>A maps to NM_003356.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr11:18566343 C>G did not map to a codon.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr7:100486655 T>G maps to NM_001015072.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:186336961 C>T maps to NM_018359.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr9:114691848 G>T maps to NM_003358.1 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr9:114694548 C>T maps to NM_003358.1 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:39506117 G>A maps to NM_003359.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:128867284 T>C maps to NM_020120.3 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr2:128937437 A>G maps to NM_020120.3 T1298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr2:128931513 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:128945048 G>A maps to NM_020120.3 P1501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr2:128886623 T>C maps to NM_020120.3 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr2:128939843 C>T maps to NM_020120.3 A1408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:128927912 T>G maps to NM_020120.3 A991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr13:96508429 A>G maps to NM_020121.3 I1330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:96675373 A>G maps to NM_020121.3 C135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:96592218 C>A maps to NM_020121.3 E602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr13:96529619 T>C did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr13:96536924 A>G maps to NM_020121.3 R1016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:64109748 G>A maps to NM_006759.3 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr2:234669064 T>C maps to NM_000463.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:234545533 G>A maps to NM_019075.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:234637852 G>A maps to NM_019093.2 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:234637982 G>T maps to NM_019093.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr2:234638614 T>C maps to NM_019093.2 C281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:234622134 G>A maps to NM_019078.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:234602180 C>T maps to NM_001072.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:234601854 G>T maps to NM_001072.3 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:234591314 C>A maps to ENST00000373460 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr2:234591342 C>A maps to ENST00000373460 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:234591342 C>T maps to ENST00000373460 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr2:234591342 C>A maps to ENST00000373460 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:234526659 C>T maps to NM_019076.4 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:234526853 C>A maps to NM_019076.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr2:234580966 A>G maps to NM_021027.2 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr2:234580975 A>G maps to NM_021027.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:234581113 A>G maps to NM_021027.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr4:70465029 A>G maps to ENST00000514019 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr4:70465029 A>G maps to ENST00000514019 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:70505003 C>A maps to ENST00000514019 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr4:69817091 G>A maps to NM_024743.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:69795691 G>A maps to NM_024743.3 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr4:69816940 G>A maps to NM_024743.3 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr4:69817091 G>T maps to NM_024743.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:70079939 C>T maps to NM_001073.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr4:70078407 T>C maps to NM_001073.1 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:70080139 G>A maps to NM_001073.1 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr4:70079941 G>T maps to NM_001073.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:69433614 A>G maps to NM_001076.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr4:69433614 A>G maps to NM_001076.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:69536113 C>A maps to NM_001076.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr4:69433614 A>G maps to NM_001076.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr4:70155426 C>G maps to NM_053039.1 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr4:70146929 G>T maps to NM_053039.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:70146229 G>A maps to NM_053039.1 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr4:70152498 T>A maps to NM_053039.1 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr4:70146739 C>T maps to NM_053039.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr4:70146871 T>G maps to NM_053039.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:70355203 C>A maps to NM_021139.2 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr4:70352408 C>T maps to NM_021139.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr4:70361045 G>A maps to NM_021139.2 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr5:35954327 C>T maps to NM_152404.3 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr5:35954450 G>A maps to NM_152404.3 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:35957311 C>T maps to NM_152404.3 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr5:35965796 T>C maps to NM_152404.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:35965529 A>G maps to NM_152404.3 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:35955919 G>A maps to NM_152404.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr5:36039771 A>C maps to NM_174914.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:36049154 C>A maps to NM_174914.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6704-01A-11D-1835-10 chr5:36049460 A>G maps to NM_174914.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr5:36066804 A>G maps to NM_174914.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:115597095 T>C maps to NM_003360.3 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:115597107 G>A maps to NM_003360.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6899-01A-11D-1924-10 chr1:162469946 G>A maps to NM_175866.4 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:4929418 G>A maps to ENST00000398240 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:4956751 G>A maps to ENST00000398240 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:34826766 T>C maps to NM_017754.3 A878A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:34827057 A>G maps to NM_017754.3 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:34831937 T>C maps to NM_017754.3 S1125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:34802601 G>A maps to NM_017754.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr12:100441857 G>A maps to NM_015054.1 Q1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr12:100492201 G>T maps to NM_015054.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:100491189 G>A maps to NM_015054.1 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:100451901 A>G maps to NM_015054.1 D1051D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:100476886 T>C maps to NM_015054.1 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:6475441 C>T maps to NM_152896.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr5:176409472 T>C maps to ENST00000377219 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr5:176396008 A>G maps to ENST00000377219 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr5:176402448 C>A maps to ENST00000377219 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr5:176402430 A>G maps to ENST00000377219 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6748-01A-11D-1835-10 chr5:176409472 T>C maps to ENST00000377219 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr5:176395630 A>G maps to ENST00000377219 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr5:176409472 T>C maps to ENST00000377219 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr5:176409535 A>G maps to ENST00000377219 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:176332330 A>G maps to ENST00000377219 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:150290456 G>T maps to NM_025218.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr6:150291230 C>A maps to NM_025218.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:150290456 G>T maps to NM_025218.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr6:150267520 G>A maps to NM_025217.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:150387034 C>A maps to NM_024518.1 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:132401560 G>A maps to NM_003565.2 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:132395266 G>A maps to NM_003565.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr12:132403156 C>A maps to NM_003565.2 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:19699445 C>T maps to NM_014683.3 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:19746536 T>C did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr17:19705137 G>A maps to NM_014683.3 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:19685217 G>A maps to NM_014683.3 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:41746625 C>A maps to NM_017886.2 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:41746560 G>A maps to NM_017886.2 D923D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:41439611 G>A maps to NM_017886.2 D1212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:41973480 A>G maps to NM_017886.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:41759286 A>G maps to NM_017886.2 N796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:41841704 A>G maps to NM_017886.2 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr3:41973390 T>C maps to NM_017886.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:20357531 G>T maps to ENST00000424589 C399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:20359875 C>T maps to ENST00000424589 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:20360286 G>A maps to ENST00000424589 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:20355365 G>A maps to ENST00000424589 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr16:20348684 A>G maps to ENST00000424589 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr21:43510426 T>C maps to NM_173568.3 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr21:43504272 C>T maps to NM_173568.3 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr21:43547820 C>T maps to NM_173568.3 N1318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:124453977 C>T maps to NM_000373.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:124456718 C>A maps to NM_000373.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:121151188 A>G maps to NM_001080533.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:121154464 C>T maps to NM_001080533.1 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:17759753 G>T maps to ENST00000428389 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:17732649 T>C maps to ENST00000428389 G1499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:17759345 G>A maps to ENST00000428389 C658C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:17785521 C>T maps to ENST00000428389 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:17759345 G>A maps to ENST00000428389 C658C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:17746903 C>T maps to ENST00000428389 W1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr9:35375188 C>T maps to ENST00000396787 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:35236522 C>A maps to ENST00000396787 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:35398613 G>T maps to ENST00000396787 E1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:35377553 C>T maps to ENST00000396787 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:35400378 T>C maps to ENST00000396787 S1404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:35236478 C>T maps to ENST00000396787 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr9:35295792 C>A maps to ENST00000396787 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr15:54529887 G>A maps to ENST00000260323 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr15:54305199 G>T maps to ENST00000260323 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr15:54305921 C>T maps to ENST00000260323 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:54685323 C>T maps to ENST00000260323 L1598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr15:54306677 C>A maps to ENST00000260323 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr15:54838962 C>T maps to ENST00000260323 R1914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr15:54919260 G>T maps to ENST00000260323 E2199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:54306884 G>A maps to ENST00000260323 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:54307944 G>T maps to ENST00000260323 E949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:54305930 C>A maps to ENST00000260323 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:54307640 A>T maps to ENST00000260323 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:54919260 G>T maps to ENST00000260323 E2199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:54614184 C>T maps to ENST00000260323 A1439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr15:54542601 C>T maps to ENST00000260323 H1136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr15:54825264 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:54919088 C>A maps to ENST00000260323 C2141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:54847641 C>T maps to ENST00000260323 R1964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr15:54305889 C>T maps to ENST00000260323 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr15:54527275 A>G maps to ENST00000260323 R1040R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:54556373 G>T maps to ENST00000260323 E1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:73838563 C>T maps to ENST00000412096 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:73835924 G>T maps to ENST00000412096 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:73832932 G>A maps to ENST00000412096 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr17:73831810 C>T maps to ENST00000412096 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:73826530 C>T maps to ENST00000412096 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:73831952 G>T maps to ENST00000412096 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr15:91483666 T>C maps to NM_018671.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr17:33495229 C>T maps to NM_173167.2 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr17:33513322 C>T maps to NM_173167.2 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:33491038 G>T maps to NM_173167.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:33482322 G>A maps to NM_173167.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr17:33482367 C>T maps to NM_173167.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr17:33482455 C>T maps to NM_173167.2 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr17:33477161 C>T maps to NM_173167.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr17:33498465 C>A maps to NM_173167.2 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr17:33482457 A>G maps to NM_173167.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:99226440 G>A maps to ENST00000409347 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:99226429 C>T maps to ENST00000409347 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:99227328 C>T maps to ENST00000409347 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr5:176304685 G>A maps to NM_133369.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:176289754 C>T maps to NM_133369.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:176297474 G>T maps to NM_133369.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:73044510 G>A maps to NM_170744.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:73059018 C>T maps to NM_170744.3 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr10:73047361 C>T maps to NM_170744.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr10:73051465 G>A maps to NM_170744.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr10:73048334 G>A maps to NM_170744.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr10:73044585 C>T maps to NM_170744.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr4:96091459 C>T maps to NM_003728.3 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:96163628 G>A maps to NM_003728.3 D353D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr4:96140246 G>T maps to NM_003728.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:96163631 G>A maps to NM_003728.3 C352C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:96171788 A>G maps to NM_003728.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr4:96137312 G>A maps to NM_003728.3 Y565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr6:40998214 G>A maps to NM_173561.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:40998407 C>T maps to NM_173561.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:41002621 G>A maps to NM_173561.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:41001726 G>T maps to NM_173561.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:40998152 G>A maps to NM_173561.2 H436H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:41000722 G>A maps to NM_173561.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr8:35616882 G>T maps to ENST00000416672 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:35541225 G>A maps to ENST00000416672 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:35406888 T>C maps to ENST00000416672 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:35541072 G>A maps to ENST00000416672 W193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr8:35406877 G>T maps to ENST00000416672 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:35406822 C>T maps to ENST00000416672 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr8:35616878 G>T maps to ENST00000416672 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:35606169 G>A maps to ENST00000416672 W636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:35583700 G>A maps to ENST00000416672 Q450Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:35544090 A>G maps to ENST00000416672 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:35608158 G>A maps to ENST00000416672 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr8:35606140 G>A maps to ENST00000416672 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr8:35544187 C>T maps to ENST00000416672 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:167721285 C>A maps to NM_018974.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr6:167728837 G>A maps to NM_018974.3 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:167721363 C>T maps to NM_018974.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr6:167709567 G>A maps to NM_018974.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:1273285 C>T maps to NM_001080461.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr17:73812971 G>A maps to NM_001080419.1 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr17:73805870 C>A maps to NM_001080419.1 C121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:1453263 G>A maps to ENST00000508903 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:1448917 A>C maps to NM_001037125.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr22:24891419 C>T maps to NM_016327.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr19:18963026 C>T maps to ENST00000418384 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:18968310 C>T maps to ENST00000418384 Y728Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:18974258 C>A maps to ENST00000418384 I882I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:18956814 C>T maps to ENST00000418384 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:18976406 A>G maps to ENST00000418384 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr10:12041943 C>T maps to NM_015542.2 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:11998360 G>A maps to NM_015542.2 H844H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:11994151 G>A maps to NM_015542.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr10:12021097 T>C maps to NM_015542.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr13:115057114 C>T maps to NM_023011.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr13:115067440 G>T maps to NM_023011.2 G415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:115057114 C>T maps to NM_023011.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:118986825 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:118985826 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:118985489 C>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:118971919 G>A did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:118971919 G>A did not map to a codon.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr23:118971919 G>A did not map to a codon.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr23:118971919 G>A did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:118971918 C>T did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:118971919 G>A did not map to a codon.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:36157719 G>A maps to NM_007000.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:36159534 C>T maps to NM_007000.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:36159450 C>A maps to NM_007000.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:76144402 G>A maps to NM_030570.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr7:76140016 C>T maps to NM_030570.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:48146626 C>T maps to NM_003364.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr2:158978098 A>T maps to NM_001135098.1 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:158958583 A>T maps to NM_001135098.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:158974430 C>T maps to NM_001135098.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr2:158980294 T>C maps to NM_001135098.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:74519614 G>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:74513338 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:74516221 G>T did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:74513339 G>A did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:74519698 G>A did not map to a codon.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr23:74519722 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:74494337 T>C did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr20:33891827 T>G maps to NM_018244.4 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr20:33934981 G>A maps to NM_018244.4 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:33971870 C>T maps to NM_018244.4 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr20:33969721 C>T maps to NM_018244.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3538-01A-01W-0831-10 chr8:97247743 C>T maps to NM_006294.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:97244159 G>A maps to NM_006294.3 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:21994489 T>C maps to NM_003366.2 *454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:29698766 G>A maps to NM_006003.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:16134111 G>A maps to NM_001089591.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:229772123 G>A maps to NM_014777.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr1:229771436 T>C maps to NM_014777.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:229771001 G>T maps to NM_014777.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:229795043 A>G maps to NM_014777.2 *1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:229794968 C>A maps to NM_014777.2 I1500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:229772039 G>A maps to NM_014777.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:43918701 C>T maps to NM_001077663.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:43918254 G>A maps to NM_001077663.1 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr9:131151566 C>T maps to NM_001135947.1 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:131150101 C>A maps to NM_001135947.1 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:126219596 C>T maps to NM_001165974.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr3:126224579 G>A maps to NM_001165974.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:45480611 G>A maps to NM_000374.4 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:45480121 G>A maps to NM_000374.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr10:127484731 C>T maps to NM_000375.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:127503672 T>C maps to NM_000375.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:17327090 G>A maps to NM_018467.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:161011477 T>C maps to NM_007122.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr1:161011477 T>C maps to NM_007122.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr19:35761351 T>G maps to NM_003367.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:17552727 G>A maps to NM_153676.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr11:17523512 A>C maps to NM_153676.3 Y733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr11:17539022 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:17537802 G>A maps to NM_153676.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:72916201 C>T maps to NM_173477.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:72915904 C>T maps to NM_173477.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:72915949 G>A maps to NM_173477.2 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6166-01A-11D-1650-10 chr17:72915795 A>G maps to NM_173477.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr17:72916060 G>A maps to NM_173477.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr1:216595321 G>A maps to ENST00000366943 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:215848445 A>T maps to ENST00000366943 P4269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:215824086 G>A maps to ENST00000366943 T4730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:216166365 C>T maps to ENST00000366943 P2267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3524-01A-02W-0831-10 chr1:215990449 G>A maps to ENST00000366943 C3153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr1:216074119 G>A maps to ENST00000366943 G2476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr1:215848855 C>A maps to ENST00000366943 E4133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr1:215901416 G>A maps to ENST00000366943 D4007D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:215802242 G>A maps to ENST00000366943 S5168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr1:216221978 T>C maps to ENST00000366943 T2020T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr1:215848631 G>A maps to ENST00000366943 A4207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr1:216496916 C>T maps to ENST00000366943 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:216371875 C>A maps to ENST00000366943 E1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr1:215848823 C>T maps to ENST00000366943 S4143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:215820912 C>T maps to ENST00000366943 E4914E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:215901722 G>A maps to ENST00000366943 R3905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:216040484 G>A maps to ENST00000366943 F2903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:216496928 G>A maps to ENST00000366943 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:215972339 G>A maps to ENST00000366943 G3289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:216424431 T>G maps to ENST00000366943 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr1:215916600 G>A maps to ENST00000366943 S3822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr1:215932063 T>C maps to ENST00000366943 G3754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr1:215901722 G>A maps to ENST00000366943 R3905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:216369957 C>T maps to ENST00000366943 G1396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:216498727 C>T maps to ENST00000366943 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:215933090 T>C maps to ENST00000366943 Q3714Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:215960057 G>A maps to ENST00000366943 A3447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:215932063 T>C maps to ENST00000366943 G3754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:215802170 G>T maps to ENST00000366943 G5192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:215822069 G>A maps to ENST00000366943 G4794G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:216019259 T>C maps to ENST00000366943 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:215808007 C>A maps to ENST00000366943 S5030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr1:215848466 A>G maps to ENST00000366943 P4262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:216258112 T>C maps to ENST00000366943 E1698E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:216363607 A>G maps to ENST00000366943 G1451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:215963505 A>G maps to ENST00000366943 C3359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:215963505 A>G maps to ENST00000366943 C3359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr1:216591939 G>A maps to ENST00000366943 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr1:216538319 A>T maps to ENST00000366943 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr1:216062202 A>T maps to ENST00000366943 Y2596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr1:215848550 C>T maps to ENST00000366943 T4234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:216591939 G>A maps to ENST00000366943 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr1:215963505 A>G maps to ENST00000366943 C3359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr1:216497640 A>G maps to ENST00000366943 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr1:215972432 C>T maps to ENST00000366943 R3258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:216424242 A>G did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:216497640 A>G maps to ENST00000366943 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:215814064 G>A maps to ENST00000366943 R4935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:216246481 T>C maps to ENST00000366943 G1911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:216138764 T>C maps to ENST00000366943 K2338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:17361126 G>A maps to NM_031941.3 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:17361159 C>T maps to NM_031941.3 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:17373555 G>A maps to NM_031941.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:17373555 G>A maps to NM_031941.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:17370541 C>A did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr19:17367456 A>G maps to NM_031941.3 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr10:105152190 C>T maps to NM_032747.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:76715053 G>A maps to NM_003715.2 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:76726329 G>T maps to NM_003715.2 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:76692235 T>C maps to NM_003715.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr4:76727712 A>C maps to NM_003715.2 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:84793793 C>T maps to NM_005153.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr16:84792970 A>G maps to NM_005153.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:84801925 G>T maps to NM_005153.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr16:84812658 C>T maps to NM_005153.2 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr16:84806209 C>T maps to NM_005153.2 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:47101910 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:47103932 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:47098862 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:47100030 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:47101516 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:47102830 C>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:47100030 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:47099756 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:47098811 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr23:47106743 A>T did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:47100743 C>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:47101536 G>T did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:47107229 C>T did not map to a codon.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr23:47104273 G>A did not map to a codon.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr3:179462840 C>T maps to NM_003940.2 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:179437747 G>T maps to NM_003940.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:179439263 G>A maps to NM_003940.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:179418811 C>T maps to NM_003940.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr18:196733 C>T maps to NM_005151.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:62783575 G>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr12:62708650 C>T maps to ENST00000280377 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr12:62785021 T>C maps to ENST00000280377 D682D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3681-01A-01W-0900-09 chr21:30415811 G>A maps to NM_006447.2 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr21:30411451 G>T maps to NM_006447.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr21:30419139 T>A maps to NM_006447.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr21:30412970 T>G maps to NM_006447.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr8:11994863 G>T maps to NM_201402.2 S469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:11994817 G>A maps to NM_201402.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr8:11995018 T>G maps to NM_201402.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:11994916 G>A maps to NM_201402.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:49152538 C>T maps to ENST00000434032 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:49148411 C>T maps to ENST00000434032 R1170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr3:49154035 G>A maps to ENST00000434032 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr3:49154035 G>A maps to ENST00000434032 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr3:49151427 C>T maps to ENST00000434032 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr3:49148450 G>T maps to ENST00000434032 G1157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:119243716 G>A maps to NM_004205.4 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:119229957 C>T maps to NM_004205.4 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr9:132630547 C>T maps to NM_001008563.3 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:161134864 C>T maps to NM_012475.4 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:20908272 C>T maps to ENST00000455117 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr1:55591190 C>T maps to NM_015306.2 T1254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr1:55563297 G>C maps to NM_015306.2 R1896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:55614159 T>C maps to NM_015306.2 K648K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:55590162 G>A maps to NM_015306.2 R1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:55622701 G>T maps to NM_015306.2 Y455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr1:55537531 C>T maps to NM_015306.2 S2585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:55600044 G>A maps to NM_015306.2 N1081N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:55558493 A>G maps to NM_015306.2 A2150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr1:55612631 A>G maps to NM_015306.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:55624691 A>G maps to NM_015306.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:55603289 C>T maps to NM_015306.2 K1033K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr1:55558493 A>G maps to NM_015306.2 A2150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:55558493 A>G maps to NM_015306.2 A2150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr21:17250152 A>G maps to ENST00000285681 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr21:17163835 C>T maps to ENST00000285681 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr21:17198654 T>C maps to ENST00000285681 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:17250703 G>A maps to ENST00000285681 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr21:17135220 G>A maps to ENST00000285681 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr21:17203796 T>C maps to ENST00000285681 D614D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr21:17205755 C>T maps to ENST00000285681 R695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr21:17250697 G>A maps to ENST00000285681 E1056E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr21:17250150 G>T maps to ENST00000285681 G978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr21:17199458 G>T maps to ENST00000285681 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:17250152 A>G maps to ENST00000285681 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr21:17250152 A>G maps to ENST00000285681 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr21:17250185 C>T maps to ENST00000285681 I989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr21:17250152 A>G maps to ENST00000285681 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr21:17150265 A>G maps to ENST00000285681 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr21:17250152 A>G maps to ENST00000285681 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr23:132159666 C>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr23:132160290 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:132159624 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:132160836 C>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:132159666 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:132160052 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:132161157 A>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:132161521 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:132161862 T>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:132161062 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:132160552 C>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:132160803 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:132161008 C>A did not map to a codon.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr23:132160272 G>A did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr11:113670057 A>G maps to NM_020886.2 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:113673917 C>A maps to NM_020886.2 E942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:113704981 G>A maps to NM_020886.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:113677251 G>A maps to NM_020886.2 Q787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:113674517 A>G did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:113723234 C>A maps to NM_020886.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr11:113704161 G>A maps to NM_020886.2 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr11:113701643 T>C maps to NM_020886.2 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr11:113679896 A>G maps to NM_020886.2 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr11:113670045 T>C maps to NM_020886.2 R1050R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:57642592 G>A maps to NM_020903.2 K850K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr19:57641533 G>A maps to NM_020903.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:57640948 G>A maps to NM_020903.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:57642088 T>C maps to NM_020903.2 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:57640519 G>A maps to NM_020903.2 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:57642199 A>G maps to NM_020903.2 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:109519147 C>T maps to NM_032663.3 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr16:23119413 C>A maps to NM_020718.3 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr16:23080808 G>A maps to NM_020718.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:23080122 C>T maps to NM_020718.3 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr17:58299882 G>A maps to NM_032582.3 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr17:58258969 T>C maps to NM_032582.3 S1421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr17:58286132 C>G maps to NM_032582.3 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:78184289 G>A maps to NM_015017.3 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr1:78180332 A>T maps to NM_015017.3 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:61436102 T>C maps to NM_014709.3 R2950R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:61622008 C>T maps to NM_014709.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:61416048 A>C maps to NM_014709.3 T3343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:61546366 G>A maps to NM_014709.3 R1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:61546366 G>A maps to NM_014709.3 R1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:61415542 G>A maps to NM_014709.3 D3445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:61544863 G>A maps to NM_014709.3 G1069G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:61575065 G>A maps to NM_014709.3 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:61484359 G>A maps to NM_014709.3 I1990I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr2:61647900 A>G maps to NM_014709.3 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr2:61436102 T>C maps to NM_014709.3 R2950R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr2:61436102 T>C maps to NM_014709.3 R2950R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr2:61493278 A>G maps to NM_014709.3 N1819N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr2:61493278 A>G maps to NM_014709.3 N1819N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr2:61538675 A>T maps to NM_014709.3 P1272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:61473529 C>T maps to NM_014709.3 T2159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:61622317 A>G maps to NM_014709.3 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:61607471 C>T maps to NM_014709.3 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr11:77909003 C>A maps to NM_020798.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr11:77918659 A>G maps to NM_020798.2 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:77917030 C>T maps to NM_020798.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr11:77916967 G>A maps to NM_020798.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr17:76832229 G>T maps to NM_025090.3 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:76794503 A>G maps to NM_025090.3 *1124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:219418411 G>A maps to NM_020935.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:219411754 A>G maps to NM_020935.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr4:144134772 A>G maps to NM_032557.5 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr4:144135702 C>T maps to NM_032557.5 Y858Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr4:144135717 G>A maps to NM_032557.5 R863R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:144134766 G>A maps to NM_032557.5 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr4:144135039 A>G maps to NM_032557.5 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:144135649 C>T maps to NM_032557.5 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:144130725 A>G maps to NM_032557.5 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:49349074 C>T maps to NM_003363.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:49349074 C>T maps to NM_003363.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr3:49337908 T>C maps to NM_003363.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr3:49362401 T>C maps to NM_003363.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr3:49316276 G>A maps to NM_003363.3 N901N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr3:49337908 T>C maps to NM_003363.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:49362401 T>C maps to NM_003363.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:234394475 C>A maps to NM_018218.2 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:234405462 C>A maps to NM_018218.2 E922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:234405439 A>G maps to NM_018218.2 D929D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:234407198 C>A maps to NM_018218.2 E915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:234432050 C>A maps to NM_018218.2 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:6189713 T>C maps to ENST00000404835 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:6196399 A>G maps to ENST00000404835 S1219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr7:6189266 C>T maps to ENST00000404835 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr7:6183787 G>T maps to ENST00000404835 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:9615366 C>A maps to NM_153210.3 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:9604817 G>A maps to NM_153210.3 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr17:9615300 C>T maps to NM_153210.3 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:9631301 C>T maps to NM_153210.3 G789G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:95927366 C>T maps to NM_032147.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:95922630 C>A maps to NM_032147.2 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00W-01A-01W-A005-10 chr12:95927075 T>C maps to NM_032147.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr12:95927654 A>G maps to NM_032147.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:95927075 T>C maps to NM_032147.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:95927297 T>C maps to NM_032147.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:99894072 T>C maps to NM_001080481.1 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:99894093 C>T maps to NM_001080481.1 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr6:99916431 T>C maps to NM_001080481.1 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr6:99894072 T>C maps to NM_001080481.1 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr4:53497228 A>G did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:11957977 C>T maps to ENST00000399455 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:11863743 C>T maps to NM_017944.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:11964231 C>T maps to ENST00000399455 I895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr11:11974327 G>A maps to ENST00000399455 L1215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr11:11941792 C>A maps to ENST00000399455 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:22084233 A>G maps to NM_032236.5 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:22005927 A>T maps to NM_032236.5 T1030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:22079134 C>A maps to NM_032236.5 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:22032326 C>T maps to NM_032236.5 K759K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:22084254 C>T maps to NM_032236.5 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr1:22021621 T>C maps to NM_032236.5 K940K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr1:22021621 T>C maps to NM_032236.5 K940K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:41766426 C>T maps to NM_018561.3 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:41773962 C>T maps to ENST00000373009 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:41771616 G>T maps to ENST00000373009 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr6:41766552 G>A maps to ENST00000373009 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00D-01A-01W-A005-10 chr12:6961370 C>T maps to NM_001098536.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:6972377 C>T maps to NM_001098536.1 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:6964647 C>T maps to NM_001098536.1 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr12:6964654 C>T maps to NM_001098536.1 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:55515256 T>G did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:55515253 G>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:55513874 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:55514577 T>C did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:55514325 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr23:55513444 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:55514506 T>C did not map to a codon.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr4:120182997 T>C maps to NM_019050.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:120212330 G>T maps to NM_019050.2 E755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr4:120213810 T>C maps to NM_019050.2 C889C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr4:120192532 T>C maps to NM_019050.2 H506H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:120188537 T>C maps to NM_019050.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr4:120189480 T>C maps to NM_019050.2 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:75276418 C>T maps to NM_152586.3 G1255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr10:75279709 C>T maps to NM_152586.3 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr10:75276601 A>G maps to NM_152586.3 D1194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr17:5072276 G>A maps to NM_004505.2 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr17:5041491 C>T maps to NM_004505.2 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:11569531 C>T maps to NM_001080491.2 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr10:11505267 G>A maps to NM_001080491.2 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:11505056 G>T maps to NM_001080491.2 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:11531161 G>A maps to NM_001080491.2 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:8996317 G>A maps to NM_003470.2 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:9000434 C>A maps to NM_003470.2 E426*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3663-01A-01D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:9024252 C>T maps to ENST00000381886 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr16:8988947 C>T maps to NM_003470.2 A993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:8997211 G>A maps to NM_003470.2 Y584Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AU-6004-01A-11D-1719-10. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-AY-5543-01A-01D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr16:9024252 C>T maps to ENST00000381886 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr16:8990872 T>C maps to NM_003470.2 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr16:8990872 T>C maps to NM_003470.2 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:8989006 C>A maps to NM_003470.2 E974*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CK-4947-01B-11D-1650-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr16:9024252 C>A maps to ENST00000381886 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr16:8990872 T>C maps to NM_003470.2 K934K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D5-6540-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr16:9024252 C>A maps to ENST00000381886 A35A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D5-6541-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr16:8990872 T>C maps to NM_003470.2 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:9010358 C>A maps to NM_003470.2 V302V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G4-6317-01A-11D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr16:9024252 C>T maps to ENST00000381886 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:9017177 G>A maps to NM_003470.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr15:50782024 C>T maps to NM_005154.3 R640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:50773953 C>T maps to NM_005154.3 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:40990743 G>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:41025391 A>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:41055598 T>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:41075505 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:41045840 C>T did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:41010221 C>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:40988386 C>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr23:41077660 G>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:41025166 G>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:41075682 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:41025218 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:41075438 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:41027379 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:41073881 C>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:41045781 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:41047290 A>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:41075558 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:41091689 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr23:41078482 A>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:40982911 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:41064703 G>A did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:41069808 A>C did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:41000436 A>C did not map to a codon.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr23:41088662 G>A did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:41055977 T>G did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:41057838 A>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:41076577 G>A did not map to a codon.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr23:41022041 G>A did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr23:40996080 C>T did not map to a codon.
Sequencing variant TCGA-D5-6537-01A-11D-1719-10 chr23:41075554 A>G did not map to a codon.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr23:41075554 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:41082526 T>C did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:41075427 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:41084096 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:40988349 C>A did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:41029360 G>A did not map to a codon.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr24:14922747 A>G did not map to a codon.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr24:14847975 A>C did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr24:14958900 A>G did not map to a codon.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr24:14924967 C>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr24:14952970 A>G did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr24:14922684 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr24:14883078 A>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr24:14903482 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr24:14953039 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr24:14928228 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:14848047 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:14898676 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:31232712 A>G maps to NM_005800.4 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:31205222 G>A maps to NM_005800.4 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:149275058 C>T maps to NM_005715.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr6:149395059 C>T maps to NM_005715.2 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:149342550 C>T maps to NM_005715.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr6:149395152 G>A maps to NM_005715.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3517-01A-01W-0831-10 chr23:129045023 T>C did not map to a codon.
Sequencing variant TCGA-AA-3548-01A-01W-0831-10 chr23:129045801 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:129041401 G>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:129045117 A>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:129059952 A>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:129058786 G>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:129054459 G>T did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:129054485 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:129060228 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:52604200 G>T maps to NM_021645.5 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr13:52604307 C>T maps to NM_021645.5 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr13:52603875 C>A maps to NM_021645.5 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:52604115 G>A maps to NM_021645.5 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr13:52604736 T>G maps to NM_021645.5 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr13:52604308 G>T maps to NM_021645.5 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr13:52604307 C>T maps to NM_021645.5 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr13:52604325 T>C maps to NM_021645.5 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr13:52604325 T>C maps to NM_021645.5 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr13:52604307 C>A maps to NM_021645.5 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr12:101679364 T>C maps to NM_014503.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:101711339 C>T maps to NM_014503.2 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:101689349 G>A maps to NM_014503.2 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr12:101750778 G>A maps to NM_014503.2 A1870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr12:101727083 G>A maps to NM_014503.2 Q1141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:101731936 T>C maps to NM_014503.2 S1250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:101767193 C>T maps to NM_014503.2 T2298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:101750394 C>T maps to NM_014503.2 R1820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr12:101745882 A>G maps to NM_014503.2 K1645K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr12:101689307 T>C maps to NM_014503.2 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:101711393 C>T maps to NM_014503.2 P897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:117783847 G>T maps to NM_032334.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr8:117784035 T>G maps to NM_032334.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:71555167 C>A maps to NM_020368.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:30221678 G>T maps to NM_018428.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr17:30202393 A>G maps to NM_018428.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:144803525 T>C did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr6:144761493 C>T maps to NM_007124.2 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:144782342 C>T maps to NM_007124.2 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:145073036 A>G maps to NM_007124.2 L2768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:144783941 C>T maps to NM_007124.2 V1002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:144854328 G>T maps to NM_007124.2 E2056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr6:144749961 G>A maps to NM_007124.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:145160379 G>A maps to NM_007124.2 S3379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:144801042 C>A maps to NM_007124.2 A1144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr6:145079101 T>C maps to NM_007124.2 H2824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:144814435 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:144869848 G>A maps to NM_007124.2 S2223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:144808751 G>A maps to NM_007124.2 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr6:145157011 A>G maps to NM_007124.2 S3254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr6:144780374 C>A maps to NM_007124.2 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr17:80333069 G>A maps to NM_018949.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr17:80332523 G>A maps to NM_018949.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr24:15471662 C>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr24:15417989 G>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr24:15582093 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr24:15363004 T>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:15362958 A>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:75719855 A>G maps to NM_003369.3 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A285-01A-11D-A16V-10 chr11:75599919 A>G maps to NM_003369.3 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:106761670 G>A maps to ENST00000283148 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr23:47516688 G>C did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:47517023 C>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:70818711 T>C maps to NM_018052.3 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:70726859 G>A maps to NM_018052.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:8064967 G>A maps to ENST00000488857 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr1:7837258 G>T maps to NM_004781.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr1:7837299 C>T maps to NM_004781.3 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr1:171675510 A>G maps to NM_003762.4 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr2:85818882 G>A maps to NM_006634.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:155119262 A>G did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:116228012 C>T maps to NM_001172412.1 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:116202303 C>T maps to NM_001172412.1 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr1:160389360 C>T maps to NM_020335.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr1:160390204 C>T maps to NM_020335.2 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:160388955 T>A maps to NM_020335.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr18:9937029 C>T maps to NM_003574.5 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:56993357 T>C maps to NM_004738.4 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr6:31746773 C>T maps to NM_006295.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr6:30890921 C>T maps to NM_001167734.1 R773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr6:30883003 T>A maps to NM_001167734.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr6:30882663 G>A maps to NM_001167734.1 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:30883805 T>C maps to NM_001167734.1 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr6:30891009 T>C did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr14:77242546 C>T maps to NM_014909.4 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr14:77229328 C>T maps to NM_014909.4 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:77242318 C>T maps to NM_014909.4 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:77229439 G>A maps to NM_014909.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr14:77242594 C>T maps to NM_014909.4 H297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:213125141 C>T maps to NM_001136474.1 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:213125129 C>T maps to NM_001136474.1 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:41170780 C>T maps to NM_006373.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr16:78011555 C>T maps to NM_020927.1 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:77822782 C>T maps to NM_020927.1 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:77910269 C>A maps to NM_020927.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:77859153 T>G maps to NM_020927.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:77910269 C>A maps to NM_020927.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr19:6857115 T>C maps to NM_005428.2 *846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:6836548 G>A maps to NM_005428.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:6836518 G>A maps to NM_005428.2 R618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01G-01A-01W-A005-10 chr19:6829914 C>T maps to NM_005428.2 R462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr19:6822291 C>T maps to NM_005428.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr19:6822291 C>T maps to NM_005428.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:6822321 G>A maps to NM_005428.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr19:6833227 C>T maps to NM_005428.2 N514N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr9:136640121 G>A maps to NM_001134398.1 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:136726542 C>A maps to NM_001134398.1 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr9:136633569 G>A maps to NM_001134398.1 N861N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr9:136804242 A>G maps to NM_001134398.1 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:136633629 G>A maps to NM_001134398.1 D841D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr9:136637157 C>A maps to NM_001134398.1 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr9:136637155 C>T maps to NM_001134398.1 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:108185360 C>T maps to NM_006113.4 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:108322086 G>A maps to NM_006113.4 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr1:108313292 C>A maps to NM_006113.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr1:108160194 G>T maps to NM_006113.4 C658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:118893629 C>T maps to NM_001112704.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:118897420 G>A maps to NM_001112704.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:118897444 G>A maps to NM_001112704.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:101188867 G>A maps to NM_001078.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:101200199 A>G maps to NM_001078.3 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:101197006 G>A maps to NM_001078.3 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:82832970 A>G maps to NM_004385.4 L1383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr5:82836264 A>G maps to NM_004385.4 G2481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:82833015 T>C maps to NM_004385.4 N1398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3519-01A-02W-0831-10 chr5:82835286 T>G maps to NM_004385.4 Y2155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr5:82835326 G>T maps to NM_004385.4 E2169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr5:82834547 C>A maps to NM_004385.4 S1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr5:82837005 T>C maps to NM_004385.4 G2728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:82835478 A>G maps to NM_004385.4 E2219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr5:82786247 C>T maps to NM_004385.4 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr5:82835862 A>G maps to NM_004385.4 A2347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr5:82833948 A>G maps to NM_004385.4 T1709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:82816371 C>T maps to NM_004385.4 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:82835676 C>A maps to NM_004385.4 P2285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr5:82833363 A>G maps to NM_004385.4 T1514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr5:82875805 C>T maps to NM_004385.4 C3296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr5:82833615 A>G maps to NM_004385.4 E1598E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr5:82834216 T>C maps to NM_004385.4 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:82816186 G>T maps to NM_004385.4 E688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:82834354 G>T maps to NM_004385.4 E1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:82835781 C>A maps to NM_004385.4 I2320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:82817832 C>T maps to NM_004385.4 I1236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:82836240 C>T maps to NM_004385.4 S2473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:82868305 T>A maps to NM_004385.4 I3269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:82836579 G>T maps to NM_004385.4 V2586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:82836687 C>T maps to NM_004385.4 I2622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr5:82833279 C>T maps to NM_004385.4 Y1486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr5:82815321 A>T maps to NM_004385.4 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr5:82834216 T>C maps to NM_004385.4 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr10:75854133 G>A maps to NM_014000.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:75849785 G>A maps to NM_014000.2 W394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr10:75871734 C>G maps to NM_014000.2 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:75871761 C>T maps to NM_014000.2 D947D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:35062243 C>T maps to NM_007126.3 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr9:35057428 C>T maps to NM_007126.3 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr8:67577183 A>G maps to NM_025054.4 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:67576840 G>A maps to NM_025054.4 R785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:67547088 G>A maps to NM_025054.4 R1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:67577554 G>A maps to NM_025054.4 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr8:67577753 A>G maps to NM_025054.4 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:67578476 T>C maps to NM_025054.4 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr8:67547317 C>T maps to NM_025054.4 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:7811791 A>C did not map to a codon.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr23:7811918 G>A did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:7811738 C>T did not map to a codon.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr23:7811704 C>T did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr23:8138136 T>G did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:8138189 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:8434413 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr5:133316483 G>A maps to NM_003374.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr10:76973800 T>C maps to NM_001184783.1 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr10:76973800 T>C maps to NM_001184783.1 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:48240449 G>A maps to NM_001017535.1 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3848-01A-01W-0900-09 chr12:48238690 C>T maps to NM_001017535.1 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr12:48258872 G>A maps to NM_001017535.1 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:43745335 C>T maps to NM_001025366.2 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:177608560 C>A maps to NM_005429.2 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:177608447 G>A maps to NM_005429.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr4:177608585 C>T maps to NM_005429.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr3:156983344 T>C maps to NM_001167912.1 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:157146155 A>G maps to NM_001167912.1 H217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:157099072 G>A maps to NM_001167912.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:157146113 G>A maps to NM_001167912.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:156979030 G>T maps to NM_001167912.1 V798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr3:157146155 A>G maps to NM_001167912.1 H217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:157146155 A>G maps to NM_001167912.1 H217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr3:157146155 A>G maps to NM_001167912.1 H217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:56060346 G>A maps to NM_007146.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:95660168 C>T maps to NM_017599.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:95681598 C>T maps to NM_017599.3 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:95694097 T>G maps to NM_017599.3 Y663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:95656693 C>A maps to NM_017599.3 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:135630781 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:135618391 C>T did not map to a codon.
Sequencing variant TCGA-AA-3514-01A-02W-0831-10 chr23:135631052 C>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:135618201 C>T did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:135630882 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:135632930 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:135630957 T>A did not map to a codon.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr23:135631087 C>T did not map to a codon.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr23:135630844 G>C did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:135618255 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:135630768 A>T did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:117589556 G>T maps to NM_182645.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr6:117589517 C>T maps to NM_182645.2 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr3:87018004 G>A maps to NM_016206.2 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr3:87027952 C>T did not map to a codon.
Alternatively spliced codon TCGA-AA-A01R-01A-21W-A096-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr3:11606330 G>A maps to NM_014667.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr3:10188196 G>T did not map to a codon.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr3:10188258 A>G maps to NM_000551.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:10188321 T>A did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr3:10188222 A>G maps to NM_000551.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr3:10183611 A>G maps to NM_000551.2 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr3:10188273 T>A maps to NM_000551.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:10188195 A>G did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr3:10188222 A>G maps to NM_000551.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr3:10191546 C>A maps to NM_000551.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr3:10188315 G>A maps to NM_000551.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr3:10191528 T>C maps to NM_000551.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:10183783 C>T maps to NM_000551.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr3:10188273 T>C maps to NM_000551.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr3:10183680 C>T maps to NM_000551.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:10191627 A>G maps to NM_000551.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr3:10191477 T>C maps to NM_000551.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:10188273 T>C maps to NM_000551.2 S139S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AZ-5407-01A-01D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr3:10188198 T>C maps to NM_000551.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:10188261 A>G maps to NM_000551.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:10191513 A>G maps to NM_000551.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:10188318 A>G maps to NM_000551.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:10191647 G>T maps to NM_000551.2 *214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr3:10191598 C>T maps to NM_000551.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:10191594 A>G maps to NM_000551.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr3:10188288 A>G maps to NM_000551.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr3:10191537 A>G maps to NM_000551.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr3:10191627 A>G maps to NM_000551.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr3:10188321 T>C did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:10191495 C>T maps to NM_000551.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr3:10191646 T>C maps to NM_000551.2 *214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:10188252 A>G maps to NM_000551.2 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr3:10188255 T>C maps to NM_000551.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:10191642 A>G maps to NM_000551.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr3:10191627 A>G maps to NM_000551.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr3:10188288 A>G maps to NM_000551.2 G144G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CM-6678-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:10191489 A>G maps to NM_000551.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr3:10191633 A>G maps to NM_000551.2 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr3:10183587 C>T maps to NM_000551.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr3:10188216 A>G maps to NM_000551.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr3:10188243 G>T maps to NM_000551.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr3:10188222 A>G maps to NM_000551.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr3:10188273 T>C maps to NM_000551.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr3:10191627 A>G maps to NM_000551.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:10191480 G>T maps to NM_000551.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:10188240 T>C maps to NM_000551.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:10188273 T>C maps to NM_000551.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:38035435 T>C maps to NM_015873.3 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr10:17278291 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:17272654 G>A maps to NM_003380.3 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr14:77895396 C>T maps to ENST00000445370 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:42576526 C>T maps to NM_004624.3 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:42560742 C>A maps to NM_004624.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:42576577 C>T maps to NM_004624.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr7:158835761 A>G maps to ENST00000402066 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:158896486 G>A maps to ENST00000402066 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr7:158829590 C>T maps to ENST00000402066 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:36982144 C>T maps to NM_053276.3 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:37032713 G>A maps to NM_053276.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr2:37010496 G>T maps to NM_053276.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr2:37035991 G>A maps to NM_053276.3 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:36970261 C>T maps to NM_053276.3 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:37041347 C>T maps to NM_053276.3 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:37028482 G>A maps to NM_053276.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr9:2643742 C>A maps to NM_003383.3 C312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:2652885 T>C maps to NM_003383.3 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr9:2639949 A>G maps to NM_003383.3 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:2643959 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:2639886 C>T maps to NM_003383.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:150573500 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:150573467 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:150572105 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:5908931 T>C maps to NM_001017921.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:4689224 G>A maps to NM_001144939.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr17:4688707 G>A maps to NM_182566.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:57967482 G>T maps to NM_020633.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr19:57967605 C>T maps to NM_020633.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:57967605 C>T maps to NM_020633.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:53762393 G>T maps to NM_173856.2 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:53762647 C>A maps to NM_173856.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:53762225 G>T maps to NM_173856.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:53770297 G>A maps to NM_173857.2 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:53770309 A>C maps to NM_173857.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:133034985 C>T maps to NM_004666.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:133014265 A>C maps to NM_004666.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:133004293 G>A maps to NM_004666.2 C509C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr6:133013415 G>A maps to NM_004666.2 Y378Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:133070851 C>T maps to NM_004665.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:133072550 C>T maps to NM_004665.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:133078824 C>T maps to NM_004665.2 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:133077059 A>G maps to NM_004665.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:133065592 G>T maps to NM_004665.2 S470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:133065626 G>A maps to NM_004665.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:55540718 C>T maps to NM_030796.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr3:51475499 G>T maps to ENST00000273612 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:51517769 A>G maps to ENST00000273612 H25H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:51505004 C>A maps to ENST00000273612 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr22:24095095 G>C maps to ENST00000405618 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr22:24095293 G>A maps to ENST00000405618 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr22:24095296 G>A maps to ENST00000405618 H48H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr11:118947732 C>A maps to NM_021729.4 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:118949546 C>A maps to NM_021729.4 Y701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:118949008 C>T maps to NM_021729.4 R629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr11:118944625 G>A maps to NM_021729.4 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:118944072 C>T maps to NM_021729.4 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr9:79966343 T>C maps to ENST00000376646 G2467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:79955336 C>T maps to ENST00000376646 D2299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr9:79938133 C>T maps to ENST00000376646 S1994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:79946948 A>G maps to ENST00000376646 P2005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:79930289 G>T maps to ENST00000376646 E1512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr9:79824435 T>C maps to ENST00000376646 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr9:79895138 G>A maps to ENST00000376646 T963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr9:79824435 T>C maps to ENST00000376646 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr9:79824435 T>C maps to ENST00000376646 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:79875038 C>T maps to ENST00000376646 R776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr9:79824435 T>C maps to ENST00000376646 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr9:79840891 G>A maps to ENST00000376646 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:100729396 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:100733226 C>T maps to NM_017890.3 T2359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:100523465 T>C maps to NM_017890.3 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr8:100866137 C>T maps to NM_017890.3 Y3532Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:100115277 C>T maps to NM_017890.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr8:100287354 T>C maps to NM_017890.3 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:100779199 T>C did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:100533169 C>T maps to NM_017890.3 G1584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr8:100733268 G>A maps to NM_017890.3 V2373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr8:100514003 A>G maps to NM_017890.3 G1320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr8:100050688 T>C maps to NM_017890.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr8:100479762 T>C maps to NM_017890.3 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr8:100829925 A>G maps to NM_017890.3 E2777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr8:100829925 A>G maps to NM_017890.3 E2777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:100866407 A>G maps to NM_017890.3 G3622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr8:100479762 T>C maps to NM_017890.3 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:100847785 T>A maps to NM_017890.3 V3279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:100866458 T>C maps to NM_017890.3 Y3639Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:100821643 G>A maps to NM_017890.3 W2686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr8:100287354 T>C maps to NM_017890.3 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr8:100479762 T>C maps to NM_017890.3 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr8:100711918 A>C maps to NM_017890.3 P2096P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr8:100654047 C>T maps to NM_017890.3 Q1769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr8:100866129 C>A maps to NM_017890.3 R3530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr8:100454774 T>C maps to NM_017890.3 P1119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:100454786 T>C maps to NM_017890.3 I1123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr8:100454774 T>C maps to NM_017890.3 P1119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr15:62217668 C>A maps to NM_020821.2 E2199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr15:62327168 A>G maps to NM_020821.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr15:62250828 C>T maps to NM_020821.2 V1381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:62277143 C>A maps to NM_020821.2 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:62299514 C>A maps to NM_020821.2 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:62238024 A>G maps to NM_020821.2 D1679D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr15:62261603 T>A maps to NM_020821.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr15:62261603 T>A maps to NM_020821.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:12336563 G>A maps to NM_015378.2 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr1:12336515 G>A maps to NM_015378.2 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:12568999 C>T maps to NM_015378.2 Y4363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr1:12569044 C>T maps to NM_015378.2 S4378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:12336785 G>A maps to NM_015378.2 P1047P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:12374303 G>A maps to NM_015378.2 T2356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:12433906 A>G maps to NM_015378.2 K3637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:12418602 C>T maps to NM_015378.2 R3363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:12379632 C>A maps to NM_015378.2 T2498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:12401883 C>T maps to NM_015378.2 L2892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:12428625 C>T maps to NM_015378.2 R3518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:12414213 G>A maps to NM_015378.2 G3205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:12414216 G>A maps to NM_015378.2 T3206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:12414210 T>C maps to NM_015378.2 N3204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:12382624 C>A maps to NM_015378.2 S2579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:12318084 C>T maps to NM_015378.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:12416557 T>C maps to NM_015378.2 Y3325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr20:2845024 C>T maps to NM_022575.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:2845218 G>A maps to NM_022575.2 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr20:2847207 C>T maps to NM_022575.2 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr20:2847207 C>A maps to NM_022575.2 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:41191387 G>T maps to NM_020857.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr15:41195208 T>C maps to NM_020857.2 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:70922260 A>G maps to NM_004896.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr11:134113184 C>T maps to NM_052875.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:134095129 C>T maps to NM_052875.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr8:145650189 G>A maps to NM_183057.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:145649326 T>C maps to NM_183057.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:110929927 C>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:122745822 T>C maps to NM_022916.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:122735535 G>A maps to NM_022916.4 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr15:91545372 G>A maps to NM_018668.3 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:46712943 G>A maps to NM_018206.4 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:52997719 G>A maps to NM_016075.2 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr11:60901523 C>T maps to NM_017966.4 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr11:60900012 T>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:73085477 G>A maps to NM_001077621.1 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr15:42459012 A>G maps to ENST00000348544 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:42465939 G>T maps to ENST00000348544 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:38796482 A>G maps to NM_014396.3 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr7:38796518 G>A maps to NM_014396.3 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr7:38791873 G>A maps to NM_014396.3 Q610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:150064114 C>T maps to NM_007259.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3511-01A-21D-1835-10 chr18:61060662 A>T maps to NM_004869.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr18:61071018 G>A maps to NM_004869.3 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:61067904 T>C maps to NM_004869.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:33218697 G>A maps to NM_022553.4 R698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:33236863 G>A maps to NM_022553.4 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr6:33219348 A>G maps to NM_022553.4 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr6:33236353 G>A maps to NM_022553.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr6:33219348 A>G maps to NM_022553.4 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr17:559186 C>A maps to NM_001128159.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr17:600714 A>G maps to NM_001128159.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr17:465782 G>A maps to NM_001128159.2 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr17:531357 C>T maps to NM_001128159.2 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:423083 C>T maps to NM_001128159.2 Q770Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr17:613825 G>A maps to NM_001128159.2 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr17:422475 C>A maps to NM_001128159.2 P797P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:64211055 C>T maps to NM_016516.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:64161083 C>A maps to NM_016516.2 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:64211013 A>G maps to NM_016516.2 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:151158393 C>T maps to ENST00000354473 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:184577783 T>C maps to ENST00000437079 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:184586774 G>A maps to ENST00000437079 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:184542483 G>T maps to ENST00000437079 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:184631343 T>C maps to ENST00000437079 Y728Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr3:184647446 C>T maps to ENST00000437079 R932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr14:97327072 G>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:58275998 T>C maps to NM_001130480.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:50510882 G>A maps to NM_016440.3 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr23:107310218 A>G did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr23:107320395 G>T did not map to a codon.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr23:107320508 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:107301289 G>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:107310234 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr23:107304721 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:107316576 C>T did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:107319386 G>A did not map to a codon.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr23:107310216 C>T did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:107310218 A>G did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:107310216 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr12:118520169 G>A maps to NM_019086.5 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr12:118533515 C>T maps to NM_019086.5 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:118511738 C>T maps to NM_019086.5 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr11:124618609 C>A maps to NM_014312.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:65253400 G>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:65244884 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:65242110 G>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:65247910 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:54545537 G>A maps to NM_198481.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr19:54544289 G>A maps to NM_198481.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr7:54617630 C>T maps to ENST00000404951 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr7:54617711 A>G maps to ENST00000404951 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr20:36572573 C>T maps to NM_080607.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr20:36560133 G>T maps to NM_080607.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:25059545 T>C maps to NM_014588.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:25060076 C>T maps to NM_014588.4 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr14:74711918 A>G maps to NM_182894.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:74727456 G>A maps to NM_182894.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr6:142519711 C>T maps to NM_016485.3 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr6:142468453 C>T maps to NM_016485.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:117699421 C>T maps to NM_024626.2 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr14:68129193 C>T maps to NM_006370.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr17:26696573 G>A maps to NM_000638.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:26696672 G>A maps to NM_000638.3 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:26696684 C>T maps to NM_000638.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr10:116045770 C>T maps to NM_198496.1 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr10:116049198 C>T maps to NM_198496.1 Y691Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr10:116048757 C>A maps to NM_198496.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:116032510 G>A maps to NM_198496.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr16:22157663 C>T maps to NM_173615.3 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr16:22132344 G>A maps to NM_173615.3 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:22108213 C>T maps to NM_173615.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:98834431 G>T maps to NM_144992.4 G654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:98887243 G>A maps to NM_144992.4 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:98804463 A>G maps to NM_144992.4 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr2:98920175 T>C maps to NM_144992.4 P1144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:98866854 T>C maps to NM_144992.4 N916N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr11:124012398 C>T maps to NM_014622.4 D658D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr11:124013276 G>T maps to NM_014622.4 E718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr11:123994161 G>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr11:123988583 T>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:49842380 G>A maps to NM_198570.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:49842341 C>T maps to NM_198570.3 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr7:49815048 G>A maps to NM_198570.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr2:215301417 C>T maps to NM_001080500.2 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr2:215279273 C>T maps to NM_001080500.2 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:61048483 C>T maps to NM_152718.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:61032042 C>A maps to NM_152718.2 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr11:61032609 G>A maps to NM_152718.2 C680C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr11:61058327 G>A maps to NM_152718.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr11:61036436 G>A maps to NM_152718.2 H613H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:61053834 G>A maps to NM_152718.2 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:6128638 G>A maps to NM_000552.3 R1315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr12:6094750 C>T maps to NM_000552.3 T2293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3692-01A-01W-0900-09 chr12:6127534 T>G maps to NM_000552.3 A1683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr12:6127639 A>G maps to NM_000552.3 P1648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:6128116 C>T maps to NM_000552.3 G1489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr12:6128293 C>T maps to NM_000552.3 K1430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr12:6061673 C>T maps to NM_000552.3 T2666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:6103593 C>T maps to NM_000552.3 T2081T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:6181579 G>A maps to NM_000552.3 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr12:6091077 C>T maps to NM_000552.3 Q2387Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00U-01A-01W-A005-10 chr12:6061625 T>C maps to NM_000552.3 G2682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:6094277 C>T maps to NM_000552.3 T2303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:6128572 C>T maps to NM_000552.3 P1337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:6105277 C>A maps to NM_000552.3 E1985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:6140711 C>T maps to NM_000552.3 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:6167117 C>T maps to NM_000552.3 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:6167195 A>G maps to NM_000552.3 Y516Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr12:6122773 G>A maps to NM_000552.3 Y1831Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr12:6182857 G>A maps to NM_000552.3 C308C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr10:28900837 C>A maps to NM_016628.3 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr10:28824555 C>T maps to NM_016628.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:28900724 G>A maps to NM_016628.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr10:28900851 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:28879761 G>A did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:28903548 G>A maps to NM_016628.3 Q497Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:88259886 A>G maps to ENST00000342368 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr10:88259616 G>A maps to ENST00000342368 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr10:88232059 A>G maps to ENST00000342368 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr14:100803479 C>A maps to NM_173701.1 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:119575578 T>C maps to NM_015836.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:119575583 A>G maps to NM_015836.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr1:119619179 G>T maps to NM_015836.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:48544177 C>T did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:48546485 G>A did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:48544174 G>A did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr6:110424760 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr6:110423268 A>C maps to NM_003931.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:27741442 A>G maps to NM_006990.2 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:27755288 G>A maps to NM_006990.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:27736336 A>G maps to NM_006990.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr1:27744915 C>T maps to NM_006990.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:27739085 A>G maps to NM_006990.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:27256962 A>G maps to NM_006646.5 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr13:27256971 G>A maps to NM_006646.5 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:123336646 T>C maps to NM_003941.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:123349205 A>G maps to NM_003941.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:123332423 G>A maps to NM_003941.2 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr7:123332589 C>T maps to NM_003941.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:123346375 G>A maps to NM_003941.2 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr12:14943561 A>G maps to NM_016312.2 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr12:14947558 G>A maps to NM_016312.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:14946788 A>G maps to NM_016312.2 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:14941975 G>T maps to NM_016312.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr22:42415688 C>A maps to NM_152613.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr22:42394827 G>A maps to NM_152613.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr13:41639195 G>A maps to NM_007187.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr13:41639403 A>G maps to NM_007187.3 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:102612898 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:102612837 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr7:70853322 C>T maps to NM_022479.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3562-01A-02W-0831-10 chr7:70886057 G>A maps to NM_022479.1 W310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:71142269 G>A maps to NM_022479.1 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr7:70853283 C>T maps to NM_022479.1 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr7:70800611 G>A maps to NM_022479.1 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr7:71175891 C>A maps to NM_022479.1 Y549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr7:71135051 C>A maps to NM_022479.1 Y454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr7:71130574 G>A maps to NM_022479.1 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:71135018 T>A maps to NM_022479.1 C443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr7:71134988 A>G maps to NM_022479.1 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr7:73249092 G>A maps to NM_152559.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr7:73279950 G>T maps to NM_182504.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr2:224760308 A>G maps to NM_020830.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:224743393 C>T maps to NM_020830.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:224809983 G>A maps to NM_020830.3 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr2:224744948 A>G maps to NM_020830.3 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:224743432 T>C maps to NM_020830.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:52332384 C>T maps to NM_052950.3 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr4:85657480 C>A did not map to a codon.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr4:85636509 T>C maps to NM_014991.4 G2634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr4:85676502 G>A maps to NM_014991.4 S1825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:85758090 A>G maps to NM_014991.4 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr4:85708676 C>A maps to NM_014991.4 G1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:85600378 G>A maps to NM_014991.4 D3280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:85750272 G>A maps to NM_014991.4 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr4:85707193 G>A maps to NM_014991.4 L1334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:85672857 A>G maps to NM_014991.4 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:85729569 A>G maps to NM_014991.4 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:85614145 G>A maps to NM_014991.4 R2981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:85710983 G>A maps to NM_014991.4 I1188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:85781681 G>A maps to NM_014991.4 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:85747965 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:85594124 C>A maps to NM_014991.4 E3493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr4:85660272 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr4:85687085 T>G maps to NM_014991.4 R1689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr4:85742699 G>A maps to NM_014991.4 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr14:55429707 T>C maps to NM_007086.3 E831E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr14:55467348 T>A maps to NM_007086.3 K272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:55453894 A>G maps to NM_007086.3 H579H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr4:10084746 C>T maps to NM_017491.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:10099421 G>A maps to NM_017491.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr10:122643321 A>G maps to NM_018117.11 K590K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:122664870 C>T maps to NM_018117.11 D1078D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:122665440 C>T maps to NM_018117.11 H1115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr10:122624603 G>T maps to NM_018117.11 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:122619678 G>A maps to NM_018117.11 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:122662710 C>T maps to NM_018117.11 C966C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:122643378 C>T maps to NM_018117.11 N609N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:122650313 C>A maps to NM_018117.11 I810I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:122665413 C>T maps to NM_018117.11 A1106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr10:122662744 G>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr10:122649409 A>G maps to NM_018117.11 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:122661811 C>T maps to NM_018117.11 Q911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr2:203760820 T>C maps to NM_018256.3 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr2:203759313 G>T maps to NM_018256.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:48458717 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:48463305 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:48458878 C>A did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:48463284 G>C did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:48460281 C>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:48460473 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:48463284 G>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:48460473 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:48458723 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:9515781 T>C maps to NM_145054.4 D337D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:9511482 C>T maps to NM_145054.4 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:9503461 C>T maps to NM_145054.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr17:9515745 G>A maps to NM_145054.4 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:177071647 C>T maps to NM_170710.4 N760N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:177082099 C>T maps to NM_170710.4 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:177046286 G>T maps to NM_170710.4 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:177093624 G>T maps to NM_170710.4 E1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:177100690 C>T maps to NM_170710.4 F1310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr4:177067310 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:177072974 G>T maps to NM_170710.4 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr4:177081144 G>A maps to NM_170710.4 R866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:177093635 A>G maps to NM_170710.4 K1110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:989856 G>A maps to NM_024100.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:984406 G>A maps to NM_024100.3 W18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:39276476 C>T maps to NM_025132.3 G1205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:39280182 T>A maps to NM_025132.3 C1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr4:39187400 G>A maps to NM_025132.3 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr4:39206809 T>C maps to NM_025132.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr4:39206809 T>C maps to NM_025132.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:102675298 C>T maps to ENST00000454394 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr14:102676048 T>C maps to ENST00000454394 C545C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr16:737322 G>A maps to ENST00000248142 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:735685 G>A maps to ENST00000248142 H687H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:739514 G>A maps to ENST00000248142 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:739417 G>A maps to ENST00000248142 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:739514 G>A maps to ENST00000248142 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr16:739274 C>A maps to ENST00000248142 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:737725 G>A maps to ENST00000248142 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr14:100847785 C>A maps to NM_001161476.1 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:100934476 C>T maps to NM_001161476.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:100950403 C>A maps to NM_001161476.1 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr14:100934416 A>C maps to NM_001161476.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:224619250 T>C maps to NM_025160.6 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:224581668 C>T maps to NM_025160.6 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:224585867 G>A maps to NM_025160.6 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:170089026 A>G maps to NM_182552.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:170059579 C>T maps to NM_182552.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr6:170002338 C>T maps to NM_182552.3 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr6:170059261 G>A maps to NM_182552.3 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr6:170047944 G>A maps to NM_182552.3 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr1:118483460 G>A maps to NM_006784.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:118501964 C>T maps to NM_006784.2 C909C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:128522060 C>A maps to NM_001006622.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:128477303 T>C maps to NM_018383.4 Q765Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr2:128467308 G>A maps to NM_018383.4 R1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:128479501 C>A maps to NM_018383.4 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:128482767 T>G maps to NM_018383.4 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:128482007 C>T maps to NM_018383.4 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:128476859 C>T maps to NM_018383.4 G913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr9:131397113 G>A maps to NM_052844.3 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr9:131397430 C>T maps to NM_052844.3 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:20153692 C>T maps to NM_001006657.1 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr2:20153613 G>T maps to NM_001006657.1 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr2:20153613 G>T maps to NM_001006657.1 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr2:20153613 G>A maps to NM_001006657.1 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr2:20153613 G>A maps to NM_001006657.1 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr5:110428247 C>A maps to NM_139281.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:110439605 C>A maps to NM_139281.2 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr5:110462473 G>T maps to NM_139281.2 E917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr5:110428108 T>C maps to NM_139281.2 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:110454737 G>A maps to NM_139281.2 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:127618523 C>T maps to NM_001045476.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr21:44270305 C>T maps to NM_018669.4 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr21:44293770 A>T maps to NM_018669.4 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:76729030 C>A maps to NM_018268.2 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:76732203 C>T maps to NM_018268.2 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:29135494 T>C maps to NM_015131.1 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:29136954 G>A maps to NM_015131.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:29136954 G>A maps to NM_015131.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:29152515 G>A maps to NM_015131.1 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:117575372 C>T did not map to a codon.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr23:117527094 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:117544905 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:117532356 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:117527163 A>G did not map to a codon.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr23:117570666 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:117543545 C>T did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:117526614 G>T did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:117576280 C>T did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:117527154 T>G did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:117576246 G>T did not map to a codon.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr23:117526613 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:117526614 G>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:48933275 C>T did not map to a codon.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr23:48933107 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:48932851 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:48935403 G>T did not map to a codon.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr23:48934127 G>A did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr23:48933301 T>C did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:48932826 C>T did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr1:109538233 A>G maps to NM_001142550.1 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr1:109553926 C>T maps to NM_001142550.1 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr1:109524461 C>T maps to NM_001142550.1 W772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:109538233 A>T maps to NM_001142550.1 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr1:109538233 A>G maps to NM_001142550.1 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr3:39104579 C>T maps to NM_020839.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr3:39125662 T>C maps to NM_020839.2 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:39127099 T>C maps to NM_020839.2 H491H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:39111231 G>A maps to NM_020839.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:167218063 C>A maps to NM_178824.3 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr3:167247000 C>A maps to NM_178824.3 G397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:167277989 A>G maps to NM_178824.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr3:167277926 G>A maps to NM_178824.3 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:167254676 A>T maps to NM_178824.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:167254676 A>G maps to NM_178824.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr3:167322161 A>G maps to NM_178824.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr3:167319913 C>T did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr3:167277926 G>A maps to NM_178824.3 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr3:167293906 C>T maps to NM_178824.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:137005841 A>G maps to NM_052821.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr9:137013407 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:137007762 C>T maps to NM_052821.3 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr3:113098287 T>C maps to NM_001164496.1 E721E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:113098287 T>C maps to NM_001164496.1 E721E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:113120559 A>G maps to NM_001164496.1 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr3:196288166 A>G maps to NM_182627.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:196281105 A>C maps to NM_182627.1 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr3:196288166 A>G maps to NM_182627.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr2:74652024 G>A maps to NM_032118.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:74955896 G>A maps to NM_030581.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:74923710 A>C maps to NM_030581.3 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:74919551 G>A maps to NM_030581.3 I896I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:74920198 G>A maps to NM_030581.3 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr3:122133655 G>A maps to NM_019069.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr3:122133814 A>G maps to NM_019069.3 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr3:122133511 C>T maps to NM_019069.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr3:122134075 A>T maps to NM_019069.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:122133607 A>C maps to NM_019069.3 Y256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr3:122133814 A>G maps to NM_019069.3 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr3:49051279 T>C maps to NM_018031.3 C801C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr7:158734752 G>T maps to NM_018051.4 V972V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr7:158672578 C>T maps to NM_018051.4 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:158664011 G>A maps to NM_018051.4 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr15:78580638 G>A maps to NM_025234.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr15:78581976 A>T maps to NM_025234.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:36593663 C>T maps to NM_001083961.1 D1082D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:36573978 C>T maps to NM_001083961.1 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:36580181 C>T maps to NM_001083961.1 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:36592919 C>T maps to NM_001083961.1 C1029C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:36592211 G>A maps to NM_001083961.1 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:85592279 C>T maps to NM_145172.3 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr1:85560132 A>G maps to NM_145172.3 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:85546975 C>T maps to NM_145172.3 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:85551531 C>T maps to NM_145172.3 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:85598535 A>T did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:85589819 C>T maps to NM_145172.3 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr1:85538767 G>A maps to NM_145172.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:241958511 C>T maps to NM_144625.4 R991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:241946596 G>A maps to NM_144625.4 W863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:241834443 C>T maps to NM_144625.4 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:43675503 G>T maps to NM_001195831.1 G616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:43638429 A>G maps to NM_001195831.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:43675503 G>T maps to NM_001195831.1 G616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr12:122406015 C>T maps to NM_144668.4 C904C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr12:122372175 C>T maps to NM_144668.4 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:122361779 G>T maps to NM_144668.4 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:122392186 T>C maps to NM_144668.4 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:122398589 C>T maps to NM_144668.4 R745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:122386922 G>T maps to NM_144668.4 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr12:122359396 G>A maps to NM_144668.4 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr12:122399888 G>A maps to NM_144668.4 E771E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr12:122369782 C>T maps to NM_144668.4 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr8:124121761 G>T maps to NM_145647.3 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:124096453 G>A maps to NM_145647.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:124146368 C>T maps to NM_145647.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:228786134 G>A maps to NM_178821.1 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr2:228769718 T>C maps to NM_178821.1 H241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr2:228758588 C>T maps to NM_178821.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:228755987 A>C maps to NM_178821.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:54363650 T>C maps to NM_015285.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:54424439 T>C maps to NM_015285.2 S872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:54339844 G>A maps to NM_015285.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr18:54483286 G>A maps to NM_015285.2 Q1072Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr18:54591321 C>T maps to NM_015285.2 A1232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:37701188 C>T maps to NM_018034.2 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:37379474 G>A maps to NM_018034.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:37701208 T>C maps to NM_018034.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr5:37396644 A>G maps to NM_018034.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr15:53992109 G>A maps to NM_182758.2 C534C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr15:53908347 A>G maps to NM_182758.2 D685D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr15:53907755 C>A maps to NM_182758.2 G883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:53908293 A>C maps to NM_182758.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:53992097 G>A maps to NM_182758.2 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:53907948 G>A maps to NM_182758.2 H818H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:54015027 C>T maps to NM_182758.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:53889438 C>T maps to NM_182758.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:53889317 C>A maps to NM_182758.2 E1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:54005063 C>A maps to NM_182758.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:85188945 C>T maps to NM_032856.2 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:62603450 C>T maps to NM_018093.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:190340091 A>G maps to NM_032168.1 K814K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr2:190339474 T>C maps to NM_032168.1 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:190332357 C>T maps to NM_032168.1 R538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:190327258 C>T maps to NM_032168.1 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:44136209 A>G maps to NM_024908.3 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:111983959 C>T maps to NM_024102.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:67306259 A>G maps to NM_024763.4 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr1:67288096 G>A maps to NM_024763.4 Q815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:3552543 G>A maps to NM_017818.3 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:3547634 C>T maps to NM_017818.3 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:1639341 C>T maps to NM_001163809.1 R1779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:1629653 C>T maps to NM_001163809.1 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:1631567 G>A maps to NM_001163809.1 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr17:1640792 C>T maps to NM_001163809.1 S1880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr17:1629794 G>T maps to NM_001163809.1 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:1635699 A>T maps to NM_001163809.1 G1413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:12781593 C>T maps to NM_032332.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr9:140458997 C>T maps to NM_138778.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr9:140459009 C>T maps to NM_138778.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr7:151093008 C>T maps to ENST00000426624 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:33666303 C>T maps to NM_173479.3 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:33639751 C>T maps to NM_173479.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:33663283 G>T maps to NM_173479.3 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:33628608 C>T maps to NM_173479.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:703646 A>G maps to NM_145294.4 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr16:716915 G>A maps to NM_145294.4 K1672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr16:711949 C>T maps to NM_145294.4 Y1308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr16:717522 G>T maps to NM_145294.4 P1727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:710628 C>T maps to NM_145294.4 P1102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:705117 C>A maps to NM_145294.4 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:712759 C>T maps to NM_145294.4 V1409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:134871019 G>A maps to NM_014149.3 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:134873274 C>T maps to NM_014149.3 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:134894381 T>C maps to NM_014149.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:134896161 C>T maps to NM_014149.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr7:134870953 G>C maps to NM_014149.3 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr7:134893597 A>G maps to NM_014149.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr2:68361856 G>A maps to NM_138458.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr15:90276309 G>A maps to NM_020212.1 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:90274677 C>A maps to NM_020212.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr2:160112722 A>C maps to NM_001128212.1 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr1:27620581 C>T maps to ENST00000319394 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:27587577 C>T maps to ENST00000319394 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:27609861 G>A maps to ENST00000319394 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr8:124448697 C>T maps to NM_018024.1 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr11:9608075 G>A maps to NM_003390.3 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:9598793 G>A maps to NM_003390.3 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr11:9608328 C>T maps to NM_003390.3 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr11:9598749 C>T maps to NM_003390.3 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:9598749 C>A maps to NM_003390.3 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:141418981 G>A maps to NM_001105558.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr7:141408743 C>T maps to NM_001105558.1 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02J-01A-01W-A00E-09 chr7:141424002 C>T maps to NM_001105558.1 H383H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr7:141423048 C>T maps to NM_001105558.1 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:141424848 A>C maps to NM_001105558.1 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr7:141424950 G>T maps to NM_001105558.1 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr16:84351893 G>A maps to NM_021197.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr16:84328645 A>C maps to NM_021197.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:44258494 C>T maps to NM_080753.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr20:43752513 G>A maps to NM_080869.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:44404239 C>T maps to NM_080614.1 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:44166704 G>A maps to ENST00000396669 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr20:44187578 C>T maps to NM_130896.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:44236777 C>A maps to NM_147198.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:683777 C>T maps to NM_053284.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr17:48917620 G>A maps to NM_175575.5 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:48918217 C>T maps to NM_175575.5 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:48917338 C>A maps to NM_175575.5 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:48917608 C>T maps to NM_175575.5 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:48918166 C>T maps to NM_175575.5 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:48917023 C>A maps to NM_175575.5 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr17:48917551 G>A maps to NM_175575.5 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr17:48917437 C>T maps to NM_175575.5 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:48917263 G>A maps to NM_175575.5 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr17:48918274 C>T maps to NM_175575.5 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr4:6302673 C>T maps to NM_006005.3 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:6303726 C>T maps to NM_006005.3 Y735Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:6290748 G>A maps to NM_006005.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:6293665 C>T maps to NM_006005.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr4:6302712 C>T maps to NM_006005.3 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:6279412 C>T maps to NM_006005.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr15:83499778 C>T maps to NM_001080435.1 C690C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr15:83499628 A>T maps to NM_001080435.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr15:83491930 G>A maps to NM_001080435.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr4:1980539 A>G maps to NM_133335.3 R1334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr4:1940242 G>A maps to NM_133335.3 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:1953848 G>A maps to NM_133335.3 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr4:1962775 C>T maps to NM_133335.3 N1090N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:1957708 G>T did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr4:1936967 G>C maps to NM_133335.3 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr4:1962766 A>G maps to NM_133335.3 E1087E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:38162192 G>A maps to NM_023034.1 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:38162808 G>A maps to NM_023034.1 C799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr8:38139034 G>A maps to NM_023034.1 R1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:38133163 C>A maps to NM_023034.1 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:1993285 C>A maps to NM_005663.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr4:1985174 C>T maps to NM_005663.3 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr4:1985604 C>T maps to NM_005663.3 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:1993325 C>T maps to NM_005663.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr4:1993433 G>A maps to NM_005663.3 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr12:65514229 A>G maps to NM_007191.4 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr12:65445152 T>C maps to NM_007191.4 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr12:65445170 G>T maps to NM_007191.4 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:175431879 C>T maps to NM_003387.4 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:175437115 T>C maps to NM_003387.4 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr2:175440058 G>A maps to NM_003387.4 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr2:175427330 C>T did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:38421096 A>T maps to NM_133264.4 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr17:38434452 A>C maps to NM_133264.4 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr17:38421195 C>T maps to NM_133264.4 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr17:38420889 C>A maps to NM_133264.4 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr7:29928928 C>T maps to NM_001080529.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:29923940 G>A maps to NM_001080529.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6922-01A-11D-1924-10 chr7:29923775 G>A maps to NM_001080529.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:66426282 C>T maps to NM_017983.5 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr17:66426282 C>T maps to NM_017983.5 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr7:5239272 A>G maps to NM_015610.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:5256730 G>A maps to NM_015610.3 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:5239272 A>G maps to NM_015610.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr7:5239272 A>G maps to NM_015610.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr7:5239272 A>G maps to NM_015610.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:134239718 C>T maps to NM_003882.2 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr8:134225385 C>T maps to NM_003882.2 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:134232989 C>T maps to NM_003882.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr8:134237747 C>T maps to NM_003882.2 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:134233082 C>T maps to NM_003882.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr8:134239718 C>T maps to NM_003882.2 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:134225273 C>T maps to NM_003882.2 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:15535154 G>T maps to ENST00000389282 A1545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:68564332 G>A maps to NM_001002292.3 N538N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr1:68624835 C>A maps to NM_024911.6 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr12:992667 A>G maps to NM_001184985.1 E1459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr12:992667 A>G maps to NM_001184985.1 E1459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr12:939280 C>A maps to NM_001184985.1 Y422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:970361 G>T maps to NM_001184985.1 G602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03J-01A-21W-A096-10 chr12:936417 G>A maps to NM_001184985.1 K381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:939271 A>G maps to NM_001184985.1 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:968599 A>G maps to NM_001184985.1 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:977147 G>A maps to NM_001184985.1 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:988758 A>G maps to NM_018979.3 V798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:994658 G>A maps to NM_001184985.1 Q1823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr12:977132 T>C maps to NM_001184985.1 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr12:939271 A>G maps to NM_001184985.1 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr12:992667 A>G maps to NM_001184985.1 E1459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr12:992667 A>G maps to NM_001184985.1 E1459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr12:992667 A>G maps to NM_001184985.1 E1459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:96051649 G>A maps to ENST00000297954 P1575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:96019249 G>A maps to ENST00000297954 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr9:96024184 G>A maps to ENST00000297954 P1052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr9:95997219 G>A maps to ENST00000297954 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr9:96051772 C>T maps to ENST00000297954 G1616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr9:95992141 G>A maps to ENST00000297954 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr9:96030987 C>G maps to ENST00000297954 P1331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:96070769 G>A maps to ENST00000297954 A2177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr9:95947801 C>T maps to ENST00000297954 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:96054861 G>A maps to ENST00000297954 P1742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr9:96026242 G>A maps to ENST00000297954 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr23:54275418 A>G did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:54321219 G>A did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:54275418 A>G did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:54275998 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:54275455 G>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:54275305 C>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:54276013 C>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:54228596 A>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:54275997 T>C did not map to a codon.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr23:54282312 G>C did not map to a codon.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr23:54319391 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:54264902 C>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:54321244 T>C did not map to a codon.
Sequencing variant TCGA-AA-3875-01A-01W-0900-09 chr23:54276547 C>G did not map to a codon.
Sequencing variant TCGA-AA-3971-01A-01W-0995-10 chr23:54278060 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:54324821 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr23:54335607 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:54275454 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:54263466 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:54337635 A>C did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:54319694 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:54275996 G>A did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr23:54228594 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:54275178 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:54277852 A>G did not map to a codon.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr23:54263399 C>T did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:54282212 C>T did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:54228594 T>C did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr23:54225052 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr23:54259356 T>C did not map to a codon.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr23:54228595 G>A did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:54337723 C>T did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:54263399 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:54275997 T>C did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:54263400 A>G did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr17:40933192 C>T maps to NM_032387.4 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr17:40945635 G>A maps to NM_032387.4 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:40947528 C>A maps to NM_032387.4 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr17:40934873 G>A maps to NM_032387.4 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr17:40934801 G>A maps to NM_032387.4 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:40936554 C>T maps to NM_032387.4 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr17:40934939 G>A maps to NM_032387.4 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:219747041 C>T maps to NM_025216.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:49360089 G>A maps to NM_003394.3 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr12:49360144 G>T maps to NM_003394.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr11:75902768 C>T maps to NM_004626.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:75902621 G>A maps to NM_004626.2 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr11:75898249 G>A maps to NM_004626.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr11:75907590 G>C maps to NM_004626.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr7:120979254 T>C maps to NM_057168.1 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr7:120971762 G>A maps to NM_057168.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr7:116918295 G>A maps to NM_003391.2 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-7000-01A-11D-1924-10 chr7:116918232 G>A maps to NM_003391.2 N353N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr7:116955223 A>G maps to NM_003391.2 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr1:113058939 C>T maps to NM_024494.2 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr1:113062996 C>T maps to NM_024494.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:44845961 C>T maps to NM_030753.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr17:44851031 A>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:228246913 C>T maps to ENST00000366753 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:228246811 C>T maps to ENST00000366753 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:22456345 T>C did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr1:22446806 C>T maps to NM_030761.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:55504335 G>A maps to NM_003392.3 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:55514947 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr3:55513588 C>T maps to NM_003392.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr3:55504149 C>T maps to NM_003392.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr12:1755090 C>T maps to NM_032642.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr2:219736387 G>A maps to NM_006522.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:13896043 G>A maps to NM_004625.3 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:13860668 C>T maps to NM_004625.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr3:13896087 C>A maps to NM_004625.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr22:46318840 G>A maps to NM_058238.2 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr22:46327019 C>T maps to NM_058238.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr22:46327043 G>A maps to NM_058238.2 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:137424706 G>A maps to NM_058244.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:137424670 G>A maps to NM_058244.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr17:44952530 G>T maps to NM_003396.1 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr17:44952581 G>C maps to NM_003396.1 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:7606671 G>A maps to NM_018081.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr21:40763716 A>G maps to NM_004627.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:31007869 G>T maps to NM_000553.4 E1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr8:31012198 A>G maps to NM_000553.4 K1249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:118481133 C>T maps to ENST00000441406 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr12:118490203 G>A maps to ENST00000441406 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:118474207 C>T maps to ENST00000441406 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr17:6023708 C>T maps to NM_015253.1 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr17:6021507 G>T maps to NM_015253.1 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr17:5991340 C>T maps to NM_015253.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr17:5991334 C>T maps to NM_015253.1 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr12:108603984 C>T maps to ENST00000261400 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:108600075 C>T maps to ENST00000261400 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:108626649 C>T maps to ENST00000261400 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:108620897 C>T maps to ENST00000261400 C312C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr12:108604020 C>T maps to ENST00000261400 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr12:108589987 C>T maps to ENST00000261400 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr12:108620879 G>A maps to ENST00000261400 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr12:108642020 G>A maps to ENST00000261400 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr12:108642089 G>A maps to ENST00000261400 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr12:108604002 C>T maps to ENST00000261400 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr11:32413590 A>G maps to NM_024426.4 C453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:32410609 C>T maps to NM_024426.4 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr11:32410609 C>T maps to NM_024426.4 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr11:32421568 G>A maps to NM_024426.4 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:32414301 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr11:32450100 C>T maps to NM_024426.4 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr11:32413575 T>C maps to NM_024426.4 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr11:32414260 T>C maps to NM_024426.4 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr11:32456324 T>C maps to NM_024426.4 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr11:32413565 G>T maps to NM_024426.4 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr11:32413563 C>T maps to NM_024426.4 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr11:32413575 T>C maps to NM_024426.4 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr11:32413590 A>G maps to NM_024426.4 C453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr11:32413554 G>A maps to NM_024426.4 H465H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr11:32414248 A>G maps to NM_024426.4 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr11:32421541 G>A maps to NM_024426.4 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:32413575 T>C maps to NM_024426.4 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:32450148 G>T maps to NM_024426.4 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr6:160176144 G>A maps to NM_004906.3 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:160160024 C>T maps to NM_004906.3 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr6:160164785 C>T maps to NM_004906.3 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:160169260 C>T maps to NM_004906.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:34984482 C>T maps to ENST00000270288 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:34983946 C>T maps to ENST00000270288 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:34991074 C>T maps to ENST00000270288 C622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:167812321 G>A maps to NM_001161661.1 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:167891846 G>A maps to NM_001161661.1 S1016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:167891717 G>A maps to NM_001161661.1 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr4:184114754 A>G maps to ENST00000448232 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:184166598 C>T maps to ENST00000448232 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:184186251 C>T maps to ENST00000448232 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr4:184205539 C>T maps to ENST00000448232 C1039C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:184186922 T>C did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr4:184190312 C>T maps to ENST00000448232 C799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:10046903 C>T did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:10062211 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:10085432 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:10106863 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:10096746 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:10035412 G>A did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:10046903 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:10090716 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr23:10062251 C>T did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:10058860 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr23:10084547 G>A did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr23:10084547 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:10106819 G>A did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:10104727 G>A did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:10085224 C>A did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:10094285 A>C did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:10085223 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:10090697 G>A did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:10094324 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:10085306 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:10107474 A>G did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:10085203 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:10090778 G>T did not map to a codon.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr23:10084545 A>G did not map to a codon.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr23:10058925 C>T did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr23:10102589 G>A did not map to a codon.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr23:10085307 C>A did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:10085495 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:10085222 G>T did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:10084545 A>G did not map to a codon.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr23:10085307 C>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:78466519 T>C maps to NM_016373.1 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr16:78143678 G>A maps to NM_016373.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:78198080 G>A maps to NM_016373.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:78198180 G>T maps to NM_016373.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr16:78142371 C>T maps to NM_016373.1 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:78420818 T>C maps to NM_016373.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:87393742 G>A maps to NM_007013.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:87437502 T>C maps to NM_007013.3 N371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:87460617 G>T maps to NM_007013.3 E717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr16:69971485 C>T maps to NM_007014.3 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:69922110 G>A maps to NM_007014.3 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr16:69951728 G>A maps to NM_007014.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:69921976 G>T maps to NM_007014.3 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:69971485 C>T maps to NM_007014.3 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr16:69833187 T>C maps to NM_007014.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr3:149260150 G>A maps to NM_001168278.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:7686171 G>A maps to NM_020196.2 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:7692706 C>T maps to NM_020196.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:7685287 C>T maps to NM_020196.2 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:52841633 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:52842195 A>G did not map to a codon.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr23:52844155 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:52844153 T>A did not map to a codon.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr23:52844155 A>G did not map to a codon.
Multiple mappings detected for codon TCGA-AA-3815-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr22:29191303 G>T maps to NM_001079539.1 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr3:46063022 G>A maps to NM_005283.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr2:31588393 G>A maps to NM_000379.3 R825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:31593229 C>T maps to NM_000379.3 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:31596795 G>A maps to NM_000379.3 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr2:31602774 C>T maps to NM_000379.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr2:31609388 T>A maps to NM_000379.3 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:31600016 C>T maps to NM_000379.3 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr2:31590893 T>A maps to NM_000379.3 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:31560635 G>T maps to NM_000379.3 A1274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:2688595 A>C did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:2700136 A>T did not map to a codon.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr23:2729396 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:2729383 G>A did not map to a codon.
Sequencing variant TCGA-CA-5797-01A-01D-1650-10 chr23:2729381 A>G did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:2700141 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:123019981 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:123034433 T>G did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:123019858 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:123041015 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:123041018 T>G did not map to a codon.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr23:123034387 T>C did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:123020044 A>G did not map to a codon.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr23:123020277 C>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:123020047 T>C did not map to a codon.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr3:39226543 G>A maps to NM_194293.2 Q1465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:39228788 G>A maps to NM_194293.2 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:39229228 G>A maps to NM_194293.2 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:39229169 G>A maps to NM_194293.2 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:39229340 G>A maps to NM_194293.2 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:39229808 A>G maps to NM_194293.2 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr3:39227069 G>A maps to NM_194293.2 D1289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:39226496 G>T maps to NM_194293.2 A1480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:39230339 C>T maps to NM_194293.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:39227882 T>C maps to NM_194293.2 E1018E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:39228089 C>T maps to NM_194293.2 P949P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:39230144 G>A maps to NM_194293.2 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:39228298 G>A maps to NM_194293.2 Q880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr2:168099806 C>T maps to NM_152381.5 D635D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr2:168103075 C>A maps to NM_152381.5 S1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:168105422 T>G maps to NM_152381.5 T2507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:168107950 C>A maps to NM_152381.5 S3350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr2:167992543 T>A maps to NM_152381.5 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3814-01A-01W-0900-09 chr2:168098325 C>A maps to NM_152381.5 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr2:168107295 C>T maps to NM_152381.5 R3132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:168102642 C>T maps to NM_152381.5 R1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:168103973 C>G maps to NM_152381.5 G2024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:168074698 C>T maps to NM_152381.5 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:168100850 C>T maps to NM_152381.5 F983F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:168106529 C>T maps to NM_152381.5 T2876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:168106679 C>T maps to NM_152381.5 F2926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:168074698 C>T maps to NM_152381.5 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:168102323 C>A maps to NM_152381.5 I1474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:168102398 C>T maps to NM_152381.5 F1499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:168099143 C>T maps to NM_152381.5 C414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:168106475 C>T maps to NM_152381.5 I2858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr2:168102642 C>T maps to NM_152381.5 R1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:168074794 G>A maps to NM_152381.5 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:168102210 C>T maps to NM_152381.5 R1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:168107672 C>T maps to NM_152381.5 D3257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:168115455 C>T maps to ENST00000420519 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr2:168101375 A>G maps to NM_152381.5 Q1158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:168103652 T>C maps to NM_152381.5 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr2:168103445 C>A maps to NM_152381.5 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr2:168103652 T>C maps to NM_152381.5 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr2:168100067 C>A maps to NM_152381.5 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:167760372 A>G maps to NM_152381.5 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr2:168110646 C>A maps to ENST00000420519 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr2:168103652 T>C maps to NM_152381.5 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:168107292 C>T maps to NM_152381.5 R3131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6932-01A-11D-1924-10 chr2:168114747 A>G maps to ENST00000420519 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr2:168103652 T>C maps to NM_152381.5 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:167992447 G>A maps to NM_152381.5 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:37587352 T>G did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:37587421 G>A did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:37587397 A>G did not map to a codon.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr23:37587110 A>G did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:37545303 G>A did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:37553709 G>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:37553797 A>C did not map to a codon.
Sequencing variant TCGA-F4-6855-01A-11D-1924-10 chr23:37553697 G>A did not map to a codon.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr23:37587070 T>C did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:37545260 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:56015611 T>C maps to NM_052898.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:56436158 C>A maps to NM_052898.1 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr8:56436527 G>A maps to NM_052898.1 E565E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:56436131 C>T maps to NM_052898.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:56436131 C>T maps to NM_052898.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr8:56270265 C>T maps to NM_052898.1 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr8:6690411 G>A maps to NM_207411.4 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:6681154 T>C maps to NM_207411.4 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr8:10755877 G>A maps to NM_173683.3 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3502-01A-01D-1408-10 chr8:10756046 C>T maps to NM_173683.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3521-01A-01W-0831-10 chr8:10755506 G>A maps to NM_173683.3 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr8:10756046 C>T maps to NM_173683.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:10756220 G>A maps to NM_173683.3 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:10755923 G>A maps to NM_173683.3 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:10756223 G>T maps to NM_173683.3 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:10755899 G>A maps to NM_173683.3 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr8:11058359 C>T maps to NM_173683.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:11058359 C>T maps to NM_173683.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:11058455 C>T maps to NM_173683.3 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:30584608 C>T maps to NM_001011718.1 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:71646499 C>A maps to NM_001011720.1 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:100169620 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:100169967 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:100177877 G>A did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr23:100183110 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:100183245 A>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:100169387 C>T did not map to a codon.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr23:100169996 T>G did not map to a codon.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr23:100169862 A>G did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:100169862 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr23:100169861 A>G did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr9:100455963 C>A maps to NM_000380.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr9:100437843 G>A maps to NM_000380.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:100437825 C>T maps to NM_000380.3 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:14189440 A>G maps to NM_004628.4 N827N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:14211971 C>T maps to NM_004628.4 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr10:111640662 G>A maps to NM_020383.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr10:111630636 A>G maps to NM_020383.3 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:128896704 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:128879236 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:128884527 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:128901640 C>T did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:128902349 C>T did not map to a codon.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr23:128880302 G>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:61715885 A>G maps to NM_003400.3 D681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:61709555 A>G maps to NM_003400.3 Y977Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:61709609 A>G maps to NM_003400.3 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:61720164 T>C maps to NM_003400.3 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:21374437 G>A maps to NM_022459.4 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:21383303 G>A maps to NM_022459.4 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr13:21396328 C>A maps to NM_022459.4 G314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr13:21395946 G>A maps to NM_022459.4 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr13:21396413 G>T maps to NM_022459.4 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:21383346 G>A maps to NM_022459.4 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr13:21357983 A>G maps to NM_022459.4 D1111D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3662-01A-01D-1719-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr6:43496661 A>C maps to NM_020750.2 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr6:43538650 C>T maps to NM_020750.2 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:43501740 G>A maps to NM_020750.2 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr6:43535016 A>G maps to NM_020750.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr16:28167539 C>A maps to NM_015171.2 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:28117810 A>G maps to NM_015171.2 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr16:28115977 C>T maps to NM_015171.2 T945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:21856608 C>T maps to ENST00000434536 R821R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:21835303 C>T maps to ENST00000434536 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:21856608 C>T maps to ENST00000434536 R821R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr8:21861448 C>T maps to ENST00000434536 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr12:64814243 A>G maps to NM_007235.3 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:64824068 T>C did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr12:64823857 C>T maps to NM_007235.3 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr1:180601396 C>A maps to NM_004736.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:180775218 C>T maps to NM_004736.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:180772530 C>T maps to NM_004736.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:180772621 C>T maps to NM_004736.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:180805752 C>T maps to NM_004736.3 R468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr1:180794314 C>T maps to NM_004736.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:180832842 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:180793937 C>T maps to NM_004736.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr19:44047603 A>G maps to NM_006297.2 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:44056176 C>T maps to NM_006297.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:104173450 G>A maps to NM_005432.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr14:104165698 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:82499369 G>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:82649045 C>A maps to NM_022406.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr2:216981419 G>A maps to NM_021141.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr2:216983870 C>T maps to NM_021141.3 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:217055002 G>A maps to NM_021141.3 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4323-01A-21D-1835-10 chr2:216997080 C>T maps to NM_021141.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr22:42059785 G>A maps to NM_001469.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr22:42049656 A>G maps to NM_001469.3 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr22:42049656 A>G maps to NM_001469.3 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr12:58350549 T>C maps to NM_033276.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr3:142075776 G>A maps to NM_019001.3 Q1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr3:142140332 A>G maps to NM_019001.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:142139902 G>A maps to NM_019001.3 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:142139905 A>C maps to NM_019001.3 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr3:142144354 A>G maps to NM_019001.3 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr3:142051901 T>C maps to NM_019001.3 A1323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr3:142031517 A>G maps to NM_019001.3 H1580H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr20:21321450 G>A maps to NM_012255.3 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr20:21314589 C>T maps to NM_012255.3 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr20:21327097 T>C maps to NM_012255.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:21314187 G>T maps to NM_012255.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:21319705 G>T maps to NM_012255.3 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:21337283 G>T maps to NM_012255.3 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:21312957 G>A maps to NM_012255.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:74563070 G>A maps to NM_182969.1 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:74563070 G>A maps to NM_182969.1 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr11:74556289 G>T maps to NM_182969.1 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr3:38438609 C>G maps to NM_005108.3 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6652-01A-11D-1771-10 chr16:17228526 C>T maps to NM_022166.3 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr16:17202800 G>A maps to NM_022166.3 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr16:17235123 G>A maps to NM_022166.3 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:17232259 G>A maps to NM_022166.3 C572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr16:17211512 G>T maps to NM_022166.3 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3808-01A-01W-0995-10 chr17:48432334 C>A maps to NM_022167.2 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr17:48435635 C>T maps to NM_022167.2 D670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:101984915 G>A maps to NM_001130145.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr12:32900292 G>A maps to NM_001040436.1 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:32903720 A>G maps to NM_001040436.1 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr12:32900292 G>A maps to NM_001040436.1 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr12:32902923 T>C maps to NM_001040436.1 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:43162855 T>C maps to NM_004559.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr1:43166658 C>A maps to NM_004559.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr1:43166658 C>T maps to NM_004559.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr1:43162404 A>G maps to NM_004559.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr1:43162404 A>G maps to NM_004559.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr1:43166658 C>T maps to NM_004559.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr1:43166658 C>A maps to NM_004559.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6321-01A-11D-1719-10 chr1:43162404 A>G maps to NM_004559.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:7194426 G>A maps to NM_015982.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr3:183471989 C>A maps to NM_018023.4 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr3:183525886 C>T maps to NM_018023.4 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:183521881 C>T maps to NM_018023.4 C1230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:183474382 G>A maps to NM_018023.4 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr3:183469922 G>A maps to NM_018023.4 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr3:183515753 C>T maps to NM_018023.4 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:183439909 C>T maps to NM_018023.4 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:183503950 C>T maps to NM_018023.4 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr3:183442220 T>A maps to NM_018023.4 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr3:183515811 C>T maps to NM_018023.4 Q1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr3:183439758 T>C maps to NM_018023.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr18:751799 A>G maps to NM_005433.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr18:724567 G>T maps to NM_005433.3 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6809-01A-11D-1835-10 chr18:746048 C>T maps to NM_005433.3 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr11:66055105 G>A maps to ENST00000376904 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:66055549 A>G did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:38799469 G>A maps to NM_001039672.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr1:54331940 G>A maps to NM_018982.4 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:54337050 G>A maps to NM_018982.4 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:54337056 C>A maps to NM_018982.4 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:11038555 T>C maps to NM_024029.3 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:32530611 G>T maps to NM_032312.3 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:67751761 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:67751721 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr23:67731808 G>A did not map to a codon.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr7:44247006 G>A maps to NM_006555.3 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr14:75264759 G>A maps to NM_019589.2 E920E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:75248057 C>T maps to NM_019589.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr14:75265443 A>C maps to NM_019589.2 R1148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr14:75276204 A>G maps to NM_019589.2 P1548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr14:75248503 G>A maps to NM_019589.2 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:75264718 C>T maps to NM_019589.2 Q907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr10:27411888 C>T maps to NM_139312.1 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr10:27406519 C>T maps to NM_139312.1 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr17:57466719 G>C did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr2:30381547 C>T maps to NM_001127399.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr2:135745498 C>A maps to NM_025052.3 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:135738767 A>T maps to NM_025052.3 C1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:135743548 A>G maps to NM_025052.3 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr2:135744689 A>T maps to NM_025052.3 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:135738833 A>G maps to NM_025052.3 P1159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:135756508 C>A maps to NM_025052.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:135779400 C>T did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:135779320 A>G maps to NM_025052.3 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr2:135779368 A>G maps to NM_025052.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr2:135779320 A>G maps to NM_025052.3 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:135738767 A>G maps to NM_025052.3 C1181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr2:135756431 C>T maps to NM_025052.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr4:69184445 G>A maps to NM_001031732.2 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr4:69203141 A>C maps to NM_001031732.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:69188581 C>A maps to NM_001031732.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr4:69188540 G>A maps to NM_001031732.2 H509H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:112870065 G>T maps to NM_022828.3 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr5:112862483 T>C did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr5:112874844 G>T maps to NM_022828.3 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:112902949 C>T maps to NM_022828.3 R1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:112876708 G>T maps to NM_022828.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:112868682 C>A maps to NM_022828.3 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr5:112860680 G>A maps to NM_022828.3 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr5:112878120 C>T maps to NM_022828.3 C472C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr5:112878200 G>A did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr20:61834286 G>A maps to NM_017798.3 N335N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:61833788 C>T maps to NM_017798.3 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:61834724 G>A maps to NM_017798.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:61834283 C>T maps to NM_017798.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:29069682 C>T maps to NM_016258.2 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:64100029 G>A maps to ENST00000339066 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:64087908 G>A maps to ENST00000339066 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:64099318 G>A maps to ENST00000339066 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr7:75959466 G>T maps to NM_012479.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr7:75958908 G>A maps to NM_012479.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:75958977 C>T maps to NM_012479.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:75959484 G>A maps to NM_012479.3 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr7:75959097 G>A maps to NM_012479.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01D-01A-01W-A00E-09 chr2:9770512 G>A maps to NM_006826.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr8:101936215 C>T maps to NM_003406.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr1:155629627 T>C maps to ENST00000368339 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:21875174 C>T did not map to a codon.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr23:21875006 G>A did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:21875625 G>A did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:21875209 A>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:21874823 C>T did not map to a codon.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr23:21874909 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr17:74077645 G>A maps to NM_180990.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr18:72914150 G>A maps to NM_175907.4 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:174125844 G>T maps to NM_016653.2 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:100350395 G>T maps to ENST00000349350 E890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr7:100348383 T>C maps to ENST00000349350 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr7:100391523 G>T maps to ENST00000349350 G2623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr7:100361491 G>A maps to ENST00000349350 S1350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:100358105 C>T maps to ENST00000349350 F1263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:100348392 C>T maps to ENST00000349350 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:100344188 G>A maps to ENST00000349350 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr7:100366290 C>T maps to ENST00000349350 G1700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr2:98341694 G>A maps to NM_001079.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:98341658 G>A maps to NM_001079.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:98341592 G>A maps to NM_001079.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr2:98341592 G>A maps to NM_001079.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr2:98340853 C>T maps to NM_001079.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr2:98354128 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:167023706 G>A maps to ENST00000307529 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:167045889 C>T maps to ENST00000307529 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:167023648 C>A maps to ENST00000307529 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:167023730 A>C maps to ENST00000307529 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:167000070 A>G maps to ENST00000307529 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3819-01A-01W-0900-09 chr23:2408075 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:2406843 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr3:111312928 A>G maps to NM_024508.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:111313012 T>C maps to NM_024508.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:50278686 G>A maps to NM_014838.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr22:50279862 C>T maps to NM_014838.2 S851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr22:50278539 C>T maps to NM_014838.2 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr22:50278044 C>T maps to NM_014838.2 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:56186852 G>A maps to NM_030776.2 H268H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:56185304 G>A maps to NM_030776.2 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:56190020 G>A maps to NM_030776.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr20:56185391 C>T maps to NM_030776.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:56179642 C>A maps to NM_030776.2 G426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr20:56186912 G>T maps to NM_030776.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr14:64989824 C>T maps to NM_001123329.1 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr14:64989160 C>T maps to NM_001123329.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:64990006 A>G maps to NM_001123329.1 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr8:81411958 T>G maps to NM_001105539.1 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr8:81430746 T>C maps to NM_001105539.1 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3976-01A-01W-0995-10 chr3:101384530 G>T maps to NM_014415.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:101370010 C>A maps to NM_014415.3 *1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:101384047 T>C maps to NM_014415.3 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:101378773 C>T maps to NM_014415.3 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr6:31868965 G>A maps to NM_181842.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:113935068 G>A maps to NM_001018011.1 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr11:114118067 G>A maps to NM_001018011.1 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:114057704 C>T maps to NM_001018011.1 C466C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr11:114121252 G>A maps to NM_001018011.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr1:16269105 A>G maps to ENST00000375733 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:16272312 G>A maps to ENST00000375733 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:151694691 C>T maps to NM_020861.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:151686763 G>A maps to NM_020861.1 D479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:114070330 G>A maps to NM_001164342.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:114070444 G>A maps to NM_001164342.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr3:114057989 G>T maps to NM_001164342.1 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:114069919 G>A maps to NM_001164342.1 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:114070510 G>A maps to NM_001164342.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr3:114069889 C>T maps to NM_001164342.1 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr3:114069415 A>G maps to NM_001164342.1 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:114070036 C>T maps to NM_001164342.1 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr6:109798127 G>A maps to NM_014797.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:109787671 G>A maps to NM_014797.2 C492C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr6:109797432 G>A maps to NM_014797.2 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr6:109796638 A>G maps to NM_014797.2 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr6:109787446 G>A maps to NM_014797.2 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr6:109796638 A>G maps to NM_014797.2 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr9:125682003 C>T maps to NM_020924.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr11:62520293 G>A maps to NM_024784.3 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr19:36206025 C>T maps to NM_014383.1 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr23:119388225 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:119389241 A>G did not map to a codon.
Sequencing variant TCGA-AA-3552-01A-01W-0831-10 chr23:119388317 G>A did not map to a codon.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr23:119388044 A>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:119388208 G>A did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr23:119387316 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:119389248 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr23:119388770 A>G did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr23:119387934 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:119388199 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:119389224 T>A did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:119387869 G>T did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:119387867 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:119388325 T>C did not map to a codon.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr23:119387868 A>G did not map to a codon.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr23:119388044 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr23:119388838 G>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:119388044 A>G did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr3:141164556 A>G maps to NM_001080412.2 K1109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:141161265 C>T maps to NM_001080412.2 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:141164533 A>C maps to NM_001080412.2 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr3:141161265 C>T maps to NM_001080412.2 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr12:57398095 C>T maps to NM_014830.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr12:57397009 A>G maps to NM_014830.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr12:57398095 C>T maps to NM_014830.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr12:57396583 C>T maps to NM_014830.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr17:7369826 G>T maps to NM_020899.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:7366995 C>T maps to NM_020899.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr17:7369208 G>A maps to NM_020899.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3695-01A-01W-0900-09 chr1:22828007 T>C maps to NM_014870.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:22828001 C>T maps to NM_014870.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr1:22843790 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:22818022 G>A maps to NM_014870.3 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:197168889 T>C maps to NM_194314.2 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:197150124 G>A maps to NM_194314.2 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:197160903 C>A maps to NM_194314.2 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:130131656 G>A maps to ENST00000397753 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:59028170 A>G maps to NM_032792.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:62421621 A>G maps to NM_025224.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:62421804 G>T maps to NM_025224.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr20:62421648 C>T maps to NM_025224.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:62421515 C>A maps to NM_025224.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:62422083 T>C maps to NM_025224.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6607-01A-11D-1835-10 chr20:62421305 G>A maps to NM_025224.2 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:62421522 G>A maps to NM_025224.2 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr20:62421201 C>T maps to NM_025224.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr20:62421705 C>T maps to NM_025224.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:62407139 G>A maps to NM_025224.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:42704549 C>A maps to NM_145166.3 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr1:6647545 C>G maps to NM_005341.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr4:4304087 G>A maps to NM_145291.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr4:4303943 C>T maps to NM_145291.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:4322568 C>T maps to NM_145291.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:4304189 G>A maps to NM_145291.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:37441318 C>T maps to NM_014872.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:125673990 C>A maps to NM_006626.4 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:4054813 G>A maps to NM_015898.2 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6167-01A-11D-1650-10 chr19:4053967 C>T did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr1:154988272 C>T maps to ENST00000417934 C413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:154987864 C>T maps to ENST00000417934 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:154987402 T>A maps to ENST00000417934 C123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr18:45567043 G>A maps to NM_001039360.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:45566338 C>T maps to NM_001039360.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr18:45567052 A>G maps to NM_001039360.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr18:45556140 G>A maps to NM_001039360.2 C450C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr18:45566671 C>T maps to NM_001039360.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr18:45566673 G>A maps to NM_001039360.2 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:33059216 C>T maps to NM_001040441.1 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr6:33423692 T>C maps to NM_152735.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr1:37947424 C>T maps to NM_025079.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:37948136 C>T maps to NM_025079.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr1:37949076 C>T maps to NM_025079.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr23:64722642 A>C did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:64721734 G>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:64708943 G>A did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:64708998 G>T did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:64722709 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:64719058 A>G did not map to a codon.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr11:110036356 C>T maps to NM_033390.1 F849F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr11:110023656 G>T maps to NM_033390.1 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:110023656 G>T maps to NM_033390.1 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:110007608 T>C maps to NM_033390.1 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr6:149777944 G>A maps to NM_207360.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr6:149777983 C>T maps to NM_207360.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:46549949 G>A maps to ENST00000242848 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr13:46543188 G>A maps to ENST00000242848 R1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr13:46549949 G>A maps to ENST00000242848 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr13:46549496 G>A maps to ENST00000242848 R797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr13:46549463 G>A maps to ENST00000242848 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3956-01A-02W-0995-10 chr13:46559497 G>A maps to ENST00000242848 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr13:46563174 A>C maps to ENST00000242848 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr13:46577301 G>A maps to ENST00000242848 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr13:46541938 G>A maps to ENST00000242848 R1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr13:46542109 G>A maps to ENST00000242848 R1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:46541926 G>A maps to ENST00000242848 R1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr13:46549682 G>A maps to ENST00000242848 R735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr13:46559497 G>A maps to ENST00000242848 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr13:46585551 C>A maps to ENST00000242848 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr13:46537997 T>G maps to ENST00000242848 R1551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr13:46559693 G>A maps to ENST00000242848 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr14:89061336 T>C maps to NM_207662.3 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:89034473 C>T maps to NM_024824.4 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:88666312 C>T maps to ENST00000452588 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:88666312 C>T maps to ENST00000452588 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:88677774 C>T maps to ENST00000452588 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr16:88677719 C>G maps to ENST00000452588 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:144547901 G>A maps to NM_015117.2 C764C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr8:144620384 G>T maps to NM_015117.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:144620597 C>T maps to NM_015117.2 W313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr8:144620717 T>C maps to NM_015117.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:47597289 C>T maps to NM_015168.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:47572526 G>A maps to NM_015168.1 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:47575670 G>A maps to NM_015168.1 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr19:47575730 C>T maps to NM_015168.1 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:47569729 C>A maps to NM_015168.1 T1265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr2:113074147 A>G maps to NM_198581.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3489-01A-21D-1835-10 chr2:113074147 A>G maps to NM_198581.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:113089875 A>G maps to NM_198581.2 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr2:113067706 A>G maps to NM_198581.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr2:113082196 A>G maps to NM_198581.2 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:113074147 A>G maps to NM_198581.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:113079390 T>C maps to NM_198581.2 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr2:113089707 A>G maps to NM_198581.2 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:11873135 G>A maps to NM_014153.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr16:11861399 G>A maps to NM_014153.3 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr16:11868328 C>T maps to NM_014153.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr16:11873071 C>A maps to NM_014153.3 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:11856529 C>T maps to NM_014153.3 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr16:11861399 G>A maps to NM_014153.3 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr16:11868229 C>A maps to NM_014153.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:11861399 G>A maps to NM_014153.3 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr22:41751550 C>T maps to ENST00000351589 Q721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr22:41721852 C>T maps to ENST00000351589 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr22:41742148 C>T maps to ENST00000351589 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr22:41753327 C>T maps to ENST00000351589 D959D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6569-01A-11D-1771-10 chr22:41716693 C>T maps to ENST00000351589 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr2:112995975 G>A maps to NM_032494.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:112991807 A>C maps to NM_032494.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:138764960 T>C maps to ENST00000464606 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr7:138739998 G>A maps to ENST00000464606 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr7:138732495 A>G maps to ENST00000464606 T973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr7:138768748 C>T maps to ENST00000464606 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6808-01A-11D-1835-10 chr7:138749703 C>A maps to ENST00000464606 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr7:129664309 T>C maps to NM_016478.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:129662245 G>A maps to NM_016478.3 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr7:129662197 C>T maps to NM_016478.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr23:64137728 G>A did not map to a codon.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr23:64141740 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:64140042 C>A did not map to a codon.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr23:64141803 A>G did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr1:52943383 A>G maps to NM_001009881.2 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr1:52897012 C>T maps to NM_001009881.2 Q1461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:52891132 T>C maps to NM_001009881.2 A1586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:52962690 C>T maps to NM_001009881.2 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:52981600 C>A maps to NM_001009881.2 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:52911463 C>A maps to NM_001009881.2 E1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:52933861 C>A maps to NM_001009881.2 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:52911509 A>G maps to NM_001009881.2 N1257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr23:117959514 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:117960386 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr23:117960136 C>G did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:117960025 C>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:117959820 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr23:117959653 G>A did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:117960306 C>G did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:117960367 G>A did not map to a codon.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr23:117960040 C>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:117959502 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:117959704 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:117959490 G>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:73524354 G>A did not map to a codon.
Sequencing variant TCGA-AA-3560-01A-01W-0831-10 chr23:73524328 C>T did not map to a codon.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr23:73524138 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:87448107 C>T maps to NM_015144.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:87448148 T>A did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:87446040 C>T maps to NM_015144.2 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:111698216 C>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:111698682 G>T did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:111698857 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:111698386 T>C did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:103359036 G>A did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:103359040 A>G did not map to a codon.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr23:103359872 C>G did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr18:60242325 G>A maps to NM_017742.4 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:60242298 G>A maps to NM_017742.4 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr18:60191493 C>A maps to NM_017742.4 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr18:60242481 T>C maps to NM_017742.4 N1056N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr10:81192472 G>A maps to NM_153367.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr23:77913792 T>A did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:77913075 T>A did not map to a codon.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr23:77913569 C>T did not map to a codon.
Sequencing variant TCGA-AA-3860-01A-02W-0900-09 chr23:77913702 G>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:77912655 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:77913561 G>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:77912934 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr23:77913137 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:77912624 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:77913127 C>T did not map to a codon.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr23:77913719 C>A did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:77913139 T>A did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:77913137 A>G did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:77913766 G>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:77913778 T>C did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr23:77913663 G>T did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr9:88916208 G>A maps to NM_024617.3 Q1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:88955926 T>C maps to NM_024617.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:88940426 C>A maps to NM_024617.3 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr9:88924129 T>C maps to NM_024617.3 E1219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:88959937 C>T maps to NM_024617.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr9:88924129 T>C maps to NM_024617.3 E1219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr9:88924129 T>C maps to NM_024617.3 E1219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:37356931 A>G maps to NM_032226.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr9:37304240 C>T maps to NM_032226.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:122958550 G>A maps to NM_017612.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr12:122967854 T>C maps to NM_017612.2 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr12:122958600 G>A maps to NM_017612.2 Q523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr12:122958628 G>A maps to NM_017612.2 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr5:80600713 G>A maps to NM_032280.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:80600771 G>T maps to NM_032280.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:99998765 G>A maps to NM_017984.3 D606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr7:99998705 C>T maps to NM_017984.3 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr3:28454696 T>C maps to NM_001040432.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr3:28476696 C>T maps to NM_001040432.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:28476738 A>G maps to NM_001040432.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr3:28520394 G>T maps to NM_001040432.1 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3807-01A-01W-0995-10 chr2:207175896 T>C maps to NM_020923.1 I2215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:207172821 G>A maps to NM_020923.1 K1190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:207172771 C>T maps to NM_020923.1 R1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:207171055 G>T maps to NM_020923.1 G602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:207171873 G>A maps to NM_020923.1 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:207162061 A>G maps to NM_020923.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:207172323 G>A maps to NM_020923.1 K1024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:207171448 G>T maps to NM_020923.1 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:207175935 G>A maps to NM_020923.1 S2228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:207171240 C>T maps to NM_020923.1 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:207171573 G>A maps to NM_020923.1 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:207174175 G>T maps to NM_020923.1 G1642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:207172206 C>T maps to NM_020923.1 H985H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr2:207175654 C>T maps to NM_020923.1 L2135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr9:131483666 G>A maps to ENST00000372667 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr9:131483566 G>A maps to ENST00000372667 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr6:158093883 G>A maps to NM_024630.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:158014056 G>A maps to NM_024630.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr6:157963721 C>A maps to NM_024630.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:74644584 A>G did not map to a codon.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr23:74742740 A>G did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:74725662 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:74648996 G>T did not map to a codon.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr23:74742768 C>T did not map to a codon.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr23:74670729 G>A did not map to a codon.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr23:74742740 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:74636992 G>T did not map to a codon.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr23:74636957 C>A did not map to a codon.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr23:74742740 A>G did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:74698736 G>C did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr10:99211893 C>T maps to NM_198046.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr12:77244666 C>T maps to NM_015336.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:77220824 T>C maps to NM_015336.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr1:27179293 C>A maps to NM_032283.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr3:195936354 G>A maps to NM_001039617.1 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:17067514 C>T maps to NM_016353.4 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:17072743 A>G did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr13:21999791 A>G maps to ENST00000400590 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr13:21987847 C>A maps to ENST00000400590 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr9:14639923 G>A maps to NM_178566.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr14:77605988 C>T maps to NM_174976.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:113675209 A>G maps to NM_173570.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr3:44968225 G>A maps to NM_016598.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:45000748 G>A maps to NM_016598.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr3:44975391 G>A maps to NM_016598.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:6628283 C>T maps to NM_018106.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:6624665 G>A maps to NM_018106.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:85024143 C>T maps to NM_001145548.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr16:85011533 C>T maps to NM_001145548.1 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr22:20130976 C>T maps to NM_013373.3 D608D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr22:20129049 G>A maps to NM_013373.3 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr22:20126824 T>C maps to NM_013373.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:128962993 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:128957706 C>A did not map to a codon.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr23:128945381 C>A did not map to a codon.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr23:128957685 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:128948649 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:128957779 C>T did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:128946753 G>A did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:128940434 C>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr10:31815670 C>T maps to NM_001174096.1 R953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:31791291 C>T maps to NM_001174096.1 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:31816023 G>A maps to NM_001174096.1 E1070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:145157253 T>C maps to NM_014795.3 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:145156917 C>T maps to NM_014795.3 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:145157127 G>A maps to NM_014795.3 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr2:145157094 A>G maps to NM_014795.3 N553N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr2:145156008 G>A maps to NM_014795.3 T915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr2:145147230 G>A maps to NM_014795.3 G1144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:131503843 G>A maps to NM_006336.2 N569N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr9:131513412 C>T maps to NM_006336.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr9:131517835 G>A maps to NM_006336.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:131503115 C>T maps to NM_006336.2 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:131515801 G>A maps to NM_006336.2 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr9:131515111 G>A maps to NM_006336.2 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:82626244 G>A maps to NM_024699.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr8:82626170 G>A maps to NM_024699.2 G154G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AZ-6608-01A-11D-1835-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr2:220073734 A>T maps to NM_138802.1 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr2:220072682 C>T maps to NM_138802.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:38029399 C>T maps to NM_021943.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:74975591 T>A maps to ENST00000437241 K87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:80423543 G>A maps to NM_019006.2 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:80423582 G>A maps to NM_019006.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr8:135596240 C>T maps to NM_020863.3 K907K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr8:135669909 G>A maps to NM_020863.3 H30H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01X-01A-21W-A096-10 chr8:135669909 G>A maps to NM_020863.3 H30H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr8:135614704 A>G maps to NM_020863.3 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:135521992 C>A did not map to a codon.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr8:135649767 C>T maps to NM_020863.3 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr8:135614917 C>T maps to NM_020863.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr12:72020201 A>T maps to NM_144982.4 S1385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr12:72057078 G>T maps to NM_144982.4 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3975-01A-01W-0995-10 chr12:72025984 G>A maps to NM_144982.4 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:72057138 C>T maps to NM_144982.4 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr12:72057141 C>T maps to NM_144982.4 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:72056907 T>C maps to NM_144982.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr12:72030317 C>T maps to NM_144982.4 Q684Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr12:72014072 A>G maps to NM_144982.4 D1589D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr12:72041552 A>G maps to NM_144982.4 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr12:72013842 A>G maps to NM_144982.4 L1638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:72829329 G>A maps to NM_006885.3 A2417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:72829347 C>T maps to NM_006885.3 A2411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:72830262 C>T maps to NM_006885.3 P2106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:72832374 G>A maps to NM_006885.3 R1402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:72993489 C>T maps to NM_006885.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr16:72821254 C>T maps to NM_006885.3 T3640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:72923738 C>T maps to NM_006885.3 Q1113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr16:72984472 G>A maps to NM_006885.3 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:72827529 C>T maps to NM_006885.3 T3017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr16:72984448 A>G maps to NM_006885.3 C1045C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr16:72829497 G>A maps to NM_006885.3 D2361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr16:72984577 G>A maps to NM_006885.3 H1002H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:72822712 C>T maps to NM_006885.3 L3154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr16:72822520 C>T maps to NM_006885.3 P3218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:72821749 G>A maps to NM_006885.3 S3475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr16:72830610 C>T maps to NM_006885.3 K1990K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:72991335 C>T maps to NM_006885.3 T903T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:72992127 G>A maps to NM_006885.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr16:72832083 C>T maps to NM_006885.3 L1499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr16:72821070 T>A maps to NM_006885.3 R3702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:72828552 G>A maps to NM_006885.3 H2676H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr16:72822535 C>A maps to NM_006885.3 P3213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr8:77767190 G>A maps to NM_024721.4 P2678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:77617726 A>G maps to NM_024721.4 E468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr8:77775546 G>T maps to NM_024721.4 V3199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:77775342 C>T maps to NM_024721.4 P3131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr8:77768426 C>T maps to NM_024721.4 H3090H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr8:77765384 G>A maps to NM_024721.4 P2076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr8:77616658 C>T maps to NM_024721.4 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr8:77776233 C>T maps to NM_024721.4 F3428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:77617310 G>T maps to NM_024721.4 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:77690640 C>T maps to NM_024721.4 I1097I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:77765037 T>C maps to NM_024721.4 L1961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:77690640 C>A maps to NM_024721.4 I1097I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:77764976 C>T maps to NM_024721.4 G1940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:77775615 C>A maps to NM_024721.4 I3222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr8:77617273 C>T maps to NM_024721.4 C317C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr8:77775879 G>T maps to NM_024721.4 L3310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr8:77761758 T>C maps to NM_024721.4 C1219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:77618140 C>T maps to NM_024721.4 D606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:77767691 G>T maps to NM_024721.4 L2845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:77768339 G>A maps to NM_024721.4 Q3061Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:77761833 G>T maps to NM_024721.4 P1244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr8:77766446 A>G maps to NM_024721.4 P2430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr8:77618291 C>T maps to NM_024721.4 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr8:77763467 C>T maps to NM_024721.4 F1437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr8:77775768 T>G maps to NM_024721.4 Y3273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr8:77767440 C>T maps to NM_024721.4 L2762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:77776509 C>A maps to NM_024721.4 C3520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:77616664 C>T maps to NM_024721.4 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:77617219 T>C maps to NM_024721.4 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr8:77775702 T>C maps to NM_024721.4 A3251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6679-01A-11D-1835-10 chr8:77766446 A>G maps to NM_024721.4 P2430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr8:77763680 T>C maps to NM_024721.4 S1508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr8:77768387 G>A maps to NM_024721.4 T3077T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:77765303 T>A maps to NM_024721.4 P2049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr8:77767448 G>A maps to NM_024721.4 P2764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr8:77767043 T>C maps to NM_024721.4 N2629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr8:77775450 T>A maps to NM_024721.4 P3167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:77776197 C>T maps to NM_024721.4 D3416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr8:77617450 G>A maps to NM_024721.4 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:77775762 T>C maps to NM_024721.4 A3271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:75203655 A>T maps to NM_153688.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr16:75203859 C>A maps to NM_153688.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr16:75200702 T>C maps to NM_153688.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr15:42742521 C>A maps to NM_022473.1 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr15:42729492 C>T maps to NM_022473.1 Q1538Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr15:42743575 G>A maps to NM_022473.1 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:42740763 G>A maps to NM_022473.1 R858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:42742855 T>C maps to NM_022473.1 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr15:42738795 C>A maps to NM_022473.1 G1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:42720268 G>A maps to NM_022473.1 R1626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr15:42734424 C>T maps to NM_022473.1 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr15:42742519 C>T maps to NM_022473.1 E627E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:42734268 A>G did not map to a codon.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr15:42727683 A>G maps to NM_022473.1 H1570H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:42717100 T>A maps to NM_022473.1 V1684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr19:44831843 T>C maps to ENST00000412927 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:44833199 A>G maps to ENST00000412927 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:44833061 C>T maps to ENST00000412927 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:44840774 C>T did not map to a codon.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:44831843 T>A maps to ENST00000412927 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr19:36831200 C>T maps to NM_020917.2 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:36831764 G>A maps to NM_020917.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:36831623 G>A maps to NM_020917.2 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr18:5291168 T>C maps to NM_003409.3 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:5291873 C>T maps to NM_003409.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr18:5291248 G>A maps to NM_003409.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr18:5291117 G>A maps to NM_003409.3 C363C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:5290967 A>G maps to NM_003409.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr18:5291558 G>A maps to NM_003409.3 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:178359049 G>T maps to NM_030613.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:178359168 T>C maps to NM_030613.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr5:178358337 T>C maps to NM_030613.2 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:178358868 C>A maps to NM_030613.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr19:57065074 C>T maps to NM_020828.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:57060378 C>T maps to NM_020828.1 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:57065209 T>C maps to NM_020828.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:57065902 T>C maps to NM_020828.1 H583H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:57066158 G>T maps to NM_020828.1 G669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:57065935 C>A maps to NM_020828.1 C594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:57066509 G>T maps to NM_020828.1 E786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:57059203 C>A maps to NM_020828.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:4995092 C>T maps to NM_153018.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:38125944 A>G maps to NM_014898.2 C499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr19:38125901 G>A maps to NM_014898.2 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr14:69256810 C>T maps to NM_004926.2 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr2:43452621 G>C maps to NM_006887.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr2:43452500 G>A maps to NM_006887.4 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr9:115806462 A>G maps to NM_003408.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01S-01A-21W-A096-10 chr9:115805265 C>T maps to NM_003408.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr8:144332450 G>C maps to NM_173832.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6649-01A-11D-1771-10 chr4:188924680 T>C maps to NM_174900.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr4:188924572 C>A maps to NM_174900.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:188924164 C>T maps to NM_174900.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:29644681 G>T maps to NM_001109809.2 C33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:29644655 A>G did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:29640582 C>T maps to NM_001109809.2 W435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr6:29640603 G>T maps to NM_001109809.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:50701311 G>A maps to NM_199427.2 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr20:50776803 C>T maps to NM_018197.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr20:50701515 G>A maps to NM_199427.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr20:50705171 C>T maps to NM_199427.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr20:50769311 C>T maps to NM_018197.2 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:50701668 C>T maps to NM_199427.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:50782552 C>A maps to NM_018197.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:50769311 C>T maps to NM_018197.2 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:50701242 G>A maps to NM_199427.2 C597C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr20:50768792 C>T maps to NM_018197.2 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr20:50769704 A>G maps to NM_018197.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr20:50769440 G>A maps to NM_018197.2 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:36883828 A>T maps to NM_133466.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr19:36883819 G>A maps to NM_133466.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr16:68598238 A>C maps to NM_133458.2 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr11:58377436 C>T maps to NM_053023.4 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr11:58377432 C>T maps to NM_053023.4 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr11:58384962 G>A maps to NM_053023.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr11:64852250 C>T maps to NM_006782.3 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:88599613 G>A maps to NM_153813.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr16:88594443 C>T maps to NM_153813.2 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:88598566 C>T maps to NM_153813.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:106814337 C>T maps to NM_012082.3 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:106811027 C>T maps to NM_012082.3 Y272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr8:106814109 C>T maps to NM_012082.3 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:106813644 T>G maps to NM_012082.3 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:106814997 G>A maps to NM_012082.3 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr8:106814982 C>T maps to NM_012082.3 D891D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr8:106331190 A>T maps to NM_012082.3 K8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:106813419 C>T maps to NM_012082.3 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr8:106331178 C>A maps to NM_012082.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr8:106815474 T>C maps to NM_012082.3 A1055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr5:32403301 C>T maps to NM_016107.3 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr5:32407064 C>T maps to NM_016107.3 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:32403337 C>T maps to NM_016107.3 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr5:32390542 T>C maps to NM_016107.3 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:32364303 A>G maps to NM_016107.3 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:32404046 C>T maps to NM_016107.3 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr5:32407031 T>A maps to NM_016107.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr5:32420111 A>G maps to NM_016107.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr5:32364128 A>G maps to NM_016107.3 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:3813929 G>A maps to NM_015174.1 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:3831778 C>T maps to NM_015174.1 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:3831745 C>T maps to NM_015174.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:3825360 G>A maps to NM_015174.1 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr19:3831805 C>T maps to NM_015174.1 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr23:24190893 C>A did not map to a codon.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr23:24226334 A>G did not map to a codon.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr23:24226376 T>A did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:24227042 C>T did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:24228884 C>T did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:24225530 C>T did not map to a codon.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr23:24228601 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:24225909 T>C did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:24225447 G>A did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:24228884 C>T did not map to a codon.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr23:24226376 T>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:24229387 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:24227164 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr23:24226334 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:24229003 G>A did not map to a codon.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr23:24226376 T>C did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:24228949 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr24:2829684 C>T did not map to a codon.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr24:2843565 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:2843628 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:2843688 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr24:2847972 G>A did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr14:73464717 G>C maps to NM_021260.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr14:73444742 G>A maps to NM_021260.2 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr14:73440842 G>A maps to NM_021260.2 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:73444936 G>A maps to NM_021260.2 C475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr5:79770570 G>A maps to NM_014733.3 A1461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr5:79739027 C>T maps to NM_014733.3 Q836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr5:79741095 G>T maps to NM_014733.3 E866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:79733119 G>T maps to NM_014733.3 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:79732783 G>T maps to NM_014733.3 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr15:41105092 C>T maps to NM_001077268.1 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr15:41099918 A>C maps to NM_001077268.1 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28K-01A-21D-A16V-10 chr15:41105041 A>G maps to NM_001077268.1 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr15:41102860 G>A maps to NM_001077268.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:15115414 G>T maps to NM_022340.2 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:15115690 T>C maps to NM_022340.2 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr14:68244361 A>G maps to NM_015346.3 L1630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:68233121 G>T maps to NM_015346.3 R1945R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr14:68248233 C>T maps to NM_015346.3 W1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr14:68233121 G>T maps to NM_015346.3 R1945R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr14:68268817 C>T maps to NM_015346.3 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:68252692 A>G maps to NM_015346.3 T1062T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr14:68215239 G>A maps to NM_015346.3 S2511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr14:68244359 C>T maps to NM_015346.3 L1630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr14:68228247 C>T maps to NM_015346.3 T2141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:99504522 G>T maps to NM_001002261.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr10:99502892 C>T maps to NM_001002261.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:2343240 G>A maps to NM_020972.2 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr4:2306575 G>A maps to NM_020972.2 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr4:2306614 C>T maps to NM_020972.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr4:2306716 G>A maps to NM_020972.2 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:52811773 C>T maps to NM_004799.2 Q1387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:52704075 T>C maps to NM_004799.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:52761567 T>G maps to NM_004799.2 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:52704732 T>C maps to NM_004799.2 H548H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr1:52704336 C>T maps to NM_004799.2 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr1:52704915 T>C maps to NM_004799.2 N609N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:52703331 C>T maps to NM_004799.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr1:52703331 C>T maps to NM_004799.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:10418871 G>A maps to NM_001103167.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr20:62364982 C>T maps to NM_032527.4 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr20:62366598 C>A maps to NM_032527.4 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr20:62340012 C>T maps to NM_032527.4 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:124267528 C>A maps to NM_007222.3 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr8:124267208 T>C maps to NM_007222.3 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr8:124265702 A>G maps to NM_007222.3 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr8:124267385 T>A maps to NM_007222.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr8:124266545 C>T maps to NM_007222.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr8:123966173 A>G maps to NM_014943.3 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr8:123965810 C>T maps to NM_014943.3 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr8:123965499 C>T maps to NM_014943.3 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr8:123965192 C>T maps to NM_014943.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr8:123964577 G>A maps to NM_014943.3 T276T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AA-3870-01A-01W-0995-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr20:39832956 A>G maps to NM_015035.3 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr3:147128225 C>T maps to NM_003412.3 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3531-01A-01W-0831-10 chr3:147128621 G>A maps to NM_003412.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3534-01A-01W-0831-10 chr3:147131208 G>A maps to NM_003412.3 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:147128189 G>A maps to NM_003412.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr3:147128528 C>T maps to NM_003412.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr3:147131190 T>C maps to NM_003412.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Q-01A-01W-A005-10 chr13:100635130 G>A maps to NM_007129.2 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:136651154 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:136652142 G>T did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:136649489 G>A did not map to a codon.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr23:136649340 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:136648917 G>A did not map to a codon.
Sequencing variant TCGA-AD-6965-01A-11D-1924-10 chr23:136651153 A>G did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:136651150 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:136649644 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:136649489 G>A did not map to a codon.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr23:136649846 C>A did not map to a codon.
Sequencing variant TCGA-CM-5868-01A-01D-1650-10 chr23:136652076 T>C did not map to a codon.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr23:136649759 C>T did not map to a codon.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr23:136649487 G>A did not map to a codon.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr23:136649469 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:136648908 G>C did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:136649551 C>T did not map to a codon.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr3:147120550 G>A maps to NM_001168379.1 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr3:147108845 C>T maps to NM_001168379.1 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:147109007 G>A maps to NM_001168379.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr3:147108935 C>T maps to NM_001168379.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:100617630 C>A maps to NM_033132.3 *664Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:58102357 C>T maps to NM_001010879.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr19:57286448 C>T maps to NM_001146326.1 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr19:57286124 T>C maps to NM_001146326.1 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:57293401 C>A maps to NM_001146326.1 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:57286127 G>A maps to NM_001146326.1 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:57286067 G>A maps to NM_001146326.1 C524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr19:57286709 A>G maps to NM_001146326.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr19:57286124 T>C maps to NM_001146326.1 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:57647131 A>G maps to NM_052882.1 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:57649840 C>T maps to NM_052882.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:57648307 G>T maps to NM_052882.1 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:99631504 A>G maps to NM_003439.1 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr7:99631625 C>T maps to NM_003439.1 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:25258303 G>A maps to NM_001012981.4 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr16:25255382 G>A maps to NM_001012981.4 H568H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:25251703 G>A maps to NM_001012981.4 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr16:25258103 A>G maps to NM_001012981.4 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:25266614 C>T maps to NM_001012981.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr6:28327686 G>A maps to NM_024493.2 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr6:28327545 C>T maps to NM_024493.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr7:99128860 C>A maps to NM_014569.3 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:99128950 T>C maps to NM_014569.3 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:101139340 T>C did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:101138577 C>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:101139377 C>A did not map to a codon.
Sequencing variant TCGA-AA-3526-01A-02W-0831-10 chr23:101138824 T>C did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:101138886 T>G did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:101139326 G>A did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:101141679 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:101139184 G>A did not map to a codon.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr23:101159301 G>A did not map to a codon.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr23:101138612 G>T did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:101138642 C>A did not map to a codon.
Sequencing variant TCGA-DM-A28C-01A-11D-A16V-10 chr23:101138612 G>T did not map to a codon.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr23:101138611 C>T did not map to a codon.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr23:101138612 G>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr3:178745575 G>A maps to NM_022470.3 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr8:40438781 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr8:40683147 G>T maps to NM_024645.2 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr22:30127249 C>T maps to NM_019103.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr10:81037007 C>T maps to NM_020338.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr10:81066066 A>C maps to NM_020338.3 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr10:81058852 C>T maps to NM_020338.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:81058852 C>T maps to NM_020338.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:81060578 C>T maps to NM_020338.3 N633N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr10:81070898 C>T maps to NM_020338.3 A1018A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr7:44800100 C>T maps to NM_031449.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:44805020 G>A maps to NM_031449.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr7:44796658 G>A maps to NM_031449.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr7:44800160 C>T maps to NM_031449.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr7:44806213 G>C maps to NM_031449.3 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr7:44797099 C>T maps to NM_031449.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr7:44796129 C>T maps to NM_031449.3 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:35579879 C>T maps to NM_024772.3 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:35579795 C>T maps to NM_024772.3 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr13:20656173 C>T maps to NM_001190965.1 R1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr13:20641082 C>T maps to NM_001190965.1 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr13:20656973 G>T maps to NM_001190965.1 G1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr13:20641013 A>G maps to NM_001190965.1 S1052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr13:20567730 T>C maps to NM_001190965.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:20567814 A>G maps to NM_001190965.1 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr13:20641010 A>G maps to NM_001190965.1 V1051V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:70464160 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:70461114 G>A did not map to a codon.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr23:70462269 C>T did not map to a codon.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr23:70469000 G>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:70468030 C>A did not map to a codon.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr23:70464682 T>C did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:70464684 A>C did not map to a codon.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr23:70469416 C>A did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:70464686 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:70463818 G>A did not map to a codon.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr23:70468621 G>A did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:70470283 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:70471428 C>T did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:70469364 G>A did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:70465586 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:70466244 C>T did not map to a codon.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr1:35884110 A>C maps to NM_005095.2 A1459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:35824812 G>T maps to NM_005095.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:35847149 C>T maps to NM_005095.2 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:35852755 A>G maps to NM_005095.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr1:35881235 G>A maps to NM_005095.2 R1410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr1:35853092 T>C maps to NM_005095.2 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr13:20398910 T>C maps to NM_001142684.1 E572E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr13:20411899 C>A maps to NM_001142684.1 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr1:35474489 G>A maps to NM_007167.3 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:35478182 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:35484955 C>T maps to NM_007167.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:35454438 A>G maps to NM_007167.3 Y748Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr3:50380622 C>T maps to NM_015896.2 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr3:50382647 A>G maps to NM_015896.2 H36H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr10:226017 T>C maps to NM_006624.4 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:255930 C>T maps to NM_006624.4 C73C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr10:282809 G>A maps to NM_006624.4 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr10:287974 G>A maps to NM_006624.4 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:267194 T>C maps to NM_006624.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:42914309 C>A did not map to a codon.
Sequencing variant TCGA-CM-6680-01A-11D-1835-10 chr17:4646745 C>T maps to NM_001136046.1 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr10:75184857 G>A maps to NM_001024593.1 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr20:45867832 C>T maps to ENST00000471951 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr20:45905319 G>A maps to ENST00000471951 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:45874842 G>A maps to ENST00000471951 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr20:45848945 C>T maps to ENST00000471951 T1150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr20:45918994 G>T maps to ENST00000471951 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr20:45874806 C>T maps to ENST00000471951 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr20:45874938 T>G maps to ENST00000471951 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:45905196 C>T maps to ENST00000471951 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr20:45874806 C>T maps to ENST00000471951 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr12:133732963 G>T maps to NM_015394.4 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:133733161 C>T maps to NM_015394.4 R444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr12:133733502 C>T maps to NM_015394.4 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:21910600 A>C maps to NM_173531.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr19:19790214 G>A maps to NM_033204.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:64167353 C>A maps to NM_016220.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:64168766 A>G maps to NM_016220.3 E695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr19:48789802 G>T maps to NM_153608.1 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A029-01A-01W-A00E-09 chr19:48790080 G>A maps to NM_153608.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:48789753 C>T maps to NM_153608.1 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:6731962 C>A maps to ENST00000330442 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:9677545 C>T maps to NM_001008727.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:9677341 A>G maps to NM_001008727.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:9676720 C>T maps to NM_001008727.2 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:9677248 G>A maps to NM_001008727.2 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:9677488 C>T maps to NM_001008727.2 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:247320482 C>T maps to NM_003431.2 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr1:247320092 A>G maps to NM_003431.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:58946279 G>A maps to NM_003433.3 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr19:58945400 T>C maps to NM_003433.3 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:58945448 G>A maps to NM_003433.3 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:58945217 A>G maps to NM_003433.3 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr20:18297204 G>A maps to ENST00000401790 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr20:18297138 G>A maps to ENST00000401790 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:58132122 C>A maps to NM_003435.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:58579639 C>T maps to NM_007134.1 H620H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:58579648 G>A maps to NM_007134.1 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr19:58579675 T>C maps to NM_007134.1 C632C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3989-01A-01W-0995-10 chr19:58571402 G>A maps to NM_003436.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:58579352 A>T maps to NM_007134.1 K525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr19:58578961 C>A maps to NM_007134.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5863-01A-21D-1835-10 chr19:58578496 A>G maps to NM_007134.1 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:12298666 C>T maps to NM_003437.3 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:12296604 G>A maps to NM_003437.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:64292366 A>G maps to ENST00000307355 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:64291327 T>C maps to NM_001160183.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:19823206 G>A maps to NM_021030.2 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:19822870 G>A maps to NM_021030.2 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:19822282 G>A maps to NM_021030.2 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:19822450 G>A maps to NM_021030.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:19822366 G>A maps to NM_021030.2 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:19822450 G>A maps to NM_021030.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:19824903 G>A maps to NM_021030.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:19823038 G>A maps to NM_021030.2 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr19:19823198 A>G maps to NM_021030.2 H297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:19823206 G>A maps to NM_021030.2 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr12:133682198 T>C maps to NM_003440.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:366975 T>A maps to NM_003441.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr4:367320 G>C maps to NM_003441.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:219509531 G>A maps to NM_001105537.1 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr2:219507208 G>A maps to NM_001105537.1 R1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr2:219508127 C>T maps to NM_001105537.1 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr2:219509156 T>C maps to NM_001105537.1 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr11:9496100 G>A maps to NM_003442.5 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:9537830 C>T maps to NM_003442.5 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr11:9534058 C>T maps to NM_003442.5 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr11:9516258 C>T maps to NM_003442.5 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr3:124952690 G>T maps to NM_021964.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:124952498 A>G maps to NM_021964.2 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:125007036 T>C maps to NM_021964.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr19:58213199 G>A maps to NM_001085384.1 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:44500545 T>C maps to NM_003445.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:44501037 G>A maps to NM_003445.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:44501457 A>G maps to NM_003445.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:47272073 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:47272184 G>T did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr23:47272584 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:47272629 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:47230118 G>T did not map to a codon.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr23:47271998 A>G did not map to a codon.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr8:146157868 G>A maps to NM_006958.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr8:146157254 C>T maps to NM_006958.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr8:146156563 G>A maps to NM_006958.2 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:146156528 A>G maps to NM_006958.2 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr8:146156734 G>A maps to NM_006958.2 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr8:146156612 G>A maps to NM_006958.2 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:146157866 C>T maps to NM_006958.2 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:53572704 A>C maps to NM_001102603.1 L361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:53571383 A>G maps to NM_001102603.1 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:53572487 G>T maps to NM_001102603.1 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:53572976 C>T maps to NM_001102603.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr6:28053333 G>T maps to NM_003447.3 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr3:44598649 G>A maps to NM_018651.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr3:44612303 C>T maps to NM_018651.2 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr3:44612848 G>A maps to NM_018651.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:44611751 C>A maps to NM_018651.2 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:44609809 A>G maps to NM_018651.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr3:44609833 C>T maps to NM_018651.2 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr9:97063210 C>T maps to NM_194320.2 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr9:97062481 T>C maps to NM_194320.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:97063195 C>T maps to NM_194320.2 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr9:97063279 C>T maps to NM_194320.2 H480H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:52090211 G>T maps to NM_007147.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:52090219 C>T maps to NM_007147.2 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:52091191 C>T maps to NM_007147.2 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr19:52090219 C>T maps to NM_007147.2 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:9491969 T>C maps to NM_001172651.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:9492110 T>C maps to NM_001172651.1 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:44981599 C>T maps to NM_013256.3 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:44981374 T>C maps to NM_013256.3 Q441Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr19:44981548 A>G maps to NM_013256.3 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:44981653 A>C maps to NM_013256.3 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:47836715 G>T did not map to a codon.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr23:47836310 T>C did not map to a codon.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:47842709 C>A did not map to a codon.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr23:47837005 G>A did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:47835879 G>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:47836220 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:47835716 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:47836637 G>T did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:47836714 C>T did not map to a codon.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr23:47836154 T>C did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:47836640 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:47837066 A>G did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:47836716 T>C did not map to a codon.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr23:47836154 T>C did not map to a codon.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr23:47836310 T>C did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:47836714 C>A did not map to a codon.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr23:47836714 C>A did not map to a codon.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr23:47836154 T>C did not map to a codon.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr23:47836716 T>A did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:47836714 C>T did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:47836714 C>T did not map to a codon.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr6:27419999 A>G maps to NM_007149.2 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr6:27420083 G>A maps to NM_007149.2 Y418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:27419467 G>A maps to NM_007149.2 R624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr6:27420011 C>T maps to NM_007149.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6603-01A-11D-1835-10 chr6:27419705 A>C maps to NM_007149.2 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5538-01A-01D-1650-10 chr6:27420011 C>T maps to NM_007149.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:152089272 G>T did not map to a codon.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr23:152138984 A>G did not map to a codon.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr23:152113883 C>T did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:152086612 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:152087588 A>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:152089272 G>A did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:152100301 C>T did not map to a codon.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr23:152101440 C>T did not map to a codon.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr23:152113970 T>C did not map to a codon.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr23:152089282 T>C did not map to a codon.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr23:152090756 C>T did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:152089283 C>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr6:28244319 C>A maps to NM_001023560.2 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr9:104171426 T>C maps to NM_003452.2 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr9:104171366 A>G maps to NM_003452.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr9:104171603 A>G maps to NM_003452.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr9:104171609 C>T maps to NM_003452.2 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr9:104170232 T>C maps to NM_003452.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:104171366 A>G maps to NM_003452.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr16:71509779 G>A maps to NM_006961.3 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:28116256 C>T maps to NM_006298.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr6:28121314 G>A maps to NM_006298.2 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:28121621 G>T maps to NM_006298.2 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:28200587 C>T maps to ENST00000425468 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:3381544 T>C maps to NM_001130520.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:44684350 C>T maps to NM_006991.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr3:44684350 C>T maps to NM_006991.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00Z-01A-01W-A005-10 chr3:44672678 C>T maps to NM_006991.3 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:12243601 G>A maps to NM_021143.2 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:3274188 T>C maps to NM_198088.2 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr11:123601254 G>A maps to NM_003455.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr11:123597093 G>A maps to NM_003455.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr11:123600515 G>A maps to NM_003455.2 H140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr11:123601389 T>C maps to NM_003455.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr11:123597490 T>C maps to NM_003455.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr11:123596974 G>A maps to NM_003455.2 H559H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr11:123597490 T>C maps to NM_003455.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr16:3163439 A>G maps to NM_001042428.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr16:3169794 G>A maps to NM_001042428.1 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr17:30678932 T>C did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:22155438 A>G maps to NM_007153.3 H799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6548-01A-11D-1835-10 chr19:22156896 G>T maps to NM_007153.3 Y313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:22154865 T>C maps to NM_007153.3 K990K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:22157208 A>C maps to NM_007153.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr19:22154964 G>C maps to NM_007153.3 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr19:58152732 C>T maps to NM_006385.3 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:148951211 C>T maps to NM_012256.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:7021701 A>G maps to NM_013249.2 H404H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr11:7022352 C>T maps to NM_013249.2 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:7023973 G>T maps to NM_013249.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr11:7022735 C>A maps to NM_013249.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr11:6977668 G>A maps to NM_013250.2 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr11:6977521 T>C maps to NM_013250.2 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr11:6977032 G>A maps to NM_013250.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr11:6953809 G>T maps to NM_013250.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:52198078 A>G maps to NM_006526.2 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:52198654 C>T maps to NM_006526.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr20:52193040 G>A maps to NM_006526.2 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr20:52198621 G>A maps to NM_006526.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr20:52198378 G>A maps to NM_006526.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr20:52188348 T>G maps to NM_006526.2 A1027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:52192434 C>T maps to NM_006526.2 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr20:52193349 C>T maps to NM_006526.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr20:52199014 A>G maps to NM_006526.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr20:52198882 G>A maps to NM_006526.2 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr20:52193349 C>T maps to NM_006526.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr20:52199014 A>G maps to NM_006526.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr20:52194909 T>A maps to NM_006526.2 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:45499271 C>T maps to NM_006963.4 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:44470959 C>T maps to NM_013359.2 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-4105-01A-02D-1771-10 chr19:44536130 C>T maps to NM_001129996.1 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr19:44536078 A>G maps to NM_001129996.1 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:44536261 T>C maps to NM_001129996.1 H185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-3779-01A-01D-1719-10 chr19:44536132 G>A maps to NM_001129996.1 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:44536078 A>G maps to NM_001129996.1 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:44536775 G>T maps to NM_001129996.1 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:44536078 A>G maps to NM_001129996.1 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr19:44536078 A>G maps to NM_001129996.1 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:44571012 T>C maps to NM_013361.4 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:44570289 C>A maps to NM_013361.4 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:44610705 C>T maps to NM_013398.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:44612265 A>G maps to NM_013398.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:44612226 C>T maps to NM_013398.2 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5860-01A-01D-1650-10 chr19:44611666 G>T maps to NM_013398.2 G452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr19:44611668 A>G maps to NM_013398.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:44635940 C>T maps to NM_013362.2 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:44679969 C>T maps to NM_001032372.1 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:44680371 C>T maps to NM_001032372.1 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:44739599 T>C maps to NM_182490.1 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:44739644 C>T maps to NM_182490.1 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:44739435 C>T maps to NM_182490.1 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:44739728 C>T maps to NM_182490.1 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:44933155 G>A maps to NM_014518.2 Y600Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr19:44934174 C>A maps to NM_014518.2 G261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr16:71482763 A>G maps to NM_145911.1 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:44515613 T>C maps to NM_006300.3 *475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:44513273 G>T maps to NM_006300.3 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr19:44515438 G>A maps to NM_006300.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr17:5009163 G>A maps to NM_014519.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:5012885 G>A maps to NM_014519.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3818-01A-01W-0900-09 chr19:44778579 G>A maps to NM_181756.1 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3855-01A-01W-0995-10 chr19:44777070 G>A maps to NM_181756.1 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:44777751 C>A maps to NM_181756.1 C313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr19:44660680 C>G maps to NM_006630.2 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr19:44661284 C>T maps to NM_006630.2 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:44791952 A>G maps to NM_004234.4 C545C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:44792270 G>T maps to NM_004234.4 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr19:44792825 A>G maps to NM_004234.4 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:44791913 A>G maps to NM_004234.4 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr18:74620329 C>T maps to NM_007345.3 D782D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr18:74620473 G>A maps to NM_007345.3 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr18:74580768 C>T maps to NM_007345.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr18:74649214 C>T maps to NM_007345.3 D1564D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr18:74563807 G>A maps to NM_007345.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr18:74620425 G>A maps to NM_007345.3 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr18:74587520 C>T maps to NM_007345.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:74606990 C>T maps to NM_007345.3 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28H-01A-11D-A16V-10 chr18:74563798 C>T maps to NM_007345.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:244218335 G>A maps to NM_205768.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr1:244217658 C>T maps to NM_205768.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:44053362 G>A maps to NM_001099284.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr10:44052591 G>T maps to NM_001099284.1 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:44052384 C>T maps to NM_001099284.1 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr18:32917196 T>A maps to NM_006965.2 *369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr10:38241528 T>C maps to NM_145011.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr10:38241636 A>G maps to NM_145011.2 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr10:38241807 C>T maps to NM_145011.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr8:146107211 C>T maps to NM_021061.3 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr8:145947486 T>A maps to NM_138367.1 K520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr8:145947898 A>T maps to NM_138367.1 C382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr8:145947415 G>A maps to NM_138367.1 H543H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:20002988 C>A maps to NM_021047.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:20002577 T>C maps to NM_021047.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:20003001 G>T maps to NM_021047.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:19989319 G>T maps to NM_021047.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:24310223 C>A maps to NM_203282.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr19:24309497 T>C maps to NM_203282.2 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:24289437 A>G maps to NM_203282.2 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6854-01A-11D-1924-10 chr19:24309356 A>G maps to NM_203282.2 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:58452369 A>C maps to NM_005773.2 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr19:58453319 G>A maps to NM_005773.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:58453448 C>A maps to NM_005773.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr19:22271024 C>A maps to NM_033468.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr19:22271838 A>G maps to NM_033468.2 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:37005546 T>C maps to NM_001166038.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr16:3336042 C>T maps to NM_005741.4 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr16:3336042 C>T maps to NM_005741.4 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:57723919 C>T maps to NM_003417.4 C485C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr19:9525381 G>A maps to NM_006631.2 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6137-01A-11D-1771-10 chr19:9524700 T>C maps to NM_006631.2 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:9523994 G>A maps to NM_006631.2 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:9524082 C>T maps to NM_006631.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:9524436 G>T maps to NM_006631.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr19:9524700 T>C maps to NM_006631.2 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:9523994 G>A maps to NM_006631.2 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:9524256 G>T maps to NM_006631.2 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr16:31926724 T>C maps to NM_003414.4 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr16:31926538 A>G maps to NM_003414.4 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3542-01A-02W-0831-10 chr16:31926952 A>G maps to NM_003414.4 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr16:31895898 G>A maps to NM_003414.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4616-01A-21D-1835-10 chr16:31927249 T>C maps to NM_003414.4 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:64388851 T>G maps to NM_021148.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:64388522 C>T maps to NM_021148.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:64377988 G>T maps to NM_021148.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:152612798 A>G did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:152612538 C>T did not map to a codon.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr23:152612701 G>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:152612436 A>C did not map to a codon.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr23:152612477 T>C did not map to a codon.
Sequencing variant TCGA-AZ-6605-01A-11D-1835-10 chr16:89790052 C>T maps to NM_001113525.1 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr16:89799949 C>T maps to NM_001113525.1 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr7:111958289 C>T maps to NM_021994.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr7:111936314 C>T maps to NM_021994.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr7:111936290 A>G maps to NM_021994.2 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr7:111936288 C>T maps to NM_021994.2 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr7:111936290 A>G maps to NM_021994.2 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:111936290 A>G maps to NM_021994.2 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5660-01A-01D-1650-10 chr19:53303873 C>T maps to NM_006969.3 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr19:53303462 A>G maps to NM_006969.3 H545H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:53304745 C>A maps to NM_006969.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:53304659 C>T maps to NM_006969.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:53303381 A>G maps to NM_006969.3 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:53303059 G>A maps to NM_006969.3 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:53303057 C>T maps to NM_006969.3 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr22:22869624 C>T maps to NM_080740.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr22:22869899 C>A maps to NM_080740.3 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr22:22869291 C>T maps to NM_080740.3 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr22:22842526 G>A maps to NM_080764.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr22:22843276 T>C maps to NM_080764.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:129361653 A>G did not map to a codon.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr23:129377604 A>G did not map to a codon.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr23:129373665 T>G did not map to a codon.
Sequencing variant TCGA-AA-3866-01A-01W-0995-10 chr23:129350044 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:129361711 G>T did not map to a codon.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr23:129377604 A>G did not map to a codon.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr23:129377604 A>G did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:129377604 A>G did not map to a codon.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr23:129349855 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr15:56996405 G>A maps to NM_017661.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr15:56999301 G>A maps to NM_017661.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr15:56970877 C>T maps to NM_017661.2 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:56970889 T>C maps to NM_017661.2 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr15:56970889 T>C maps to NM_017661.2 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:56969770 C>T did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:200376331 C>T maps to NM_012482.3 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:200377890 T>A maps to NM_012482.3 K315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr1:200376565 A>G maps to NM_012482.3 H756H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6920-01A-11D-1924-10 chr1:200376565 A>G maps to NM_012482.3 H756H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr1:200377252 T>A maps to NM_012482.3 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr1:200376310 C>T maps to NM_012482.3 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:200377285 A>G maps to NM_012482.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6654-01A-21D-1835-10 chr7:148904446 G>A maps to NM_003575.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr7:148909501 T>C maps to NM_003575.2 H335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:44352519 T>C maps to NM_181845.1 H589H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:44351562 G>A maps to NM_181845.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:44351257 G>T maps to NM_181845.1 G169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:44352078 T>C maps to NM_181845.1 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:44590833 C>T maps to NM_001037813.2 C401C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3968-01A-01W-0995-10 chr19:44892265 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:44892219 A>G maps to NM_152354.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:44891029 A>G maps to NM_152354.3 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:15611544 C>T maps to NM_020652.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01T-01A-21W-A096-10 chr17:15619397 G>A maps to NM_020652.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:15620046 C>T maps to NM_020652.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr17:18565855 G>A maps to NM_001145045.1 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:18565848 C>A maps to NM_001145045.1 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:18565806 G>A maps to NM_001145045.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01I-01A-02W-A00E-09 chr17:16470900 G>A maps to NM_020653.2 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:16456447 A>G maps to NM_020653.2 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr6:87968045 T>C maps to NM_015021.1 L1567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr6:87965347 A>G maps to NM_015021.1 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr6:87965719 G>A maps to NM_015021.1 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:87967243 A>G maps to NM_015021.1 S1299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr6:87964928 G>T maps to NM_015021.1 G528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr6:87943113 C>T maps to NM_015021.1 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:87965338 C>A maps to NM_015021.1 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:87969689 C>T maps to NM_015021.1 R2115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr6:87966379 C>T maps to NM_015021.1 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:87964994 G>T maps to NM_015021.1 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:87967222 T>C maps to NM_015021.1 N1292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr6:87967138 T>C maps to NM_015021.1 P1264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr6:87967138 T>C maps to NM_015021.1 P1264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr6:87925694 T>C maps to NM_015021.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr6:87965017 A>G maps to NM_015021.1 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr6:87971377 C>A maps to NM_015021.1 C2677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr6:87965371 A>C maps to NM_015021.1 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr6:87968045 T>C maps to NM_015021.1 L1567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr6:87967138 T>C maps to NM_015021.1 P1264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr6:87967138 T>C maps to NM_015021.1 P1264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr21:43413718 A>C maps to NM_020727.4 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr21:43411447 C>T maps to NM_020727.4 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr21:43413324 C>A maps to NM_020727.4 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr21:43411924 G>A maps to NM_020727.4 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr21:43411447 C>A maps to NM_020727.4 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr21:43411447 C>A maps to NM_020727.4 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr21:43411966 G>A maps to NM_020727.4 N746N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr21:43411447 C>A maps to NM_020727.4 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr7:99662518 A>G maps to NM_017715.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr7:99669593 G>A maps to NM_032924.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr7:99669689 C>T maps to NM_032924.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3955-01A-02W-0995-10 chr19:35435738 C>T maps to NM_001099438.1 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:35434190 T>G maps to NM_001099438.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:35434733 C>T maps to NM_001099438.1 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:35434154 C>T maps to NM_001099438.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3688-01A-01W-0900-09 chr5:150275248 C>A maps to NM_001172831.1 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr5:150277672 G>A maps to NM_001172831.1 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:35174066 C>T maps to ENST00000221282 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr19:57869021 C>T maps to ENST00000391705 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr19:57868625 T>G maps to ENST00000391705 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5255-01A-11D-1835-10 chr19:57868850 A>G maps to ENST00000391705 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:57868734 G>T maps to ENST00000391705 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr19:57867599 G>A maps to ENST00000391705 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr6:28963142 G>A maps to NM_001010877.2 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:28962971 G>A maps to NM_001010877.2 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:28963002 G>A maps to NM_001010877.2 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D8-01A-11D-A152-10 chr6:28967771 G>A maps to NM_001010877.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:9271706 C>A maps to NM_020933.4 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:9271877 G>A maps to NM_020933.4 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:9271884 C>T maps to NM_020933.4 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:9271874 G>A maps to NM_020933.4 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr6:43307265 G>A maps to NM_014345.2 F1490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr6:43322665 C>T maps to NM_014345.2 W802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr6:43307302 G>T maps to NM_014345.2 S1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr6:43308152 G>A maps to NM_014345.2 R1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr6:43325340 A>G maps to NM_014345.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:43323669 C>A maps to NM_014345.2 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr6:43316178 G>A maps to NM_014345.2 F985F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr6:43305519 C>T maps to NM_014345.2 P2072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:44139886 G>A maps to NM_006973.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:53393493 C>T maps to NM_207333.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02O-01A-21W-A096-10 chr19:53384811 G>T maps to NM_207333.2 Y189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6678-01A-11D-1835-10 chr19:53432563 A>G maps to NM_203307.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:28295165 C>A maps to NM_030899.4 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr6:28297345 G>A maps to NM_030899.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:58983133 C>T maps to NM_014347.2 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3986-01A-02W-0995-10 chr19:58983148 C>T maps to NM_014347.2 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:58967480 G>A maps to NM_207395.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3837-01A-01W-0900-09 chr1:90475678 C>T maps to NM_182976.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:90482906 C>T maps to NM_182976.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:90487883 C>T maps to NM_182976.2 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr1:90473297 C>T maps to NM_182976.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:58639919 A>G maps to NM_024620.3 C317C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:58640348 C>T maps to NM_024620.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:58639601 G>A maps to NM_024620.3 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr19:58639288 G>A maps to NM_024620.3 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr19:58640423 G>T maps to NM_024620.3 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:142143641 A>C maps to NM_014487.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr19:54080794 C>T maps to NM_001079907.1 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:54080875 G>A maps to NM_001079907.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:54081001 G>A maps to NM_001079907.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:14817544 T>A maps to NM_032433.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:14829330 G>T maps to NM_032433.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:14805847 C>T maps to NM_032433.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:14815942 G>A maps to NM_032433.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:45131461 C>T maps to NM_018102.3 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr20:45130462 A>G maps to NM_018102.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr20:45130556 G>T maps to NM_018102.3 S474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr20:45130660 T>C maps to NM_018102.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr20:45131124 T>G maps to NM_018102.3 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr20:44598327 C>T maps to NM_022095.3 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3973-01A-01W-0995-10 chr20:44588070 C>T maps to NM_022095.3 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3980-01A-02W-0995-10 chr20:44588937 G>A maps to NM_022095.3 H643H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr20:44586495 G>A maps to NM_022095.3 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01F-01A-01W-A005-10 chr20:44590782 C>T maps to NM_022095.3 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr20:44588009 G>A maps to NM_022095.3 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr20:44596969 G>A maps to NM_022095.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr20:44580824 G>A maps to NM_022095.3 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr20:44580806 G>A maps to NM_022095.3 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr20:25656944 G>A maps to NM_015655.2 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr20:25657017 G>A maps to NM_015655.2 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:25666238 C>A maps to NM_015655.2 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr10:38343822 T>C maps to NM_006954.1 C257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr10:38345397 T>A maps to NM_006954.1 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:38306265 G>T maps to NM_006954.1 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:38344641 T>C maps to NM_006954.1 C530C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr10:43088585 T>C maps to NM_006955.1 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr10:43089674 A>G maps to NM_006955.1 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr10:43127400 C>A maps to NM_006955.1 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:43088555 A>G maps to NM_006955.1 C614C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr10:43127437 C>T maps to NM_006955.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4682-01B-01D-1408-10 chr8:146003459 G>A maps to NM_030580.3 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:146003459 G>A maps to NM_030580.3 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:32349787 C>A maps to ENST00000375200 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5796-01A-01D-1650-10 chr20:32345069 C>T maps to ENST00000375200 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr20:32358032 C>T maps to ENST00000375200 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:2463856 G>A maps to NM_024325.4 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr20:2464937 A>G maps to NM_024325.4 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:2465150 T>C maps to NM_024325.4 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr20:2465120 G>A maps to NM_024325.4 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr19:37368229 C>A maps to NM_003419.3 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:37368661 T>C maps to NM_003419.3 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:37368949 C>A maps to NM_003419.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:37368334 T>G maps to NM_003419.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:176489068 C>A maps to ENST00000503039 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:53644547 C>T maps to NM_001172674.1 K512K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6924-01A-11D-1924-10 chr19:53643749 A>C maps to NM_001172674.1 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:44692630 A>G maps to NM_003420.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr3:44700502 G>A maps to NM_003420.3 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:52468331 G>A maps to ENST00000391795 N532N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:52468594 C>A maps to ENST00000391795 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:178139257 G>A maps to NM_005649.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr5:178139210 T>C maps to NM_005649.2 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:178310671 G>T maps to NM_058230.2 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:178506333 C>T maps to NM_014594.1 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr5:178506422 C>T maps to NM_014594.1 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr5:178506762 G>T maps to NM_014594.1 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr5:178505838 G>T maps to NM_014594.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr5:178506884 C>T maps to NM_014594.1 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:7584232 T>C maps to NM_018083.4 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:7585372 C>T maps to NM_018083.4 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:64136626 C>T maps to NM_199451.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr10:64136077 C>A maps to NM_199451.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02K-01A-21W-A096-10 chr10:64425963 T>C did not map to a codon.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr10:64415161 T>C maps to NM_199452.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr10:64148187 G>A maps to NM_199451.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:64416175 C>T maps to NM_199451.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3696-01A-01W-0900-09 chr5:71757113 G>A maps to NM_152625.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr5:71756420 C>T maps to NM_152625.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:71752358 G>A maps to NM_152625.1 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr5:71756813 C>G maps to NM_152625.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr5:71756477 C>T maps to NM_152625.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr5:71756672 G>A maps to NM_152625.1 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr10:38406403 G>T maps to NM_003421.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr10:38406697 G>T maps to NM_003421.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr10:38406697 G>T maps to NM_003421.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr10:38406504 G>A maps to NM_003421.2 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr19:37118175 G>A maps to NM_032825.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:37101594 A>G maps to NM_032825.3 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00L-01A-01W-A005-10 chr19:37100893 T>C maps to NM_032825.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5341-01A-01D-1408-10 chr19:37118019 G>A maps to NM_032825.3 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:37733803 C>T maps to NM_152604.1 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:37734187 C>T maps to NM_152604.1 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr12:6782539 G>A maps to NM_001135734.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:6781652 G>A maps to NM_001135734.1 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr12:6778352 G>T maps to NM_001135734.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr12:6787459 G>A maps to NM_001135734.1 T173T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D5-6529-01A-11D-1771-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr12:6777068 T>C maps to ENST00000407384 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr12:6787597 T>A maps to NM_001135734.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28E-01A-11D-A16V-10 chr12:6787345 A>G maps to NM_001135734.1 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr12:54769669 G>A maps to NM_001130967.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3810-01A-01W-0995-10 chr2:180307982 C>T maps to NM_152520.4 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr2:180308129 G>A maps to NM_152520.4 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr3:21552374 G>T maps to NM_024697.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:21478483 C>T maps to NM_024697.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr3:21552485 C>T maps to NM_024697.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr3:21462732 G>A maps to NM_024697.2 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr3:21462858 G>A maps to NM_024697.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr6:27368950 C>T maps to NM_001076781.1 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr6:27369094 C>T maps to NM_001076781.1 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr7:99091169 A>C maps to NM_032164.2 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr7:99091607 G>A maps to NM_032164.2 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:99096339 C>T maps to NM_032164.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr8:28218518 G>A maps to NM_018660.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr8:28214250 C>T maps to NM_018660.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3554-01A-01W-0833-10 chr8:28206718 G>A maps to NM_018660.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr8:28214286 G>A maps to NM_018660.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr8:28206256 G>T maps to NM_018660.2 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr18:32953519 T>C maps to NM_145756.2 A154A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A6-6781-01A-22D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:32825305 C>T maps to NM_001135178.2 R213*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-A010-01A-01W-A00E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr18:32826087 A>G maps to NM_001135178.2 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr18:32826114 G>A maps to NM_001135178.2 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr18:32844145 A>G maps to NM_001166012.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr7:148876649 C>T maps to NM_170686.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr19:44384222 C>T maps to ENST00000324394 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:44377213 T>C maps to ENST00000324394 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:44377825 G>A maps to ENST00000324394 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:44384168 G>T maps to ENST00000324394 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr18:72775184 G>A maps to NM_017757.2 A1836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:72601875 G>T maps to NM_017757.2 E1711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr18:72775409 C>A maps to NM_017757.2 V1911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr18:72347441 C>A maps to NM_017757.2 V1489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr18:72775187 G>A maps to NM_017757.2 A1837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr18:72344507 C>A maps to NM_017757.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr18:72347613 C>T maps to NM_017757.2 R1547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr18:72589218 A>G maps to NM_017757.2 K1648K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:72345839 C>T maps to NM_017757.2 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr11:46723111 C>T maps to NM_024741.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:46726300 C>T maps to NM_024741.2 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr11:46726491 C>T maps to NM_024741.2 C414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr23:47308220 T>C did not map to a codon.
Sequencing variant TCGA-AA-3549-01A-02W-0831-10 chr23:47307382 C>T did not map to a codon.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr23:47307753 C>T did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:47308728 C>T did not map to a codon.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr23:47308221 A>T did not map to a codon.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr23:47308222 C>T did not map to a codon.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr23:47308789 C>T did not map to a codon.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr23:47308222 C>T did not map to a codon.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr23:47307086 A>G did not map to a codon.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr23:47307088 C>A did not map to a codon.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr23:47308221 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:47307155 G>A did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:8576573 C>T maps to NM_001146175.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:53612951 C>A maps to NM_001164309.1 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr19:53611926 G>A maps to NM_001164309.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:58087211 G>A maps to NM_017879.1 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:58419941 A>G maps to NM_152475.2 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr19:58437733 C>T maps to NM_133460.1 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:58437969 G>A maps to NM_133460.1 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr19:58438840 C>T maps to NM_133460.1 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:58438380 G>A maps to NM_133460.1 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:58438596 C>A maps to NM_133460.1 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:58005131 G>T maps to NM_001098491.1 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:58005260 C>T maps to NM_001098491.1 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr19:58004770 T>A maps to NM_001098491.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:37618888 A>G maps to NM_144689.3 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr16:49671355 G>A maps to NM_015069.2 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3852-01A-01W-0900-09 chr16:49670278 G>T maps to NM_015069.2 G928G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr16:49559352 C>T maps to NM_015069.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr16:49669690 C>T maps to NM_015069.2 E1124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr16:49671409 C>T maps to NM_015069.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr16:49671030 G>A maps to NM_015069.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr16:49670998 C>T maps to NM_015069.2 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr16:49672159 A>G maps to NM_015069.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:49670668 G>A maps to NM_015069.2 C798C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr16:49671835 A>G maps to NM_015069.2 Y409Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr16:49671862 G>A maps to NM_015069.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:148801662 G>A maps to NM_001001661.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr7:148800955 C>T maps to NM_001001661.2 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:148801954 G>A maps to NM_001001661.2 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:148801627 C>T maps to NM_001001661.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:148801588 G>A maps to NM_001001661.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:148802284 C>T maps to NM_001001661.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr7:148801345 C>T maps to NM_001001661.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr19:9639397 C>T maps to NM_024106.1 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:9639303 C>A maps to NM_024106.1 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr19:9643590 G>T maps to NM_024106.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:21720372 G>A maps to NM_001001415.2 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:21719703 G>A maps to NM_001001415.2 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr19:21720810 T>C maps to NM_001001415.2 C652C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:21990498 A>G maps to NM_003423.2 H780H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:22001992 C>A maps to NM_003423.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:21990936 G>A maps to NM_003423.2 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:21990768 G>T maps to NM_003423.2 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:21991701 A>G maps to NM_003423.2 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:21992217 A>G maps to NM_003423.2 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:21991566 T>C maps to NM_003423.2 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:21239752 G>A maps to NM_025189.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:21216934 G>A maps to NM_025189.3 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6317-01A-11D-1719-10 chr19:21239632 G>A maps to NM_025189.3 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr19:21365714 T>C maps to NM_133473.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:21366168 C>T maps to NM_133473.2 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:21366735 G>T maps to NM_133473.2 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr19:21326370 A>T maps to NM_133473.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr19:52537422 A>G maps to NM_014650.2 H503H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:52537437 G>A maps to NM_014650.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:52538025 A>T maps to NM_014650.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:52537683 A>T maps to NM_014650.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr19:12127300 A>G maps to NM_001080411.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:12126542 G>T maps to NM_001080411.1 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr16:3433124 G>A maps to ENST00000396852 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6541-01A-11D-1719-10 chr16:3440118 A>C maps to ENST00000396852 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:23688782 G>A maps to NM_001077195.1 C364C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:31137577 G>A maps to NM_182755.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6751-01A-11D-1835-10 chr10:31137716 A>G maps to NM_182755.2 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr19:11979194 G>A maps to NM_152262.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:11979243 C>T maps to NM_152262.2 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr19:11979243 C>T maps to NM_152262.2 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:12383928 G>A maps to NM_001164276.1 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:12383977 G>T maps to NM_001164276.1 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:12384424 A>G maps to NM_001164276.1 H263H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:12383989 A>G maps to NM_001164276.1 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:11942521 T>C maps to NM_152357.2 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:11942552 C>T maps to NM_152357.2 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:11943056 C>T maps to NM_152357.2 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:11943730 G>T maps to NM_152357.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr19:11942239 T>G maps to NM_152357.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:11891608 C>T maps to NM_152355.2 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:11892193 C>T maps to NM_152355.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr19:12461942 T>C maps to NM_030824.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:12474427 T>C maps to NM_030824.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr19:12461942 T>C maps to NM_030824.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:12460898 G>A maps to NM_030824.2 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:12461060 A>G maps to NM_030824.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:12461669 A>G maps to NM_030824.2 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:12461669 A>G maps to NM_030824.2 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:12461669 A>G maps to NM_030824.2 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:12461669 A>T maps to NM_030824.2 C243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:12541760 G>A maps to NM_005815.4 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:12542022 G>A maps to NM_005815.4 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr3:44489113 A>T maps to NM_181489.5 C683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:44496672 G>A maps to NM_181489.5 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:44488945 G>A maps to NM_181489.5 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A282-01A-12D-A16V-10 chr3:44489659 C>T maps to NM_181489.5 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:58991855 G>A maps to NM_017908.2 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:134483203 G>C did not map to a codon.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr23:134494390 A>G did not map to a codon.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr23:134493887 C>T did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:134494550 C>A did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:134494390 A>G did not map to a codon.
Sequencing variant TCGA-CA-6716-01A-11D-1835-10 chr23:134493888 A>G did not map to a codon.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr23:134494390 A>G did not map to a codon.
Sequencing variant TCGA-F4-6805-01A-11D-1835-10 chr23:134493888 A>G did not map to a codon.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr23:134494334 G>A did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:134494861 G>A did not map to a codon.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr19:44417682 G>A maps to NM_003425.3 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:44418342 C>T maps to NM_003425.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:44417739 T>C maps to NM_003425.3 E616E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:44417543 G>A maps to NM_003425.3 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr6:56993580 G>T maps to NM_001031623.2 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr6:57012185 G>T maps to NM_001031623.2 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr6:57012977 G>T maps to NM_001031623.2 E699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr6:57012439 G>C maps to NM_001031623.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr5:178373478 C>A maps to NM_182594.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr5:178392047 A>C maps to NM_182594.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr5:178373409 G>A maps to NM_182594.2 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr5:178391968 T>A maps to NM_182594.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr5:178391869 C>T maps to NM_182594.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr5:178373482 C>T maps to NM_182594.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:57802427 C>T maps to NM_006635.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:37129788 T>C maps to NM_153257.2 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:37130562 A>C maps to NM_153257.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr9:109694728 G>A maps to NM_021224.4 G2005G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:109690167 C>T maps to NM_021224.4 N1325N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr9:109686819 C>T maps to NM_021224.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3693-01A-01W-0900-09 chr9:109773302 A>T maps to NM_021224.4 K2505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr9:109690563 G>A maps to NM_021224.4 Q1457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr9:109687836 G>A maps to NM_021224.4 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr9:109734349 G>A maps to NM_021224.4 L2164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr9:109765624 A>G maps to NM_021224.4 E2369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:109687182 A>G maps to NM_021224.4 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr9:109687407 T>C maps to NM_021224.4 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr9:109687543 C>T maps to NM_021224.4 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6890-01A-11D-1924-10 chr9:109688116 G>T maps to NM_021224.4 E642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr9:109686963 C>T maps to NM_021224.4 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5403-01A-01D-1650-10 chr9:109687287 T>C maps to NM_021224.4 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:109686567 A>G maps to NM_021224.4 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr9:109687140 C>A maps to NM_021224.4 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr7:149462735 C>T maps to NM_207336.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:149462735 C>T maps to NM_207336.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr7:149462939 C>T maps to NM_207336.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:53344822 G>A maps to NM_001008801.1 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:53344877 G>T maps to NM_001008801.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr19:53345296 C>A maps to NM_001008801.1 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:53344376 T>C maps to NM_001008801.1 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:57088933 G>A maps to NM_001001668.3 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:57036803 G>A maps to NM_020813.2 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:57036734 T>C maps to NM_020813.2 C433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:57036969 G>T maps to NM_020813.2 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:57036231 G>T maps to NM_020813.2 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:57036914 A>C maps to NM_020813.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr19:57036305 T>G maps to NM_020813.2 Y290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:50549892 A>G maps to NM_015428.1 V731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:50549241 A>G maps to NM_015428.1 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:50549091 C>T maps to NM_015428.1 C464C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr19:50549779 C>A maps to NM_015428.1 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr5:121487750 A>G maps to NM_207317.1 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:57187987 C>T maps to NM_033273.1 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr7:57187708 G>A maps to NM_033273.1 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:57188026 G>A maps to NM_033273.1 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr16:30408768 T>G maps to ENST00000495929 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:30409410 C>T maps to ENST00000495929 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4070-01A-01W-1073-09 chr16:30409515 A>C maps to ENST00000495929 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3685-01A-02W-0900-09 chr19:52825982 C>T maps to NM_144684.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr19:52825585 T>C maps to NM_144684.2 H361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr19:52825580 C>T maps to NM_144684.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:52825120 T>C maps to NM_144684.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:52825090 A>T maps to NM_144684.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr9:114289968 G>A maps to NM_133464.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr9:114304129 C>T maps to NM_133464.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr9:114304653 C>A maps to NM_133464.2 S480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:95609787 A>G maps to NM_031486.1 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr9:95618555 A>G maps to NM_031486.1 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr10:44111739 C>T maps to NM_145312.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr10:44112442 A>C maps to NM_145312.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr10:48371036 C>T maps to NM_153034.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr10:48370726 G>A maps to NM_153034.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:11916813 G>T maps to NM_152356.3 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3543-01A-01W-0833-10 chr19:11917211 C>T maps to NM_152356.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr19:11917052 G>A maps to NM_152356.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:11917409 G>A maps to NM_152356.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:11917898 C>T maps to NM_152356.3 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:11917052 G>A maps to NM_152356.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:11917898 C>T maps to NM_152356.3 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:11917172 T>C maps to NM_152356.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr19:22846611 T>C maps to NM_020855.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr19:21607392 C>T maps to NM_001076678.2 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:21606246 G>A maps to NM_001076678.2 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3667-01A-01W-0900-09 chr19:21606562 A>T maps to NM_001076678.2 K368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr1:247464357 C>T maps to NM_032752.1 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3870-01A-01W-0995-10 chr1:247492715 G>T maps to NM_032752.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:247464282 C>T maps to NM_032752.1 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr1:247464519 G>A maps to NM_032752.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5656-01A-21D-1835-10 chr19:58868368 C>T maps to NM_198458.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:58867516 G>A maps to NM_198458.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3558-01A-01W-0831-10 chr16:4812664 G>A maps to NM_021646.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr16:4812574 T>C maps to NM_021646.1 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr16:4802757 C>T maps to NM_021646.1 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr3:44761795 G>T maps to NM_033210.4 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:44763637 C>T maps to NM_033210.4 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr10:77159664 G>A maps to NM_032772.4 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr10:77158920 G>A maps to NM_032772.4 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00R-01A-01W-A005-10 chr19:19917814 G>A maps to NM_001099269.2 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:19905834 A>G maps to NM_001099269.2 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:32844765 A>C maps to NM_014910.4 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:32844585 G>T maps to NM_014910.4 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:32873646 G>A maps to NM_014910.4 K840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:32844470 C>T maps to NM_014910.4 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:32844623 T>A maps to NM_014910.4 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr9:99521928 G>A maps to NM_014930.1 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr2:27844027 C>T maps to NM_032434.2 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:27839181 T>G maps to NM_032434.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr20:62594020 C>T maps to NM_020713.1 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:62595266 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr20:62598814 C>T maps to NM_020713.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr20:62593954 C>A maps to NM_020713.1 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr20:62595543 G>T maps to NM_020713.1 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5657-01A-01D-1650-10 chr2:27600888 A>G maps to NM_144631.4 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr2:27601910 C>T maps to NM_144631.4 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr2:27601233 A>C maps to NM_144631.4 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr2:95815326 T>C maps to NM_032788.1 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr2:95815896 C>T maps to NM_032788.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr18:74153390 C>T maps to ENST00000443185 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr18:74154044 G>T maps to ENST00000443185 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr18:74092164 C>T maps to ENST00000443185 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6310-01A-11D-1719-10 chr8:146032711 G>A maps to NM_213605.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr8:146033599 C>T maps to NM_213605.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr10:97917911 C>T maps to NM_014803.3 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr10:97919075 A>G maps to NM_014803.3 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr10:97919913 C>T maps to NM_014803.3 R1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:97917666 G>T maps to NM_014803.3 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr10:97916586 C>T maps to NM_014803.3 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr4:10445425 G>A maps to NM_053042.2 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr4:10445768 C>T maps to NM_053042.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr4:10445657 A>G maps to NM_053042.2 H765H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr4:10447232 T>A maps to NM_053042.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:10447325 C>T maps to NM_053042.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr4:10446980 C>T maps to NM_053042.2 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr18:14105368 G>A maps to NM_145287.3 Y390Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr18:14105587 C>T maps to NM_145287.3 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr18:14105754 C>A maps to NM_145287.3 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DA-01A-11D-A152-10 chr18:14105209 C>T maps to NM_145287.3 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr18:22805217 G>A maps to NM_015461.2 C888C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr18:22804563 G>T maps to NM_015461.2 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3561-01A-01W-0831-10 chr18:22806392 G>A maps to NM_015461.2 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr18:22806162 G>A maps to NM_015461.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr18:22806876 C>T maps to NM_015461.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr18:22804911 G>A maps to NM_015461.2 C990C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6196-01A-11D-1719-10 chr18:22804449 G>A maps to NM_015461.2 N1144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr18:22806156 A>T maps to NM_015461.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr18:22806605 T>A maps to NM_015461.2 K426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr18:22806399 T>C maps to NM_015461.2 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr18:22804982 G>T maps to NM_015461.2 R967R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6459-01A-11D-1771-10 chr18:22775207 T>A maps to NM_015461.2 K1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr18:22804380 G>A maps to NM_015461.2 D1167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:56113510 G>A maps to NM_153219.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr19:42729055 G>A maps to NM_133444.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A017-01A-01W-A00E-09 chr19:42730141 A>G maps to NM_133444.1 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:37880732 C>A maps to NM_032453.1 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr19:52918503 G>A maps to NM_032423.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:52909828 T>C maps to NM_032423.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr19:52918614 T>C maps to NM_032423.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:52919691 C>A maps to NM_032423.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:52918518 C>T maps to NM_032423.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:52909855 C>T maps to NM_032423.2 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:52909864 C>T maps to NM_032423.2 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:37037947 T>C maps to NM_001145649.1 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:37037800 C>T maps to NM_001145649.1 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:37037815 A>G maps to NM_001145649.1 H548H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr19:58117658 C>T maps to NM_020880.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3842-01A-01W-0995-10 chr19:58117894 C>T maps to NM_020880.3 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:58118428 T>G maps to NM_020880.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:58117598 G>T maps to NM_020880.3 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr19:58118455 C>T maps to NM_020880.3 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:58117828 A>G maps to NM_020880.3 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:58117436 G>T maps to NM_020880.3 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:58118242 C>G maps to NM_020880.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr19:58118230 A>G maps to NM_020880.3 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr18:56651322 C>T maps to NM_018181.4 A1177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr18:56601735 G>A maps to NM_018181.4 Q806Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:56606845 G>T maps to NM_018181.4 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr18:56648795 G>T maps to NM_018181.4 E1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr18:56586289 G>A maps to NM_018181.4 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3678-01A-01W-0900-09 chr18:56587705 G>A maps to NM_018181.4 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3684-01A-02W-0900-09 chr18:56651514 G>A maps to NM_018181.4 G1241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr18:56585740 C>T maps to NM_018181.4 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr18:56586955 G>A maps to NM_018181.4 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr18:56601783 G>A maps to NM_018181.4 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr18:56586799 G>A maps to NM_018181.4 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr18:56651568 C>T maps to NM_018181.4 G1259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr18:56586448 C>A maps to NM_018181.4 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr18:56587228 C>A maps to NM_018181.4 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:52941546 C>A maps to NM_001143939.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:52941372 C>T maps to NM_001143939.1 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr19:30936460 G>T maps to NM_014717.1 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3831-01A-01W-0900-09 chr19:30935836 C>T maps to NM_014717.1 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3844-01A-01W-0995-10 chr19:30934981 G>T maps to NM_014717.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:31039276 C>A maps to NM_014717.1 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr19:31038871 G>A maps to NM_014717.1 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:31038886 C>T maps to NM_014717.1 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr19:30935476 C>T maps to NM_014717.1 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr19:31025760 C>T maps to NM_014717.1 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr19:30935012 C>T maps to NM_014717.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:31025823 C>A maps to NM_014717.1 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:38102600 T>C maps to NM_152606.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:38091995 A>G maps to NM_152606.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:57840245 C>T maps to NM_213598.3 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:57835174 G>A maps to NM_213598.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr19:57839811 C>T maps to NM_213598.3 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5666-01A-01D-1650-10 chr19:40520079 C>T maps to NM_178544.3 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:40520805 T>C maps to NM_178544.3 H543H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6625-01A-21D-1771-10 chr19:40513218 C>T maps to NM_178544.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr19:57889114 A>G maps to NM_173631.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr19:57889114 A>G maps to NM_173631.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:57889483 C>T maps to NM_173631.2 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:57911214 A>G maps to NM_001172773.1 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:57910182 C>T maps to NM_001172773.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:57910486 G>T maps to NM_001172773.1 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:57910926 C>T maps to NM_001172773.1 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:58046621 G>A maps to ENST00000376233 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:58048662 T>C maps to ENST00000376233 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:58049724 G>A maps to ENST00000376233 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr19:58050195 C>T maps to ENST00000376233 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:58049967 T>C maps to ENST00000376233 N532N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:58058531 C>T maps to NM_001039654.1 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr19:58197990 T>C maps to ENST00000356715 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:58197978 C>A maps to ENST00000356715 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr19:58319998 A>G maps to NM_024762.3 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr19:2827727 C>T maps to NM_001102651.1 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:2834307 C>T maps to NM_001102651.1 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:2852845 T>A maps to NM_152791.4 C261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr19:2877778 C>T maps to NM_024967.1 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:2877778 C>T maps to NM_024967.1 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:2878236 C>T maps to NM_024967.1 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:2877778 C>T maps to NM_024967.1 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6168-01A-11D-1650-10 chr19:2877843 C>T maps to NM_024967.1 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:7075715 G>T maps to NM_024341.2 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:8932717 G>A maps to NM_144693.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:8922048 C>A maps to NM_144693.1 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr19:8922718 C>T maps to NM_144693.1 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:9453039 G>T maps to NM_032497.1 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:9452609 T>C maps to NM_032497.1 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:9452609 T>C maps to NM_032497.1 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr19:9584951 C>T maps to NM_152476.2 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:9581065 A>G did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:9578673 C>A maps to NM_152476.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:9581974 T>C maps to NM_152476.2 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6315-01A-11D-1719-10 chr19:9581066 C>T did not map to a codon.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:9721004 G>A maps to NM_152289.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6626-01A-11D-1771-10 chr19:9721463 T>C maps to NM_152289.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:12430286 A>G maps to NM_145276.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr19:12429506 C>T maps to NM_145276.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:12430162 C>A maps to NM_145276.2 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr19:12433522 G>A maps to NM_145276.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr19:12638452 G>A maps to NM_144976.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr19:12638452 G>T maps to NM_144976.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr19:12638452 G>A maps to NM_144976.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:36673442 G>A maps to ENST00000355114 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:36673931 G>A maps to ENST00000355114 C333C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:36673952 T>C maps to ENST00000355114 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:36963831 T>A maps to NM_001145343.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3712-01A-21D-1719-10 chr19:37440552 A>G maps to NM_198539.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:37441366 C>T maps to NM_198539.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:37440702 C>A maps to NM_198539.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6163-01A-11D-1650-10 chr19:37440552 A>G maps to NM_198539.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XF-01A-11D-A152-10 chr19:37440552 A>G maps to NM_198539.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3680-01A-01W-0900-09 chr19:37903657 G>A maps to NM_152484.2 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:37904508 C>A maps to NM_152484.2 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:37904737 T>C maps to NM_152484.2 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr19:37904155 A>G maps to NM_152484.2 C468C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6529-01A-11D-1771-10 chr19:37917208 C>T maps to NM_152484.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:37904311 T>C maps to NM_152484.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:2916211 A>G maps to NM_173480.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:2917611 T>C maps to NM_173480.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D0-01A-11D-A152-10 chr19:2917848 T>C maps to NM_173480.2 H410H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr19:2917752 G>A maps to NM_173480.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:38057031 C>A maps to NM_016536.3 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:38055643 T>C maps to NM_016536.3 E562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:38056738 A>G maps to NM_016536.3 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr8:125989892 C>A maps to NM_152412.2 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:125989805 G>A maps to NM_152412.2 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr8:125989166 C>T maps to NM_152412.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr8:125990078 C>T maps to NM_152412.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:38229550 C>A maps to NM_001172690.1 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02H-01A-01W-A00E-09 chr19:38229638 A>G maps to NM_001172690.1 C584C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:38230052 C>T maps to NM_001172690.1 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr19:38229944 G>T maps to NM_001172690.1 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:42584809 A>G maps to ENST00000222339 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6747-01A-11D-1835-10 chr19:42584798 C>T maps to ENST00000222339 R771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:42584317 G>A maps to ENST00000222339 E610E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr19:42584551 C>T maps to ENST00000222339 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr19:44039550 C>T maps to ENST00000458714 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:44039454 G>A maps to ENST00000458714 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr19:52376611 C>A maps to NM_032679.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:53015008 G>T maps to NM_001099694.1 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:56156246 C>T maps to NM_016535.3 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:56895473 A>G maps to NM_144690.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:56895549 T>C maps to NM_144690.1 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr19:56895624 T>C maps to NM_144690.1 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6538-01A-11D-1719-10 chr19:56895624 T>C maps to NM_144690.1 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D4-01A-21D-A152-10 chr19:56895792 A>G maps to NM_144690.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr19:56934914 T>C maps to NM_001159861.1 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3939-01A-01W-0995-10 chr19:56934606 C>T maps to NM_001159861.1 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:56934924 G>T maps to NM_001159861.1 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:56935407 G>T maps to NM_001159861.1 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:56934999 G>T maps to NM_001159861.1 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:56925356 A>G maps to NM_001159861.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr19:58929135 G>A maps to NM_173548.1 K417K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:58928562 G>A maps to NM_173548.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:58928325 G>A maps to NM_173548.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6898-01A-11D-1924-10 chr19:58921330 G>A maps to NM_173548.1 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:37643396 G>A maps to ENST00000356958 C468C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:37642892 A>T maps to ENST00000356958 C636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6534-01A-21D-1924-10 chr19:37643416 C>A maps to ENST00000356958 G462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6323-01A-11D-1719-10 chr19:37643414 T>C maps to ENST00000356958 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:37643414 T>C maps to ENST00000356958 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:37680605 T>C maps to NM_152279.3 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr19:37677526 G>A maps to NM_152279.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:37677178 G>A maps to NM_152279.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr15:85326065 T>C maps to NM_014630.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr15:85326445 C>T maps to NM_014630.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:85334027 G>A maps to NM_014630.2 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr15:85326619 C>T maps to NM_014630.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3930-01A-01W-0995-10 chr15:85345485 C>T maps to NM_014630.2 A1222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:26496948 C>T maps to NM_015871.4 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr17:5087518 A>G maps to NM_032530.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:5087092 C>T maps to NM_032530.1 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:5087173 G>T maps to NM_032530.1 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:86724 G>T maps to NM_182524.2 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr4:87060 A>T maps to NM_182524.2 K556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr8:192900 C>T maps to NM_001042416.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:3487476 C>T maps to NM_152457.1 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr16:3486861 C>T maps to NM_152457.1 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6901-01A-11D-1924-10 chr16:3486516 C>T maps to NM_152457.1 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr16:2049728 G>T maps to ENST00000431526 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr19:35250004 T>C maps to NM_001007248.2 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:35250826 G>T maps to NM_001007248.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:53269613 G>A maps to NM_198457.2 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:53270576 C>T maps to NM_198457.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr19:53270576 C>T maps to NM_198457.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:53269131 G>T maps to NM_198457.2 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr12:133502192 G>A maps to NM_001164715.1 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr12:133509731 C>A maps to NM_001164715.1 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr12:133502966 C>T maps to NM_001164715.1 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr12:133509731 C>A maps to NM_001164715.1 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:58490988 G>T maps to NM_025027.3 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:58512096 C>T maps to NM_025027.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:58490544 T>C maps to NM_025027.3 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:38188958 A>G maps to NM_032689.4 H691H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr5:123984306 G>A maps to NM_020747.2 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5664-01A-21D-1835-10 chr5:123983880 C>A maps to NM_020747.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr5:123983265 C>T maps to NM_020747.2 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr5:123982611 T>C maps to NM_020747.2 K1155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr5:123983880 C>A maps to NM_020747.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6532-01A-11D-1719-10 chr5:124080250 T>C maps to NM_020747.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr5:123984381 C>T maps to NM_020747.2 K565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr5:124079872 G>A maps to NM_020747.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr15:64966951 A>G maps to NM_015042.1 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3812-01A-01W-0900-09 chr15:64968010 C>T maps to NM_015042.1 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr15:64972936 G>T maps to NM_015042.1 G1346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr15:64966240 T>C maps to NM_015042.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr15:64967845 A>G maps to NM_015042.1 E931E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr15:64966201 C>A maps to NM_015042.1 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:52869875 A>T maps to NM_001161425.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr19:52869554 A>G maps to NM_001161425.1 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0X9-01A-11D-A152-10 chr19:52869000 C>T maps to NM_001161425.1 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:53209020 A>G maps to NM_001161500.1 N429N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr19:52447855 C>T maps to NM_001031721.3 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:52447579 G>A maps to NM_001031721.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:52448888 T>C maps to NM_001031721.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:52519830 C>T maps to NM_025040.3 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:52521311 C>A maps to NM_025040.3 G63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:52520063 C>A maps to NM_025040.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr19:52520550 G>A maps to NM_025040.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr19:52496180 A>G maps to ENST00000354939 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:52496291 C>T maps to ENST00000354939 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr19:52497551 A>G maps to ENST00000354939 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr19:52496180 A>G maps to ENST00000354939 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:52505089 C>A maps to ENST00000354939 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:52618352 T>C maps to NM_178523.3 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00W-01A-01W-A005-10 chr19:52618565 G>A maps to NM_178523.3 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:52619333 T>C maps to NM_178523.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3850-01A-01W-0995-10 chr9:116811414 C>T maps to ENST00000374126 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr9:116811036 C>T maps to ENST00000374126 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr9:116769708 C>T maps to ENST00000374126 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr9:116778981 C>T maps to ENST00000374126 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:116750696 G>A maps to ENST00000374126 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr9:116778438 G>A maps to NM_133374.2 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr9:116810207 C>T maps to ENST00000374126 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:40528598 G>T maps to NM_001145082.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02Y-01A-43W-A096-10 chr3:40558150 C>T maps to NM_175888.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr3:40573866 T>C maps to NM_001098414.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr8:144733631 G>A maps to NM_014789.3 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr8:144732473 G>A maps to NM_014789.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr8:144733544 C>T maps to NM_014789.3 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr17:16527217 C>A maps to NM_020787.3 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:16527347 G>A maps to NM_020787.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:16525931 G>T maps to NM_020787.3 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr17:16526903 A>G maps to NM_020787.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:12256363 G>A maps to ENST00000439556 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:12256779 G>A maps to ENST00000439556 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr19:12256483 G>A maps to ENST00000439556 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:20807437 A>G maps to NM_001076675.2 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr19:20807827 G>T maps to NM_001076675.2 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:20807524 C>T maps to NM_001076675.2 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:20808246 G>A maps to NM_001076675.2 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:20808313 A>G maps to NM_001076675.2 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:20808153 C>A maps to NM_001076675.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:11728545 G>T maps to NM_145295.3 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:11727837 G>T maps to NM_145295.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:55992823 C>T maps to NM_033113.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:55995151 G>A maps to NM_033113.2 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr16:30794931 G>A maps to NM_001080417.1 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:30794631 C>T maps to NM_001080417.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr23:47919227 C>A did not map to a codon.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr23:47919257 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:47918546 C>T did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:47918982 C>T did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:47918102 A>G did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:47919499 A>C did not map to a codon.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr23:47919499 A>C did not map to a codon.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr23:47918883 T>C did not map to a codon.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr23:47919499 A>G did not map to a codon.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr23:47919499 A>G did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr2:71576842 C>A maps to NM_014497.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr2:71661876 C>T maps to NM_014497.3 F1959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:71654129 G>T maps to NM_014497.3 E1711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr2:71655743 A>G maps to NM_014497.3 E1871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:71576572 A>G maps to NM_014497.3 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr2:71650828 G>A maps to NM_014497.3 K1395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:179051457 C>T maps to NM_016331.1 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr12:48741899 T>G did not map to a codon.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:40961709 C>T maps to NM_198494.2 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:40922639 A>G maps to NM_023070.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr1:40928627 G>A maps to NM_023070.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3666-01A-02W-0900-09 chr1:91406697 C>T maps to NM_201269.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr1:91405938 G>A maps to NM_201269.1 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6676-01A-11D-1835-10 chr1:91406751 C>T maps to NM_201269.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6536-01A-11D-1719-10 chr1:91405545 C>A maps to NM_201269.1 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3496-01A-21D-1835-10 chr23:22292136 C>A did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:22291567 C>T did not map to a codon.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr23:22291389 G>A did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr23:22291525 A>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:22291206 T>C did not map to a codon.
Sequencing variant TCGA-AA-A00O-01A-02W-A00E-09 chr23:22292060 C>T did not map to a codon.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr23:22291937 C>T did not map to a codon.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr23:22291623 A>C did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:22291295 C>T did not map to a codon.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr23:22291294 C>T did not map to a codon.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr16:31089502 C>T maps to NM_014699.3 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:31089135 T>A maps to NM_014699.3 C497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:31090506 A>G maps to NM_014699.3 A954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr1:182026715 G>A maps to NM_001009992.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3994-01A-01W-1073-09 chr1:182025762 C>T maps to NM_001009992.1 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr1:182026704 C>T maps to NM_001009992.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:182025981 G>A maps to NM_001009992.1 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr1:182025500 G>A maps to NM_001009992.1 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:182027106 C>T maps to NM_001009992.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6533-01A-11D-1719-10 chr1:182027121 G>A maps to NM_001009992.1 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr19:52394554 A>G maps to NM_023074.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:52394722 A>T maps to NM_023074.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr17:47394439 A>G maps to NM_014897.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr17:47389291 G>A maps to NM_014897.2 C387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr19:11597869 C>T maps to NM_138783.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-5254-01A-21D-1835-10 chr19:11597655 G>A maps to NM_138783.3 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:11597866 G>A maps to NM_138783.3 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr3:88188630 T>C maps to NM_018293.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr3:88189921 G>T maps to NM_018293.2 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr3:88188772 G>T maps to NM_018293.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr3:88189014 C>T maps to NM_018293.2 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:99170243 C>A maps to NM_001083956.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:99170460 G>T maps to NM_001083956.1 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr9:40774704 T>C maps to NM_033160.5 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6161-01A-11D-1650-10 chr9:40773966 T>C maps to NM_033160.5 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr9:40773966 T>C maps to NM_033160.5 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr3:44635987 T>C maps to NM_173658.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:44635760 G>T maps to NM_173658.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr3:44636188 G>A maps to NM_173658.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:44636416 A>G maps to NM_173658.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3544-01A-01W-0831-10 chr3:42950351 G>A maps to NM_001134656.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr3:42956029 A>C maps to NM_001134656.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5916-01A-11D-1650-10 chr3:42949626 T>C maps to NM_001134656.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr12:124496762 T>C maps to NM_152437.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:53668848 G>A maps to NM_024733.3 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:53668644 T>G maps to NM_024733.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:53669073 G>A maps to NM_024733.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:53668817 G>A maps to NM_024733.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:56953250 T>C maps to ENST00000342634 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr19:56952983 T>C maps to ENST00000342634 E588E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AA-3833-01A-01W-0900-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AA-3833-01A-01W-0900-09 chr16:31073153 G>A maps to ENST00000417110 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr16:31072582 G>T maps to NM_001172669.1 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D6-01A-21D-A152-10 chr16:31072582 G>T maps to NM_001172669.1 R579R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DM-A1DB-01A-11D-A152-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr16:31073255 T>C maps to ENST00000417110 P148P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G4-6304-01A-11D-1924-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-G4-6304-01A-11D-1924-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:31075327 C>T maps to NM_001172669.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr1:247263801 G>A maps to NM_024804.2 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr1:247201098 C>T maps to NM_033213.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr1:247201652 A>G maps to NM_033213.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6169-01A-11D-1650-10 chr1:247201188 T>C maps to NM_033213.3 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:247201263 A>G maps to NM_033213.3 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:58232649 G>A maps to ENST00000335820 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01Z-01A-11W-A096-10 chr19:58232421 G>A maps to ENST00000335820 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5864-01A-01D-1650-10 chr19:58232976 T>C maps to ENST00000335820 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr1:249142141 G>T maps to NM_024836.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr1:249141613 C>T maps to NM_024836.1 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr1:249142327 C>T maps to NM_024836.1 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr23:46359847 T>G did not map to a codon.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr23:46387830 G>A did not map to a codon.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr23:46359327 A>G did not map to a codon.
Sequencing variant TCGA-AY-6386-01A-21D-1719-10 chr23:46359327 A>G did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:46359974 C>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:46360547 A>G did not map to a codon.
Sequencing variant TCGA-CK-4948-01B-11D-1650-10 chr23:46359377 C>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:23836141 A>G maps to NM_138330.2 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:23836536 C>A maps to NM_138330.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:23837134 G>A maps to NM_138330.2 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr19:23837044 A>G maps to NM_138330.2 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr19:23837044 A>G maps to NM_138330.2 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr19:23845843 C>A maps to NM_138330.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr19:23845885 C>T maps to NM_138330.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:22363867 T>C maps to NM_001001411.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:53741624 C>A maps to NM_182609.2 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:53740272 T>C maps to NM_182609.2 K569K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:53740848 A>G maps to NM_182609.2 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:53740364 C>A maps to NM_182609.2 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:227842154 A>G maps to NM_178549.3 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:227843091 G>T maps to NM_178549.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr7:63981568 T>C maps to NM_178558.4 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr7:64004783 G>A maps to NM_178558.4 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:23926802 G>A maps to NM_138286.2 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:23937667 C>T maps to NM_138286.2 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3664-01A-01W-0900-09 chr19:20118010 C>T maps to NM_033196.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:20117755 G>A maps to NM_033196.2 H185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:26694135 C>A maps to ENST00000436292 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr1:26694240 G>A maps to ENST00000436292 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr1:26691361 G>A maps to ENST00000436292 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:41012930 C>T maps to NM_152373.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:41012978 T>C maps to NM_152373.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:151258838 T>C maps to NM_020832.1 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr1:151261167 C>T maps to NM_020832.1 R760R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr1:151262973 G>A maps to NM_020832.1 R1048R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr16:30581464 G>A maps to NM_145271.3 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:30582812 C>T maps to NM_145271.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6963-01A-11D-1924-10 chr16:30581356 G>A maps to NM_145271.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr16:30581503 G>A maps to NM_145271.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr16:30582445 T>C did not map to a codon.
Sequencing variant TCGA-A6-5659-01A-01D-1650-10 chr16:30615770 A>G maps to NM_138447.1 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01P-01A-21W-A096-10 chr16:30616046 G>A maps to NM_138447.1 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr16:30620849 C>T maps to NM_138447.1 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr16:30616649 G>A maps to NM_138447.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6928-01A-11D-1924-10 chr16:30616696 G>A maps to NM_138447.1 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6806-01A-11D-1835-10 chr16:30616391 G>A maps to NM_138447.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr1:43317460 C>T maps to ENST00000442768 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:249150611 T>C maps to NM_001136036.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr1:249148145 C>T maps to NM_001136036.2 K386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr1:249149985 G>A maps to NM_001136036.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:249148222 G>A maps to NM_001136036.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr1:247162734 A>G maps to NM_020394.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-5543-01A-01D-1650-10 chr1:247150498 C>A maps to NM_020394.3 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr1:247150759 G>A maps to NM_020394.3 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr8:144378456 G>A maps to NM_030895.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr1:120165483 C>T maps to NM_001080470.1 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr1:120165750 G>A maps to NM_001080470.1 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:9406188 G>A maps to NM_198535.1 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr19:9407215 A>G maps to NM_198535.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:9406285 A>G maps to NM_198535.1 C598C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr8:146054927 T>C maps to ENST00000446747 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr8:146068063 C>T maps to ENST00000446747 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5662-01A-01D-1650-10 chr22:24086466 T>C maps to NM_021916.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr22:24086367 G>A maps to NM_021916.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr22:24086475 G>T maps to NM_021916.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:12059837 G>A maps to NM_144566.1 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr19:12059852 A>G maps to NM_144566.1 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr19:12060191 T>C maps to NM_144566.1 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:53086679 T>C maps to NM_001172655.1 H522H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:53086622 T>C maps to NM_001172655.1 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr8:81555313 C>T maps to NM_001033723.2 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr8:144775907 C>T maps to NM_173831.3 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr19:21493303 C>T maps to NM_021269.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5915-01A-11D-1650-10 chr19:21493303 C>T maps to NM_021269.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr19:21477068 A>G maps to NM_021269.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:12575429 G>A maps to ENST00000428311 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:12575093 G>A maps to ENST00000428311 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6715-01A-21D-1835-10 chr19:12575034 C>T maps to ENST00000428311 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2683-01A-01W-0831-10 chr19:57133713 G>C maps to NM_021216.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3518-01A-02W-0833-10 chr19:57133932 C>T maps to NM_021216.4 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:57133428 C>A maps to NM_021216.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01V-01A-23W-A096-10 chr19:57132798 G>A maps to NM_021216.4 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:57133566 C>A maps to NM_021216.4 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4744-01A-01D-1408-10 chr19:57134061 C>T maps to NM_021216.4 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr15:90611583 C>T maps to NM_198526.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr15:90611595 C>T maps to NM_198526.2 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr15:90611532 C>T maps to NM_198526.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr15:90610447 C>T maps to NM_198526.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr15:90610962 C>G maps to NM_198526.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr15:90610818 G>A maps to NM_198526.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6138-01A-11D-1771-10 chr23:84519370 G>A did not map to a codon.
Sequencing variant TCGA-A6-6651-01A-21D-1835-10 chr23:84526561 A>G did not map to a codon.
Sequencing variant TCGA-AA-3872-01A-01W-0995-10 chr23:84510341 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01Q-01A-01W-A005-10 chr23:84526265 A>G did not map to a codon.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr23:84525921 T>C did not map to a codon.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr23:84526378 T>C did not map to a codon.
Sequencing variant TCGA-D5-6539-01A-11D-1719-10 chr23:84526277 T>C did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:84525077 G>A did not map to a codon.
Sequencing variant TCGA-AA-3979-01A-01W-0995-10 chr19:21300958 A>T maps to NM_182515.3 K497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:21301035 C>T maps to NM_182515.3 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:57529148 G>T maps to NM_001159279.1 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr7:57529400 G>T maps to NM_001159279.1 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr7:57528613 G>A maps to NM_001159279.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr4:437343 G>T maps to NM_133474.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr4:435606 A>G maps to NM_133474.2 H883H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr4:436839 G>T maps to NM_133474.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr4:436275 C>T maps to NM_133474.2 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A03F-01A-11W-A096-10 chr4:437165 C>A maps to NM_133474.2 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr4:436595 C>A maps to NM_133474.2 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr4:438146 T>A maps to NM_133474.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr4:266134 C>A maps to ENST00000419098 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr4:265633 C>A maps to ENST00000419098 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr4:266042 G>T maps to ENST00000419098 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D9-01A-11D-A152-10 chr7:63680105 C>G maps to NM_001159524.1 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:20736533 G>A maps to NM_001159293.1 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr22:20760156 C>T maps to NM_003426.2 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr22:20755612 C>T maps to NM_003426.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr22:20760915 C>T maps to NM_003426.2 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr22:20760534 C>T maps to NM_003426.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr12:53581355 C>T maps to NM_001004304.3 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr12:53580193 C>T maps to NM_001004304.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3941-01A-01W-0995-10 chr7:149191480 C>T maps to NM_001163474.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:149191148 G>A maps to NM_001163474.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:149171702 G>A maps to NM_001163474.1 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr7:149191525 G>A maps to NM_001163474.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6888-01A-11D-1924-10 chr19:57955799 T>C maps to NM_001023561.2 H428H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:57953257 T>C maps to NM_001023561.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr19:57956660 G>A maps to NM_001023561.2 Q715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr17:80788308 G>A maps to NM_024702.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6929-01A-31D-1924-10 chr16:3367301 G>A maps to NM_153028.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2678-01A-01W-0831-10 chr23:134421634 T>C did not map to a codon.
Sequencing variant TCGA-AA-3655-01A-02D-1719-10 chr23:134421770 C>A did not map to a codon.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr23:134424934 C>A did not map to a codon.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr23:134421428 T>C did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:134421768 A>T did not map to a codon.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr23:134426282 A>G did not map to a codon.
Sequencing variant TCGA-G4-6307-01A-11D-1719-10 chr23:134421215 G>T did not map to a codon.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr6:35261692 G>A did not map to a codon.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:35258056 C>T maps to NM_003427.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr6:35260379 C>T maps to NM_003427.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6781-01A-22D-1924-10 chr19:53958360 A>G maps to NM_001008401.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3851-01A-01W-0995-10 chr19:53959593 T>A maps to NM_001008401.3 C611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:53959938 C>T maps to NM_001008401.3 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr19:53958360 A>G maps to NM_001008401.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5541-01A-01D-1650-10 chr19:53958360 A>G maps to NM_001008401.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28F-01A-11D-A16V-10 chr19:53958981 G>A maps to NM_001008401.3 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6299-01A-11D-1771-10 chr19:12088964 G>T maps to NM_001012753.1 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr16:30567324 G>A maps to NM_033410.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr16:30566562 C>T maps to NM_033410.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AU-6004-01A-11D-1719-10 chr16:30567201 G>A maps to NM_033410.3 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:53911827 G>A maps to NM_001040185.1 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3854-01A-01W-0900-09 chr19:52794360 C>A maps to NM_001010851.2 Y439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:52793572 G>T maps to NM_001010851.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:2933758 G>A maps to NM_021217.2 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:2934029 G>T maps to NM_021217.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A0XD-01A-12D-A152-10 chr19:2936655 G>A maps to NM_021217.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr15:35273928 G>A maps to NM_014106.3 Y569Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:57985397 G>A maps to NM_001024596.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr19:57988665 A>C maps to NM_001024596.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:57987133 G>A maps to NM_001024596.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:57985397 G>A maps to NM_001024596.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr19:57985283 G>A maps to NM_001024596.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr15:90897924 A>G maps to NM_001004309.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:90903824 A>G maps to NM_001004309.2 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr7:150094450 G>A maps to NM_173680.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr7:150093790 G>A maps to NM_173680.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:58265515 C>T maps to NM_173632.3 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr7:149129634 G>A maps to ENST00000440594 C577C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr7:149153083 C>T maps to ENST00000440594 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr7:149133891 G>A maps to ENST00000440594 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr7:149129328 G>A maps to ENST00000440594 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr16:89293415 T>C maps to NM_182531.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr16:89293952 A>G maps to NM_182531.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr16:89294854 T>A maps to NM_182531.2 L692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:40580706 G>A maps to NM_001142577.1 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:40581661 G>T maps to NM_001142577.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:40580706 G>A maps to NM_001142577.1 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:40542374 G>A maps to NM_001005851.2 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:38160388 C>A maps to NM_152605.3 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr9:99581826 C>A maps to NM_001001662.1 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6677-01A-11D-1835-10 chr9:99607277 G>A maps to NM_001001662.1 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr9:99607277 G>A maps to NM_001001662.1 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr16:30594000 G>A maps to NM_152458.6 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6172-01A-11D-1650-10 chr16:30594261 C>T maps to NM_152458.6 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr16:30594462 G>A maps to NM_152458.6 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3846-01A-01W-0995-10 chr7:148769443 G>A maps to NM_152411.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:56599997 C>T maps to NM_001002836.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr7:99084676 G>T maps to NM_213603.2 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr7:99084622 A>T maps to NM_213603.2 K264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr7:99084988 C>T maps to NM_213603.2 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr19:37309361 T>G maps to NM_206894.2 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr19:37309859 G>A maps to NM_206894.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr19:37309703 G>T maps to NM_206894.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr19:37310147 A>G maps to NM_206894.2 H366H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr19:37314611 A>G maps to NM_206894.2 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:37310014 G>A maps to NM_206894.2 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:12739965 A>G maps to NM_153358.2 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr19:12738843 A>G maps to NM_153358.2 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:35451892 G>A maps to NM_175872.4 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr19:38028447 A>C maps to NM_001013659.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:38023361 C>A maps to NM_001013659.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:38028600 C>A maps to NM_001013659.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr19:12502428 G>T maps to NM_001080821.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4746-01A-01D-1408-10 chr19:58806557 C>T maps to NM_021089.2 R462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr19:58805761 A>G maps to NM_021089.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr3:113955339 G>A maps to NM_007136.3 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr3:113955600 G>A maps to NM_007136.3 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3867-01A-01W-0995-10 chr3:113955339 G>A maps to NM_007136.3 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr3:113955270 G>A maps to NM_007136.3 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr3:113955567 C>T maps to NM_007136.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr3:113955305 G>A maps to NM_007136.3 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr7:127014097 A>C maps to NM_176814.3 L431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3662-01A-01D-1719-10 chr2:185802430 C>A maps to NM_194250.1 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr2:185802430 C>A maps to NM_194250.1 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3715-01A-01W-0900-09 chr2:185800767 T>C maps to NM_194250.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00A-01A-01W-A005-10 chr2:185731161 G>T maps to NM_194250.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr2:185800788 G>A maps to NM_194250.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:185798362 C>T maps to NM_194250.1 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr2:185801409 T>C maps to NM_194250.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6600-01A-11D-1771-10 chr2:185800533 C>T maps to NM_194250.1 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:185802430 C>A maps to NM_194250.1 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6606-01A-11D-1835-10 chr2:185801469 G>A maps to NM_194250.1 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr2:185800758 C>T maps to NM_194250.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr7:88963897 G>A maps to NM_181646.2 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:88966255 T>C maps to NM_181646.2 G1320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr7:88965868 G>A maps to NM_181646.2 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr7:88965814 C>G maps to NM_181646.2 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3982-01A-02W-0995-10 chr7:88964470 T>A maps to NM_181646.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:88965847 A>G maps to NM_181646.2 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:88956666 G>T maps to NM_181646.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr7:88965517 T>C maps to NM_181646.2 P1074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5914-01A-11D-1650-10 chr7:88962983 A>T maps to NM_181646.2 K230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4752-01A-01D-1408-10 chr7:88964350 C>T maps to NM_181646.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6719-01A-11D-1835-10 chr19:57764520 C>T maps to NM_001023563.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr19:53058499 C>T maps to NM_001039886.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr19:53057719 C>T maps to NM_001039886.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:53058232 C>T maps to NM_001039886.3 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:53056666 A>G maps to NM_001039886.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr19:53057888 A>T maps to NM_001039886.3 K574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:53058568 C>T maps to NM_001039886.3 F800F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:53056493 G>T maps to NM_001039886.3 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:53058475 C>T maps to NM_001039886.3 G769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-3809-01A-01W-0995-10 chr23:47775967 C>T did not map to a codon.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:47774588 C>A did not map to a codon.
Sequencing variant TCGA-AA-3947-01A-01W-0995-10 chr23:47774359 T>G did not map to a codon.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr23:47775429 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:47775548 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:47775735 T>C did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:53994484 C>A maps to NM_001004301.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1DB-01A-11D-A152-10 chr19:53995081 T>C maps to NM_001004301.3 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr19:53454163 A>G maps to NM_001031665.1 N288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr19:53453374 G>A maps to NM_001031665.1 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:53454613 A>G maps to NM_001031665.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr19:53454061 G>A maps to NM_001031665.1 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01K-01A-01W-A00E-09 chr19:53459333 A>G maps to NM_001031665.1 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:53459300 C>T maps to NM_001031665.1 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:53453506 T>C maps to NM_001031665.1 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3555-01A-01W-0831-10 chr16:71894310 G>A maps to ENST00000425432 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr19:11833235 A>G maps to NM_001080493.2 H371H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00E-01A-01W-A005-10 chr4:146700558 G>A maps to ENST00000508784 Q830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr4:146686150 G>A maps to ENST00000508784 T1073T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr4:146695709 G>A maps to ENST00000508784 F936F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr4:146770590 G>A maps to ENST00000508784 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr4:146823555 G>T maps to ENST00000508784 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6293-01A-11D-1719-10 chr4:146791553 C>A maps to ENST00000508784 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3811-01A-01W-0995-10 chr13:115091731 G>A maps to NM_032436.2 P805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr13:115090561 G>A maps to NM_032436.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr13:115089703 C>A maps to NM_032436.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6586-01A-11D-1771-10 chr13:115090738 T>C maps to NM_032436.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr19:37382458 C>A maps to NM_001171979.1 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr19:53117460 C>T maps to NM_018300.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr17:33289302 G>T maps to NM_052857.3 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr17:33289310 C>A maps to NM_052857.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2671-01A-01D-1408-10 chr20:57767711 G>A maps to NM_178457.1 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5665-01A-01D-1650-10 chr20:57829767 C>T maps to NM_178457.1 D1668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr20:57829672 G>T maps to NM_178457.1 E1637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr20:57769658 C>T maps to NM_178457.1 P1195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr20:57829431 G>A maps to NM_178457.1 S1556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3710-01A-01W-0995-10 chr20:57829575 C>A maps to NM_178457.1 P1604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr20:57829431 G>A maps to NM_178457.1 S1556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A022-01A-21W-A096-10 chr20:57782043 C>A maps to NM_178457.1 R1320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr20:57829185 C>A maps to NM_178457.1 S1474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr20:57767573 C>T maps to NM_178457.1 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6170-01A-11D-1650-10 chr20:57766697 C>T maps to NM_178457.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3845-01A-01W-0995-10 chr19:57176194 C>T maps to NM_001005850.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr19:57176275 G>A maps to NM_001005850.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:57175726 G>A maps to NM_001005850.1 C302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr19:57175780 G>T maps to NM_001005850.1 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-6746-01A-11D-1835-10 chr19:57176296 C>T maps to NM_001005850.1 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:52659759 T>C maps to NM_001102657.1 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:52660035 T>C maps to NM_001102657.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:102793061 C>T maps to NM_018335.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr14:102808332 C>T maps to NM_018335.3 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr14:102798053 C>T maps to NM_018335.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr14:102805543 G>A maps to NM_018335.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:52570384 T>C maps to NM_001136499.1 Q250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:52570666 C>T maps to NM_001136499.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr19:52569913 G>T maps to NM_001136499.1 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6703-01A-11D-1835-10 chr19:52568395 C>T maps to NM_001136499.1 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:52568371 C>T maps to NM_001136499.1 G921G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:12187588 A>C maps to NM_001136501.1 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr19:53854855 C>T maps to NM_138374.1 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:9868917 C>A maps to NM_001077624.1 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:9868896 C>A maps to NM_001077624.1 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6782-01A-11D-1835-10 chr19:21132355 A>T maps to NM_003429.4 K346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr19:21132210 A>T maps to NM_003429.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:21132978 T>C maps to NM_003429.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr19:21117753 G>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr19:21132334 G>T maps to NM_003429.4 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6309-01A-21D-1835-10 chr3:32032199 T>C maps to NM_001137674.1 C543C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr7:149559143 G>A maps to NM_001099220.1 G965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3952-01A-01W-0995-10 chr7:149561288 G>A maps to NM_001099220.1 A1142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A004-01A-01W-A00E-09 chr7:149545091 C>T maps to NM_001099220.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr7:149557532 G>A maps to NM_001099220.1 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6304-01A-11D-1924-10 chr7:149545160 C>T maps to NM_001099220.1 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:12155012 C>A maps to NM_001080404.1 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr19:52888545 T>C maps to NM_001145434.1 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3861-01A-01W-0995-10 chr19:52888041 G>T maps to NM_001145434.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:52887660 C>A maps to NM_001145434.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr19:52887903 T>C maps to NM_001145434.1 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5861-01A-01D-1650-10 chr19:52887801 T>C maps to NM_001145434.1 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5539-01A-01D-1650-10 chr19:52887264 A>G maps to NM_001145434.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr19:23545249 A>G maps to NM_003430.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:23543485 A>G maps to NM_003430.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5540-01A-01D-1650-10 chr19:23545419 G>A maps to NM_003430.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6540-01A-11D-1719-10 chr19:23542267 G>A maps to NM_003430.2 G1171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6923-01A-11D-1924-10 chr19:23542956 C>A maps to NM_003430.2 E942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6926-01A-11D-1924-10 chr19:23545267 T>C maps to NM_003430.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr19:23543569 A>G maps to NM_003430.2 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6306-01A-11D-1771-10 chr19:23542725 C>A maps to NM_003430.2 E1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:23542612 G>A maps to NM_003430.2 G1056G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr7:64863707 A>G maps to NM_152626.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr7:64863782 T>C maps to NM_152626.2 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr19:22574577 C>A maps to NM_001098626.1 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:22574926 T>C maps to NM_001098626.1 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:22575727 A>C maps to NM_001098626.1 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:22575480 C>A maps to NM_001098626.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3984-01A-02W-0995-10 chr19:22940501 C>A maps to ENST00000397104 E646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:22941593 C>A maps to ENST00000397104 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:22939843 C>T maps to ENST00000397104 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr19:22940460 T>C maps to ENST00000397104 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6165-01A-11D-1650-10 chr19:22941351 G>T maps to ENST00000397104 Y362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr20:47866062 G>A maps to NM_021035.2 C1166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:47864844 T>C maps to NM_021035.2 Q1572Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:47881339 G>T maps to NM_021035.2 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-4071-01A-01W-1073-09 chr20:47888150 C>T maps to NM_021035.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr20:47865201 G>A maps to NM_021035.2 F1453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr20:47863848 C>T maps to NM_021035.2 T1904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1D7-01A-11D-A152-10 chr20:47864561 G>A maps to NM_021035.2 L1667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr7:100867079 C>A maps to NM_006349.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr7:100866804 C>T maps to NM_006349.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr1:86171988 G>A maps to NM_017953.3 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr1:86171988 G>A maps to NM_017953.3 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A28G-01A-11D-A16V-10 chr16:75127560 C>A maps to ENST00000320619 Y172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr22:29383092 T>C maps to NM_032173.2 N10N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr22:29445467 C>T maps to NM_032173.2 C333C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6162-01A-11D-1650-10 chr22:29446743 C>T maps to NM_032173.2 R759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr22:29440866 C>T maps to NM_032173.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6570-01A-11D-1771-10 chr22:29383170 C>T maps to NM_032173.2 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6142-01A-11D-1771-10 chr19:5456200 C>T maps to NM_181710.3 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A02W-01A-01W-A00E-09 chr19:5456386 G>A maps to NM_181710.3 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr19:5455795 A>G maps to NM_181710.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HA-01A-11D-A152-10 chr19:5455879 C>T maps to NM_181710.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr11:60643041 A>C maps to NM_207341.2 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00F-01A-01W-A005-10 chr11:60638571 C>T maps to NM_207341.2 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr16:21222703 C>T maps to NM_003460.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00J-01A-02W-A005-10 chr16:21218203 G>T maps to NM_003460.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:21213535 G>A maps to NM_003460.1 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr16:21218179 G>T maps to NM_003460.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr16:21213511 G>A maps to NM_003460.1 N400N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3877-01A-01W-0995-10 chr7:76062946 C>T maps to NM_001110354.1 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr7:76054539 G>T maps to NM_001110354.1 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3821-01A-01W-0995-10 chr1:238048708 C>T maps to NM_021186.3 W381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:238049173 G>A maps to NM_021186.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr1:238050843 G>T maps to NM_021186.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr1:238048533 G>A maps to NM_021186.3 H414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:38029297 T>G maps to NM_199321.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3525-01A-02W-0833-10 chr17:38031646 A>G maps to NM_199321.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:38032950 G>A maps to NM_199321.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6608-01A-11D-1835-10 chr17:38031673 C>T maps to NM_199321.2 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr17:38026960 G>T maps to NM_199321.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6856-01A-11D-1924-10 chr17:38029309 G>T maps to NM_199321.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3972-01A-01W-0995-10 chr3:102196368 C>T maps to NM_175056.1 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr3:102175051 G>T maps to NM_175056.1 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr3:102187822 T>C maps to NM_175056.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6303-01A-11D-1771-10 chr3:102175053 A>T maps to NM_175056.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr10:126631406 T>C maps to NM_017580.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr10:126631406 T>C maps to NM_017580.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr10:126631611 G>T maps to NM_017580.2 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr1:71544342 A>G maps to NM_203350.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:71532565 A>G maps to NM_203350.2 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6599-01A-11D-1771-10 chr1:71546660 G>A maps to NM_203350.2 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:71538204 C>A maps to NM_203350.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5862-01A-01D-1650-10 chr1:71532484 T>C maps to NM_203350.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr2:135965173 G>A maps to NM_032143.2 R947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3977-01A-01W-0995-10 chr2:135965173 G>A maps to NM_032143.2 R947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr2:136073100 C>T did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr2:135957925 A>G maps to NM_032143.2 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6674-01A-11D-1835-10 chr2:135957953 T>C maps to NM_032143.2 S1066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr23:15822297 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:15808622 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:15840962 T>C did not map to a codon.
Sequencing variant TCGA-CK-4952-01A-01D-1719-10 chr23:15821891 G>A did not map to a codon.
Sequencing variant TCGA-F4-6460-01A-11D-1771-10 chr23:15821890 C>T did not map to a codon.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:58549260 G>A maps to NM_182572.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:58564896 C>A maps to NM_182572.3 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6588-01A-11D-1771-10 chr19:58549471 C>T maps to NM_182572.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5344-01A-21D-1719-10 chr16:3142119 C>T maps to NM_032805.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A024-01A-02W-A00E-09 chr6:28097694 T>C maps to NM_025231.1 H338H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5348-01A-21D-1719-10 chr6:28094583 G>T maps to NM_025231.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr19:58601565 C>A maps to NM_001145542.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr19:58601580 C>T maps to NM_001145542.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6675-01A-11D-1835-10 chr19:58629718 C>T maps to NM_001145542.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6931-01A-11D-1924-10 chr19:58597595 C>A maps to NM_001145542.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6648-01A-11D-1771-10 chr15:85147193 G>A maps to NM_181877.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr15:85165003 C>T maps to NM_181877.3 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr15:85164373 C>T maps to NM_181877.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3950-01A-02W-0995-10 chr1:33954216 T>C maps to NM_145238.3 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr1:33960901 G>A maps to NM_145238.3 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DM-A1HB-01A-21D-A183-10 chr1:33957279 A>G maps to NM_145238.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr7:99654964 C>T maps to NM_145914.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AY-6197-01A-11D-1719-10 chr7:99661540 C>T maps to NM_145914.2 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2672-01A-01W-0833-10 chr19:58849785 A>G maps to NM_181846.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr19:58846399 C>T maps to NM_181846.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3815-01A-01W-0995-10 chr15:43656212 G>A maps to NM_152455.3 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr15:43661271 C>T maps to NM_152455.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr15:43653554 C>A maps to NM_152455.3 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:58187551 A>C maps to NM_152677.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr19:58187716 C>A maps to NM_152677.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4747-01A-01D-1408-10 chr19:58189912 T>A maps to NM_152677.2 C314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr19:56733582 G>A maps to NM_024303.1 H284H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6653-01A-11D-1771-10 chr19:56701327 C>T maps to NM_001080456.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr19:56701276 A>G maps to NM_001080456.2 C469C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr20:44511728 C>A maps to NM_080603.4 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr20:44511465 T>C maps to NM_080603.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6171-01A-11D-1650-10 chr20:44511965 G>A maps to NM_080603.4 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-2676-01A-01W-0833-10 chr2:187713710 C>T maps to NM_182521.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr2:187692974 T>C maps to NM_182521.2 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00K-01A-02W-A005-10 chr2:187713824 C>T maps to NM_182521.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr2:187698729 T>C maps to NM_182521.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4681-01A-01D-1408-10 chr2:187692974 T>C maps to NM_182521.2 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr2:187698690 G>A maps to NM_182521.2 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr2:187697902 G>A maps to NM_182521.2 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-4743-01A-01D-1719-10 chr2:187692974 T>C maps to NM_182521.2 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-5349-01A-21D-1719-10 chr2:187692974 T>C maps to NM_182521.2 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3697-01A-01D-1719-10 chr20:44507215 C>A maps to NM_080752.3 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr20:44507212 C>T maps to NM_080752.3 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr20:44505802 G>A maps to NM_080752.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-5537-01A-21D-1924-10 chr20:44507206 C>T maps to NM_080752.3 D670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr19:13919921 G>A maps to NM_023072.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3864-01A-01W-0995-10 chr1:45506186 G>A maps to NM_020883.1 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6964-01A-11D-1924-10 chr1:45484701 A>G maps to NM_020883.1 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr1:45484214 G>A maps to NM_020883.1 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3663-01A-01D-1719-10 chr6:116987863 C>T maps to NM_145062.2 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr6:116973254 G>A maps to NM_145062.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr6:116987881 G>A maps to NM_145062.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-6780-01A-11D-1835-10 chr11:113607418 T>C maps to NM_004724.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4950-01A-01D-1719-10 chr11:113639611 G>C maps to NM_004724.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G4-6628-01A-11D-1835-10 chr11:113631634 G>A maps to NM_004724.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A6-5661-01A-01D-1650-10 chr23:57936270 G>A did not map to a codon.
Sequencing variant TCGA-AA-3949-01A-01W-0995-10 chr23:57935789 C>T did not map to a codon.
Sequencing variant TCGA-AA-3966-01A-01W-1073-09 chr23:57935162 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:57934494 C>A did not map to a codon.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr23:57935324 G>A did not map to a codon.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr23:57936020 G>A did not map to a codon.
Sequencing variant TCGA-CA-6717-01A-11D-1835-10 chr23:57934488 A>C did not map to a codon.
Sequencing variant TCGA-D5-6535-01A-11D-1719-10 chr23:57935895 T>C did not map to a codon.
Sequencing variant TCGA-AA-3492-01A-01D-1408-10 chr23:57619451 A>G did not map to a codon.
Sequencing variant TCGA-AD-5900-01A-11D-1650-10 chr23:57619831 G>A did not map to a codon.
Sequencing variant TCGA-A6-6141-01A-11D-1771-10 chr3:126189753 G>A maps to NM_025112.4 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A01R-01A-21W-A096-10 chr3:126160628 G>A maps to NM_025112.4 G791G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-5913-01A-11D-1650-10 chr3:126180752 G>A maps to NM_025112.4 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F4-6807-01A-11D-1835-10 chr3:126185148 G>A maps to NM_025112.4 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr1:53282203 G>A maps to NM_024646.2 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6889-01A-11D-1924-10 chr1:53237298 T>C maps to NM_024646.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6598-01A-11D-1771-10 chr1:53237287 C>T maps to NM_024646.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr7:143086970 C>T maps to NM_001010972.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3510-01A-01D-1408-10 chr17:3917764 G>A maps to NM_015113.3 F2730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3660-01A-01D-1719-10 chr17:3953082 T>C maps to NM_015113.3 P1978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3672-01A-01W-0900-09 chr17:3937342 G>A maps to NM_015113.3 L2184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3713-01A-21D-1719-10 chr17:3974200 G>A maps to NM_015113.3 D1284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A00N-01A-02W-A00E-09 chr17:3957381 G>A maps to NM_015113.3 S1801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-A010-01A-01W-A00E-09 chr17:3935528 G>A maps to NM_015113.3 C2261C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AD-6895-01A-11D-1924-10 chr17:4020434 C>T maps to NM_015113.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-4315-01A-01D-1408-10 chr17:3962534 G>A maps to NM_015113.3 R1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CA-6718-01A-11D-1835-10 chr17:3969813 G>T maps to NM_015113.3 S1392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CK-4947-01B-11D-1650-10 chr17:3920844 G>A maps to NM_015113.3 L2607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3516-01A-02W-0833-10 chr1:78098061 G>T maps to NM_015534.4 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AA-3556-01A-01W-0831-10 chr1:78098028 G>A maps to NM_015534.4 N337N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-5407-01A-01D-1719-10 chr1:78041806 A>G maps to NM_015534.4 D759D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AZ-6601-01A-11D-1771-10 chr1:78097671 G>T maps to NM_015534.4 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CM-6164-01A-11D-1650-10 chr1:78098226 T>C maps to NM_015534.4 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6927-01A-21D-1924-10 chr1:78099026 G>A maps to NM_015534.4 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D5-6930-01A-11D-1924-10 chr1:78098555 G>A maps to NM_015534.4 R162*. Only missense variants will be evaluated by CHASM.
