Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 17 7788214 7788214 + Missense_Mutation SNP G G C TCGA-FD-A3N5-01A-11D-A21A-08 TCGA-FD-A3N5-10A-01D-A21A-08 g.chr17:7788214G>C c.90G>C c.(88-90)gaG>gaC p.E30D BLCA 17 7792337 7792337 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr17:7792337G>A c.19G>A c.(19-21)Gtg>Atg p.V7M BLCA 17 7793025 7793025 + Missense_Mutation SNP G G C TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr17:7793025G>C c.144G>C c.(142-144)aaG>aaC p.K48N BLCA 17 7793898 7793898 + Nonsense_Mutation SNP G G T TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr17:7793898G>T c.223G>T c.(223-225)Gag>Tag p.E75* BLCA 17 7797534 7797534 + Silent SNP C C T TCGA-DK-A3IS-01A-21D-A21A-08 TCGA-DK-A3IS-10A-01D-A21A-08 g.chr17:7797534C>T c.1026C>T c.(1024-1026)gtC>gtT p.V342V BLCA 17 7797579 7797579 + Missense_Mutation SNP G G T TCGA-K4-A3WV-01A-11D-A22Z-08 TCGA-K4-A3WV-10A-01D-A22Z-08 g.chr17:7797579G>T c.1071G>T c.(1069-1071)aaG>aaT p.K357N BLCA 17 7800409 7800409 + Missense_Mutation SNP C C G TCGA-GV-A3QI-01A-11D-A21Z-08 TCGA-GV-A3QI-10A-01D-A21Z-08 g.chr17:7800409C>G c.1716C>G c.(1714-1716)atC>atG p.I572M BLCA 17 7801368 7801368 + Missense_Mutation SNP G G A TCGA-K4-A4AC-01A-21D-A26M-08 TCGA-K4-A4AC-10A-01D-A26K-08 g.chr17:7801368G>A c.1999G>A c.(1999-2001)Gaa>Aaa p.E667K BLCA 17 7802344 7802344 + Missense_Mutation SNP G G A TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr17:7802344G>A c.2167G>A c.(2167-2169)Gag>Aag p.E723K BLCA 17 7802505 7802505 + Silent SNP C C T TCGA-DK-A3IL-01A-11D-A20D-08 TCGA-DK-A3IL-10A-01D-A20D-08 g.chr17:7802505C>T c.2328C>T c.(2326-2328)taC>taT p.Y776Y BLCA 17 7804619 7804619 + Missense_Mutation SNP G G A TCGA-GU-A42P-01A-11D-A23U-08 TCGA-GU-A42P-10A-01D-A23U-08 g.chr17:7804619G>A c.3178G>A c.(3178-3180)Ggg>Agg p.G1060R BLCA 17 7804619 7804619 + Missense_Mutation SNP G G C TCGA-KQ-A41O-01A-12D-A34U-08 TCGA-KQ-A41O-10D-01D-A34X-08 g.chr17:7804619G>C c.3178G>C c.(3178-3180)Ggg>Cgg p.G1060R BLCA 17 7804636 7804636 + Silent SNP C C G TCGA-R3-A69X-01A-22D-A30E-08 TCGA-R3-A69X-10A-01D-A30H-08 g.chr17:7804636C>G c.3195C>G c.(3193-3195)ctC>ctG p.L1065L BLCA 17 7806657 7806657 + Missense_Mutation SNP C C T TCGA-CF-A1HS-01A-11D-A13W-08 TCGA-CF-A1HS-10A-01D-A13W-08 g.chr17:7806657C>T c.3563C>T c.(3562-3564)gCg>gTg p.A1188V BLCA 17 7808955 7808955 + Missense_Mutation SNP G G C TCGA-FD-A3SR-01A-11D-A22Z-08 TCGA-FD-A3SR-10A-01D-A22Z-08 g.chr17:7808955G>C c.4155G>C c.(4153-4155)aaG>aaC p.K1385N BLCA 17 7809948 7809948 + Missense_Mutation SNP C C G TCGA-E7-A6ME-01A-22D-A32B-08 TCGA-E7-A6ME-10B-01D-A329-08 g.chr17:7809948C>G c.4436C>G c.(4435-4437)cCt>cGt p.P1479R BLCA 17 7810216 7810216 + Silent SNP T T C TCGA-E7-A519-01A-11D-A26M-08 TCGA-E7-A519-10A-01D-A26K-08 g.chr17:7810216T>C c.4533T>C c.(4531-4533)cgT>cgC p.R1511R BLCA 17 7810488 7810488 + Missense_Mutation SNP C C G TCGA-PQ-A6FN-01A-11D-A31L-08 TCGA-PQ-A6FN-10A-01D-A31J-08 g.chr17:7810488C>G c.4711C>G c.(4711-4713)Ctt>Gtt p.L1571V BLCA 17 7812116 7812116 + Missense_Mutation SNP T T A TCGA-ZF-AA56-01A-31D-A391-08 TCGA-ZF-AA56-10A-01D-A394-08 g.chr17:7812116T>A c.5363T>A c.(5362-5364)aTg>aAg p.M1788K BLCA 17 7812129 7812129 + Silent SNP C C T TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr17:7812129C>T c.5376C>T c.(5374-5376)ttC>ttT p.F1792F BRCA 17 7788214 7788214 + Missense_Mutation SNP G G C TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr17:7788214G>C c.90G>C c.(88-90)gaG>gaC p.E30D BRCA 17 7796626 7796626 + Missense_Mutation SNP C C G TCGA-E2-A1IN-01A-11D-A13L-09 TCGA-E2-A1IN-10A-01D-A188-09 g.chr17:7796626C>G c.532C>G c.(532-534)Cct>Gct p.P178A BRCA 17 7796726 7796726 + Missense_Mutation SNP C C T TCGA-AR-A1AI-01A-11D-A12Q-09 TCGA-AR-A1AI-10A-01D-A12Q-09 g.chr17:7796726C>T c.632C>T c.(631-633)gCg>gTg p.A211V BRCA 17 7796758 7796758 + Missense_Mutation SNP G G C TCGA-A8-A0AB-01A-11W-A050-09 TCGA-A8-A0AB-10A-01W-A055-09 g.chr17:7796758G>C c.664G>C c.(664-666)Gag>Cag p.E222Q BRCA 17 7797876 7797876 + Missense_Mutation SNP G G C TCGA-BH-A1FC-01A-11D-A13L-09 TCGA-BH-A1FC-11A-32D-A188-09 g.chr17:7797876G>C c.1219G>C c.(1219-1221)Gat>Cat p.D407H BRCA 17 7798780 7798780 + Nonsense_Mutation SNP C C T TCGA-BH-A0BP-01A-11D-A10Y-09 TCGA-BH-A0BP-10A-01D-A110-09 g.chr17:7798780C>T c.1627C>T c.(1627-1629)Caa>Taa p.Q543* BRCA 17 7800445 7800445 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr17:7800445G>T c.1752G>T c.(1750-1752)aaG>aaT p.K584N BRCA 17 7800561 7800561 + Missense_Mutation SNP G G A TCGA-A2-A0YM-01A-11D-A10G-09 TCGA-A2-A0YM-10A-01D-A10G-09 g.chr17:7800561G>A c.1868G>A c.(1867-1869)cGt>cAt p.R623H BRCA 17 7801884 7801884 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr17:7801884G>A c.2122G>A c.(2122-2124)Gat>Aat p.D708N BRCA 17 7802461 7802461 + Missense_Mutation SNP G G A TCGA-AC-A3W6-01A-12D-A228-09 TCGA-AC-A3W6-10A-01D-A22A-09 g.chr17:7802461G>A c.2284G>A c.(2284-2286)Gag>Aag p.E762K BRCA 17 7808966 7808966 + Frame_Shift_Del DEL G G - TCGA-D8-A1XJ-01A-11D-A14K-09 TCGA-D8-A1XJ-10A-01W-A16I-09 g.chr17:7808966delG c.4166delG c.(4165-4167)cggfs p.R1389fs BRCA 17 7808967 7808967 + Silent SNP G G A TCGA-BH-A2L8-01A-11D-A18P-09 TCGA-BH-A2L8-10A-01D-A18P-09 g.chr17:7808967G>A c.4167G>A c.(4165-4167)cgG>cgA p.R1389R BRCA 17 7809182 7809182 + Silent SNP C C A TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr17:7809182C>A c.4233C>A c.(4231-4233)ggC>ggA p.G1411G BRCA 17 7809929 7809929 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr17:7809929A>C c.4417A>C c.(4417-4419)Acc>Ccc p.T1473P BRCA 17 7809938 7809938 + Missense_Mutation SNP G G A TCGA-BH-A2L8-01A-11D-A18P-09 TCGA-BH-A2L8-10A-01D-A18P-09 g.chr17:7809938G>A c.4426G>A c.(4426-4428)Gat>Aat p.D1476N BRCA 17 7812031 7812031 + Missense_Mutation SNP T T G TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr17:7812031T>G c.5278T>G c.(5278-5280)Tgg>Ggg p.W1760G CESC 17 7792996 7792996 + Missense_Mutation SNP C C G TCGA-EK-A2RN-01A-12D-A20U-09 TCGA-EK-A2RN-10A-01D-A20U-09 g.chr17:7792996C>G c.115C>G c.(115-117)Cgg>Ggg p.R39G CESC 17 7802458 7802458 + Missense_Mutation SNP G G A TCGA-UC-A7PF-01A-11D-A351-09 TCGA-UC-A7PF-11A-31D-A351-09 g.chr17:7802458G>A c.2281G>A c.(2281-2283)Gat>Aat p.D761N CESC 17 7802461 7802461 + Missense_Mutation SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr17:7802461G>A c.2284G>A c.(2284-2286)Gag>Aag p.E762K CESC 17 7803244 7803244 + Missense_Mutation SNP C C G TCGA-C5-A1BQ-01C-11D-A20U-09 TCGA-C5-A1BQ-10A-01D-A20U-09 g.chr17:7803244C>G c.2575C>G c.(2575-2577)Ctg>Gtg p.L859V CESC 17 7804021 7804021 + Missense_Mutation SNP G G A TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr17:7804021G>A c.2950G>A c.(2950-2952)Gtt>Att p.V984I CESC 17 7804195 7804195 + Nonsense_Mutation SNP C C T TCGA-DS-A0VM-01A-11D-A10S-08 TCGA-DS-A0VM-10A-01D-A10S-08 g.chr17:7804195C>T c.3004C>T c.(3004-3006)Cga>Tga p.R1002* CESC 17 7807175 7807175 + Missense_Mutation SNP C C A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr17:7807175C>A c.3760C>A c.(3760-3762)Cat>Aat p.H1254N CESC 17 7810527 7810527 + Missense_Mutation SNP G G C TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr17:7810527G>C c.4750G>C c.(4750-4752)Gag>Cag p.E1584Q CESC 17 7814210 7814210 + Missense_Mutation SNP G G A TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr17:7814210G>A c.5800G>A c.(5800-5802)Gcc>Acc p.A1934T CHOL 17 7798770 7798770 + Silent SNP C C T TCGA-W5-AA31-01A-11D-A417-09 TCGA-W5-AA31-10A-01D-A41A-09 g.chr17:7798770C>T c.1617C>T c.(1615-1617)ccC>ccT p.P539P COAD 17 7793077 7793077 + Nonsense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr17:7793077C>T c.196C>T c.(196-198)Cga>Tga p.R66* COAD 17 7793078 7793078 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr17:7793078G>A c.197G>A c.(196-198)cGa>cAa p.R66Q COAD 17 7794001 7794001 + Frame_Shift_Del DEL A A - TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr17:7794001delA c.326delA c.(325-327)gaafs p.E109fs COAD 17 7794343 7794343 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr17:7794343A>C c.470A>C c.(469-471)cAc>cCc p.H157P COAD 17 7796733 7796733 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr17:7796733G>A c.639G>A c.(637-639)gcG>gcA p.A213A COAD 17 7797756 7797756 + Frame_Shift_Del DEL G G - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr17:7797756delG c.1099delG c.(1099-1101)gggfs p.G367fs COAD 17 7797864 7797864 + Missense_Mutation SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr17:7797864C>A c.1207C>A c.(1207-1209)Ctc>Atc p.L403I COAD 17 7798702 7798703 + Frame_Shift_Ins INS - - G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr17:7798702_7798703insG c.1549_1550insG c.(1549-1551)tggfs p.W517fs COAD 17 7798703 7798703 + Frame_Shift_Del DEL G G - TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr17:7798703delG c.1550delG c.(1549-1551)tggfs p.W517fs COAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs COAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs COAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs COAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs COAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs COAD 17 7801400 7801400 + Missense_Mutation SNP G G T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr17:7801400G>T c.2031G>T c.(2029-2031)aaG>aaT p.K677N COAD 17 7801872 7801872 + Missense_Mutation SNP G G A TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr17:7801872G>A c.2110G>A c.(2110-2112)Gag>Aag p.E704K COAD 17 7802466 7802466 + Frame_Shift_Del DEL G G - TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr17:7802466delG c.2289delG c.(2287-2289)atgfs p.M763fs COAD 17 7802694 7802694 + Missense_Mutation SNP C C A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr17:7802694C>A c.2377C>A c.(2377-2379)Cca>Aca p.P793T COAD 17 7803967 7803967 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr17:7803967C>T c.2896C>T c.(2896-2898)Cgg>Tgg p.R966W COAD 17 7806657 7806657 + Missense_Mutation SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr17:7806657C>T c.3563C>T c.(3562-3564)gCg>gTg p.A1188V COAD 17 7806730 7806730 + Silent SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr17:7806730G>A c.3636G>A c.(3634-3636)ggG>ggA p.G1212G COAD 17 7807153 7807153 + Missense_Mutation SNP G G T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr17:7807153G>T c.3738G>T c.(3736-3738)aaG>aaT p.K1246N COAD 17 7808983 7808983 + Missense_Mutation SNP C C A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:7808983C>A c.4183C>A c.(4183-4185)Cca>Aca p.P1395T COAD 17 7810227 7810227 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr17:7810227C>T c.4544C>T c.(4543-4545)cCg>cTg p.P1515L COAD 17 7810508 7810508 + Silent SNP A A G TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr17:7810508A>G c.4731A>G c.(4729-4731)gaA>gaG p.E1577E COAD 17 7810671 7810671 + Splice_Site SNP G G A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr17:7810671G>A c.4789G>A c.(4789-4791)Gct>Act p.A1597T COAD 17 7812504 7812504 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr17:7812504C>T c.5438C>T c.(5437-5439)gCg>gTg p.A1813V COAD 17 7813746 7813746 + Splice_Site SNP T T C TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:7813746T>C c.5591T>C c.(5590-5592)gTt>gCt p.V1864A COAD 17 7814170 7814170 + Nonsense_Mutation SNP C C A TCGA-F4-6854-01A-11D-1924-10 TCGA-F4-6854-10A-01D-1924-10 g.chr17:7814170C>A c.5760C>A c.(5758-5760)taC>taA p.Y1920* COAD 17 7814196 7814196 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr17:7814196C>T c.5786C>T c.(5785-5787)cCg>cTg p.P1929L COAD 17 7814810 7814812 + In_Frame_Del DEL GAA GAA - TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr17:7814810_7814812delGAA c.5910_5912delGAA c.(5908-5913)gtgaag>gtg p.K1972del COADREAD 17 7793077 7793077 + Nonsense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr17:7793077C>T c.196C>T c.(196-198)Cga>Tga p.R66* COADREAD 17 7793078 7793078 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr17:7793078G>A c.197G>A c.(196-198)cGa>cAa p.R66Q COADREAD 17 7794001 7794001 + Frame_Shift_Del DEL A A - TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr17:7794001delA c.326delA c.(325-327)gaafs p.E109fs COADREAD 17 7794343 7794343 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr17:7794343A>C c.470A>C c.(469-471)cAc>cCc p.H157P COADREAD 17 7796733 7796733 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr17:7796733G>A c.639G>A c.(637-639)gcG>gcA p.A213A COADREAD 17 7797756 7797756 + Frame_Shift_Del DEL G G - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr17:7797756delG c.1099delG c.(1099-1101)gggfs p.G367fs COADREAD 17 7797864 7797864 + Missense_Mutation SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr17:7797864C>A c.1207C>A c.(1207-1209)Ctc>Atc p.L403I COADREAD 17 7798702 7798703 + Frame_Shift_Ins INS - - G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr17:7798702_7798703insG c.1549_1550insG c.(1549-1551)tggfs p.W517fs COADREAD 17 7798703 7798703 + Frame_Shift_Del DEL G G - TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr17:7798703delG c.1550delG c.(1549-1551)tggfs p.W517fs COADREAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs COADREAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs COADREAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs COADREAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs COADREAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs COADREAD 17 7801400 7801400 + Missense_Mutation SNP G G T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr17:7801400G>T c.2031G>T c.(2029-2031)aaG>aaT p.K677N COADREAD 17 7801872 7801872 + Missense_Mutation SNP G G A TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr17:7801872G>A c.2110G>A c.(2110-2112)Gag>Aag p.E704K COADREAD 17 7802466 7802466 + Frame_Shift_Del DEL G G - TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr17:7802466delG c.2289delG c.(2287-2289)atgfs p.M763fs COADREAD 17 7802694 7802694 + Missense_Mutation SNP C C A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr17:7802694C>A c.2377C>A c.(2377-2379)Cca>Aca p.P793T COADREAD 17 7803967 7803967 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr17:7803967C>T c.2896C>T c.(2896-2898)Cgg>Tgg p.R966W COADREAD 17 7804220 7804220 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr17:7804220G>A c.3029G>A c.(3028-3030)cGa>cAa p.R1010Q COADREAD 17 7806657 7806657 + Missense_Mutation SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr17:7806657C>T c.3563C>T c.(3562-3564)gCg>gTg p.A1188V COADREAD 17 7806730 7806730 + Silent SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr17:7806730G>A c.3636G>A c.(3634-3636)ggG>ggA p.G1212G COADREAD 17 7807153 7807153 + Missense_Mutation SNP G G T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr17:7807153G>T c.3738G>T c.(3736-3738)aaG>aaT p.K1246N COADREAD 17 7808983 7808983 + Missense_Mutation SNP C C A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:7808983C>A c.4183C>A c.(4183-4185)Cca>Aca p.P1395T COADREAD 17 7810227 7810227 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr17:7810227C>T c.4544C>T c.(4543-4545)cCg>cTg p.P1515L COADREAD 17 7810508 7810508 + Silent SNP A A G TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr17:7810508A>G c.4731A>G c.(4729-4731)gaA>gaG p.E1577E COADREAD 17 7810508 7810508 + Silent SNP A A G TCGA-DY-A1H8-01A-21D-A152-10 TCGA-DY-A1H8-10A-01D-A152-10 g.chr17:7810508A>G c.4731A>G c.(4729-4731)gaA>gaG p.E1577E COADREAD 17 7810671 7810671 + Splice_Site SNP G G A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr17:7810671G>A c.4789G>A c.(4789-4791)Gct>Act p.A1597T COADREAD 17 7811765 7811765 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr17:7811765C>T c.5198C>T c.(5197-5199)tCg>tTg p.S1733L COADREAD 17 7812504 7812504 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr17:7812504C>T c.5438C>T c.(5437-5439)gCg>gTg p.A1813V COADREAD 17 7813746 7813746 + Splice_Site SNP T T C TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:7813746T>C c.5591T>C c.(5590-5592)gTt>gCt p.V1864A COADREAD 17 7814170 7814170 + Nonsense_Mutation SNP C C A TCGA-F4-6854-01A-11D-1924-10 TCGA-F4-6854-10A-01D-1924-10 g.chr17:7814170C>A c.5760C>A c.(5758-5760)taC>taA p.Y1920* COADREAD 17 7814196 7814196 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr17:7814196C>T c.5786C>T c.(5785-5787)cCg>cTg p.P1929L COADREAD 17 7814810 7814812 + In_Frame_Del DEL GAA GAA - TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr17:7814810_7814812delGAA c.5910_5912delGAA c.(5908-5913)gtgaag>gtg p.K1972del DLBC 17 7792326 7792326 + Missense_Mutation SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr17:7792326C>T c.8C>T c.(7-9)gCg>gTg p.A3V DLBC 17 7796805 7796805 + Silent SNP C C G TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr17:7796805C>G c.711C>G c.(709-711)tcC>tcG p.S237S DLBC 17 7798425 7798425 + Missense_Mutation SNP T T C TCGA-GS-A9TY-01A-11D-A38X-10 TCGA-GS-A9TY-10A-01D-A38X-10 g.chr17:7798425T>C c.1460T>C c.(1459-1461)cTg>cCg p.L487P DLBC 17 7807904 7807904 + Missense_Mutation SNP G G A TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr17:7807904G>A c.4039G>A c.(4039-4041)Gtt>Att p.V1347I ESCA 17 7796665 7796665 + Missense_Mutation SNP G G C TCGA-L5-A8NG-01A-11D-A37C-09 TCGA-L5-A8NG-11A-11D-A37F-09 g.chr17:7796665G>C c.571G>C c.(571-573)Gcc>Ccc p.A191P ESCA 17 7797811 7797811 + Missense_Mutation SNP G G A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr17:7797811G>A c.1154G>A c.(1153-1155)tGc>tAc p.C385Y ESCA 17 7797888 7797888 + Missense_Mutation SNP G G T TCGA-R6-A6L4-01A-11D-A31U-09 TCGA-R6-A6L4-10A-01D-A31U-09 g.chr17:7797888G>T c.1231G>T c.(1231-1233)Gac>Tac p.D411Y ESCA 17 7798284 7798284 + Missense_Mutation SNP A A G TCGA-L5-A4OU-01A-11D-A28B-09 TCGA-L5-A4OU-11A-11D-A28E-09 g.chr17:7798284A>G c.1319A>G c.(1318-1320)gAa>gGa p.E440G ESCA 17 7798335 7798335 + Missense_Mutation SNP A A T TCGA-L5-A8NV-01A-11D-A37C-09 TCGA-L5-A8NV-11A-11D-A37F-09 g.chr17:7798335A>T c.1370A>T c.(1369-1371)gAg>gTg p.E457V ESCA 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs ESCA 17 7801849 7801849 + Missense_Mutation SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr17:7801849G>A c.2087G>A c.(2086-2088)cGc>cAc p.R696H ESCA 17 7803295 7803295 + Missense_Mutation SNP C C T TCGA-LN-A5U7-01A-11D-A31U-09 TCGA-LN-A5U7-10A-01D-A31U-09 g.chr17:7803295C>T c.2626C>T c.(2626-2628)Cgc>Tgc p.R876C ESCA 17 7807298 7807300 + In_Frame_Del DEL GAA GAA - TCGA-S8-A6BV-01A-21D-A31U-09 TCGA-S8-A6BV-10A-01D-A31U-09 g.chr17:7807298_7807300delGAA c.3883_3885delGAA c.(3883-3885)gaadel p.E1296del ESCA 17 7809966 7809966 + Missense_Mutation SNP G G A TCGA-LN-A49X-01A-31D-A27G-09 TCGA-LN-A49X-10A-01D-A27G-09 g.chr17:7809966G>A c.4454G>A c.(4453-4455)cGc>cAc p.R1485H GBM 17 7811263 7811263 + Missense_Mutation SNP G G A TCGA-28-5216-01A-01D-1486-08 TCGA-28-5216-10A-01D-1486-08 g.chr17:7811263G>A c.5078G>A c.(5077-5079)cGg>cAg p.R1693Q GBMLGG 17 7802784 7802784 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:7802784C>T c.2467C>T c.(2467-2469)Cgg>Tgg p.R823W GBMLGG 17 7803351 7803351 + Splice_Site SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:7803351G>T c.2682G>T c.(2680-2682)aaG>aaT p.K894N GBMLGG 17 7811263 7811263 + Missense_Mutation SNP G G A TCGA-28-5216-01A-01D-1486-08 TCGA-28-5216-10A-01D-1486-08 g.chr17:7811263G>A c.5078G>A c.(5077-5079)cGg>cAg p.R1693Q GBMLGG 17 7814264 7814264 + Nonsense_Mutation SNP C C T TCGA-E1-A7YI-01A-11D-A34A-08 TCGA-E1-A7YI-10A-01D-A34A-08 g.chr17:7814264C>T c.5854C>T c.(5854-5856)Cag>Tag p.Q1952* HNSC 17 7793095 7793095 + Splice_Site SNP G G T TCGA-UF-A7JO-01A-11D-A34J-08 TCGA-UF-A7JO-10A-01D-A34M-08 g.chr17:7793095G>T c.e2+1 HNSC 17 7794330 7794330 + Missense_Mutation SNP G G A TCGA-CV-6936-01A-11D-1912-08 TCGA-CV-6936-10A-01D-1912-08 g.chr17:7794330G>A c.457G>A c.(457-459)Gag>Aag p.E153K HNSC 17 7797825 7797826 + Frame_Shift_Ins INS - - A TCGA-CN-6024-01A-11D-1683-08 TCGA-CN-6024-10A-01D-1683-08 g.chr17:7797825_7797826insA c.1168_1169insA c.(1168-1170)gaafs p.E390fs HNSC 17 7797866 7797866 + Silent SNP C C T TCGA-P3-A6T3-01A-11D-A34J-08 TCGA-P3-A6T3-10A-01D-A34M-08 g.chr17:7797866C>T c.1209C>T c.(1207-1209)ctC>ctT p.L403L HNSC 17 7800404 7800404 + Missense_Mutation SNP G G C TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr17:7800404G>C c.1711G>C c.(1711-1713)Gaa>Caa p.E571Q HNSC 17 7800529 7800529 + Silent SNP G G A TCGA-IQ-7630-01A-11D-2078-08 TCGA-IQ-7630-10A-01D-2078-08 g.chr17:7800529G>A c.1836G>A c.(1834-1836)ccG>ccA p.P612P HNSC 17 7802768 7802768 + Silent SNP G G A TCGA-CV-7263-01A-11D-2012-08 TCGA-CV-7263-10A-01D-2013-08 g.chr17:7802768G>A c.2451G>A c.(2449-2451)acG>acA p.T817T HNSC 17 7806008 7806008 + Silent SNP G G A TCGA-CV-5441-01A-01D-1512-08 TCGA-CV-5441-11A-01D-1512-08 g.chr17:7806008G>A c.3333G>A c.(3331-3333)acG>acA p.T1111T HNSC 17 7806800 7806800 + Missense_Mutation SNP C C G TCGA-DQ-5630-01A-01D-1870-08 TCGA-DQ-5630-10A-01D-1870-08 g.chr17:7806800C>G c.3706C>G c.(3706-3708)Cta>Gta p.L1236V HNSC 17 7807798 7807798 + Missense_Mutation SNP G G C TCGA-TN-A7HJ-01A-12D-A34J-08 TCGA-TN-A7HJ-10A-01D-A34M-08 g.chr17:7807798G>C c.3933G>C c.(3931-3933)gaG>gaC p.E1311D HNSC 17 7808456 7808456 + Missense_Mutation SNP G G C TCGA-CN-A6V1-01A-12D-A34J-08 TCGA-CN-A6V1-10B-01D-A34M-08 g.chr17:7808456G>C c.4111G>C c.(4111-4113)Gat>Cat p.D1371H HNSC 17 7809901 7809901 + Silent SNP G G T TCGA-CV-A6JM-01A-11D-A31L-08 TCGA-CV-A6JM-10A-01D-A31J-08 g.chr17:7809901G>T c.4389G>T c.(4387-4389)ctG>ctT p.L1463L HNSC 17 7810280 7810280 + Missense_Mutation SNP T T C TCGA-CN-5373-01A-01D-1434-08 TCGA-CN-5373-10A-01D-1434-08 g.chr17:7810280T>C c.4597T>C c.(4597-4599)Tct>Cct p.S1533P HNSC 17 7810759 7810759 + Missense_Mutation SNP G G C TCGA-CR-6484-01A-11D-1870-08 TCGA-CR-6484-10A-01D-1870-08 g.chr17:7810759G>C c.4877G>C c.(4876-4878)gGa>gCa p.G1626A HNSC 17 7812049 7812049 + Missense_Mutation SNP G G T TCGA-BA-4077-01B-01D-1434-08 TCGA-BA-4077-10A-01D-1434-08 g.chr17:7812049G>T c.5296G>T c.(5296-5298)Gat>Tat p.D1766Y HNSC 17 7813774 7813774 + Silent SNP C C T TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr17:7813774C>T c.5619C>T c.(5617-5619)agC>agT p.S1873S HNSC 17 7814165 7814165 + Splice_Site SNP G G A TCGA-UF-A719-01A-12D-A34J-08 TCGA-UF-A719-10A-01D-A34M-08 g.chr17:7814165G>A c.5755G>A c.(5755-5757)Gcc>Acc p.A1919T HNSC 17 7814256 7814256 + Missense_Mutation SNP A A G TCGA-CR-7370-01A-11D-2129-08 TCGA-CR-7370-10A-01D-2129-08 g.chr17:7814256A>G c.5846A>G c.(5845-5847)aAt>aGt p.N1949S KICH 17 7793910 7793910 + Missense_Mutation SNP T T C TCGA-KN-8425-01A-11D-2310-10 TCGA-KN-8425-11A-01D-2310-10 g.chr17:7793910T>C c.235T>C c.(235-237)Tct>Cct p.S79P KICH 17 7814222 7814222 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr17:7814222G>A c.5812G>A c.(5812-5814)Gca>Aca p.A1938T KIPAN 17 7793910 7793910 + Missense_Mutation SNP T T C TCGA-KN-8425-01A-11D-2310-10 TCGA-KN-8425-11A-01D-2310-10 g.chr17:7793910T>C c.235T>C c.(235-237)Tct>Cct p.S79P KIPAN 17 7794342 7794342 + Missense_Mutation SNP C C G TCGA-PJ-A5Z8-01A-11D-A28G-10 TCGA-PJ-A5Z8-10A-01D-A28G-10 g.chr17:7794342C>G c.469C>G c.(469-471)Cac>Gac p.H157D KIPAN 17 7797756 7797756 + Missense_Mutation SNP G G A TCGA-B0-4712-01A-01D-1501-10 TCGA-B0-4712-11A-02D-1501-10 g.chr17:7797756G>A c.1099G>A c.(1099-1101)Ggg>Agg p.G367R KIPAN 17 7801818 7801818 + Missense_Mutation SNP C C A TCGA-B0-5400-01A-01D-1501-10 TCGA-B0-5400-11A-01D-1501-10 g.chr17:7801818C>A c.2056C>A c.(2056-2058)Cta>Ata p.L686I KIPAN 17 7802423 7802423 + Missense_Mutation SNP T T A TCGA-CJ-4886-01A-01D-1373-10 TCGA-CJ-4886-11A-01D-1373-10 g.chr17:7802423T>A c.2246T>A c.(2245-2247)tTc>tAc p.F749Y KIPAN 17 7805978 7805978 + Nonsense_Mutation SNP C C A TCGA-AK-3451-01A-02D-1251-10 TCGA-AK-3451-10A-01D-1251-10 g.chr17:7805978C>A c.3303C>A c.(3301-3303)taC>taA p.Y1101* KIPAN 17 7806304 7806304 + Silent SNP C C T TCGA-BP-4961-01A-01D-1462-08 TCGA-BP-4961-11A-01D-1462-08 g.chr17:7806304C>T c.3420C>T c.(3418-3420)ggC>ggT p.G1140G KIPAN 17 7814222 7814222 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr17:7814222G>A c.5812G>A c.(5812-5814)Gca>Aca p.A1938T KIRC 17 7797756 7797756 + Missense_Mutation SNP G G A TCGA-B0-4712-01A-01D-1501-10 TCGA-B0-4712-11A-02D-1501-10 g.chr17:7797756G>A c.1099G>A c.(1099-1101)Ggg>Agg p.G367R KIRC 17 7801818 7801818 + Missense_Mutation SNP C C A TCGA-B0-5400-01A-01D-1501-10 TCGA-B0-5400-11A-01D-1501-10 g.chr17:7801818C>A c.2056C>A c.(2056-2058)Cta>Ata p.L686I KIRC 17 7802423 7802423 + Missense_Mutation SNP T T A TCGA-CJ-4886-01A-01D-1373-10 TCGA-CJ-4886-11A-01D-1373-10 g.chr17:7802423T>A c.2246T>A c.(2245-2247)tTc>tAc p.F749Y KIRC 17 7805978 7805978 + Nonsense_Mutation SNP C C A TCGA-AK-3451-01A-02D-1251-10 TCGA-AK-3451-10A-01D-1251-10 g.chr17:7805978C>A c.3303C>A c.(3301-3303)taC>taA p.Y1101* KIRC 17 7806304 7806304 + Silent SNP C C T TCGA-BP-4961-01A-01D-1462-08 TCGA-BP-4961-11A-01D-1462-08 g.chr17:7806304C>T c.3420C>T c.(3418-3420)ggC>ggT p.G1140G KIRP 17 7794342 7794342 + Missense_Mutation SNP C C G TCGA-PJ-A5Z8-01A-11D-A28G-10 TCGA-PJ-A5Z8-10A-01D-A28G-10 g.chr17:7794342C>G c.469C>G c.(469-471)Cac>Gac p.H157D LGG 17 7802784 7802784 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:7802784C>T c.2467C>T c.(2467-2469)Cgg>Tgg p.R823W LGG 17 7803351 7803351 + Splice_Site SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:7803351G>T c.2682G>T c.(2680-2682)aaG>aaT p.K894N LGG 17 7814264 7814264 + Nonsense_Mutation SNP C C T TCGA-E1-A7YI-01A-11D-A34A-08 TCGA-E1-A7YI-10A-01D-A34A-08 g.chr17:7814264C>T c.5854C>T c.(5854-5856)Cag>Tag p.Q1952* LIHC 17 7793914 7793914 + Missense_Mutation SNP A A G TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr17:7793914A>G c.239A>G c.(238-240)gAg>gGg p.E80G LIHC 17 7798461 7798461 + Missense_Mutation SNP G G A TCGA-WQ-A9G7-01A-11D-A36X-10 TCGA-WQ-A9G7-10A-01D-A370-10 g.chr17:7798461G>A c.1496G>A c.(1495-1497)cGa>cAa p.R499Q LIHC 17 7798720 7798720 + Missense_Mutation SNP G G A TCGA-ED-A66Y-01A-11D-A30V-10 TCGA-ED-A66Y-10A-01D-A30V-10 g.chr17:7798720G>A c.1567G>A c.(1567-1569)Gca>Aca p.A523T LIHC 17 7802659 7802659 + Splice_Site SNP A A G TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr17:7802659A>G c.e15-1 LIHC 17 7803881 7803881 + Missense_Mutation SNP T T C TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chr17:7803881T>C c.2810T>C c.(2809-2811)tTg>tCg p.L937S LIHC 17 7804563 7804563 + Splice_Site SNP A A G TCGA-DD-A39X-01A-11D-A20W-10 TCGA-DD-A39X-11A-11D-A20W-10 g.chr17:7804563A>G c.3122A>G c.(3121-3123)gAg>gGg p.E1041G LIHC 17 7806316 7806316 + Silent SNP T T C TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr17:7806316T>C c.3432T>C c.(3430-3432)aaT>aaC p.N1144N LIHC 17 7809999 7809999 + Missense_Mutation SNP C C A TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr17:7809999C>A c.4487C>A c.(4486-4488)tCt>tAt p.S1496Y LIHC 17 7810554 7810554 + Missense_Mutation SNP A A G TCGA-BC-A3KG-01A-11D-A20W-10 TCGA-BC-A3KG-10A-01D-A20W-10 g.chr17:7810554A>G c.4777A>G c.(4777-4779)Atg>Gtg p.M1593V LIHC 17 7811224 7811224 + Missense_Mutation SNP G G T TCGA-FV-A3R2-01A-11D-A22F-10 TCGA-FV-A3R2-11A-11D-A22F-10 g.chr17:7811224G>T c.5039G>T c.(5038-5040)gGt>gTt p.G1680V LUAD 17 7794055 7794055 + Missense_Mutation SNP A A C TCGA-17-Z028-01A-01W-0746-08 TCGA-17-Z028-11A-01W-0746-08 g.chr17:7794055A>C c.380A>C c.(379-381)cAa>cCa p.Q127P LUAD 17 7794291 7794291 + Missense_Mutation SNP C C G TCGA-78-7539-01A-11D-2063-08 TCGA-78-7539-10A-01D-2063-08 g.chr17:7794291C>G c.418C>G c.(418-420)Ctg>Gtg p.L140V LUAD 17 7796626 7796626 + Missense_Mutation SNP C C T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr17:7796626C>T c.532C>T c.(532-534)Cct>Tct p.P178S LUAD 17 7796813 7796813 + Missense_Mutation SNP C C T TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr17:7796813C>T c.719C>T c.(718-720)cCc>cTc p.P240L LUAD 17 7797466 7797466 + Missense_Mutation SNP G G A TCGA-MP-A4TK-01A-11D-A24P-08 TCGA-MP-A4TK-10A-01D-A24P-08 g.chr17:7797466G>A c.958G>A c.(958-960)Gag>Aag p.E320K LUAD 17 7797526 7797526 + Missense_Mutation SNP G G T TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr17:7797526G>T c.1018G>T c.(1018-1020)Ggc>Tgc p.G340C LUAD 17 7797908 7797908 + Silent SNP A A G TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr17:7797908A>G c.1251A>G c.(1249-1251)aaA>aaG p.K417K LUAD 17 7798322 7798322 + Missense_Mutation SNP G G A TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr17:7798322G>A c.1357G>A c.(1357-1359)Gat>Aat p.D453N LUAD 17 7801419 7801419 + Splice_Site SNP C C T TCGA-17-Z043-01A-01W-0746-08 TCGA-17-Z043-11A-01W-0746-08 g.chr17:7801419C>T c.2050C>T c.(2050-2052)Cga>Tga p.R684* LUAD 17 7801902 7801902 + Missense_Mutation SNP C C G TCGA-44-8119-01A-11D-2238-08 TCGA-44-8119-10A-01D-2238-08 g.chr17:7801902C>G c.2140C>G c.(2140-2142)Ccc>Gcc p.P714A LUAD 17 7802665 7802665 + Missense_Mutation SNP A A C TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr17:7802665A>C c.2348A>C c.(2347-2349)cAc>cCc p.H783P LUAD 17 7803213 7803213 + Splice_Site SNP G G A TCGA-73-4658-01A-01D-1753-08 TCGA-73-4658-11A-01D-1753-08 g.chr17:7803213G>A c.e16-1 LUAD 17 7803982 7803982 + Missense_Mutation SNP G G A TCGA-17-Z033-01A-01W-0746-08 TCGA-17-Z033-11A-01W-0746-08 g.chr17:7803982G>A c.2911G>A c.(2911-2913)Gat>Aat p.D971N LUAD 17 7803999 7803999 + Missense_Mutation SNP G G T TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chr17:7803999G>T c.2928G>T c.(2926-2928)atG>atT p.M976I LUAD 17 7806656 7806656 + Missense_Mutation SNP G G T TCGA-53-A4EZ-01A-12D-A24P-08 TCGA-53-A4EZ-10A-01D-A24P-08 g.chr17:7806656G>T c.3562G>T c.(3562-3564)Gcg>Tcg p.A1188S LUAD 17 7807240 7807240 + Silent SNP C C T TCGA-62-A471-01A-12D-A24D-08 TCGA-62-A471-10A-01D-A24F-08 g.chr17:7807240C>T c.3825C>T c.(3823-3825)gaC>gaT p.D1275D LUAD 17 7807859 7807859 + Missense_Mutation SNP G G C TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr17:7807859G>C c.3994G>C c.(3994-3996)Gac>Cac p.D1332H LUAD 17 7809241 7809241 + Missense_Mutation SNP C C G TCGA-55-8301-01A-11D-2284-08 TCGA-55-8301-10A-01D-2284-08 g.chr17:7809241C>G c.4292C>G c.(4291-4293)cCa>cGa p.P1431R LUAD 17 7809893 7809893 + Missense_Mutation SNP C C T TCGA-17-Z011-01A-01W-0746-08 TCGA-17-Z011-11A-01W-0746-08 g.chr17:7809893C>T c.4381C>T c.(4381-4383)Cgc>Tgc p.R1461C LUAD 17 7809897 7809897 + Missense_Mutation SNP A A G TCGA-05-5420-01A-01D-1625-08 TCGA-05-5420-11A-01D-1625-08 g.chr17:7809897A>G c.4385A>G c.(4384-4386)cAt>cGt p.H1462R LUAD 17 7812610 7812610 + Frame_Shift_Del DEL G G - TCGA-93-A4JQ-01A-11D-A24P-08 TCGA-93-A4JQ-10A-01D-A24P-08 g.chr17:7812610delG c.5544delG c.(5542-5544)aagfs p.K1848fs LUSC 17 7793959 7793959 + Missense_Mutation SNP A A G TCGA-39-5021-01A-01D-1441-08 TCGA-39-5021-11A-01D-1441-08 g.chr17:7793959A>G c.284A>G c.(283-285)tAt>tGt p.Y95C LUSC 17 7798755 7798755 + Silent SNP A A T TCGA-34-5231-01A-21D-1817-08 TCGA-34-5231-10A-01D-1817-08 g.chr17:7798755A>T c.1602A>T c.(1600-1602)ccA>ccT p.P534P LUSC 17 7801302 7801302 + Missense_Mutation SNP G G T TCGA-60-2724-01A-01D-1522-08 TCGA-60-2724-11A-01D-1522-08 g.chr17:7801302G>T c.1933G>T c.(1933-1935)Ggg>Tgg p.G645W LUSC 17 7802420 7802420 + Missense_Mutation SNP G G T TCGA-21-5787-01A-01D-1632-08 TCGA-21-5787-10A-01D-1632-08 g.chr17:7802420G>T c.2243G>T c.(2242-2244)cGc>cTc p.R748L LUSC 17 7806032 7806032 + Silent SNP C C A TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chr17:7806032C>A c.3357C>A c.(3355-3357)atC>atA p.I1119I OV 17 7796604 7796604 + Splice_Site SNP G G T TCGA-61-1895-01A-01W-0639-09 TCGA-61-1895-11A-01W-0639-09 g.chr17:7796604G>T c.510G>T c.(508-510)agG>agT p.R170S OV 17 7798346 7798346 + Missense_Mutation SNP G G C TCGA-24-1843-01A-01W-0639-09 TCGA-24-1843-10A-01W-0639-09 g.chr17:7798346G>C c.1381G>C c.(1381-1383)Gta>Cta p.V461L OV 17 7812541 7812541 + Silent SNP C C G TCGA-61-1900-01A-01W-0639-09 TCGA-61-1900-11A-01W-0640-09 g.chr17:7812541C>G c.5475C>G c.(5473-5475)ccC>ccG p.P1825P OV 17 7813861 7813861 + Silent SNP C C T TCGA-29-1763-01A-02W-0633-09 TCGA-29-1763-10A-01W-0633-09 g.chr17:7813861C>T c.5706C>T c.(5704-5706)agC>agT p.S1902S PAAD 17 7794054 7794055 + Frame_Shift_Ins INS - - A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7794054_7794055insA c.379_380insA c.(379-381)caafs p.Q127fs PAAD 17 7796784 7796784 + Silent SNP G G A TCGA-2L-AAQM-01A-11D-A397-08 TCGA-2L-AAQM-11A-11D-A39A-08 g.chr17:7796784G>A c.690G>A c.(688-690)tcG>tcA p.S230S PAAD 17 7797171 7797171 + Missense_Mutation SNP G G A TCGA-OE-A75W-01A-12D-A32N-08 TCGA-OE-A75W-10A-01D-A32N-08 g.chr17:7797171G>A c.842G>A c.(841-843)cGc>cAc p.R281H PAAD 17 7800528 7800528 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7800528C>A c.1835C>A c.(1834-1836)cCg>cAg p.P612Q PAAD 17 7803329 7803329 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7803329G>A c.2660G>A c.(2659-2661)cGa>cAa p.R887Q PAAD 17 7806616 7806616 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7806616C>T c.3522C>T c.(3520-3522)ggC>ggT p.G1174G PAAD 17 7810228 7810228 + Silent SNP G G A TCGA-HZ-A77O-01A-11D-A33T-08 TCGA-HZ-A77O-10A-01D-A33W-08 g.chr17:7810228G>A c.4545G>A c.(4543-4545)ccG>ccA p.P1515P PAAD 17 7810694 7810694 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7810694A>G c.4812A>G c.(4810-4812)ccA>ccG p.P1604P PAAD 17 7811277 7811277 + Nonsense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7811277C>T c.5092C>T c.(5092-5094)Cga>Tga p.R1698* PAAD 17 7812062 7812062 + Missense_Mutation SNP C C T TCGA-HZ-8637-01A-11D-2396-08 TCGA-HZ-8637-10A-01D-2396-08 g.chr17:7812062C>T c.5309C>T c.(5308-5310)gCc>gTc p.A1770V PAAD 17 7814233 7814233 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7814233G>A c.5823G>A c.(5821-5823)ggG>ggA p.G1941G PCPG 17 7802767 7802767 + Missense_Mutation SNP C C T TCGA-QT-A5XL-01A-11D-A35D-08 TCGA-QT-A5XL-10A-01D-A35B-08 g.chr17:7802767C>T c.2450C>T c.(2449-2451)aCg>aTg p.T817M PCPG 17 7803968 7803968 + Missense_Mutation SNP G G A TCGA-QR-A70U-01A-11D-A35D-08 TCGA-QR-A70U-10A-01D-A35B-08 g.chr17:7803968G>A c.2897G>A c.(2896-2898)cGg>cAg p.R966Q PRAD 17 7798765 7798765 + Frame_Shift_Del DEL C C - TCGA-V1-A8WN-01A-11D-A377-08 TCGA-V1-A8WN-10A-01D-A37A-08 g.chr17:7798765delC c.1612delC c.(1612-1614)cccfs p.P539fs PRAD 17 7801306 7801307 + Frame_Shift_Ins INS - - T TCGA-CH-5762-01A-11D-1576-08 TCGA-CH-5762-11A-01D-1576-08 g.chr17:7801306_7801307insT c.1937_1938insT c.(1936-1941)aattacfs p.Y647fs PRAD 17 7802839 7802839 + Missense_Mutation SNP G G T TCGA-HC-A9TE-01A-11D-A41K-08 TCGA-HC-A9TE-10A-01D-A41N-08 g.chr17:7802839G>T c.2522G>T c.(2521-2523)gGc>gTc p.G841V PRAD 17 7804250 7804250 + Missense_Mutation SNP A A G TCGA-Y6-A8TL-01A-21D-A377-08 TCGA-Y6-A8TL-10A-01D-A37A-08 g.chr17:7804250A>G c.3059A>G c.(3058-3060)aAt>aGt p.N1020S PRAD 17 7806622 7806622 + Silent SNP C C T TCGA-HC-7212-01A-11D-2114-08 TCGA-HC-7212-10A-01D-2115-08 g.chr17:7806622C>T c.3528C>T c.(3526-3528)gcC>gcT p.A1176A PRAD 17 7811746 7811746 + Nonsense_Mutation SNP G G T TCGA-J9-A52B-01A-11D-A26M-08 TCGA-J9-A52B-10A-01D-A26K-08 g.chr17:7811746G>T c.5179G>T c.(5179-5181)Gaa>Taa p.E1727* READ 17 7804220 7804220 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr17:7804220G>A c.3029G>A c.(3028-3030)cGa>cAa p.R1010Q READ 17 7810508 7810508 + Silent SNP A A G TCGA-DY-A1H8-01A-21D-A152-10 TCGA-DY-A1H8-10A-01D-A152-10 g.chr17:7810508A>G c.4731A>G c.(4729-4731)gaA>gaG p.E1577E READ 17 7811765 7811765 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr17:7811765C>T c.5198C>T c.(5197-5199)tCg>tTg p.S1733L SARC 17 7802799 7802799 + Nonsense_Mutation SNP G G T TCGA-DX-A7EO-01A-11D-A36J-09 TCGA-DX-A7EO-10A-01D-A36M-09 g.chr17:7802799G>T c.2482G>T c.(2482-2484)Gag>Tag p.E828* SARC 17 7810224 7810224 + Missense_Mutation SNP T T G TCGA-DX-A8BG-01A-12D-A417-09 TCGA-DX-A8BG-10B-01D-A41A-09 g.chr17:7810224T>G c.4541T>G c.(4540-4542)aTg>aGg p.M1514R SARC 17 7810227 7810227 + Missense_Mutation SNP C C T TCGA-DX-A8BG-01A-12D-A417-09 TCGA-DX-A8BG-10B-01D-A41A-09 g.chr17:7810227C>T c.4544C>T c.(4543-4545)cCg>cTg p.P1515L SARC 17 7810447 7810447 + Missense_Mutation SNP C C G TCGA-DX-A8BG-01A-12D-A417-09 TCGA-DX-A8BG-10B-01D-A41A-09 g.chr17:7810447C>G c.4670C>G c.(4669-4671)aCt>aGt p.T1557S SKCM 17 7793966 7793966 + Silent SNP C C A TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr17:7793966C>A c.291C>A c.(289-291)acC>acA p.T97T SKCM 17 7796822 7796822 + Missense_Mutation SNP C C T TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr17:7796822C>T c.728C>T c.(727-729)cCa>cTa p.P243L SKCM 17 7797852 7797852 + Missense_Mutation SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr17:7797852C>T c.1195C>T c.(1195-1197)Cgt>Tgt p.R399C SKCM 17 7798689 7798689 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr17:7798689C>T c.1536C>T c.(1534-1536)atC>atT p.I512I SKCM 17 7798840 7798840 + Missense_Mutation SNP T T C TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr17:7798840T>C c.1687T>C c.(1687-1689)Tcc>Ccc p.S563P SKCM 17 7801392 7801392 + Missense_Mutation SNP G G A TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr17:7801392G>A c.2023G>A c.(2023-2025)Gaa>Aaa p.E675K SKCM 17 7802714 7802714 + Silent SNP C C T TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr17:7802714C>T c.2397C>T c.(2395-2397)aaC>aaT p.N799N SKCM 17 7802801 7802801 + Missense_Mutation SNP G G T TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr17:7802801G>T c.2484G>T c.(2482-2484)gaG>gaT p.E828D SKCM 17 7803245 7803245 + Missense_Mutation SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr17:7803245T>C c.2576T>C c.(2575-2577)cTg>cCg p.L859P SKCM 17 7803628 7803628 + Silent SNP T T C TCGA-EB-A5SG-06A-11D-A30X-08 TCGA-EB-A5SG-10A-01D-A30X-08 g.chr17:7803628T>C c.2703T>C c.(2701-2703)ggT>ggC p.G901G SKCM 17 7803930 7803930 + Silent SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr17:7803930C>T c.2859C>T c.(2857-2859)atC>atT p.I953I SKCM 17 7806015 7806015 + Silent SNP C C T TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr17:7806015C>T c.3340C>T c.(3340-3342)Ctg>Ttg p.L1114L SKCM 17 7806292 7806292 + Silent SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr17:7806292C>T c.3408C>T c.(3406-3408)acC>acT p.T1136T SKCM 17 7806313 7806313 + Silent SNP C C T TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr17:7806313C>T c.3429C>T c.(3427-3429)atC>atT p.I1143I SKCM 17 7807809 7807809 + Missense_Mutation SNP C C T TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr17:7807809C>T c.3944C>T c.(3943-3945)cCt>cTt p.P1315L SKCM 17 7808417 7808417 + Splice_Site SNP G G A TCGA-FS-A1ZC-06A-11D-A197-08 TCGA-FS-A1ZC-10A-01D-A199-08 g.chr17:7808417G>A c.e26-1 SKCM 17 7808467 7808467 + Silent SNP C C T TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr17:7808467C>T c.4122C>T c.(4120-4122)ttC>ttT p.F1374F SKCM 17 7808467 7808467 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr17:7808467C>T c.4122C>T c.(4120-4122)ttC>ttT p.F1374F SKCM 17 7809173 7809173 + Splice_Site SNP G G A TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr17:7809173G>A c.e28-1 SKCM 17 7810332 7810332 + Missense_Mutation SNP C C T TCGA-EE-A2MK-06A-11D-A196-08 TCGA-EE-A2MK-10A-01D-A198-08 g.chr17:7810332C>T c.4649C>T c.(4648-4650)cCc>cTc p.P1550L SKCM 17 7811260 7811260 + Missense_Mutation SNP C C G TCGA-EB-A5SG-06A-11D-A30X-08 TCGA-EB-A5SG-10A-01D-A30X-08 g.chr17:7811260C>G c.5075C>G c.(5074-5076)cCa>cGa p.P1692R SKCM 17 7811272 7811272 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr17:7811272G>A c.5087G>A c.(5086-5088)gGg>gAg p.G1696E SKCM 17 7811803 7811803 + Missense_Mutation SNP T T G TCGA-EE-A2MG-06A-11D-A197-08 TCGA-EE-A2MG-10A-01D-A199-08 g.chr17:7811803T>G c.5236T>G c.(5236-5238)Tat>Gat p.Y1746D

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 17 7798702 7798702 single base substitution T G downstream_gene_variant BLCA-CN 17 7798702 7798702 single base substitution T G exon_variant BLCA-CN 17 7798702 7798702 single base substitution T G missense_variant W387G 1159T>G BLCA-CN 17 7798702 7798702 single base substitution T G missense_variant W517G 1549T>G BLCA-CN 17 7798702 7798702 single base substitution T G missense_variant W576G 1726T>G BLCA-US 17 7788146 7788148 deletion of <=200bp GAG - inframe_deletion E8 BLCA-US 17 7788146 7788148 deletion of <=200bp GAG - upstream_gene_variant BLCA-US 17 7788214 7788214 single base substitution G C missense_variant E30D 90G>C BLCA-US 17 7788214 7788214 single base substitution G C upstream_gene_variant BLCA-US 17 7792337 7792337 single base substitution G A intron_variant BLCA-US 17 7792337 7792337 single base substitution G A missense_variant V7M 19G>A BLCA-US 17 7792337 7792337 single base substitution G A upstream_gene_variant BLCA-US 17 7797534 7797534 single base substitution C T downstream_gene_variant BLCA-US 17 7797534 7797534 single base substitution C T exon_variant BLCA-US 17 7797534 7797534 single base substitution C T synonymous_variant V212V 636C>T BLCA-US 17 7797534 7797534 single base substitution C T synonymous_variant V342V 1026C>T BLCA-US 17 7797534 7797534 single base substitution C T synonymous_variant V401V 1203C>T BLCA-US 17 7797534 7797534 single base substitution C T synonymous_variant V69V 207C>T BLCA-US 17 7797534 7797534 single base substitution C T upstream_gene_variant BLCA-US 17 7797579 7797579 single base substitution G T downstream_gene_variant BLCA-US 17 7797579 7797579 single base substitution G T exon_variant BLCA-US 17 7797579 7797579 single base substitution G T missense_variant K227N 681G>T BLCA-US 17 7797579 7797579 single base substitution G T missense_variant K357N 1071G>T BLCA-US 17 7797579 7797579 single base substitution G T missense_variant K416N 1248G>T BLCA-US 17 7797579 7797579 single base substitution G T missense_variant K84N 252G>T BLCA-US 17 7797579 7797579 single base substitution G T upstream_gene_variant BLCA-US 17 7800409 7800409 single base substitution C G downstream_gene_variant BLCA-US 17 7800409 7800409 single base substitution C G missense_variant I442M 1326C>G BLCA-US 17 7800409 7800409 single base substitution C G missense_variant I572M 1716C>G BLCA-US 17 7800409 7800409 single base substitution C G missense_variant I631M 1893C>G BLCA-US 17 7802505 7802505 single base substitution C T downstream_gene_variant BLCA-US 17 7802505 7802505 single base substitution C T synonymous_variant Y776Y 2328C>T BLCA-US 17 7802505 7802505 single base substitution C T synonymous_variant Y835Y 2505C>T BLCA-US 17 7802505 7802505 single base substitution C T upstream_gene_variant BLCA-US 17 7806657 7806657 single base substitution C T missense_variant A1188V 3563C>T BLCA-US 17 7806657 7806657 single base substitution C T missense_variant A1247V 3740C>T BLCA-US 17 7806657 7806657 single base substitution C T upstream_gene_variant BLCA-US 17 7808955 7808955 single base substitution G C 3_prime_UTR_variant BLCA-US 17 7808955 7808955 single base substitution G C downstream_gene_variant BLCA-US 17 7808955 7808955 single base substitution G C exon_variant BLCA-US 17 7808955 7808955 single base substitution G C missense_variant K1385N 4155G>C BLCA-US 17 7808955 7808955 single base substitution G C missense_variant K1444N 4332G>C BLCA-US 17 7808955 7808955 single base substitution G C upstream_gene_variant BRCA-EU 17 7783527 7783527 single base substitution G A upstream_gene_variant BRCA-EU 17 7786577 7786577 single base substitution C G upstream_gene_variant BRCA-EU 17 7787214 7787214 deletion of <=200bp A - upstream_gene_variant BRCA-EU 17 7787214 7787214 single base substitution A T upstream_gene_variant BRCA-EU 17 7788497 7788497 single base substitution G A intron_variant BRCA-EU 17 7788497 7788497 single base substitution G A upstream_gene_variant BRCA-EU 17 7789532 7789532 single base substitution G C intron_variant BRCA-EU 17 7789532 7789532 single base substitution G C upstream_gene_variant BRCA-EU 17 7790040 7790040 single base substitution G C intron_variant BRCA-EU 17 7790040 7790040 single base substitution G C upstream_gene_variant BRCA-EU 17 7790592 7790592 single base substitution C A intron_variant BRCA-EU 17 7790592 7790592 single base substitution C A upstream_gene_variant BRCA-EU 17 7793237 7793237 single base substitution C A intron_variant BRCA-EU 17 7793237 7793237 single base substitution C A upstream_gene_variant BRCA-EU 17 7795617 7795617 single base substitution C A downstream_gene_variant BRCA-EU 17 7795617 7795617 single base substitution C A intron_variant BRCA-EU 17 7795617 7795617 single base substitution C A upstream_gene_variant BRCA-EU 17 7799685 7799685 single base substitution G A downstream_gene_variant BRCA-EU 17 7799685 7799685 single base substitution G A intron_variant BRCA-EU 17 7800051 7800051 single base substitution G A downstream_gene_variant BRCA-EU 17 7800051 7800051 single base substitution G A intron_variant BRCA-EU 17 7800473 7800473 single base substitution G T downstream_gene_variant BRCA-EU 17 7800473 7800473 single base substitution G T missense_variant D464Y 1390G>T BRCA-EU 17 7800473 7800473 single base substitution G T missense_variant D594Y 1780G>T BRCA-EU 17 7800473 7800473 single base substitution G T missense_variant D653Y 1957G>T BRCA-EU 17 7800586 7800586 single base substitution G A downstream_gene_variant BRCA-EU 17 7800586 7800586 single base substitution G A missense_variant M501I 1503G>A BRCA-EU 17 7800586 7800586 single base substitution G A missense_variant M631I 1893G>A BRCA-EU 17 7800586 7800586 single base substitution G A missense_variant M690I 2070G>A BRCA-EU 17 7801951 7801951 single base substitution G T downstream_gene_variant BRCA-EU 17 7801951 7801951 single base substitution G T intron_variant BRCA-EU 17 7806225 7806225 single base substitution G C downstream_gene_variant BRCA-EU 17 7806225 7806225 single base substitution G C intron_variant BRCA-EU 17 7806225 7806225 single base substitution G C upstream_gene_variant BRCA-EU 17 7807064 7807064 single base substitution G T intron_variant BRCA-EU 17 7807064 7807064 single base substitution G T upstream_gene_variant BRCA-EU 17 7807098 7807098 single base substitution T C intron_variant BRCA-EU 17 7807098 7807098 single base substitution T C upstream_gene_variant BRCA-EU 17 7807471 7807471 single base substitution C T exon_variant BRCA-EU 17 7807471 7807471 single base substitution C T intron_variant BRCA-EU 17 7807471 7807471 single base substitution C T upstream_gene_variant BRCA-EU 17 7807874 7807874 single base substitution C G 3_prime_UTR_variant BRCA-EU 17 7807874 7807874 single base substitution C G exon_variant BRCA-EU 17 7807874 7807874 single base substitution C G missense_variant L1337V 4009C>G BRCA-EU 17 7807874 7807874 single base substitution C G missense_variant L1396V 4186C>G BRCA-EU 17 7807874 7807874 single base substitution C G upstream_gene_variant BRCA-EU 17 7809710 7809710 single base substitution G A downstream_gene_variant BRCA-EU 17 7809710 7809710 single base substitution G A intron_variant BRCA-EU 17 7809710 7809710 single base substitution G A upstream_gene_variant BRCA-EU 17 7810925 7810925 single base substitution A C 3_prime_UTR_variant BRCA-EU 17 7810925 7810925 single base substitution A C downstream_gene_variant BRCA-EU 17 7810925 7810925 single base substitution A C exon_variant BRCA-EU 17 7810925 7810925 single base substitution A C intron_variant BRCA-EU 17 7810925 7810925 single base substitution A C missense_variant E1644A 4931A>C BRCA-EU 17 7810925 7810925 single base substitution A C missense_variant E1703A 5108A>C BRCA-EU 17 7810925 7810925 single base substitution A C upstream_gene_variant BRCA-EU 17 7810972 7810972 single base substitution G A 3_prime_UTR_variant BRCA-EU 17 7810972 7810972 single base substitution G A downstream_gene_variant BRCA-EU 17 7810972 7810972 single base substitution G A exon_variant BRCA-EU 17 7810972 7810972 single base substitution G A intron_variant BRCA-EU 17 7810972 7810972 single base substitution G A missense_variant E1660K 4978G>A BRCA-EU 17 7810972 7810972 single base substitution G A missense_variant E1719K 5155G>A BRCA-EU 17 7810972 7810972 single base substitution G A upstream_gene_variant BRCA-EU 17 7812558 7812558 single base substitution C T 3_prime_UTR_variant BRCA-EU 17 7812558 7812558 single base substitution C T downstream_gene_variant BRCA-EU 17 7812558 7812558 single base substitution C T missense_variant A123V 368C>T BRCA-EU 17 7812558 7812558 single base substitution C T missense_variant A150V 449C>T BRCA-EU 17 7812558 7812558 single base substitution C T missense_variant A159V 476C>T BRCA-EU 17 7812558 7812558 single base substitution C T missense_variant A1797V 5390C>T BRCA-EU 17 7812558 7812558 single base substitution C T missense_variant A1831V 5492C>T BRCA-EU 17 7812558 7812558 single base substitution C T missense_variant A1890V 5669C>T BRCA-EU 17 7812558 7812558 single base substitution C T upstream_gene_variant BRCA-EU 17 7812616 7812616 single base substitution G A 3_prime_UTR_variant BRCA-EU 17 7812616 7812616 single base substitution G A downstream_gene_variant BRCA-EU 17 7812616 7812616 single base substitution G A synonymous_variant S142S 426G>A BRCA-EU 17 7812616 7812616 single base substitution G A synonymous_variant S169S 507G>A BRCA-EU 17 7812616 7812616 single base substitution G A synonymous_variant S178S 534G>A BRCA-EU 17 7812616 7812616 single base substitution G A synonymous_variant S1816S 5448G>A BRCA-EU 17 7812616 7812616 single base substitution G A synonymous_variant S1850S 5550G>A BRCA-EU 17 7812616 7812616 single base substitution G A synonymous_variant S1909S 5727G>A BRCA-EU 17 7812616 7812616 single base substitution G A upstream_gene_variant BRCA-EU 17 7814593 7814593 single base substitution G T downstream_gene_variant BRCA-EU 17 7814593 7814593 single base substitution G T intron_variant BRCA-EU 17 7816106 7816106 deletion of <=200bp A - downstream_gene_variant BRCA-EU 17 7816200 7816204 deletion of <=200bp TTAGA - downstream_gene_variant BRCA-EU 17 7816220 7816220 single base substitution G A downstream_gene_variant BRCA-EU 17 7816270 7816270 single base substitution G T downstream_gene_variant BRCA-EU 17 7817049 7817049 single base substitution C T downstream_gene_variant BRCA-EU 17 7819163 7819163 single base substitution A G downstream_gene_variant BRCA-EU 17 7819357 7819357 single base substitution G T downstream_gene_variant BRCA-FR 17 7800586 7800586 single base substitution G A downstream_gene_variant BRCA-FR 17 7800586 7800586 single base substitution G A missense_variant M501I 1503G>A BRCA-FR 17 7800586 7800586 single base substitution G A missense_variant M631I 1893G>A BRCA-FR 17 7800586 7800586 single base substitution G A missense_variant M690I 2070G>A BRCA-FR 17 7810972 7810972 single base substitution G A 3_prime_UTR_variant BRCA-FR 17 7810972 7810972 single base substitution G A downstream_gene_variant BRCA-FR 17 7810972 7810972 single base substitution G A exon_variant BRCA-FR 17 7810972 7810972 single base substitution G A intron_variant BRCA-FR 17 7810972 7810972 single base substitution G A missense_variant E1660K 4978G>A BRCA-FR 17 7810972 7810972 single base substitution G A missense_variant E1719K 5155G>A BRCA-FR 17 7810972 7810972 single base substitution G A upstream_gene_variant BRCA-KR 17 7819034 7819034 single base substitution C T downstream_gene_variant BRCA-UK 17 7786577 7786577 single base substitution C G upstream_gene_variant BRCA-US 17 7788214 7788214 single base substitution G C missense_variant E30D 90G>C BRCA-US 17 7788214 7788214 single base substitution G C upstream_gene_variant BRCA-US 17 7793748 7793748 deletion of <=200bp A - exon_variant BRCA-US 17 7793748 7793748 deletion of <=200bp A - intron_variant BRCA-US 17 7793748 7793748 deletion of <=200bp A - upstream_gene_variant BRCA-US 17 7796626 7796626 single base substitution C G downstream_gene_variant BRCA-US 17 7796626 7796626 single base substitution C G exon_variant BRCA-US 17 7796626 7796626 single base substitution C G missense_variant P178A 532C>G BRCA-US 17 7796626 7796626 single base substitution C G missense_variant P237A 709C>G BRCA-US 17 7796626 7796626 single base substitution C G missense_variant P52A 154C>G BRCA-US 17 7796626 7796626 single base substitution C G upstream_gene_variant BRCA-US 17 7796726 7796726 single base substitution C T downstream_gene_variant BRCA-US 17 7796726 7796726 single base substitution C T exon_variant BRCA-US 17 7796726 7796726 single base substitution C T missense_variant A211V 632C>T BRCA-US 17 7796726 7796726 single base substitution C T missense_variant A270V 809C>T BRCA-US 17 7796726 7796726 single base substitution C T missense_variant A85V 254C>T BRCA-US 17 7796726 7796726 single base substitution C T upstream_gene_variant BRCA-US 17 7796758 7796758 single base substitution G C downstream_gene_variant BRCA-US 17 7796758 7796758 single base substitution G C exon_variant BRCA-US 17 7796758 7796758 single base substitution G C missense_variant E222Q 664G>C BRCA-US 17 7796758 7796758 single base substitution G C missense_variant E281Q 841G>C BRCA-US 17 7796758 7796758 single base substitution G C missense_variant E96Q 286G>C BRCA-US 17 7796758 7796758 single base substitution G C upstream_gene_variant BRCA-US 17 7797876 7797876 single base substitution G C downstream_gene_variant BRCA-US 17 7797876 7797876 single base substitution G C exon_variant BRCA-US 17 7797876 7797876 single base substitution G C missense_variant D277H 829G>C BRCA-US 17 7797876 7797876 single base substitution G C missense_variant D407H 1219G>C BRCA-US 17 7797876 7797876 single base substitution G C missense_variant D466H 1396G>C BRCA-US 17 7798764 7798764 single base substitution A C downstream_gene_variant BRCA-US 17 7798764 7798764 single base substitution A C exon_variant BRCA-US 17 7798764 7798764 single base substitution A C synonymous_variant P407P 1221A>C BRCA-US 17 7798764 7798764 single base substitution A C synonymous_variant P537P 1611A>C BRCA-US 17 7798764 7798764 single base substitution A C synonymous_variant P596P 1788A>C BRCA-US 17 7798780 7798780 single base substitution C T downstream_gene_variant BRCA-US 17 7798780 7798780 single base substitution C T exon_variant BRCA-US 17 7798780 7798780 single base substitution C T stop_gained Q413* 1237C>T BRCA-US 17 7798780 7798780 single base substitution C T stop_gained Q543* 1627C>T BRCA-US 17 7798780 7798780 single base substitution C T stop_gained Q602* 1804C>T BRCA-US 17 7800445 7800445 single base substitution G T downstream_gene_variant BRCA-US 17 7800445 7800445 single base substitution G T missense_variant K454N 1362G>T BRCA-US 17 7800445 7800445 single base substitution G T missense_variant K584N 1752G>T BRCA-US 17 7800445 7800445 single base substitution G T missense_variant K643N 1929G>T BRCA-US 17 7800561 7800561 single base substitution G A downstream_gene_variant BRCA-US 17 7800561 7800561 single base substitution G A missense_variant R493H 1478G>A BRCA-US 17 7800561 7800561 single base substitution G A missense_variant R623H 1868G>A BRCA-US 17 7800561 7800561 single base substitution G A missense_variant R682H 2045G>A BRCA-US 17 7801857 7801859 deletion of <=200bp AAG - downstream_gene_variant BRCA-US 17 7801857 7801859 deletion of <=200bp AAG - inframe_deletion K699 BRCA-US 17 7801857 7801859 deletion of <=200bp AAG - inframe_deletion K758 BRCA-US 17 7801884 7801884 single base substitution G A downstream_gene_variant BRCA-US 17 7801884 7801884 single base substitution G A missense_variant D708N 2122G>A BRCA-US 17 7801884 7801884 single base substitution G A missense_variant D767N 2299G>A BRCA-US 17 7802461 7802461 single base substitution G A downstream_gene_variant BRCA-US 17 7802461 7802461 single base substitution G A missense_variant E762K 2284G>A BRCA-US 17 7802461 7802461 single base substitution G A missense_variant E821K 2461G>A BRCA-US 17 7802461 7802461 single base substitution G A upstream_gene_variant BRCA-US 17 7808966 7808966 deletion of <=200bp G - 3_prime_UTR_variant BRCA-US 17 7808966 7808966 deletion of <=200bp G - downstream_gene_variant BRCA-US 17 7808966 7808966 deletion of <=200bp G - exon_variant BRCA-US 17 7808966 7808966 deletion of <=200bp G - frameshift_variant R1389 BRCA-US 17 7808966 7808966 deletion of <=200bp G - frameshift_variant R1448 BRCA-US 17 7808966 7808966 deletion of <=200bp G - upstream_gene_variant BRCA-US 17 7808967 7808967 single base substitution G A 3_prime_UTR_variant BRCA-US 17 7808967 7808967 single base substitution G A downstream_gene_variant BRCA-US 17 7808967 7808967 single base substitution G A exon_variant BRCA-US 17 7808967 7808967 single base substitution G A synonymous_variant R1389R 4167G>A BRCA-US 17 7808967 7808967 single base substitution G A synonymous_variant R1448R 4344G>A BRCA-US 17 7808967 7808967 single base substitution G A upstream_gene_variant BRCA-US 17 7809182 7809182 single base substitution C A 3_prime_UTR_variant BRCA-US 17 7809182 7809182 single base substitution C A downstream_gene_variant BRCA-US 17 7809182 7809182 single base substitution C A synonymous_variant G1411G 4233C>A BRCA-US 17 7809182 7809182 single base substitution C A synonymous_variant G1470G 4410C>A BRCA-US 17 7809182 7809182 single base substitution C A upstream_gene_variant BRCA-US 17 7809929 7809929 single base substitution A C 3_prime_UTR_variant BRCA-US 17 7809929 7809929 single base substitution A C downstream_gene_variant BRCA-US 17 7809929 7809929 single base substitution A C missense_variant T1473P 4417A>C BRCA-US 17 7809929 7809929 single base substitution A C missense_variant T1532P 4594A>C BRCA-US 17 7809929 7809929 single base substitution A C upstream_gene_variant BRCA-US 17 7809938 7809938 single base substitution G A 3_prime_UTR_variant BRCA-US 17 7809938 7809938 single base substitution G A downstream_gene_variant BRCA-US 17 7809938 7809938 single base substitution G A missense_variant D1476N 4426G>A BRCA-US 17 7809938 7809938 single base substitution G A missense_variant D1535N 4603G>A BRCA-US 17 7809938 7809938 single base substitution G A upstream_gene_variant BRCA-US 17 7812031 7812031 single base substitution T G 3_prime_UTR_variant BRCA-US 17 7812031 7812031 single base substitution T G downstream_gene_variant BRCA-US 17 7812031 7812031 single base substitution T G missense_variant W1726G 5176T>G BRCA-US 17 7812031 7812031 single base substitution T G missense_variant W1760G 5278T>G BRCA-US 17 7812031 7812031 single base substitution T G missense_variant W1819G 5455T>G BRCA-US 17 7812031 7812031 single base substitution T G missense_variant W52G 154T>G BRCA-US 17 7812031 7812031 single base substitution T G missense_variant W79G 235T>G BRCA-US 17 7812031 7812031 single base substitution T G missense_variant W88G 262T>G BRCA-US 17 7812031 7812031 single base substitution T G upstream_gene_variant BTCA-JP 17 7796738 7796738 single base substitution C T downstream_gene_variant BTCA-JP 17 7796738 7796738 single base substitution C T exon_variant BTCA-JP 17 7796738 7796738 single base substitution C T missense_variant A215V 644C>T BTCA-JP 17 7796738 7796738 single base substitution C T missense_variant A274V 821C>T BTCA-JP 17 7796738 7796738 single base substitution C T missense_variant A89V 266C>T BTCA-JP 17 7796738 7796738 single base substitution C T upstream_gene_variant BTCA-JP 17 7797354 7797354 single base substitution T C downstream_gene_variant BTCA-JP 17 7797354 7797354 single base substitution T C intron_variant BTCA-JP 17 7797354 7797354 single base substitution T C upstream_gene_variant BTCA-JP 17 7798765 7798765 deletion of <=200bp C - downstream_gene_variant BTCA-JP 17 7798765 7798765 deletion of <=200bp C - exon_variant BTCA-JP 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P408 BTCA-JP 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P538 BTCA-JP 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P597 BTCA-JP 17 7798765 7798765 insertion of <=200bp - CC downstream_gene_variant BTCA-JP 17 7798765 7798765 insertion of <=200bp - CC exon_variant BTCA-JP 17 7798765 7798765 insertion of <=200bp - CC frameshift_variant P408P? BTCA-JP 17 7798765 7798765 insertion of <=200bp - CC frameshift_variant P538P? BTCA-JP 17 7798765 7798765 insertion of <=200bp - CC frameshift_variant P597P? BTCA-JP 17 7798765 7798765 insertion of <=200bp - C downstream_gene_variant BTCA-JP 17 7798765 7798765 insertion of <=200bp - C exon_variant BTCA-JP 17 7798765 7798765 insertion of <=200bp - C frameshift_variant P408P? BTCA-JP 17 7798765 7798765 insertion of <=200bp - C frameshift_variant P538P? BTCA-JP 17 7798765 7798765 insertion of <=200bp - C frameshift_variant P597P? BTCA-JP 17 7801754 7801754 single base substitution A G downstream_gene_variant BTCA-JP 17 7801754 7801754 single base substitution A G intron_variant BTCA-JP 17 7803329 7803329 single base substitution G A downstream_gene_variant BTCA-JP 17 7803329 7803329 single base substitution G A missense_variant R887Q 2660G>A BTCA-JP 17 7803329 7803329 single base substitution G A missense_variant R946Q 2837G>A BTCA-JP 17 7803329 7803329 single base substitution G A upstream_gene_variant BTCA-JP 17 7804339 7804339 single base substitution G A downstream_gene_variant BTCA-JP 17 7804339 7804339 single base substitution G A intron_variant BTCA-JP 17 7804339 7804339 single base substitution G A upstream_gene_variant BTCA-JP 17 7806563 7806563 single base substitution A C intron_variant BTCA-JP 17 7806563 7806563 single base substitution A C upstream_gene_variant BTCA-JP 17 7810943 7810943 deletion of <=200bp G - 3_prime_UTR_variant BTCA-JP 17 7810943 7810943 deletion of <=200bp G - downstream_gene_variant BTCA-JP 17 7810943 7810943 deletion of <=200bp G - exon_variant BTCA-JP 17 7810943 7810943 deletion of <=200bp G - frameshift_variant R1650 BTCA-JP 17 7810943 7810943 deletion of <=200bp G - frameshift_variant R1709 BTCA-JP 17 7810943 7810943 deletion of <=200bp G - intron_variant BTCA-JP 17 7810943 7810943 deletion of <=200bp G - upstream_gene_variant BTCA-JP 17 7819163 7819163 single base substitution A T downstream_gene_variant CESC-US 17 7792996 7792996 single base substitution C G missense_variant R39G 115C>G CESC-US 17 7792996 7792996 single base substitution C G missense_variant R98G 292C>G CESC-US 17 7792996 7792996 single base substitution C G upstream_gene_variant CESC-US 17 7793747 7793747 insertion of <=200bp - A exon_variant CESC-US 17 7793747 7793747 insertion of <=200bp - A intron_variant CESC-US 17 7793747 7793747 insertion of <=200bp - A upstream_gene_variant CESC-US 17 7802458 7802458 single base substitution G A downstream_gene_variant CESC-US 17 7802458 7802458 single base substitution G A missense_variant D761N 2281G>A CESC-US 17 7802458 7802458 single base substitution G A missense_variant D820N 2458G>A CESC-US 17 7802458 7802458 single base substitution G A upstream_gene_variant CESC-US 17 7802461 7802461 single base substitution G A downstream_gene_variant CESC-US 17 7802461 7802461 single base substitution G A missense_variant E762K 2284G>A CESC-US 17 7802461 7802461 single base substitution G A missense_variant E821K 2461G>A CESC-US 17 7802461 7802461 single base substitution G A upstream_gene_variant CESC-US 17 7803244 7803244 single base substitution C G downstream_gene_variant CESC-US 17 7803244 7803244 single base substitution C G missense_variant L859V 2575C>G CESC-US 17 7803244 7803244 single base substitution C G missense_variant L918V 2752C>G CESC-US 17 7803244 7803244 single base substitution C G upstream_gene_variant CESC-US 17 7804021 7804021 single base substitution G A downstream_gene_variant CESC-US 17 7804021 7804021 single base substitution G A missense_variant V1043I 3127G>A CESC-US 17 7804021 7804021 single base substitution G A missense_variant V984I 2950G>A CESC-US 17 7804021 7804021 single base substitution G A upstream_gene_variant CESC-US 17 7804195 7804195 single base substitution C T downstream_gene_variant CESC-US 17 7804195 7804195 single base substitution C T stop_gained R1002* 3004C>T CESC-US 17 7804195 7804195 single base substitution C T stop_gained R1061* 3181C>T CESC-US 17 7804195 7804195 single base substitution C T upstream_gene_variant CESC-US 17 7807175 7807175 single base substitution C A exon_variant CESC-US 17 7807175 7807175 single base substitution C A missense_variant H1254N 3760C>A CESC-US 17 7807175 7807175 single base substitution C A missense_variant H1313N 3937C>A CESC-US 17 7807175 7807175 single base substitution C A upstream_gene_variant CESC-US 17 7810527 7810527 single base substitution G C 3_prime_UTR_variant CESC-US 17 7810527 7810527 single base substitution G C downstream_gene_variant CESC-US 17 7810527 7810527 single base substitution G C missense_variant E1584Q 4750G>C CESC-US 17 7810527 7810527 single base substitution G C missense_variant E1643Q 4927G>C CESC-US 17 7810527 7810527 single base substitution G C upstream_gene_variant CESC-US 17 7814210 7814210 single base substitution G A 3_prime_UTR_variant CESC-US 17 7814210 7814210 single base substitution G A downstream_gene_variant CESC-US 17 7814210 7814210 single base substitution G A exon_variant CESC-US 17 7814210 7814210 single base substitution G A missense_variant A1900T 5698G>A CESC-US 17 7814210 7814210 single base substitution G A missense_variant A1934T 5800G>A CESC-US 17 7814210 7814210 single base substitution G A missense_variant A1993T 5977G>A CESC-US 17 7814210 7814210 single base substitution G A missense_variant G171D 512G>A CESC-US 17 7814210 7814210 single base substitution G A missense_variant G249D 746G>A CESC-US 17 7814210 7814210 single base substitution G A missense_variant G277D 830G>A CESC-US 17 7819061 7819061 single base substitution G A downstream_gene_variant CLLE-ES 17 7818719 7818719 single base substitution C T downstream_gene_variant COAD-US 17 7792326 7792326 single base substitution C T intron_variant COAD-US 17 7792326 7792326 single base substitution C T missense_variant A3V 8C>T COAD-US 17 7792326 7792326 single base substitution C T upstream_gene_variant COAD-US 17 7793077 7793077 single base substitution C T exon_variant COAD-US 17 7793077 7793077 single base substitution C T stop_gained R125* 373C>T COAD-US 17 7793077 7793077 single base substitution C T stop_gained R66* 196C>T COAD-US 17 7793077 7793077 single base substitution C T upstream_gene_variant COAD-US 17 7793078 7793078 single base substitution G A exon_variant COAD-US 17 7793078 7793078 single base substitution G A missense_variant R125Q 374G>A COAD-US 17 7793078 7793078 single base substitution G A missense_variant R66Q 197G>A COAD-US 17 7793078 7793078 single base substitution G A upstream_gene_variant COAD-US 17 7793929 7793929 single base substitution G A downstream_gene_variant COAD-US 17 7793929 7793929 single base substitution G A exon_variant COAD-US 17 7793929 7793929 single base substitution G A missense_variant R144Q 431G>A COAD-US 17 7793929 7793929 single base substitution G A missense_variant R85Q 254G>A COAD-US 17 7793929 7793929 single base substitution G A upstream_gene_variant COAD-US 17 7797122 7797122 deletion of <=200bp G - downstream_gene_variant COAD-US 17 7797122 7797122 deletion of <=200bp G - splice_acceptor_variant COAD-US 17 7797122 7797122 deletion of <=200bp G - upstream_gene_variant COAD-US 17 7797756 7797756 deletion of <=200bp G - downstream_gene_variant COAD-US 17 7797756 7797756 deletion of <=200bp G - exon_variant COAD-US 17 7797756 7797756 deletion of <=200bp G - frameshift_variant G237 COAD-US 17 7797756 7797756 deletion of <=200bp G - frameshift_variant G367 COAD-US 17 7797756 7797756 deletion of <=200bp G - frameshift_variant G426 COAD-US 17 7797756 7797756 deletion of <=200bp G - frameshift_variant G88 COAD-US 17 7797756 7797756 deletion of <=200bp G - upstream_gene_variant COAD-US 17 7797863 7797863 single base substitution C A downstream_gene_variant COAD-US 17 7797863 7797863 single base substitution C A exon_variant COAD-US 17 7797863 7797863 single base substitution C A missense_variant H272Q 816C>A COAD-US 17 7797863 7797863 single base substitution C A missense_variant H402Q 1206C>A COAD-US 17 7797863 7797863 single base substitution C A missense_variant H461Q 1383C>A COAD-US 17 7797863 7797863 single base substitution C A upstream_gene_variant COAD-US 17 7798702 7798702 insertion of <=200bp - G downstream_gene_variant COAD-US 17 7798702 7798702 insertion of <=200bp - G exon_variant COAD-US 17 7798702 7798702 insertion of <=200bp - G frameshift_variant W387V? COAD-US 17 7798702 7798702 insertion of <=200bp - G frameshift_variant W517V? COAD-US 17 7798702 7798702 insertion of <=200bp - G frameshift_variant W576V? COAD-US 17 7798703 7798703 deletion of <=200bp G - downstream_gene_variant COAD-US 17 7798703 7798703 deletion of <=200bp G - exon_variant COAD-US 17 7798703 7798703 deletion of <=200bp G - frameshift_variant W387 COAD-US 17 7798703 7798703 deletion of <=200bp G - frameshift_variant W517 COAD-US 17 7798703 7798703 deletion of <=200bp G - frameshift_variant W576 COAD-US 17 7798765 7798765 deletion of <=200bp C - downstream_gene_variant COAD-US 17 7798765 7798765 deletion of <=200bp C - exon_variant COAD-US 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P408 COAD-US 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P538 COAD-US 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P597 COAD-US 17 7802466 7802466 deletion of <=200bp G - downstream_gene_variant COAD-US 17 7802466 7802466 deletion of <=200bp G - frameshift_variant M763 COAD-US 17 7802466 7802466 deletion of <=200bp G - frameshift_variant M822 COAD-US 17 7802466 7802466 deletion of <=200bp G - upstream_gene_variant COAD-US 17 7806657 7806657 single base substitution C T missense_variant A1188V 3563C>T COAD-US 17 7806657 7806657 single base substitution C T missense_variant A1247V 3740C>T COAD-US 17 7806657 7806657 single base substitution C T upstream_gene_variant COAD-US 17 7806730 7806730 single base substitution G A synonymous_variant G1212G 3636G>A COAD-US 17 7806730 7806730 single base substitution G A synonymous_variant G1271G 3813G>A COAD-US 17 7806730 7806730 single base substitution G A upstream_gene_variant COAD-US 17 7808983 7808983 single base substitution C A 3_prime_UTR_variant COAD-US 17 7808983 7808983 single base substitution C A downstream_gene_variant COAD-US 17 7808983 7808983 single base substitution C A missense_variant P1395T 4183C>A COAD-US 17 7808983 7808983 single base substitution C A missense_variant P1454T 4360C>A COAD-US 17 7808983 7808983 single base substitution C A upstream_gene_variant COAD-US 17 7812622 7812622 single base substitution G A 3_prime_UTR_variant COAD-US 17 7812622 7812622 single base substitution G A downstream_gene_variant COAD-US 17 7812622 7812622 single base substitution G A synonymous_variant A144A 432G>A COAD-US 17 7812622 7812622 single base substitution G A synonymous_variant A171A 513G>A COAD-US 17 7812622 7812622 single base substitution G A synonymous_variant A180A 540G>A COAD-US 17 7812622 7812622 single base substitution G A synonymous_variant A1818A 5454G>A COAD-US 17 7812622 7812622 single base substitution G A synonymous_variant A1852A 5556G>A COAD-US 17 7812622 7812622 single base substitution G A synonymous_variant A1911A 5733G>A COAD-US 17 7812622 7812622 single base substitution G A upstream_gene_variant COAD-US 17 7813746 7813746 single base substitution T C downstream_gene_variant COAD-US 17 7813746 7813746 single base substitution T C exon_variant COAD-US 17 7813746 7813746 single base substitution T C intron_variant COAD-US 17 7813746 7813746 single base substitution T C missense_variant V1830A 5489T>C COAD-US 17 7813746 7813746 single base substitution T C missense_variant V1864A 5591T>C COAD-US 17 7813746 7813746 single base substitution T C missense_variant V1923A 5768T>C COAD-US 17 7813746 7813746 single base substitution T C splice_region_variant COAD-US 17 7814170 7814170 single base substitution C A 3_prime_UTR_variant COAD-US 17 7814170 7814170 single base substitution C A downstream_gene_variant COAD-US 17 7814170 7814170 single base substitution C A exon_variant COAD-US 17 7814170 7814170 single base substitution C A missense_variant P158T 472C>A COAD-US 17 7814170 7814170 single base substitution C A missense_variant P236T 706C>A COAD-US 17 7814170 7814170 single base substitution C A missense_variant P264T 790C>A COAD-US 17 7814170 7814170 single base substitution C A stop_gained Y1886* 5658C>A COAD-US 17 7814170 7814170 single base substitution C A stop_gained Y1920* 5760C>A COAD-US 17 7814170 7814170 single base substitution C A stop_gained Y1979* 5937C>A COAD-US 17 7814196 7814196 single base substitution C T 3_prime_UTR_variant COAD-US 17 7814196 7814196 single base substitution C T downstream_gene_variant COAD-US 17 7814196 7814196 single base substitution C T exon_variant COAD-US 17 7814196 7814196 single base substitution C T missense_variant P1895L 5684C>T COAD-US 17 7814196 7814196 single base substitution C T missense_variant P1929L 5786C>T COAD-US 17 7814196 7814196 single base substitution C T missense_variant P1988L 5963C>T COAD-US 17 7814196 7814196 single base substitution C T synonymous_variant S166S 498C>T COAD-US 17 7814196 7814196 single base substitution C T synonymous_variant S244S 732C>T COAD-US 17 7814196 7814196 single base substitution C T synonymous_variant S272S 816C>T COCA-CN 17 7793078 7793078 single base substitution G A exon_variant COCA-CN 17 7793078 7793078 single base substitution G A missense_variant R125Q 374G>A COCA-CN 17 7793078 7793078 single base substitution G A missense_variant R66Q 197G>A COCA-CN 17 7793078 7793078 single base substitution G A upstream_gene_variant COCA-CN 17 7794269 7794269 single base substitution G A downstream_gene_variant COCA-CN 17 7794269 7794269 single base substitution G A synonymous_variant Q132Q 396G>A COCA-CN 17 7794269 7794269 single base substitution G A synonymous_variant Q191Q 573G>A COCA-CN 17 7794269 7794269 single base substitution G A synonymous_variant Q6Q 18G>A COCA-CN 17 7794269 7794269 single base substitution G A upstream_gene_variant COCA-CN 17 7797109 7797109 single base substitution G A downstream_gene_variant COCA-CN 17 7797109 7797109 single base substitution G A intron_variant COCA-CN 17 7797109 7797109 single base substitution G A upstream_gene_variant COCA-CN 17 7797190 7797190 single base substitution G T downstream_gene_variant COCA-CN 17 7797190 7797190 single base substitution G T exon_variant COCA-CN 17 7797190 7797190 single base substitution G T missense_variant K14N 42G>T COCA-CN 17 7797190 7797190 single base substitution G T missense_variant K161N 483G>T COCA-CN 17 7797190 7797190 single base substitution G T missense_variant K287N 861G>T COCA-CN 17 7797190 7797190 single base substitution G T missense_variant K346N 1038G>T COCA-CN 17 7797190 7797190 single base substitution G T upstream_gene_variant COCA-CN 17 7798345 7798345 single base substitution C T downstream_gene_variant COCA-CN 17 7798345 7798345 single base substitution C T exon_variant COCA-CN 17 7798345 7798345 single base substitution C T synonymous_variant R330R 990C>T COCA-CN 17 7798345 7798345 single base substitution C T synonymous_variant R460R 1380C>T COCA-CN 17 7798345 7798345 single base substitution C T synonymous_variant R519R 1557C>T COCA-CN 17 7800352 7800352 single base substitution T G downstream_gene_variant COCA-CN 17 7800352 7800352 single base substitution T G intron_variant COCA-CN 17 7800463 7800463 single base substitution C A downstream_gene_variant COCA-CN 17 7800463 7800463 single base substitution C A synonymous_variant P460P 1380C>A COCA-CN 17 7800463 7800463 single base substitution C A synonymous_variant P590P 1770C>A COCA-CN 17 7800463 7800463 single base substitution C A synonymous_variant P649P 1947C>A COCA-CN 17 7801822 7801822 single base substitution T G downstream_gene_variant COCA-CN 17 7801822 7801822 single base substitution T G missense_variant I687S 2060T>G COCA-CN 17 7801822 7801822 single base substitution T G missense_variant I746S 2237T>G COCA-CN 17 7801961 7801961 single base substitution G A downstream_gene_variant COCA-CN 17 7801961 7801961 single base substitution G A intron_variant COCA-CN 17 7802550 7802550 single base substitution C T downstream_gene_variant COCA-CN 17 7802550 7802550 single base substitution C T intron_variant COCA-CN 17 7802550 7802550 single base substitution C T upstream_gene_variant COCA-CN 17 7803395 7803395 single base substitution T C downstream_gene_variant COCA-CN 17 7803395 7803395 single base substitution T C intron_variant COCA-CN 17 7803395 7803395 single base substitution T C upstream_gene_variant COCA-CN 17 7807212 7807212 single base substitution G A exon_variant COCA-CN 17 7807212 7807212 single base substitution G A missense_variant R1266Q 3797G>A COCA-CN 17 7807212 7807212 single base substitution G A missense_variant R1325Q 3974G>A COCA-CN 17 7807212 7807212 single base substitution G A upstream_gene_variant COCA-CN 17 7807875 7807875 single base substitution T C 3_prime_UTR_variant COCA-CN 17 7807875 7807875 single base substitution T C exon_variant COCA-CN 17 7807875 7807875 single base substitution T C missense_variant L1337P 4010T>C COCA-CN 17 7807875 7807875 single base substitution T C missense_variant L1396P 4187T>C COCA-CN 17 7807875 7807875 single base substitution T C upstream_gene_variant COCA-CN 17 7808571 7808571 single base substitution A C exon_variant COCA-CN 17 7808571 7808571 single base substitution A C intron_variant COCA-CN 17 7808571 7808571 single base substitution A C upstream_gene_variant COCA-CN 17 7809271 7809271 single base substitution T G 3_prime_UTR_variant COCA-CN 17 7809271 7809271 single base substitution T G downstream_gene_variant COCA-CN 17 7809271 7809271 single base substitution T G missense_variant V1441G 4322T>G COCA-CN 17 7809271 7809271 single base substitution T G missense_variant V1500G 4499T>G COCA-CN 17 7809271 7809271 single base substitution T G upstream_gene_variant COCA-CN 17 7810040 7810040 single base substitution G T downstream_gene_variant COCA-CN 17 7810040 7810040 single base substitution G T intron_variant COCA-CN 17 7810040 7810040 single base substitution G T upstream_gene_variant COCA-CN 17 7810055 7810055 single base substitution C T downstream_gene_variant COCA-CN 17 7810055 7810055 single base substitution C T intron_variant COCA-CN 17 7810055 7810055 single base substitution C T upstream_gene_variant COCA-CN 17 7811410 7811410 single base substitution T C downstream_gene_variant COCA-CN 17 7811410 7811410 single base substitution T C intron_variant COCA-CN 17 7811410 7811410 single base substitution T C upstream_gene_variant COCA-CN 17 7811731 7811731 single base substitution C G 3_prime_UTR_variant COCA-CN 17 7811731 7811731 single base substitution C G downstream_gene_variant COCA-CN 17 7811731 7811731 single base substitution C G exon_variant COCA-CN 17 7811731 7811731 single base substitution C G missense_variant L14V 40C>G COCA-CN 17 7811731 7811731 single base substitution C G missense_variant L1688V 5062C>G COCA-CN 17 7811731 7811731 single base substitution C G missense_variant L1722V 5164C>G COCA-CN 17 7811731 7811731 single base substitution C G missense_variant L1781V 5341C>G COCA-CN 17 7811731 7811731 single base substitution C G missense_variant L41V 121C>G COCA-CN 17 7811731 7811731 single base substitution C G missense_variant L50V 148C>G COCA-CN 17 7811731 7811731 single base substitution C G upstream_gene_variant COCA-CN 17 7812703 7812703 single base substitution G A downstream_gene_variant COCA-CN 17 7812703 7812703 single base substitution G A intron_variant COCA-CN 17 7812703 7812703 single base substitution G A splice_donor_variant COCA-CN 17 7812703 7812703 single base substitution G A upstream_gene_variant COCA-CN 17 7819149 7819149 single base substitution T C downstream_gene_variant ESAD-UK 17 7785548 7785548 single base substitution G A upstream_gene_variant ESAD-UK 17 7787141 7787141 single base substitution C T upstream_gene_variant ESAD-UK 17 7791107 7791107 single base substitution G A intron_variant ESAD-UK 17 7791107 7791107 single base substitution G A upstream_gene_variant ESAD-UK 17 7796590 7796590 single base substitution T G downstream_gene_variant ESAD-UK 17 7796590 7796590 single base substitution T G intron_variant ESAD-UK 17 7796590 7796590 single base substitution T G upstream_gene_variant ESAD-UK 17 7801994 7801994 single base substitution C T downstream_gene_variant ESAD-UK 17 7801994 7801994 single base substitution C T intron_variant ESAD-UK 17 7802910 7802910 single base substitution C A downstream_gene_variant ESAD-UK 17 7802910 7802910 single base substitution C A intron_variant ESAD-UK 17 7802910 7802910 single base substitution C A upstream_gene_variant ESAD-UK 17 7803456 7803456 single base substitution G A downstream_gene_variant ESAD-UK 17 7803456 7803456 single base substitution G A intron_variant ESAD-UK 17 7803456 7803456 single base substitution G A upstream_gene_variant ESAD-UK 17 7806722 7806722 single base substitution C T missense_variant R1210W 3628C>T ESAD-UK 17 7806722 7806722 single base substitution C T missense_variant R1269W 3805C>T ESAD-UK 17 7806722 7806722 single base substitution C T upstream_gene_variant ESAD-UK 17 7806951 7806951 single base substitution C T intron_variant ESAD-UK 17 7806951 7806951 single base substitution C T upstream_gene_variant ESAD-UK 17 7808776 7808776 single base substitution T G downstream_gene_variant ESAD-UK 17 7808776 7808776 single base substitution T G intron_variant ESAD-UK 17 7808776 7808776 single base substitution T G upstream_gene_variant ESAD-UK 17 7811107 7811107 single base substitution C G downstream_gene_variant ESAD-UK 17 7811107 7811107 single base substitution C G exon_variant ESAD-UK 17 7811107 7811107 single base substitution C G intron_variant ESAD-UK 17 7811107 7811107 single base substitution C G upstream_gene_variant ESAD-UK 17 7811275 7811275 single base substitution G A 3_prime_UTR_variant ESAD-UK 17 7811275 7811275 single base substitution G A downstream_gene_variant ESAD-UK 17 7811275 7811275 single base substitution G A exon_variant ESAD-UK 17 7811275 7811275 single base substitution G A missense_variant R1663Q 4988G>A ESAD-UK 17 7811275 7811275 single base substitution G A missense_variant R1697Q 5090G>A ESAD-UK 17 7811275 7811275 single base substitution G A missense_variant R16Q 47G>A ESAD-UK 17 7811275 7811275 single base substitution G A missense_variant R1756Q 5267G>A ESAD-UK 17 7811275 7811275 single base substitution G A missense_variant R25Q 74G>A ESAD-UK 17 7811275 7811275 single base substitution G A upstream_gene_variant ESAD-UK 17 7816113 7816113 insertion of <=200bp - G downstream_gene_variant ESAD-UK 17 7816248 7816248 single base substitution G A downstream_gene_variant ESAD-UK 17 7818763 7818763 single base substitution A C downstream_gene_variant ESCA-CN 17 7804342 7804342 single base substitution C A downstream_gene_variant ESCA-CN 17 7804342 7804342 single base substitution C A intron_variant ESCA-CN 17 7804342 7804342 single base substitution C A upstream_gene_variant ESCA-CN 17 7819092 7819092 single base substitution G A downstream_gene_variant GBM-US 17 7811263 7811263 single base substitution G A 3_prime_UTR_variant GBM-US 17 7811263 7811263 single base substitution G A downstream_gene_variant GBM-US 17 7811263 7811263 single base substitution G A exon_variant GBM-US 17 7811263 7811263 single base substitution G A missense_variant R12Q 35G>A GBM-US 17 7811263 7811263 single base substitution G A missense_variant R1659Q 4976G>A GBM-US 17 7811263 7811263 single base substitution G A missense_variant R1693Q 5078G>A GBM-US 17 7811263 7811263 single base substitution G A missense_variant R1752Q 5255G>A GBM-US 17 7811263 7811263 single base substitution G A missense_variant R21Q 62G>A GBM-US 17 7811263 7811263 single base substitution G A upstream_gene_variant KIRC-US 17 7797756 7797756 single base substitution G A downstream_gene_variant KIRC-US 17 7797756 7797756 single base substitution G A exon_variant KIRC-US 17 7797756 7797756 single base substitution G A missense_variant G237R 709G>A KIRC-US 17 7797756 7797756 single base substitution G A missense_variant G367R 1099G>A KIRC-US 17 7797756 7797756 single base substitution G A missense_variant G426R 1276G>A KIRC-US 17 7797756 7797756 single base substitution G A missense_variant G88R 262G>A KIRC-US 17 7797756 7797756 single base substitution G A upstream_gene_variant KIRC-US 17 7797795 7797795 single base substitution G A downstream_gene_variant KIRC-US 17 7797795 7797795 single base substitution G A exon_variant KIRC-US 17 7797795 7797795 single base substitution G A missense_variant D101N 301G>A KIRC-US 17 7797795 7797795 single base substitution G A missense_variant D250N 748G>A KIRC-US 17 7797795 7797795 single base substitution G A missense_variant D380N 1138G>A KIRC-US 17 7797795 7797795 single base substitution G A missense_variant D439N 1315G>A KIRC-US 17 7797795 7797795 single base substitution G A upstream_gene_variant KIRC-US 17 7801818 7801818 single base substitution C A downstream_gene_variant KIRC-US 17 7801818 7801818 single base substitution C A missense_variant L686I 2056C>A KIRC-US 17 7801818 7801818 single base substitution C A missense_variant L745I 2233C>A KIRC-US 17 7802423 7802423 single base substitution T A downstream_gene_variant KIRC-US 17 7802423 7802423 single base substitution T A missense_variant F749Y 2246T>A KIRC-US 17 7802423 7802423 single base substitution T A missense_variant F808Y 2423T>A KIRC-US 17 7802423 7802423 single base substitution T A upstream_gene_variant KIRC-US 17 7805978 7805978 single base substitution C A downstream_gene_variant KIRC-US 17 7805978 7805978 single base substitution C A stop_gained Y1101* 3303C>A KIRC-US 17 7805978 7805978 single base substitution C A stop_gained Y1160* 3480C>A KIRC-US 17 7805978 7805978 single base substitution C A upstream_gene_variant KIRC-US 17 7806304 7806304 single base substitution C T downstream_gene_variant KIRC-US 17 7806304 7806304 single base substitution C T synonymous_variant G1140G 3420C>T KIRC-US 17 7806304 7806304 single base substitution C T synonymous_variant G1199G 3597C>T KIRC-US 17 7806304 7806304 single base substitution C T upstream_gene_variant KIRP-US 17 7788146 7788148 deletion of <=200bp GAG - inframe_deletion E8 KIRP-US 17 7788146 7788148 deletion of <=200bp GAG - upstream_gene_variant KIRP-US 17 7794342 7794342 single base substitution C G downstream_gene_variant KIRP-US 17 7794342 7794342 single base substitution C G missense_variant H157D 469C>G KIRP-US 17 7794342 7794342 single base substitution C G missense_variant H216D 646C>G KIRP-US 17 7794342 7794342 single base substitution C G missense_variant H31D 91C>G KIRP-US 17 7794342 7794342 single base substitution C G upstream_gene_variant KIRP-US 17 7801857 7801859 deletion of <=200bp AAG - downstream_gene_variant KIRP-US 17 7801857 7801859 deletion of <=200bp AAG - inframe_deletion K699 KIRP-US 17 7801857 7801859 deletion of <=200bp AAG - inframe_deletion K758 LAML-KR 17 7813853 7813853 single base substitution G A 3_prime_UTR_variant LAML-KR 17 7813853 7813853 single base substitution G A downstream_gene_variant LAML-KR 17 7813853 7813853 single base substitution G A exon_variant LAML-KR 17 7813853 7813853 single base substitution G A intron_variant LAML-KR 17 7813853 7813853 single base substitution G A missense_variant E1866K 5596G>A LAML-KR 17 7813853 7813853 single base substitution G A missense_variant E1900K 5698G>A LAML-KR 17 7813853 7813853 single base substitution G A missense_variant E1959K 5875G>A LAML-KR 17 7813853 7813853 single base substitution G A missense_variant R215Q 644G>A LAML-KR 17 7813853 7813853 single base substitution G A missense_variant R243Q 728G>A LAML-KR 17 7814693 7814693 single base substitution T G downstream_gene_variant LAML-KR 17 7814693 7814693 single base substitution T G intron_variant LGG-US 17 7796794 7796794 single base substitution A C downstream_gene_variant LGG-US 17 7796794 7796794 single base substitution A C exon_variant LGG-US 17 7796794 7796794 single base substitution A C missense_variant I108L 322A>C LGG-US 17 7796794 7796794 single base substitution A C missense_variant I234L 700A>C LGG-US 17 7796794 7796794 single base substitution A C missense_variant I293L 877A>C LGG-US 17 7796794 7796794 single base substitution A C upstream_gene_variant LICA-CN 17 7806653 7806653 single base substitution C T missense_variant R1187C 3559C>T LICA-CN 17 7806653 7806653 single base substitution C T missense_variant R1246C 3736C>T LICA-CN 17 7806653 7806653 single base substitution C T upstream_gene_variant LICA-FR 17 7798765 7798765 deletion of <=200bp C - downstream_gene_variant LICA-FR 17 7798765 7798765 deletion of <=200bp C - exon_variant LICA-FR 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P408 LICA-FR 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P538 LICA-FR 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P597 LICA-FR 17 7802681 7802681 single base substitution C T downstream_gene_variant LICA-FR 17 7802681 7802681 single base substitution C T synonymous_variant F788F 2364C>T LICA-FR 17 7802681 7802681 single base substitution C T synonymous_variant F847F 2541C>T LICA-FR 17 7802681 7802681 single base substitution C T upstream_gene_variant LICA-FR 17 7812076 7812076 single base substitution C G 3_prime_UTR_variant LICA-FR 17 7812076 7812076 single base substitution C G downstream_gene_variant LICA-FR 17 7812076 7812076 single base substitution C G missense_variant P103A 307C>G LICA-FR 17 7812076 7812076 single base substitution C G missense_variant P1741A 5221C>G LICA-FR 17 7812076 7812076 single base substitution C G missense_variant P1775A 5323C>G LICA-FR 17 7812076 7812076 single base substitution C G missense_variant P1834A 5500C>G LICA-FR 17 7812076 7812076 single base substitution C G missense_variant P67A 199C>G LICA-FR 17 7812076 7812076 single base substitution C G missense_variant P94A 280C>G LICA-FR 17 7812076 7812076 single base substitution C G upstream_gene_variant LICA-FR 17 7816584 7816584 single base substitution A G downstream_gene_variant LIHC-US 17 7798720 7798720 single base substitution G A downstream_gene_variant LIHC-US 17 7798720 7798720 single base substitution G A exon_variant LIHC-US 17 7798720 7798720 single base substitution G A missense_variant A393T 1177G>A LIHC-US 17 7798720 7798720 single base substitution G A missense_variant A523T 1567G>A LIHC-US 17 7798720 7798720 single base substitution G A missense_variant A582T 1744G>A LIHC-US 17 7809999 7809999 single base substitution C A 3_prime_UTR_variant LIHC-US 17 7809999 7809999 single base substitution C A downstream_gene_variant LIHC-US 17 7809999 7809999 single base substitution C A missense_variant S1496Y 4487C>A LIHC-US 17 7809999 7809999 single base substitution C A missense_variant S1555Y 4664C>A LIHC-US 17 7809999 7809999 single base substitution C A upstream_gene_variant LIHC-US 17 7811224 7811224 single base substitution G T 3_prime_UTR_variant LIHC-US 17 7811224 7811224 single base substitution G T downstream_gene_variant LIHC-US 17 7811224 7811224 single base substitution G T exon_variant LIHC-US 17 7811224 7811224 single base substitution G T missense_variant G1646V 4937G>T LIHC-US 17 7811224 7811224 single base substitution G T missense_variant G1680V 5039G>T LIHC-US 17 7811224 7811224 single base substitution G T missense_variant G1739V 5216G>T LIHC-US 17 7811224 7811224 single base substitution G T missense_variant G8V 23G>T LIHC-US 17 7811224 7811224 single base substitution G T upstream_gene_variant LINC-JP 17 7790016 7790016 single base substitution G A intron_variant LINC-JP 17 7790016 7790016 single base substitution G A upstream_gene_variant LINC-JP 17 7794437 7794437 single base substitution C A downstream_gene_variant LINC-JP 17 7794437 7794437 single base substitution C A intron_variant LINC-JP 17 7794437 7794437 single base substitution C A upstream_gene_variant LINC-JP 17 7797792 7797792 single base substitution C T downstream_gene_variant LINC-JP 17 7797792 7797792 single base substitution C T exon_variant LINC-JP 17 7797792 7797792 single base substitution C T stop_gained Q100* 298C>T LINC-JP 17 7797792 7797792 single base substitution C T stop_gained Q249* 745C>T LINC-JP 17 7797792 7797792 single base substitution C T stop_gained Q379* 1135C>T LINC-JP 17 7797792 7797792 single base substitution C T stop_gained Q438* 1312C>T LINC-JP 17 7797792 7797792 single base substitution C T upstream_gene_variant LINC-JP 17 7798204 7798204 single base substitution T G downstream_gene_variant LINC-JP 17 7798204 7798204 single base substitution T G intron_variant LINC-JP 17 7798460 7798460 single base substitution C T downstream_gene_variant LINC-JP 17 7798460 7798460 single base substitution C T exon_variant LINC-JP 17 7798460 7798460 single base substitution C T stop_gained R369* 1105C>T LINC-JP 17 7798460 7798460 single base substitution C T stop_gained R499* 1495C>T LINC-JP 17 7798460 7798460 single base substitution C T stop_gained R558* 1672C>T LINC-JP 17 7798870 7798870 single base substitution C G downstream_gene_variant LINC-JP 17 7798870 7798870 single base substitution C G exon_variant LINC-JP 17 7798870 7798870 single base substitution C G intron_variant LINC-JP 17 7798970 7798970 single base substitution T G downstream_gene_variant LINC-JP 17 7798970 7798970 single base substitution T G intron_variant LINC-JP 17 7802628 7802628 single base substitution T G downstream_gene_variant LINC-JP 17 7802628 7802628 single base substitution T G intron_variant LINC-JP 17 7802628 7802628 single base substitution T G upstream_gene_variant LINC-JP 17 7808401 7808401 single base substitution C T intron_variant LINC-JP 17 7808401 7808401 single base substitution C T upstream_gene_variant LINC-JP 17 7812433 7812433 single base substitution C T downstream_gene_variant LINC-JP 17 7812433 7812433 single base substitution C T intron_variant LINC-JP 17 7812433 7812433 single base substitution C T upstream_gene_variant LINC-JP 17 7814828 7814828 single base substitution G A 3_prime_UTR_variant LINC-JP 17 7814828 7814828 single base substitution G A downstream_gene_variant LINC-JP 17 7814828 7814828 single base substitution G A exon_variant LINC-JP 17 7814828 7814828 single base substitution G A missense_variant G214S 640G>A LINC-JP 17 7814828 7814828 single base substitution G A missense_variant G320S 958G>A LINC-JP 17 7814828 7814828 single base substitution G A missense_variant M1942I 5826G>A LINC-JP 17 7814828 7814828 single base substitution G A missense_variant M1976I 5928G>A LINC-JP 17 7814828 7814828 single base substitution G A missense_variant M2035I 6105G>A LINC-JP 17 7817335 7817335 single base substitution A C downstream_gene_variant LIRI-JP 17 7783338 7783338 single base substitution G A upstream_gene_variant LIRI-JP 17 7783908 7783908 single base substitution G A upstream_gene_variant LIRI-JP 17 7783909 7783909 single base substitution A T upstream_gene_variant LIRI-JP 17 7784609 7784610 deletion of <=200bp AG - upstream_gene_variant LIRI-JP 17 7792314 7792314 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 17 7792314 7792314 single base substitution G A intron_variant LIRI-JP 17 7792314 7792314 single base substitution G A upstream_gene_variant LIRI-JP 17 7793423 7793423 single base substitution G A intron_variant LIRI-JP 17 7793423 7793423 single base substitution G A upstream_gene_variant LIRI-JP 17 7796655 7796655 single base substitution C T downstream_gene_variant LIRI-JP 17 7796655 7796655 single base substitution C T exon_variant LIRI-JP 17 7796655 7796655 single base substitution C T synonymous_variant T187T 561C>T LIRI-JP 17 7796655 7796655 single base substitution C T synonymous_variant T246T 738C>T LIRI-JP 17 7796655 7796655 single base substitution C T synonymous_variant T61T 183C>T LIRI-JP 17 7796655 7796655 single base substitution C T upstream_gene_variant LIRI-JP 17 7803829 7803829 single base substitution G A downstream_gene_variant LIRI-JP 17 7803829 7803829 single base substitution G A intron_variant LIRI-JP 17 7803829 7803829 single base substitution G A upstream_gene_variant LIRI-JP 17 7805607 7805607 single base substitution G A downstream_gene_variant LIRI-JP 17 7805607 7805607 single base substitution G A intron_variant LIRI-JP 17 7805607 7805607 single base substitution G A upstream_gene_variant LIRI-JP 17 7812986 7812986 single base substitution A C downstream_gene_variant LIRI-JP 17 7812986 7812986 single base substitution A C exon_variant LIRI-JP 17 7812986 7812986 single base substitution A C intron_variant LIRI-JP 17 7813152 7813152 single base substitution C G downstream_gene_variant LIRI-JP 17 7813152 7813152 single base substitution C G exon_variant LIRI-JP 17 7813152 7813152 single base substitution C G intron_variant LIRI-JP 17 7813653 7813653 single base substitution T C downstream_gene_variant LIRI-JP 17 7813653 7813653 single base substitution T C exon_variant LIRI-JP 17 7813653 7813653 single base substitution T C intron_variant LIRI-JP 17 7814805 7814805 single base substitution C T 3_prime_UTR_variant LIRI-JP 17 7814805 7814805 single base substitution C T downstream_gene_variant LIRI-JP 17 7814805 7814805 single base substitution C T exon_variant LIRI-JP 17 7814805 7814805 single base substitution C T missense_variant A206V 617C>T LIRI-JP 17 7814805 7814805 single base substitution C T missense_variant A312V 935C>T LIRI-JP 17 7814805 7814805 single base substitution C T missense_variant L1935F 5803C>T LIRI-JP 17 7814805 7814805 single base substitution C T missense_variant L1969F 5905C>T LIRI-JP 17 7814805 7814805 single base substitution C T missense_variant L2028F 6082C>T LUSC-KR 17 7796988 7796988 single base substitution G T downstream_gene_variant LUSC-KR 17 7796988 7796988 single base substitution G T intron_variant LUSC-KR 17 7796988 7796988 single base substitution G T upstream_gene_variant LUSC-KR 17 7805738 7805738 single base substitution C G downstream_gene_variant LUSC-KR 17 7805738 7805738 single base substitution C G intron_variant LUSC-KR 17 7805738 7805738 single base substitution C G upstream_gene_variant LUSC-KR 17 7806147 7806147 single base substitution T A downstream_gene_variant LUSC-KR 17 7806147 7806147 single base substitution T A intron_variant LUSC-KR 17 7806147 7806147 single base substitution T A upstream_gene_variant LUSC-KR 17 7810241 7810241 single base substitution G T 3_prime_UTR_variant LUSC-KR 17 7810241 7810241 single base substitution G T downstream_gene_variant LUSC-KR 17 7810241 7810241 single base substitution G T missense_variant D1520Y 4558G>T LUSC-KR 17 7810241 7810241 single base substitution G T missense_variant D1579Y 4735G>T LUSC-KR 17 7810241 7810241 single base substitution G T upstream_gene_variant LUSC-KR 17 7812574 7812574 single base substitution C T 3_prime_UTR_variant LUSC-KR 17 7812574 7812574 single base substitution C T downstream_gene_variant LUSC-KR 17 7812574 7812574 single base substitution C T synonymous_variant A128A 384C>T LUSC-KR 17 7812574 7812574 single base substitution C T synonymous_variant A155A 465C>T LUSC-KR 17 7812574 7812574 single base substitution C T synonymous_variant A164A 492C>T LUSC-KR 17 7812574 7812574 single base substitution C T synonymous_variant A1802A 5406C>T LUSC-KR 17 7812574 7812574 single base substitution C T synonymous_variant A1836A 5508C>T LUSC-KR 17 7812574 7812574 single base substitution C T synonymous_variant A1895A 5685C>T LUSC-KR 17 7812574 7812574 single base substitution C T upstream_gene_variant LUSC-US 17 7793959 7793959 single base substitution A G downstream_gene_variant LUSC-US 17 7793959 7793959 single base substitution A G exon_variant LUSC-US 17 7793959 7793959 single base substitution A G missense_variant Y154C 461A>G LUSC-US 17 7793959 7793959 single base substitution A G missense_variant Y95C 284A>G LUSC-US 17 7793959 7793959 single base substitution A G upstream_gene_variant LUSC-US 17 7798755 7798755 single base substitution A T downstream_gene_variant LUSC-US 17 7798755 7798755 single base substitution A T exon_variant LUSC-US 17 7798755 7798755 single base substitution A T synonymous_variant P404P 1212A>T LUSC-US 17 7798755 7798755 single base substitution A T synonymous_variant P534P 1602A>T LUSC-US 17 7798755 7798755 single base substitution A T synonymous_variant P593P 1779A>T LUSC-US 17 7801302 7801302 single base substitution G T downstream_gene_variant LUSC-US 17 7801302 7801302 single base substitution G T missense_variant G515W 1543G>T LUSC-US 17 7801302 7801302 single base substitution G T missense_variant G645W 1933G>T LUSC-US 17 7801302 7801302 single base substitution G T missense_variant G704W 2110G>T LUSC-US 17 7802420 7802420 single base substitution G T downstream_gene_variant LUSC-US 17 7802420 7802420 single base substitution G T missense_variant R748L 2243G>T LUSC-US 17 7802420 7802420 single base substitution G T missense_variant R807L 2420G>T LUSC-US 17 7802420 7802420 single base substitution G T upstream_gene_variant LUSC-US 17 7806032 7806032 single base substitution C A downstream_gene_variant LUSC-US 17 7806032 7806032 single base substitution C A synonymous_variant I1119I 3357C>A LUSC-US 17 7806032 7806032 single base substitution C A synonymous_variant I1178I 3534C>A LUSC-US 17 7806032 7806032 single base substitution C A upstream_gene_variant MALY-DE 17 7816384 7816384 insertion of <=200bp - T downstream_gene_variant MALY-DE 17 7818654 7818654 single base substitution G A downstream_gene_variant MELA-AU 17 7783642 7783642 single base substitution G A upstream_gene_variant MELA-AU 17 7784247 7784247 single base substitution G A upstream_gene_variant MELA-AU 17 7784362 7784362 single base substitution G A upstream_gene_variant MELA-AU 17 7784644 7784644 single base substitution G A upstream_gene_variant MELA-AU 17 7785522 7785522 single base substitution T A upstream_gene_variant MELA-AU 17 7785555 7785555 single base substitution G A upstream_gene_variant MELA-AU 17 7786020 7786021 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 17 7787578 7787578 single base substitution G A upstream_gene_variant MELA-AU 17 7787796 7787796 single base substitution G A upstream_gene_variant MELA-AU 17 7789192 7789192 single base substitution C T intron_variant MELA-AU 17 7789192 7789192 single base substitution C T upstream_gene_variant MELA-AU 17 7789927 7789927 single base substitution C T intron_variant MELA-AU 17 7789927 7789927 single base substitution C T upstream_gene_variant MELA-AU 17 7789964 7789964 single base substitution C T intron_variant MELA-AU 17 7789964 7789964 single base substitution C T upstream_gene_variant MELA-AU 17 7790558 7790558 single base substitution T C intron_variant MELA-AU 17 7790558 7790558 single base substitution T C upstream_gene_variant MELA-AU 17 7790778 7790778 single base substitution C T intron_variant MELA-AU 17 7790778 7790778 single base substitution C T upstream_gene_variant MELA-AU 17 7793112 7793112 single base substitution C T intron_variant MELA-AU 17 7793112 7793112 single base substitution C T upstream_gene_variant MELA-AU 17 7793261 7793262 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 17 7793261 7793262 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 17 7793556 7793556 single base substitution C T intron_variant MELA-AU 17 7793556 7793556 single base substitution C T upstream_gene_variant MELA-AU 17 7794221 7794221 single base substitution G A downstream_gene_variant MELA-AU 17 7794221 7794221 single base substitution G A intron_variant MELA-AU 17 7794221 7794221 single base substitution G A upstream_gene_variant MELA-AU 17 7794245 7794245 single base substitution C T downstream_gene_variant MELA-AU 17 7794245 7794245 single base substitution C T intron_variant MELA-AU 17 7794245 7794245 single base substitution C T upstream_gene_variant MELA-AU 17 7794253 7794253 single base substitution C T downstream_gene_variant MELA-AU 17 7794253 7794253 single base substitution C T splice_region_variant MELA-AU 17 7794253 7794253 single base substitution C T upstream_gene_variant MELA-AU 17 7795331 7795331 single base substitution C T downstream_gene_variant MELA-AU 17 7795331 7795331 single base substitution C T intron_variant MELA-AU 17 7795331 7795331 single base substitution C T upstream_gene_variant MELA-AU 17 7795334 7795334 single base substitution C G downstream_gene_variant MELA-AU 17 7795334 7795334 single base substitution C G intron_variant MELA-AU 17 7795334 7795334 single base substitution C G upstream_gene_variant MELA-AU 17 7795779 7795779 single base substitution G A downstream_gene_variant MELA-AU 17 7795779 7795779 single base substitution G A intron_variant MELA-AU 17 7795779 7795779 single base substitution G A upstream_gene_variant MELA-AU 17 7796478 7796478 single base substitution C T downstream_gene_variant MELA-AU 17 7796478 7796478 single base substitution C T intron_variant MELA-AU 17 7796478 7796478 single base substitution C T upstream_gene_variant MELA-AU 17 7797345 7797345 single base substitution C T downstream_gene_variant MELA-AU 17 7797345 7797345 single base substitution C T intron_variant MELA-AU 17 7797345 7797345 single base substitution C T upstream_gene_variant MELA-AU 17 7797672 7797672 single base substitution C T downstream_gene_variant MELA-AU 17 7797672 7797672 single base substitution C T intron_variant MELA-AU 17 7797672 7797672 single base substitution C T upstream_gene_variant MELA-AU 17 7797690 7797690 single base substitution C T downstream_gene_variant MELA-AU 17 7797690 7797690 single base substitution C T intron_variant MELA-AU 17 7797690 7797690 single base substitution C T upstream_gene_variant MELA-AU 17 7797960 7797960 single base substitution A G downstream_gene_variant MELA-AU 17 7797960 7797960 single base substitution A G exon_variant MELA-AU 17 7797960 7797960 single base substitution A G intron_variant MELA-AU 17 7798185 7798185 single base substitution C T downstream_gene_variant MELA-AU 17 7798185 7798185 single base substitution C T intron_variant MELA-AU 17 7798458 7798458 single base substitution C T downstream_gene_variant MELA-AU 17 7798458 7798458 single base substitution C T exon_variant MELA-AU 17 7798458 7798458 single base substitution C T missense_variant P368L 1103C>T MELA-AU 17 7798458 7798458 single base substitution C T missense_variant P498L 1493C>T MELA-AU 17 7798458 7798458 single base substitution C T missense_variant P557L 1670C>T MELA-AU 17 7798628 7798628 single base substitution C T downstream_gene_variant MELA-AU 17 7798628 7798628 single base substitution C T intron_variant MELA-AU 17 7799105 7799105 single base substitution C T downstream_gene_variant MELA-AU 17 7799105 7799105 single base substitution C T intron_variant MELA-AU 17 7799121 7799121 single base substitution C T downstream_gene_variant MELA-AU 17 7799121 7799121 single base substitution C T intron_variant MELA-AU 17 7800325 7800325 single base substitution C T downstream_gene_variant MELA-AU 17 7800325 7800325 single base substitution C T intron_variant MELA-AU 17 7800331 7800331 single base substitution C T downstream_gene_variant MELA-AU 17 7800331 7800331 single base substitution C T intron_variant MELA-AU 17 7800879 7800879 single base substitution G A downstream_gene_variant MELA-AU 17 7800879 7800879 single base substitution G A intron_variant MELA-AU 17 7801811 7801811 single base substitution C T downstream_gene_variant MELA-AU 17 7801811 7801811 single base substitution C T splice_region_variant MELA-AU 17 7801971 7801971 single base substitution C T downstream_gene_variant MELA-AU 17 7801971 7801971 single base substitution C T intron_variant MELA-AU 17 7803234 7803234 single base substitution C T downstream_gene_variant MELA-AU 17 7803234 7803234 single base substitution C T synonymous_variant F855F 2565C>T MELA-AU 17 7803234 7803234 single base substitution C T synonymous_variant F914F 2742C>T MELA-AU 17 7803234 7803234 single base substitution C T upstream_gene_variant MELA-AU 17 7803235 7803235 single base substitution C T downstream_gene_variant MELA-AU 17 7803235 7803235 single base substitution C T missense_variant H856Y 2566C>T MELA-AU 17 7803235 7803235 single base substitution C T missense_variant H915Y 2743C>T MELA-AU 17 7803235 7803235 single base substitution C T upstream_gene_variant MELA-AU 17 7803581 7803581 single base substitution C T downstream_gene_variant MELA-AU 17 7803581 7803581 single base substitution C T intron_variant MELA-AU 17 7803581 7803581 single base substitution C T upstream_gene_variant MELA-AU 17 7803930 7803930 single base substitution C T downstream_gene_variant MELA-AU 17 7803930 7803930 single base substitution C T synonymous_variant I1012I 3036C>T MELA-AU 17 7803930 7803930 single base substitution C T synonymous_variant I953I 2859C>T MELA-AU 17 7803930 7803930 single base substitution C T upstream_gene_variant MELA-AU 17 7804329 7804329 single base substitution G A downstream_gene_variant MELA-AU 17 7804329 7804329 single base substitution G A intron_variant MELA-AU 17 7804329 7804329 single base substitution G A upstream_gene_variant MELA-AU 17 7804395 7804395 single base substitution C T downstream_gene_variant MELA-AU 17 7804395 7804395 single base substitution C T intron_variant MELA-AU 17 7804395 7804395 single base substitution C T upstream_gene_variant MELA-AU 17 7804533 7804533 single base substitution C T downstream_gene_variant MELA-AU 17 7804533 7804533 single base substitution C T intron_variant MELA-AU 17 7804533 7804533 single base substitution C T upstream_gene_variant MELA-AU 17 7804705 7804705 single base substitution C T downstream_gene_variant MELA-AU 17 7804705 7804705 single base substitution C T intron_variant MELA-AU 17 7804705 7804705 single base substitution C T upstream_gene_variant MELA-AU 17 7805075 7805075 single base substitution C T downstream_gene_variant MELA-AU 17 7805075 7805075 single base substitution C T intron_variant MELA-AU 17 7805075 7805075 single base substitution C T upstream_gene_variant MELA-AU 17 7805204 7805204 single base substitution G A downstream_gene_variant MELA-AU 17 7805204 7805204 single base substitution G A intron_variant MELA-AU 17 7805204 7805204 single base substitution G A upstream_gene_variant MELA-AU 17 7805282 7805283 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 17 7805282 7805283 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 17 7805282 7805283 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 17 7805392 7805392 single base substitution T C downstream_gene_variant MELA-AU 17 7805392 7805392 single base substitution T C intron_variant MELA-AU 17 7805392 7805392 single base substitution T C upstream_gene_variant MELA-AU 17 7806908 7806908 single base substitution C G intron_variant MELA-AU 17 7806908 7806908 single base substitution C G upstream_gene_variant MELA-AU 17 7807269 7807269 single base substitution C T exon_variant MELA-AU 17 7807269 7807269 single base substitution C T missense_variant S1285F 3854C>T MELA-AU 17 7807269 7807269 single base substitution C T missense_variant S1344F 4031C>T MELA-AU 17 7807269 7807269 single base substitution C T upstream_gene_variant MELA-AU 17 7807368 7807368 single base substitution C T intron_variant MELA-AU 17 7807368 7807368 single base substitution C T upstream_gene_variant MELA-AU 17 7807506 7807506 single base substitution T A 3_prime_UTR_variant MELA-AU 17 7807506 7807506 single base substitution T A exon_variant MELA-AU 17 7807506 7807506 single base substitution T A intron_variant MELA-AU 17 7807506 7807506 single base substitution T A upstream_gene_variant MELA-AU 17 7807696 7807696 single base substitution C T 3_prime_UTR_variant MELA-AU 17 7807696 7807696 single base substitution C T exon_variant MELA-AU 17 7807696 7807696 single base substitution C T intron_variant MELA-AU 17 7807696 7807696 single base substitution C T upstream_gene_variant MELA-AU 17 7808061 7808061 single base substitution G A intron_variant MELA-AU 17 7808061 7808061 single base substitution G A upstream_gene_variant MELA-AU 17 7808781 7808781 single base substitution G T downstream_gene_variant MELA-AU 17 7808781 7808781 single base substitution G T intron_variant MELA-AU 17 7808781 7808781 single base substitution G T upstream_gene_variant MELA-AU 17 7809451 7809451 single base substitution C T downstream_gene_variant MELA-AU 17 7809451 7809451 single base substitution C T intron_variant MELA-AU 17 7809451 7809451 single base substitution C T upstream_gene_variant MELA-AU 17 7809550 7809550 single base substitution C T downstream_gene_variant MELA-AU 17 7809550 7809550 single base substitution C T intron_variant MELA-AU 17 7809550 7809550 single base substitution C T upstream_gene_variant MELA-AU 17 7809735 7809735 single base substitution G A downstream_gene_variant MELA-AU 17 7809735 7809735 single base substitution G A intron_variant MELA-AU 17 7809735 7809735 single base substitution G A upstream_gene_variant MELA-AU 17 7810272 7810272 single base substitution G C 3_prime_UTR_variant MELA-AU 17 7810272 7810272 single base substitution G C downstream_gene_variant MELA-AU 17 7810272 7810272 single base substitution G C missense_variant R1530T 4589G>C MELA-AU 17 7810272 7810272 single base substitution G C missense_variant R1589T 4766G>C MELA-AU 17 7810272 7810272 single base substitution G C upstream_gene_variant MELA-AU 17 7810332 7810332 single base substitution C T 3_prime_UTR_variant MELA-AU 17 7810332 7810332 single base substitution C T downstream_gene_variant MELA-AU 17 7810332 7810332 single base substitution C T missense_variant P1550L 4649C>T MELA-AU 17 7810332 7810332 single base substitution C T missense_variant P1609L 4826C>T MELA-AU 17 7810332 7810332 single base substitution C T upstream_gene_variant MELA-AU 17 7810436 7810436 single base substitution C T downstream_gene_variant MELA-AU 17 7810436 7810436 single base substitution C T splice_region_variant MELA-AU 17 7810436 7810436 single base substitution C T upstream_gene_variant MELA-AU 17 7810728 7810729 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 17 7810728 7810729 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 17 7810728 7810729 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P1616F 4846CC>TT MELA-AU 17 7810728 7810729 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P1675F 5023CC>TT MELA-AU 17 7810728 7810729 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 17 7810854 7810854 single base substitution C T downstream_gene_variant MELA-AU 17 7810854 7810854 single base substitution C T exon_variant MELA-AU 17 7810854 7810854 single base substitution C T intron_variant MELA-AU 17 7810854 7810854 single base substitution C T upstream_gene_variant MELA-AU 17 7810861 7810861 single base substitution C T downstream_gene_variant MELA-AU 17 7810861 7810861 single base substitution C T exon_variant MELA-AU 17 7810861 7810861 single base substitution C T intron_variant MELA-AU 17 7810861 7810861 single base substitution C T upstream_gene_variant MELA-AU 17 7810864 7810864 single base substitution G A downstream_gene_variant MELA-AU 17 7810864 7810864 single base substitution G A exon_variant MELA-AU 17 7810864 7810864 single base substitution G A intron_variant MELA-AU 17 7810864 7810864 single base substitution G A upstream_gene_variant MELA-AU 17 7811318 7811318 single base substitution C T 3_prime_UTR_variant MELA-AU 17 7811318 7811318 single base substitution C T downstream_gene_variant MELA-AU 17 7811318 7811318 single base substitution C T exon_variant MELA-AU 17 7811318 7811318 single base substitution C T synonymous_variant I1677I 5031C>T MELA-AU 17 7811318 7811318 single base substitution C T synonymous_variant I1711I 5133C>T MELA-AU 17 7811318 7811318 single base substitution C T synonymous_variant I1770I 5310C>T MELA-AU 17 7811318 7811318 single base substitution C T synonymous_variant I30I 90C>T MELA-AU 17 7811318 7811318 single base substitution C T synonymous_variant I39I 117C>T MELA-AU 17 7811318 7811318 single base substitution C T synonymous_variant I3I 9C>T MELA-AU 17 7811318 7811318 single base substitution C T upstream_gene_variant MELA-AU 17 7811503 7811503 single base substitution C T downstream_gene_variant MELA-AU 17 7811503 7811503 single base substitution C T intron_variant MELA-AU 17 7811503 7811503 single base substitution C T upstream_gene_variant MELA-AU 17 7812531 7812531 single base substitution C T 3_prime_UTR_variant MELA-AU 17 7812531 7812531 single base substitution C T downstream_gene_variant MELA-AU 17 7812531 7812531 single base substitution C T missense_variant P114L 341C>T MELA-AU 17 7812531 7812531 single base substitution C T missense_variant P141L 422C>T MELA-AU 17 7812531 7812531 single base substitution C T missense_variant P150L 449C>T MELA-AU 17 7812531 7812531 single base substitution C T missense_variant P1788L 5363C>T MELA-AU 17 7812531 7812531 single base substitution C T missense_variant P1822L 5465C>T MELA-AU 17 7812531 7812531 single base substitution C T missense_variant P1881L 5642C>T MELA-AU 17 7812531 7812531 single base substitution C T upstream_gene_variant MELA-AU 17 7813091 7813091 single base substitution C T downstream_gene_variant MELA-AU 17 7813091 7813091 single base substitution C T exon_variant MELA-AU 17 7813091 7813091 single base substitution C T intron_variant MELA-AU 17 7813122 7813122 single base substitution C T downstream_gene_variant MELA-AU 17 7813122 7813122 single base substitution C T exon_variant MELA-AU 17 7813122 7813122 single base substitution C T intron_variant MELA-AU 17 7813577 7813577 single base substitution C T downstream_gene_variant MELA-AU 17 7813577 7813577 single base substitution C T exon_variant MELA-AU 17 7813577 7813577 single base substitution C T intron_variant MELA-AU 17 7814332 7814332 single base substitution C T downstream_gene_variant MELA-AU 17 7814332 7814332 single base substitution C T intron_variant MELA-AU 17 7814473 7814473 single base substitution C T downstream_gene_variant MELA-AU 17 7814473 7814473 single base substitution C T intron_variant MELA-AU 17 7814661 7814661 single base substitution C T downstream_gene_variant MELA-AU 17 7814661 7814661 single base substitution C T intron_variant MELA-AU 17 7815379 7815380 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 17 7815379 7815380 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 17 7815379 7815380 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 17 7815425 7815426 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 17 7815425 7815426 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 17 7815425 7815426 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 17 7815723 7815723 single base substitution G T 3_prime_UTR_variant MELA-AU 17 7815723 7815723 single base substitution G T downstream_gene_variant MELA-AU 17 7815723 7815723 single base substitution G T exon_variant MELA-AU 17 7815896 7815896 single base substitution C T 3_prime_UTR_variant MELA-AU 17 7815896 7815896 single base substitution C T downstream_gene_variant MELA-AU 17 7815896 7815896 single base substitution C T exon_variant MELA-AU 17 7818126 7818126 single base substitution C T downstream_gene_variant MELA-AU 17 7818400 7818400 single base substitution A T downstream_gene_variant MELA-AU 17 7818764 7818764 single base substitution G A downstream_gene_variant MELA-AU 17 7819627 7819627 single base substitution C T downstream_gene_variant ORCA-IN 17 7816784 7816784 single base substitution C T downstream_gene_variant ORCA-IN 17 7817444 7817444 single base substitution C G downstream_gene_variant ORCA-IN 17 7818213 7818213 single base substitution C G downstream_gene_variant OV-AU 17 7789386 7789386 single base substitution C A intron_variant OV-AU 17 7789386 7789386 single base substitution C A upstream_gene_variant OV-AU 17 7791851 7791851 single base substitution G C intron_variant OV-AU 17 7791851 7791851 single base substitution G C upstream_gene_variant OV-AU 17 7792373 7792373 single base substitution A G intron_variant OV-AU 17 7792373 7792373 single base substitution A G missense_variant R19G 55A>G OV-AU 17 7792373 7792373 single base substitution A G upstream_gene_variant OV-AU 17 7792973 7792973 single base substitution G A intron_variant OV-AU 17 7792973 7792973 single base substitution G A upstream_gene_variant OV-AU 17 7801525 7801525 single base substitution G T downstream_gene_variant OV-AU 17 7801525 7801525 single base substitution G T intron_variant OV-AU 17 7805523 7805523 single base substitution G A downstream_gene_variant OV-AU 17 7805523 7805523 single base substitution G A intron_variant OV-AU 17 7805523 7805523 single base substitution G A upstream_gene_variant OV-AU 17 7818685 7818685 single base substitution C G downstream_gene_variant OV-AU 17 7820249 7820249 single base substitution G C downstream_gene_variant PACA-AU 17 7796653 7796653 single base substitution A T downstream_gene_variant PACA-AU 17 7796653 7796653 single base substitution A T exon_variant PACA-AU 17 7796653 7796653 single base substitution A T missense_variant T187S 559A>T PACA-AU 17 7796653 7796653 single base substitution A T missense_variant T246S 736A>T PACA-AU 17 7796653 7796653 single base substitution A T missense_variant T61S 181A>T PACA-AU 17 7796653 7796653 single base substitution A T upstream_gene_variant PACA-AU 17 7806471 7806475 deletion of <=200bp TCTCT - intron_variant PACA-AU 17 7806471 7806475 deletion of <=200bp TCTCT - upstream_gene_variant PACA-CA 17 7785745 7785745 single base substitution C T upstream_gene_variant PACA-CA 17 7793513 7793513 single base substitution C T intron_variant PACA-CA 17 7793513 7793513 single base substitution C T upstream_gene_variant PACA-CA 17 7793611 7793611 single base substitution C T intron_variant PACA-CA 17 7793611 7793611 single base substitution C T upstream_gene_variant PACA-CA 17 7798995 7798995 single base substitution C G downstream_gene_variant PACA-CA 17 7798995 7798995 single base substitution C G intron_variant PACA-CA 17 7799927 7799927 single base substitution T C downstream_gene_variant PACA-CA 17 7799927 7799927 single base substitution T C intron_variant PACA-CA 17 7800126 7800126 single base substitution G A downstream_gene_variant PACA-CA 17 7800126 7800126 single base substitution G A intron_variant PACA-CA 17 7801714 7801714 single base substitution C A downstream_gene_variant PACA-CA 17 7801714 7801714 single base substitution C A intron_variant PACA-CA 17 7803811 7803811 single base substitution G T downstream_gene_variant PACA-CA 17 7803811 7803811 single base substitution G T intron_variant PACA-CA 17 7803811 7803811 single base substitution G T upstream_gene_variant PACA-CA 17 7808580 7808580 single base substitution T C exon_variant PACA-CA 17 7808580 7808580 single base substitution T C intron_variant PACA-CA 17 7808580 7808580 single base substitution T C upstream_gene_variant PACA-CA 17 7810440 7810440 single base substitution G A downstream_gene_variant PACA-CA 17 7810440 7810440 single base substitution G A splice_region_variant PACA-CA 17 7810440 7810440 single base substitution G A upstream_gene_variant PACA-CA 17 7812671 7812671 single base substitution G A downstream_gene_variant PACA-CA 17 7812671 7812671 single base substitution G A intron_variant PACA-CA 17 7812671 7812671 single base substitution G A missense_variant G197S 589G>A PACA-CA 17 7812671 7812671 single base substitution G A upstream_gene_variant PACA-CA 17 7816157 7816157 insertion of <=200bp - A downstream_gene_variant PACA-CA 17 7817253 7817253 insertion of <=200bp - A downstream_gene_variant PAEN-AU 17 7802175 7802175 insertion of <=200bp - A downstream_gene_variant PAEN-AU 17 7802175 7802175 insertion of <=200bp - A intron_variant PAEN-AU 17 7802175 7802175 insertion of <=200bp - A upstream_gene_variant PBCA-DE 17 7798601 7798601 single base substitution C T downstream_gene_variant PBCA-DE 17 7798601 7798601 single base substitution C T intron_variant PBCA-DE 17 7799248 7799248 insertion of <=200bp - A downstream_gene_variant PBCA-DE 17 7799248 7799248 insertion of <=200bp - A intron_variant PBCA-DE 17 7806123 7806123 deletion of <=200bp A - downstream_gene_variant PBCA-DE 17 7806123 7806123 deletion of <=200bp A - intron_variant PBCA-DE 17 7806123 7806123 deletion of <=200bp A - upstream_gene_variant PBCA-DE 17 7807665 7807665 single base substitution G A 3_prime_UTR_variant PBCA-DE 17 7807665 7807665 single base substitution G A exon_variant PBCA-DE 17 7807665 7807665 single base substitution G A intron_variant PBCA-DE 17 7807665 7807665 single base substitution G A upstream_gene_variant PBCA-DE 17 7816294 7816294 single base substitution C G downstream_gene_variant PBCA-DE 17 7818063 7818063 single base substitution G A downstream_gene_variant PRAD-UK 17 7788898 7788898 single base substitution C G intron_variant PRAD-UK 17 7788898 7788898 single base substitution C G upstream_gene_variant PRAD-UK 17 7793119 7793119 single base substitution T A intron_variant PRAD-UK 17 7793119 7793119 single base substitution T A upstream_gene_variant PRAD-UK 17 7806327 7806327 single base substitution C T downstream_gene_variant PRAD-UK 17 7806327 7806327 single base substitution C T missense_variant A1148V 3443C>T PRAD-UK 17 7806327 7806327 single base substitution C T missense_variant A1207V 3620C>T PRAD-UK 17 7806327 7806327 single base substitution C T upstream_gene_variant PRAD-US 17 7788146 7788148 deletion of <=200bp GAG - inframe_deletion E8 PRAD-US 17 7788146 7788148 deletion of <=200bp GAG - upstream_gene_variant PRAD-US 17 7788212 7788214 deletion of <=200bp GAG - inframe_deletion E30 PRAD-US 17 7788212 7788214 deletion of <=200bp GAG - upstream_gene_variant PRAD-US 17 7801306 7801306 insertion of <=200bp - T downstream_gene_variant PRAD-US 17 7801306 7801306 insertion of <=200bp - T frameshift_variant N516I? PRAD-US 17 7801306 7801306 insertion of <=200bp - T frameshift_variant N646I? PRAD-US 17 7801306 7801306 insertion of <=200bp - T frameshift_variant N705I? PRAD-US 17 7806622 7806622 single base substitution C T synonymous_variant A1176A 3528C>T PRAD-US 17 7806622 7806622 single base substitution C T synonymous_variant A1235A 3705C>T PRAD-US 17 7806622 7806622 single base substitution C T upstream_gene_variant PRAD-US 17 7811746 7811746 single base substitution G T 3_prime_UTR_variant PRAD-US 17 7811746 7811746 single base substitution G T downstream_gene_variant PRAD-US 17 7811746 7811746 single base substitution G T exon_variant PRAD-US 17 7811746 7811746 single base substitution G T stop_gained E1693* 5077G>T PRAD-US 17 7811746 7811746 single base substitution G T stop_gained E1727* 5179G>T PRAD-US 17 7811746 7811746 single base substitution G T stop_gained E1786* 5356G>T PRAD-US 17 7811746 7811746 single base substitution G T stop_gained E19* 55G>T PRAD-US 17 7811746 7811746 single base substitution G T stop_gained E46* 136G>T PRAD-US 17 7811746 7811746 single base substitution G T stop_gained E55* 163G>T PRAD-US 17 7811746 7811746 single base substitution G T upstream_gene_variant READ-US 17 7792380 7792380 single base substitution C A intron_variant READ-US 17 7792380 7792380 single base substitution C A missense_variant S21Y 62C>A READ-US 17 7792380 7792380 single base substitution C A upstream_gene_variant READ-US 17 7793078 7793078 single base substitution G A exon_variant READ-US 17 7793078 7793078 single base substitution G A missense_variant R125Q 374G>A READ-US 17 7793078 7793078 single base substitution G A missense_variant R66Q 197G>A READ-US 17 7793078 7793078 single base substitution G A upstream_gene_variant RECA-EU 17 7804015 7804015 single base substitution C G downstream_gene_variant RECA-EU 17 7804015 7804015 single base substitution C G missense_variant L1041V 3121C>G RECA-EU 17 7804015 7804015 single base substitution C G missense_variant L982V 2944C>G RECA-EU 17 7804015 7804015 single base substitution C G upstream_gene_variant SKCA-BR 17 7786441 7786441 single base substitution G A upstream_gene_variant SKCA-BR 17 7788625 7788625 insertion of <=200bp - CCCGCCGCCG intron_variant SKCA-BR 17 7788625 7788625 insertion of <=200bp - CCCGCCGCCG upstream_gene_variant SKCA-BR 17 7788814 7788814 single base substitution T C intron_variant SKCA-BR 17 7788814 7788814 single base substitution T C upstream_gene_variant SKCA-BR 17 7792649 7792649 single base substitution A G intron_variant SKCA-BR 17 7792649 7792649 single base substitution A G upstream_gene_variant SKCA-BR 17 7797222 7797222 single base substitution T G downstream_gene_variant SKCA-BR 17 7797222 7797222 single base substitution T G exon_variant SKCA-BR 17 7797222 7797222 single base substitution T G missense_variant L172R 515T>G SKCA-BR 17 7797222 7797222 single base substitution T G missense_variant L25R 74T>G SKCA-BR 17 7797222 7797222 single base substitution T G missense_variant L298R 893T>G SKCA-BR 17 7797222 7797222 single base substitution T G missense_variant L357R 1070T>G SKCA-BR 17 7797222 7797222 single base substitution T G upstream_gene_variant SKCA-BR 17 7798709 7798709 single base substitution A G downstream_gene_variant SKCA-BR 17 7798709 7798709 single base substitution A G exon_variant SKCA-BR 17 7798709 7798709 single base substitution A G missense_variant E389G 1166A>G SKCA-BR 17 7798709 7798709 single base substitution A G missense_variant E519G 1556A>G SKCA-BR 17 7798709 7798709 single base substitution A G missense_variant E578G 1733A>G SKCA-BR 17 7804822 7804823 deletion of <=200bp GT - downstream_gene_variant SKCA-BR 17 7804822 7804823 deletion of <=200bp GT - intron_variant SKCA-BR 17 7804822 7804823 deletion of <=200bp GT - upstream_gene_variant SKCA-BR 17 7805262 7805262 single base substitution T G downstream_gene_variant SKCA-BR 17 7805262 7805262 single base substitution T G intron_variant SKCA-BR 17 7805262 7805262 single base substitution T G upstream_gene_variant SKCA-BR 17 7806493 7806493 single base substitution C T intron_variant SKCA-BR 17 7806493 7806493 single base substitution C T upstream_gene_variant SKCA-BR 17 7806529 7806529 single base substitution A G intron_variant SKCA-BR 17 7806529 7806529 single base substitution A G upstream_gene_variant SKCA-BR 17 7808226 7808226 single base substitution G C intron_variant SKCA-BR 17 7808226 7808226 single base substitution G C upstream_gene_variant SKCA-BR 17 7809271 7809271 single base substitution T G 3_prime_UTR_variant SKCA-BR 17 7809271 7809271 single base substitution T G downstream_gene_variant SKCA-BR 17 7809271 7809271 single base substitution T G missense_variant V1441G 4322T>G SKCA-BR 17 7809271 7809271 single base substitution T G missense_variant V1500G 4499T>G SKCA-BR 17 7809271 7809271 single base substitution T G upstream_gene_variant SKCA-BR 17 7812537 7812537 single base substitution A C 3_prime_UTR_variant SKCA-BR 17 7812537 7812537 single base substitution A C downstream_gene_variant SKCA-BR 17 7812537 7812537 single base substitution A C missense_variant H116P 347A>C SKCA-BR 17 7812537 7812537 single base substitution A C missense_variant H143P 428A>C SKCA-BR 17 7812537 7812537 single base substitution A C missense_variant H152P 455A>C SKCA-BR 17 7812537 7812537 single base substitution A C missense_variant H1790P 5369A>C SKCA-BR 17 7812537 7812537 single base substitution A C missense_variant H1824P 5471A>C SKCA-BR 17 7812537 7812537 single base substitution A C missense_variant H1883P 5648A>C SKCA-BR 17 7812537 7812537 single base substitution A C upstream_gene_variant SKCA-BR 17 7812676 7812676 single base substitution C T downstream_gene_variant SKCA-BR 17 7812676 7812676 single base substitution C T intron_variant SKCA-BR 17 7812676 7812676 single base substitution C T synonymous_variant P198P 594C>T SKCA-BR 17 7812676 7812676 single base substitution C T upstream_gene_variant SKCA-BR 17 7819072 7819072 single base substitution A C downstream_gene_variant SKCM-US 17 7793966 7793966 single base substitution C A downstream_gene_variant SKCM-US 17 7793966 7793966 single base substitution C A exon_variant SKCM-US 17 7793966 7793966 single base substitution C A synonymous_variant T156T 468C>A SKCM-US 17 7793966 7793966 single base substitution C A synonymous_variant T97T 291C>A SKCM-US 17 7793966 7793966 single base substitution C A upstream_gene_variant SKCM-US 17 7796803 7796803 single base substitution T C downstream_gene_variant SKCM-US 17 7796803 7796803 single base substitution T C exon_variant SKCM-US 17 7796803 7796803 single base substitution T C missense_variant S111P 331T>C SKCM-US 17 7796803 7796803 single base substitution T C missense_variant S237P 709T>C SKCM-US 17 7796803 7796803 single base substitution T C missense_variant S296P 886T>C SKCM-US 17 7796803 7796803 single base substitution T C upstream_gene_variant SKCM-US 17 7796822 7796822 single base substitution C T downstream_gene_variant SKCM-US 17 7796822 7796822 single base substitution C T exon_variant SKCM-US 17 7796822 7796822 single base substitution C T missense_variant P117L 350C>T SKCM-US 17 7796822 7796822 single base substitution C T missense_variant P243L 728C>T SKCM-US 17 7796822 7796822 single base substitution C T missense_variant P302L 905C>T SKCM-US 17 7796822 7796822 single base substitution C T upstream_gene_variant SKCM-US 17 7797852 7797852 single base substitution C T downstream_gene_variant SKCM-US 17 7797852 7797852 single base substitution C T exon_variant SKCM-US 17 7797852 7797852 single base substitution C T missense_variant R269C 805C>T SKCM-US 17 7797852 7797852 single base substitution C T missense_variant R399C 1195C>T SKCM-US 17 7797852 7797852 single base substitution C T missense_variant R458C 1372C>T SKCM-US 17 7797852 7797852 single base substitution C T upstream_gene_variant SKCM-US 17 7798689 7798689 single base substitution C T downstream_gene_variant SKCM-US 17 7798689 7798689 single base substitution C T exon_variant SKCM-US 17 7798689 7798689 single base substitution C T synonymous_variant I382I 1146C>T SKCM-US 17 7798689 7798689 single base substitution C T synonymous_variant I512I 1536C>T SKCM-US 17 7798689 7798689 single base substitution C T synonymous_variant I571I 1713C>T SKCM-US 17 7798840 7798840 single base substitution T C downstream_gene_variant SKCM-US 17 7798840 7798840 single base substitution T C exon_variant SKCM-US 17 7798840 7798840 single base substitution T C missense_variant S433P 1297T>C SKCM-US 17 7798840 7798840 single base substitution T C missense_variant S563P 1687T>C SKCM-US 17 7798840 7798840 single base substitution T C missense_variant S622P 1864T>C SKCM-US 17 7801392 7801392 single base substitution G A downstream_gene_variant SKCM-US 17 7801392 7801392 single base substitution G A missense_variant E675K 2023G>A SKCM-US 17 7801392 7801392 single base substitution G A missense_variant E734K 2200G>A SKCM-US 17 7802714 7802714 single base substitution C T downstream_gene_variant SKCM-US 17 7802714 7802714 single base substitution C T synonymous_variant N799N 2397C>T SKCM-US 17 7802714 7802714 single base substitution C T synonymous_variant N858N 2574C>T SKCM-US 17 7802714 7802714 single base substitution C T upstream_gene_variant SKCM-US 17 7802801 7802801 single base substitution G T downstream_gene_variant SKCM-US 17 7802801 7802801 single base substitution G T missense_variant E828D 2484G>T SKCM-US 17 7802801 7802801 single base substitution G T missense_variant E887D 2661G>T SKCM-US 17 7802801 7802801 single base substitution G T upstream_gene_variant SKCM-US 17 7803245 7803245 single base substitution T C downstream_gene_variant SKCM-US 17 7803245 7803245 single base substitution T C missense_variant L859P 2576T>C SKCM-US 17 7803245 7803245 single base substitution T C missense_variant L918P 2753T>C SKCM-US 17 7803245 7803245 single base substitution T C upstream_gene_variant SKCM-US 17 7803628 7803628 single base substitution T C downstream_gene_variant SKCM-US 17 7803628 7803628 single base substitution T C synonymous_variant G901G 2703T>C SKCM-US 17 7803628 7803628 single base substitution T C synonymous_variant G960G 2880T>C SKCM-US 17 7803628 7803628 single base substitution T C upstream_gene_variant SKCM-US 17 7803930 7803930 single base substitution C T downstream_gene_variant SKCM-US 17 7803930 7803930 single base substitution C T synonymous_variant I1012I 3036C>T SKCM-US 17 7803930 7803930 single base substitution C T synonymous_variant I953I 2859C>T SKCM-US 17 7803930 7803930 single base substitution C T upstream_gene_variant SKCM-US 17 7804297 7804297 single base substitution C T downstream_gene_variant SKCM-US 17 7804297 7804297 single base substitution C T missense_variant P1036S 3106C>T SKCM-US 17 7804297 7804297 single base substitution C T missense_variant P1095S 3283C>T SKCM-US 17 7804297 7804297 single base substitution C T upstream_gene_variant SKCM-US 17 7806015 7806015 single base substitution C T downstream_gene_variant SKCM-US 17 7806015 7806015 single base substitution C T synonymous_variant L1114L 3340C>T SKCM-US 17 7806015 7806015 single base substitution C T synonymous_variant L1173L 3517C>T SKCM-US 17 7806015 7806015 single base substitution C T upstream_gene_variant SKCM-US 17 7806292 7806292 single base substitution C T downstream_gene_variant SKCM-US 17 7806292 7806292 single base substitution C T synonymous_variant T1136T 3408C>T SKCM-US 17 7806292 7806292 single base substitution C T synonymous_variant T1195T 3585C>T SKCM-US 17 7806292 7806292 single base substitution C T upstream_gene_variant SKCM-US 17 7806313 7806313 single base substitution C T downstream_gene_variant SKCM-US 17 7806313 7806313 single base substitution C T synonymous_variant I1143I 3429C>T SKCM-US 17 7806313 7806313 single base substitution C T synonymous_variant I1202I 3606C>T SKCM-US 17 7806313 7806313 single base substitution C T upstream_gene_variant SKCM-US 17 7807809 7807809 single base substitution C T 3_prime_UTR_variant SKCM-US 17 7807809 7807809 single base substitution C T exon_variant SKCM-US 17 7807809 7807809 single base substitution C T missense_variant P1315L 3944C>T SKCM-US 17 7807809 7807809 single base substitution C T missense_variant P1374L 4121C>T SKCM-US 17 7807809 7807809 single base substitution C T upstream_gene_variant SKCM-US 17 7808417 7808417 single base substitution G A splice_acceptor_variant SKCM-US 17 7808417 7808417 single base substitution G A upstream_gene_variant SKCM-US 17 7808467 7808467 single base substitution C T 3_prime_UTR_variant SKCM-US 17 7808467 7808467 single base substitution C T exon_variant SKCM-US 17 7808467 7808467 single base substitution C T synonymous_variant F1374F 4122C>T SKCM-US 17 7808467 7808467 single base substitution C T synonymous_variant F1433F 4299C>T SKCM-US 17 7808467 7808467 single base substitution C T upstream_gene_variant SKCM-US 17 7808948 7808948 single base substitution A G 3_prime_UTR_variant SKCM-US 17 7808948 7808948 single base substitution A G downstream_gene_variant SKCM-US 17 7808948 7808948 single base substitution A G exon_variant SKCM-US 17 7808948 7808948 single base substitution A G missense_variant Q1383R 4148A>G SKCM-US 17 7808948 7808948 single base substitution A G missense_variant Q1442R 4325A>G SKCM-US 17 7808948 7808948 single base substitution A G upstream_gene_variant SKCM-US 17 7809173 7809173 single base substitution G A downstream_gene_variant SKCM-US 17 7809173 7809173 single base substitution G A splice_acceptor_variant SKCM-US 17 7809173 7809173 single base substitution G A upstream_gene_variant SKCM-US 17 7810332 7810332 single base substitution C T 3_prime_UTR_variant SKCM-US 17 7810332 7810332 single base substitution C T downstream_gene_variant SKCM-US 17 7810332 7810332 single base substitution C T missense_variant P1550L 4649C>T SKCM-US 17 7810332 7810332 single base substitution C T missense_variant P1609L 4826C>T SKCM-US 17 7810332 7810332 single base substitution C T upstream_gene_variant SKCM-US 17 7811260 7811260 single base substitution C G 3_prime_UTR_variant SKCM-US 17 7811260 7811260 single base substitution C G downstream_gene_variant SKCM-US 17 7811260 7811260 single base substitution C G exon_variant SKCM-US 17 7811260 7811260 single base substitution C G missense_variant P11R 32C>G SKCM-US 17 7811260 7811260 single base substitution C G missense_variant P1658R 4973C>G SKCM-US 17 7811260 7811260 single base substitution C G missense_variant P1692R 5075C>G SKCM-US 17 7811260 7811260 single base substitution C G missense_variant P1751R 5252C>G SKCM-US 17 7811260 7811260 single base substitution C G missense_variant P20R 59C>G SKCM-US 17 7811260 7811260 single base substitution C G upstream_gene_variant SKCM-US 17 7811272 7811272 single base substitution G A 3_prime_UTR_variant SKCM-US 17 7811272 7811272 single base substitution G A downstream_gene_variant SKCM-US 17 7811272 7811272 single base substitution G A exon_variant SKCM-US 17 7811272 7811272 single base substitution G A missense_variant G15E 44G>A SKCM-US 17 7811272 7811272 single base substitution G A missense_variant G1662E 4985G>A SKCM-US 17 7811272 7811272 single base substitution G A missense_variant G1696E 5087G>A SKCM-US 17 7811272 7811272 single base substitution G A missense_variant G1755E 5264G>A SKCM-US 17 7811272 7811272 single base substitution G A missense_variant G24E 71G>A SKCM-US 17 7811272 7811272 single base substitution G A upstream_gene_variant SKCM-US 17 7811803 7811803 single base substitution T G 3_prime_UTR_variant SKCM-US 17 7811803 7811803 single base substitution T G downstream_gene_variant SKCM-US 17 7811803 7811803 single base substitution T G exon_variant SKCM-US 17 7811803 7811803 single base substitution T G missense_variant Y1712D 5134T>G SKCM-US 17 7811803 7811803 single base substitution T G missense_variant Y1746D 5236T>G SKCM-US 17 7811803 7811803 single base substitution T G missense_variant Y1805D 5413T>G SKCM-US 17 7811803 7811803 single base substitution T G missense_variant Y38D 112T>G SKCM-US 17 7811803 7811803 single base substitution T G missense_variant Y65D 193T>G SKCM-US 17 7811803 7811803 single base substitution T G missense_variant Y74D 220T>G SKCM-US 17 7811803 7811803 single base substitution T G upstream_gene_variant STAD-US 17 7794025 7794025 single base substitution G A downstream_gene_variant STAD-US 17 7794025 7794025 single base substitution G A missense_variant R117Q 350G>A STAD-US 17 7794025 7794025 single base substitution G A missense_variant R176Q 527G>A STAD-US 17 7794025 7794025 single base substitution G A upstream_gene_variant STAD-US 17 7794048 7794048 deletion of <=200bp G - downstream_gene_variant STAD-US 17 7794048 7794048 deletion of <=200bp G - frameshift_variant G125 STAD-US 17 7794048 7794048 deletion of <=200bp G - frameshift_variant G184 STAD-US 17 7794048 7794048 deletion of <=200bp G - upstream_gene_variant STAD-US 17 7794305 7794305 single base substitution G T downstream_gene_variant STAD-US 17 7794305 7794305 single base substitution G T synonymous_variant L144L 432G>T STAD-US 17 7794305 7794305 single base substitution G T synonymous_variant L18L 54G>T STAD-US 17 7794305 7794305 single base substitution G T synonymous_variant L203L 609G>T STAD-US 17 7794305 7794305 single base substitution G T upstream_gene_variant STAD-US 17 7794347 7794347 single base substitution G A downstream_gene_variant STAD-US 17 7794347 7794347 single base substitution G A synonymous_variant T158T 474G>A STAD-US 17 7794347 7794347 single base substitution G A synonymous_variant T217T 651G>A STAD-US 17 7794347 7794347 single base substitution G A synonymous_variant T32T 96G>A STAD-US 17 7794347 7794347 single base substitution G A upstream_gene_variant STAD-US 17 7796827 7796827 deletion of <=200bp C - downstream_gene_variant STAD-US 17 7796827 7796827 deletion of <=200bp C - exon_variant STAD-US 17 7796827 7796827 deletion of <=200bp C - frameshift_variant P119 STAD-US 17 7796827 7796827 deletion of <=200bp C - frameshift_variant P245 STAD-US 17 7796827 7796827 deletion of <=200bp C - frameshift_variant P304 STAD-US 17 7796827 7796827 deletion of <=200bp C - upstream_gene_variant STAD-US 17 7797156 7797156 single base substitution G A downstream_gene_variant STAD-US 17 7797156 7797156 single base substitution G A exon_variant STAD-US 17 7797156 7797156 single base substitution G A missense_variant R150Q 449G>A STAD-US 17 7797156 7797156 single base substitution G A missense_variant R276Q 827G>A STAD-US 17 7797156 7797156 single base substitution G A missense_variant R335Q 1004G>A STAD-US 17 7797156 7797156 single base substitution G A missense_variant R3Q 8G>A STAD-US 17 7797156 7797156 single base substitution G A upstream_gene_variant STAD-US 17 7797857 7797857 single base substitution C A downstream_gene_variant STAD-US 17 7797857 7797857 single base substitution C A exon_variant STAD-US 17 7797857 7797857 single base substitution C A synonymous_variant A270A 810C>A STAD-US 17 7797857 7797857 single base substitution C A synonymous_variant A400A 1200C>A STAD-US 17 7797857 7797857 single base substitution C A synonymous_variant A459A 1377C>A STAD-US 17 7797857 7797857 single base substitution C A upstream_gene_variant STAD-US 17 7798346 7798346 single base substitution G A downstream_gene_variant STAD-US 17 7798346 7798346 single base substitution G A exon_variant STAD-US 17 7798346 7798346 single base substitution G A missense_variant V331I 991G>A STAD-US 17 7798346 7798346 single base substitution G A missense_variant V461I 1381G>A STAD-US 17 7798346 7798346 single base substitution G A missense_variant V520I 1558G>A STAD-US 17 7798700 7798700 single base substitution G A downstream_gene_variant STAD-US 17 7798700 7798700 single base substitution G A exon_variant STAD-US 17 7798700 7798700 single base substitution G A missense_variant R386Q 1157G>A STAD-US 17 7798700 7798700 single base substitution G A missense_variant R516Q 1547G>A STAD-US 17 7798700 7798700 single base substitution G A missense_variant R575Q 1724G>A STAD-US 17 7798765 7798765 deletion of <=200bp C - downstream_gene_variant STAD-US 17 7798765 7798765 deletion of <=200bp C - exon_variant STAD-US 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P408 STAD-US 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P538 STAD-US 17 7798765 7798765 deletion of <=200bp C - frameshift_variant P597 STAD-US 17 7802494 7802494 single base substitution G A downstream_gene_variant STAD-US 17 7802494 7802494 single base substitution G A missense_variant V773I 2317G>A STAD-US 17 7802494 7802494 single base substitution G A missense_variant V832I 2494G>A STAD-US 17 7802494 7802494 single base substitution G A upstream_gene_variant STAD-US 17 7803219 7803219 single base substitution G T downstream_gene_variant STAD-US 17 7803219 7803219 single base substitution G T missense_variant E850D 2550G>T STAD-US 17 7803219 7803219 single base substitution G T missense_variant E909D 2727G>T STAD-US 17 7803219 7803219 single base substitution G T upstream_gene_variant STAD-US 17 7803346 7803346 single base substitution T C downstream_gene_variant STAD-US 17 7803346 7803346 single base substitution T C missense_variant S893P 2677T>C STAD-US 17 7803346 7803346 single base substitution T C missense_variant S952P 2854T>C STAD-US 17 7803346 7803346 single base substitution T C upstream_gene_variant STAD-US 17 7805989 7805989 single base substitution G A downstream_gene_variant STAD-US 17 7805989 7805989 single base substitution G A missense_variant R1105H 3314G>A STAD-US 17 7805989 7805989 single base substitution G A missense_variant R1164H 3491G>A STAD-US 17 7805989 7805989 single base substitution G A upstream_gene_variant STAD-US 17 7807305 7807305 single base substitution A G exon_variant STAD-US 17 7807305 7807305 single base substitution A G missense_variant D1297G 3890A>G STAD-US 17 7807305 7807305 single base substitution A G missense_variant D1356G 4067A>G STAD-US 17 7807305 7807305 single base substitution A G upstream_gene_variant STAD-US 17 7809005 7809005 single base substitution G A 3_prime_UTR_variant STAD-US 17 7809005 7809005 single base substitution G A downstream_gene_variant STAD-US 17 7809005 7809005 single base substitution G A missense_variant R1402Q 4205G>A STAD-US 17 7809005 7809005 single base substitution G A missense_variant R1461Q 4382G>A STAD-US 17 7809005 7809005 single base substitution G A upstream_gene_variant STAD-US 17 7809229 7809229 deletion of <=200bp G - 3_prime_UTR_variant STAD-US 17 7809229 7809229 deletion of <=200bp G - downstream_gene_variant STAD-US 17 7809229 7809229 deletion of <=200bp G - frameshift_variant W1427 STAD-US 17 7809229 7809229 deletion of <=200bp G - frameshift_variant W1486 STAD-US 17 7809229 7809229 deletion of <=200bp G - upstream_gene_variant STAD-US 17 7809236 7809236 single base substitution G A 3_prime_UTR_variant STAD-US 17 7809236 7809236 single base substitution G A downstream_gene_variant STAD-US 17 7809236 7809236 single base substitution G A missense_variant M1429I 4287G>A STAD-US 17 7809236 7809236 single base substitution G A missense_variant M1488I 4464G>A STAD-US 17 7809236 7809236 single base substitution G A upstream_gene_variant STAD-US 17 7810228 7810228 single base substitution G A 3_prime_UTR_variant STAD-US 17 7810228 7810228 single base substitution G A downstream_gene_variant STAD-US 17 7810228 7810228 single base substitution G A synonymous_variant P1515P 4545G>A STAD-US 17 7810228 7810228 single base substitution G A synonymous_variant P1574P 4722G>A STAD-US 17 7810228 7810228 single base substitution G A upstream_gene_variant STAD-US 17 7810789 7810789 single base substitution G T 3_prime_UTR_variant STAD-US 17 7810789 7810789 single base substitution G T downstream_gene_variant STAD-US 17 7810789 7810789 single base substitution G T exon_variant STAD-US 17 7810789 7810789 single base substitution G T missense_variant G1636V 4907G>T STAD-US 17 7810789 7810789 single base substitution G T missense_variant G1695V 5084G>T STAD-US 17 7810789 7810789 single base substitution G T upstream_gene_variant STAD-US 17 7812021 7812021 single base substitution C T 3_prime_UTR_variant STAD-US 17 7812021 7812021 single base substitution C T downstream_gene_variant STAD-US 17 7812021 7812021 single base substitution C T synonymous_variant G1722G 5166C>T STAD-US 17 7812021 7812021 single base substitution C T synonymous_variant G1756G 5268C>T STAD-US 17 7812021 7812021 single base substitution C T synonymous_variant G1815G 5445C>T STAD-US 17 7812021 7812021 single base substitution C T synonymous_variant G48G 144C>T STAD-US 17 7812021 7812021 single base substitution C T synonymous_variant G75G 225C>T STAD-US 17 7812021 7812021 single base substitution C T synonymous_variant G84G 252C>T STAD-US 17 7812021 7812021 single base substitution C T upstream_gene_variant STAD-US 17 7813796 7813796 single base substitution C T 3_prime_UTR_variant STAD-US 17 7813796 7813796 single base substitution C T downstream_gene_variant STAD-US 17 7813796 7813796 single base substitution C T exon_variant STAD-US 17 7813796 7813796 single base substitution C T intron_variant STAD-US 17 7813796 7813796 single base substitution C T missense_variant P196L 587C>T STAD-US 17 7813796 7813796 single base substitution C T missense_variant P224L 671C>T STAD-US 17 7813796 7813796 single base substitution C T missense_variant R1847C 5539C>T STAD-US 17 7813796 7813796 single base substitution C T missense_variant R1881C 5641C>T STAD-US 17 7813796 7813796 single base substitution C T missense_variant R1940C 5818C>T STAD-US 17 7813856 7813856 single base substitution C T 3_prime_UTR_variant STAD-US 17 7813856 7813856 single base substitution C T downstream_gene_variant STAD-US 17 7813856 7813856 single base substitution C T exon_variant STAD-US 17 7813856 7813856 single base substitution C T intron_variant STAD-US 17 7813856 7813856 single base substitution C T missense_variant A216V 647C>T STAD-US 17 7813856 7813856 single base substitution C T missense_variant A244V 731C>T STAD-US 17 7813856 7813856 single base substitution C T missense_variant R1867C 5599C>T STAD-US 17 7813856 7813856 single base substitution C T missense_variant R1901C 5701C>T STAD-US 17 7813856 7813856 single base substitution C T missense_variant R1960C 5878C>T STAD-US 17 7814196 7814196 single base substitution C T 3_prime_UTR_variant STAD-US 17 7814196 7814196 single base substitution C T downstream_gene_variant STAD-US 17 7814196 7814196 single base substitution C T exon_variant STAD-US 17 7814196 7814196 single base substitution C T missense_variant P1895L 5684C>T STAD-US 17 7814196 7814196 single base substitution C T missense_variant P1929L 5786C>T STAD-US 17 7814196 7814196 single base substitution C T missense_variant P1988L 5963C>T STAD-US 17 7814196 7814196 single base substitution C T synonymous_variant S166S 498C>T STAD-US 17 7814196 7814196 single base substitution C T synonymous_variant S244S 732C>T STAD-US 17 7814196 7814196 single base substitution C T synonymous_variant S272S 816C>T STAD-US 17 7814252 7814252 single base substitution G A 3_prime_UTR_variant STAD-US 17 7814252 7814252 single base substitution G A downstream_gene_variant STAD-US 17 7814252 7814252 single base substitution G A exon_variant STAD-US 17 7814252 7814252 single base substitution G A missense_variant A1914T 5740G>A STAD-US 17 7814252 7814252 single base substitution G A missense_variant A1948T 5842G>A STAD-US 17 7814252 7814252 single base substitution G A missense_variant A2007T 6019G>A STAD-US 17 7814252 7814252 single base substitution G A missense_variant R185H 554G>A STAD-US 17 7814252 7814252 single base substitution G A missense_variant R291H 872G>A STAD-US 17 7814810 7814812 deletion of <=200bp GAA - 3_prime_UTR_variant STAD-US 17 7814810 7814812 deletion of <=200bp GAA - downstream_gene_variant STAD-US 17 7814810 7814812 deletion of <=200bp GAA - exon_variant STAD-US 17 7814810 7814812 deletion of <=200bp GAA - inframe_deletion E208 STAD-US 17 7814810 7814812 deletion of <=200bp GAA - inframe_deletion E314 STAD-US 17 7814810 7814812 deletion of <=200bp GAA - inframe_deletion VK1936V STAD-US 17 7814810 7814812 deletion of <=200bp GAA - inframe_deletion VK1970V STAD-US 17 7814810 7814812 deletion of <=200bp GAA - inframe_deletion VK2029V STAD-US 17 7814849 7814849 single base substitution C T 3_prime_UTR_variant STAD-US 17 7814849 7814849 single base substitution C T downstream_gene_variant STAD-US 17 7814849 7814849 single base substitution C T exon_variant STAD-US 17 7814849 7814849 single base substitution C T missense_variant R221W 661C>T STAD-US 17 7814849 7814849 single base substitution C T missense_variant R327W 979C>T STAD-US 17 7814849 7814849 single base substitution C T synonymous_variant D1949D 5847C>T STAD-US 17 7814849 7814849 single base substitution C T synonymous_variant D1983D 5949C>T STAD-US 17 7814849 7814849 single base substitution C T synonymous_variant D2042D 6126C>T THCA-SA 17 7788343 7788343 insertion of <=200bp - CCG inframe_insertion F73FR THCA-SA 17 7788343 7788343 insertion of <=200bp - CCG upstream_gene_variant THCA-SA 17 7815712 7815712 single base substitution C T 3_prime_UTR_variant THCA-SA 17 7815712 7815712 single base substitution C T downstream_gene_variant THCA-SA 17 7815712 7815712 single base substitution C T exon_variant THCA-US 17 7797853 7797853 single base substitution G A downstream_gene_variant THCA-US 17 7797853 7797853 single base substitution G A exon_variant THCA-US 17 7797853 7797853 single base substitution G A missense_variant R269H 806G>A THCA-US 17 7797853 7797853 single base substitution G A missense_variant R399H 1196G>A THCA-US 17 7797853 7797853 single base substitution G A missense_variant R458H 1373G>A THCA-US 17 7797853 7797853 single base substitution G A upstream_gene_variant THCA-US 17 7798683 7798683 single base substitution G C downstream_gene_variant THCA-US 17 7798683 7798683 single base substitution G C exon_variant THCA-US 17 7798683 7798683 single base substitution G C missense_variant Q380H 1140G>C THCA-US 17 7798683 7798683 single base substitution G C missense_variant Q510H 1530G>C THCA-US 17 7798683 7798683 single base substitution G C missense_variant Q569H 1707G>C THCA-US 17 7800502 7800502 single base substitution G C downstream_gene_variant THCA-US 17 7800502 7800502 single base substitution G C missense_variant K473N 1419G>C THCA-US 17 7800502 7800502 single base substitution G C missense_variant K603N 1809G>C THCA-US 17 7800502 7800502 single base substitution G C missense_variant K662N 1986G>C UCEC-US 17 7792988 7792988 single base substitution A G missense_variant D36G 107A>G UCEC-US 17 7792988 7792988 single base substitution A G missense_variant D95G 284A>G UCEC-US 17 7792988 7792988 single base substitution A G upstream_gene_variant UCEC-US 17 7793982 7793982 single base substitution C T downstream_gene_variant UCEC-US 17 7793982 7793982 single base substitution C T exon_variant UCEC-US 17 7793982 7793982 single base substitution C T stop_gained R103* 307C>T UCEC-US 17 7793982 7793982 single base substitution C T stop_gained R162* 484C>T UCEC-US 17 7793982 7793982 single base substitution C T upstream_gene_variant UCEC-US 17 7796726 7796726 single base substitution C T downstream_gene_variant UCEC-US 17 7796726 7796726 single base substitution C T exon_variant UCEC-US 17 7796726 7796726 single base substitution C T missense_variant A211V 632C>T UCEC-US 17 7796726 7796726 single base substitution C T missense_variant A270V 809C>T UCEC-US 17 7796726 7796726 single base substitution C T missense_variant A85V 254C>T UCEC-US 17 7796726 7796726 single base substitution C T upstream_gene_variant UCEC-US 17 7797129 7797129 single base substitution G A downstream_gene_variant UCEC-US 17 7797129 7797129 single base substitution G A exon_variant UCEC-US 17 7797129 7797129 single base substitution G A missense_variant G141D 422G>A UCEC-US 17 7797129 7797129 single base substitution G A missense_variant G267D 800G>A UCEC-US 17 7797129 7797129 single base substitution G A missense_variant G326D 977G>A UCEC-US 17 7797129 7797129 single base substitution G A upstream_gene_variant UCEC-US 17 7797492 7797492 single base substitution T C downstream_gene_variant UCEC-US 17 7797492 7797492 single base substitution T C exon_variant UCEC-US 17 7797492 7797492 single base substitution T C synonymous_variant S198S 594T>C UCEC-US 17 7797492 7797492 single base substitution T C synonymous_variant S328S 984T>C UCEC-US 17 7797492 7797492 single base substitution T C synonymous_variant S387S 1161T>C UCEC-US 17 7797492 7797492 single base substitution T C synonymous_variant S55S 165T>C UCEC-US 17 7797492 7797492 single base substitution T C upstream_gene_variant UCEC-US 17 7797535 7797535 single base substitution C T downstream_gene_variant UCEC-US 17 7797535 7797535 single base substitution C T exon_variant UCEC-US 17 7797535 7797535 single base substitution C T missense_variant R213C 637C>T UCEC-US 17 7797535 7797535 single base substitution C T missense_variant R343C 1027C>T UCEC-US 17 7797535 7797535 single base substitution C T missense_variant R402C 1204C>T UCEC-US 17 7797535 7797535 single base substitution C T missense_variant R70C 208C>T UCEC-US 17 7797535 7797535 single base substitution C T upstream_gene_variant UCEC-US 17 7797818 7797818 deletion of <=200bp G - downstream_gene_variant UCEC-US 17 7797818 7797818 deletion of <=200bp G - exon_variant UCEC-US 17 7797818 7797818 deletion of <=200bp G - frameshift_variant Q108 UCEC-US 17 7797818 7797818 deletion of <=200bp G - frameshift_variant Q257 UCEC-US 17 7797818 7797818 deletion of <=200bp G - frameshift_variant Q387 UCEC-US 17 7797818 7797818 deletion of <=200bp G - frameshift_variant Q446 UCEC-US 17 7797818 7797818 deletion of <=200bp G - upstream_gene_variant UCEC-US 17 7800406 7800406 single base substitution A C downstream_gene_variant UCEC-US 17 7800406 7800406 single base substitution A C missense_variant E441D 1323A>C UCEC-US 17 7800406 7800406 single base substitution A C missense_variant E571D 1713A>C UCEC-US 17 7800406 7800406 single base substitution A C missense_variant E630D 1890A>C UCEC-US 17 7800528 7800528 single base substitution C T downstream_gene_variant UCEC-US 17 7800528 7800528 single base substitution C T missense_variant P482L 1445C>T UCEC-US 17 7800528 7800528 single base substitution C T missense_variant P612L 1835C>T UCEC-US 17 7800528 7800528 single base substitution C T missense_variant P671L 2012C>T UCEC-US 17 7801815 7801815 single base substitution G T downstream_gene_variant UCEC-US 17 7801815 7801815 single base substitution G T stop_gained E685* 2053G>T UCEC-US 17 7801815 7801815 single base substitution G T stop_gained E744* 2230G>T UCEC-US 17 7802419 7802419 single base substitution C T downstream_gene_variant UCEC-US 17 7802419 7802419 single base substitution C T missense_variant R748C 2242C>T UCEC-US 17 7802419 7802419 single base substitution C T missense_variant R807C 2419C>T UCEC-US 17 7802419 7802419 single base substitution C T upstream_gene_variant UCEC-US 17 7803219 7803219 single base substitution G T downstream_gene_variant UCEC-US 17 7803219 7803219 single base substitution G T missense_variant E850D 2550G>T UCEC-US 17 7803219 7803219 single base substitution G T missense_variant E909D 2727G>T UCEC-US 17 7803219 7803219 single base substitution G T upstream_gene_variant UCEC-US 17 7803251 7803251 single base substitution C T downstream_gene_variant UCEC-US 17 7803251 7803251 single base substitution C T missense_variant S861L 2582C>T UCEC-US 17 7803251 7803251 single base substitution C T missense_variant S920L 2759C>T UCEC-US 17 7803251 7803251 single base substitution C T upstream_gene_variant UCEC-US 17 7803698 7803698 single base substitution C T downstream_gene_variant UCEC-US 17 7803698 7803698 single base substitution C T missense_variant L925F 2773C>T UCEC-US 17 7803698 7803698 single base substitution C T missense_variant L984F 2950C>T UCEC-US 17 7803698 7803698 single base substitution C T upstream_gene_variant UCEC-US 17 7803987 7803987 single base substitution C A downstream_gene_variant UCEC-US 17 7803987 7803987 single base substitution C A synonymous_variant V1031V 3093C>A UCEC-US 17 7803987 7803987 single base substitution C A synonymous_variant V972V 2916C>A UCEC-US 17 7803987 7803987 single base substitution C A upstream_gene_variant UCEC-US 17 7803995 7803995 single base substitution A G downstream_gene_variant UCEC-US 17 7803995 7803995 single base substitution A G missense_variant N1034S 3101A>G UCEC-US 17 7803995 7803995 single base substitution A G missense_variant N975S 2924A>G UCEC-US 17 7803995 7803995 single base substitution A G upstream_gene_variant UCEC-US 17 7804274 7804274 single base substitution G A downstream_gene_variant UCEC-US 17 7804274 7804274 single base substitution G A missense_variant C1028Y 3083G>A UCEC-US 17 7804274 7804274 single base substitution G A missense_variant C1087Y 3260G>A UCEC-US 17 7804274 7804274 single base substitution G A upstream_gene_variant UCEC-US 17 7804674 7804674 single base substitution G A downstream_gene_variant UCEC-US 17 7804674 7804674 single base substitution G A missense_variant R1078Q 3233G>A UCEC-US 17 7804674 7804674 single base substitution G A missense_variant R1137Q 3410G>A UCEC-US 17 7804674 7804674 single base substitution G A upstream_gene_variant UCEC-US 17 7805993 7805993 single base substitution C T downstream_gene_variant UCEC-US 17 7805993 7805993 single base substitution C T synonymous_variant I1106I 3318C>T UCEC-US 17 7805993 7805993 single base substitution C T synonymous_variant I1165I 3495C>T UCEC-US 17 7805993 7805993 single base substitution C T upstream_gene_variant UCEC-US 17 7806042 7806042 single base substitution A G downstream_gene_variant UCEC-US 17 7806042 7806042 single base substitution A G missense_variant N1123D 3367A>G UCEC-US 17 7806042 7806042 single base substitution A G missense_variant N1182D 3544A>G UCEC-US 17 7806042 7806042 single base substitution A G upstream_gene_variant UCEC-US 17 7806657 7806657 single base substitution C T missense_variant A1188V 3563C>T UCEC-US 17 7806657 7806657 single base substitution C T missense_variant A1247V 3740C>T UCEC-US 17 7806657 7806657 single base substitution C T upstream_gene_variant UCEC-US 17 7806722 7806722 single base substitution C T missense_variant R1210W 3628C>T UCEC-US 17 7806722 7806722 single base substitution C T missense_variant R1269W 3805C>T UCEC-US 17 7806722 7806722 single base substitution C T upstream_gene_variant UCEC-US 17 7806817 7806817 single base substitution C T synonymous_variant N1241N 3723C>T UCEC-US 17 7806817 7806817 single base substitution C T synonymous_variant N1300N 3900C>T UCEC-US 17 7806817 7806817 single base substitution C T upstream_gene_variant UCEC-US 17 7807196 7807196 single base substitution G A exon_variant UCEC-US 17 7807196 7807196 single base substitution G A missense_variant A1261T 3781G>A UCEC-US 17 7807196 7807196 single base substitution G A missense_variant A1320T 3958G>A UCEC-US 17 7807196 7807196 single base substitution G A upstream_gene_variant UCEC-US 17 7807783 7807783 single base substitution C A 3_prime_UTR_variant UCEC-US 17 7807783 7807783 single base substitution C A exon_variant UCEC-US 17 7807783 7807783 single base substitution C A synonymous_variant I1306I 3918C>A UCEC-US 17 7807783 7807783 single base substitution C A synonymous_variant I1365I 4095C>A UCEC-US 17 7807783 7807783 single base substitution C A upstream_gene_variant UCEC-US 17 7807889 7807889 single base substitution C T 3_prime_UTR_variant UCEC-US 17 7807889 7807889 single base substitution C T exon_variant UCEC-US 17 7807889 7807889 single base substitution C T missense_variant R1342W 4024C>T UCEC-US 17 7807889 7807889 single base substitution C T missense_variant R1401W 4201C>T UCEC-US 17 7807889 7807889 single base substitution C T upstream_gene_variant UCEC-US 17 7808417 7808417 single base substitution G T splice_acceptor_variant UCEC-US 17 7808417 7808417 single base substitution G T upstream_gene_variant UCEC-US 17 7808449 7808449 single base substitution G T 3_prime_UTR_variant UCEC-US 17 7808449 7808449 single base substitution G T exon_variant UCEC-US 17 7808449 7808449 single base substitution G T missense_variant E1368D 4104G>T UCEC-US 17 7808449 7808449 single base substitution G T missense_variant E1427D 4281G>T UCEC-US 17 7808449 7808449 single base substitution G T upstream_gene_variant UCEC-US 17 7809893 7809893 single base substitution C T 3_prime_UTR_variant UCEC-US 17 7809893 7809893 single base substitution C T downstream_gene_variant UCEC-US 17 7809893 7809893 single base substitution C T missense_variant R1461C 4381C>T UCEC-US 17 7809893 7809893 single base substitution C T missense_variant R1520C 4558C>T UCEC-US 17 7809893 7809893 single base substitution C T upstream_gene_variant UCEC-US 17 7809937 7809937 single base substitution C T 3_prime_UTR_variant UCEC-US 17 7809937 7809937 single base substitution C T downstream_gene_variant UCEC-US 17 7809937 7809937 single base substitution C T synonymous_variant A1475A 4425C>T UCEC-US 17 7809937 7809937 single base substitution C T synonymous_variant A1534A 4602C>T UCEC-US 17 7809937 7809937 single base substitution C T upstream_gene_variant UCEC-US 17 7810214 7810214 single base substitution C T 3_prime_UTR_variant UCEC-US 17 7810214 7810214 single base substitution C T downstream_gene_variant UCEC-US 17 7810214 7810214 single base substitution C T missense_variant R1511C 4531C>T UCEC-US 17 7810214 7810214 single base substitution C T missense_variant R1570C 4708C>T UCEC-US 17 7810214 7810214 single base substitution C T upstream_gene_variant UCEC-US 17 7811008 7811008 single base substitution T G 3_prime_UTR_variant UCEC-US 17 7811008 7811008 single base substitution T G downstream_gene_variant UCEC-US 17 7811008 7811008 single base substitution T G exon_variant UCEC-US 17 7811008 7811008 single base substitution T G intron_variant UCEC-US 17 7811008 7811008 single base substitution T G missense_variant L1672V 5014T>G UCEC-US 17 7811008 7811008 single base substitution T G missense_variant L1731V 5191T>G UCEC-US 17 7811008 7811008 single base substitution T G upstream_gene_variant UCEC-US 17 7811274 7811274 single base substitution C T 3_prime_UTR_variant UCEC-US 17 7811274 7811274 single base substitution C T downstream_gene_variant UCEC-US 17 7811274 7811274 single base substitution C T exon_variant UCEC-US 17 7811274 7811274 single base substitution C T stop_gained R16* 46C>T UCEC-US 17 7811274 7811274 single base substitution C T stop_gained R1663* 4987C>T UCEC-US 17 7811274 7811274 single base substitution C T stop_gained R1697* 5089C>T UCEC-US 17 7811274 7811274 single base substitution C T stop_gained R1756* 5266C>T UCEC-US 17 7811274 7811274 single base substitution C T stop_gained R25* 73C>T UCEC-US 17 7811274 7811274 single base substitution C T upstream_gene_variant UCEC-US 17 7811726 7811726 single base substitution A G 3_prime_UTR_variant UCEC-US 17 7811726 7811726 single base substitution A G downstream_gene_variant UCEC-US 17 7811726 7811726 single base substitution A G exon_variant UCEC-US 17 7811726 7811726 single base substitution A G missense_variant H12R 35A>G UCEC-US 17 7811726 7811726 single base substitution A G missense_variant H1686R 5057A>G UCEC-US 17 7811726 7811726 single base substitution A G missense_variant H1720R 5159A>G UCEC-US 17 7811726 7811726 single base substitution A G missense_variant H1779R 5336A>G UCEC-US 17 7811726 7811726 single base substitution A G missense_variant H39R 116A>G UCEC-US 17 7811726 7811726 single base substitution A G missense_variant H48R 143A>G UCEC-US 17 7811726 7811726 single base substitution A G upstream_gene_variant UCEC-US 17 7811750 7811750 single base substitution G T 3_prime_UTR_variant UCEC-US 17 7811750 7811750 single base substitution G T downstream_gene_variant UCEC-US 17 7811750 7811750 single base substitution G T exon_variant UCEC-US 17 7811750 7811750 single base substitution G T missense_variant R1694L 5081G>T UCEC-US 17 7811750 7811750 single base substitution G T missense_variant R1728L 5183G>T UCEC-US 17 7811750 7811750 single base substitution G T missense_variant R1787L 5360G>T UCEC-US 17 7811750 7811750 single base substitution G T missense_variant R20L 59G>T UCEC-US 17 7811750 7811750 single base substitution G T missense_variant R47L 140G>T UCEC-US 17 7811750 7811750 single base substitution G T missense_variant R56L 167G>T UCEC-US 17 7811750 7811750 single base substitution G T upstream_gene_variant UCEC-US 17 7812640 7812640 single base substitution C T 3_prime_UTR_variant UCEC-US 17 7812640 7812640 single base substitution C T downstream_gene_variant UCEC-US 17 7812640 7812640 single base substitution C T synonymous_variant N150N 450C>T UCEC-US 17 7812640 7812640 single base substitution C T synonymous_variant N177N 531C>T UCEC-US 17 7812640 7812640 single base substitution C T synonymous_variant N1824N 5472C>T UCEC-US 17 7812640 7812640 single base substitution C T synonymous_variant N1858N 5574C>T UCEC-US 17 7812640 7812640 single base substitution C T synonymous_variant N186N 558C>T UCEC-US 17 7812640 7812640 single base substitution C T synonymous_variant N1917N 5751C>T UCEC-US 17 7812640 7812640 single base substitution C T upstream_gene_variant UCEC-US 17 7813831 7813831 single base substitution C T 3_prime_UTR_variant UCEC-US 17 7813831 7813831 single base substitution C T downstream_gene_variant UCEC-US 17 7813831 7813831 single base substitution C T exon_variant UCEC-US 17 7813831 7813831 single base substitution C T intron_variant UCEC-US 17 7813831 7813831 single base substitution C T missense_variant R208C 622C>T UCEC-US 17 7813831 7813831 single base substitution C T missense_variant R236C 706C>T UCEC-US 17 7813831 7813831 single base substitution C T synonymous_variant I1858I 5574C>T UCEC-US 17 7813831 7813831 single base substitution C T synonymous_variant I1892I 5676C>T UCEC-US 17 7813831 7813831 single base substitution C T synonymous_variant I1951I 5853C>T UCEC-US 17 7813839 7813839 single base substitution G A 3_prime_UTR_variant UCEC-US 17 7813839 7813839 single base substitution G A downstream_gene_variant UCEC-US 17 7813839 7813839 single base substitution G A exon_variant UCEC-US 17 7813839 7813839 single base substitution G A intron_variant UCEC-US 17 7813839 7813839 single base substitution G A missense_variant R1861H 5582G>A UCEC-US 17 7813839 7813839 single base substitution G A missense_variant R1895H 5684G>A UCEC-US 17 7813839 7813839 single base substitution G A missense_variant R1954H 5861G>A UCEC-US 17 7813839 7813839 single base substitution G A synonymous_variant P210P 630G>A UCEC-US 17 7813839 7813839 single base substitution G A synonymous_variant P238P 714G>A UCEC-US 17 7813890 7813890 single base substitution C T 3_prime_UTR_variant UCEC-US 17 7813890 7813890 single base substitution C T downstream_gene_variant UCEC-US 17 7813890 7813890 single base substitution C T exon_variant UCEC-US 17 7813890 7813890 single base substitution C T intron_variant UCEC-US 17 7813890 7813890 single base substitution C T missense_variant T1878M 5633C>T UCEC-US 17 7813890 7813890 single base substitution C T missense_variant T1912M 5735C>T UCEC-US 17 7813890 7813890 single base substitution C T missense_variant T1971M 5912C>T UCEC-US 17 7813890 7813890 single base substitution C T synonymous_variant H227H 681C>T UCEC-US 17 7813890 7813890 single base substitution C T synonymous_variant H255H 765C>T UCEC-US 17 7814819 7814819 single base substitution G A 3_prime_UTR_variant UCEC-US 17 7814819 7814819 single base substitution G A downstream_gene_variant UCEC-US 17 7814819 7814819 single base substitution G A exon_variant UCEC-US 17 7814819 7814819 single base substitution G A missense_variant E211K 631G>A UCEC-US 17 7814819 7814819 single base substitution G A missense_variant E317K 949G>A UCEC-US 17 7814819 7814819 single base substitution G A synonymous_variant E1939E 5817G>A UCEC-US 17 7814819 7814819 single base substitution G A synonymous_variant E1973E 5919G>A UCEC-US 17 7814819 7814819 single base substitution G A synonymous_variant E2032E 6096G>A UCEC-US 17 7814976 7814976 single base substitution C T 3_prime_UTR_variant UCEC-US 17 7814976 7814976 single base substitution C T downstream_gene_variant UCEC-US 17 7814976 7814976 single base substitution C T exon_variant UCEC-US 17 7814976 7814976 single base substitution C T missense_variant A263V 788C>T UCEC-US 17 7814976 7814976 single base substitution C T missense_variant A369V 1106C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand SH-0622 COSM437716 c.2095_2097delAAG p.K703delK Deletion - In frame 17:7898539-7898541 + RK064_C01 COSM1630470 c.561C>T p.T187T Substitution - coding silent 17:7893337-7893337 + TCGA-EE-A3AA-06 COSM3523264 c.2859C>T p.I953I Substitution - coding silent 17:7900612-7900612 + Pat_53_B COSM2803226 c.5762C>T p.P1921L Substitution - Missense 17:7910854-7910854 + cSCCP4 COSM139045 c.1168G>T p.E390* Substitution - Nonsense 17:7894507-7894507 + TCGA-AZ-4615-01 COSM3691902 c.254G>A p.R85Q Substitution - Missense 17:7890611-7890611 + Pat_16_A COSM473486 c.1099G>A p.G367R Substitution - Missense 17:7894438-7894438 + CHC155T COSM217148 c.5323C>G p.P1775A Substitution - Missense 17:7908758-7908758 + Pat_22_B COSM5853719 c.5540C>G p.S1847C Substitution - Missense 17:7909288-7909288 + 2521244 COSM5895168 c.709_710insC p.G238fs*12 Insertion - Frameshift 17:7893485-7893486 + TCGA-BH-A2L8-01 COSM3820881 c.4426G>A p.D1476N Substitution - Missense 17:7906620-7906620 + TCGA-BS-A0UF-01 COSM985438 c.1713A>C p.E571D Substitution - Missense 17:7897088-7897088 + TCGA-DD-A3A0-01 COSM4934694 c.4487C>A p.S1496Y Substitution - Missense 17:7906681-7906681 + TCGA-AP-A059-01 COSM417942 c.3563C>T p.A1188V Substitution - Missense 17:7903339-7903339 + MD-220 COSM301930 c.721G>C p.A241P Substitution - Missense 17:7893497-7893497 + SC_9068 COSM5567466 c.4586C>G p.S1529C Substitution - Missense 17:7906951-7906951 + D28 COSM5544692 c.1222C>T p.P408S Substitution - Missense 17:7894561-7894561 + SNUH_G15_S1 COSM3680603 c.467A>C p.Y156S Substitution - Missense 17:7891022-7891022 + BD6T COSM5499281 c.1612_1613insCC p.R540fs*17 Insertion - Frameshift 17:7895447-7895448 + DLBCL793 COSM1580705 c.861G>T p.K287N Substitution - Missense 17:7893872-7893872 + TCGA-BH-A0BP-01 COSM437714 c.1627C>T p.Q543* Substitution - Nonsense 17:7895462-7895462 + TCGA-AA-3713-01 COSM417942 c.3563C>T p.A1188V Substitution - Missense 17:7903339-7903339 + TCGA-CJ-4886-01 COSM3362399 c.2246T>A p.F749Y Substitution - Missense 17:7899105-7899105 + TCGA-EE-A2MG-06 COSM3523310 c.5236T>G p.Y1746D Substitution - Missense 17:7908485-7908485 + TCGA-AM-5821-01 COSM3755974 c.8C>T p.A3V Substitution - Missense 17:7889008-7889008 + T2940 COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + TCGA-HF-7132-01 COSM4070382 c.3314G>A p.R1105H Substitution - Missense 17:7902671-7902671 + TCGA-AA-3715-01 COSM268881 c.1207C>A p.L403I Substitution - Missense 17:7894546-7894546 + CSCC-62-T COSM4546693 c.3877G>C p.V1293L Substitution - Missense 17:7903974-7903974 + 18 COSM5745317 c.2887C>T p.H963Y Substitution - Missense 17:7900640-7900640 + 8066081 COSM3388270 c.559A>T p.T187S Substitution - Missense 17:7893335-7893335 + TCGA-BG-A0LX-01 COSM985516 c.4425C>T p.A1475A Substitution - coding silent 17:7906619-7906619 + TCGA-A8-A0A6-01 COSM3820880 c.4417A>C p.T1473P Substitution - Missense 17:7906611-7906611 + CSCC-38-T COSM4569713 c.1789T>C p.S597P Substitution - Missense 17:7897164-7897164 + PT34 COSM5910911 c.3479C>T p.P1160L Substitution - Missense 17:7903045-7903045 + 388 COSM4427425 c.100+4A>G p.? Unknown 17:7889104-7889104 + HCT-15 COSM1679535 c.521C>A p.A174D Substitution - Missense 17:7893297-7893297 + YUSIV COSM5387554 c.540C>T p.I180I Substitution - coding silent 17:7893316-7893316 + T3152 COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + TCGA-EL-A3H1-01 COSM3370954 c.1809G>C p.K603N Substitution - Missense 17:7897184-7897184 + PR-00-1165 COSM243668 c.5793C>T p.Y1931Y Substitution - coding silent 17:7910885-7910885 + PT44 COSM5926953 c.793+5G>A p.? Unknown 17:7893574-7893574 + S02120 COSM5673566 c.1088C>T p.P363L Substitution - Missense 17:7894427-7894427 + TCGA-AX-A060-01 COSM985531 c.5183G>T p.R1728L Substitution - Missense 17:7908432-7908432 + TCGA-28-5216-01 COSM3403345 c.5078G>A p.R1693Q Substitution - Missense 17:7907945-7907945 + BCM723T COSM5348366 c.1618delC p.R540fs*16 Deletion - Frameshift 17:7895453-7895453 + TCGA-BR-7851-01 COSM2802859 c.474G>A p.T158T Substitution - coding silent 17:7891029-7891029 + TCGA-PJ-A5Z8-01 COSM3989400 c.469C>G p.H157D Substitution - Missense 17:7891024-7891024 + SNUH_G15_S1 COSM3680609 c.4590A>C p.R1530S Substitution - Missense 17:7906955-7906955 + TCGA-EM-A3FM-01 COSM3370952 c.1196G>A p.R399H Substitution - Missense 17:7894535-7894535 + CRC-17T COSM4130771 c.4322T>G p.V1441G Substitution - Missense 17:7905953-7905953 + ML_50_T_01 COSM5038592 c.1556A>G p.E519G Substitution - Missense 17:7895391-7895391 + BZ16 COSM5758372 c.973G>A p.D325N Substitution - Missense 17:7894163-7894163 + LUAD-S01478 COSM399763 c.5471A>C p.H1824P Substitution - Missense 17:7909219-7909219 + TCGA-F5-6814-01 COSM1387346 c.197G>A p.R66Q Substitution - Missense 17:7889760-7889760 + TCGA-B5-A11E-01 COSM985428 c.800G>A p.G267D Substitution - Missense 17:7893811-7893811 + T368 COSM417942 c.3563C>T p.A1188V Substitution - Missense 17:7903339-7903339 + TCGA-DO-A2HM-01 COSM3370953 c.1530G>C p.Q510H Substitution - Missense 17:7895365-7895365 + TCGA-ER-A193-06 COSM3523247 c.1195C>T p.R399C Substitution - Missense 17:7894534-7894534 + 587220 COSM1200965 c.292G>A p.G98R Substitution - Missense 17:7890649-7890649 + TCGA-BR-8382-01 COSM4070396 c.5641C>T p.R1881C Substitution - Missense 17:7910478-7910478 + pfg008T COSM1640884 c.2690G>T p.R897M Substitution - Missense 17:7900297-7900297 + BD124T COSM5490947 c.4949delG p.E1652fs*27 Deletion - Frameshift 17:7907625-7907625 + TCGA-EE-A2MK-06 COSM3523306 c.4649C>T p.P1550L Substitution - Missense 17:7907014-7907014 + TCGA-AA-3715-01 COSM268880 c.639G>A p.A213A Substitution - coding silent 17:7893415-7893415 + TCGA-BR-7707-01 COSM1200966 c.5701C>T p.R1901C Substitution - Missense 17:7910538-7910538 + TCGA-D8-A27G-01 COSM3820879 c.4233C>A p.G1411G Substitution - coding silent 17:7905864-7905864 + pfg059T COSM4749524 c.4265A>G p.N1422S Substitution - Missense 17:7905896-7905896 + Pat_66_A COSM5853699 c.826C>T p.R276* Substitution - Nonsense 17:7893837-7893837 + CCK81 COSM2803188 c.4471C>T p.R1491C Substitution - Missense 17:7906665-7906665 + PT46 COSM5929715 c.4838G>A p.R1613K Substitution - Missense 17:7907402-7907402 + cSCCP8 COSM140785 c.4243C>T p.R1415C Substitution - Missense 17:7905874-7905874 + Pat_70_B COSM437716 c.2095_2097delAAG p.K703delK Deletion - In frame 17:7898539-7898541 + BD165T COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + S02352 COSM5672148 c.5489A>C p.H1830P Substitution - Missense 17:7909237-7909237 + Pat_16_A COSM985495 c.3781G>A p.A1261T Substitution - Missense 17:7903878-7903878 + S00838 COSM5661505 c.5202G>T p.G1734G Substitution - coding silent 17:7908451-7908451 + TCGA-D9-A6EC-06 COSM4401373 c.2576T>C p.L859P Substitution - Missense 17:7899927-7899927 + TCGA-D3-A1Q6-06 COSM3523283 c.3429C>T p.I1143I Substitution - coding silent 17:7902995-7902995 + TCGA-EB-A5SG-06 COSM3890616 c.2703T>C p.G901G Substitution - coding silent 17:7900310-7900310 + ESO-0292 COSM1241005 c.613T>C p.S205P Substitution - Missense 17:7893389-7893389 + PT51 COSM5938389 c.1457C>T p.P486L Substitution - Missense 17:7895104-7895104 + LUAD-NYU201 COSM371330 c.700A>C p.I234L Substitution - Missense 17:7893476-7893476 + 61 COSM5740856 c.5662C>T p.R1888* Substitution - Nonsense 17:7910499-7910499 + TCGA-UC-A7PF-01 COSM4830188 c.2281G>A p.D761N Substitution - Missense 17:7899140-7899140 + TCGA-BS-A0UM-01 COSM985518 c.4531C>T p.R1511C Substitution - Missense 17:7906896-7906896 + 2334196 COSM319433 c.4015A>C p.K1339Q Substitution - Missense 17:7904562-7904562 + TCGA-CD-5804-01 COSM4070392 c.4287G>A p.M1429I Substitution - Missense 17:7905918-7905918 + TCGA-AN-A046-01 COSM3820856 c.1752G>T p.K584N Substitution - Missense 17:7897127-7897127 + CSCC-44-T COSM4494346 c.253C>T p.R85W Substitution - Missense 17:7890610-7890610 + TCGA-B5-A11J-01 COSM985423 c.307C>T p.R103* Substitution - Nonsense 17:7890664-7890664 + TCGA-EE-A181-06 COSM3523308 c.5087G>A p.G1696E Substitution - Missense 17:7907954-7907954 + 6948_PT COSM5755167 c.4210G>A p.G1404R Substitution - Missense 17:7905692-7905692 + TCGA-BR-4292-01 COSM4070393 c.4907G>T p.G1636V Substitution - Missense 17:7907471-7907471 + TCGA-CG-5728-01 COSM985462 c.2550G>T p.E850D Substitution - Missense 17:7899901-7899901 + PTC-28C COSM371330 c.700A>C p.I234L Substitution - Missense 17:7893476-7893476 + pfg025T COSM1640881 c.811C>T p.R271W Substitution - Missense 17:7893822-7893822 + TCGA-ER-A194-01 COSM3523268 c.3106C>T p.P1036S Substitution - Missense 17:7900979-7900979 + TCGA-ED-A66Y-01 COSM4926454 c.1567G>A p.A523T Substitution - Missense 17:7895402-7895402 + CSCC-31-T COSM4494609 c.4192C>T p.P1398S Substitution - Missense 17:7905674-7905674 + TCGA-BS-A0UF-01 COSM985472 c.2916C>A p.V972V Substitution - coding silent 17:7900669-7900669 + TCGA-B5-A11X-01 COSM985502 c.4024C>T p.R1342W Substitution - Missense 17:7904571-7904571 + CSCC-31-T COSM4451830 c.1251A>T p.K417N Substitution - Missense 17:7894590-7894590 + B96-Tumor COSM3932770 c.1549T>G p.W517G Substitution - Missense 17:7895384-7895384 + TCGA-A5-A0VP-01 COSM985460 c.2242C>T p.R748C Substitution - Missense 17:7899101-7899101 + TCGA-D1-A17Q-01 COSM985491 c.3723C>T p.N1241N Substitution - coding silent 17:7903499-7903499 + PT43 COSM301930 c.721G>C p.A241P Substitution - Missense 17:7893497-7893497 + TCGA-B0-4712-01 COSM473486 c.1099G>A p.G367R Substitution - Missense 17:7894438-7894438 + TCGA-A3-3363-01 COSM1494088 c.5117G>A p.R1706Q Substitution - Missense 17:7907984-7907984 + TCGA-BR-8487-01 COSM4070361 c.2317G>A p.V773I Substitution - Missense 17:7899176-7899176 + J30_T COSM3958895 c.4558G>T p.D1520Y Substitution - Missense 17:7906923-7906923 + 2521260 COSM274532 c.2896C>T p.R966W Substitution - Missense 17:7900649-7900649 + TCGA-BR-6452-01 COSM1387384 c.5786C>T p.P1929L Substitution - Missense 17:7910878-7910878 + TCGA-29-1763-01 COSM1324719 c.5706C>T p.S1902S Substitution - coding silent 17:7910543-7910543 + TCGA-A6-6780-01 COSM3686134 c.794-1delG p.? Unknown 17:7893804-7893804 + TCGA-BH-A2L8-01 COSM3820877 c.4167G>A p.R1389R Substitution - coding silent 17:7905649-7905649 + TCGA-D1-A15X-01 COSM985540 c.5735C>T p.T1912M Substitution - Missense 17:7910572-7910572 + YUKAT COSM5387560 c.2368G>A p.V790M Substitution - Missense 17:7899367-7899367 + TCGA-A5-A0GB-01 COSM985419 c.107A>G p.D36G Substitution - Missense 17:7889670-7889670 + DN120A6 COSM5789893 c.4978G>A p.E1660K Substitution - Missense 17:7907654-7907654 + ATL019 COSM5706654 c.3017C>T p.A1006V Substitution - Missense 17:7900890-7900890 + SB_07 COSM5753272 c.2246delT p.F749fs*11 Deletion - Frameshift 17:7899105-7899105 + 8057501 COSM3388270 c.559A>T p.T187S Substitution - Missense 17:7893335-7893335 + WSU-HN30 COSM301930 c.721G>C p.A241P Substitution - Missense 17:7893497-7893497 + AMO1 COSM1235988 c.2593A>G p.I865V Substitution - Missense 17:7899944-7899944 + TCGA-BR-4184-01 COSM4070395 c.5268C>T p.G1756G Substitution - coding silent 17:7908703-7908703 + pfg076T COSM4749522 c.2824G>C p.E942Q Substitution - Missense 17:7900577-7900577 + 423 COSM4432507 c.1290G>T p.W430C Substitution - Missense 17:7894937-7894937 + TCGA-BS-A0UA-01 COSM985489 c.3628C>T p.R1210W Substitution - Missense 17:7903404-7903404 + PT35 COSM5913859 c.1504-6C>T p.? Unknown 17:7895333-7895333 + TCGA-BP-4340-01 COSM3362398 c.1138G>A p.D380N Substitution - Missense 17:7894477-7894477 + TCGA-P5-A5EX-01 COSM371330 c.700A>C p.I234L Substitution - Missense 17:7893476-7893476 + PTC-77C COSM4130754 c.1098C>A p.A366A Substitution - coding silent 17:7894437-7894437 + T97 COSM239308 c.1730delT p.M577fs*33 Deletion - Frameshift 17:7897105-7897105 + TCGA-EE-A3J7-06 COSM3890612 c.2397C>T p.N799N Substitution - coding silent 17:7899396-7899396 + TCGA-JX-A3Q0-01 COSM4823936 c.5800G>A p.A1934T Substitution - Missense 17:7910892-7910892 + TCGA-EE-A2MR-06 COSM2803151 c.4122C>T p.F1374F Substitution - coding silent 17:7905149-7905149 + T3174 COSM4671983 c.4244G>A p.R1415H Substitution - Missense 17:7905875-7905875 + TCGA-66-2734-01 COSM708757 c.3357C>A p.I1119I Substitution - coding silent 17:7902714-7902714 + LOVO COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + TCGA-AD-6895-01 COSM1387384 c.5786C>T p.P1929L Substitution - Missense 17:7910878-7910878 + T2944 COSM4671978 c.1732T>C p.Y578H Substitution - Missense 17:7897107-7897107 + CHC1774T COSM4802394 c.2364C>T p.F788F Substitution - coding silent 17:7899363-7899363 + T578 COSM4671980 c.2750A>C p.N917T Substitution - Missense 17:7900357-7900357 + EGC8 COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + 587224 COSM1200966 c.5701C>T p.R1901C Substitution - Missense 17:7910538-7910538 + Pat_11_B COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + 169 COSM3730018 c.1611_1612insC p.R540fs*47 Insertion - Frameshift 17:7895446-7895447 + TCGA-AY-6197-01 COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + 587376 COSM1200970 c.3010T>G p.F1004V Substitution - Missense 17:7900883-7900883 + AA1816 COSM4168800 c.5677G>A p.A1893T Substitution - Missense 17:7910514-7910514 + YUGURT COSM5387561 c.3397C>T p.L1133F Substitution - Missense 17:7902963-7902963 + TCGA-AX-A0J1-01 COSM985434 c.1161delG p.G388fs*96 Deletion - Frameshift 17:7894500-7894500 + 6948_CLM COSM5755167 c.4210G>A p.G1404R Substitution - Missense 17:7905692-7905692 + TCGA-AA-A00N-01 COSM274531 c.2031G>T p.K677N Substitution - Missense 17:7898082-7898082 + CHC155T COSM217148 c.5323C>G p.P1775A Substitution - Missense 17:7908758-7908758 + TCGA-24-1843-01 COSM1324722 c.1381G>C p.V461L Substitution - Missense 17:7895028-7895028 + 4095_T COSM3958888 c.2012C>G p.P671R Substitution - Missense 17:7898063-7898063 + BD124T COSM5493520 c.644C>T p.A215V Substitution - Missense 17:7893420-7893420 + LN18 COSM5712768 c.5054G>T p.R1685L Substitution - Missense 17:7907921-7907921 + 165 COSM985540 c.5735C>T p.T1912M Substitution - Missense 17:7910572-7910572 + TCGA-BS-A0UJ-01 COSM985486 c.3367A>G p.N1123D Substitution - Missense 17:7902724-7902724 + 130 COSM3732910 c.5183G>A p.R1728Q Substitution - Missense 17:7908432-7908432 + PA285 COSM1163181 c.4778T>C p.M1593T Substitution - Missense 17:7907237-7907237 + C086 COSM1200963 c.5053C>T p.R1685* Substitution - Nonsense 17:7907920-7907920 + Pat_31_A COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + T3064 COSM4671976 c.242G>A p.R81Q Substitution - Missense 17:7890599-7890599 + 949_T COSM3958889 c.2405G>T p.R802L Substitution - Missense 17:7899404-7899404 + LC_C6 COSM1189395 c.435G>C p.E145D Substitution - Missense 17:7890990-7890990 + ESO-1133 COSM1248204 c.911A>T p.K304M Substitution - Missense 17:7893922-7893922 + PTC-46C COSM4130771 c.4322T>G p.V1441G Substitution - Missense 17:7905953-7905953 + TCGA-B5-A11N-01 COSM985529 c.5159A>G p.H1720R Substitution - Missense 17:7908408-7908408 + T228 COSM4671987 c.5950G>A p.G1984R Substitution - Missense 17:7911532-7911532 + SC_9081 COSM5567882 c.614C>T p.S205L Substitution - Missense 17:7893390-7893390 + TCGA-B5-A11E-01 COSM985462 c.2550G>T p.E850D Substitution - Missense 17:7899901-7899901 + TCGA-D3-A51G-06 COSM3523260 c.2484G>T p.E828D Substitution - Missense 17:7899483-7899483 + SCC-15 COSM301930 c.721G>C p.A241P Substitution - Missense 17:7893497-7893497 + TCGA-DK-A3IS-01 COSM1303443 c.1026C>T p.V342V Substitution - coding silent 17:7894216-7894216 + Pat_55_A COSM5853700 c.1105G>A p.E369K Substitution - Missense 17:7894444-7894444 + TCGA-RP-A695-06 COSM4896210 c.728C>T p.P243L Substitution - Missense 17:7893504-7893504 + TCGA-F4-6854-01 COSM1387383 c.5760C>A p.Y1920* Substitution - Nonsense 17:7910852-7910852 + TCGA-A2-A0T5-01 COSM3820855 c.1611A>C p.P537P Substitution - coding silent 17:7895446-7895446 + 381_T COSM3958887 c.1441C>G p.H481D Substitution - Missense 17:7895088-7895088 + TCGA-AP-A0LG-01 COSM985421 c.252C>T p.Y84Y Substitution - coding silent 17:7890609-7890609 + ACINAR01 COSM1735417 c.5195C>T p.S1732F Substitution - Missense 17:7908444-7908444 + TCGA-EE-A2MS-06 COSM3523251 c.1687T>C p.S563P Substitution - Missense 17:7895522-7895522 + TCGA-EE-A2GI-06 COSM2803151 c.4122C>T p.F1374F Substitution - coding silent 17:7905149-7905149 + HRA19 COSM4637772 c.2684T>G p.F895C Substitution - Missense 17:7900291-7900291 + TCGA-AZ-6601-01 COSM1387372 c.4183C>A p.P1395T Substitution - Missense 17:7905665-7905665 + TCGA-FS-A1ZC-06 COSM3523297 c.4073-1G>A p.? Unknown 17:7905099-7905099 + AOCS-155-3-5 COSM4139921 c.55A>G p.R19G Substitution - Missense 17:7889055-7889055 + CSCC-29-T COSM4488168 c.3107C>T p.P1036L Substitution - Missense 17:7900980-7900980 + YUOMEGA COSM5387562 c.3758T>C p.I1253T Substitution - Missense 17:7903855-7903855 + SNU-C2B COSM2803178 c.4250G>A p.R1417Q Substitution - Missense 17:7905881-7905881 + 19M COSM985468 c.2582C>T p.S861L Substitution - Missense 17:7899933-7899933 + YUDEXA COSM1709759 c.2467C>T p.R823W Substitution - Missense 17:7899466-7899466 + TCGA-BS-A0UV-01 COSM985470 c.2773C>T p.L925F Substitution - Missense 17:7900380-7900380 + CAL27 COSM2803082 c.3563C>A p.A1188E Substitution - Missense 17:7903339-7903339 + 1342576 COSM51320 c.4729G>A p.E1577K Substitution - Missense 17:7907188-7907188 + TCGA-FU-A3HZ-01 COSM4839690 c.3760C>A p.H1254N Substitution - Missense 17:7903857-7903857 + LUAD-S01405 COSM398975 c.188G>A p.G63E Substitution - Missense 17:7889751-7889751 + TCGA-D5-6927-01 COSM1387358 c.2289delG p.L765fs*1 Deletion - Frameshift 17:7899148-7899148 + Pat_65_A COSM437716 c.2095_2097delAAG p.K703delK Deletion - In frame 17:7898539-7898541 + LAU149 COSM232032 c.3128C>T p.P1043L Substitution - Missense 17:7901251-7901251 + A673 COSM4580204 c.1156C>G p.Q386E Substitution - Missense 17:7894495-7894495 + CHC1774T COSM4802394 c.2364C>T p.F788F Substitution - coding silent 17:7899363-7899363 + BD122T COSM5521000 c.2660G>A p.R887Q Substitution - Missense 17:7900011-7900011 + TCGA-EB-A3XB-01 COSM3523301 c.4148A>G p.Q1383R Substitution - Missense 17:7905630-7905630 + 23 COSM5016544 c.1958_1965delGGAGGGAC p.W653fs*4 Deletion - Frameshift 17:7898009-7898016 + CHEWS033 COSM4580205 c.1776C>T p.P592P Substitution - coding silent 17:7897151-7897151 + TCGA-CK-5913-01 COSM3691909 c.5556G>A p.A1852A Substitution - coding silent 17:7909304-7909304 + S02291 COSM5686979 c.2468G>T p.R823L Substitution - Missense 17:7899467-7899467 + TCGA-A5-A0GB-01 COSM985534 c.5574C>T p.N1858N Substitution - coding silent 17:7909322-7909322 + 23 COSM5016543 c.1949_1955delTAGTAAA p.L650fs*17 Deletion - Frameshift 17:7898000-7898006 + SWE-2B COSM1178238 c.1200C>A p.A400A Substitution - coding silent 17:7894539-7894539 + pfg143T COSM4765036 c.1612_1613insC p.R540fs*47 Insertion - Frameshift 17:7895447-7895448 + TCGA-J9-A52B-01 COSM4876972 c.5179G>T p.E1727* Substitution - Nonsense 17:7908428-7908428 + TCGA-AA-A00N-01 COSM274532 c.2896C>T p.R966W Substitution - Missense 17:7900649-7900649 + LIM2551 COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + TCGA-EE-A29D-06 COSM3523250 c.1536C>T p.I512I Substitution - coding silent 17:7895371-7895371 + HX32T COSM3717738 c.1495C>T p.R499* Substitution - Nonsense 17:7895142-7895142 + SNUH_G76_S1 COSM4419972 c.4092G>A p.S1364S Substitution - coding silent 17:7905119-7905119 + PT46 COSM5929716 c.2626C>T p.R876C Substitution - Missense 17:7899977-7899977 + PR-09-2517 COSM243669 c.4034A>C p.K1345T Substitution - Missense 17:7904581-7904581 + TCGA-CG-5718-01 COSM4070329 c.827G>A p.R276Q Substitution - Missense 17:7893838-7893838 + TCGA-HU-A4GX-01 COSM4070397 c.5842G>A p.A1948T Substitution - Missense 17:7910934-7910934 + CSCC-11-T COSM4272963 c.4583C>T p.S1528F Substitution - Missense 17:7906948-7906948 + TCGA-BS-A0UV-01 COSM985440 c.1835C>T p.P612L Substitution - Missense 17:7897210-7897210 + TCGA-B5-A0JY-01 COSM985542 c.5919G>A p.E1973E Substitution - coding silent 17:7911501-7911501 + T2932 COSM2803081 c.3560G>A p.R1187H Substitution - Missense 17:7903336-7903336 + TCGA-D1-A0ZO-01 COSM985495 c.3781G>A p.A1261T Substitution - Missense 17:7903878-7903878 + T3080 COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + T3091 COSM4671979 c.2422G>A p.A808T Substitution - Missense 17:7899421-7899421 + sysucc-1370T COSM5470778 c.5164C>G p.L1722V Substitution - Missense 17:7908413-7908413 + H1155 COSM1195473 c.5630C>T p.A1877V Substitution - Missense 17:7910467-7910467 + DLBCL799 COSM1580705 c.861G>T p.K287N Substitution - Missense 17:7893872-7893872 + TCGA-HU-A4H5-01 COSM4070328 c.432G>T p.L144L Substitution - coding silent 17:7890987-7890987 + TCGA-A6-6653-01 COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + KM12 COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + TCGA-EE-A3AG-06 COSM3523252 c.2023G>A p.E675K Substitution - Missense 17:7898074-7898074 + Patient_2_Relapse COSM5414982 c.2096A>G p.K699R Substitution - Missense 17:7898540-7898540 + TCGA-HU-A4H4-01 COSM473501 c.4545G>A p.P1515P Substitution - coding silent 17:7906910-7906910 + TCGA-21-5787-01 COSM708762 c.2243G>T p.R748L Substitution - Missense 17:7899102-7899102 + TCGA-A6-2676-01 COSM265557 c.5910_5912delGAA p.K1972delK Deletion - In frame 17:7911492-7911494 + TCGA-DS-A0VM-01 COSM460183 c.3004C>T p.R1002* Substitution - Nonsense 17:7900877-7900877 + AOCS-091-1-3 COSM4139922 c.101-9G>A p.? Unknown 17:7889655-7889655 + HX20T COSM3717735 c.1135C>T p.Q379* Substitution - Nonsense 17:7894474-7894474 + TCGA-D3-A5GN-06 COSM3523246 c.291C>A p.T97T Substitution - coding silent 17:7890648-7890648 + TCGA-61-1895-01 COSM1324723 c.510G>T p.R170S Substitution - Missense 17:7893286-7893286 + TCGA-A6-6781-01 COSM1387345 c.196C>T p.R66* Substitution - Nonsense 17:7889759-7889759 + 66 COSM5015436 c.1577C>T p.A526V Substitution - Missense 17:7895412-7895412 + CSCC-31-T COSM4445638 c.5590+9C>T p.? Unknown 17:7909347-7909347 + T3225 COSM4671984 c.4254G>T p.K1418N Substitution - Missense 17:7905885-7905885 + MO_1128 COSM5554531 c.3522C>T p.G1174G Substitution - coding silent 17:7903298-7903298 + 66 COSM5743822 c.1049G>A p.G350D Substitution - Missense 17:7894239-7894239 + TCGA-B5-A11Y-01 COSM985527 c.5089C>T p.R1697* Substitution - Nonsense 17:7907956-7907956 + TCGA-AZ-4315-01 COSM1387346 c.197G>A p.R66Q Substitution - Missense 17:7889760-7889760 + S01873 COSM5672148 c.5489A>C p.H1830P Substitution - Missense 17:7909237-7909237 + 8066067 COSM3388270 c.559A>T p.T187S Substitution - Missense 17:7893335-7893335 + TCGA-AP-A051-01 COSM985430 c.984T>C p.S328S Substitution - coding silent 17:7894174-7894174 + TCGA-C5-A1BQ-01 COSM4841648 c.2575C>G p.L859V Substitution - Missense 17:7899926-7899926 + RK308_C01 COSM3742489 c.5905C>T p.L1969F Substitution - Missense 17:7911487-7911487 + PT37 COSM5921127 c.4453C>T p.R1485C Substitution - Missense 17:7906647-7906647 + 0067_CRUK_PC_0067_T1_DNA COSM4421042 c.3443C>T p.A1148V Substitution - Missense 17:7903009-7903009 + TCGA-AX-A0J0-01 COSM985499 c.3918C>A p.I1306I Substitution - coding silent 17:7904465-7904465 + 1 COSM5015435 c.473C>T p.T158M Substitution - Missense 17:7891028-7891028 + 587226 COSM1200963 c.5053C>T p.R1685* Substitution - Nonsense 17:7907920-7907920 + CSCC-7-T COSM4479361 c.2141C>T p.P714L Substitution - Missense 17:7898585-7898585 + 23 COSM5016545 c.1968_1986del19 p.L656fs*7 Deletion - Frameshift 17:7898019-7898037 + CSCC-38-T COSM4475175 c.1791C>T p.S597S Substitution - coding silent 17:7897166-7897166 + TCGA-AK-3451-01 COSM473495 c.3303C>A p.Y1101* Substitution - Nonsense 17:7902660-7902660 + HCC119T COSM1610929 c.1707+10C>G p.? Unknown 17:7895552-7895552 + WA55 COSM237193 c.1494C>T p.P498P Substitution - coding silent 17:7895141-7895141 + Pat_15_B COSM437716 c.2095_2097delAAG p.K703delK Deletion - In frame 17:7898539-7898541 + TCGA-FU-A23L-01 COSM301930 c.721G>C p.A241P Substitution - Missense 17:7893497-7893497 + 234 COSM3730018 c.1611_1612insC p.R540fs*47 Insertion - Frameshift 17:7895446-7895447 + TCGA-AA-A010-01 COSM279871 c.470A>C p.H157P Substitution - Missense 17:7891025-7891025 + TCGA-AA-3492-01 COSM1387348 c.1099delG p.E368fs*116 Deletion - Frameshift 17:7894438-7894438 + TCGA-G4-6628-01 COSM1387363 c.3636G>A p.G1212G Substitution - coding silent 17:7903412-7903412 + PT35 COSM5913860 c.682G>C p.V228L Substitution - Missense 17:7893458-7893458 + PTC-70C COSM4130771 c.4322T>G p.V1441G Substitution - Missense 17:7905953-7905953 + TCGA-CD-8536-01 COSM4070330 c.1381G>A p.V461I Substitution - Missense 17:7895028-7895028 + TCGA-IR-A3LK-01 COSM3820861 c.2284G>A p.E762K Substitution - Missense 17:7899143-7899143 + TCGA-CG-5723-01 COSM4070362 c.2677T>C p.S893P Substitution - Missense 17:7900028-7900028 + sysucc-311T COSM1580705 c.861G>T p.K287N Substitution - Missense 17:7893872-7893872 + PT49 COSM5936281 c.1615C>T p.P539S Substitution - Missense 17:7895450-7895450 + TCGA-B5-A0K6-01 COSM985478 c.3233G>A p.R1078Q Substitution - Missense 17:7901356-7901356 + HONE1 COSM4995788 c.121C>A p.L41M Substitution - Missense 17:7889684-7889684 + ID46 COSM1166744 c.929T>C p.V310A Substitution - Missense 17:7894119-7894119 + PD11345a COSM5789893 c.4978G>A p.E1660K Substitution - Missense 17:7907654-7907654 + SNU-175 COSM2803186 c.4382G>A p.R1461H Substitution - Missense 17:7906576-7906576 + TCGA-AP-A0LQ-01 COSM985538 c.5684G>A p.R1895H Substitution - Missense 17:7910521-7910521 + TCGA-39-5021-01 COSM708770 c.284A>G p.Y95C Substitution - Missense 17:7890641-7890641 + TCGA-A2-A0YM-01 COSM437715 c.1868G>A p.R623H Substitution - Missense 17:7897243-7897243 + PTC-28C COSM4130767 c.2547G>T p.R849S Substitution - Missense 17:7899898-7899898 + LUAD-RT-S01831 COSM384314 c.725T>C p.L242P Substitution - Missense 17:7893501-7893501 + TCGA-BS-A0UJ-01 COSM985474 c.2924A>G p.N975S Substitution - Missense 17:7900677-7900677 + HCC173T COSM3717744 c.5928G>A p.M1976I Substitution - Missense 17:7911510-7911510 + TCGA-FS-A1ZD-06 COSM3890610 c.709T>C p.S237P Substitution - Missense 17:7893485-7893485 + 164 COSM301930 c.721G>C p.A241P Substitution - Missense 17:7893497-7893497 + TCGA-A8-A0AB-01 COSM437713 c.664G>C p.E222Q Substitution - Missense 17:7893440-7893440 + HCC173 COSM3717744 c.5928G>A p.M1976I Substitution - Missense 17:7911510-7911510 + PT13 COSM5896303 c.1688C>T p.S563F Substitution - Missense 17:7895523-7895523 + TCGA-GV-A3QI-01 COSM1303444 c.1716C>G p.I572M Substitution - Missense 17:7897091-7897091 + CH-54-T2 COSM5651050 c.155G>A p.R52Q Substitution - Missense 17:7889718-7889718 + ESCC_109 COSM985468 c.2582C>T p.S861L Substitution - Missense 17:7899933-7899933 + TCGA-A6-6653-01 COSM1387350 c.1550delG p.E519fs*4 Deletion - Frameshift 17:7895385-7895385 + sysucc-783T COSM5484173 c.3797G>A p.R1266Q Substitution - Missense 17:7903894-7903894 + LUAD-S01356 COSM398050 c.4243C>A p.R1415S Substitution - Missense 17:7905874-7905874 + 4436_CLM COSM5755167 c.4210G>A p.G1404R Substitution - Missense 17:7905692-7905692 + TCGA-BR-7707-01 COSM4070386 c.3890A>G p.D1297G Substitution - Missense 17:7903987-7903987 + TCGA-A3-3363-01 COSM473495 c.3303C>A p.Y1101* Substitution - Nonsense 17:7902660-7902660 + ESO-717 COSM1242127 c.1664T>C p.V555A Substitution - Missense 17:7895499-7895499 + 587302 COSM1200964 c.2363T>C p.F788S Substitution - Missense 17:7899362-7899362 + SNU-C2B COSM2803193 c.4580G>A p.R1527H Substitution - Missense 17:7906945-7906945 + Pat_08_B COSM5853714 c.3943C>T p.P1315S Substitution - Missense 17:7904490-7904490 + TCGA-HU-A4GQ-01 COSM4070332 c.1547G>A p.R516Q Substitution - Missense 17:7895382-7895382 + TCGA-EB-A5SG-06 COSM3890626 c.5075C>G p.P1692R Substitution - Missense 17:7907942-7907942 + TCGA-AZ-4615-01 COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + TCGA-RP-A695-06 COSM4897041 c.4225-1G>A p.? Unknown 17:7905855-7905855 + 8014573 COSM3388270 c.559A>T p.T187S Substitution - Missense 17:7893335-7893335 + TCGA-C8-A12U-01 COSM437716 c.2095_2097delAAG p.K703delK Deletion - In frame 17:7898539-7898541 + TCGA-BH-A1FC-01 COSM1480129 c.1219G>C p.D407H Substitution - Missense 17:7894558-7894558 + TCGA-DK-A3IL-01 COSM1303445 c.2328C>T p.Y776Y Substitution - coding silent 17:7899187-7899187 + 1_RESISTANT COSM437716 c.2095_2097delAAG p.K703delK Deletion - In frame 17:7898539-7898541 + TCGA-G4-6320-01 COSM3691903 c.1206C>A p.H402Q Substitution - Missense 17:7894545-7894545 + S00501 COSM310077 c.3097T>C p.Y1033H Substitution - Missense 17:7900970-7900970 + CSCC-44-T COSM4500083 c.5397C>A p.L1799L Substitution - coding silent 17:7909145-7909145 + TCGA-61-1900-01 COSM1324720 c.5475C>G p.P1825P Substitution - coding silent 17:7909223-7909223 + 8057513 COSM3388270 c.559A>T p.T187S Substitution - Missense 17:7893335-7893335 + TCGA-CF-A1HS-01 COSM417942 c.3563C>T p.A1188V Substitution - Missense 17:7903339-7903339 + HSJD_DIPG003 COSM301930 c.721G>C p.A241P Substitution - Missense 17:7893497-7893497 + T3118 COSM1387351 c.1612delC p.R540fs*16 Deletion - Frameshift 17:7895447-7895447 + BD124T COSM4765036 c.1612_1613insC p.R540fs*47 Insertion - Frameshift 17:7895447-7895448 + SC_9090 COSM5547649 c.4278_4311del34 p.W1427fs*7 Deletion - Frameshift 17:7905909-7905942 + sysucc-1317T COSM5449061 c.4010T>C p.L1337P Substitution - Missense 17:7904557-7904557 + S02376 COSM5696992 c.4737G>T p.Q1579H Substitution - Missense 17:7907196-7907196 + 587332 COSM1200967 c.5861C>A p.P1954H Substitution - Missense 17:7910953-7910953 + 3N44-VS-3T44 COSM4982215 c.5292G>A p.Q1764Q Substitution - coding silent 17:7908727-7908727 + 587342 COSM1200968 c.1356G>T p.E452D Substitution - Missense 17:7895003-7895003 + TCGA-BR-8680-01 COSM4070389 c.4205G>A p.R1402Q Substitution - Missense 17:7905687-7905687 + 423 COSM4432506 c.1289delG p.E431fs*53 Deletion - Frameshift 17:7894936-7894936 + Pat_63_B COSM5853713 c.3862G>A p.V1288M Substitution - Missense 17:7903959-7903959 + MOLT-4 COSM985518 c.4531C>T p.R1511C Substitution - Missense 17:7906896-7906896 + PD8964a COSM5782218 c.4931A>C p.E1644A Substitution - Missense 17:7907607-7907607 + TCGA-EI-6917-01 COSM3421985 c.62C>A p.S21Y Substitution - Missense 17:7889062-7889062 + YUKIL COSM174799 c.5198C>T p.S1733L Substitution - Missense 17:7908447-7908447 + C135 COSM4617827 c.5494C>T p.R1832C Substitution - Missense 17:7909242-7909242 + Pat_26_A COSM437716 c.2095_2097delAAG p.K703delK Deletion - In frame 17:7898539-7898541 + STC232 COSM5055846 c.4004G>A p.R1335Q Substitution - Missense 17:7904551-7904551 + OV207 COSM252435 c.1379G>A p.R460H Substitution - Missense 17:7895026-7895026 + TCGA-D1-A177-01 COSM985425 c.359A>G p.K120R Substitution - Missense 17:7890716-7890716 + WA23 COSM239307 c.841C>T p.R281C Substitution - Missense 17:7893852-7893852 + A3 COSM5350421 c.2398T>A p.W800R Substitution - Missense 17:7899397-7899397 + TCGA-AP-A051-01 COSM985508 c.4104G>T p.E1368D Substitution - Missense 17:7905131-7905131 + IPMN11 COSM248766 c.3002C>G p.T1001S Substitution - Missense 17:7900875-7900875 + STC297 COSM4070398 c.5949C>T p.D1983D Substitution - coding silent 17:7911531-7911531 + 401 COSM4429619 c.3526G>A p.A1176T Substitution - Missense 17:7903302-7903302 + AML_14y_08_DX COSM5956834 c.5698G>A p.E1900K Substitution - Missense 17:7910535-7910535 + 2521252 COSM5895205 c.5882-4_5882-3insC p.? Unknown 17:7911460-7911461 + TCGA-EE-A2MS-06 COSM3523282 c.3408C>T p.T1136T Substitution - coding silent 17:7902974-7902974 + 587342 COSM1200969 c.3421C>A p.L1141M Substitution - Missense 17:7902987-7902987 + TCGA-A5-A0VP-01 COSM985432 c.1027C>T p.R343C Substitution - Missense 17:7894217-7894217 + 180 COSM3721237 c.442G>C p.E148Q Substitution - Missense 17:7890997-7890997 + TCGA-AC-A23H-01 COSM3820860 c.2122G>A p.D708N Substitution - Missense 17:7898566-7898566 + T3724 COSM4671981 c.3548G>A p.R1183Q Substitution - Missense 17:7903324-7903324 + TCGA-D1-A15X-01 COSM985476 c.3083G>A p.C1028Y Substitution - Missense 17:7900956-7900956 + TCGA-AR-A1AI-01 COSM437712 c.632C>T p.A211V Substitution - Missense 17:7893408-7893408 + 24 COSM4778192 c.3406A>C p.T1136P Substitution - Missense 17:7902972-7902972 + TCGA-60-2724-01 COSM708767 c.1933G>T p.G645W Substitution - Missense 17:7897984-7897984 + D11 COSM5006787 c.3089A>C p.N1030T Substitution - Missense 17:7900962-7900962 + TCGA-D1-A103-01 COSM437712 c.632C>T p.A211V Substitution - Missense 17:7893408-7893408 + 1115153 COSM473501 c.4545G>A p.P1515P Substitution - coding silent 17:7906910-7906910 + T36 COSM4671982 c.3561C>T p.R1187R Substitution - coding silent 17:7903337-7903337 + T3446 COSM4671985 c.4358+2T>C p.? Unknown 17:7905991-7905991 + CSCC-32-T COSM4570178 c.2240T>C p.L747P Substitution - Missense 17:7899099-7899099 + T3094 COSM4671986 c.5338G>A p.A1780T Substitution - Missense 17:7908773-7908773 + T407 COSM4671977 c.854G>A p.R285Q Substitution - Missense 17:7893865-7893865 + SC_9109 COSM5572847 c.2216A>G p.Y739C Substitution - Missense 17:7899075-7899075 + SNUH_G16_S1 COSM4000331 c.3462T>C p.F1154F Substitution - coding silent 17:7903028-7903028 + TCGA-AZ-6601-01 COSM1387381 c.5591T>C p.V1864A Substitution - Missense 17:7910428-7910428 + TCGA-A2-A0T5-01 COSM3820882 c.5278T>G p.W1760G Substitution - Missense 17:7908713-7908713 + SH-0622 COSM5017884 c.822delC p.R276fs*19 Deletion - Frameshift 17:7893833-7893833 + C0075T COSM4151785 c.2944C>G p.L982V Substitution - Missense 17:7900697-7900697 + TCGA-D1-A17C-01 COSM985446 c.2053G>T p.E685* Substitution - Nonsense 17:7898497-7898497 + TCGA-AX-A0J0-01 COSM985521 c.5014T>G p.L1672V Substitution - Missense 17:7907690-7907690 + DLBCL785 COSM1580707 c.2678C>T p.S893F Substitution - Missense 17:7900029-7900029 + SC_9055 COSM5569300 c.5007A>G p.T1669T Substitution - coding silent 17:7907683-7907683 + TCGA-CJ-5677-01 COSM473492 c.3126C>T p.S1042S Substitution - coding silent 17:7901249-7901249 + TCGA-E2-A1IN-01 COSM1480128 c.532C>G p.P178A Substitution - Missense 17:7893308-7893308 + T3090 COSM2802859 c.474G>A p.T158T Substitution - coding silent 17:7891029-7891029 + Pat_14_B COSM5853715 c.4001C>T p.A1334V Substitution - Missense 17:7904548-7904548 + SWE-22 COSM460183 c.3004C>T p.R1002* Substitution - Nonsense 17:7900877-7900877 + S00501 COSM310077 c.3097T>C p.Y1033H Substitution - Missense 17:7900970-7900970 + CRC-37T COSM5479666 c.1380C>T p.R460R Substitution - coding silent 17:7895027-7895027 + HCA7 COSM4630361 c.1029C>T p.R343R Substitution - coding silent 17:7894219-7894219 + 722_T COSM3958886 c.31G>T p.A11S Substitution - Missense 17:7889031-7889031 + LUAD-RT-S01777 COSM381998 c.4876G>T p.G1626* Substitution - Nonsense 17:7907440-7907440 + TCGA-AP-A056-01 COSM985506 c.4073-1G>T p.? Unknown 17:7905099-7905099 + CHC155T COSM217148 c.5323C>G p.P1775A Substitution - Missense 17:7908758-7908758 + pfg008T COSM1640884 c.2690G>T p.R897M Substitution - Missense 17:7900297-7900297 + TCGA-CG-5728-01 COSM4070327 c.350G>A p.R117Q Substitution - Missense 17:7890707-7890707 + CSCC-35-T COSM4499996 c.5382C>T p.A1794A Substitution - coding silent 17:7908817-7908817 + 12M COSM5577338 c.750C>T p.I250I Substitution - coding silent 17:7893526-7893526 + TCGA-34-5231-01 COSM708768 c.1602A>T p.P534P Substitution - coding silent 17:7895437-7895437 + TCGA-DK-A1AC-01 COSM1303442 c.19G>A p.V7M Substitution - Missense 17:7889019-7889019 + TCGA-AA-3713-01 COSM1387349 c.1549_1550insG p.E519fs*68 Insertion - Frameshift 17:7895384-7895385 + SW48 COSM2803196 c.4769G>A p.G1590E Substitution - Missense 17:7907228-7907228 + TCGA-K4-A3WV-01 COSM3796182 c.1071G>T p.K357N Substitution - Missense 17:7894261-7894261 + SW1417 COSM2803084 c.3577C>T p.R1193* Substitution - Nonsense 17:7903353-7903353 + TCGA-EK-A2RN-01 COSM4823217 c.115C>G p.R39G Substitution - Missense 17:7889678-7889678 + PT37 COSM5921128 c.2979-6C>A p.? Unknown 17:7900846-7900846 + DLBCL705 COSM1580706 c.1432T>C p.Y478H Substitution - Missense 17:7895079-7895079 + STC291 COSM5055849 c.5836G>A p.A1946T Substitution - Missense 17:7910928-7910928 + LUAD-B02594 COSM336538 c.1246G>T p.G416C Substitution - Missense 17:7894585-7894585 + PD5951a COSM5791377 c.1780G>T p.D594Y Substitution - Missense 17:7897155-7897155 + HCC119 COSM1610929 c.1707+10C>G p.? Unknown 17:7895552-7895552 + S0029 COSM5882946 c.1336G>A p.E446K Substitution - Missense 17:7894983-7894983 + TCGA-D7-A4YV-01 COSM4070398 c.5949C>T p.D1983D Substitution - coding silent 17:7911531-7911531 + TCGA-D8-A1XJ-01 COSM5833450 c.4166delG p.N1390fs*35 Deletion - Frameshift 17:7905648-7905648 + WA19 COSM239309 c.2366T>G p.L789R Substitution - Missense 17:7899365-7899365 + HCC049T COSM5812035 c.3559C>T p.R1187C Substitution - Missense 17:7903335-7903335 + TCGA-AC-A3W6-01 COSM3820861 c.2284G>A p.E762K Substitution - Missense 17:7899143-7899143 + TCGA-A5-A0GP-01 COSM985536 c.5676C>T p.I1892I Substitution - coding silent 17:7910513-7910513 + A673 COSM4580206 c.1869T>G p.R623R Substitution - coding silent 17:7897244-7897244 + TCGA-D1-A16X-01 COSM985468 c.2582C>T p.S861L Substitution - Missense 17:7899933-7899933 + TCGA-ER-A2NC-06 COSM3523281 c.3340C>T p.L1114L Substitution - coding silent 17:7902697-7902697 + P03-595 COSM243667 c.4359-2A>G p.? Unknown 17:7906551-7906551 + PT24_2 COSM5904636 c.3679G>T p.D1227Y Substitution - Missense 17:7903455-7903455 + TCGA-FD-A3SR-01 COSM3796189 c.4155G>C p.K1385N Substitution - Missense 17:7905637-7905637 + C086 COSM5528626 c.4734C>T p.N1578N Substitution - coding silent 17:7907193-7907193 + TCGA-FV-A3R2-01 COSM4929309 c.5039G>T p.G1680V Substitution - Missense 17:7907906-7907906 + TCGA-HC-7212-01 COSM3672611 c.3528C>T p.A1176A Substitution - coding silent 17:7903304-7903304 + TCGA-D1-A17Q-01 COSM985484 c.3318C>T p.I1106I Substitution - coding silent 17:7902675-7902675 + TCGA-BP-4961-01 COSM473498 c.3420C>T p.G1140G Substitution - coding silent 17:7902986-7902986 + TCGA-CD-A4MG-01 COSM1178238 c.1200C>A p.A400A Substitution - coding silent 17:7894539-7894539 + TCGA-B0-5400-01 COSM473489 c.2056C>A p.L686I Substitution - Missense 17:7898500-7898500 + ESCC_150 COSM5644974 c.3564G>A p.A1188A Substitution - coding silent 17:7903340-7903340 + TCGA-EE-A3AF-06 COSM3523290 c.3944C>T p.P1315L Substitution - Missense 17:7904491-7904491 + TCGA-BS-A0UL-01 COSM985514 c.4381C>T p.R1461C Substitution - Missense 17:7906575-7906575 + H1299 COSM985540 c.5735C>T p.T1912M Substitution - Missense 17:7910572-7910572 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.25601 17p13.1 602120

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAG - InFrameDeletion p.K762delK c.2284_2286delAAG 17 7801857 BRCA A C IntronicSNV . c.5767+330A>C 17 7812986 HC A C Missense p.K1398Q c.4192A>C 17 7807880 SCLC A C Missense p.Q186P c.557A>C 17 7794055 LUAD - A Frameshift p.I450Nfs*5 c.1348dupA 17 7797826 HNSC A G Missense p.D95G c.284A>G 17 7792988 UCEC A G Missense p.H1521R c.4562A>G 17 7809897 LUAD A G Missense p.N2008S c.6023A>G 17 7814256 HNSC A G Missense p.Y154C c.461A>G 17 7793959 LUSC A T Missense p.K363M c.1088A>T 17 7797240 ESCA A T Synonymous p.P593P c.1779A>T 17 7798755 LUSC C A Missense p.L745I c.2233C>A 17 7801818 RCCC C A Missense p.N258K c.774C>A 17 7796691 STAD C A Nonsense p.Y1160* c.3480C>A 17 7805978 RCCC C A Synonymous p.A1513A c.4539C>A 17 7809874 STAD C A Synonymous p.I1178I c.3534C>A 17 7806032 LUSC C A Synonymous p.P113P c.339C>A 17 7793043 STAD C - Frameshift p.P305Lfs*49 c.914delC 17 7796827 STAD C G Missense p.I631M c.1893C>G 17 7800409 BLCA C G Missense p.L1295V c.3883C>G 17 7806800 HNSC C G Missense p.P1834A c.5500C>G 17 7812076 HC C G Missense p.P237A c.709C>G 17 7796626 BRCA C G Missense p.R694G c.2080C>G 17 7800596 CM C T IntronicSNV . c.1681-72C>T 17 7798585 NSCLC C T IntronicSNV . c.4250-17C>T 17 7808401 STAD C T Missense p.A1247V c.3740C>T 17 7806657 BLCA C T Missense p.A270V c.809C>T 17 7796726 BRCA C T Missense p.L1630F c.4888C>T 17 7810488 CM C T Missense p.P1049L c.3146C>T 17 7804040 CM C T Missense p.P1095S c.3283C>T 17 7804297 CM C T Missense p.P1374L c.4121C>T 17 7807809 CM C T Missense p.P1609L c.4826C>T 17 7810332 CM C T Missense p.P299L c.896C>T 17 7796813 LUAD C T Missense p.R1269W c.3805C>T 17 7806722 UCEC C T Missense p.R1401W c.4201C>T 17 7807889 UCEC C T Missense p.R1520C c.4558C>T 17 7809893 UCEC C T Missense p.R1570C c.4708C>T 17 7810214 UCEC C T Missense p.R330W c.988C>T 17 7797140 STAD C T Missense p.R402C c.1204C>T 17 7797535 UCEC C T Missense p.R458C c.1372C>T 17 7797852 CM C T Missense p.R807C c.2419C>T 17 7802419 UCEC C T Missense p.S920L c.2759C>T 17 7803251 CM C T Nonsense p.Q602* c.1804C>T 17 7798780 BRCA C T Nonsense p.R162* c.484C>T 17 7793982 UCEC C T Nonsense p.R1756* c.5266C>T 17 7811274 UCEC C T Nonsense p.R743* c.2227C>T 17 7801419 LUAD C T Synonymous p.A1235A c.3705C>T 17 7806622 PRAD C T Synonymous p.A1534A c.4602C>T 17 7809937 UCEC C T Synonymous p.F1433F c.4299C>T 17 7808467 CM C T Synonymous p.G1199G c.3597C>T 17 7806304 RCCC C T Synonymous p.I1202I c.3606C>T 17 7806313 CM C T Synonymous p.L1173L c.3517C>T 17 7806015 CM C T Synonymous p.L1845L c.5533C>T 17 7812109 CM C T Synonymous p.N1917N c.5751C>T 17 7812640 UCEC C T Synonymous p.N858N c.2574C>T 17 7802714 CM C T Synonymous p.T1195T c.3585C>T 17 7806292 CM C T Synonymous p.V401V c.1203C>T 17 7797534 BLCA C T Synonymous p.Y835Y c.2505C>T 17 7802505 BLCA GAG - InFrameDeletion p.E14delE c.40_42delGAG 17 7788146 BLCA GAG - InFrameDeletion p.E14delE c.40_42delGAG 17 7788146 BRCA GAG - InFrameDeletion p.E14delE c.40_42delGAG 17 7788146 PRAD GAG - InFrameDeletion p.E14delE c.40_42delGAG 17 7788146 THCA GAG - InFrameDeletion p.E35delE c.104_106delAGG 17 7788212 PRAD GAG - InFrameDeletion p.E35delE c.104_106delAGG 17 7788212 THCA G A Missense p.A1320T c.3958G>A 17 7807196 UCEC G A Missense p.D1030N c.3088G>A 17 7803982 LUAD G A Missense p.D439N c.1315G>A 17 7797795 RCCC G A Missense p.E212K c.634G>A 17 7794330 HNSC G A Missense p.E734K c.2200G>A 17 7801392 CM G A Missense p.G1755E c.5264G>A 17 7811272 CM G A Missense p.G426R c.1276G>A 17 7797756 RCCC G A Missense p.R1137Q c.3410G>A 17 7804674 UCEC G A Missense p.R1752Q c.5255G>A 17 7811263 GBM G A Missense p.R176Q c.527G>A 17 7794025 STAD G A Missense p.R1954H c.5861G>A 17 7813839 UCEC G A Missense p.R335Q c.1004G>A 17 7797156 STAD G A Missense p.R458H c.1373G>A 17 7797853 THCA G A Missense p.R682H c.2045G>A 17 7800561 BRCA G A SpliceAcceptorSNV . c.2722-1G>A 17 7803213 LUAD G A SpliceAcceptorSNV . c.4250-1G>A 17 7808417 CM G A Synonymous p.P671P c.2013G>A 17 7800529 HNSC G A Synonymous p.R413R c.1239G>A 17 7797570 CM G A Synonymous p.T1170T c.3510G>A 17 7806008 HNSC G A Synonymous p.T876T c.2628G>A 17 7802768 HNSC G C Missense p.D466H c.1396G>C 17 7797876 BRCA G C Missense p.E281Q c.841G>C 17 7796758 BRCA G C Missense p.E30D c.90G>C 17 7788214 BLCA G C Missense p.G1685A c.5054G>C 17 7810759 HNSC G C Missense p.K662N c.1986G>C 17 7800502 THCA G C Missense p.Q569H c.1707G>C 17 7798683 THCA G C Missense p.R1802T c.5405G>C 17 7811795 BRCA G - Frameshift p.Q186Kfs*14 c.555delG 17 7794048 STAD G T Missense p.D1825Y c.5473G>T 17 7812049 HNSC G T Missense p.E909D c.2727G>T 17 7803219 STAD G T Missense p.G1695V c.5084G>T 17 7810789 STAD G T Missense p.G399C c.1195G>T 17 7797526 LUAD G T Missense p.G704W c.2110G>T 17 7801302 LUSC G T Missense p.R1787L c.5360G>T 17 7811750 UCEC G T Missense p.R807L c.2420G>T 17 7802420 LUSC G T Missense p.R956M c.2867G>T 17 7803615 STAD G T Missense p.W866L c.2597G>T 17 7802737 STAD G T Nonsense p.E1786* c.5356G>T 17 7811746 PRAD G T Nonsense p.E744* c.2230G>T 17 7801815 UCEC G T Synonymous p.T721T c.2163G>T 17 7801355 HNSC T A Missense p.F808Y c.2423T>A 17 7802423 RCCC T C Missense p.S1592P c.4774T>C 17 7810280 HNSC T C Missense p.S296P c.886T>C 17 7796803 CM T C Missense p.S296P c.886T>C 17 7796803 HNSC T C Missense p.S622P c.1864T>C 17 7798840 CM T C Missense p.Y1092H c.3274T>C 17 7804288 SCLC - T Frameshift p.Y706Lfs*13 c.2116dupT 17 7801307 PRAD T G Missense p.Y1805D c.5413T>G 17 7811803 CM T G Synonymous p.L465L c.1395T>G 17 7797875 LUAD