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 10 101637013 101637013 + Silent SNP G G A TCGA-XF-AAN0-01A-11D-A42E-08 TCGA-XF-AAN0-10A-01D-A42H-08 g.chr10:101637013G>A c.4629C>T c.(4627-4629)ctC>ctT p.L1543L BLCA 10 101639649 101639649 + Silent SNP G G T TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr10:101639649G>T c.4467C>A c.(4465-4467)ctC>ctA p.L1489L BLCA 10 101639932 101639932 + Missense_Mutation SNP G G A TCGA-ZF-A9R9-01A-11D-A38G-08 TCGA-ZF-A9R9-10A-01D-A38J-08 g.chr10:101639932G>A c.4184C>T c.(4183-4185)aCc>aTc p.T1395I BLCA 10 101645608 101645608 + Missense_Mutation SNP C C T TCGA-5N-A9KM-01A-11D-A42E-08 TCGA-5N-A9KM-10A-01D-A42H-08 g.chr10:101645608C>T c.3634G>A c.(3634-3636)Ggc>Agc p.G1212S BLCA 10 101648614 101648614 + Missense_Mutation SNP G G A TCGA-DK-AA6T-01A-11D-A391-08 TCGA-DK-AA6T-10A-01D-A394-08 g.chr10:101648614G>A c.3253C>T c.(3253-3255)Cgc>Tgc p.R1085C BLCA 10 101657854 101657854 + Missense_Mutation SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr10:101657854C>T c.2909G>A c.(2908-2910)cGa>cAa p.R970Q BLCA 10 101715193 101715193 + Missense_Mutation SNP G G C TCGA-GU-A42Q-01A-11D-A23U-08 TCGA-GU-A42Q-10A-01D-A23U-08 g.chr10:101715193G>C c.2038C>G c.(2038-2040)Cat>Gat p.H680D BLCA 10 101715548 101715548 + Silent SNP C C T TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chr10:101715548C>T c.1683G>A c.(1681-1683)aaG>aaA p.K561K BLCA 10 101715783 101715783 + Missense_Mutation SNP G G T TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr10:101715783G>T c.1448C>A c.(1447-1449)tCt>tAt p.S483Y BLCA 10 101715892 101715892 + Missense_Mutation SNP G G A TCGA-2F-A9KQ-01A-11D-A38G-08 TCGA-2F-A9KQ-11A-11D-A38J-08 g.chr10:101715892G>A c.1339C>T c.(1339-1341)Ctt>Ttt p.L447F BLCA 10 101715925 101715925 + Missense_Mutation SNP T T A TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr10:101715925T>A c.1306A>T c.(1306-1308)Agc>Tgc p.S436C BLCA 10 101716810 101716810 + Missense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr10:101716810G>C c.421C>G c.(421-423)Cag>Gag p.Q141E BLCA 10 101716848 101716848 + Nonsense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr10:101716848G>C c.383C>G c.(382-384)tCa>tGa p.S128* BLCA 10 101716853 101716853 + Silent SNP G G C TCGA-FD-A43P-01A-31D-A23U-08 TCGA-FD-A43P-10A-01D-A23U-08 g.chr10:101716853G>C c.378C>G c.(376-378)ctC>ctG p.L126L BRCA 10 101637038 101637038 + Nonsense_Mutation SNP G G T TCGA-A2-A25A-01A-12D-A16D-09 TCGA-A2-A25A-10A-01D-A16D-09 g.chr10:101637038G>T c.4604C>A c.(4603-4605)tCa>tAa p.S1535* BRCA 10 101639792 101639792 + Missense_Mutation SNP A A G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr10:101639792A>G c.4324T>C c.(4324-4326)Tcc>Ccc p.S1442P BRCA 10 101643811 101643811 + Missense_Mutation SNP T T G TCGA-A7-A0DA-01A-31D-A10Y-09 TCGA-A7-A0DA-10A-01D-A110-09 g.chr10:101643811T>G c.3954A>C c.(3952-3954)aaA>aaC p.K1318N BRCA 10 101643877 101643877 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr10:101643877G>T c.3888C>A c.(3886-3888)ttC>ttA p.F1296L BRCA 10 101643927 101643927 + Missense_Mutation SNP G G T TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr10:101643927G>T c.3838C>A c.(3838-3840)Ctc>Atc p.L1280I BRCA 10 101646291 101646291 + Silent SNP G G C TCGA-GM-A2D9-01A-11D-A18P-09 TCGA-GM-A2D9-11A-42D-A18P-09 g.chr10:101646291G>C c.3384C>G c.(3382-3384)ctC>ctG p.L1128L BRCA 10 101648689 101648689 + Missense_Mutation SNP C C T TCGA-AN-A0AT-01A-11D-A045-09 TCGA-AN-A0AT-10A-01W-A055-09 g.chr10:101648689C>T c.3178G>A c.(3178-3180)Gtg>Atg p.V1060M BRCA 10 101659737 101659737 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr10:101659737C>T c.2641G>A c.(2641-2643)Gaa>Aaa p.E881K BRCA 10 101668763 101668763 + Missense_Mutation SNP G G A TCGA-AN-A0FJ-01A-11W-A019-09 TCGA-AN-A0FJ-10A-01W-A021-09 g.chr10:101668763G>A c.2401C>T c.(2401-2403)Cgg>Tgg p.R801W BRCA 10 101715245 101715245 + Silent SNP G G C TCGA-AC-A23C-01A-12D-A167-09 TCGA-AC-A23C-10A-01D-A167-09 g.chr10:101715245G>C c.1986C>G c.(1984-1986)ctC>ctG p.L662L BRCA 10 101715753 101715753 + Missense_Mutation SNP C C T TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr10:101715753C>T c.1478G>A c.(1477-1479)aGa>aAa p.R493K BRCA 10 101728874 101728874 + Missense_Mutation SNP C C T TCGA-BH-A0GZ-01A-11W-A071-09 TCGA-BH-A0GZ-10A-01W-A071-09 g.chr10:101728874C>T c.266G>A c.(265-267)cGa>cAa p.R89Q CESC 10 101637012 101637012 + Missense_Mutation SNP C C T TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr10:101637012C>T c.4630G>A c.(4630-4632)Gag>Aag p.E1544K CESC 10 101645515 101645515 + Missense_Mutation SNP G G C TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr10:101645515G>C c.3727C>G c.(3727-3729)Cca>Gca p.P1243A CESC 10 101656053 101656053 + Missense_Mutation SNP G G T TCGA-LP-A5U2-01A-11D-A28B-09 TCGA-LP-A5U2-10A-01D-A28E-09 g.chr10:101656053G>T c.3022C>A c.(3022-3024)Ctg>Atg p.L1008M CESC 10 101715391 101715391 + Missense_Mutation SNP G G A TCGA-C5-A1M8-01A-21D-A13W-08 TCGA-C5-A1M8-10A-01D-A13W-08 g.chr10:101715391G>A c.1840C>T c.(1840-1842)Cgt>Tgt p.R614C CESC 10 101715662 101715662 + Missense_Mutation SNP C C T TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr10:101715662C>T c.1569G>A c.(1567-1569)atG>atA p.M523I CESC 10 101716192 101716192 + Missense_Mutation SNP C C T TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr10:101716192C>T c.1039G>A c.(1039-1041)Gag>Aag p.E347K CHOL 10 101639890 101639890 + Missense_Mutation SNP G G T TCGA-W6-AA0S-01A-11D-A417-09 TCGA-W6-AA0S-10A-01D-A41A-09 g.chr10:101639890G>T c.4226C>A c.(4225-4227)cCg>cAg p.P1409Q CHOL 10 101716493 101716493 + Silent SNP G G T TCGA-W5-AA2Q-01A-11D-A417-09 TCGA-W5-AA2Q-10A-01D-A41A-09 g.chr10:101716493G>T c.738C>A c.(736-738)acC>acA p.T246T COAD 10 101639642 101639642 + Missense_Mutation SNP C C G TCGA-AA-3543-01A-01W-0833-10 TCGA-AA-3543-10A-01W-0833-10 g.chr10:101639642C>G c.4474G>C c.(4474-4476)Gga>Cga p.G1492R COAD 10 101639727 101639727 + Silent SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:101639727C>T c.4389G>A c.(4387-4389)ccG>ccA p.P1463P COAD 10 101639943 101639943 + Silent SNP A A G TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr10:101639943A>G c.4173T>C c.(4171-4173)gcT>gcC p.A1391A COAD 10 101639996 101639996 + Missense_Mutation SNP A A G TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:101639996A>G c.4120T>C c.(4120-4122)Ttc>Ctc p.F1374L COAD 10 101643936 101643936 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:101643936G>A c.3829C>T c.(3829-3831)Cgg>Tgg p.R1277W COAD 10 101646058 101646058 + Splice_Site SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:101646058G>A c.3617C>T c.(3616-3618)tCg>tTg p.S1206L COAD 10 101646214 101646214 + Missense_Mutation SNP C C T TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr10:101646214C>T c.3461G>A c.(3460-3462)cGg>cAg p.R1154Q COAD 10 101646215 101646215 + Silent SNP G G T TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr10:101646215G>T c.3460C>A c.(3460-3462)Cgg>Agg p.R1154R COAD 10 101646304 101646304 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr10:101646304C>T c.3371G>A c.(3370-3372)cGc>cAc p.R1124H COAD 10 101648644 101648644 + Silent SNP G G T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr10:101648644G>T c.3223C>A c.(3223-3225)Cgg>Agg p.R1075R COAD 10 101654743 101654743 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:101654743G>T c.3116C>A c.(3115-3117)tCt>tAt p.S1039Y COAD 10 101654779 101654779 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:101654779T>C c.3080A>G c.(3079-3081)gAa>gGa p.E1027G COAD 10 101659759 101659759 + Silent SNP A A G TCGA-CK-5912-01A-11D-1650-10 TCGA-CK-5912-10A-01D-1650-10 g.chr10:101659759A>G c.2619T>C c.(2617-2619)caT>caC p.H873H COAD 10 101659760 101659760 + Missense_Mutation SNP T T C TCGA-F4-6569-01A-11D-1771-10 TCGA-F4-6569-10A-01D-1771-10 g.chr10:101659760T>C c.2618A>G c.(2617-2619)cAt>cGt p.H873R COAD 10 101659796 101659796 + Missense_Mutation SNP T T C TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr10:101659796T>C c.2582A>G c.(2581-2583)gAg>gGg p.E861G COAD 10 101668830 101668830 + Silent SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr10:101668830C>T c.2334G>A c.(2332-2334)gaG>gaA p.E778E COAD 10 101715177 101715177 + Missense_Mutation SNP A A C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr10:101715177A>C c.2054T>G c.(2053-2055)cTg>cGg p.L685R COAD 10 101715363 101715363 + Missense_Mutation SNP G G T TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr10:101715363G>T c.1868C>A c.(1867-1869)cCc>cAc p.P623H COAD 10 101715377 101715377 + Silent SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr10:101715377C>T c.1854G>A c.(1852-1854)ccG>ccA p.P618P COAD 10 101715699 101715699 + Missense_Mutation SNP G G A TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr10:101715699G>A c.1532C>T c.(1531-1533)aCg>aTg p.T511M COAD 10 101715823 101715823 + Frame_Shift_Del DEL T T - TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr10:101715823delT c.1408delA c.(1408-1410)actfs p.T470fs COAD 10 101715927 101715927 + Missense_Mutation SNP C C A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr10:101715927C>A c.1304G>T c.(1303-1305)gGg>gTg p.G435V COAD 10 101716082 101716082 + Silent SNP C C T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr10:101716082C>T c.1149G>A c.(1147-1149)ggG>ggA p.G383G COAD 10 101716420 101716420 + Silent SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:101716420G>T c.811C>A c.(811-813)Cga>Aga p.R271R COAD 10 101716439 101716439 + Silent SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr10:101716439G>A c.792C>T c.(790-792)ttC>ttT p.F264F COAD 10 101716493 101716493 + Silent SNP G G C TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr10:101716493G>C c.738C>G c.(736-738)acC>acG p.T246T COAD 10 101716730 101716730 + Silent SNP C C T TCGA-AA-3989-01A-01W-0995-10 TCGA-AA-3989-10A-01W-0999-10 g.chr10:101716730C>T c.501G>A c.(499-501)agG>agA p.R167R COAD 10 101716765 101716766 + Frame_Shift_Ins INS - - C TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr10:101716765_101716766insC c.465_466insG c.(463-468)gggcttfs p.L156fs COAD 10 101716911 101716911 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:101716911C>T c.320G>A c.(319-321)cGa>cAa p.R107Q COAD 10 101731833 101731833 + Missense_Mutation SNP C C G TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr10:101731833C>G c.49G>C c.(49-51)Gta>Cta p.V17L COADREAD 10 101639642 101639642 + Missense_Mutation SNP C C G TCGA-AA-3543-01A-01W-0833-10 TCGA-AA-3543-10A-01W-0833-10 g.chr10:101639642C>G c.4474G>C c.(4474-4476)Gga>Cga p.G1492R COADREAD 10 101639727 101639727 + Silent SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:101639727C>T c.4389G>A c.(4387-4389)ccG>ccA p.P1463P COADREAD 10 101639943 101639943 + Silent SNP A A G TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr10:101639943A>G c.4173T>C c.(4171-4173)gcT>gcC p.A1391A COADREAD 10 101639996 101639996 + Missense_Mutation SNP A A G TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:101639996A>G c.4120T>C c.(4120-4122)Ttc>Ctc p.F1374L COADREAD 10 101643936 101643936 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:101643936G>A c.3829C>T c.(3829-3831)Cgg>Tgg p.R1277W COADREAD 10 101646058 101646058 + Splice_Site SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:101646058G>A c.3617C>T c.(3616-3618)tCg>tTg p.S1206L COADREAD 10 101646214 101646214 + Missense_Mutation SNP C C T TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr10:101646214C>T c.3461G>A c.(3460-3462)cGg>cAg p.R1154Q COADREAD 10 101646215 101646215 + Silent SNP G G T TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr10:101646215G>T c.3460C>A c.(3460-3462)Cgg>Agg p.R1154R COADREAD 10 101646304 101646304 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr10:101646304C>T c.3371G>A c.(3370-3372)cGc>cAc p.R1124H COADREAD 10 101648644 101648644 + Silent SNP G G T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr10:101648644G>T c.3223C>A c.(3223-3225)Cgg>Agg p.R1075R COADREAD 10 101654743 101654743 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:101654743G>T c.3116C>A c.(3115-3117)tCt>tAt p.S1039Y COADREAD 10 101654779 101654779 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:101654779T>C c.3080A>G c.(3079-3081)gAa>gGa p.E1027G COADREAD 10 101659759 101659759 + Silent SNP A A G TCGA-CK-5912-01A-11D-1650-10 TCGA-CK-5912-10A-01D-1650-10 g.chr10:101659759A>G c.2619T>C c.(2617-2619)caT>caC p.H873H COADREAD 10 101659760 101659760 + Missense_Mutation SNP T T C TCGA-F4-6569-01A-11D-1771-10 TCGA-F4-6569-10A-01D-1771-10 g.chr10:101659760T>C c.2618A>G c.(2617-2619)cAt>cGt p.H873R COADREAD 10 101659796 101659796 + Missense_Mutation SNP T T C TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr10:101659796T>C c.2582A>G c.(2581-2583)gAg>gGg p.E861G COADREAD 10 101667793 101667793 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:101667793G>A c.2513C>T c.(2512-2514)tCg>tTg p.S838L COADREAD 10 101668830 101668830 + Silent SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr10:101668830C>T c.2334G>A c.(2332-2334)gaG>gaA p.E778E COADREAD 10 101715177 101715177 + Missense_Mutation SNP A A C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr10:101715177A>C c.2054T>G c.(2053-2055)cTg>cGg p.L685R COADREAD 10 101715363 101715363 + Missense_Mutation SNP G G T TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr10:101715363G>T c.1868C>A c.(1867-1869)cCc>cAc p.P623H COADREAD 10 101715377 101715377 + Silent SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr10:101715377C>T c.1854G>A c.(1852-1854)ccG>ccA p.P618P COADREAD 10 101715699 101715699 + Missense_Mutation SNP G G A TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr10:101715699G>A c.1532C>T c.(1531-1533)aCg>aTg p.T511M COADREAD 10 101715823 101715823 + Frame_Shift_Del DEL T T - TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr10:101715823delT c.1408delA c.(1408-1410)actfs p.T470fs COADREAD 10 101715927 101715927 + Missense_Mutation SNP C C A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr10:101715927C>A c.1304G>T c.(1303-1305)gGg>gTg p.G435V COADREAD 10 101716082 101716082 + Silent SNP C C T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr10:101716082C>T c.1149G>A c.(1147-1149)ggG>ggA p.G383G COADREAD 10 101716420 101716420 + Silent SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:101716420G>T c.811C>A c.(811-813)Cga>Aga p.R271R COADREAD 10 101716439 101716439 + Silent SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr10:101716439G>A c.792C>T c.(790-792)ttC>ttT p.F264F COADREAD 10 101716493 101716493 + Silent SNP G G C TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr10:101716493G>C c.738C>G c.(736-738)acC>acG p.T246T COADREAD 10 101716730 101716730 + Silent SNP C C T TCGA-AA-3989-01A-01W-0995-10 TCGA-AA-3989-10A-01W-0999-10 g.chr10:101716730C>T c.501G>A c.(499-501)agG>agA p.R167R COADREAD 10 101716765 101716766 + Frame_Shift_Ins INS - - C TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr10:101716765_101716766insC c.465_466insG c.(463-468)gggcttfs p.L156fs COADREAD 10 101716911 101716911 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:101716911C>T c.320G>A c.(319-321)cGa>cAa p.R107Q COADREAD 10 101731833 101731833 + Missense_Mutation SNP C C G TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr10:101731833C>G c.49G>C c.(49-51)Gta>Cta p.V17L ESCA 10 101637038 101637038 + Nonsense_Mutation SNP G G T TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chr10:101637038G>T c.4604C>A c.(4603-4605)tCa>tAa p.S1535* ESCA 10 101654708 101654708 + Missense_Mutation SNP T T C TCGA-R6-A8WG-01A-11D-A37C-09 TCGA-R6-A8WG-10A-01D-A37F-09 g.chr10:101654708T>C c.3151A>G c.(3151-3153)Atc>Gtc p.I1051V ESCA 10 101658499 101658499 + Splice_Site SNP C C G TCGA-JY-A6FD-01A-11D-A33E-09 TCGA-JY-A6FD-10A-01D-A33H-09 g.chr10:101658499C>G c.e8+1 ESCA 10 101715538 101715538 + Missense_Mutation SNP C C T TCGA-L5-A8NU-01A-11D-A36J-09 TCGA-L5-A8NU-11A-11D-A36M-09 g.chr10:101715538C>T c.1693G>A c.(1693-1695)Ggg>Agg p.G565R ESCA 10 101716195 101716195 + Missense_Mutation SNP C C A TCGA-LN-A49Y-01A-11D-A27G-09 TCGA-LN-A49Y-10A-01D-A27G-09 g.chr10:101716195C>A c.1036G>T c.(1036-1038)Gcc>Tcc p.A346S ESCA 10 101716851 101716851 + Missense_Mutation SNP G G A TCGA-JY-A938-01A-11D-A37C-09 TCGA-JY-A938-10A-01D-A37F-09 g.chr10:101716851G>A c.380C>T c.(379-381)tCc>tTc p.S127F GBM 10 101654794 101654794 + Missense_Mutation SNP A A G TCGA-27-2519-01A-01D-1494-08 TCGA-27-2519-10A-01D-1494-08 g.chr10:101654794A>G c.3065T>C c.(3064-3066)gTa>gCa p.V1022A GBM 10 101715528 101715528 + Missense_Mutation SNP G G C TCGA-27-1834-01A-01W-0643-08 TCGA-27-1834-10A-01W-0644-08 g.chr10:101715528G>C c.1703C>G c.(1702-1704)aCa>aGa p.T568R GBM 10 101716663 101716663 + Nonsense_Mutation SNP G G A TCGA-32-1979-01A-01D-1696-08 TCGA-32-1979-10A-01D-1696-08 g.chr10:101716663G>A c.568C>T c.(568-570)Cga>Tga p.R190* GBM 10 101716779 101716779 + Missense_Mutation SNP C C T TCGA-32-1977-01A-01D-1353-08 TCGA-32-1977-10C-01D-1353-08 g.chr10:101716779C>T c.452G>A c.(451-453)cGg>cAg p.R151Q GBMLGG 10 101646233 101646233 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:101646233C>A c.3442G>T c.(3442-3444)Gag>Tag p.E1148* GBMLGG 10 101654794 101654794 + Missense_Mutation SNP A A G TCGA-27-2519-01A-01D-1494-08 TCGA-27-2519-10A-01D-1494-08 g.chr10:101654794A>G c.3065T>C c.(3064-3066)gTa>gCa p.V1022A GBMLGG 10 101667847 101667847 + Missense_Mutation SNP G G A TCGA-DU-6406-01A-11D-1705-08 TCGA-DU-6406-10A-01D-1705-08 g.chr10:101667847G>A c.2459C>T c.(2458-2460)cCa>cTa p.P820L GBMLGG 10 101715528 101715528 + Missense_Mutation SNP G G C TCGA-27-1834-01A-01W-0643-08 TCGA-27-1834-10A-01W-0644-08 g.chr10:101715528G>C c.1703C>G c.(1702-1704)aCa>aGa p.T568R GBMLGG 10 101715654 101715654 + Missense_Mutation SNP C C A TCGA-S9-A7IY-01A-11D-A34A-08 TCGA-S9-A7IY-10A-01D-A34A-08 g.chr10:101715654C>A c.1577G>T c.(1576-1578)gGt>gTt p.G526V GBMLGG 10 101716663 101716663 + Nonsense_Mutation SNP G G A TCGA-32-1979-01A-01D-1696-08 TCGA-32-1979-10A-01D-1696-08 g.chr10:101716663G>A c.568C>T c.(568-570)Cga>Tga p.R190* GBMLGG 10 101716779 101716779 + Missense_Mutation SNP C C T TCGA-32-1977-01A-01D-1353-08 TCGA-32-1977-10C-01D-1353-08 g.chr10:101716779C>T c.452G>A c.(451-453)cGg>cAg p.R151Q HNSC 10 101639776 101639776 + Missense_Mutation SNP C C A TCGA-CN-4735-01A-01D-1434-08 TCGA-CN-4735-10A-01D-1434-08 g.chr10:101639776C>A c.4340G>T c.(4339-4341)gGg>gTg p.G1447V HNSC 10 101639864 101639864 + Missense_Mutation SNP G G C TCGA-CV-5440-01A-01D-1512-08 TCGA-CV-5440-11A-01D-1512-08 g.chr10:101639864G>C c.4252C>G c.(4252-4254)Ctc>Gtc p.L1418V HNSC 10 101639891 101639891 + Missense_Mutation SNP G G A TCGA-CV-A45P-01A-11D-A24D-08 TCGA-CV-A45P-10A-01D-A24F-08 g.chr10:101639891G>A c.4225C>T c.(4225-4227)Ccg>Tcg p.P1409S HNSC 10 101639929 101639929 + Missense_Mutation SNP G G A TCGA-CN-A63Y-01A-11D-A30E-08 TCGA-CN-A63Y-10A-01D-A30H-08 g.chr10:101639929G>A c.4187C>T c.(4186-4188)tCg>tTg p.S1396L HNSC 10 101639938 101639938 + Missense_Mutation SNP G G C TCGA-CV-A45P-01A-11D-A24D-08 TCGA-CV-A45P-10A-01D-A24F-08 g.chr10:101639938G>C c.4178C>G c.(4177-4179)tCc>tGc p.S1393C HNSC 10 101646294 101646294 + Missense_Mutation SNP C C G TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr10:101646294C>G c.3381G>C c.(3379-3381)aaG>aaC p.K1127N HNSC 10 101648654 101648654 + Silent SNP C C T TCGA-KU-A6H7-01A-11D-A31L-08 TCGA-KU-A6H7-10A-01D-A31J-08 g.chr10:101648654C>T c.3213G>A c.(3211-3213)gaG>gaA p.E1071E HNSC 10 101657950 101657950 + Missense_Mutation SNP T T A TCGA-CR-6492-01A-12D-2078-08 TCGA-CR-6492-10A-01D-2078-08 g.chr10:101657950T>A c.2813A>T c.(2812-2814)aAt>aTt p.N938I HNSC 10 101658519 101658519 + Splice_Site SNP T T C TCGA-CN-4727-01A-01D-1434-08 TCGA-CN-4727-10A-01D-1434-08 g.chr10:101658519T>C c.e8-2 HNSC 10 101715080 101715080 + Silent SNP G G C TCGA-CV-A463-01A-11D-A25Y-08 TCGA-CV-A463-10A-01D-A25Y-08 g.chr10:101715080G>C c.2151C>G c.(2149-2151)ctC>ctG p.L717L HNSC 10 101715220 101715220 + Missense_Mutation SNP C C G TCGA-CV-5440-01A-01D-1512-08 TCGA-CV-5440-11A-01D-1512-08 g.chr10:101715220C>G c.2011G>C c.(2011-2013)Gag>Cag p.E671Q HNSC 10 101715433 101715433 + Missense_Mutation SNP C C G TCGA-CV-5440-01A-01D-1512-08 TCGA-CV-5440-11A-01D-1512-08 g.chr10:101715433C>G c.1798G>C c.(1798-1800)Gag>Cag p.E600Q HNSC 10 101715777 101715777 + Nonsense_Mutation SNP G G C TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr10:101715777G>C c.1454C>G c.(1453-1455)tCa>tGa p.S485* HNSC 10 101715869 101715869 + Missense_Mutation SNP T T A TCGA-CN-A63U-01A-11D-A30E-08 TCGA-CN-A63U-10A-01D-A30H-08 g.chr10:101715869T>A c.1362A>T c.(1360-1362)agA>agT p.R454S HNSC 10 101716099 101716099 + Nonsense_Mutation SNP C C A TCGA-CN-A63T-01A-11D-A28R-08 TCGA-CN-A63T-10A-01D-A28U-08 g.chr10:101716099C>A c.1132G>T c.(1132-1134)Gag>Tag p.E378* HNSC 10 101716803 101716803 + Missense_Mutation SNP G G A TCGA-P3-A6T3-01A-11D-A34J-08 TCGA-P3-A6T3-10A-01D-A34M-08 g.chr10:101716803G>A c.428C>T c.(427-429)cCg>cTg p.P143L HNSC 10 101716889 101716889 + Silent SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr10:101716889G>A c.342C>T c.(340-342)ggC>ggT p.G114G HNSC 10 101731794 101731794 + Missense_Mutation SNP C C T TCGA-CN-6019-01A-11D-1683-08 TCGA-CN-6019-10A-01D-1683-08 g.chr10:101731794C>T c.88G>A c.(88-90)Gag>Aag p.E30K HNSC 10 101731859 101731859 + Missense_Mutation SNP C C T TCGA-CN-A642-01A-12D-A30E-08 TCGA-CN-A642-10A-01D-A30H-08 g.chr10:101731859C>T c.23G>A c.(22-24)cGa>cAa p.R8Q KICH 10 101716912 101716912 + Nonsense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr10:101716912G>A c.319C>T c.(319-321)Cga>Tga p.R107* KIPAN 10 101646325 101646325 + Missense_Mutation SNP G G C TCGA-BQ-7044-01A-11D-1961-08 TCGA-BQ-7044-11A-01D-1961-08 g.chr10:101646325G>C c.3350C>G c.(3349-3351)cCc>cGc p.P1117R KIPAN 10 101715031 101715031 + Missense_Mutation SNP C C A TCGA-B4-5832-01A-11D-1669-08 TCGA-B4-5832-10A-01D-1669-08 g.chr10:101715031C>A c.2200G>T c.(2200-2202)Gat>Tat p.D734Y KIPAN 10 101715503 101715503 + Missense_Mutation SNP G G T TCGA-PJ-A5Z8-01A-11D-A28G-10 TCGA-PJ-A5Z8-10A-01D-A28G-10 g.chr10:101715503G>T c.1728C>A c.(1726-1728)caC>caA p.H576Q KIPAN 10 101716912 101716912 + Nonsense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr10:101716912G>A c.319C>T c.(319-321)Cga>Tga p.R107* KIRC 10 101715031 101715031 + Missense_Mutation SNP C C A TCGA-B4-5832-01A-11D-1669-08 TCGA-B4-5832-10A-01D-1669-08 g.chr10:101715031C>A c.2200G>T c.(2200-2202)Gat>Tat p.D734Y KIRP 10 101646325 101646325 + Missense_Mutation SNP G G C TCGA-BQ-7044-01A-11D-1961-08 TCGA-BQ-7044-11A-01D-1961-08 g.chr10:101646325G>C c.3350C>G c.(3349-3351)cCc>cGc p.P1117R KIRP 10 101715503 101715503 + Missense_Mutation SNP G G T TCGA-PJ-A5Z8-01A-11D-A28G-10 TCGA-PJ-A5Z8-10A-01D-A28G-10 g.chr10:101715503G>T c.1728C>A c.(1726-1728)caC>caA p.H576Q LGG 10 101646233 101646233 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:101646233C>A c.3442G>T c.(3442-3444)Gag>Tag p.E1148* LGG 10 101667847 101667847 + Missense_Mutation SNP G G A TCGA-DU-6406-01A-11D-1705-08 TCGA-DU-6406-10A-01D-1705-08 g.chr10:101667847G>A c.2459C>T c.(2458-2460)cCa>cTa p.P820L LGG 10 101715654 101715654 + Missense_Mutation SNP C C A TCGA-S9-A7IY-01A-11D-A34A-08 TCGA-S9-A7IY-10A-01D-A34A-08 g.chr10:101715654C>A c.1577G>T c.(1576-1578)gGt>gTt p.G526V LIHC 10 101668878 101668878 + Silent SNP A A G TCGA-DD-A1ED-01A-11D-A152-10 TCGA-DD-A1ED-10A-01D-A152-10 g.chr10:101668878A>G c.2286T>C c.(2284-2286)tcT>tcC p.S762S LIHC 10 101715378 101715378 + Missense_Mutation SNP G G A TCGA-DD-AADG-01A-11D-A40R-10 TCGA-DD-AADG-10A-01D-A40U-10 g.chr10:101715378G>A c.1853C>T c.(1852-1854)cCg>cTg p.P618L LUAD 10 101636983 101636983 + Missense_Mutation SNP C C G TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr10:101636983C>G c.4659G>C c.(4657-4659)gaG>gaC p.E1553D LUAD 10 101639582 101639582 + Missense_Mutation SNP C C A TCGA-50-6594-01A-11D-1753-08 TCGA-50-6594-11A-01D-1753-08 g.chr10:101639582C>A c.4534G>T c.(4534-4536)Gca>Tca p.A1512S LUAD 10 101646282 101646282 + Missense_Mutation SNP G G C TCGA-05-4395-01A-01D-1265-08 TCGA-05-4395-10A-01D-1265-08 g.chr10:101646282G>C c.3393C>G c.(3391-3393)ttC>ttG p.F1131L LUAD 10 101646372 101646372 + Silent SNP C C T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr10:101646372C>T c.3303G>A c.(3301-3303)cgG>cgA p.R1101R LUAD 10 101648681 101648681 + Silent SNP A A G TCGA-86-8672-01A-21D-2393-08 TCGA-86-8672-10A-01D-2393-08 g.chr10:101648681A>G c.3186T>C c.(3184-3186)gcT>gcC p.A1062A LUAD 10 101648710 101648710 + Splice_Site SNP C C A TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chr10:101648710C>A c.3157G>T c.(3157-3159)Gag>Tag p.E1053* LUAD 10 101656083 101656083 + Missense_Mutation SNP T T C TCGA-91-6829-01A-21D-1855-08 TCGA-91-6829-11A-01D-1855-08 g.chr10:101656083T>C c.2992A>G c.(2992-2994)Atc>Gtc p.I998V LUAD 10 101715478 101715478 + Missense_Mutation SNP C C G TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr10:101715478C>G c.1753G>C c.(1753-1755)Gag>Cag p.E585Q LUAD 10 101715910 101715910 + Missense_Mutation SNP C C T TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr10:101715910C>T c.1321G>A c.(1321-1323)Gaa>Aaa p.E441K LUAD 10 101716089 101716089 + Missense_Mutation SNP G G A TCGA-73-4668-01A-01D-1265-08 TCGA-73-4668-11A-01D-1265-08 g.chr10:101716089G>A c.1142C>T c.(1141-1143)gCa>gTa p.A381V LUAD 10 101716274 101716274 + Missense_Mutation SNP C C A TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr10:101716274C>A c.957G>T c.(955-957)agG>agT p.R319S LUAD 10 101716378 101716378 + Silent SNP G G A TCGA-44-7660-01A-11D-2063-08 TCGA-44-7660-10A-01D-2063-08 g.chr10:101716378G>A c.853C>T c.(853-855)Ctg>Ttg p.L285L LUAD 10 101716642 101716642 + Missense_Mutation SNP C C A TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr10:101716642C>A c.589G>T c.(589-591)Ggt>Tgt p.G197C LUAD 10 101716779 101716779 + Missense_Mutation SNP C C A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr10:101716779C>A c.452G>T c.(451-453)cGg>cTg p.R151L LUSC 10 101636941 101636941 + Silent SNP G G A TCGA-66-2791-01A-01D-0983-08 TCGA-66-2791-11A-01D-0983-08 g.chr10:101636941G>A c.4701C>T c.(4699-4701)ccC>ccT p.P1567P LUSC 10 101643884 101643884 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr10:101643884C>T c.3881G>A c.(3880-3882)cGg>cAg p.R1294Q LUSC 10 101656026 101656026 + Nonsense_Mutation SNP G G A TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr10:101656026G>A c.3049C>T c.(3049-3051)Cag>Tag p.Q1017* LUSC 10 101656145 101656145 + Missense_Mutation SNP T T C TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr10:101656145T>C c.2930A>G c.(2929-2931)tAc>tGc p.Y977C LUSC 10 101668899 101668899 + Missense_Mutation SNP C C T TCGA-60-2713-01A-01D-1522-08 TCGA-60-2713-11A-01D-1522-08 g.chr10:101668899C>T c.2265G>A c.(2263-2265)atG>atA p.M755I LUSC 10 101715112 101715112 + Missense_Mutation SNP T T G TCGA-37-3783-01A-01D-1267-08 TCGA-37-3783-10A-01D-1267-08 g.chr10:101715112T>G c.2119A>C c.(2119-2121)Atg>Ctg p.M707L LUSC 10 101715737 101715737 + Missense_Mutation SNP C C A TCGA-66-2756-01A-01D-1522-08 TCGA-66-2756-11A-01D-1522-08 g.chr10:101715737C>A c.1494G>T c.(1492-1494)caG>caT p.Q498H LUSC 10 101716838 101716838 + Silent SNP C C A TCGA-46-6026-01A-11D-1817-08 TCGA-46-6026-10A-01D-1817-08 g.chr10:101716838C>A c.393G>T c.(391-393)cgG>cgT p.R131R OV 10 101639945 101639945 + Missense_Mutation SNP C C T TCGA-24-2038-01A-01W-0722-08 TCGA-24-2038-10A-01W-0722-08 g.chr10:101639945C>T c.4171G>A c.(4171-4173)Gct>Act p.A1391T OV 10 101643914 101643914 + Missense_Mutation SNP T T C TCGA-20-1683-01A-01W-0633-09 TCGA-20-1683-10A-01W-0633-09 g.chr10:101643914T>C c.3851A>G c.(3850-3852)tAt>tGt p.Y1284C OV 10 101646214 101646214 + Missense_Mutation SNP C C T TCGA-10-0934-01A-02W-0420-08 TCGA-10-0934-11A-01W-0420-08 g.chr10:101646214C>T c.3461G>A c.(3460-3462)cGg>cAg p.R1154Q OV 10 101659761 101659761 + Missense_Mutation SNP G G T TCGA-61-2111-01A-01W-0722-08 TCGA-61-2111-11A-01W-0723-08 g.chr10:101659761G>T c.2617C>A c.(2617-2619)Cat>Aat p.H873N OV 10 101715848 101715848 + Silent SNP G G A TCGA-61-2613-01A-01W-1092-09 TCGA-61-2613-11A-01W-1092-09 g.chr10:101715848G>A c.1383C>T c.(1381-1383)ccC>ccT p.P461P OV 10 101716493 101716493 + Silent SNP G G T TCGA-04-1338-01A-01W-0484-10 TCGA-04-1338-11A-01W-0485-10 g.chr10:101716493G>T c.738C>A c.(736-738)acC>acA p.T246T OV 10 101731833 101731833 + Missense_Mutation SNP C C T TCGA-24-2019-01A-02W-0722-08 TCGA-24-2019-10A-01W-0722-08 g.chr10:101731833C>T c.49G>A c.(49-51)Gta>Ata p.V17I PAAD 10 101646207 101646207 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:101646207G>T c.3468C>A c.(3466-3468)aaC>aaA p.N1156K PAAD 10 101654741 101654741 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:101654741A>G c.3118T>C c.(3118-3120)Ttt>Ctt p.F1040L PAAD 10 101659757 101659757 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:101659757T>C c.2621A>G c.(2620-2622)gAt>gGt p.D874G PRAD 10 101636947 101636947 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:101636947G>A c.4695C>T c.(4693-4695)taC>taT p.Y1565Y PRAD 10 101636968 101636968 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:101636968C>T c.4674G>A c.(4672-4674)gaG>gaA p.E1558E PRAD 10 101639889 101639889 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:101639889C>T c.4227G>A c.(4225-4227)ccG>ccA p.P1409P PRAD 10 101731785 101731785 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:101731785C>T c.97G>A c.(97-99)Gca>Aca p.A33T READ 10 101667793 101667793 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:101667793G>A c.2513C>T c.(2512-2514)tCg>tTg p.S838L SARC 10 101716781 101716781 + Silent SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr10:101716781G>A c.450C>T c.(448-450)gcC>gcT p.A150A SKCM 10 101637062 101637062 + Missense_Mutation SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr10:101637062C>T c.4580G>A c.(4579-4581)cGa>cAa p.R1527Q SKCM 10 101639683 101639683 + Missense_Mutation SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr10:101639683G>A c.4433C>T c.(4432-4434)tCc>tTc p.S1478F SKCM 10 101639890 101639890 + Missense_Mutation SNP G G A TCGA-EB-A5SG-06A-11D-A30X-08 TCGA-EB-A5SG-10A-01D-A30X-08 g.chr10:101639890G>A c.4226C>T c.(4225-4227)cCg>cTg p.P1409L SKCM 10 101639994 101639994 + Silent SNP G G A TCGA-D3-A3MV-06A-11D-A21A-08 TCGA-D3-A3MV-10A-01D-A21A-08 g.chr10:101639994G>A c.4122C>T c.(4120-4122)ttC>ttT p.F1374F SKCM 10 101640031 101640031 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr10:101640031G>A c.4085C>T c.(4084-4086)tCc>tTc p.S1362F SKCM 10 101640083 101640083 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr10:101640083G>A c.4033C>T c.(4033-4035)Ccc>Tcc p.P1345S SKCM 10 101643875 101643875 + Missense_Mutation SNP T T C TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr10:101643875T>C c.3890A>G c.(3889-3891)aAt>aGt p.N1297S SKCM 10 101643911 101643911 + Missense_Mutation SNP G G A TCGA-EE-A29Q-06A-11D-A197-08 TCGA-EE-A29Q-10A-01D-A199-08 g.chr10:101643911G>A c.3854C>T c.(3853-3855)cCc>cTc p.P1285L SKCM 10 101643929 101643929 + Missense_Mutation SNP G G A TCGA-GN-A267-06A-21D-A196-08 TCGA-GN-A267-10A-01D-A198-08 g.chr10:101643929G>A c.3836C>T c.(3835-3837)tCc>tTc p.S1279F SKCM 10 101646230 101646230 + Missense_Mutation SNP C C T TCGA-D3-A2JD-06A-11D-A19A-08 TCGA-D3-A2JD-10A-01D-A19A-08 g.chr10:101646230C>T c.3445G>A c.(3445-3447)Gag>Aag p.E1149K SKCM 10 101646231 101646231 + Silent SNP C C T TCGA-D3-A2JD-06A-11D-A19A-08 TCGA-D3-A2JD-10A-01D-A19A-08 g.chr10:101646231C>T c.3444G>A c.(3442-3444)gaG>gaA p.E1148E SKCM 10 101646249 101646249 + Silent SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr10:101646249C>T c.3426G>A c.(3424-3426)aaG>aaA p.K1142K SKCM 10 101646372 101646372 + Silent SNP C C T TCGA-GN-A267-06A-21D-A196-08 TCGA-GN-A267-10A-01D-A198-08 g.chr10:101646372C>T c.3303G>A c.(3301-3303)cgG>cgA p.R1101R SKCM 10 101648593 101648593 + Missense_Mutation SNP A A G TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr10:101648593A>G c.3274T>C c.(3274-3276)Ttc>Ctc p.F1092L SKCM 10 101654768 101654768 + Nonsense_Mutation SNP G G A TCGA-EE-A2A6-06A-11D-A197-08 TCGA-EE-A2A6-10A-01D-A199-08 g.chr10:101654768G>A c.3091C>T c.(3091-3093)Cga>Tga p.R1031* SKCM 10 101659801 101659801 + Silent SNP C C T TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr10:101659801C>T c.2577G>A c.(2575-2577)cgG>cgA p.R859R SKCM 10 101715157 101715157 + Missense_Mutation SNP G G A TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr10:101715157G>A c.2074C>T c.(2074-2076)Ccc>Tcc p.P692S SKCM 10 101715158 101715158 + Silent SNP G G A TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr10:101715158G>A c.2073C>T c.(2071-2073)tgC>tgT p.C691C SKCM 10 101715232 101715232 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:101715232G>A c.1999C>T c.(1999-2001)Cgt>Tgt p.R667C SKCM 10 101715238 101715238 + Nonsense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr10:101715238G>A c.1993C>T c.(1993-1995)Cga>Tga p.R665* SKCM 10 101715817 101715817 + Nonsense_Mutation SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr10:101715817G>A c.1414C>T c.(1414-1416)Cag>Tag p.Q472* SKCM 10 101715887 101715887 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:101715887G>A c.1344C>T c.(1342-1344)ccC>ccT p.P448P SKCM 10 101715970 101715970 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr10:101715970G>A c.1261C>T c.(1261-1263)Cat>Tat p.H421Y SKCM 10 101716029 101716029 + Missense_Mutation SNP G G A TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr10:101716029G>A c.1202C>T c.(1201-1203)cCc>cTc p.P401L SKCM 10 101716582 101716582 + Nonsense_Mutation SNP G G A TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr10:101716582G>A c.649C>T c.(649-651)Caa>Taa p.Q217* SKCM 10 101716647 101716647 + Missense_Mutation SNP G G A TCGA-FS-A1ZP-06A-11D-A197-08 TCGA-FS-A1ZP-10A-01D-A199-08 g.chr10:101716647G>A c.584C>T c.(583-585)cCa>cTa p.P195L SKCM 10 101728986 101728986 + Missense_Mutation SNP G G A TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr10:101728986G>A c.154C>T c.(154-156)Ccc>Tcc p.P52S SKCM 10 101731860 101731860 + Nonsense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr10:101731860G>A c.22C>T c.(22-24)Cga>Tga p.R8* SKCM 10 101731860 101731860 + Nonsense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-11A-11D-A23B-08 g.chr10:101731860G>A c.22C>T c.(22-24)Cga>Tga p.R8*

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 10 101715220 101715220 single base substitution C G missense_variant E671Q 2011G>C BLCA-US 10 101639649 101639649 single base substitution G T synonymous_variant L1489L 4467C>A BLCA-US 10 101639649 101639649 single base substitution G T synonymous_variant L1513L 4539C>A BLCA-US 10 101639649 101639649 single base substitution G T synonymous_variant L425L 1275C>A BLCA-US 10 101639649 101639649 single base substitution G T synonymous_variant L735L 2205C>A BOCA-UK 10 101645595 101645595 single base substitution T C downstream_gene_variant BOCA-UK 10 101645595 101645595 single base substitution T C missense_variant N1216S 3647A>G BOCA-UK 10 101645595 101645595 single base substitution T C missense_variant N1240S 3719A>G BOCA-UK 10 101645595 101645595 single base substitution T C missense_variant N152S 455A>G BOCA-UK 10 101645595 101645595 single base substitution T C missense_variant N462S 1385A>G BRCA-EU 10 101631963 101631963 single base substitution T G downstream_gene_variant BRCA-EU 10 101632237 101632237 single base substitution C G downstream_gene_variant BRCA-EU 10 101632436 101632436 single base substitution C A downstream_gene_variant BRCA-EU 10 101633336 101633359 deletion of <=200bp GCAGAGCTGGAAGGGTAATTTGAC - downstream_gene_variant BRCA-EU 10 101634999 101634999 single base substitution T G downstream_gene_variant BRCA-EU 10 101635920 101635920 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 10 101635920 101635920 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 101636687 101636687 single base substitution C A 3_prime_UTR_variant BRCA-EU 10 101637063 101637063 single base substitution G A stop_gained R1527* 4579C>T BRCA-EU 10 101637063 101637063 single base substitution G A stop_gained R1551* 4651C>T BRCA-EU 10 101637063 101637063 single base substitution G A stop_gained R463* 1387C>T BRCA-EU 10 101637063 101637063 single base substitution G A stop_gained R773* 2317C>T BRCA-EU 10 101637547 101637547 single base substitution G T intron_variant BRCA-EU 10 101637769 101637769 single base substitution C T intron_variant BRCA-EU 10 101638015 101638015 single base substitution C T intron_variant BRCA-EU 10 101638821 101638821 single base substitution G A intron_variant BRCA-EU 10 101640074 101640074 single base substitution G C missense_variant P1348A 4042C>G BRCA-EU 10 101640074 101640074 single base substitution G C missense_variant P1372A 4114C>G BRCA-EU 10 101640074 101640074 single base substitution G C missense_variant P284A 850C>G BRCA-EU 10 101640074 101640074 single base substitution G C missense_variant P594A 1780C>G BRCA-EU 10 101640972 101640972 single base substitution C T intron_variant BRCA-EU 10 101642781 101642781 single base substitution G T downstream_gene_variant BRCA-EU 10 101642781 101642781 single base substitution G T intron_variant BRCA-EU 10 101644213 101644223 deletion of <=200bp TCTTGTGACAA - downstream_gene_variant BRCA-EU 10 101644213 101644223 deletion of <=200bp TCTTGTGACAA - intron_variant BRCA-EU 10 101644438 101644438 single base substitution G A downstream_gene_variant BRCA-EU 10 101644438 101644438 single base substitution G A intron_variant BRCA-EU 10 101645024 101645024 single base substitution T G downstream_gene_variant BRCA-EU 10 101645024 101645024 single base substitution T G intron_variant BRCA-EU 10 101645850 101645850 single base substitution T C downstream_gene_variant BRCA-EU 10 101645850 101645850 single base substitution T C intron_variant BRCA-EU 10 101646027 101646027 single base substitution A C downstream_gene_variant BRCA-EU 10 101646027 101646027 single base substitution A C intron_variant BRCA-EU 10 101647590 101647590 deletion of <=200bp T - intron_variant BRCA-EU 10 101647860 101647860 single base substitution G A intron_variant BRCA-EU 10 101653363 101653363 single base substitution C T downstream_gene_variant BRCA-EU 10 101653363 101653363 single base substitution C T intron_variant BRCA-EU 10 101653363 101653363 single base substitution C T upstream_gene_variant BRCA-EU 10 101654337 101654337 single base substitution T C 5_prime_UTR_variant BRCA-EU 10 101654337 101654337 single base substitution T C downstream_gene_variant BRCA-EU 10 101654337 101654337 single base substitution T C intron_variant BRCA-EU 10 101654613 101654613 single base substitution C G downstream_gene_variant BRCA-EU 10 101654613 101654613 single base substitution C G intron_variant BRCA-EU 10 101656544 101656544 single base substitution G A downstream_gene_variant BRCA-EU 10 101656544 101656544 single base substitution G A intron_variant BRCA-EU 10 101658132 101658132 deletion of <=200bp T - intron_variant BRCA-EU 10 101658132 101658132 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 101660088 101660088 single base substitution G A intron_variant BRCA-EU 10 101660088 101660088 single base substitution G A upstream_gene_variant BRCA-EU 10 101660258 101660258 insertion of <=200bp - AC intron_variant BRCA-EU 10 101660258 101660258 insertion of <=200bp - AC upstream_gene_variant BRCA-EU 10 101660398 101660398 insertion of <=200bp - T intron_variant BRCA-EU 10 101660398 101660398 insertion of <=200bp - T upstream_gene_variant BRCA-EU 10 101662164 101662164 single base substitution T C intron_variant BRCA-EU 10 101662164 101662164 single base substitution T C upstream_gene_variant BRCA-EU 10 101662335 101662335 single base substitution G A intron_variant BRCA-EU 10 101662335 101662335 single base substitution G A upstream_gene_variant BRCA-EU 10 101662444 101662444 single base substitution G A intron_variant BRCA-EU 10 101662444 101662444 single base substitution G A upstream_gene_variant BRCA-EU 10 101665026 101665026 single base substitution T C intron_variant BRCA-EU 10 101665222 101665222 single base substitution G A intron_variant BRCA-EU 10 101668131 101668131 single base substitution C A intron_variant BRCA-EU 10 101668577 101668577 single base substitution A C intron_variant BRCA-EU 10 101668885 101668885 single base substitution G C missense_variant S48C 143C>G BRCA-EU 10 101668885 101668885 single base substitution G C missense_variant S6C 17C>G BRCA-EU 10 101668885 101668885 single base substitution G C missense_variant S760C 2279C>G BRCA-EU 10 101669201 101669201 single base substitution G C intron_variant BRCA-EU 10 101669902 101669902 single base substitution T G intron_variant BRCA-EU 10 101672210 101672210 single base substitution T C intron_variant BRCA-EU 10 101673708 101673708 insertion of <=200bp - A intron_variant BRCA-EU 10 101673708 101673708 insertion of <=200bp - A splice_donor_variant BRCA-EU 10 101679686 101679686 single base substitution G C intron_variant BRCA-EU 10 101680159 101680159 single base substitution A T intron_variant BRCA-EU 10 101681444 101681444 single base substitution C G intron_variant BRCA-EU 10 101681605 101681605 single base substitution G C intron_variant BRCA-EU 10 101682010 101682010 single base substitution G A intron_variant BRCA-EU 10 101682117 101682117 single base substitution A C intron_variant BRCA-EU 10 101683043 101683043 single base substitution G A intron_variant BRCA-EU 10 101685184 101685184 deletion of <=200bp T - intron_variant BRCA-EU 10 101691742 101691742 single base substitution C A intron_variant BRCA-EU 10 101691742 101691742 single base substitution C A upstream_gene_variant BRCA-EU 10 101691829 101691832 deletion of <=200bp AAAG - intron_variant BRCA-EU 10 101691829 101691832 deletion of <=200bp AAAG - upstream_gene_variant BRCA-EU 10 101692610 101692610 single base substitution G T intron_variant BRCA-EU 10 101692610 101692610 single base substitution G T upstream_gene_variant BRCA-EU 10 101693110 101693110 single base substitution C T intron_variant BRCA-EU 10 101693110 101693110 single base substitution C T upstream_gene_variant BRCA-EU 10 101693592 101693592 single base substitution C G intron_variant BRCA-EU 10 101693592 101693592 single base substitution C G upstream_gene_variant BRCA-EU 10 101694303 101694303 single base substitution G A intron_variant BRCA-EU 10 101694303 101694303 single base substitution G A upstream_gene_variant BRCA-EU 10 101694759 101694759 single base substitution G T intron_variant BRCA-EU 10 101694759 101694759 single base substitution G T upstream_gene_variant BRCA-EU 10 101695406 101695406 single base substitution C G intron_variant BRCA-EU 10 101695406 101695406 single base substitution C G upstream_gene_variant BRCA-EU 10 101695633 101695633 single base substitution T A intron_variant BRCA-EU 10 101695633 101695633 single base substitution T A upstream_gene_variant BRCA-EU 10 101695693 101695693 single base substitution G C intron_variant BRCA-EU 10 101695693 101695693 single base substitution G C upstream_gene_variant BRCA-EU 10 101696183 101696183 single base substitution C G intron_variant BRCA-EU 10 101696949 101696949 single base substitution C A intron_variant BRCA-EU 10 101699119 101699119 single base substitution T C intron_variant BRCA-EU 10 101699503 101699503 single base substitution A C intron_variant BRCA-EU 10 101699557 101699557 single base substitution C G intron_variant BRCA-EU 10 101699635 101699635 single base substitution C T intron_variant BRCA-EU 10 101699994 101699994 single base substitution C G intron_variant BRCA-EU 10 101700072 101700072 single base substitution C G intron_variant BRCA-EU 10 101701132 101701132 single base substitution G C intron_variant BRCA-EU 10 101701220 101701220 single base substitution C A intron_variant BRCA-EU 10 101702029 101702029 single base substitution C A intron_variant BRCA-EU 10 101704923 101704923 single base substitution A C intron_variant BRCA-EU 10 101705414 101705414 single base substitution T A intron_variant BRCA-EU 10 101706249 101706249 single base substitution G A intron_variant BRCA-EU 10 101707952 101707952 single base substitution C T intron_variant BRCA-EU 10 101708909 101708909 single base substitution T A intron_variant BRCA-EU 10 101712444 101712444 single base substitution G C intron_variant BRCA-EU 10 101712700 101712700 single base substitution C G intron_variant BRCA-EU 10 101714416 101714416 single base substitution G A intron_variant BRCA-EU 10 101715036 101715036 single base substitution A G missense_variant L732P 2195T>C BRCA-EU 10 101716093 101716093 single base substitution T C missense_variant T380A 1138A>G BRCA-EU 10 101717099 101717099 single base substitution A C intron_variant BRCA-EU 10 101721421 101721421 single base substitution T C intron_variant BRCA-EU 10 101722847 101722847 single base substitution A G intron_variant BRCA-EU 10 101725577 101725577 single base substitution A G intron_variant BRCA-EU 10 101730811 101730811 single base substitution G C intron_variant BRCA-EU 10 101731040 101731040 single base substitution G C intron_variant BRCA-EU 10 101734606 101734606 single base substitution G A intron_variant BRCA-EU 10 101735406 101735406 deletion of <=200bp A - intron_variant BRCA-EU 10 101738487 101738487 single base substitution C G intron_variant BRCA-EU 10 101738612 101738612 single base substitution G A intron_variant BRCA-EU 10 101739736 101739736 single base substitution C A intron_variant BRCA-EU 10 101742989 101742989 single base substitution A G intron_variant BRCA-EU 10 101743627 101743627 single base substitution G C intron_variant BRCA-EU 10 101745373 101745373 single base substitution G T intron_variant BRCA-EU 10 101745374 101745374 single base substitution A G intron_variant BRCA-EU 10 101745953 101745953 single base substitution T G intron_variant BRCA-EU 10 101747007 101747007 single base substitution C G intron_variant BRCA-EU 10 101747615 101747615 single base substitution C T intron_variant BRCA-EU 10 101749104 101749104 single base substitution C G intron_variant BRCA-EU 10 101750370 101750370 single base substitution A T intron_variant BRCA-EU 10 101752255 101752255 single base substitution G A intron_variant BRCA-EU 10 101753190 101753190 single base substitution T C intron_variant BRCA-EU 10 101754384 101754384 single base substitution T G intron_variant BRCA-EU 10 101754554 101754554 single base substitution C T intron_variant BRCA-EU 10 101755420 101755420 single base substitution A G intron_variant BRCA-EU 10 101755640 101755640 single base substitution C T intron_variant BRCA-EU 10 101764835 101764835 single base substitution G A intron_variant BRCA-EU 10 101764987 101764987 single base substitution C A intron_variant BRCA-EU 10 101766773 101766773 single base substitution G C intron_variant BRCA-EU 10 101767194 101767194 single base substitution C T intron_variant BRCA-EU 10 101767610 101767610 single base substitution G C intron_variant BRCA-EU 10 101767955 101767955 single base substitution A G intron_variant BRCA-EU 10 101768093 101768093 single base substitution C G intron_variant BRCA-EU 10 101768112 101768113 deletion of <=200bp TG - intron_variant BRCA-EU 10 101768588 101768588 single base substitution G C intron_variant BRCA-EU 10 101769085 101769085 single base substitution C T intron_variant BRCA-EU 10 101769292 101769292 single base substitution G A intron_variant BRCA-EU 10 101770370 101770370 single base substitution A G upstream_gene_variant BRCA-EU 10 101771238 101771238 single base substitution A T upstream_gene_variant BRCA-EU 10 101771848 101771848 single base substitution C T upstream_gene_variant BRCA-EU 10 101773135 101773135 deletion of <=200bp A - upstream_gene_variant BRCA-EU 10 101774021 101774021 single base substitution G A upstream_gene_variant BRCA-EU 10 101774174 101774174 single base substitution G A upstream_gene_variant BRCA-EU 10 101774241 101774241 single base substitution G C upstream_gene_variant BRCA-FR 10 101631370 101631370 single base substitution G A downstream_gene_variant BRCA-FR 10 101637129 101637129 single base substitution G A intron_variant BRCA-FR 10 101638015 101638015 single base substitution C T intron_variant BRCA-FR 10 101649274 101649274 single base substitution C T intron_variant BRCA-FR 10 101649274 101649274 single base substitution C T upstream_gene_variant BRCA-FR 10 101653732 101653732 single base substitution T A downstream_gene_variant BRCA-FR 10 101653732 101653732 single base substitution T A intron_variant BRCA-FR 10 101653732 101653732 single base substitution T A upstream_gene_variant BRCA-FR 10 101660088 101660088 single base substitution G A intron_variant BRCA-FR 10 101660088 101660088 single base substitution G A upstream_gene_variant BRCA-FR 10 101662164 101662164 single base substitution T C intron_variant BRCA-FR 10 101662164 101662164 single base substitution T C upstream_gene_variant BRCA-FR 10 101679686 101679686 single base substitution G C intron_variant BRCA-FR 10 101680159 101680159 single base substitution A T intron_variant BRCA-FR 10 101694303 101694303 single base substitution G A intron_variant BRCA-FR 10 101694303 101694303 single base substitution G A upstream_gene_variant BRCA-FR 10 101694700 101694700 single base substitution A G intron_variant BRCA-FR 10 101694700 101694700 single base substitution A G upstream_gene_variant BRCA-FR 10 101701132 101701132 single base substitution G C intron_variant BRCA-FR 10 101706249 101706249 single base substitution G A intron_variant BRCA-FR 10 101712444 101712444 single base substitution G C intron_variant BRCA-FR 10 101721409 101721409 single base substitution C G intron_variant BRCA-FR 10 101731463 101731463 single base substitution G A intron_variant BRCA-FR 10 101752255 101752255 single base substitution G A intron_variant BRCA-FR 10 101758281 101758281 single base substitution G C intron_variant BRCA-FR 10 101772838 101772838 single base substitution C T upstream_gene_variant BRCA-FR 10 101774174 101774174 single base substitution G A upstream_gene_variant BRCA-FR 10 101774241 101774241 single base substitution G C upstream_gene_variant BRCA-KR 10 101716364 101716364 single base substitution T A synonymous_variant T289T 867A>T BRCA-UK 10 101637610 101637610 single base substitution G C intron_variant BRCA-UK 10 101638821 101638821 single base substitution G A intron_variant BRCA-UK 10 101645850 101645850 single base substitution T C downstream_gene_variant BRCA-UK 10 101645850 101645850 single base substitution T C intron_variant BRCA-UK 10 101655933 101655933 single base substitution G T downstream_gene_variant BRCA-UK 10 101655933 101655933 single base substitution G T intron_variant BRCA-UK 10 101665494 101665494 single base substitution G C intron_variant BRCA-UK 10 101665935 101665935 single base substitution G A intron_variant BRCA-UK 10 101666546 101666546 single base substitution G C intron_variant BRCA-UK 10 101670602 101670602 single base substitution G C intron_variant BRCA-UK 10 101682956 101682956 single base substitution G C intron_variant BRCA-UK 10 101699985 101699985 single base substitution G A intron_variant BRCA-UK 10 101704923 101704923 single base substitution A C intron_variant BRCA-UK 10 101718144 101718144 single base substitution G A intron_variant BRCA-US 10 101637038 101637038 single base substitution G T stop_gained S1535* 4604C>A BRCA-US 10 101637038 101637038 single base substitution G T stop_gained S1559* 4676C>A BRCA-US 10 101637038 101637038 single base substitution G T stop_gained S471* 1412C>A BRCA-US 10 101637038 101637038 single base substitution G T stop_gained S781* 2342C>A BRCA-US 10 101639792 101639792 single base substitution A G missense_variant S1442P 4324T>C BRCA-US 10 101639792 101639792 single base substitution A G missense_variant S1466P 4396T>C BRCA-US 10 101639792 101639792 single base substitution A G missense_variant S378P 1132T>C BRCA-US 10 101639792 101639792 single base substitution A G missense_variant S688P 2062T>C BRCA-US 10 101643811 101643811 single base substitution T G downstream_gene_variant BRCA-US 10 101643811 101643811 single base substitution T G missense_variant K1318N 3954A>C BRCA-US 10 101643811 101643811 single base substitution T G missense_variant K1342N 4026A>C BRCA-US 10 101643811 101643811 single base substitution T G missense_variant K254N 762A>C BRCA-US 10 101643811 101643811 single base substitution T G missense_variant K564N 1692A>C BRCA-US 10 101643877 101643877 single base substitution G T downstream_gene_variant BRCA-US 10 101643877 101643877 single base substitution G T missense_variant F1296L 3888C>A BRCA-US 10 101643877 101643877 single base substitution G T missense_variant F1320L 3960C>A BRCA-US 10 101643877 101643877 single base substitution G T missense_variant F232L 696C>A BRCA-US 10 101643877 101643877 single base substitution G T missense_variant F542L 1626C>A BRCA-US 10 101643927 101643927 single base substitution G T downstream_gene_variant BRCA-US 10 101643927 101643927 single base substitution G T missense_variant L1280I 3838C>A BRCA-US 10 101643927 101643927 single base substitution G T missense_variant L1304I 3910C>A BRCA-US 10 101643927 101643927 single base substitution G T missense_variant L216I 646C>A BRCA-US 10 101643927 101643927 single base substitution G T missense_variant L526I 1576C>A BRCA-US 10 101646291 101646291 single base substitution G C exon_variant BRCA-US 10 101646291 101646291 single base substitution G C synonymous_variant L1128L 3384C>G BRCA-US 10 101646291 101646291 single base substitution G C synonymous_variant L1152L 3456C>G BRCA-US 10 101646291 101646291 single base substitution G C synonymous_variant L374L 1122C>G BRCA-US 10 101646291 101646291 single base substitution G C synonymous_variant L64L 192C>G BRCA-US 10 101648689 101648689 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 10 101648689 101648689 single base substitution C T exon_variant BRCA-US 10 101648689 101648689 single base substitution C T missense_variant V1060M 3178G>A BRCA-US 10 101648689 101648689 single base substitution C T missense_variant V1084M 3250G>A BRCA-US 10 101648689 101648689 single base substitution C T missense_variant V306M 916G>A BRCA-US 10 101659737 101659737 single base substitution C T missense_variant E127K 379G>A BRCA-US 10 101659737 101659737 single base substitution C T missense_variant E169K 505G>A BRCA-US 10 101659737 101659737 single base substitution C T missense_variant E881K 2641G>A BRCA-US 10 101659737 101659737 single base substitution C T upstream_gene_variant BRCA-US 10 101668763 101668763 single base substitution G A missense_variant R47W 139C>T BRCA-US 10 101668763 101668763 single base substitution G A missense_variant R801W 2401C>T BRCA-US 10 101668763 101668763 single base substitution G A missense_variant R89W 265C>T BRCA-US 10 101715245 101715245 single base substitution G C synonymous_variant L662L 1986C>G BRCA-US 10 101715753 101715753 single base substitution C T missense_variant R493K 1478G>A BRCA-US 10 101728874 101728874 single base substitution C T missense_variant R89Q 266G>A BTCA-JP 10 101643631 101643631 single base substitution G A downstream_gene_variant BTCA-JP 10 101643631 101643631 single base substitution G A intron_variant BTCA-JP 10 101643724 101643724 deletion of <=200bp T - downstream_gene_variant BTCA-JP 10 101643724 101643724 deletion of <=200bp T - intron_variant BTCA-JP 10 101658089 101658089 single base substitution C T intron_variant BTCA-JP 10 101658089 101658089 single base substitution C T upstream_gene_variant BTCA-JP 10 101658123 101658123 deletion of <=200bp A - intron_variant BTCA-JP 10 101658123 101658123 deletion of <=200bp A - upstream_gene_variant BTCA-JP 10 101658631 101658631 single base substitution T C intron_variant BTCA-JP 10 101658631 101658631 single base substitution T C upstream_gene_variant BTCA-JP 10 101689799 101689799 single base substitution A T 5_prime_UTR_variant BTCA-JP 10 101689799 101689799 single base substitution A T intron_variant BTCA-JP 10 101714816 101714816 single base substitution G A intron_variant BTCA-JP 10 101714818 101714818 single base substitution A G intron_variant CESC-US 10 101637012 101637012 single base substitution C T missense_variant E1544K 4630G>A CESC-US 10 101637012 101637012 single base substitution C T missense_variant E1568K 4702G>A CESC-US 10 101637012 101637012 single base substitution C T missense_variant E480K 1438G>A CESC-US 10 101637012 101637012 single base substitution C T missense_variant E790K 2368G>A CESC-US 10 101645515 101645515 single base substitution G C downstream_gene_variant CESC-US 10 101645515 101645515 single base substitution G C missense_variant P1243A 3727C>G CESC-US 10 101645515 101645515 single base substitution G C missense_variant P1267A 3799C>G CESC-US 10 101645515 101645515 single base substitution G C missense_variant P179A 535C>G CESC-US 10 101645515 101645515 single base substitution G C missense_variant P489A 1465C>G CESC-US 10 101656053 101656053 single base substitution G T downstream_gene_variant CESC-US 10 101656053 101656053 single base substitution G T intron_variant CESC-US 10 101656053 101656053 single base substitution G T missense_variant L1008M 3022C>A CESC-US 10 101656053 101656053 single base substitution G T missense_variant L1032M 3094C>A CESC-US 10 101656053 101656053 single base substitution G T missense_variant L254M 760C>A CESC-US 10 101715391 101715391 single base substitution G A missense_variant R614C 1840C>T CESC-US 10 101715662 101715662 single base substitution C T missense_variant M523I 1569G>A CESC-US 10 101716192 101716192 single base substitution C T missense_variant E347K 1039G>A CESC-US 10 101716973 101716973 single base substitution G T intron_variant CLLE-ES 10 101632068 101632068 single base substitution G T downstream_gene_variant CLLE-ES 10 101650612 101650612 single base substitution C T intron_variant CLLE-ES 10 101650612 101650612 single base substitution C T upstream_gene_variant CLLE-ES 10 101668575 101668576 multiple base substitution (>=2bp and <=200bp) TA AG intron_variant CLLE-ES 10 101715145 101715145 insertion of <=200bp - G frameshift_variant V696A? CLLE-ES 10 101715397 101715397 single base substitution G C missense_variant P612A 1834C>G CLLE-ES 10 101724403 101724403 single base substitution G A intron_variant CLLE-ES 10 101736186 101736190 deletion of <=200bp CAGCA - intron_variant CLLE-ES 10 101761065 101761065 single base substitution G T intron_variant COAD-US 10 101639682 101639682 single base substitution G A synonymous_variant S1478S 4434C>T COAD-US 10 101639682 101639682 single base substitution G A synonymous_variant S1502S 4506C>T COAD-US 10 101639682 101639682 single base substitution G A synonymous_variant S414S 1242C>T COAD-US 10 101639682 101639682 single base substitution G A synonymous_variant S724S 2172C>T COAD-US 10 101639727 101639727 single base substitution C T synonymous_variant P1463P 4389G>A COAD-US 10 101639727 101639727 single base substitution C T synonymous_variant P1487P 4461G>A COAD-US 10 101639727 101639727 single base substitution C T synonymous_variant P399P 1197G>A COAD-US 10 101639727 101639727 single base substitution C T synonymous_variant P709P 2127G>A COAD-US 10 101639877 101639877 single base substitution A C missense_variant C1413W 4239T>G COAD-US 10 101639877 101639877 single base substitution A C missense_variant C1437W 4311T>G COAD-US 10 101639877 101639877 single base substitution A C missense_variant C349W 1047T>G COAD-US 10 101639877 101639877 single base substitution A C missense_variant C659W 1977T>G COAD-US 10 101646058 101646058 single base substitution G A downstream_gene_variant COAD-US 10 101646058 101646058 single base substitution G A missense_variant S1206L 3617C>T COAD-US 10 101646058 101646058 single base substitution G A missense_variant S1230L 3689C>T COAD-US 10 101646058 101646058 single base substitution G A missense_variant S142L 425C>T COAD-US 10 101646058 101646058 single base substitution G A missense_variant S452L 1355C>T COAD-US 10 101657880 101657880 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 10 101657880 101657880 single base substitution G A downstream_gene_variant COAD-US 10 101657880 101657880 single base substitution G A synonymous_variant N207N 621C>T COAD-US 10 101657880 101657880 single base substitution G A synonymous_variant N961N 2883C>T COAD-US 10 101715292 101715292 single base substitution G T missense_variant L647M 1939C>A COAD-US 10 101715823 101715823 deletion of <=200bp T - frameshift_variant T470 COAD-US 10 101715927 101715927 single base substitution C A missense_variant G435V 1304G>T COAD-US 10 101716082 101716082 single base substitution C T synonymous_variant G383G 1149G>A COAD-US 10 101716590 101716590 single base substitution G A missense_variant S214F 641C>T COCA-CN 10 101634115 101634115 single base substitution A G downstream_gene_variant COCA-CN 10 101636901 101636901 single base substitution C T 3_prime_UTR_variant COCA-CN 10 101640048 101640048 single base substitution G T synonymous_variant S1356S 4068C>A COCA-CN 10 101640048 101640048 single base substitution G T synonymous_variant S1380S 4140C>A COCA-CN 10 101640048 101640048 single base substitution G T synonymous_variant S292S 876C>A COCA-CN 10 101640048 101640048 single base substitution G T synonymous_variant S602S 1806C>A COCA-CN 10 101645575 101645575 single base substitution C T downstream_gene_variant COCA-CN 10 101645575 101645575 single base substitution C T missense_variant E1223K 3667G>A COCA-CN 10 101645575 101645575 single base substitution C T missense_variant E1247K 3739G>A COCA-CN 10 101645575 101645575 single base substitution C T missense_variant E159K 475G>A COCA-CN 10 101645575 101645575 single base substitution C T missense_variant E469K 1405G>A COCA-CN 10 101657728 101657728 single base substitution G A downstream_gene_variant COCA-CN 10 101657728 101657728 single base substitution G A intron_variant COCA-CN 10 101658568 101658568 single base substitution A C intron_variant COCA-CN 10 101658568 101658568 single base substitution A C upstream_gene_variant COCA-CN 10 101661999 101661999 single base substitution A T intron_variant COCA-CN 10 101661999 101661999 single base substitution A T upstream_gene_variant COCA-CN 10 101668986 101668986 single base substitution T C intron_variant COCA-CN 10 101682285 101682285 single base substitution A T intron_variant COCA-CN 10 101689997 101689997 single base substitution T G 5_prime_UTR_variant COCA-CN 10 101689997 101689997 single base substitution T G intron_variant COCA-CN 10 101690296 101690296 single base substitution T C 5_prime_UTR_variant COCA-CN 10 101690296 101690296 single base substitution T C intron_variant COCA-CN 10 101690388 101690388 single base substitution C A 5_prime_UTR_variant COCA-CN 10 101690388 101690388 single base substitution C A intron_variant COCA-CN 10 101690537 101690537 single base substitution G T 5_prime_UTR_variant COCA-CN 10 101690537 101690537 single base substitution G T intron_variant COCA-CN 10 101690637 101690637 single base substitution C G 5_prime_UTR_variant COCA-CN 10 101690637 101690637 single base substitution C G intron_variant COCA-CN 10 101694871 101694871 single base substitution G A intron_variant COCA-CN 10 101694871 101694871 single base substitution G A upstream_gene_variant COCA-CN 10 101699189 101699189 single base substitution C A intron_variant COCA-CN 10 101713599 101713599 single base substitution C T intron_variant COCA-CN 10 101728800 101728800 single base substitution G A intron_variant COCA-CN 10 101750589 101750589 single base substitution C T intron_variant COCA-CN 10 101750591 101750591 single base substitution T C intron_variant COCA-CN 10 101750595 101750595 single base substitution C T intron_variant COCA-CN 10 101752563 101752563 single base substitution A G intron_variant COCA-CN 10 101757025 101757025 single base substitution A G intron_variant COCA-CN 10 101757861 101757861 single base substitution G A intron_variant EOPC-DE 10 101637433 101637433 single base substitution C T intron_variant EOPC-DE 10 101660238 101660238 single base substitution A G intron_variant EOPC-DE 10 101660238 101660238 single base substitution A G upstream_gene_variant EOPC-DE 10 101669569 101669569 single base substitution A C intron_variant EOPC-DE 10 101688538 101688538 single base substitution A C intron_variant EOPC-DE 10 101688541 101688541 single base substitution C A intron_variant EOPC-DE 10 101710899 101710899 single base substitution C T intron_variant EOPC-DE 10 101748332 101748332 single base substitution G T intron_variant ESAD-UK 10 101632672 101632672 single base substitution T C downstream_gene_variant ESAD-UK 10 101640921 101640921 single base substitution G A intron_variant ESAD-UK 10 101641932 101641932 single base substitution T C downstream_gene_variant ESAD-UK 10 101641932 101641932 single base substitution T C intron_variant ESAD-UK 10 101644011 101644011 single base substitution C A downstream_gene_variant ESAD-UK 10 101644011 101644011 single base substitution C A intron_variant ESAD-UK 10 101644395 101644395 single base substitution G C downstream_gene_variant ESAD-UK 10 101644395 101644395 single base substitution G C intron_variant ESAD-UK 10 101644910 101644910 single base substitution T C downstream_gene_variant ESAD-UK 10 101644910 101644910 single base substitution T C intron_variant ESAD-UK 10 101649076 101649076 single base substitution T C exon_variant ESAD-UK 10 101649076 101649076 single base substitution T C intron_variant ESAD-UK 10 101649311 101649311 single base substitution T G intron_variant ESAD-UK 10 101649311 101649311 single base substitution T G upstream_gene_variant ESAD-UK 10 101649588 101649588 single base substitution G A intron_variant ESAD-UK 10 101649588 101649588 single base substitution G A upstream_gene_variant ESAD-UK 10 101649750 101649750 single base substitution T C intron_variant ESAD-UK 10 101649750 101649750 single base substitution T C upstream_gene_variant ESAD-UK 10 101650219 101650219 single base substitution C T intron_variant ESAD-UK 10 101650219 101650219 single base substitution C T upstream_gene_variant ESAD-UK 10 101657802 101657802 single base substitution C T downstream_gene_variant ESAD-UK 10 101657802 101657802 single base substitution C T intron_variant ESAD-UK 10 101659273 101659273 single base substitution C T intron_variant ESAD-UK 10 101659273 101659273 single base substitution C T upstream_gene_variant ESAD-UK 10 101667142 101667142 single base substitution T A intron_variant ESAD-UK 10 101667156 101667156 single base substitution G T intron_variant ESAD-UK 10 101672566 101672566 insertion of <=200bp - GTCAC intron_variant ESAD-UK 10 101672575 101672575 single base substitution C T intron_variant ESAD-UK 10 101674430 101674430 single base substitution G A intron_variant ESAD-UK 10 101674430 101674430 single base substitution G A upstream_gene_variant ESAD-UK 10 101674798 101674798 single base substitution C T intron_variant ESAD-UK 10 101674798 101674798 single base substitution C T upstream_gene_variant ESAD-UK 10 101674863 101674863 single base substitution A T intron_variant ESAD-UK 10 101674863 101674863 single base substitution A T upstream_gene_variant ESAD-UK 10 101674884 101674887 deletion of <=200bp ATAC - intron_variant ESAD-UK 10 101674884 101674887 deletion of <=200bp ATAC - upstream_gene_variant ESAD-UK 10 101674938 101674938 single base substitution C A intron_variant ESAD-UK 10 101674938 101674938 single base substitution C A upstream_gene_variant ESAD-UK 10 101682720 101682720 single base substitution C T intron_variant ESAD-UK 10 101684187 101684187 single base substitution G A intron_variant ESAD-UK 10 101684247 101684247 single base substitution T G intron_variant ESAD-UK 10 101691125 101691125 single base substitution G A intron_variant ESAD-UK 10 101691125 101691125 single base substitution G A upstream_gene_variant ESAD-UK 10 101691476 101691476 single base substitution G A intron_variant ESAD-UK 10 101691476 101691476 single base substitution G A upstream_gene_variant ESAD-UK 10 101699813 101699813 single base substitution G A intron_variant ESAD-UK 10 101702770 101702770 single base substitution T C intron_variant ESAD-UK 10 101703888 101703888 single base substitution C T intron_variant ESAD-UK 10 101704431 101704431 single base substitution G A intron_variant ESAD-UK 10 101705236 101705236 single base substitution T A intron_variant ESAD-UK 10 101706671 101706671 single base substitution T C intron_variant ESAD-UK 10 101708749 101708749 insertion of <=200bp - ATAAATAAATAC intron_variant ESAD-UK 10 101714369 101714369 single base substitution C T intron_variant ESAD-UK 10 101714456 101714456 single base substitution G A intron_variant ESAD-UK 10 101715100 101715100 single base substitution C T missense_variant A711T 2131G>A ESAD-UK 10 101717912 101717912 single base substitution G A intron_variant ESAD-UK 10 101719970 101719970 single base substitution A C intron_variant ESAD-UK 10 101722374 101722374 single base substitution C T intron_variant ESAD-UK 10 101724606 101724606 single base substitution C T intron_variant ESAD-UK 10 101724646 101724646 deletion of <=200bp T - intron_variant ESAD-UK 10 101728704 101728704 single base substitution T A intron_variant ESAD-UK 10 101729236 101729236 single base substitution C T intron_variant ESAD-UK 10 101729569 101729569 single base substitution C T intron_variant ESAD-UK 10 101731443 101731443 single base substitution A C intron_variant ESAD-UK 10 101735479 101735480 deletion of <=200bp AG - intron_variant ESAD-UK 10 101737030 101737030 single base substitution T A intron_variant ESAD-UK 10 101738128 101738128 single base substitution C T intron_variant ESAD-UK 10 101739524 101739524 single base substitution G A intron_variant ESAD-UK 10 101740154 101740154 single base substitution A C intron_variant ESAD-UK 10 101740885 101740885 single base substitution T A intron_variant ESAD-UK 10 101742432 101742432 single base substitution G T intron_variant ESAD-UK 10 101748953 101748953 single base substitution T A intron_variant ESAD-UK 10 101751918 101751918 single base substitution G A intron_variant ESAD-UK 10 101761868 101761868 single base substitution A C intron_variant ESAD-UK 10 101764828 101764828 single base substitution C T intron_variant ESAD-UK 10 101769751 101769751 single base substitution G C upstream_gene_variant ESAD-UK 10 101770246 101770246 single base substitution G A upstream_gene_variant ESAD-UK 10 101774201 101774201 single base substitution C A upstream_gene_variant ESCA-CN 10 101716642 101716644 deletion of <=200bp CTT - disruptive_inframe_deletion EG196G ESCA-CN 10 101716750 101716750 single base substitution C G missense_variant D161H 481G>C GBM-US 10 101654794 101654794 single base substitution A G 5_prime_UTR_variant GBM-US 10 101654794 101654794 single base substitution A G downstream_gene_variant GBM-US 10 101654794 101654794 single base substitution A G missense_variant V1022A 3065T>C GBM-US 10 101654794 101654794 single base substitution A G missense_variant V1046A 3137T>C GBM-US 10 101654794 101654794 single base substitution A G missense_variant V268A 803T>C GBM-US 10 101715528 101715528 single base substitution G C missense_variant T568R 1703C>G GBM-US 10 101716663 101716663 single base substitution G A stop_gained R190* 568C>T GBM-US 10 101716779 101716779 single base substitution C T missense_variant R151Q 452G>A KIRC-US 10 101728908 101728908 single base substitution T G missense_variant T78P 232A>C KIRP-US 10 101646325 101646325 single base substitution G C exon_variant KIRP-US 10 101646325 101646325 single base substitution G C missense_variant P1117R 3350C>G KIRP-US 10 101646325 101646325 single base substitution G C missense_variant P1141R 3422C>G KIRP-US 10 101646325 101646325 single base substitution G C missense_variant P363R 1088C>G KIRP-US 10 101646325 101646325 single base substitution G C missense_variant P53R 158C>G KIRP-US 10 101715503 101715503 single base substitution G T missense_variant H576Q 1728C>A LAML-KR 10 101651621 101651621 single base substitution G C intron_variant LAML-KR 10 101651621 101651621 single base substitution G C upstream_gene_variant LAML-KR 10 101668570 101668570 single base substitution T C intron_variant LAML-KR 10 101683815 101683815 single base substitution A G intron_variant LGG-US 10 101731881 101731881 single base substitution T C start_lost M1V 1A>G LICA-CN 10 101659705 101659705 single base substitution C A missense_variant K137N 411G>T LICA-CN 10 101659705 101659705 single base substitution C A missense_variant K179N 537G>T LICA-CN 10 101659705 101659705 single base substitution C A missense_variant K891N 2673G>T LICA-CN 10 101659705 101659705 single base substitution C A upstream_gene_variant LICA-FR 10 101740682 101740682 single base substitution G A intron_variant LICA-FR 10 101756519 101756519 single base substitution A G intron_variant LICA-FR 10 101761171 101761171 insertion of <=200bp - T intron_variant LIHC-US 10 101656127 101656127 single base substitution T C downstream_gene_variant LIHC-US 10 101656127 101656127 single base substitution T C intron_variant LIHC-US 10 101656127 101656127 single base substitution T C missense_variant D1007G 3020A>G LIHC-US 10 101656127 101656127 single base substitution T C missense_variant D229G 686A>G LIHC-US 10 101656127 101656127 single base substitution T C missense_variant D983G 2948A>G LINC-JP 10 101646171 101646171 single base substitution C T exon_variant LINC-JP 10 101646171 101646171 single base substitution C T synonymous_variant L104L 312G>A LINC-JP 10 101646171 101646171 single base substitution C T synonymous_variant L1168L 3504G>A LINC-JP 10 101646171 101646171 single base substitution C T synonymous_variant L1192L 3576G>A LINC-JP 10 101646171 101646171 single base substitution C T synonymous_variant L414L 1242G>A LINC-JP 10 101648614 101648614 single base substitution G A exon_variant LINC-JP 10 101648614 101648614 single base substitution G A missense_variant R1085C 3253C>T LINC-JP 10 101648614 101648614 single base substitution G A missense_variant R1109C 3325C>T LINC-JP 10 101648614 101648614 single base substitution G A missense_variant R21C 61C>T LINC-JP 10 101648614 101648614 single base substitution G A missense_variant R331C 991C>T LINC-JP 10 101656292 101656292 single base substitution T C downstream_gene_variant LINC-JP 10 101656292 101656292 single base substitution T C intron_variant LINC-JP 10 101658123 101658123 deletion of <=200bp A - intron_variant LINC-JP 10 101658123 101658123 deletion of <=200bp A - upstream_gene_variant LINC-JP 10 101672167 101672167 single base substitution T C intron_variant LINC-JP 10 101673872 101673872 single base substitution A G intron_variant LINC-JP 10 101673872 101673872 single base substitution A G upstream_gene_variant LINC-JP 10 101673975 101673975 single base substitution C T intron_variant LINC-JP 10 101673975 101673975 single base substitution C T upstream_gene_variant LINC-JP 10 101678469 101678469 single base substitution A C intron_variant LINC-JP 10 101678469 101678469 single base substitution A C upstream_gene_variant LINC-JP 10 101680518 101680518 single base substitution A G intron_variant LINC-JP 10 101686703 101686703 single base substitution C T intron_variant LINC-JP 10 101688610 101688610 single base substitution A G intron_variant LINC-JP 10 101688975 101688975 deletion of <=200bp A - intron_variant LINC-JP 10 101702745 101702745 single base substitution A G intron_variant LINC-JP 10 101709724 101709724 deletion of <=200bp C - intron_variant LINC-JP 10 101712921 101712921 single base substitution G C intron_variant LINC-JP 10 101714818 101714818 single base substitution A G intron_variant LINC-JP 10 101727871 101727871 single base substitution T G intron_variant LINC-JP 10 101734123 101734123 single base substitution A C intron_variant LINC-JP 10 101737545 101737545 single base substitution C T intron_variant LINC-JP 10 101755085 101755085 single base substitution C A intron_variant LINC-JP 10 101772826 101772826 single base substitution C G upstream_gene_variant LINC-JP 10 101773682 101773682 single base substitution G A upstream_gene_variant LIRI-JP 10 101630964 101630964 single base substitution C A downstream_gene_variant LIRI-JP 10 101635571 101635571 single base substitution T C 3_prime_UTR_variant LIRI-JP 10 101635571 101635571 single base substitution T C downstream_gene_variant LIRI-JP 10 101636777 101636777 single base substitution T A 3_prime_UTR_variant LIRI-JP 10 101639324 101639324 single base substitution A T intron_variant LIRI-JP 10 101640377 101640377 single base substitution T C intron_variant LIRI-JP 10 101650405 101650405 single base substitution T C intron_variant LIRI-JP 10 101650405 101650405 single base substitution T C upstream_gene_variant LIRI-JP 10 101653015 101653015 single base substitution C T downstream_gene_variant LIRI-JP 10 101653015 101653015 single base substitution C T intron_variant LIRI-JP 10 101653015 101653015 single base substitution C T upstream_gene_variant LIRI-JP 10 101655041 101655041 single base substitution G A downstream_gene_variant LIRI-JP 10 101655041 101655041 single base substitution G A intron_variant LIRI-JP 10 101656746 101656746 single base substitution G A downstream_gene_variant LIRI-JP 10 101656746 101656746 single base substitution G A intron_variant LIRI-JP 10 101657780 101657780 single base substitution G T downstream_gene_variant LIRI-JP 10 101657780 101657780 single base substitution G T intron_variant LIRI-JP 10 101660957 101660957 single base substitution T C intron_variant LIRI-JP 10 101660957 101660957 single base substitution T C upstream_gene_variant LIRI-JP 10 101660991 101660991 single base substitution T C intron_variant LIRI-JP 10 101660991 101660991 single base substitution T C upstream_gene_variant LIRI-JP 10 101663374 101663374 single base substitution C T intron_variant LIRI-JP 10 101663570 101663570 single base substitution A C intron_variant LIRI-JP 10 101665097 101665097 single base substitution C T intron_variant LIRI-JP 10 101669708 101669708 single base substitution T C intron_variant LIRI-JP 10 101671447 101671447 single base substitution T G intron_variant LIRI-JP 10 101671508 101671508 single base substitution G A intron_variant LIRI-JP 10 101671995 101671995 single base substitution G C intron_variant LIRI-JP 10 101675859 101675859 single base substitution T C intron_variant LIRI-JP 10 101675859 101675859 single base substitution T C upstream_gene_variant LIRI-JP 10 101676488 101676488 single base substitution A G intron_variant LIRI-JP 10 101676488 101676488 single base substitution A G upstream_gene_variant LIRI-JP 10 101676580 101676580 single base substitution A G intron_variant LIRI-JP 10 101676580 101676580 single base substitution A G upstream_gene_variant LIRI-JP 10 101677897 101677897 single base substitution C A intron_variant LIRI-JP 10 101677897 101677897 single base substitution C A upstream_gene_variant LIRI-JP 10 101679194 101679194 single base substitution C A intron_variant LIRI-JP 10 101679785 101679785 single base substitution T G intron_variant LIRI-JP 10 101681411 101681411 single base substitution G C intron_variant LIRI-JP 10 101683593 101683593 single base substitution G C intron_variant LIRI-JP 10 101684643 101684644 deletion of <=200bp AG - intron_variant LIRI-JP 10 101686096 101686096 single base substitution T C intron_variant LIRI-JP 10 101686324 101686324 single base substitution G C intron_variant LIRI-JP 10 101686836 101686836 single base substitution A G intron_variant LIRI-JP 10 101688303 101688303 single base substitution A G intron_variant LIRI-JP 10 101689469 101689469 single base substitution T G 5_prime_UTR_variant LIRI-JP 10 101689469 101689469 single base substitution T G intron_variant LIRI-JP 10 101689796 101689796 single base substitution T C 5_prime_UTR_variant LIRI-JP 10 101689796 101689796 single base substitution T C intron_variant LIRI-JP 10 101690035 101690035 single base substitution C A 5_prime_UTR_variant LIRI-JP 10 101690035 101690035 single base substitution C A intron_variant LIRI-JP 10 101690222 101690222 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 10 101690222 101690222 single base substitution T C intron_variant LIRI-JP 10 101693516 101693516 single base substitution C T intron_variant LIRI-JP 10 101693516 101693516 single base substitution C T upstream_gene_variant LIRI-JP 10 101698389 101698389 single base substitution C T intron_variant LIRI-JP 10 101698405 101698405 deletion of <=200bp T - intron_variant LIRI-JP 10 101704337 101704337 single base substitution G A intron_variant LIRI-JP 10 101704998 101704998 single base substitution G C intron_variant LIRI-JP 10 101707233 101707233 single base substitution T C intron_variant LIRI-JP 10 101708382 101708382 single base substitution C A intron_variant LIRI-JP 10 101710496 101710496 single base substitution G C intron_variant LIRI-JP 10 101713252 101713252 single base substitution T C intron_variant LIRI-JP 10 101722351 101722351 single base substitution G A intron_variant LIRI-JP 10 101724254 101724254 deletion of <=200bp G - intron_variant LIRI-JP 10 101726397 101726397 single base substitution T A intron_variant LIRI-JP 10 101729963 101729963 single base substitution T C intron_variant LIRI-JP 10 101730885 101730885 single base substitution G A intron_variant LIRI-JP 10 101733086 101733086 single base substitution T G intron_variant LIRI-JP 10 101734560 101734560 single base substitution C T intron_variant LIRI-JP 10 101735109 101735109 single base substitution T C intron_variant LIRI-JP 10 101735278 101735278 single base substitution T C intron_variant LIRI-JP 10 101735985 101735985 single base substitution T C intron_variant LIRI-JP 10 101736923 101736923 single base substitution C T intron_variant LIRI-JP 10 101737760 101737760 single base substitution C A intron_variant LIRI-JP 10 101740352 101740352 single base substitution C T intron_variant LIRI-JP 10 101741070 101741070 single base substitution C A intron_variant LIRI-JP 10 101742821 101742821 single base substitution C T intron_variant LIRI-JP 10 101744995 101744995 single base substitution T C intron_variant LIRI-JP 10 101745912 101745912 single base substitution A C intron_variant LIRI-JP 10 101746552 101746552 single base substitution T G intron_variant LIRI-JP 10 101747262 101747262 single base substitution A C intron_variant LIRI-JP 10 101747967 101747967 single base substitution A C intron_variant LIRI-JP 10 101748317 101748317 single base substitution G A intron_variant LIRI-JP 10 101748422 101748422 single base substitution T C intron_variant LIRI-JP 10 101749224 101749224 single base substitution T G intron_variant LIRI-JP 10 101754668 101754668 single base substitution T C intron_variant LIRI-JP 10 101755172 101755172 single base substitution G A intron_variant LIRI-JP 10 101755858 101755858 single base substitution C A intron_variant LIRI-JP 10 101758035 101758035 single base substitution C A intron_variant LIRI-JP 10 101765474 101765474 single base substitution G A intron_variant LIRI-JP 10 101767071 101767071 single base substitution C T intron_variant LIRI-JP 10 101767738 101767738 single base substitution T C intron_variant LUSC-KR 10 101630743 101630743 single base substitution T A downstream_gene_variant LUSC-KR 10 101639579 101639579 single base substitution C G missense_variant E1513Q 4537G>C LUSC-KR 10 101639579 101639579 single base substitution C G missense_variant E1537Q 4609G>C LUSC-KR 10 101639579 101639579 single base substitution C G missense_variant E449Q 1345G>C LUSC-KR 10 101639579 101639579 single base substitution C G missense_variant E759Q 2275G>C LUSC-KR 10 101640767 101640767 single base substitution G C intron_variant LUSC-KR 10 101645309 101645309 single base substitution T G downstream_gene_variant LUSC-KR 10 101645309 101645309 single base substitution T G intron_variant LUSC-KR 10 101646368 101646368 single base substitution C A exon_variant LUSC-KR 10 101646368 101646368 single base substitution C A missense_variant V1103F 3307G>T LUSC-KR 10 101646368 101646368 single base substitution C A missense_variant V1127F 3379G>T LUSC-KR 10 101646368 101646368 single base substitution C A missense_variant V349F 1045G>T LUSC-KR 10 101646368 101646368 single base substitution C A missense_variant V39F 115G>T LUSC-KR 10 101648346 101648346 single base substitution T C intron_variant LUSC-KR 10 101655450 101655450 single base substitution C T downstream_gene_variant LUSC-KR 10 101655450 101655450 single base substitution C T intron_variant LUSC-KR 10 101659365 101659365 single base substitution C G intron_variant LUSC-KR 10 101659365 101659365 single base substitution C G upstream_gene_variant LUSC-KR 10 101665138 101665138 single base substitution C T intron_variant LUSC-KR 10 101666248 101666248 single base substitution G A intron_variant LUSC-KR 10 101670946 101670946 single base substitution T G intron_variant LUSC-KR 10 101671507 101671507 single base substitution C T intron_variant LUSC-KR 10 101673161 101673161 single base substitution C A intron_variant LUSC-KR 10 101679476 101679476 single base substitution G A intron_variant LUSC-KR 10 101679686 101679686 single base substitution G C intron_variant LUSC-KR 10 101685447 101685447 single base substitution C G intron_variant LUSC-KR 10 101688988 101688988 single base substitution C A intron_variant LUSC-KR 10 101698635 101698635 single base substitution C T intron_variant LUSC-KR 10 101705711 101705711 single base substitution C T intron_variant LUSC-KR 10 101711784 101711784 single base substitution T C intron_variant LUSC-KR 10 101715334 101715334 single base substitution G A missense_variant P633S 1897C>T LUSC-KR 10 101718918 101718918 single base substitution T C intron_variant LUSC-KR 10 101719272 101719272 single base substitution C A intron_variant LUSC-KR 10 101724025 101724025 single base substitution C A intron_variant LUSC-KR 10 101731103 101731103 single base substitution C A intron_variant LUSC-KR 10 101736676 101736676 single base substitution C T intron_variant LUSC-KR 10 101737206 101737206 single base substitution G A intron_variant LUSC-KR 10 101743462 101743462 single base substitution G C intron_variant LUSC-KR 10 101743471 101743471 single base substitution G A intron_variant LUSC-KR 10 101743479 101743479 single base substitution G T intron_variant LUSC-KR 10 101745308 101745308 single base substitution G C intron_variant LUSC-KR 10 101752299 101752299 single base substitution T A intron_variant LUSC-KR 10 101757502 101757502 single base substitution G A intron_variant LUSC-KR 10 101758610 101758610 single base substitution G A intron_variant LUSC-KR 10 101760535 101760535 single base substitution G C intron_variant LUSC-KR 10 101761979 101761979 single base substitution C A intron_variant LUSC-KR 10 101765127 101765127 single base substitution C A intron_variant LUSC-KR 10 101766150 101766150 single base substitution G C intron_variant LUSC-KR 10 101767879 101767879 single base substitution A G intron_variant LUSC-US 10 101636941 101636941 single base substitution G A synonymous_variant P1567P 4701C>T LUSC-US 10 101636941 101636941 single base substitution G A synonymous_variant P1591P 4773C>T LUSC-US 10 101636941 101636941 single base substitution G A synonymous_variant P503P 1509C>T LUSC-US 10 101636941 101636941 single base substitution G A synonymous_variant P813P 2439C>T LUSC-US 10 101643884 101643884 single base substitution C T downstream_gene_variant LUSC-US 10 101643884 101643884 single base substitution C T missense_variant R1294Q 3881G>A LUSC-US 10 101643884 101643884 single base substitution C T missense_variant R1318Q 3953G>A LUSC-US 10 101643884 101643884 single base substitution C T missense_variant R230Q 689G>A LUSC-US 10 101643884 101643884 single base substitution C T missense_variant R540Q 1619G>A LUSC-US 10 101656026 101656026 single base substitution G A downstream_gene_variant LUSC-US 10 101656026 101656026 single base substitution G A intron_variant LUSC-US 10 101656026 101656026 single base substitution G A stop_gained Q1017* 3049C>T LUSC-US 10 101656026 101656026 single base substitution G A stop_gained Q1041* 3121C>T LUSC-US 10 101656026 101656026 single base substitution G A stop_gained Q263* 787C>T LUSC-US 10 101656145 101656145 single base substitution T C downstream_gene_variant LUSC-US 10 101656145 101656145 single base substitution T C intron_variant LUSC-US 10 101656145 101656145 single base substitution T C missense_variant Y1001C 3002A>G LUSC-US 10 101656145 101656145 single base substitution T C missense_variant Y223C 668A>G LUSC-US 10 101656145 101656145 single base substitution T C missense_variant Y977C 2930A>G LUSC-US 10 101668899 101668899 single base substitution C T missense_variant M43I 129G>A LUSC-US 10 101668899 101668899 single base substitution C T missense_variant M755I 2265G>A LUSC-US 10 101668899 101668899 single base substitution C T start_lost M1I 3G>A LUSC-US 10 101715112 101715112 single base substitution T G missense_variant M707L 2119A>C LUSC-US 10 101715737 101715737 single base substitution C A missense_variant Q498H 1494G>T LUSC-US 10 101716838 101716838 single base substitution C A synonymous_variant R131R 393G>T MALY-DE 10 101631801 101631801 single base substitution G A downstream_gene_variant MALY-DE 10 101650158 101650158 single base substitution G A intron_variant MALY-DE 10 101650158 101650158 single base substitution G A upstream_gene_variant MALY-DE 10 101664133 101664133 single base substitution G A intron_variant MALY-DE 10 101692662 101692662 single base substitution G A intron_variant MALY-DE 10 101692662 101692662 single base substitution G A upstream_gene_variant MALY-DE 10 101703623 101703623 single base substitution C T intron_variant MALY-DE 10 101704657 101704657 deletion of <=200bp A - intron_variant MALY-DE 10 101705053 101705053 single base substitution A C intron_variant MALY-DE 10 101708295 101708295 single base substitution A G intron_variant MALY-DE 10 101725357 101725357 single base substitution C T intron_variant MALY-DE 10 101726541 101726541 single base substitution T C intron_variant MALY-DE 10 101727291 101727294 deletion of <=200bp AAAT - intron_variant MALY-DE 10 101754685 101754685 single base substitution T C intron_variant MALY-DE 10 101768590 101768590 single base substitution C G intron_variant MALY-DE 10 101769277 101769277 single base substitution G A intron_variant MALY-DE 10 101771993 101771993 single base substitution T G upstream_gene_variant MELA-AU 10 101630522 101630522 single base substitution C T downstream_gene_variant MELA-AU 10 101630876 101630876 single base substitution C T downstream_gene_variant MELA-AU 10 101630955 101630955 single base substitution C T downstream_gene_variant MELA-AU 10 101631248 101631248 single base substitution G A downstream_gene_variant MELA-AU 10 101632003 101632003 single base substitution G A downstream_gene_variant MELA-AU 10 101632515 101632515 single base substitution C T downstream_gene_variant MELA-AU 10 101632903 101632904 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 10 101632976 101632976 single base substitution G A downstream_gene_variant MELA-AU 10 101632987 101632987 single base substitution G A downstream_gene_variant MELA-AU 10 101633595 101633595 single base substitution G A downstream_gene_variant MELA-AU 10 101633729 101633729 single base substitution G A downstream_gene_variant MELA-AU 10 101634117 101634117 single base substitution G A downstream_gene_variant MELA-AU 10 101634669 101634669 single base substitution C T downstream_gene_variant MELA-AU 10 101634940 101634940 single base substitution A T downstream_gene_variant MELA-AU 10 101635362 101635362 single base substitution G A 3_prime_UTR_variant MELA-AU 10 101635362 101635362 single base substitution G A downstream_gene_variant MELA-AU 10 101635954 101635954 single base substitution C T 3_prime_UTR_variant MELA-AU 10 101635954 101635954 single base substitution C T downstream_gene_variant MELA-AU 10 101636191 101636191 single base substitution G A 3_prime_UTR_variant MELA-AU 10 101636191 101636191 single base substitution G A downstream_gene_variant MELA-AU 10 101636523 101636523 single base substitution G A 3_prime_UTR_variant MELA-AU 10 101636523 101636523 single base substitution G A downstream_gene_variant MELA-AU 10 101636564 101636564 single base substitution C T 3_prime_UTR_variant MELA-AU 10 101637022 101637022 single base substitution G A synonymous_variant L1540L 4620C>T MELA-AU 10 101637022 101637022 single base substitution G A synonymous_variant L1564L 4692C>T MELA-AU 10 101637022 101637022 single base substitution G A synonymous_variant L476L 1428C>T MELA-AU 10 101637022 101637022 single base substitution G A synonymous_variant L786L 2358C>T MELA-AU 10 101638073 101638073 single base substitution C T intron_variant MELA-AU 10 101638260 101638260 single base substitution G A intron_variant MELA-AU 10 101638338 101638338 single base substitution G A intron_variant MELA-AU 10 101638692 101638692 single base substitution A T intron_variant MELA-AU 10 101638904 101638904 single base substitution G A intron_variant MELA-AU 10 101639049 101639049 single base substitution T G intron_variant MELA-AU 10 101639434 101639435 multiple base substitution (>=2bp and <=200bp) TG CA intron_variant MELA-AU 10 101639846 101639846 single base substitution G A missense_variant P1424S 4270C>T MELA-AU 10 101639846 101639846 single base substitution G A missense_variant P1448S 4342C>T MELA-AU 10 101639846 101639846 single base substitution G A missense_variant P360S 1078C>T MELA-AU 10 101639846 101639846 single base substitution G A missense_variant P670S 2008C>T MELA-AU 10 101639938 101639938 single base substitution G A missense_variant S1393F 4178C>T MELA-AU 10 101639938 101639938 single base substitution G A missense_variant S1417F 4250C>T MELA-AU 10 101639938 101639938 single base substitution G A missense_variant S329F 986C>T MELA-AU 10 101639938 101639938 single base substitution G A missense_variant S639F 1916C>T MELA-AU 10 101640416 101640416 single base substitution G A intron_variant MELA-AU 10 101640667 101640667 single base substitution G A intron_variant MELA-AU 10 101641392 101641392 single base substitution T A downstream_gene_variant MELA-AU 10 101641392 101641392 single base substitution T A intron_variant MELA-AU 10 101641860 101641860 single base substitution G A downstream_gene_variant MELA-AU 10 101641860 101641860 single base substitution G A intron_variant MELA-AU 10 101642427 101642427 single base substitution A G downstream_gene_variant MELA-AU 10 101642427 101642427 single base substitution A G intron_variant MELA-AU 10 101642936 101642936 single base substitution G A downstream_gene_variant MELA-AU 10 101642936 101642936 single base substitution G A intron_variant MELA-AU 10 101642997 101642997 single base substitution C A downstream_gene_variant MELA-AU 10 101642997 101642997 single base substitution C A intron_variant MELA-AU 10 101643316 101643316 single base substitution G A downstream_gene_variant MELA-AU 10 101643316 101643316 single base substitution G A intron_variant MELA-AU 10 101643342 101643343 multiple base substitution (>=2bp and <=200bp) AA GC downstream_gene_variant MELA-AU 10 101643342 101643343 multiple base substitution (>=2bp and <=200bp) AA GC intron_variant MELA-AU 10 101643494 101643494 single base substitution G A downstream_gene_variant MELA-AU 10 101643494 101643494 single base substitution G A intron_variant MELA-AU 10 101643928 101643928 single base substitution G A downstream_gene_variant MELA-AU 10 101643928 101643928 single base substitution G A synonymous_variant S1279S 3837C>T MELA-AU 10 101643928 101643928 single base substitution G A synonymous_variant S1303S 3909C>T MELA-AU 10 101643928 101643928 single base substitution G A synonymous_variant S215S 645C>T MELA-AU 10 101643928 101643928 single base substitution G A synonymous_variant S525S 1575C>T MELA-AU 10 101644834 101644834 single base substitution G A downstream_gene_variant MELA-AU 10 101644834 101644834 single base substitution G A intron_variant MELA-AU 10 101646359 101646359 single base substitution G A exon_variant MELA-AU 10 101646359 101646359 single base substitution G A missense_variant P1106S 3316C>T MELA-AU 10 101646359 101646359 single base substitution G A missense_variant P1130S 3388C>T MELA-AU 10 101646359 101646359 single base substitution G A missense_variant P352S 1054C>T MELA-AU 10 101646359 101646359 single base substitution G A missense_variant P42S 124C>T MELA-AU 10 101646400 101646400 single base substitution G A intron_variant MELA-AU 10 101647290 101647290 single base substitution A T intron_variant MELA-AU 10 101647391 101647391 single base substitution T A intron_variant MELA-AU 10 101647631 101647631 single base substitution G A intron_variant MELA-AU 10 101649493 101649493 single base substitution C A intron_variant MELA-AU 10 101649493 101649493 single base substitution C A upstream_gene_variant MELA-AU 10 101650031 101650031 single base substitution G A intron_variant MELA-AU 10 101650031 101650031 single base substitution G A upstream_gene_variant MELA-AU 10 101650325 101650325 single base substitution G A intron_variant MELA-AU 10 101650325 101650325 single base substitution G A upstream_gene_variant MELA-AU 10 101650383 101650383 single base substitution C G intron_variant MELA-AU 10 101650383 101650383 single base substitution C G upstream_gene_variant MELA-AU 10 101651849 101651850 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 101651849 101651850 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 101653205 101653205 single base substitution G A downstream_gene_variant MELA-AU 10 101653205 101653205 single base substitution G A intron_variant MELA-AU 10 101653205 101653205 single base substitution G A upstream_gene_variant MELA-AU 10 101653485 101653485 single base substitution G A downstream_gene_variant MELA-AU 10 101653485 101653485 single base substitution G A intron_variant MELA-AU 10 101653485 101653485 single base substitution G A upstream_gene_variant MELA-AU 10 101653486 101653486 single base substitution A C downstream_gene_variant MELA-AU 10 101653486 101653486 single base substitution A C intron_variant MELA-AU 10 101653486 101653486 single base substitution A C upstream_gene_variant MELA-AU 10 101653561 101653561 single base substitution T C downstream_gene_variant MELA-AU 10 101653561 101653561 single base substitution T C intron_variant MELA-AU 10 101653561 101653561 single base substitution T C upstream_gene_variant MELA-AU 10 101653641 101653641 single base substitution G A downstream_gene_variant MELA-AU 10 101653641 101653641 single base substitution G A intron_variant MELA-AU 10 101653641 101653641 single base substitution G A upstream_gene_variant MELA-AU 10 101653732 101653732 single base substitution T A downstream_gene_variant MELA-AU 10 101653732 101653732 single base substitution T A intron_variant MELA-AU 10 101653732 101653732 single base substitution T A upstream_gene_variant MELA-AU 10 101655090 101655090 single base substitution G A downstream_gene_variant MELA-AU 10 101655090 101655090 single base substitution G A intron_variant MELA-AU 10 101655907 101655907 single base substitution T C downstream_gene_variant MELA-AU 10 101655907 101655907 single base substitution T C intron_variant MELA-AU 10 101656106 101656106 single base substitution G A downstream_gene_variant MELA-AU 10 101656106 101656106 single base substitution G A intron_variant MELA-AU 10 101656106 101656106 single base substitution G A missense_variant S1014F 3041C>T MELA-AU 10 101656106 101656106 single base substitution G A missense_variant S236F 707C>T MELA-AU 10 101656106 101656106 single base substitution G A missense_variant S990F 2969C>T MELA-AU 10 101656872 101656872 single base substitution G A downstream_gene_variant MELA-AU 10 101656872 101656872 single base substitution G A intron_variant MELA-AU 10 101657263 101657263 single base substitution A G downstream_gene_variant MELA-AU 10 101657263 101657263 single base substitution A G intron_variant MELA-AU 10 101657301 101657301 single base substitution T C downstream_gene_variant MELA-AU 10 101657301 101657301 single base substitution T C intron_variant MELA-AU 10 101658313 101658313 single base substitution G A intron_variant MELA-AU 10 101658313 101658313 single base substitution G A upstream_gene_variant MELA-AU 10 101659042 101659042 deletion of <=200bp A - intron_variant MELA-AU 10 101659042 101659042 deletion of <=200bp A - upstream_gene_variant MELA-AU 10 101660066 101660066 single base substitution G T intron_variant MELA-AU 10 101660066 101660066 single base substitution G T upstream_gene_variant MELA-AU 10 101660219 101660219 single base substitution C T intron_variant MELA-AU 10 101660219 101660219 single base substitution C T upstream_gene_variant MELA-AU 10 101660226 101660226 single base substitution T C intron_variant MELA-AU 10 101660226 101660226 single base substitution T C upstream_gene_variant MELA-AU 10 101661133 101661133 single base substitution G A intron_variant MELA-AU 10 101661133 101661133 single base substitution G A upstream_gene_variant MELA-AU 10 101661326 101661326 single base substitution C T intron_variant MELA-AU 10 101661326 101661326 single base substitution C T upstream_gene_variant MELA-AU 10 101663091 101663091 single base substitution T G intron_variant MELA-AU 10 101663666 101663666 single base substitution G A intron_variant MELA-AU 10 101663913 101663913 single base substitution G A intron_variant MELA-AU 10 101663989 101663989 single base substitution G A intron_variant MELA-AU 10 101664563 101664563 single base substitution G A intron_variant MELA-AU 10 101665875 101665876 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 101666594 101666594 single base substitution G A intron_variant MELA-AU 10 101667064 101667064 single base substitution G A intron_variant MELA-AU 10 101667287 101667287 single base substitution G A intron_variant MELA-AU 10 101667591 101667591 single base substitution G A intron_variant MELA-AU 10 101667710 101667710 single base substitution T C intron_variant MELA-AU 10 101669140 101669140 single base substitution A C intron_variant MELA-AU 10 101669456 101669456 single base substitution G A intron_variant MELA-AU 10 101669931 101669931 single base substitution C T intron_variant MELA-AU 10 101670017 101670017 single base substitution G A intron_variant MELA-AU 10 101670632 101670632 single base substitution G A intron_variant MELA-AU 10 101670967 101670967 single base substitution C A intron_variant MELA-AU 10 101671859 101671859 single base substitution A G intron_variant MELA-AU 10 101672103 101672104 deletion of <=200bp AG - intron_variant MELA-AU 10 101673290 101673290 single base substitution C T intron_variant MELA-AU 10 101673548 101673548 single base substitution A T intron_variant MELA-AU 10 101673703 101673703 single base substitution G A intron_variant MELA-AU 10 101674149 101674149 single base substitution G A intron_variant MELA-AU 10 101674149 101674149 single base substitution G A upstream_gene_variant MELA-AU 10 101674780 101674780 single base substitution G A intron_variant MELA-AU 10 101674780 101674780 single base substitution G A upstream_gene_variant MELA-AU 10 101675047 101675047 single base substitution G A intron_variant MELA-AU 10 101675047 101675047 single base substitution G A upstream_gene_variant MELA-AU 10 101675087 101675087 single base substitution T A intron_variant MELA-AU 10 101675087 101675087 single base substitution T A upstream_gene_variant MELA-AU 10 101675648 101675648 single base substitution T C intron_variant MELA-AU 10 101675648 101675648 single base substitution T C upstream_gene_variant MELA-AU 10 101675751 101675751 single base substitution G A intron_variant MELA-AU 10 101675751 101675751 single base substitution G A upstream_gene_variant MELA-AU 10 101676115 101676115 single base substitution G A intron_variant MELA-AU 10 101676115 101676115 single base substitution G A upstream_gene_variant MELA-AU 10 101676145 101676145 single base substitution G A intron_variant MELA-AU 10 101676145 101676145 single base substitution G A upstream_gene_variant MELA-AU 10 101676390 101676390 single base substitution A C intron_variant MELA-AU 10 101676390 101676390 single base substitution A C upstream_gene_variant MELA-AU 10 101676877 101676877 single base substitution G A intron_variant MELA-AU 10 101676877 101676877 single base substitution G A upstream_gene_variant MELA-AU 10 101678706 101678706 single base substitution G A intron_variant MELA-AU 10 101678706 101678706 single base substitution G A upstream_gene_variant MELA-AU 10 101678955 101678955 single base substitution C A intron_variant MELA-AU 10 101679479 101679479 single base substitution G A intron_variant MELA-AU 10 101679510 101679510 single base substitution C A intron_variant MELA-AU 10 101680022 101680022 single base substitution G A intron_variant MELA-AU 10 101680089 101680089 single base substitution C T intron_variant MELA-AU 10 101680131 101680131 single base substitution C T intron_variant MELA-AU 10 101680138 101680138 single base substitution T A intron_variant MELA-AU 10 101680476 101680476 single base substitution G A intron_variant MELA-AU 10 101680674 101680674 single base substitution G A intron_variant MELA-AU 10 101680905 101680905 single base substitution G A intron_variant MELA-AU 10 101681202 101681202 single base substitution G A intron_variant MELA-AU 10 101682908 101682908 single base substitution G A intron_variant MELA-AU 10 101682923 101682923 single base substitution G A intron_variant MELA-AU 10 101683778 101683778 single base substitution G A intron_variant MELA-AU 10 101684033 101684033 single base substitution A T intron_variant MELA-AU 10 101685659 101685659 single base substitution G A intron_variant MELA-AU 10 101686430 101686430 single base substitution G A intron_variant MELA-AU 10 101687007 101687007 single base substitution G A intron_variant MELA-AU 10 101687283 101687283 single base substitution G A intron_variant MELA-AU 10 101688029 101688029 single base substitution G A intron_variant MELA-AU 10 101688206 101688206 single base substitution G A intron_variant MELA-AU 10 101688266 101688266 single base substitution G A intron_variant MELA-AU 10 101688297 101688297 single base substitution T A intron_variant MELA-AU 10 101688968 101688968 single base substitution C A intron_variant MELA-AU 10 101689662 101689662 single base substitution A G 5_prime_UTR_variant MELA-AU 10 101689662 101689662 single base substitution A G intron_variant MELA-AU 10 101689899 101689899 single base substitution G A 5_prime_UTR_variant MELA-AU 10 101689899 101689899 single base substitution G A intron_variant MELA-AU 10 101690415 101690415 single base substitution G A 5_prime_UTR_variant MELA-AU 10 101690415 101690415 single base substitution G A intron_variant MELA-AU 10 101691549 101691549 single base substitution G A intron_variant MELA-AU 10 101691549 101691549 single base substitution G A upstream_gene_variant MELA-AU 10 101691712 101691712 single base substitution G A intron_variant MELA-AU 10 101691712 101691712 single base substitution G A upstream_gene_variant MELA-AU 10 101691746 101691746 single base substitution G A intron_variant MELA-AU 10 101691746 101691746 single base substitution G A upstream_gene_variant MELA-AU 10 101691983 101691983 single base substitution G A intron_variant MELA-AU 10 101691983 101691983 single base substitution G A upstream_gene_variant MELA-AU 10 101692692 101692692 single base substitution G A intron_variant MELA-AU 10 101692692 101692692 single base substitution G A upstream_gene_variant MELA-AU 10 101694041 101694041 single base substitution G A intron_variant MELA-AU 10 101694041 101694041 single base substitution G A upstream_gene_variant MELA-AU 10 101695190 101695190 single base substitution T C intron_variant MELA-AU 10 101695190 101695190 single base substitution T C upstream_gene_variant MELA-AU 10 101695402 101695402 single base substitution A G intron_variant MELA-AU 10 101695402 101695402 single base substitution A G upstream_gene_variant MELA-AU 10 101695575 101695575 single base substitution G A intron_variant MELA-AU 10 101695575 101695575 single base substitution G A upstream_gene_variant MELA-AU 10 101695855 101695855 single base substitution G A intron_variant MELA-AU 10 101697096 101697096 single base substitution G A intron_variant MELA-AU 10 101697146 101697146 single base substitution G A intron_variant MELA-AU 10 101697183 101697183 single base substitution G A intron_variant MELA-AU 10 101698765 101698765 single base substitution G A intron_variant MELA-AU 10 101698856 101698856 single base substitution G A intron_variant MELA-AU 10 101701025 101701025 single base substitution C T intron_variant MELA-AU 10 101701493 101701493 single base substitution G A intron_variant MELA-AU 10 101702757 101702757 single base substitution G A intron_variant MELA-AU 10 101702800 101702800 single base substitution G A intron_variant MELA-AU 10 101703134 101703134 single base substitution G T intron_variant MELA-AU 10 101704397 101704397 single base substitution G A intron_variant MELA-AU 10 101705123 101705123 single base substitution G T intron_variant MELA-AU 10 101705574 101705574 single base substitution A C intron_variant MELA-AU 10 101707940 101707940 single base substitution G A intron_variant MELA-AU 10 101708542 101708542 deletion of <=200bp A - intron_variant MELA-AU 10 101708723 101708723 insertion of <=200bp - AAAT intron_variant MELA-AU 10 101708723 101708726 deletion of <=200bp AAAT - intron_variant MELA-AU 10 101708740 101708740 single base substitution A C intron_variant MELA-AU 10 101708741 101708741 insertion of <=200bp - ATAC intron_variant MELA-AU 10 101708744 101708744 single base substitution A C intron_variant MELA-AU 10 101709225 101709225 single base substitution A C intron_variant MELA-AU 10 101709417 101709417 single base substitution G A intron_variant MELA-AU 10 101709555 101709555 single base substitution A T intron_variant MELA-AU 10 101709617 101709622 deletion of <=200bp AAAAAT - intron_variant MELA-AU 10 101710461 101710461 single base substitution G A intron_variant MELA-AU 10 101710575 101710575 single base substitution A G intron_variant MELA-AU 10 101711079 101711079 single base substitution G A intron_variant MELA-AU 10 101711269 101711269 single base substitution G A intron_variant MELA-AU 10 101711274 101711274 single base substitution G A intron_variant MELA-AU 10 101711368 101711368 single base substitution G A intron_variant MELA-AU 10 101711395 101711395 single base substitution G A intron_variant MELA-AU 10 101711618 101711618 single base substitution G A intron_variant MELA-AU 10 101712801 101712801 single base substitution G A intron_variant MELA-AU 10 101713059 101713059 single base substitution T C intron_variant MELA-AU 10 101713577 101713577 insertion of <=200bp - AAAAAAAGAAAAAG intron_variant MELA-AU 10 101713684 101713684 single base substitution T C intron_variant MELA-AU 10 101715155 101715156 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P692L 2075CC>TT MELA-AU 10 101715399 101715400 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P611L 1831CC>TT MELA-AU 10 101715849 101715849 single base substitution G A missense_variant P461L 1382C>T MELA-AU 10 101715888 101715888 single base substitution G A missense_variant P448L 1343C>T MELA-AU 10 101716270 101716270 single base substitution G A missense_variant P321S 961C>T MELA-AU 10 101716420 101716420 single base substitution G A stop_gained R271* 811C>T MELA-AU 10 101716421 101716421 single base substitution G A synonymous_variant I270I 810C>T MELA-AU 10 101716810 101716810 single base substitution G A stop_gained Q141* 421C>T MELA-AU 10 101717499 101717499 single base substitution G A intron_variant MELA-AU 10 101718366 101718366 single base substitution A T intron_variant MELA-AU 10 101718469 101718469 single base substitution G A intron_variant MELA-AU 10 101718624 101718624 single base substitution G C intron_variant MELA-AU 10 101718662 101718663 multiple base substitution (>=2bp and <=200bp) AT TA intron_variant MELA-AU 10 101718767 101718767 single base substitution A G intron_variant MELA-AU 10 101719421 101719421 single base substitution G A intron_variant MELA-AU 10 101720180 101720180 single base substitution T C intron_variant MELA-AU 10 101721476 101721476 single base substitution G A intron_variant MELA-AU 10 101724267 101724267 single base substitution G A intron_variant MELA-AU 10 101724276 101724276 single base substitution G A intron_variant MELA-AU 10 101724743 101724743 single base substitution A C intron_variant MELA-AU 10 101725364 101725364 single base substitution C T intron_variant MELA-AU 10 101725506 101725506 single base substitution G A intron_variant MELA-AU 10 101726030 101726031 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 101726031 101726031 single base substitution G A intron_variant MELA-AU 10 101726060 101726060 single base substitution C G intron_variant MELA-AU 10 101727029 101727029 single base substitution A C intron_variant MELA-AU 10 101729110 101729110 single base substitution G A intron_variant MELA-AU 10 101729425 101729425 single base substitution G A intron_variant MELA-AU 10 101730220 101730220 single base substitution G A intron_variant MELA-AU 10 101730304 101730304 single base substitution A T intron_variant MELA-AU 10 101730356 101730356 single base substitution G A intron_variant MELA-AU 10 101730711 101730711 single base substitution A C intron_variant MELA-AU 10 101731469 101731469 single base substitution G A intron_variant MELA-AU 10 101731499 101731499 single base substitution G A intron_variant MELA-AU 10 101732887 101732887 single base substitution C T intron_variant MELA-AU 10 101733442 101733442 single base substitution G A intron_variant MELA-AU 10 101733750 101733750 single base substitution G A intron_variant MELA-AU 10 101733761 101733761 single base substitution G A intron_variant MELA-AU 10 101733889 101733889 single base substitution A T intron_variant MELA-AU 10 101734892 101734892 single base substitution G A intron_variant MELA-AU 10 101735640 101735640 single base substitution A G intron_variant MELA-AU 10 101736858 101736858 single base substitution G A intron_variant MELA-AU 10 101737626 101737626 single base substitution C T intron_variant MELA-AU 10 101738423 101738423 single base substitution C T intron_variant MELA-AU 10 101738585 101738585 single base substitution G A intron_variant MELA-AU 10 101738802 101738802 single base substitution G A intron_variant MELA-AU 10 101739059 101739059 single base substitution G A intron_variant MELA-AU 10 101740962 101740962 single base substitution G A intron_variant MELA-AU 10 101741543 101741543 single base substitution G A intron_variant MELA-AU 10 101741741 101741741 single base substitution C T intron_variant MELA-AU 10 101742150 101742150 single base substitution T C intron_variant MELA-AU 10 101743135 101743135 single base substitution G C intron_variant MELA-AU 10 101743175 101743175 single base substitution G A intron_variant MELA-AU 10 101743305 101743305 single base substitution G A intron_variant MELA-AU 10 101745821 101745821 single base substitution G A intron_variant MELA-AU 10 101746035 101746035 single base substitution G A intron_variant MELA-AU 10 101746329 101746329 single base substitution G A intron_variant MELA-AU 10 101746682 101746682 single base substitution C T intron_variant MELA-AU 10 101747637 101747637 single base substitution G A intron_variant MELA-AU 10 101748181 101748181 single base substitution G A intron_variant MELA-AU 10 101749822 101749822 single base substitution G A intron_variant MELA-AU 10 101749862 101749862 single base substitution G C intron_variant MELA-AU 10 101750553 101750553 single base substitution C T intron_variant MELA-AU 10 101750557 101750557 single base substitution C T intron_variant MELA-AU 10 101750565 101750565 single base substitution C T intron_variant MELA-AU 10 101752318 101752318 single base substitution C T intron_variant MELA-AU 10 101753117 101753117 single base substitution T A intron_variant MELA-AU 10 101754209 101754209 single base substitution G A intron_variant MELA-AU 10 101754419 101754419 single base substitution G T intron_variant MELA-AU 10 101756038 101756038 single base substitution G A intron_variant MELA-AU 10 101756998 101756998 single base substitution G A intron_variant MELA-AU 10 101757034 101757034 single base substitution C T intron_variant MELA-AU 10 101757496 101757496 single base substitution G A intron_variant MELA-AU 10 101757672 101757672 single base substitution G A intron_variant MELA-AU 10 101758234 101758234 single base substitution G A intron_variant MELA-AU 10 101758426 101758426 single base substitution G A intron_variant MELA-AU 10 101758433 101758433 single base substitution G A intron_variant MELA-AU 10 101759039 101759039 single base substitution G A intron_variant MELA-AU 10 101759092 101759092 single base substitution G A intron_variant MELA-AU 10 101759833 101759833 single base substitution G A intron_variant MELA-AU 10 101759983 101759983 single base substitution G A intron_variant MELA-AU 10 101760710 101760711 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 101760713 101760713 single base substitution G A intron_variant MELA-AU 10 101760851 101760851 single base substitution G A intron_variant MELA-AU 10 101761533 101761533 single base substitution G A intron_variant MELA-AU 10 101761564 101761564 single base substitution G A intron_variant MELA-AU 10 101761946 101761946 single base substitution G A intron_variant MELA-AU 10 101762731 101762731 single base substitution C T intron_variant MELA-AU 10 101763397 101763397 single base substitution G A intron_variant MELA-AU 10 101764444 101764444 single base substitution G A intron_variant MELA-AU 10 101764447 101764447 single base substitution G A intron_variant MELA-AU 10 101764805 101764805 single base substitution G A intron_variant MELA-AU 10 101766563 101766563 single base substitution T C intron_variant MELA-AU 10 101767484 101767484 single base substitution G A intron_variant MELA-AU 10 101767663 101767663 single base substitution C T intron_variant MELA-AU 10 101767992 101767995 deletion of <=200bp AAAT - intron_variant MELA-AU 10 101768059 101768059 single base substitution A T intron_variant MELA-AU 10 101768170 101768170 single base substitution G A intron_variant MELA-AU 10 101770418 101770419 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 101770889 101770889 single base substitution T C upstream_gene_variant MELA-AU 10 101771099 101771099 single base substitution C T upstream_gene_variant MELA-AU 10 101771445 101771445 insertion of <=200bp - AAAT upstream_gene_variant MELA-AU 10 101771448 101771448 single base substitution A T upstream_gene_variant MELA-AU 10 101771634 101771634 single base substitution G A upstream_gene_variant MELA-AU 10 101771690 101771690 single base substitution A C upstream_gene_variant MELA-AU 10 101771804 101771805 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 101771925 101771925 single base substitution C T upstream_gene_variant MELA-AU 10 101772061 101772061 single base substitution G A upstream_gene_variant MELA-AU 10 101772142 101772142 single base substitution G A upstream_gene_variant MELA-AU 10 101772304 101772304 single base substitution C T upstream_gene_variant MELA-AU 10 101772366 101772366 single base substitution T A upstream_gene_variant MELA-AU 10 101772374 101772374 single base substitution T A upstream_gene_variant MELA-AU 10 101772930 101772930 single base substitution G A upstream_gene_variant MELA-AU 10 101773242 101773242 single base substitution G A upstream_gene_variant MELA-AU 10 101773265 101773265 single base substitution A C upstream_gene_variant MELA-AU 10 101773380 101773380 single base substitution C T upstream_gene_variant MELA-AU 10 101774520 101774520 single base substitution C T upstream_gene_variant ORCA-IN 10 101652659 101652659 single base substitution G A intron_variant ORCA-IN 10 101652659 101652659 single base substitution G A upstream_gene_variant ORCA-IN 10 101676184 101676184 single base substitution G A intron_variant ORCA-IN 10 101676184 101676184 single base substitution G A upstream_gene_variant ORCA-IN 10 101695137 101695137 deletion of <=200bp C - intron_variant ORCA-IN 10 101695137 101695137 deletion of <=200bp C - upstream_gene_variant ORCA-IN 10 101714242 101714242 single base substitution C T intron_variant ORCA-IN 10 101715747 101715747 single base substitution G C stop_gained S495* 1484C>G ORCA-IN 10 101716023 101716023 single base substitution G T missense_variant S403Y 1208C>A ORCA-IN 10 101720640 101720640 insertion of <=200bp - G intron_variant ORCA-IN 10 101731087 101731087 single base substitution T C intron_variant ORCA-IN 10 101731338 101731338 single base substitution G A intron_variant ORCA-IN 10 101734899 101734899 single base substitution C T intron_variant ORCA-IN 10 101741383 101741383 single base substitution C G intron_variant ORCA-IN 10 101765542 101765543 deletion of <=200bp CC - intron_variant ORCA-IN 10 101774053 101774053 single base substitution G A upstream_gene_variant OV-AU 10 101636468 101636468 single base substitution G A 3_prime_UTR_variant OV-AU 10 101636468 101636468 single base substitution G A downstream_gene_variant OV-AU 10 101637623 101637623 single base substitution G C intron_variant OV-AU 10 101640952 101640952 single base substitution T A intron_variant OV-AU 10 101647497 101647497 single base substitution A C intron_variant OV-AU 10 101647642 101647642 single base substitution C T intron_variant OV-AU 10 101649153 101649153 single base substitution G T exon_variant OV-AU 10 101649153 101649153 single base substitution G T intron_variant OV-AU 10 101649721 101649721 single base substitution C T intron_variant OV-AU 10 101649721 101649721 single base substitution C T upstream_gene_variant OV-AU 10 101651562 101651562 single base substitution G T intron_variant OV-AU 10 101651562 101651562 single base substitution G T upstream_gene_variant OV-AU 10 101673829 101673829 single base substitution G T intron_variant OV-AU 10 101673829 101673829 single base substitution G T missense_variant P2Q 5C>A OV-AU 10 101682467 101682467 single base substitution T G intron_variant OV-AU 10 101682748 101682748 single base substitution C T intron_variant OV-AU 10 101683714 101683714 single base substitution A G intron_variant OV-AU 10 101685358 101685358 single base substitution C G intron_variant OV-AU 10 101688192 101688192 single base substitution T G intron_variant OV-AU 10 101704031 101704031 single base substitution G A intron_variant OV-AU 10 101706430 101706430 single base substitution T G intron_variant OV-AU 10 101714883 101714883 single base substitution G T intron_variant OV-AU 10 101715492 101715492 single base substitution A G missense_variant M580T 1739T>C OV-AU 10 101718910 101718910 single base substitution A T intron_variant OV-AU 10 101723238 101723238 single base substitution A G intron_variant OV-AU 10 101729266 101729266 single base substitution G C intron_variant OV-AU 10 101729915 101729915 single base substitution G T intron_variant OV-AU 10 101734681 101734681 single base substitution C T intron_variant OV-AU 10 101735040 101735040 single base substitution C A intron_variant OV-AU 10 101746292 101746292 single base substitution G T intron_variant OV-AU 10 101767528 101767528 single base substitution T G intron_variant OV-AU 10 101769476 101769476 single base substitution C G intron_variant OV-AU 10 101772140 101772140 single base substitution A G upstream_gene_variant OV-AU 10 101772894 101772894 single base substitution A G upstream_gene_variant OV-AU 10 101773302 101773302 single base substitution G T upstream_gene_variant OV-AU 10 101774350 101774350 single base substitution T C upstream_gene_variant PACA-AU 10 101630999 101630999 single base substitution C A downstream_gene_variant PACA-AU 10 101638434 101638434 single base substitution T A intron_variant PACA-AU 10 101643323 101643323 single base substitution C T downstream_gene_variant PACA-AU 10 101643323 101643323 single base substitution C T intron_variant PACA-AU 10 101645231 101645231 single base substitution G A downstream_gene_variant PACA-AU 10 101645231 101645231 single base substitution G A intron_variant PACA-AU 10 101647975 101647975 single base substitution G T intron_variant PACA-AU 10 101659486 101659486 single base substitution A G intron_variant PACA-AU 10 101659486 101659486 single base substitution A G upstream_gene_variant PACA-AU 10 101661701 101661701 single base substitution C T intron_variant PACA-AU 10 101661701 101661701 single base substitution C T upstream_gene_variant PACA-AU 10 101665463 101665463 single base substitution C T intron_variant PACA-AU 10 101667069 101667069 single base substitution T C intron_variant PACA-AU 10 101670268 101670268 single base substitution C A intron_variant PACA-AU 10 101680431 101680431 single base substitution A C intron_variant PACA-AU 10 101686823 101686823 single base substitution A C intron_variant PACA-AU 10 101699229 101699229 single base substitution T A intron_variant PACA-AU 10 101703456 101703456 single base substitution C T intron_variant PACA-AU 10 101703531 101703531 single base substitution C T intron_variant PACA-AU 10 101703551 101703551 single base substitution A T intron_variant PACA-AU 10 101708494 101708494 single base substitution C T intron_variant PACA-AU 10 101716802 101716802 single base substitution C T synonymous_variant P143P 429G>A PACA-AU 10 101720275 101720275 single base substitution A C intron_variant PACA-AU 10 101722695 101722695 single base substitution C A intron_variant PACA-AU 10 101727033 101727033 single base substitution G A intron_variant PACA-AU 10 101729835 101729835 single base substitution C T intron_variant PACA-AU 10 101730514 101730514 single base substitution C T intron_variant PACA-AU 10 101732523 101732523 single base substitution G A intron_variant PACA-AU 10 101734127 101734127 single base substitution G C intron_variant PACA-AU 10 101738245 101738245 single base substitution T G intron_variant PACA-AU 10 101738653 101738653 deletion of <=200bp T - intron_variant PACA-AU 10 101739469 101739469 single base substitution A T intron_variant PACA-AU 10 101745283 101745283 single base substitution C T intron_variant PACA-AU 10 101745568 101745568 single base substitution C T intron_variant PACA-AU 10 101750410 101750410 single base substitution G A intron_variant PACA-AU 10 101758352 101758352 single base substitution A G intron_variant PACA-AU 10 101764333 101764349 deletion of <=200bp ATTAGAAAAACTGGGTC - intron_variant PACA-CA 10 101639731 101639731 single base substitution G A missense_variant T1462M 4385C>T PACA-CA 10 101639731 101639731 single base substitution G A missense_variant T1486M 4457C>T PACA-CA 10 101639731 101639731 single base substitution G A missense_variant T398M 1193C>T PACA-CA 10 101639731 101639731 single base substitution G A missense_variant T708M 2123C>T PACA-CA 10 101640105 101640105 single base substitution G A synonymous_variant F1337F 4011C>T PACA-CA 10 101640105 101640105 single base substitution G A synonymous_variant F1361F 4083C>T PACA-CA 10 101640105 101640105 single base substitution G A synonymous_variant F273F 819C>T PACA-CA 10 101640105 101640105 single base substitution G A synonymous_variant F583F 1749C>T PACA-CA 10 101646748 101646748 single base substitution C G intron_variant PACA-CA 10 101651871 101651871 single base substitution C G intron_variant PACA-CA 10 101651871 101651871 single base substitution C G upstream_gene_variant PACA-CA 10 101653297 101653297 single base substitution C G downstream_gene_variant PACA-CA 10 101653297 101653297 single base substitution C G intron_variant PACA-CA 10 101653297 101653297 single base substitution C G upstream_gene_variant PACA-CA 10 101658219 101658219 single base substitution T A intron_variant PACA-CA 10 101658219 101658219 single base substitution T A upstream_gene_variant PACA-CA 10 101658779 101658779 single base substitution G A intron_variant PACA-CA 10 101658779 101658779 single base substitution G A upstream_gene_variant PACA-CA 10 101659371 101659371 single base substitution T A intron_variant PACA-CA 10 101659371 101659371 single base substitution T A upstream_gene_variant PACA-CA 10 101660406 101660406 single base substitution T C intron_variant PACA-CA 10 101660406 101660406 single base substitution T C upstream_gene_variant PACA-CA 10 101663620 101663620 single base substitution G C intron_variant PACA-CA 10 101663626 101663626 single base substitution C A intron_variant PACA-CA 10 101667475 101667475 single base substitution A T intron_variant PACA-CA 10 101668733 101668733 single base substitution T C missense_variant M57V 169A>G PACA-CA 10 101668733 101668733 single base substitution T C missense_variant M811V 2431A>G PACA-CA 10 101668733 101668733 single base substitution T C missense_variant M99V 295A>G PACA-CA 10 101671563 101671563 single base substitution T C intron_variant PACA-CA 10 101682347 101682347 single base substitution C T intron_variant PACA-CA 10 101682529 101682529 single base substitution C T intron_variant PACA-CA 10 101682555 101682555 single base substitution C G intron_variant PACA-CA 10 101684175 101684175 single base substitution G A intron_variant PACA-CA 10 101693359 101693359 single base substitution G T intron_variant PACA-CA 10 101693359 101693359 single base substitution G T upstream_gene_variant PACA-CA 10 101693997 101693997 single base substitution G A intron_variant PACA-CA 10 101693997 101693997 single base substitution G A upstream_gene_variant PACA-CA 10 101695190 101695190 single base substitution T C intron_variant PACA-CA 10 101695190 101695190 single base substitution T C upstream_gene_variant PACA-CA 10 101695890 101695890 single base substitution A G intron_variant PACA-CA 10 101696997 101696997 single base substitution G A intron_variant PACA-CA 10 101697315 101697315 single base substitution C G intron_variant PACA-CA 10 101701715 101701715 single base substitution C T intron_variant PACA-CA 10 101702035 101702035 single base substitution A T intron_variant PACA-CA 10 101702332 101702347 deletion of <=200bp CAATACTTAAGTACCT - intron_variant PACA-CA 10 101703512 101703512 single base substitution A G intron_variant PACA-CA 10 101707949 101707949 single base substitution G C intron_variant PACA-CA 10 101708445 101708445 single base substitution C G intron_variant PACA-CA 10 101712848 101712848 single base substitution G A intron_variant PACA-CA 10 101717874 101717874 single base substitution G C intron_variant PACA-CA 10 101720973 101720973 single base substitution C A intron_variant PACA-CA 10 101722257 101722257 single base substitution G A intron_variant PACA-CA 10 101724227 101724227 single base substitution C G intron_variant PACA-CA 10 101724642 101724642 single base substitution A T intron_variant PACA-CA 10 101730521 101730521 single base substitution A T intron_variant PACA-CA 10 101730861 101730861 single base substitution G A intron_variant PACA-CA 10 101731175 101731175 single base substitution G A intron_variant PACA-CA 10 101737158 101737158 single base substitution T C intron_variant PACA-CA 10 101738736 101738736 single base substitution C T intron_variant PACA-CA 10 101738897 101738897 single base substitution T C intron_variant PACA-CA 10 101739424 101739424 single base substitution T A intron_variant PACA-CA 10 101742437 101742437 single base substitution C G intron_variant PACA-CA 10 101742790 101742790 insertion of <=200bp - A intron_variant PACA-CA 10 101743066 101743066 single base substitution C A intron_variant PACA-CA 10 101751188 101751188 single base substitution C T intron_variant PACA-CA 10 101754919 101754919 single base substitution C G intron_variant PACA-CA 10 101755696 101755696 single base substitution C T intron_variant PACA-CA 10 101758550 101758550 insertion of <=200bp - T intron_variant PACA-CA 10 101765365 101765365 single base substitution A G intron_variant PACA-CA 10 101772641 101772641 single base substitution G A upstream_gene_variant PACA-CA 10 101772642 101772642 single base substitution A T upstream_gene_variant PACA-CA 10 101772749 101772749 deletion of <=200bp T - upstream_gene_variant PAEN-AU 10 101638103 101638103 single base substitution C G intron_variant PAEN-AU 10 101690907 101690907 single base substitution A C intron_variant PAEN-AU 10 101690907 101690907 single base substitution A C upstream_gene_variant PAEN-AU 10 101693201 101693201 single base substitution G A intron_variant PAEN-AU 10 101693201 101693201 single base substitution G A upstream_gene_variant PAEN-IT 10 101665412 101665412 single base substitution C A intron_variant PAEN-IT 10 101678885 101678885 single base substitution G A intron_variant PBCA-DE 10 101640923 101640923 single base substitution T C intron_variant PBCA-DE 10 101643454 101643454 single base substitution C A downstream_gene_variant PBCA-DE 10 101643454 101643454 single base substitution C A intron_variant PBCA-DE 10 101646304 101646304 single base substitution C T exon_variant PBCA-DE 10 101646304 101646304 single base substitution C T missense_variant R1124H 3371G>A PBCA-DE 10 101646304 101646304 single base substitution C T missense_variant R1148H 3443G>A PBCA-DE 10 101646304 101646304 single base substitution C T missense_variant R370H 1109G>A PBCA-DE 10 101646304 101646304 single base substitution C T missense_variant R60H 179G>A PBCA-DE 10 101650531 101650531 single base substitution G A intron_variant PBCA-DE 10 101650531 101650531 single base substitution G A upstream_gene_variant PBCA-DE 10 101652936 101652936 single base substitution G C intron_variant PBCA-DE 10 101652936 101652936 single base substitution G C upstream_gene_variant PBCA-DE 10 101666353 101666353 single base substitution G T intron_variant PBCA-DE 10 101667724 101667724 single base substitution G C intron_variant PBCA-DE 10 101670351 101670351 single base substitution T G intron_variant PBCA-DE 10 101673033 101673033 single base substitution T A intron_variant PBCA-DE 10 101682741 101682741 single base substitution T C intron_variant PBCA-DE 10 101691797 101691797 single base substitution G A intron_variant PBCA-DE 10 101691797 101691797 single base substitution G A upstream_gene_variant PBCA-DE 10 101696732 101696732 single base substitution T C intron_variant PBCA-DE 10 101709974 101709974 single base substitution G A intron_variant PBCA-DE 10 101724114 101724114 single base substitution C G intron_variant PBCA-DE 10 101740503 101740503 single base substitution C T intron_variant PBCA-DE 10 101749602 101749608 deletion of <=200bp CTATGTA - intron_variant PBCA-DE 10 101757764 101757764 deletion of <=200bp G - intron_variant PBCA-DE 10 101766408 101766408 single base substitution C T intron_variant PBCA-DE 10 101767956 101767956 single base substitution C T intron_variant PBCA-DE 10 101771793 101771793 single base substitution C T upstream_gene_variant PBCA-DE 10 101772431 101772431 deletion of <=200bp T - upstream_gene_variant PRAD-CA 10 101650404 101650404 single base substitution T C intron_variant PRAD-CA 10 101650404 101650404 single base substitution T C upstream_gene_variant PRAD-CA 10 101650757 101650757 single base substitution G T intron_variant PRAD-CA 10 101650757 101650757 single base substitution G T upstream_gene_variant PRAD-CA 10 101655287 101655287 single base substitution G C downstream_gene_variant PRAD-CA 10 101655287 101655287 single base substitution G C intron_variant PRAD-CA 10 101655699 101655699 single base substitution C T downstream_gene_variant PRAD-CA 10 101655699 101655699 single base substitution C T intron_variant PRAD-CA 10 101688137 101688137 single base substitution G A intron_variant PRAD-CA 10 101689629 101689629 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant PRAD-CA 10 101689629 101689629 single base substitution C A intron_variant PRAD-CA 10 101689650 101689650 single base substitution T C 5_prime_UTR_variant PRAD-CA 10 101689650 101689650 single base substitution T C intron_variant PRAD-CA 10 101712518 101712518 single base substitution C T intron_variant PRAD-CA 10 101715180 101715180 single base substitution C T missense_variant S684N 2051G>A PRAD-CA 10 101719944 101719944 single base substitution G A intron_variant PRAD-CA 10 101741551 101741551 single base substitution A C intron_variant PRAD-CA 10 101742062 101742062 single base substitution G A intron_variant PRAD-CA 10 101749179 101749179 single base substitution G A intron_variant PRAD-CA 10 101750545 101750545 single base substitution C T intron_variant PRAD-CA 10 101752107 101752107 single base substitution A T intron_variant PRAD-CA 10 101767087 101767087 single base substitution T G intron_variant PRAD-CA 10 101770100 101770100 single base substitution C A upstream_gene_variant PRAD-UK 10 101630556 101630556 single base substitution C T downstream_gene_variant PRAD-UK 10 101634483 101634483 single base substitution T G downstream_gene_variant PRAD-UK 10 101635266 101635266 single base substitution G A downstream_gene_variant PRAD-UK 10 101653732 101653732 single base substitution T A downstream_gene_variant PRAD-UK 10 101653732 101653732 single base substitution T A intron_variant PRAD-UK 10 101653732 101653732 single base substitution T A upstream_gene_variant PRAD-UK 10 101655890 101655890 single base substitution C G downstream_gene_variant PRAD-UK 10 101655890 101655890 single base substitution C G intron_variant PRAD-UK 10 101659482 101659482 single base substitution C T intron_variant PRAD-UK 10 101659482 101659482 single base substitution C T upstream_gene_variant PRAD-UK 10 101670763 101670763 single base substitution G A intron_variant PRAD-UK 10 101683721 101683721 single base substitution C T intron_variant PRAD-UK 10 101693617 101693617 single base substitution C T intron_variant PRAD-UK 10 101693617 101693617 single base substitution C T upstream_gene_variant PRAD-UK 10 101693924 101693924 single base substitution G T intron_variant PRAD-UK 10 101693924 101693924 single base substitution G T upstream_gene_variant PRAD-UK 10 101695627 101695627 single base substitution T C intron_variant PRAD-UK 10 101695627 101695627 single base substitution T C upstream_gene_variant PRAD-UK 10 101731817 101731817 single base substitution G A missense_variant P22L 65C>T PRAD-UK 10 101736034 101736034 single base substitution C T intron_variant PRAD-UK 10 101745782 101745782 insertion of <=200bp - A intron_variant PRAD-UK 10 101745783 101745783 insertion of <=200bp - A intron_variant PRAD-UK 10 101769394 101769394 single base substitution C A intron_variant READ-US 10 101656065 101656065 single base substitution C A downstream_gene_variant READ-US 10 101656065 101656065 single base substitution C A intron_variant READ-US 10 101656065 101656065 single base substitution C A missense_variant V1004F 3010G>T READ-US 10 101656065 101656065 single base substitution C A missense_variant V1028F 3082G>T READ-US 10 101656065 101656065 single base substitution C A missense_variant V250F 748G>T READ-US 10 101716419 101716419 single base substitution C T missense_variant R271Q 812G>A READ-US 10 101728987 101728987 single base substitution G A synonymous_variant F51F 153C>T RECA-EU 10 101638687 101638687 single base substitution G A intron_variant RECA-EU 10 101643746 101643746 single base substitution C A downstream_gene_variant RECA-EU 10 101643746 101643746 single base substitution C A intron_variant RECA-EU 10 101646623 101646623 single base substitution T C intron_variant RECA-EU 10 101647537 101647537 single base substitution T C intron_variant RECA-EU 10 101655553 101655553 single base substitution A C downstream_gene_variant RECA-EU 10 101655553 101655553 single base substitution A C intron_variant RECA-EU 10 101655554 101655554 single base substitution T A downstream_gene_variant RECA-EU 10 101655554 101655554 single base substitution T A intron_variant RECA-EU 10 101655555 101655555 single base substitution G A downstream_gene_variant RECA-EU 10 101655555 101655555 single base substitution G A intron_variant RECA-EU 10 101665094 101665094 single base substitution G T intron_variant RECA-EU 10 101666161 101666161 single base substitution G A intron_variant RECA-EU 10 101666334 101666334 single base substitution C T intron_variant RECA-EU 10 101667491 101667491 single base substitution G T intron_variant RECA-EU 10 101671463 101671463 single base substitution T A intron_variant RECA-EU 10 101684391 101684391 single base substitution A T intron_variant RECA-EU 10 101684392 101684392 single base substitution A G intron_variant RECA-EU 10 101694863 101694863 single base substitution A G intron_variant RECA-EU 10 101694863 101694863 single base substitution A G upstream_gene_variant RECA-EU 10 101713576 101713576 single base substitution A G intron_variant RECA-EU 10 101731459 101731459 single base substitution T A intron_variant RECA-EU 10 101731994 101731994 single base substitution A C intron_variant RECA-EU 10 101734011 101734011 single base substitution C A intron_variant RECA-EU 10 101735049 101735049 single base substitution G A intron_variant RECA-EU 10 101746817 101746817 single base substitution C T intron_variant RECA-EU 10 101758401 101758401 single base substitution G A intron_variant SKCA-BR 10 101630921 101630921 single base substitution A T downstream_gene_variant SKCA-BR 10 101631765 101631765 single base substitution T C downstream_gene_variant SKCA-BR 10 101632977 101632977 single base substitution G A downstream_gene_variant SKCA-BR 10 101636247 101636247 single base substitution A G 3_prime_UTR_variant SKCA-BR 10 101636247 101636247 single base substitution A G downstream_gene_variant SKCA-BR 10 101638040 101638040 single base substitution G A intron_variant SKCA-BR 10 101640973 101640973 single base substitution G A intron_variant SKCA-BR 10 101643395 101643405 deletion of <=200bp CAAAAAAAAAA - downstream_gene_variant SKCA-BR 10 101643395 101643405 deletion of <=200bp CAAAAAAAAAA - intron_variant SKCA-BR 10 101643675 101643675 insertion of <=200bp - GT downstream_gene_variant SKCA-BR 10 101643675 101643675 insertion of <=200bp - GT intron_variant SKCA-BR 10 101650213 101650213 single base substitution C T intron_variant SKCA-BR 10 101650213 101650213 single base substitution C T upstream_gene_variant SKCA-BR 10 101651791 101651791 single base substitution G C intron_variant SKCA-BR 10 101651791 101651791 single base substitution G C upstream_gene_variant SKCA-BR 10 101651803 101651803 single base substitution G A intron_variant SKCA-BR 10 101651803 101651803 single base substitution G A upstream_gene_variant SKCA-BR 10 101651917 101651917 single base substitution A G intron_variant SKCA-BR 10 101651917 101651917 single base substitution A G upstream_gene_variant SKCA-BR 10 101652035 101652035 single base substitution C G intron_variant SKCA-BR 10 101652035 101652035 single base substitution C G upstream_gene_variant SKCA-BR 10 101657173 101657173 single base substitution C T downstream_gene_variant SKCA-BR 10 101657173 101657173 single base substitution C T intron_variant SKCA-BR 10 101662856 101662856 single base substitution C T intron_variant SKCA-BR 10 101662856 101662856 single base substitution C T upstream_gene_variant SKCA-BR 10 101662858 101662859 deletion of <=200bp AT - intron_variant SKCA-BR 10 101662858 101662859 deletion of <=200bp AT - upstream_gene_variant SKCA-BR 10 101664853 101664853 single base substitution G A intron_variant SKCA-BR 10 101668911 101668911 single base substitution G A splice_region_variant SKCA-BR 10 101672341 101672341 single base substitution A G intron_variant SKCA-BR 10 101674865 101674865 insertion of <=200bp - AAAAAATAT intron_variant SKCA-BR 10 101674865 101674865 insertion of <=200bp - AAAAAATAT upstream_gene_variant SKCA-BR 10 101675161 101675161 insertion of <=200bp - TA intron_variant SKCA-BR 10 101675161 101675161 insertion of <=200bp - TA upstream_gene_variant SKCA-BR 10 101676412 101676412 insertion of <=200bp - TA intron_variant SKCA-BR 10 101676412 101676412 insertion of <=200bp - TA upstream_gene_variant SKCA-BR 10 101678331 101678331 insertion of <=200bp - CTTTTTTT intron_variant SKCA-BR 10 101678331 101678331 insertion of <=200bp - CTTTTTTTT intron_variant SKCA-BR 10 101678331 101678331 insertion of <=200bp - CTTTTTTTT upstream_gene_variant SKCA-BR 10 101678331 101678331 insertion of <=200bp - CTTTTTTT upstream_gene_variant SKCA-BR 10 101679303 101679303 single base substitution A C intron_variant SKCA-BR 10 101681449 101681449 insertion of <=200bp - GA intron_variant SKCA-BR 10 101681449 101681450 deletion of <=200bp GA - intron_variant SKCA-BR 10 101682259 101682260 deletion of <=200bp GT - intron_variant SKCA-BR 10 101683149 101683149 insertion of <=200bp - AAAT intron_variant SKCA-BR 10 101683981 101683981 single base substitution T G intron_variant SKCA-BR 10 101687330 101687330 single base substitution A G intron_variant SKCA-BR 10 101690907 101690907 single base substitution A C intron_variant SKCA-BR 10 101690907 101690907 single base substitution A C upstream_gene_variant SKCA-BR 10 101692235 101692235 single base substitution G A intron_variant SKCA-BR 10 101692235 101692235 single base substitution G A upstream_gene_variant SKCA-BR 10 101693542 101693542 single base substitution G A intron_variant SKCA-BR 10 101693542 101693542 single base substitution G A upstream_gene_variant SKCA-BR 10 101694216 101694216 single base substitution G A intron_variant SKCA-BR 10 101694216 101694216 single base substitution G A upstream_gene_variant SKCA-BR 10 101694226 101694226 single base substitution G A intron_variant SKCA-BR 10 101694226 101694226 single base substitution G A upstream_gene_variant SKCA-BR 10 101696272 101696273 deletion of <=200bp CT - intron_variant SKCA-BR 10 101702473 101702473 single base substitution G A intron_variant SKCA-BR 10 101703137 101703141 deletion of <=200bp TTTTG - intron_variant SKCA-BR 10 101705460 101705460 single base substitution C T intron_variant SKCA-BR 10 101706858 101706858 single base substitution A C intron_variant SKCA-BR 10 101713582 101713582 single base substitution G A intron_variant SKCA-BR 10 101721022 101721024 deletion of <=200bp TTC - intron_variant SKCA-BR 10 101730854 101730854 single base substitution G A intron_variant SKCA-BR 10 101731005 101731007 deletion of <=200bp GTA - intron_variant SKCA-BR 10 101731010 101731010 single base substitution C A intron_variant SKCA-BR 10 101731068 101731068 insertion of <=200bp - TTTCC intron_variant SKCA-BR 10 101732837 101732837 insertion of <=200bp - CATTT intron_variant SKCA-BR 10 101735900 101735900 single base substitution A G intron_variant SKCA-BR 10 101738093 101738093 single base substitution C T intron_variant SKCA-BR 10 101740434 101740434 single base substitution T G intron_variant SKCA-BR 10 101741418 101741418 single base substitution A G intron_variant SKCA-BR 10 101744104 101744104 single base substitution C T intron_variant SKCA-BR 10 101744247 101744247 single base substitution A G intron_variant SKCA-BR 10 101745750 101745767 deletion of <=200bp CGCCTGCCTCGCCCTCTT - intron_variant SKCA-BR 10 101746351 101746368 deletion of <=200bp CAAAAAAAAAAAAAAAAA - intron_variant SKCA-BR 10 101751763 101751763 insertion of <=200bp - GA intron_variant SKCA-BR 10 101751772 101751772 single base substitution T C intron_variant SKCA-BR 10 101755384 101755384 single base substitution G A intron_variant SKCA-BR 10 101758336 101758336 insertion of <=200bp - CA intron_variant SKCA-BR 10 101761403 101761403 single base substitution C A intron_variant SKCA-BR 10 101761715 101761715 single base substitution G A intron_variant SKCA-BR 10 101761853 101761853 single base substitution G A intron_variant SKCA-BR 10 101761867 101761867 single base substitution G A intron_variant SKCA-BR 10 101762200 101762200 single base substitution G A intron_variant SKCA-BR 10 101762632 101762632 single base substitution A G intron_variant SKCA-BR 10 101764516 101764516 single base substitution A G intron_variant SKCA-BR 10 101770377 101770377 single base substitution C G upstream_gene_variant SKCA-BR 10 101771234 101771234 single base substitution C G upstream_gene_variant SKCA-BR 10 101773424 101773424 single base substitution C G upstream_gene_variant SKCM-US 10 101637062 101637062 single base substitution C T missense_variant R1527Q 4580G>A SKCM-US 10 101637062 101637062 single base substitution C T missense_variant R1551Q 4652G>A SKCM-US 10 101637062 101637062 single base substitution C T missense_variant R463Q 1388G>A SKCM-US 10 101637062 101637062 single base substitution C T missense_variant R773Q 2318G>A SKCM-US 10 101639683 101639683 single base substitution G A missense_variant S1478F 4433C>T SKCM-US 10 101639683 101639683 single base substitution G A missense_variant S1502F 4505C>T SKCM-US 10 101639683 101639683 single base substitution G A missense_variant S414F 1241C>T SKCM-US 10 101639683 101639683 single base substitution G A missense_variant S724F 2171C>T SKCM-US 10 101639890 101639890 single base substitution G A missense_variant P1409L 4226C>T SKCM-US 10 101639890 101639890 single base substitution G A missense_variant P1433L 4298C>T SKCM-US 10 101639890 101639890 single base substitution G A missense_variant P345L 1034C>T SKCM-US 10 101639890 101639890 single base substitution G A missense_variant P655L 1964C>T SKCM-US 10 101639994 101639994 single base substitution G A synonymous_variant F1374F 4122C>T SKCM-US 10 101639994 101639994 single base substitution G A synonymous_variant F1398F 4194C>T SKCM-US 10 101639994 101639994 single base substitution G A synonymous_variant F310F 930C>T SKCM-US 10 101639994 101639994 single base substitution G A synonymous_variant F620F 1860C>T SKCM-US 10 101640031 101640031 single base substitution G A missense_variant S1362F 4085C>T SKCM-US 10 101640031 101640031 single base substitution G A missense_variant S1386F 4157C>T SKCM-US 10 101640031 101640031 single base substitution G A missense_variant S298F 893C>T SKCM-US 10 101640031 101640031 single base substitution G A missense_variant S608F 1823C>T SKCM-US 10 101640083 101640083 single base substitution G A missense_variant P1345S 4033C>T SKCM-US 10 101640083 101640083 single base substitution G A missense_variant P1369S 4105C>T SKCM-US 10 101640083 101640083 single base substitution G A missense_variant P281S 841C>T SKCM-US 10 101640083 101640083 single base substitution G A missense_variant P591S 1771C>T SKCM-US 10 101643875 101643875 single base substitution T C downstream_gene_variant SKCM-US 10 101643875 101643875 single base substitution T C missense_variant N1297S 3890A>G SKCM-US 10 101643875 101643875 single base substitution T C missense_variant N1321S 3962A>G SKCM-US 10 101643875 101643875 single base substitution T C missense_variant N233S 698A>G SKCM-US 10 101643875 101643875 single base substitution T C missense_variant N543S 1628A>G SKCM-US 10 101643911 101643911 single base substitution G A downstream_gene_variant SKCM-US 10 101643911 101643911 single base substitution G A missense_variant P1285L 3854C>T SKCM-US 10 101643911 101643911 single base substitution G A missense_variant P1309L 3926C>T SKCM-US 10 101643911 101643911 single base substitution G A missense_variant P221L 662C>T SKCM-US 10 101643911 101643911 single base substitution G A missense_variant P531L 1592C>T SKCM-US 10 101643929 101643929 single base substitution G A downstream_gene_variant SKCM-US 10 101643929 101643929 single base substitution G A missense_variant S1279F 3836C>T SKCM-US 10 101643929 101643929 single base substitution G A missense_variant S1303F 3908C>T SKCM-US 10 101643929 101643929 single base substitution G A missense_variant S215F 644C>T SKCM-US 10 101643929 101643929 single base substitution G A missense_variant S525F 1574C>T SKCM-US 10 101646249 101646249 single base substitution C T exon_variant SKCM-US 10 101646249 101646249 single base substitution C T synonymous_variant K1142K 3426G>A SKCM-US 10 101646249 101646249 single base substitution C T synonymous_variant K1166K 3498G>A SKCM-US 10 101646249 101646249 single base substitution C T synonymous_variant K388K 1164G>A SKCM-US 10 101646249 101646249 single base substitution C T synonymous_variant K78K 234G>A SKCM-US 10 101646372 101646372 single base substitution C T exon_variant SKCM-US 10 101646372 101646372 single base substitution C T synonymous_variant R1101R 3303G>A SKCM-US 10 101646372 101646372 single base substitution C T synonymous_variant R1125R 3375G>A SKCM-US 10 101646372 101646372 single base substitution C T synonymous_variant R347R 1041G>A SKCM-US 10 101646372 101646372 single base substitution C T synonymous_variant R37R 111G>A SKCM-US 10 101648593 101648593 single base substitution A G exon_variant SKCM-US 10 101648593 101648593 single base substitution A G missense_variant F1092L 3274T>C SKCM-US 10 101648593 101648593 single base substitution A G missense_variant F1116L 3346T>C SKCM-US 10 101648593 101648593 single base substitution A G missense_variant F28L 82T>C SKCM-US 10 101648593 101648593 single base substitution A G missense_variant F338L 1012T>C SKCM-US 10 101654768 101654768 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 10 101654768 101654768 single base substitution G A downstream_gene_variant SKCM-US 10 101654768 101654768 single base substitution G A stop_gained R1031* 3091C>T SKCM-US 10 101654768 101654768 single base substitution G A stop_gained R1055* 3163C>T SKCM-US 10 101654768 101654768 single base substitution G A stop_gained R277* 829C>T SKCM-US 10 101656106 101656106 single base substitution G A downstream_gene_variant SKCM-US 10 101656106 101656106 single base substitution G A intron_variant SKCM-US 10 101656106 101656106 single base substitution G A missense_variant S1014F 3041C>T SKCM-US 10 101656106 101656106 single base substitution G A missense_variant S236F 707C>T SKCM-US 10 101656106 101656106 single base substitution G A missense_variant S990F 2969C>T SKCM-US 10 101656153 101656153 single base substitution G A downstream_gene_variant SKCM-US 10 101656153 101656153 single base substitution G A intron_variant SKCM-US 10 101656153 101656153 single base substitution G A splice_region_variant SKCM-US 10 101656153 101656153 single base substitution G A synonymous_variant V998V 2994C>T SKCM-US 10 101715232 101715232 single base substitution G A missense_variant R667C 1999C>T SKCM-US 10 101715238 101715238 single base substitution G A stop_gained R665* 1993C>T SKCM-US 10 101715388 101715388 single base substitution G A missense_variant P615S 1843C>T SKCM-US 10 101715817 101715817 single base substitution G A stop_gained Q472* 1414C>T SKCM-US 10 101715887 101715887 single base substitution G A synonymous_variant P448P 1344C>T SKCM-US 10 101715970 101715970 single base substitution G A missense_variant H421Y 1261C>T SKCM-US 10 101716029 101716029 single base substitution G A missense_variant P401L 1202C>T SKCM-US 10 101716582 101716582 single base substitution G A stop_gained Q217* 649C>T SKCM-US 10 101716647 101716647 single base substitution G A missense_variant P195L 584C>T SKCM-US 10 101728986 101728986 single base substitution G A missense_variant P52S 154C>T SKCM-US 10 101731860 101731860 single base substitution G A stop_gained R8* 22C>T STAD-US 10 101637006 101637006 single base substitution T C missense_variant K1546E 4636A>G STAD-US 10 101637006 101637006 single base substitution T C missense_variant K1570E 4708A>G STAD-US 10 101637006 101637006 single base substitution T C missense_variant K482E 1444A>G STAD-US 10 101637006 101637006 single base substitution T C missense_variant K792E 2374A>G STAD-US 10 101639731 101639731 single base substitution G A missense_variant T1462M 4385C>T STAD-US 10 101639731 101639731 single base substitution G A missense_variant T1486M 4457C>T STAD-US 10 101639731 101639731 single base substitution G A missense_variant T398M 1193C>T STAD-US 10 101639731 101639731 single base substitution G A missense_variant T708M 2123C>T STAD-US 10 101639817 101639817 single base substitution T C synonymous_variant R1433R 4299A>G STAD-US 10 101639817 101639817 single base substitution T C synonymous_variant R1457R 4371A>G STAD-US 10 101639817 101639817 single base substitution T C synonymous_variant R369R 1107A>G STAD-US 10 101639817 101639817 single base substitution T C synonymous_variant R679R 2037A>G STAD-US 10 101639896 101639896 single base substitution G T missense_variant S1407Y 4220C>A STAD-US 10 101639896 101639896 single base substitution G T missense_variant S1431Y 4292C>A STAD-US 10 101639896 101639896 single base substitution G T missense_variant S343Y 1028C>A STAD-US 10 101639896 101639896 single base substitution G T missense_variant S653Y 1958C>A STAD-US 10 101643927 101643927 single base substitution G T downstream_gene_variant STAD-US 10 101643927 101643927 single base substitution G T missense_variant L1280I 3838C>A STAD-US 10 101643927 101643927 single base substitution G T missense_variant L1304I 3910C>A STAD-US 10 101643927 101643927 single base substitution G T missense_variant L216I 646C>A STAD-US 10 101643927 101643927 single base substitution G T missense_variant L526I 1576C>A STAD-US 10 101645575 101645575 single base substitution C T downstream_gene_variant STAD-US 10 101645575 101645575 single base substitution C T missense_variant E1223K 3667G>A STAD-US 10 101645575 101645575 single base substitution C T missense_variant E1247K 3739G>A STAD-US 10 101645575 101645575 single base substitution C T missense_variant E159K 475G>A STAD-US 10 101645575 101645575 single base substitution C T missense_variant E469K 1405G>A STAD-US 10 101656041 101656041 single base substitution T C downstream_gene_variant STAD-US 10 101656041 101656041 single base substitution T C intron_variant STAD-US 10 101656041 101656041 single base substitution T C missense_variant T1012A 3034A>G STAD-US 10 101656041 101656041 single base substitution T C missense_variant T1036A 3106A>G STAD-US 10 101656041 101656041 single base substitution T C missense_variant T258A 772A>G STAD-US 10 101656136 101656136 single base substitution C T downstream_gene_variant STAD-US 10 101656136 101656136 single base substitution C T intron_variant STAD-US 10 101656136 101656136 single base substitution C T missense_variant G1004D 3011G>A STAD-US 10 101656136 101656136 single base substitution C T missense_variant G226D 677G>A STAD-US 10 101656136 101656136 single base substitution C T missense_variant G980D 2939G>A STAD-US 10 101657908 101657908 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 10 101657908 101657908 single base substitution T A downstream_gene_variant STAD-US 10 101657908 101657908 single base substitution T A missense_variant N198I 593A>T STAD-US 10 101657908 101657908 single base substitution T A missense_variant N952I 2855A>T STAD-US 10 101715303 101715303 single base substitution C T missense_variant R643H 1928G>A STAD-US 10 101715527 101715527 single base substitution T A synonymous_variant T568T 1704A>T STAD-US 10 101715673 101715673 single base substitution T C missense_variant R520G 1558A>G STAD-US 10 101715833 101715833 single base substitution G T synonymous_variant S466S 1398C>A STAD-US 10 101716033 101716033 single base substitution A T missense_variant S400T 1198T>A STAD-US 10 101716054 101716054 single base substitution C T missense_variant E393K 1177G>A STAD-US 10 101716155 101716155 single base substitution G T missense_variant S359Y 1076C>A STAD-US 10 101716831 101716831 single base substitution G T missense_variant H134N 400C>A STAD-US 10 101728939 101728939 single base substitution T C synonymous_variant G67G 201A>G STAD-US 10 101728961 101728961 single base substitution G A missense_variant T60I 179C>T STAD-US 10 101731839 101731839 single base substitution G A missense_variant P15S 43C>T THCA-SA 10 101639877 101639877 single base substitution A C missense_variant C1413W 4239T>G THCA-SA 10 101639877 101639877 single base substitution A C missense_variant C1437W 4311T>G THCA-SA 10 101639877 101639877 single base substitution A C missense_variant C349W 1047T>G THCA-SA 10 101639877 101639877 single base substitution A C missense_variant C659W 1977T>G THCA-SA 10 101657880 101657880 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant THCA-SA 10 101657880 101657880 single base substitution G A downstream_gene_variant THCA-SA 10 101657880 101657880 single base substitution G A synonymous_variant N207N 621C>T THCA-SA 10 101657880 101657880 single base substitution G A synonymous_variant N961N 2883C>T THCA-SA 10 101687950 101687950 single base substitution T C intron_variant UCEC-US 10 101636953 101636953 single base substitution C A missense_variant K1563N 4689G>T UCEC-US 10 101636953 101636953 single base substitution C A missense_variant K1587N 4761G>T UCEC-US 10 101636953 101636953 single base substitution C A missense_variant K499N 1497G>T UCEC-US 10 101636953 101636953 single base substitution C A missense_variant K809N 2427G>T UCEC-US 10 101639586 101639586 single base substitution A G synonymous_variant S1510S 4530T>C UCEC-US 10 101639586 101639586 single base substitution A G synonymous_variant S1534S 4602T>C UCEC-US 10 101639586 101639586 single base substitution A G synonymous_variant S446S 1338T>C UCEC-US 10 101639586 101639586 single base substitution A G synonymous_variant S756S 2268T>C UCEC-US 10 101639600 101639600 single base substitution C A stop_gained E1506* 4516G>T UCEC-US 10 101639600 101639600 single base substitution C A stop_gained E1530* 4588G>T UCEC-US 10 101639600 101639600 single base substitution C A stop_gained E442* 1324G>T UCEC-US 10 101639600 101639600 single base substitution C A stop_gained E752* 2254G>T UCEC-US 10 101639896 101639896 single base substitution G T missense_variant S1407Y 4220C>A UCEC-US 10 101639896 101639896 single base substitution G T missense_variant S1431Y 4292C>A UCEC-US 10 101639896 101639896 single base substitution G T missense_variant S343Y 1028C>A UCEC-US 10 101639896 101639896 single base substitution G T missense_variant S653Y 1958C>A UCEC-US 10 101640022 101640022 single base substitution G T missense_variant S1365Y 4094C>A UCEC-US 10 101640022 101640022 single base substitution G T missense_variant S1389Y 4166C>A UCEC-US 10 101640022 101640022 single base substitution G T missense_variant S301Y 902C>A UCEC-US 10 101640022 101640022 single base substitution G T missense_variant S611Y 1832C>A UCEC-US 10 101640056 101640056 single base substitution C T missense_variant D1354N 4060G>A UCEC-US 10 101640056 101640056 single base substitution C T missense_variant D1378N 4132G>A UCEC-US 10 101640056 101640056 single base substitution C T missense_variant D290N 868G>A UCEC-US 10 101640056 101640056 single base substitution C T missense_variant D600N 1798G>A UCEC-US 10 101646087 101646087 single base substitution C A downstream_gene_variant UCEC-US 10 101646087 101646087 single base substitution C A missense_variant Q1196H 3588G>T UCEC-US 10 101646087 101646087 single base substitution C A missense_variant Q1220H 3660G>T UCEC-US 10 101646087 101646087 single base substitution C A missense_variant Q132H 396G>T UCEC-US 10 101646087 101646087 single base substitution C A missense_variant Q442H 1326G>T UCEC-US 10 101646143 101646143 single base substitution G T downstream_gene_variant UCEC-US 10 101646143 101646143 single base substitution G T missense_variant L114I 340C>A UCEC-US 10 101646143 101646143 single base substitution G T missense_variant L1178I 3532C>A UCEC-US 10 101646143 101646143 single base substitution G T missense_variant L1202I 3604C>A UCEC-US 10 101646143 101646143 single base substitution G T missense_variant L424I 1270C>A UCEC-US 10 101646374 101646374 single base substitution G A exon_variant UCEC-US 10 101646374 101646374 single base substitution G A missense_variant R1101W 3301C>T UCEC-US 10 101646374 101646374 single base substitution G A missense_variant R1125W 3373C>T UCEC-US 10 101646374 101646374 single base substitution G A missense_variant R347W 1039C>T UCEC-US 10 101646374 101646374 single base substitution G A missense_variant R37W 109C>T UCEC-US 10 101654728 101654728 single base substitution A G 5_prime_UTR_variant UCEC-US 10 101654728 101654728 single base substitution A G downstream_gene_variant UCEC-US 10 101654728 101654728 single base substitution A G missense_variant L1044P 3131T>C UCEC-US 10 101654728 101654728 single base substitution A G missense_variant L1068P 3203T>C UCEC-US 10 101654728 101654728 single base substitution A G missense_variant L290P 869T>C UCEC-US 10 101654729 101654729 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 10 101654729 101654729 single base substitution G T downstream_gene_variant UCEC-US 10 101654729 101654729 single base substitution G T missense_variant L1044M 3130C>A UCEC-US 10 101654729 101654729 single base substitution G T missense_variant L1068M 3202C>A UCEC-US 10 101654729 101654729 single base substitution G T missense_variant L290M 868C>A UCEC-US 10 101654735 101654735 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 10 101654735 101654735 single base substitution G A downstream_gene_variant UCEC-US 10 101654735 101654735 single base substitution G A stop_gained R1042* 3124C>T UCEC-US 10 101654735 101654735 single base substitution G A stop_gained R1066* 3196C>T UCEC-US 10 101654735 101654735 single base substitution G A stop_gained R288* 862C>T UCEC-US 10 101654768 101654768 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 10 101654768 101654768 single base substitution G A downstream_gene_variant UCEC-US 10 101654768 101654768 single base substitution G A stop_gained R1031* 3091C>T UCEC-US 10 101654768 101654768 single base substitution G A stop_gained R1055* 3163C>T UCEC-US 10 101654768 101654768 single base substitution G A stop_gained R277* 829C>T UCEC-US 10 101656046 101656046 single base substitution T C downstream_gene_variant UCEC-US 10 101656046 101656046 single base substitution T C intron_variant UCEC-US 10 101656046 101656046 single base substitution T C missense_variant H1010R 3029A>G UCEC-US 10 101656046 101656046 single base substitution T C missense_variant H1034R 3101A>G UCEC-US 10 101656046 101656046 single base substitution T C missense_variant H256R 767A>G UCEC-US 10 101657828 101657828 single base substitution T G downstream_gene_variant UCEC-US 10 101657828 101657828 single base substitution T G intron_variant UCEC-US 10 101657828 101657828 single base substitution T G missense_variant I979L 2935A>C UCEC-US 10 101657918 101657918 single base substitution G T 5_prime_UTR_variant UCEC-US 10 101657918 101657918 single base substitution G T downstream_gene_variant UCEC-US 10 101657918 101657918 single base substitution G T missense_variant P195T 583C>A UCEC-US 10 101657918 101657918 single base substitution G T missense_variant P949T 2845C>A UCEC-US 10 101667762 101667762 single base substitution G A synonymous_variant S136S 408C>T UCEC-US 10 101667762 101667762 single base substitution G A synonymous_variant S848S 2544C>T UCEC-US 10 101667762 101667762 single base substitution G A synonymous_variant S94S 282C>T UCEC-US 10 101668726 101668726 single base substitution G A missense_variant P101L 302C>T UCEC-US 10 101668726 101668726 single base substitution G A missense_variant P59L 176C>T UCEC-US 10 101668726 101668726 single base substitution G A missense_variant P813L 2438C>T UCEC-US 10 101715312 101715312 single base substitution C T missense_variant R640Q 1919G>A UCEC-US 10 101715344 101715344 single base substitution C A missense_variant Q629H 1887G>T UCEC-US 10 101715524 101715524 single base substitution C A missense_variant E569D 1707G>T UCEC-US 10 101715865 101715865 single base substitution A G missense_variant Y456H 1366T>C UCEC-US 10 101715898 101715898 single base substitution C T missense_variant D445N 1333G>A UCEC-US 10 101716116 101716116 single base substitution C A missense_variant R372I 1115G>T UCEC-US 10 101716260 101716260 single base substitution G T missense_variant S324Y 971C>A UCEC-US 10 101716391 101716391 single base substitution C T stop_gained W280* 840G>A UCEC-US 10 101716409 101716409 single base substitution C T synonymous_variant A274A 822G>A UCEC-US 10 101716662 101716662 single base substitution C T missense_variant R190Q 569G>A UCEC-US 10 101717021 101717021 single base substitution C T intron_variant UCEC-US 10 101728976 101728976 single base substitution A C missense_variant F55C 164T>G

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AP-A0LM-01 COSM913836 c.4516G>T p.E1506* Substitution - Nonsense 10:99879843-99879843 - 07-058 COSM3735990 c.4239T>G p.C1413W Substitution - Missense 10:99880120-99880120 - TCGA-BR-8059-01 COSM4010977 c.2939G>A p.G980D Substitution - Missense 10:99896379-99896379 - J11_T COSM3978021 c.1897C>T p.P633S Substitution - Missense 10:99955577-99955577 - TCGA-CD-A4MG-01 COSM2057637 c.1928G>A p.R643H Substitution - Missense 10:99955546-99955546 - TCGA-B5-A0K6-01 COSM913864 c.429G>A p.P143P Substitution - coding silent 10:99957045-99957045 - CSCC-27-T COSM4469178 c.1587C>T p.A529A Substitution - coding silent 10:99955887-99955887 - S02065 COSM5672507 c.4522G>C p.D1508H Substitution - Missense 10:99879837-99879837 - TCGA-AA-A010-01 COSM280551 c.3829C>T p.R1277W Substitution - Missense 10:99884179-99884179 - SNUH_G16_S1 COSM3997728 c.757A>C p.R253R Substitution - coding silent 10:99956717-99956717 - 113T COSM1725296 c.4498C>G p.P1500A Substitution - Missense 10:99879861-99879861 - OSCC-GB_01040111 COSM4886172 c.1208C>A p.S403Y Substitution - Missense 10:99956266-99956266 - BHY COSM4592565 c.3307G>T p.V1103F Substitution - Missense 10:99886611-99886611 - SWE-26 COSM1179215 c.748G>A p.A250T Substitution - Missense 10:99956726-99956726 - TCGA-AA-3516-01 COSM291551 c.1854G>A p.P618P Substitution - coding silent 10:99955620-99955620 - YUPLA COSM5369917 c.1443C>T p.G481G Substitution - coding silent 10:99956031-99956031 - ESCC_BICR_012T COSM5432965 c.481G>C p.D161H Substitution - Missense 10:99956993-99956993 - PDA_082 COSM3735990 c.4239T>G p.C1413W Substitution - Missense 10:99880120-99880120 - TCGA-FR-A3R1-01 COSM3433485 c.2969C>T p.S990F Substitution - Missense 10:99896349-99896349 - TCGA-D1-A177-01 COSM913844 c.3131T>C p.L1044P Substitution - Missense 10:99894971-99894971 - SNU-175 COSM2057637 c.1928G>A p.R643H Substitution - Missense 10:99955546-99955546 - 1517_CLM COSM5753376 c.4098G>T p.E1366D Substitution - Missense 10:99880261-99880261 - TCGA-B5-A11E-01 COSM913843 c.3301C>T p.R1101W Substitution - Missense 10:99886617-99886617 - TCGA-AK-3450-01 COSM3773521 c.232A>C p.T78P Substitution - Missense 10:99969151-99969151 - CH-50-T2 COSM5650809 c.1830A>C p.P610P Substitution - coding silent 10:99955644-99955644 - ICGC_MB800 COSM215405 c.3371G>A p.R1124H Substitution - Missense 10:99886547-99886547 - 12T COSM108235 c.792C>T p.F264F Substitution - coding silent 10:99956682-99956682 - TCGA-A8-A09Z-01 COSM3806254 c.3838C>A p.L1280I Substitution - Missense 10:99884170-99884170 - CACO2 COSM2057628 c.2318C>G p.S773C Substitution - Missense 10:99909089-99909089 - MOLT-4 COSM1675490 c.910C>T p.R304W Substitution - Missense 10:99956564-99956564 - QC2-32-T2 COSM3751483 c.2883C>T p.N961N Substitution - coding silent 10:99898123-99898123 - T3267 COSM4678866 c.1666C>T p.L556L Substitution - coding silent 10:99955808-99955808 - TCGA-EB-A5SG-06 COSM1204284 c.4226C>T p.P1409L Substitution - Missense 10:99880133-99880133 - CSCC-11-T COSM1702896 c.2068C>T p.P690S Substitution - Missense 10:99955406-99955406 - 587228 COSM1204285 c.1828C>T p.P610S Substitution - Missense 10:99955646-99955646 - PM-2 COSM5619517 c.1131C>G p.D377E Substitution - Missense 10:99956343-99956343 - TCGA-CD-A4MI-01 COSM4010993 c.400C>A p.H134N Substitution - Missense 10:99957074-99957074 - 0115_CRUK_PC_0115_T1_DNA COSM5420928 c.65C>T p.P22L Substitution - Missense 10:99972060-99972060 - QC2-26-T2 COSM3735990 c.4239T>G p.C1413W Substitution - Missense 10:99880120-99880120 - TCGA-DR-A0ZM-01 COSM458928 c.1569G>A p.M523I Substitution - Missense 10:99955905-99955905 - SNUH_G10_S1 COSM3751483 c.2883C>T p.N961N Substitution - coding silent 10:99898123-99898123 - TCGA-B5-A11E-01 COSM913854 c.1887G>T p.Q629H Substitution - Missense 10:99955587-99955587 - TCGA-BQ-7044-01 COSM3985356 c.3350C>G p.P1117R Substitution - Missense 10:99886568-99886568 - LUAD-B01811 COSM333725 c.2909G>T p.R970L Substitution - Missense 10:99898097-99898097 - TCGA-LP-A5U2-01 COSM4833683 c.3022C>A p.L1008M Substitution - Missense 10:99896296-99896296 - T36 COSM5341149 c.1949C>T p.S650L Substitution - Missense 10:99955525-99955525 - LUAD-NYU408 COSM373999 c.4400G>A p.R1467Q Substitution - Missense 10:99879959-99879959 - CSCC-27-T COSM4490493 c.3648C>T p.N1216N Substitution - coding silent 10:99885837-99885837 - WSU-HN12 COSM4592565 c.3307G>T p.V1103F Substitution - Missense 10:99886611-99886611 - TCGA-EB-A3Y7-01 COSM3433487 c.2922C>T p.V974V Substitution - coding silent 10:99896396-99896396 - CSCC-44-T COSM4466010 c.1411C>T p.L471F Substitution - Missense 10:99956063-99956063 - TCGA-CG-4306-01 COSM913837 c.4220C>A p.S1407Y Substitution - Missense 10:99880139-99880139 - TCGA-D3-A3MR-06 COSM3433495 c.1202C>T p.P401L Substitution - Missense 10:99956272-99956272 - SNUH_G76_S1 COSM4419930 c.747C>T p.V249V Substitution - coding silent 10:99956727-99956727 - HCC102 COSM1602853 c.3253C>T p.R1085C Substitution - Missense 10:99888857-99888857 - 661-06-01TD COSM5418930 c.2085_2086insC p.V696fs*4 Insertion - Frameshift 10:99955388-99955389 - TCGA-AM-5820-01 COSM3735990 c.4239T>G p.C1413W Substitution - Missense 10:99880120-99880120 - WSU-HN13 COSM4592565 c.3307G>T p.V1103F Substitution - Missense 10:99886611-99886611 - TCGA-AN-A0FJ-01 COSM426918 c.2401C>T p.R801W Substitution - Missense 10:99909006-99909006 - TCGA-BS-A0UV-01 COSM913861 c.822G>A p.A274A Substitution - coding silent 10:99956652-99956652 - TCGA-FW-A3R5-06 COSM3866332 c.1344C>T p.P448P Substitution - coding silent 10:99956130-99956130 - TCGA-EE-A3J5-06 COSM3433479 c.3426G>A p.K1142K Substitution - coding silent 10:99886492-99886492 - cSCCP5 COSM137992 c.964G>A p.E322K Substitution - Missense 10:99956510-99956510 - TCGA-AM-5820-01 COSM3751483 c.2883C>T p.N961N Substitution - coding silent 10:99898123-99898123 - TCGA-CD-A489-01 COSM4010981 c.1704A>T p.T568T Substitution - coding silent 10:99955770-99955770 - AOCS-104-1-6 COSM3952755 c.1739T>C p.M580T Substitution - Missense 10:99955735-99955735 - YUFERY COSM5369915 c.2829C>T p.S943S Substitution - coding silent 10:99898177-99898177 - LUAD-E01278 COSM394055 c.2282A>T p.Q761L Substitution - Missense 10:99909125-99909125 - TCGA-A6-6653-01 COSM1345260 c.1408delA p.T470fs*20 Deletion - Frameshift 10:99956066-99956066 - TCGA-AP-A051-01 COSM913845 c.3130C>A p.L1044M Substitution - Missense 10:99894972-99894972 - T2269 COSM4678874 c.428C>T p.P143L Substitution - Missense 10:99957046-99957046 - HCC102T COSM1602853 c.3253C>T p.R1085C Substitution - Missense 10:99888857-99888857 - TCGA-04-1338-01 COSM82111 c.738C>A p.T246T Substitution - coding silent 10:99956736-99956736 - TCGA-BS-A0UF-01 COSM913852 c.2438C>T p.P813L Substitution - Missense 10:99908969-99908969 - TCGA-AP-A059-01 COSM913838 c.4094C>A p.S1365Y Substitution - Missense 10:99880265-99880265 - TCGA-D5-6928-01 COSM1345261 c.1304G>T p.G435V Substitution - Missense 10:99956170-99956170 - sysucc-311T COSM4010973 c.3667G>A p.E1223K Substitution - Missense 10:99885818-99885818 - CSCC-27-T COSM4494726 c.438C>T p.S146S Substitution - coding silent 10:99957036-99957036 - I2L-P7-Tumor-Organoid COSM5360283 c.2929T>C p.Y977H Substitution - Missense 10:99896389-99896389 - SNU-175 COSM2057559 c.4172C>A p.A1391D Substitution - Missense 10:99880187-99880187 - TCGA-AA-3833-01 COSM271217 c.1532C>T p.T511M Substitution - Missense 10:99955942-99955942 - TCGA-BR-8589-01 COSM4010983 c.1558A>G p.R520G Substitution - Missense 10:99955916-99955916 - TCGA-AP-A056-01 COSM913865 c.164T>G p.F55C Substitution - Missense 10:99969219-99969219 - WSU-HN8 COSM4592565 c.3307G>T p.V1103F Substitution - Missense 10:99886611-99886611 - pfg088T COSM4759495 c.676G>T p.V226L Substitution - Missense 10:99956798-99956798 - S02065 COSM5672509 c.1292delC p.S431fs*19 Deletion - Frameshift 10:99956182-99956182 - TCGA-A5-A0GJ-01 COSM913846 c.3124C>T p.R1042* Substitution - Nonsense 10:99894978-99894978 - ATL039 COSM5703416 c.2248C>A p.Q750K Substitution - Missense 10:99955226-99955226 - TCGA-AP-A051-01 COSM913855 c.1707G>T p.E569D Substitution - Missense 10:99955767-99955767 - T3668 COSM4678878 c.23G>A p.R8Q Substitution - Missense 10:99972102-99972102 - TCGA-BR-A44T-01 COSM4010989 c.1177G>A p.E393K Substitution - Missense 10:99956297-99956297 - TCGA-EE-A2GR-06 COSM3433489 c.1993C>T p.R665* Substitution - Nonsense 10:99955481-99955481 - TCGA-DH-A66F-01 COSM3966828 c.1A>G p.M1V Substitution - Missense 10:99972124-99972124 - CSCC-41-T COSM1702886 c.4627C>T p.L1543F Substitution - Missense 10:99877258-99877258 - TCGA-AA-3672-01 COSM266402 c.2582A>G p.E861G Substitution - Missense 10:99900039-99900039 - C086 COSM3433503 c.22C>T p.R8* Substitution - Nonsense 10:99972103-99972103 - PCSI_0083_Pa_X COSM3786301 c.2431A>G p.M811V Substitution - Missense 10:99908976-99908976 - TCGA-BR-7716-01 COSM4010979 c.2855A>T p.N952I Substitution - Missense 10:99898151-99898151 - 46M COSM5587664 c.3717G>T p.P1239P Substitution - coding silent 10:99885768-99885768 - Pat_01_B COSM3433493 c.1261C>T p.H421Y Substitution - Missense 10:99956213-99956213 - TCGA-EE-A3AC-06 COSM3433473 c.3890A>G p.N1297S Substitution - Missense 10:99884118-99884118 - CSCC-18-T COSM4462866 c.1264C>T p.P422S Substitution - Missense 10:99956210-99956210 - TCGA-CD-A4MI-01 COSM4010985 c.1398C>A p.S466S Substitution - coding silent 10:99956076-99956076 - TCGA-AP-A056-01 COSM913851 c.2544C>T p.S848S Substitution - coding silent 10:99908005-99908005 - ICGC_0010 COSM913864 c.429G>A p.P143P Substitution - coding silent 10:99957045-99957045 - SC_9058 COSM5570281 c.2016C>T p.T672T Substitution - coding silent 10:99955458-99955458 - 8014396 COSM913864 c.429G>A p.P143P Substitution - coding silent 10:99957045-99957045 - HCC2998 COSM1345252 c.3617C>T p.S1206L Substitution - Missense 10:99886301-99886301 - CACO2 COSM2057588 c.3290A>G p.E1097G Substitution - Missense 10:99886628-99886628 - CAL33 COSM4592565 c.3307G>T p.V1103F Substitution - Missense 10:99886611-99886611 - CX-1 COSM2057555 c.4203G>A p.K1401K Substitution - coding silent 10:99880156-99880156 - T2269 COSM4678876 c.58G>A p.E20K Substitution - Missense 10:99972067-99972067 - TCGA-BF-A3DL-01 COSM4904848 c.1843C>T p.P615S Substitution - Missense 10:99955631-99955631 - TCGA-AP-A05D-01 COSM913841 c.3587A>G p.Q1196R Substitution - Missense 10:99886331-99886331 - WA19 COSM237310 c.3997+7A>C p.? Unknown 10:99884004-99884004 - TCGA-20-1683-01 COSM1320809 c.3851A>G p.Y1284C Substitution - Missense 10:99884157-99884157 - LS411 COSM2057553 c.4237T>C p.C1413R Substitution - Missense 10:99880122-99880122 - TCGA-AP-A056-01 COSM913857 c.1333G>A p.D445N Substitution - Missense 10:99956141-99956141 - TCGA-AC-A23H-01 COSM3806258 c.2641G>A p.E881K Substitution - Missense 10:99899980-99899980 - TCGA-46-6026-01 COSM682518 c.393G>T p.R131R Substitution - coding silent 10:99957081-99957081 - TCGA-32-1977-01 COSM2057687 c.452G>A p.R151Q Substitution - Missense 10:99957022-99957022 - T2269 COSM426918 c.2401C>T p.R801W Substitution - Missense 10:99909006-99909006 - cSCCP7 COSM139856 c.1255C>T p.P419S Substitution - Missense 10:99956219-99956219 - BK0006 COSM4185598 c.602T>C p.L201P Substitution - Missense 10:99956872-99956872 - YURUS COSM1702890 c.2627C>T p.A876V Substitution - Missense 10:99899994-99899994 - TCGA-BR-4184-01 COSM4010968 c.4385C>T p.T1462M Substitution - Missense 10:99879974-99879974 - TCGA-AM-5820-01 COSM3751481 c.4434C>T p.S1478S Substitution - coding silent 10:99879925-99879925 - TCGA-D1-A177-01 COSM913835 c.4530T>C p.S1510S Substitution - coding silent 10:99879829-99879829 - TCGA-EE-A29E-06 COSM3433471 c.4033C>T p.P1345S Substitution - Missense 10:99880326-99880326 - TCGA-BR-6452-01 COSM4010995 c.201A>G p.G67G Substitution - coding silent 10:99969182-99969182 - H COSM5414724 c.2555G>C p.G852A Substitution - Missense 10:99900066-99900066 - TCGA-61-2111-01 COSM70505 c.2617C>A p.H873N Substitution - Missense 10:99900004-99900004 - TCGA-AM-5820-01 COSM3686469 c.1939C>A p.L647M Substitution - Missense 10:99955535-99955535 - STC263 COSM5049822 c.2792T>G p.L931R Substitution - Missense 10:99898214-99898214 - TCGA-D3-A3MV-06 COSM3433467 c.4122C>T p.F1374F Substitution - coding silent 10:99880237-99880237 - TCGA-EI-6917-01 COSM2057671 c.812G>A p.R271Q Substitution - Missense 10:99956662-99956662 - LUAD-YINHD COSM348169 c.840G>C p.W280C Substitution - Missense 10:99956634-99956634 - HCC032T COSM5809285 c.2673G>T p.K891N Substitution - Missense 10:99899948-99899948 - TCGA-27-2519-01 COSM3396861 c.3065T>C p.V1022A Substitution - Missense 10:99895037-99895037 - TCGA-AP-A059-01 COSM913842 c.3532C>A p.L1178I Substitution - Missense 10:99886386-99886386 - TCGA-AF-2690-01 COSM3414608 c.3010G>T p.V1004F Substitution - Missense 10:99896308-99896308 - TCGA-HU-A4GH-01 COSM4010987 c.1198T>A p.S400T Substitution - Missense 10:99956276-99956276 - TCGA-32-1979-01 COSM3396865 c.568C>T p.R190* Substitution - Nonsense 10:99956906-99956906 - UD-SCC-2 COSM4592565 c.3307G>T p.V1103F Substitution - Missense 10:99886611-99886611 - PCSI_0164_Pa_P_526 COSM3786299 c.4011C>T p.F1337F Substitution - coding silent 10:99880348-99880348 - TCGA-B5-A11O-01 COSM913834 c.4604C>A p.S1535* Substitution - Nonsense 10:99877281-99877281 - PTC-28C COSM1179742 c.4320C>T p.S1440S Substitution - coding silent 10:99880039-99880039 - TCGA-24-2019-01 COSM70506 c.49G>A p.V17I Substitution - Missense 10:99972076-99972076 - TCGA-AZ-4315-01 COSM1345252 c.3617C>T p.S1206L Substitution - Missense 10:99886301-99886301 - 587306 COSM1204283 c.1771G>A p.G591S Substitution - Missense 10:99955703-99955703 - TCGA-D1-A103-01 COSM913833 c.4689G>T p.K1563N Substitution - Missense 10:99877196-99877196 - 1_RESISTANT COSM1718669 c.3318_3319insC p.N1108fs*12 Insertion - Frameshift 10:99886599-99886600 - TCGA-GN-A267-06 COSM3433477 c.3836C>T p.S1279F Substitution - Missense 10:99884172-99884172 - TCGA-HF-7132-01 COSM3806254 c.3838C>A p.L1280I Substitution - Missense 10:99884170-99884170 - TCGA-FW-A3R5-06 COSM3866330 c.1999C>T p.R667C Substitution - Missense 10:99955475-99955475 - TCGA-DR-A0ZM-01 COSM458929 c.3914C>G p.S1305* Substitution - Nonsense 10:99884094-99884094 - TCGA-60-2713-01 COSM682521 c.2265G>A p.M755I Substitution - Missense 10:99909142-99909142 - 587376 COSM913843 c.3301C>T p.R1101W Substitution - Missense 10:99886617-99886617 - Pat_41_A COSM4678862 c.2867C>T p.A956V Substitution - Missense 10:99898139-99898139 - CSCC-27-T COSM3433499 c.584C>T p.P195L Substitution - Missense 10:99956890-99956890 - 1339-01-03TD COSM5417954 c.1834C>G p.P612A Substitution - Missense 10:99955640-99955640 - 587278 COSM1204287 c.4696G>A p.V1566I Substitution - Missense 10:99877189-99877189 - TCGA-D1-A167-01 COSM913849 c.2845C>A p.P949T Substitution - Missense 10:99898161-99898161 - RKO COSM4647118 c.4565A>G p.Y1522C Substitution - Missense 10:99877320-99877320 - MO_1012 COSM5550767 c.2868G>T p.A956A Substitution - coding silent 10:99898138-99898138 - TCGA-AP-A051-01 COSM913840 c.3588G>T p.Q1196H Substitution - Missense 10:99886330-99886330 - TCGA-AN-A046-01 COSM3806252 c.3888C>A p.F1296L Substitution - Missense 10:99884120-99884120 - S02273 COSM5681477 c.3528G>T p.Q1176H Substitution - Missense 10:99886390-99886390 - TCGA-D3-A5GN-06 COSM3433501 c.154C>T p.P52S Substitution - Missense 10:99969229-99969229 - B104-0 COSM1745571 c.2011G>C p.E671Q Substitution - Missense 10:99955463-99955463 - CSCC-29-T COSM4458306 c.1080C>T p.P360P Substitution - coding silent 10:99956394-99956394 - NB-0478 COSM1284573 c.451C>T p.R151W Substitution - Missense 10:99957023-99957023 - cSCCP8 COSM140647 c.199G>A p.G67R Substitution - Missense 10:99969184-99969184 - TCGA-D1-A176-01 COSM913863 c.526G>A p.G176R Substitution - Missense 10:99956948-99956948 - PT48 COSM5932594 c.2028G>A p.E676E Substitution - coding silent 10:99955446-99955446 - cSCCP4 COSM138777 c.1244A>C p.Q415P Substitution - Missense 10:99956230-99956230 - TCGA-C5-A7UH-01 COSM4856643 c.4630G>A p.E1544K Substitution - Missense 10:99877255-99877255 - TCGA-66-2756-01 COSM682519 c.1494G>T p.Q498H Substitution - Missense 10:99955980-99955980 - 223 COSM4425357 c.2700G>A p.L900L Substitution - coding silent 10:99899921-99899921 - TCGA-EE-A2A6-06 COSM913847 c.3091C>T p.R1031* Substitution - Nonsense 10:99895011-99895011 - T2932 COSM4678858 c.3848G>T p.R1283M Substitution - Missense 10:99884160-99884160 - T3064 COSM4678868 c.751C>A p.L251M Substitution - Missense 10:99956723-99956723 - PCSI_0083_Pa_P_526 COSM3786301 c.2431A>G p.M811V Substitution - Missense 10:99908976-99908976 - TCGA-PJ-A5Z8-01 COSM3985358 c.1728C>A p.H576Q Substitution - Missense 10:99955746-99955746 - TCGA-CG-5721-01 COSM4010975 c.3034A>G p.T1012A Substitution - Missense 10:99896284-99896284 - 587342 COSM1204288 c.2455-2A>G p.? Unknown 10:99908096-99908096 - 49M COSM5590642 c.3707C>T p.T1236I Substitution - Missense 10:99885778-99885778 - T3658 COSM4678870 c.582delT p.P195fs*5 Deletion - Frameshift 10:99956892-99956892 - TCGA-BH-A0GZ-01 COSM426920 c.266G>A p.R89Q Substitution - Missense 10:99969117-99969117 - LS411 COSM2057561 c.4156A>G p.N1386D Substitution - Missense 10:99880203-99880203 - YUKAT COSM5369919 c.772G>A p.E258K Substitution - Missense 10:99956702-99956702 - SNUH_G10_S1 COSM3997726 c.1332C>T p.P444P Substitution - coding silent 10:99956142-99956142 - TCGA-FW-A3R5-06 COSM3433503 c.22C>T p.R8* Substitution - Nonsense 10:99972103-99972103 - 417 COSM4431537 c.1555G>C p.E519Q Substitution - Missense 10:99955919-99955919 - TCGA-CA-6717-01 COSM1345250 c.4389G>A p.P1463P Substitution - coding silent 10:99879970-99879970 - HCC2998 COSM1675488 c.3272T>G p.L1091R Substitution - Missense 10:99888838-99888838 - TCGA-BR-8360-01 COSM4010973 c.3667G>A p.E1223K Substitution - Missense 10:99885818-99885818 - TCGA-EE-A2MJ-06 COSM3433463 c.4580G>A p.R1527Q Substitution - Missense 10:99877305-99877305 - 1_PRE-TREATMENT COSM1718669 c.3318_3319insC p.N1108fs*12 Insertion - Frameshift 10:99886599-99886600 - TCGA-18-3409-01 COSM682524 c.3881G>A p.R1294Q Substitution - Missense 10:99884127-99884127 - TCGA-BR-8680-01 COSM4010991 c.1076C>A p.S359Y Substitution - Missense 10:99956398-99956398 - LC_S38 COSM1188022 c.3699G>T p.Q1233H Substitution - Missense 10:99885786-99885786 - 1517_PT COSM5753376 c.4098G>T p.E1366D Substitution - Missense 10:99880261-99880261 - CSCC-55-T COSM4566567 c.414_415CC>TT p.(=) Unknown 10:99957059-99957060 - PAPNNX COSM3866330 c.1999C>T p.R667C Substitution - Missense 10:99955475-99955475 - TCGA-37-3783-01 COSM682520 c.2119A>C p.M707L Substitution - Missense 10:99955355-99955355 - ESO-721 COSM1250487 c.1977C>G p.S659S Substitution - coding silent 10:99955497-99955497 - TCGA-CK-5916-01 COSM3751485 c.641C>T p.S214F Substitution - Missense 10:99956833-99956833 - TCGA-EE-A2MS-06 COSM3433503 c.22C>T p.R8* Substitution - Nonsense 10:99972103-99972103 - TCGA-Q1-A73O-01 COSM4834093 c.3727C>G p.P1243A Substitution - Missense 10:99885758-99885758 - ESO-077 COSM1250486 c.3711C>G p.F1237L Substitution - Missense 10:99885774-99885774 - TCGA-EE-A2MR-06 COSM3433493 c.1261C>T p.H421Y Substitution - Missense 10:99956213-99956213 - 587222 COSM1204286 c.2177C>A p.S726* Substitution - Nonsense 10:99955297-99955297 - RKO COSM4647120 c.2260G>T p.E754* Substitution - Nonsense 10:99955214-99955214 - TCGA-EE-A29E-06 COSM3433469 c.4085C>T p.S1362F Substitution - Missense 10:99880274-99880274 - LUAD-YINHD COSM348168 c.2364C>T p.V788V Substitution - coding silent 10:99909043-99909043 - TCGA-D9-A1X3-01 COSM3433499 c.584C>T p.P195L Substitution - Missense 10:99956890-99956890 - TCGA-AA-3516-01 COSM291550 c.465_466insG p.L156fs*7 Insertion - Frameshift 10:99957008-99957009 - TCGA-A2-A25A-01 COSM913834 c.4604C>A p.S1535* Substitution - Nonsense 10:99877281-99877281 - 587228 COSM1204284 c.4226C>T p.P1409L Substitution - Missense 10:99880133-99880133 - YUDIALE COSM1702896 c.2068C>T p.P690S Substitution - Missense 10:99955406-99955406 - TCGA-AP-A059-01 COSM913837 c.4220C>A p.S1407Y Substitution - Missense 10:99880139-99880139 - B104-0-Tumor COSM1745571 c.2011G>C p.E671Q Substitution - Missense 10:99955463-99955463 - QC2-32-T2 COSM3997726 c.1332C>T p.P444P Substitution - coding silent 10:99956142-99956142 - NOKSI COSM4592565 c.3307G>T p.V1103F Substitution - Missense 10:99886611-99886611 - S00932 COSM70506 c.49G>A p.V17I Substitution - Missense 10:99972076-99972076 - TCGA-AN-A0AT-01 COSM426917 c.3178G>A p.V1060M Substitution - Missense 10:99888932-99888932 - PD13306a COSM5783482 c.4579C>T p.R1527* Substitution - Nonsense 10:99877306-99877306 - AA COSM5414724 c.2555G>C p.G852A Substitution - Missense 10:99900066-99900066 - PT38 COSM5922809 c.961C>T p.P321S Substitution - Missense 10:99956513-99956513 - TCGA-GN-A267-06 COSM3433481 c.3303G>A p.R1101R Substitution - coding silent 10:99886615-99886615 - TCGA-B0-4690-01 COSM3773521 c.232A>C p.T78P Substitution - Missense 10:99969151-99969151 - HN_62854 COSM127831 c.1891C>T p.L631L Substitution - coding silent 10:99955583-99955583 - TCGA-FS-A1ZP-06 COSM3433499 c.584C>T p.P195L Substitution - Missense 10:99956890-99956890 - Pat_01_A COSM3433493 c.1261C>T p.H421Y Substitution - Missense 10:99956213-99956213 - Pat_06_A COSM2057613 c.2782C>T p.R928C Substitution - Missense 10:99898224-99898224 - PT14_1 COSM5896979 c.1329C>T p.Y443Y Substitution - coding silent 10:99956145-99956145 - CSCC-41-T COSM4540197 c.2802G>A p.M934I Substitution - Missense 10:99898204-99898204 - PT15_1 COSM5897746 c.2069C>T p.P690L Substitution - Missense 10:99955405-99955405 - TCGA-66-2791-01 COSM682525 c.4701C>T p.P1567P Substitution - coding silent 10:99877184-99877184 - ATL072 COSM5703418 c.1963A>G p.T655A Substitution - Missense 10:99955511-99955511 - GC8_T COSM147025 c.3156+3G>A p.? Unknown 10:99894943-99894943 - 12M COSM5577418 c.69C>T p.L23L Substitution - coding silent 10:99972056-99972056 - YULAN COSM1702886 c.4627C>T p.L1543F Substitution - Missense 10:99877258-99877258 - TCGA-60-2698-01 COSM682522 c.2930A>G p.Y977C Substitution - Missense 10:99896388-99896388 - 587376 COSM1204289 c.3779G>A p.R1260Q Substitution - Missense 10:99885706-99885706 - SWE-37 COSM1179742 c.4320C>T p.S1440S Substitution - coding silent 10:99880039-99880039 - TCGA-AX-A05Z-01 COSM913862 c.569G>A p.R190Q Substitution - Missense 10:99956905-99956905 - TCGA-BS-A0TC-01 COSM913853 c.1919G>A p.R640Q Substitution - Missense 10:99955555-99955555 - T3021 COSM4678872 c.575G>A p.G192D Substitution - Missense 10:99956899-99956899 - TCGA-EE-A3JA-06 COSM3433497 c.649C>T p.Q217* Substitution - Nonsense 10:99956825-99956825 - TCGA-F5-6814-01 COSM3414610 c.153C>T p.F51F Substitution - coding silent 10:99969230-99969230 - TCGA-BR-7703-01 COSM4010970 c.4299A>G p.R1433R Substitution - coding silent 10:99880060-99880060 - PD6767a COSM1638123 c.3647A>G p.N1216S Substitution - Missense 10:99885838-99885838 - LAU50_1 COSM232197 c.4369A>C p.K1457Q Substitution - Missense 10:99879990-99879990 - LP6007409-DNA_A01 COSM5953442 c.2131G>A p.A711T Substitution - Missense 10:99955343-99955343 - SW48 COSM2057609 c.2882A>G p.N961S Substitution - Missense 10:99898124-99898124 - PT49 COSM5935576 c.1135G>A p.D379N Substitution - Missense 10:99956339-99956339 - S00932 COSM70506 c.49G>A p.V17I Substitution - Missense 10:99972076-99972076 - TCGA-DR-A0ZM-01 COSM458927 c.1039G>A p.E347K Substitution - Missense 10:99956435-99956435 - TCGA-10-0934-01 COSM70504 c.3461G>A p.R1154Q Substitution - Missense 10:99886457-99886457 - TCGA-DR-A0ZM-01 COSM458930 c.4234G>T p.E1412* Substitution - Nonsense 10:99880125-99880125 - SJACT019_D COSM4968483 c.1168G>C p.V390L Substitution - Missense 10:99956306-99956306 - TCGA-AX-A05Z-01 COSM913839 c.4060G>A p.D1354N Substitution - Missense 10:99880299-99880299 - TCGA-CA-6718-01 COSM1345262 c.1149G>A p.G383G Substitution - coding silent 10:99956325-99956325 - PA285 COSM1162896 c.2267C>T p.T756M Substitution - Missense 10:99909140-99909140 - TCGA-DK-A3WW-01 COSM3790395 c.4467C>A p.L1489L Substitution - coding silent 10:99879892-99879892 - TCGA-AA-A010-01 COSM299183 c.320G>A p.R107Q Substitution - Missense 10:99957154-99957154 - TCGA-D1-A17Q-01 COSM913848 c.3029A>G p.H1010R Substitution - Missense 10:99896289-99896289 - CSCC-27-T COSM2057557 c.4187C>T p.S1396L Substitution - Missense 10:99880172-99880172 - TCGA-EE-A29Q-06 COSM3433475 c.3854C>T p.P1285L Substitution - Missense 10:99884154-99884154 - TCGA-AA-3989-01 COSM297986 c.501G>A p.R167R Substitution - coding silent 10:99956973-99956973 - TCGA-ER-A193-06 COSM3433491 c.1414C>T p.Q472* Substitution - Nonsense 10:99956060-99956060 - TCGA-A7-A0DA-01 COSM426916 c.3954A>C p.K1318N Substitution - Missense 10:99884054-99884054 - ORL-48 COSM4592565 c.3307G>T p.V1103F Substitution - Missense 10:99886611-99886611 - TCGA-46-3769-01 COSM682523 c.3049C>T p.Q1017* Substitution - Nonsense 10:99896269-99896269 - HCC165T COSM3665435 c.3504G>A p.L1168L Substitution - coding silent 10:99886414-99886414 - YUFOLD COSM1702894 c.2119A>T p.M707L Substitution - Missense 10:99955355-99955355 - TCGA-D8-A1JA-01 COSM3806261 c.1478G>A p.R493K Substitution - Missense 10:99955996-99955996 - HCC2998 COSM1675488 c.3272T>G p.L1091R Substitution - Missense 10:99888838-99888838 - TCGA-HJ-7597-01 COSM4010997 c.179C>T p.T60I Substitution - Missense 10:99969204-99969204 - TCGA-AX-A0J1-01 COSM913860 c.840G>A p.W280* Substitution - Nonsense 10:99956634-99956634 - TCGA-D1-A17U-01 COSM913850 c.2797C>T p.L933L Substitution - coding silent 10:99898209-99898209 - TCGA-AX-A05Z-01 COSM913859 c.971C>A p.S324Y Substitution - Missense 10:99956503-99956503 - TCGA-AA-A00N-01 COSM108235 c.792C>T p.F264F Substitution - coding silent 10:99956682-99956682 - YUPAT COSM1702892 c.2437_2438CC>TT p.P813F Substitution - Missense 10:99908969-99908970 - T3064 COSM4678862 c.2867C>T p.A956V Substitution - Missense 10:99898139-99898139 - CPCG0210-F1 COSM4966557 c.2051G>A p.S684N Substitution - Missense 10:99955423-99955423 - TCGA-27-1834-01 COSM3396863 c.1703C>G p.T568R Substitution - Missense 10:99955771-99955771 - S0004 COSM5881822 c.1945C>T p.P649S Substitution - Missense 10:99955529-99955529 - KPOPBR-39-T COSM5964612 c.867A>T p.T289T Substitution - coding silent 10:99956607-99956607 - LUAD_E00522 COSM352270 c.652G>C p.D218H Substitution - Missense 10:99956822-99956822 - GBM_IV-20 COSM4967029 c.4372C>T p.Q1458* Substitution - Nonsense 10:99879987-99879987 - LUAD-YINHD COSM348167 c.2944G>C p.E982Q Substitution - Missense 10:99896374-99896374 - PTC-28C COSM4144283 c.2156T>A p.L719Q Substitution - Missense 10:99955318-99955318 - HCC165 COSM3665435 c.3504G>A p.L1168L Substitution - coding silent 10:99886414-99886414 - SNUH_G10_S1 COSM3997724 c.4500G>A p.P1500P Substitution - coding silent 10:99879859-99879859 - TCGA-HU-A4H8-01 COSM4010966 c.4636A>G p.K1546E Substitution - Missense 10:99877249-99877249 - T407 COSM4678864 c.1796A>G p.Q599R Substitution - Missense 10:99955678-99955678 - LIM1215 COSM4333516 c.3086delA p.N1029fs*8 Deletion - Frameshift 10:99895016-99895016 - SCC-9 COSM4592565 c.3307G>T p.V1103F Substitution - Missense 10:99886611-99886611 - TCGA-EE-A29D-06 COSM3433465 c.4433C>T p.S1478F Substitution - Missense 10:99879926-99879926 - TCGA-BS-A0TJ-01 COSM913856 c.1366T>C p.Y456H Substitution - Missense 10:99956108-99956108 - TCGA-AC-A23C-01 COSM1474296 c.1986C>G p.L662L Substitution - coding silent 10:99955488-99955488 - TCGA-24-2038-01 COSM70503 c.4171G>A p.A1391T Substitution - Missense 10:99880188-99880188 - TCGA-B4-5832-01 COSM1492136 c.2200G>T p.D734Y Substitution - Missense 10:99955274-99955274 - SC_9055 COSM5560080 c.2525T>C p.L842S Substitution - Missense 10:99908024-99908024 - CSB6 COSM5027281 c.1865C>T p.S622F Substitution - Missense 10:99955609-99955609 - CSCC-42-T COSM4490347 c.3624C>T p.L1208L Substitution - coding silent 10:99885861-99885861 - TCGA-B5-A11E-01 COSM913858 c.1115G>T p.R372I Substitution - Missense 10:99956359-99956359 - TCGA-C5-A1M8-01 COSM4837304 c.1840C>T p.R614C Substitution - Missense 10:99955634-99955634 - YUKLAB COSM1702888 c.4433_4434CC>TT p.S1478F Substitution - Missense 10:99879925-99879926 - TCGA-FV-A3R2-01 COSM4929362 c.2948A>G p.D983G Substitution - Missense 10:99896370-99896370 - T3306 COSM4678860 c.3522C>T p.Y1174Y Substitution - coding silent 10:99886396-99886396 - NB-1375 COSM1284574 c.2267C>A p.T756K Substitution - Missense 10:99909140-99909140 - OSCC-GB_01060111 COSM4883181 c.1484C>G p.S495* Substitution - Nonsense 10:99955990-99955990 - TCGA-EE-A29E-06 COSM3433483 c.3274T>C p.F1092L Substitution - Missense 10:99888836-99888836 - TCGA-GM-A2D9-01 COSM3806256 c.3384C>G p.L1128L Substitution - coding silent 10:99886534-99886534 - QC2-26-T2 COSM3997726 c.1332C>T p.P444P Substitution - coding silent 10:99956142-99956142 - TCGA-A8-A0A6-01 COSM3806250 c.4324T>C p.S1442P Substitution - Missense 10:99880035-99880035 - ESCC_45 COSM913845 c.3130C>A p.L1044M Substitution - Missense 10:99894972-99894972 - TCGA-BR-4280-01 COSM4010999 c.43C>T p.P15S Substitution - Missense 10:99972082-99972082 - TCGA-AP-A056-01 COSM913847 c.3091C>T p.R1031* Substitution - Nonsense 10:99895011-99895011 - HT29 COSM2057555 c.4203G>A p.K1401K Substitution - coding silent 10:99880156-99880156 - TCGA-61-2613-01 COSM1320808 c.1383C>T p.P461P Substitution - coding silent 10:99956091-99956091 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.500771 10q24.2 611282 2481904|CGAP|BC041628|G/T|coding|Trp659Cys|2107|Validated; 2481906|CGAP|BC041628|A/T|non-coding||4050|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G IntronicSNV . c.2261-17933T>C 10 101686836 HC A G Missense p.L1044P c.3131T>C 10 101654728 UCEC A G Missense p.V1022A c.3065T>C 10 101654794 GBM A G Missense p.Y456H c.1366T>C 10 101715865 UCEC A G Synonymous p.S1510S c.4530T>C 10 101639586 UCEC C A Missense p.A1512S c.4534G>T 10 101639582 LUAD C A Missense p.Q498H c.1494G>T 10 101715737 LUSC C A Missense p.R319S c.957G>T 10 101716274 LUAD C A Nonsense p.E1053* c.3157G>T 10 101648710 LUAD C A Synonymous p.R131R c.393G>T 10 101716838 LUSC C A Synonymous p.V1312V c.3936G>T 10 101643829 STAD CC TT Missense p.E1149K c.3444_3445delinsAA 10 101646230 CM C G IntronicSNV . c.269-74G>C 10 101717036 CM C G Missense p.E585Q c.1753G>C 10 101715478 LUAD C G Missense p.E600Q c.1798G>C 10 101715433 HNSC C G Missense p.E671Q c.2011G>C 10 101715220 HNSC C G Missense p.G1492R c.4474G>C 10 101639642 COREAD C T Missense p.A1391T c.4171G>A 10 101639945 OV C T Missense p.E30K c.88G>A 10 101731794 HNSC C T Missense p.E441K c.1321G>A 10 101715910 LUAD C T Missense p.G852R c.2554G>A 10 101667752 CM C T Missense p.M755I c.2265G>A 10 101668899 LUSC C T Missense p.R1124H c.3371G>A 10 101646304 MB C T Missense p.R1154Q c.3461G>A 10 101646214 OV C T Missense p.R151Q c.452G>A 10 101716779 GBM C T Missense p.R640Q c.1919G>A 10 101715312 UCEC C T Missense p.R89Q c.266G>A 10 101728874 BRCA C T Missense p.V1060M c.3178G>A 10 101648689 BRCA C T Missense p.V17I c.49G>A 10 101731833 OV C T Missense p.V17I c.49G>A 10 101731833 SCLC C T Synonymous p.K1142K c.3426G>A 10 101646249 CM C T Synonymous p.K1316K c.3948G>A 10 101643817 BRCA C T Synonymous p.P143P c.429G>A 10 101716802 PAAD C T Synonymous p.R1101R c.3303G>A 10 101646372 CM C T Synonymous p.R167R c.501G>A 10 101716730 COREAD G A Missense p.A381V c.1142C>T 10 101716089 LUAD G A Missense p.H421Y c.1261C>T 10 101715970 CM G A Missense p.L1543F c.4627C>T 10 101637015 CM G A Missense p.L361F c.1081C>T 10 101716150 CM G A Missense p.P1285L c.3854C>T 10 101643911 CM G A Missense p.P15S c.43C>T 10 101731839 STAD G A Missense p.P195L c.584C>T 10 101716647 CM G A Missense p.P401L c.1202C>T 10 101716029 CM G A Missense p.P615S c.1843C>T 10 101715388 CM G A Missense p.P644S c.1930C>T 10 101715301 CM G A Missense p.P646L c.1937C>T 10 101715294 CM G A Missense p.R1467W c.4399C>T 10 101639717 CM G A Missense p.R151W c.451C>T 10 101716780 NB G A Missense p.R801W c.2401C>T 10 101668763 BRCA G A Missense p.S1279F c.3836C>T 10 101643929 CM G A Missense p.S622F c.1865C>T 10 101715366 BRCA G A Nonsense p.Q1017* c.3049C>T 10 101656026 LUSC G A Nonsense p.Q217* c.649C>T 10 101716582 CM G A Nonsense p.Q472* c.1414C>T 10 101715817 CM G A Nonsense p.R1031* c.3091C>T 10 101654768 CM G A Nonsense p.R1042* c.3124C>T 10 101654735 UCEC G A Nonsense p.R190* c.568C>T 10 101716663 GBM G A Nonsense p.R665* c.1993C>T 10 101715238 CM G A Nonsense p.R8* c.22C>T 10 101731860 CM G A Synonymous p.F1374F c.4122C>T 10 101639994 CM G A Synonymous p.G677G c.2031C>T 10 101715200 CM G A Synonymous p.L631L c.1891C>T 10 101715340 HNSC G A Synonymous p.P1567P c.4701C>T 10 101636941 LUSC G A Synonymous p.S1370S c.4110C>T 10 101640006 CM G A Synonymous p.S592S c.1776C>T 10 101715455 CM G C Missense p.F1131L c.3393C>G 10 101646282 LUAD G C Missense p.F1237L c.3711C>G 10 101645531 ESCA G C Missense p.L1418V c.4252C>G 10 101639864 HNSC G C Missense p.T568R c.1703C>G 10 101715528 GBM G C Nonsense p.S485* c.1454C>G 10 101715777 HNSC G C Synonymous p.L662L c.1986C>G 10 101715245 BRCA G C Synonymous p.S659S c.1977C>G 10 101715254 ESCA GG AA Missense p.P692S c.2073_2074delinsTT 10 101715157 CM G T Missense p.H873N c.2617C>A 10 101659761 OV G T Missense p.S1407Y c.4220C>A 10 101639896 STAD G T Missense p.T756K c.2267C>A 10 101668897 NB G T Nonsense p.S1535* c.4604C>A 10 101637038 BRCA G T Synonymous p.T246T c.738C>A 10 101716493 OV T A 3-UTRSNV . c.4731+134A>T 10 101636777 HC T A Missense p.N938I c.2813A>T 10 101657950 HNSC T A Synonymous p.T402T c.1206A>T 10 101716025 CM T C Missense p.I998V c.2992A>G 10 101656083 LUAD T C Missense p.N1297S c.3890A>G 10 101643875 CM T C SpliceAcceptorSNV . c.2703-2A>G 10 101658519 HNSC T G IntronicSNV . c.2261-20566A>C 10 101689469 HC T G Missense p.K1318N c.3954A>C 10 101643811 BRCA T G Missense p.M707L c.2119A>C 10 101715112 LUSC T G Missense p.T78P c.232A>C 10 101728908 RCCC T G Synonymous p.P635P c.1905A>C 10 101715326 BRCA